U.S. patent application number 14/305949 was filed with the patent office on 2014-10-02 for process for production of polylactic acid resin composition.
The applicant listed for this patent is KAO CORPORATION. Invention is credited to Masahiro MORI, Akira TAKENAKA, Tomoya TSUBOI.
Application Number | 20140296399 14/305949 |
Document ID | / |
Family ID | 44355300 |
Filed Date | 2014-10-02 |
United States Patent
Application |
20140296399 |
Kind Code |
A1 |
TSUBOI; Tomoya ; et
al. |
October 2, 2014 |
PROCESS FOR PRODUCTION OF POLYLACTIC ACID RESIN COMPOSITION
Abstract
A method for producing a polylactic acid resin composition,
including the following steps (1) and (2): step (1): subjecting an
organic crystal nucleating agent to a wet pulverization in the
presence of a carboxylic acid ester having a weight-average
molecular weight of from 150 to 600 and a viscosity at 23.degree.
C. of from 1 to 500 mPs and/or a phosphoric ester having a
weight-average molecular weight of from 150 to 600 and a viscosity
at 23.degree. C. of from 1 to 500 mPas to give a finely pulverized
organic crystal nucleating agent composition; and step (2):
melt-kneading a raw material for a polylactic acid resin
composition comprising the finely pulverized organic crystal
nucleating agent composition obtained in the step (1) and a
polylactic acid resin. The polylactic acid resin composition
obtainable by the method of the present invention can be suitably
used in various industrial applications, such as daily sundries,
household electric appliance parts, packaging materials for
household electric appliance parts, and automobile parts.
Inventors: |
TSUBOI; Tomoya;
(Wakayama-shi, JP) ; TAKENAKA; Akira;
(Wakayama-shi, JP) ; MORI; Masahiro;
(Wakayama-shi, JP) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
KAO CORPORATION |
Tokyo |
|
JP |
|
|
Family ID: |
44355300 |
Appl. No.: |
14/305949 |
Filed: |
June 16, 2014 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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13522648 |
Jul 17, 2012 |
8785520 |
|
|
PCT/JP2011/051307 |
Jan 25, 2011 |
|
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14305949 |
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Current U.S.
Class: |
524/139 ;
524/145; 524/161; 524/210; 524/270 |
Current CPC
Class: |
C08K 9/04 20130101; B29B
7/72 20130101; C08K 9/10 20130101; C08K 5/0083 20130101; C08K 5/20
20130101; C08K 5/521 20130101; C08K 5/098 20130101; C08K 5/42
20130101; C08J 2367/04 20130101; C08K 5/5317 20130101; B29B 7/007
20130101; C08L 93/04 20130101; C08J 3/201 20130101; C08L 67/04
20130101; C08K 5/42 20130101; C08L 67/04 20130101; C08K 5/5317
20130101; C08L 67/04 20130101; C08K 5/0083 20130101; C08L 67/04
20130101; C08K 5/521 20130101; C08L 67/04 20130101; C08K 5/098
20130101; C08L 67/04 20130101; C08K 5/20 20130101; C08L 67/04
20130101 |
Class at
Publication: |
524/139 ;
524/161; 524/145; 524/270; 524/210 |
International
Class: |
C08L 93/04 20060101
C08L093/04; C08L 67/04 20060101 C08L067/04; C08K 5/521 20060101
C08K005/521; C08K 5/20 20060101 C08K005/20; C08K 5/5317 20060101
C08K005/5317; C08K 5/42 20060101 C08K005/42 |
Foreign Application Data
Date |
Code |
Application Number |
Feb 2, 2010 |
JP |
2010-021475 |
Claims
1. A method for producing a polylactic acid resin composition,
comprising the following steps (1) and (2): step (1): subjecting an
organic crystal nucleating agent to a wet pulverization in the
presence of a carboxylic acid ester having a weight-average
molecular weight of from 150 to 600 and a viscosity at 23.degree.
C. of from 1 to 500 mPas to give a finely pulverized organic
crystal nucleating agent composition; and step (2): melt-kneading a
raw material for a polylactic acid resin composition comprising the
finely pulverized organic crystal nucleating agent composition
obtained in the step (1) and a polylactic acid resin.
2. The method for producing a polylactic acid resin composition
according to claim 1, wherein the organic crystal nucleating agent
comprises at least one organic compound selected from the group
consisting of metal salts of dialkyl aromatic sulfonates, metal
salts of phosphoric esters, metal salts of phenylphosphonic acids,
metal salts of rosin acids, aromatic carboxylic acid amides, and
rosin acid amides.
3. The method for producing a polylactic acid resin composition
according to claim 1, wherein the organic crystal nucleating agent
comprises a metal salt of a phenylphosphonic acid.
4. The method for producing a polylactic acid resin composition
according to claim 1, wherein the finely pulverized organic crystal
nucleating agent composition has a volume-median particle size
(D.sub.50) of from 50 to 700 nm.
5. The method for producing a polylactic acid resin composition
according to claim 1, wherein the step (1) comprises subjecting the
organic crystal nucleating agent to a wet pulverization in the
presence of the carboxylic acid ester, within a range satisfying a
ratio of the weight of the organic crystal nucleating agent and a
total weight of the carboxylic acid ester, that is the organic
crystal nucleating agent/the carboxylic acid ester, of from 1/99 to
50/50.
6. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid ester is a
carboxylic acid ester having two or more ester groups in the
molecule, wherein an alcohol component constituting the carboxylic
acid ester comprises an alcohol with addition of an alkylene oxide
having 2 to 3 carbon atoms in an amount of from 0.5 to 5 mol per
one hydroxyl group in average.
7. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid esters are one or
more members selected from the group consisting of carboxylic acid
esters formed between acetic acid and an ethylene oxide adduct of
glycerol, an ethylene oxide moiety of which is added in an amount
of from 3 to 6 mol in average, carboxylic acid esters formed
between acetic acid and an ethylene oxide adduct of a polyethylene
glycol, an ethylene oxide moiety of which is added in an amount of
from 4 to 6 mol in average, carboxylic acid esters formed between
succinic acid and an ethylene oxide adduct of a polyethylene glycol
monomethyl ether, an ethylene oxide moiety of which is added in an
amount of from 2 to 3 mol in average, carboxylic acid esters formed
between adipic acid and diethylene glycol monomethyl ether, and
carboxylic acid esters formed between 1,3,6-hexanetricarboxylic
acid and diethylene glycol monomethyl ether.
8. The method for producing a polylactic acid resin composition
according to claim 1, wherein the organic crystal nucleating agent
subjected to the wet pulverization has a volume-median particle
size (D.sub.50) of from 500 nm to 5 .mu.m.
9. The method for producing a polylactic acid resin composition
according to claim 1, wherein the treatment temperature for the wet
pulverization is from 5.degree. to 250.degree. C.
10. The method for producing a polylactic acid resin composition
according to claim 1, wherein the pulverizer used in the wet
pulverization is a media pulverizer.
11. The method for producing a polylactic acid resin composition
according to claim 1, wherein in the step (2) the finely pulverized
organic crystal nucleating agent composition obtained in the step
(1) is contained in an amount of from 1 to 50 parts by weight,
based on 100 parts by weight of the polylactic acid resin.
12. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid esters are one or
more members selected from the group consisting of carboxylic acid
esters formed between acetic acid and an ethylene oxide adduct of
glycerol, an ethylene oxide moiety of which is added in an amount
of from 3 to 6 mol in average.
13. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid esters are one or
more members selected from the group consisting of carboxylic acid
esters formed between acetic acid and an ethylene oxide adduct of a
polyethylene glycol, an ethylene oxide moiety of which is added in
an amount of from 4 to 6 mol in average.
14. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid esters are one or
more members selected from the group consisting of carboxylic acid
esters formed between succinic acid and an ethylene oxide adduct of
a polyethylene glycol monomethyl ether, an ethylene oxide moiety of
which is added in an amount of from 2 to 3 mol in average.
15. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid esters are one or
more members selected from the group consisting of carboxylic acid
esters formed between adipic acid and diethylene glycol monomethyl
ether.
16. The method for producing a polylactic acid resin composition
according to claim 1, wherein the carboxylic acid esters are one or
more members selected from the group consisting of carboxylic acid
esters formed between 1,3,6-hexanetricarboxylic acid and diethylene
glycol monomethyl ether.
17. A polylactic acid resin composition obtained by the method as
defined in claim 1.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a Continuation of co-pending application
Ser. No. 13/522,648 filed on Jul. 17, 2012, which is a National
Phase of PCT International Application No. PCT/JP2011/051307 filed
on Jan. 25, 2011, which claims priority under 35 U.S.C. 119(a) to
Patent Application No. 2010-021475 filed in Japan on Feb. 2, 2010.
All of the above applications are hereby expressly incorporated by
reference into the present application.
TECHNICAL FIELD
[0002] The present invention relates to a method for producing a
polylactic acid resin composition. More specifically, the present
invention relates to a method for producing a polylactic acid resin
composition, which can be suitably used as, for example, daily
sundries, household electric appliance parts, automobile parts, or
the like, and a polylactic acid resin composition obtained by the
method.
BACKGROUND ART
[0003] A polylactic acid resin is inexpensive because L-lactic acid
used as a raw material is produced by a fermentation method using a
sugar extracted from maize, potatoes, or the like. Also, the
polylactic acid resin has a very low amount of a carbon dioxide
discharge because the raw material is plant-derived, and the
properties of the resin include strong rigidity and high
transparency. Therefore, the utilization of polylactic acid resins
is expected to be promising at present.
[0004] However, the polylactic acid resin has a slow
crystallization velocity, so that if crystallization is carried
out, a long time period is required, thereby worsening the
productivity. In view of the above, a technique of improving a
crystallization rate by blending a crystal nucleating agent or the
like in the polylactic acid resin has become known.
[0005] For example, in Patent Publication 1, a polylactic acid
resin composition having an excellent crystallization velocity is
obtained by blending a polylactic acid resin with a
phenylphosphonic (acid) derivative having a particular
structure.
[0006] In Patent Publication 2, a polylactic acid resin composition
having an excellent crystallization velocity and heat resistance is
obtained by blending a biodegradable resin with a mixture of at
least one compound selected from the compounds having a hydroxyl
group and an amide group in the molecule and a metal salt of a
phenylphosphonic acid.
[0007] In Patent Publication 3, a polylactic acid resin composition
having an excellent crystallization velocity and heat resistance is
obtained by blending a polylactic acid resin with a particular
polyester-polyol and a crystal nucleating agent, and a polylactic
acid resin composition having even higher heat resistance is
obtained by previously mixing the polyester-polyol and the crystal
nucleating agent upon melt-kneading, thereby forming the crystal
nucleating agent into fine particles.
[0008] In addition, Patent Publication 4 discloses a method
utilizing an aliphatic phosphoric ester compound having an
aliphatic chain having 12 to 28 carbon atoms or the like, as a
lubricant during molding of a polylactic acid-based resin
composition. Patent Publication 5 discloses that a secondary
workability such as stretch workability can be improved in the
production of a porous sheet by adding several aliphatic phosphoric
triesters as plasticizers together with a crystal nucleating
agent.
PRIOR ART PUBLICATIONS
Patent Publications
[0009] Patent Publication 1: WO 2005/097894 [0010] Patent
Publication 2: Japanese Patent Laid-Open No. 2008-115372 [0011]
Patent Publication 3: WO 2009/013847 [0012] Patent Publication 4:
Japanese Patent Laid-Open No. 2002-179899 (Japanese Patent Gazette
No. 3532850) [0013] Patent Publication 5: Japanese Patent Laid-Open
No. 2007-112868
SUMMARY OF THE INVENTION
Problems to be Solved by the Invention
[0014] According to the conventional techniques, it is made
possible to improve a crystallization velocity and heat resistance
of the polylactic acid resin composition. In the recent years, it
is expected to use polylactic acid resin compositions in extended
applications such as automobile applications, so that polylactic
acid resin compositions having even faster crystallization
velocities and more excellent heat resistance are earnestly
desired. In addition, in order to use the polylactic acid resin
compositions as substitutes for conventional petroleum-based
resins, the same level of moldability as the polypropylene resin or
the like is required, so that molding workability at even lower
temperatures are in demand. However, in conventional techniques,
the effects are not sufficient and further improvements are in
demand.
[0015] An object of the present invention is to provide a method
for producing a polylactic acid resin composition having a fast
crystallization velocity, excellent molding workability at low
temperatures, and excellent heat resistance, and a polylactic acid
resin composition obtained by the method.
Means to Solve the Problems
[0016] In view of the above, as a result of intensive studies in
order to solve the above problems, the present inventors have found
that in the method for producing a polylactic acid resin
composition including blending and melt-kneading a raw material for
a polylactic acid resin composition containing a polylactic acid
resin and a crystal nucleating agent, an organic crystal nucleating
agent composition obtained by subjecting an organic crystal
nucleating agent to a wet pulverization in the presence of a
carboxylic acid ester having a weight-average molecular weight of
from 150 to 600 and a viscosity at 23.degree. C. of from 1 to 500
mPs, and/or a phosphoric ester having a weight-average molecular
weight of from 150 to 600 and a viscosity at 23.degree. C. of from
1 to 500 mPs is used as the crystal nucleating agent, whereby the
resulting polylactic acid resin composition has an excellent
crystallization velocity, molding workability at low temperatures,
and heat resistance.
[0017] The present invention relates to:
[1] a method for producing a polylactic acid resin composition,
including the following steps (1) and (2): step (1): subjecting an
organic crystal nucleating agent to a wet pulverization in the
presence of a carboxylic acid ester having a weight-average
molecular weight of from 150 to 600 and a viscosity at 23.degree.
C. of from 1 to 500 mPs and/or a phosphoric ester having a
weight-average molecular weight of from 150 to 600 and a viscosity
at 23.degree. C. of from 1 to 500 mPs to give a finely pulverized
organic crystal nucleating agent composition; and step (2):
melt-kneading a raw material for a polylactic acid resin
composition containing the finely pulverized organic crystal
nucleating agent composition obtained in the step (1) and a
polylactic acid resin [2] a polylactic acid resin composition
obtainable by the method of the above [1].
Effects of the Invention
[0018] The polylactic acid resin composition obtainable by the
method of the present invention exhibits some effects of being
excellent in a crystallization velocity, molding workability at low
temperatures, and heat resistance.
MODES FOR CARRYING OUT THE INVENTION
[0019] One of the major features of the method for producing a
polylactic acid resin composition of the present invention is in
that during melt-kneading of a raw material for a polylactic acid
resin composition containing a polylactic acid resin and a crystal
nucleating agent, the use of an organic crystal nucleating agent
composition obtainable by subjecting an organic crystal nucleating
agent to a wet pulverization in the presence of a carboxylic acid
ester having a weight-average molecular weight of from 150 to 600
and a viscosity at 23.degree. C. of from 1 to 500 mPs and/or a
phosphoric ester having a weight-average molecular weight of from
150 to 600 and a viscosity at 23.degree. C. of from 1 to 500 mPs,
as the crystal nucleating agent.
[0020] In a polylactic acid resin composition of Patent Publication
3, in order to increase crystallization velocity, molding
workability at low temperatures and heat resistance, a
polyester-polyol and a crystal nucleating agent are previously
mixed upon melt-kneading to form fine crystal nucleating agent
particles. As this polyester-polyol, in order to increase
compatibility with a polylactic acid resin, which is a kind of a
polyester, and wettability with fine particles of an inorganic
natural product, such as talc, which is a crystal nucleating agent,
those having a large molecular weight and a high viscosity have
been used. However, in the present invention, surprisingly, by
subjecting an organic crystal nucleating agent to a wet
pulverization using a carboxylic acid ester and/or a phosphoric
ester each having a small molecular weight and a low viscosity to
make fine particles, it is found that the resulting organic crystal
nucleating agent composition serves to a more increased
crystallization velocity of a polylactic acid resin composition, in
other words, crystallization of the polylactic acid resin
composition is made possible in an even shorter period of time, so
that the polylactic acid resin composition having favorable molding
workability at even lower temperatures and excellent heat
resistance is obtained. The carboxylic acid ester and the
phosphoric ester usable in the present invention has a small
molecular weight and a low viscosity, so that it is considered that
they serve both as a dispersion medium and a solvent for
suppressing re-aggregation of an organic crystal nucleating agent
in the wet-pulverization step. For this reason, it is considered
that the formation of fine particles of the organic crystal
nucleating agent is accomplished, and at the same time the
resulting organic crystal nucleating agent composition is finely
dispersed in a polylactic acid resin without undergoing
re-aggregation in the melt-kneading step, because the ester is
deposited to the surface of the organic crystal nucleating agent in
the organic crystal agent composition. In view of the above, it is
considered that the crystallization cores for accelerating
crystallization in the polylactic acid resin composition are
increased, thereby improving a crystallization velocity of the
polylactic acid resin. Furthermore, since the ester existing on the
surface of the organic crystal nucleating agent composition also
functions as a plasticizer, it is considered that the finely
pulverized organic crystal nucleating agent composition effectively
acts thereto, as a result of accelerating plasticization of the
polylactic acid resin, and thereby a polylactic acid resin
composition having an even more improved crystallization velocity
and at the same time having excellent molding workability at low
temperatures and excellent heat resistance, is obtained.
Method for Producing Polylactic Acid Resin Composition
[0021] The method of the present invention includes the steps
of:
step (1): subjecting an organic crystal nucleating agent to a wet
pulverization in the presence of a carboxylic acid ester having a
weight-average molecular weight of from 150 to 600 and a viscosity
at 23.degree. C. of from 1 to 500 mPs and/or a phosphoric ester
having a weight-average molecular weight of from 150 to 600 and a
viscosity at 23.degree. C. of from 1 to 500 mPs to give a finely
pulverized organic crystal nucleating agent composition; and step
(2): melt-kneading a raw material for a polylactic acid resin
composition containing the finely pulverized organic crystal
nucleating agent composition obtained in the step (1) and a
polylactic acid resin.
[0022] [Step (1)]
[0023] The step (1) is a step of subjecting an organic crystal
nucleating agent to a wet pulverization in the presence of a
carboxylic acid ester having a weight-average molecular weight of
from 150 to 600 and a viscosity at 23.degree. C. of from 1 to 500
mPs and/or a phosphoric ester having a weight-average molecular
weight of from 150 to 600 and a viscosity at 23.degree. C. of from
1 to 500 mPs to give a finely pulverized organic crystal nucleating
agent composition (hereinafter also referred to as "finely
pulverized organic crystal nucleating agent"). Here, the
above-mentioned carboxylic acid esters and phosphoric esters usable
in the wet pulverization of the organic crystal nucleating agent
are collectively referred to herein as "pulverization aid
esters."
[0024] [Organic Crystal Nucleating Agent]
[0025] The organic crystal nucleating agent usable in the present
invention is always preferably in the form of a solid within the
range of from 20.degree. to 200.degree. C., from the viewpoint of
improving a crystallization velocity of the polylactic acid resin,
and at least one member selected from the group consisting of the
following (a) to (c) is more preferred.
(a) at least one organic compound selected from the group
consisting of compounds having an isoindolinone backbone, compounds
having a diketo-pyrrolo-pyrrole backbone, compounds having a
benzimidazolone backbone, compounds having an indigo backbone,
compounds having a phthalocyanine backbone, and compounds having a
porphyrin backbone [referred to as organic crystal nucleating agent
(a)]; (b) at least one organic compound selected from the group
consisting of carbohydrazides, melamine compounds, uracils, and
N-substituted ureas [referred to as organic crystal nucleating
agent (b)]; (c) at least one organic compound selected from the
group consisting of metal salts of dialkyl aromatic sulfonates,
metal salts of phosphoric esters, metal salts of phenylphosphonic
acids, metal salts of rosin acids, aromatic carboxylic acid amides,
and rosin acid amides [referred to as organic crystal nucleating
agent (c)].
[0026] Organic Crystal Nucleating Agent (a)
[0027] The organic crystal nucleating agent (a) includes at least
one organic compound selected from the group consisting of
compounds having an isoindolinone backbone, compounds having a
diketo-pyrrolo-pyrrole backbone, compounds having a benzimidazolone
backbone, compounds having an indigo backbone, compounds having a
phthalocyanine backbone, and compounds having a porphyrin
backbone.
[0028] The compounds having an isoindolinone backbone include
compounds having an isoindolinone backbone and substituted
compounds thereof, and specific examples include yellow pigments
PY109, PY110, PY173, and an orange pigment PO61.
[0029] The compounds having a diketo-pyrrolo-pyrrole backbone
include compounds having a diketo-pyrrolo-pyrrole backbone and
substituted compounds thereof, and specific examples include red
pigments PR254, PR255, PR264, PR270, PR272, and orange pigments
PO71, PO73.
[0030] The compounds having a benzimidazolone backbone include
compounds having a benzimidazolone backbone and substituted
compounds thereof, and specific examples include a purple pigment
PV32, red pigments PR171, PR175, PR176, PR185, PR208, yellow
pigments PY120, PY151, PY154, PY156, PY175, PY180, PY181, PY194,
and orange pigments PO36, PO60, PO62, PO72.
[0031] The compounds having an indigo backbone include compounds
having an indigo backbone and substituted compounds thereof, and
specific examples include a blue dye Vat Blue 1, blue pigments
PB66, PB63, red pigments PR88, PR181, brown pigment PBr27, and
indigo carmine
[0032] The compounds having a phthalocyanine backbone include
compounds having a phthalocyanine backbone and substituted
compounds thereof, and specific examples include phthalocyanine,
blue pigments PB15, PB15:2, PB15:3, PB15:4, PB15:5, PB15:6, PB16,
green pigments PG7, PG36, copper phthalocyanine, zinc
phthalocyanine, titanyl phthalocyanine, aluminum phthalocyanine,
vanadium phthalocyanine, cadmium phthalocyanine, antimony
phthalocyanine, chromium phthalocyanine, germanium phthalocyanine,
iron phthalocyanine, chloroaluminum phthalocyanine, chloroindium
phthalocyanine, chlorogallium phthalocyanine, magnesium
phthalocyanine, dialkyl phthalocyanine, tetramethyl phthalocyanine,
tetraphenyl phthalocyanine, uranium complexes having five isoindole
rings (Superphthalocyanine), and boron complexes consisting of
three isoindole rings. In addition, the substituted compounds
include those substituted by the following substituents, including
halides, alkylated compounds, and the like. The substituents
include halogen atoms such as chlorine, bromine, fluorine, and
iodine, alkyl groups such as a methyl group, an ethyl group, and a
propyl group, alkoxy groups such as a methoxy group and an ethoxy
group, a hydroxyl group, an amino group, and the like.
[0033] The compounds having a porphyrin backbone include compounds
having a porphyrin backbone and substituted compounds thereof, and
specific examples include chlorophyll compounds, hemin compounds,
and esters thereof. Also, substituted compounds include those
substituted by the following substituents, including alkyl groups
such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl,
sec-butyl, tert-butyl, n-pentyl, isoamyl, tert-amyl, n-hexyl,
isohexyl, n-heptyl, n-octyl, n-nonyl, n-decyl, n-undecyl,
n-dodecyl, n-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl,
n-heptadecyl, n-octadecyl, n-eicosyl, n-docosyl, and n-tetracosyl;
alkenyl groups such as vinyl, propenyl (1-, 2-), butenyl (1-, 2-,
3-), pentenyl, octenyl, and butadienyl (1-, 3-); alkynyl groups
such as ethynyl, propynyl (1-, 2-), butynyl (1-, 2-, 3-) pentynyl,
octynyl, and decynyl; cycloalkyl groups such as cyclopropyl,
cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, and cyclooctyl;
aryl groups having single ring- or condensed multi-rings such as
phenyl, biphenyl, naphthyl, anthryl, phenanthryl, acenaphthylenyl;
those substituted with a cross-linked cyclic hydrocarbon group such
as 1-adamantyl, 2-adamantyl, 2-norbornanyl, 5-norbornen-2-yl. In
addition, the substituents may be halides or sulfonates.
[0034] Organic Crystal Nucleating Agent (b)
[0035] The organic crystal nucleating agent (b) includes at least
one organic compound selected from the group consisting of
carbohydrazides, melamine compounds, uracils, and N-substituted
ureas.
[0036] The carbohydrazides include ethylenedicarbonyldibenzoyl
hydrazide, tetramethylenedicarbonyldibenzoyl hydrazide,
hexamethylenedicarbonyldibenzoyl hydrazide,
octamethylenedicarbonyldibenzoyl hydrazide,
decamethylenedicarbonyldibenzoyl hydrazide,
dodecamethylenedicarbonyldibenzoyl hydrazide,
cyclohexylenedicarbonyldibenzoyl hydrazide,
octamethylenedicarbonyldi(4-methylbenzoyl) hydrazide,
octamethylenedicarbonyldi(4-t-butylbenzoyl) hydrazide,
octamethylenedicarbonyldi(2-methylbenzoyl) hydrazide, and
octamethylenedicarbonyldi(3-methylbenzoyl) hydrazide.
[0037] The melamine compounds include melamine, substituted
melamine compounds, deammoniation condensates of melamine, salts of
melamines and acids.
[0038] The substituted melamine compounds include compounds in
which a hydrogen of an amino group of melamine is substituted, and
the substituent includes an alkyl group, an alkenyl group, a phenyl
group, a hydroxyalkyl group, a hydroxyalkyl(oxa-alkyl) group, an
aminoalkyl group, and the like.
[0039] The deammoniation condensates of melamine include melam,
melem, melon, metton, and the like.
[0040] The salts of melamines and acids include salts of at least
one melamine selected from melamine, substituted melamine
compounds, and deammoniation condensates of melamine and acids. The
acids include organic acids such as isocyanuric acid, formic acid,
acetic acid, oxalic acid, malonic acid, lactic acid, citric acid,
benzoic acid, isophthalic acid, and terephthalic acid; and
inorganic acids such as hydrochloric acid, nitric acid, sulfuric
acid, pyrosulfuric acid, methanesulfonic acid, ethanesulfonic acid,
paratoluenesulfonic acid, dodecylbenzenesulfonic acid, salts of
sulfamic acid, salts of phosphoric acid, salts of pyrophosphoric
acid, salts of polyphosphoric acid, salts of phosphonic acid, salts
of phenylphosphonic acid, salts of alkylphosphonic acid, salts of
phosphinic acid, salts of boric acid, and salts of tungstic
acid.
[0041] The uracils include uracil, 6-methyluracil, 5-methyluracil
(thymine), 6-azathymine, 6-azauracil, 5-chlorouracil,
6-benzyl-2-thiouracil, 5-cyanouracil, ethyl
2-thiouracil-5-carboxylate, 5-ethyluracil,
5,6-dihydro-6-methyluracil, 5-(hydroxymethyl)uracil, 5-iodouracil,
5-methyl-2-thiouracil, 5-nitrouracil, 5-(trifluoromethyl)uracil,
2-thiouracil, 5-fluorouracil, and the like.
[0042] The N-substituted ureas include xylenebis laurylurea,
xylenebis myristylurea, xylenebis palmitylurea, xylenebis
stearylurea, and the like.
[0043] Organic Crystal Nucleating Agent (c)
[0044] The organic crystal nucleating agent (c) includes at least
one organic compound selected from the group consisting of metal
salts of dialkyl aromatic sulfonates, metal salts of phosphoric
esters, metal salts of phenylphosphonic acids, metal salts of rosin
acids, aromatic carboxylic acid amides, and rosin acid amides.
[0045] The metal salts of dialkyl aromatic sulfonates include
barium di(dimethyl 5-sulfoisophthalate), calcium di(dimethyl
5-sulfoisophthalate), potassium dimethyl 5-sulfoisophthalate, and
the like.
[0046] The metal salts of phosphoric esters include
sodium-2,2'-methylenebis(4,6-di-t-butylphenyl) phosphate,
aluminumbis(2,2'-methylenebis-4,6-di-t-butylphenyl phosphate), and
the like.
[0047] The metal salts of phenylphosphonic acids include metal
salts of phenylphosphonic acid having a phenyl group and a
phosphonic group (--PO(OH).sub.2), each of which may have a
substituent, and the substituent of the phenyl group includes alkyl
groups having 1 to 10 carbon atoms, and alkoxycarbonyl groups of
which alkoxy moiety has 1 to 10 carbon atoms, and the like.
Specific examples of the phenylphosphonic acids include
unsubstituted phenylphosphonic acid, methylphenylphosphonic acid,
ethylphenylphosphonic acid, propylphenylphosphonic acid,
butylphenylphosphonic acid, dimethoxycarbonylphenylphosphonic acid,
diethoxycarbonylphenylphosphonic acid, and the like, and the
unsubstituted phenylphosphonic acid is preferred.
[0048] The metal salts of the phenylphosphonic acid include salts
of lithium, sodium, magnesium, aluminum, potassium, calcium,
barium, copper, zinc, iron, cobalt, nickel, or the like, and the
zinc salt is preferred.
[0049] The metal salts of the rosin acids include metal salts of
pimaric acid, sandaracopimaric acid, palustric acid, isopimaric
acid, abietic acid, dehydroabietic acid, methyldehydroabietic acid,
neoabietic acid, dihydropimaric acid, dihydroabietic acid,
tetrahydroabietic acid, and the like.
[0050] The aromatic carboxylic acid amides include
1,3,5-benzenetricarboxylic acid tris(t-butylamide) (trimesic acid
tris(t-butylamide)), m-xylylenebis 12-hydroxystearic amide,
1,3,5-benzenetricarboxylic acid tricyclohexylamide (trimesic acid
tricyclohexylamide), trimesic acid tri(2-methylcyclohexylamide),
2,6-naphthalenedicarboxylic acid dicyclohexylamide, and the
like.
[0051] The rosin acid amides include p-xylylenebis rosin acid
amide, p-phenylenediamine monorosin acid amide, and the like.
[0052] These organic crystal nucleating agents may be used alone or
in a combination of two or more kinds. For example, the organic
crystal nucleating agents (a) themselves, the organic crystal
nucleating agents (b) themselves, the organic crystal nucleating
agents (c) themselves, the organic crystal nucleating agent (a) and
the organic crystal nucleating agent (b), the organic crystal
nucleating agent (a) and the organic crystal nucleating agent (c),
the organic crystal nucleating agent (b) and the organic crystal
nucleating agent (c), or the organic crystal nucleating agent (a),
the organic crystal nucleating agent (b), and the organic crystal
nucleating agent (c) can be used in combination. Among them, the
metal salts of phenylphosphonic acid, PY109, PB15:3, PB15, and
PB15:6 are preferred, and the metal salts of phenylphosphonic acid
are more preferred, from the viewpoint of improving a
crystallization velocity, and efficiently obtaining a molded
article having excellent heat resistance.
[0053] The shape and the average particle size of the organic
crystal nucleating agent subjected to the wet pulverization are not
particularly limited, so long as the organic crystal nucleating
agent can be subjected to the wet pulverization. The organic
crystal nucleating agent has a volume-median particle size
(D.sub.50) of preferably from 500 nm to 5 .mu.m, more preferably
from 600 nm to 2 .mu.m, and even more preferably from 700 nm to 1.5
.mu.m, from the viewpoint of increasing efficiency of the wet
pulverization, thereby improving the fine pulverization of the
organic crystal nucleating agent composition obtained. Here, the
average particle size of the organic crystal nucleating agent as
used herein means a volume-median particle size (D.sub.50), which
can be measured in accordance with the method described in Examples
set forth below.
[0054] [Pulverization Aid Ester]
[0055] In the present invention, in the wet pulverization of the
above-mentioned organic crystal nucleating agent, a carboxylic acid
ester having a weight-average molecular weight of from 150 to 600
and a viscosity at 23.degree. C. of from 1 to 500 mPs, and/or a
phosphoric ester having a weight-average molecular weight of from
150 to 600 and a viscosity at 23.degree. C. of from 1 to 500 mPs is
used. Here, in the present invention, the phosphoric ester usable
in the wet pulverization has a viscosity at 23.degree. C. of from 1
to 500 mPs, while the phosphoric ester, which is the organic
crystal nucleating agent, subjected to the pulverization is a solid
at a temperature range of from 20.degree. to 200.degree. C., it is
evident that the phosphoric esters are different substances.
[0056] The carboxylic acid ester and/or the phosphoric ester usable
in the wet pulverization of the organic crystal nucleating agent in
the present invention is a carboxylic acid ester having a
weight-average molecular weight of from 150 to 600 and a viscosity
of from 1 to 500 mPs, and/or a phosphoric ester having a
weight-average molecular weight of from 150 to 600 and a viscosity
of from 1 to 500 mPs, which serves as both a solvent and a
dispersant upon the fine pulverization of the organic crystal
nucleating agent. By subjecting the organic crystal nucleating
agent to the wet pulverization in the presence of the carboxylic
acid ester and/or the phosphoric ester as described above, the
aggregation of the organic crystal nucleating agent during the
pulverization step is suppressed, thereby making it possible to be
finely pulverized. Further, a crystallization velocity, molding
workability at low temperatures, and heat resistance of a
polylactic acid resin composition obtained from this finely
pulverized organic crystal nucleating agent composition are also
improved. The reasons therefor are considered to be as follows. The
finely pulverized organic crystal nucleating agent composition in
the present invention has a small particle size, and the carboxylic
acid ester and/or the phosphoric ester each having a specified
molecular weight and a specified viscosity exists on its surface,
so that the finely pulverized organic crystal nucleating agent
composition is finely dispersed in the polylactic acid resin
composition without being re-aggregated, whereby consequently the
polylactic acid resin composition has an increased number of
crystal nuclei to a large number. The ester acts as a plasticizer
to accelerate the plasticization of the polylactic acid resin,
whereby consequently the finely pulverized organic crystal
nucleating agent composition effectively act, so that a polylactic
acid resin composition having an even more improved crystallization
velocity, and at the same having excellent molding workability at
low temperatures and heat resistance is obtained.
[0057] (Carboxylic Acid Ester Having Weight-Average Molecular
Weight of from 150 to 600 and Viscosity at 23.degree. C. of from 1
to 500 mPas)
[0058] The above-mentioned carboxylic acid ester has a
weight-average molecular weight of from 150 to 600. When the
carboxylic acid ester has a weight-average molecular weight of 600
or less, its volume is large, so that the fine pulverization of the
organic crystal nucleating agent would not be insufficient. On the
other hand, when the molecular weight is 150 or more, the
plasticizing effect to the polylactic acid resin acts, so that a
polylactic acid resin composition having a sufficient
crystallization velocity can be obtained. The above-mentioned
carboxylic acid ester has a weight-average molecular weight of
preferably from 250 to 600, more preferably from 300 to 600, even
more preferably from 350 to 550, and even more preferably from 400
to 500, from the viewpoint of finely pulverizing the organic
crystal nucleating agent, and from the viewpoint of a plasticizing
effect to the polylactic acid resin. Here, in the present
specification, the weight-average molecular weights of the esters
usable in the wet pulverization of the organic crystal nucleating
agent can be measured in accordance with the method described in
Examples set forth below.
[0059] The above-mentioned carboxylic acid ester has a viscosity at
23.degree. C. of from 1 to 500 mPas. When the carboxylic acid ester
has a viscosity of 500 mPs or less, there are no risk that the
viscosity is too high so that it is made difficult to finely
pulverize the organic crystal nucleating agent. On the other hand,
when the carboxylic acid ester has a viscosity of 1 mPs or more, a
plasticizing effect to the polylactic acid resin is favorable, so
that a polylactic acid resin composition having a sufficient
crystallization velocity can be obtained. The above-mentioned
carboxylic acid ester has a viscosity at 23.degree. C. of
preferably from 1 to 400 mPs, more preferably from 2 to 200 mPs,
even more preferably from 3 to 100 mPs, even more preferably from 3
to 50 mPs, from the viewpoint of finely pulverizing the organic
crystal nucleating agent, and from the viewpoint of a plasticizing
effect to the polylactic acid resin. Here, in the present
specification, the viscosity of the ester usable in the wet
pulverization of the organic crystal nucleating agent can be
measured in accordance with the method described in Examples set
forth below.
[0060] The carboxylic acid ester having a weight-average molecular
weight of from 150 to 600 and a viscosity at 23.degree. C. of from
1 to 500 mPs is obtained by polycondensation of an alcohol
component and a carboxylic acid component given below.
[0061] As the alcohol component, a mono-alcohol, a polyhydric
alcohol or the like can be contained, and it is desired to contain
a mono-alcohol having preferably from 3 to 18 carbon atoms, more
preferably from 3 to 16 carbon atoms, and even more preferably from
3 to 14 carbon atoms, from the viewpoint of fine pulverization of
the organic crystal nucleating agent and compatibility with the
polylactic acid resin, plasticity of the polylactic acid resin,
volatile resistance of the above-mentioned carboxylic acid ester.
In addition, from the same viewpoint, it is preferable to contain
an alkylene oxide adduct of an alcohol with addition of an
alkyleneoxy group having 2 or 3 carbon atoms in an amount of
preferably from 0.5 to 5 mol, more preferably from 1.0 to 4 mol,
and even more preferably from 2 to 3 mol, in an average number of
moles added, per one hydroxyl group of the alcohol (hereinafter
also referred to as alkylene oxide adduct of an alcohol). When the
average number of moles added of the alkyleneoxy group having from
2 to 3 carbon atoms is 0.5 mol or more, sufficient plasticity can
be given to the polylactic acid resin, and when the average number
of moles added is 5 mol or less, bleeding resistance of the
above-mentioned carboxylic acid ester becomes favorable. The
alkyleneoxy group having 2 or 3 carbon atoms is preferably an
ethyleneoxy group, from the viewpoint of plasticization efficiency
to the polylactic acid resin.
[0062] In addition, the functional group bound to the ester group
other than the alkyleneoxy group, in a case of a mono-alcohol, is
desirably a hydrocarbon group having preferably from 1 to 8 carbon
atoms, more preferably from 1 to 6 carbon atoms, even more
preferably from 1 to 4 carbon atoms, and even more preferably from
1 to 2 carbon atoms, from the viewpoint of compatibility with the
polylactic acid resin. In a case of a polyhydric alcohol, the
functional group is desirably a hydrocarbon group having preferably
from 1 to 8 carbon atoms, more preferably from 1 to 6 carbon atoms,
and even more preferably from 1 to 4 carbon atoms, from the
viewpoint of compatibility with the polylactic acid resin.
[0063] Here, the alcohol constituting the above-mentioned ester
group may be used alone or in two or more kinds. It is preferable
that the alcohol component contains an alkylene oxide adduct of the
alcohol mentioned above, it is more preferable that all the
alcohols are alkylene oxide adducts of the alcohol mentioned above,
and it is even more preferable that all the alcohols are alkylene
oxide adducts of the identical alcohol mentioned above.
[0064] In addition, the alcohol component may contain an aromatic
alcohol from the viewpoint of volatile resistance of the
above-mentioned carboxylic acid ester. Since the aromatic alcohol
has excellent compatibility to the polylactic acid resin as
compared to the aliphatic alcohol having the same number of carbon
atoms, the weight-average molecular weight can be increased while
keeping bleeding resistance. The aromatic alcohol includes benzyl
alcohol and the like, and of the two or more ester groups contained
in the ester compound, it is desired that the aromatic alcohol is
constituted by, out of the two or more ester groups contained in
the ester compound, ester groups preferably that exceeds 0 and is
equal to or less than 1.5, more preferably that exceeds 0 and is
equal to or less than 1.2, and even more preferably that exceeds 0
and is equal to or less than 1.0.
[0065] A carboxylic acid compound contained in the carboxylic acid
component includes known carboxylic acids, anhydrides thereof, and
alkyl (1 to 3 carbon atoms) esters of the acids, and the like. The
carboxylic acid compound is preferably carboxylic acids having 1 to
6 carbon atoms, and more preferably carboxylic acids having 2 to 5
carbon atoms, from the viewpoint of fine pulverization of the
organic crystal nucleating agent, compatibility with the polylactic
acid resin, plasticization, and volatile resistance of the
carboxylic acid ester. Specifically, monocarboxylic acids having 1
to 6 carbon atoms include acetic acid, propanoic acid, butanoic
acid, pentanoic acid, and hexanoic acid; and dicarboxylic acids
having 2 to 6 carbon atoms include oxalic acid, malonic acid,
succinic acid, glutaric acid, and adipic acid. Among them, the
dicarboxylic acids having 2 to 6 carbon atoms are preferred, oxalic
acid, malonic acid, succinic acid, glutaric acid, and adipic acid
are more preferred, and succinic acid, glutaric acid, and adipic
acid are even more preferred, from the viewpoint of compatibility
of the ester obtained with the organic crystal nucleating agent and
the polylactic acid resin, plasticization, and volatile resistance
of the carboxylic acid ester. Here, carboxylic acids, anhydrides
thereof, an alkyl esters of the acids are collectively referred to
herein as carboxylic acid compounds.
[0066] The polycondensation of the alcohol component and the
carboxylic acid component can be carried out in accordance with a
known method. For example, in a case where the carboxylic acid
ester usable in the present invention is a polycarboxylic acid
ether ester, the carboxylic acid ester is obtained by directly
reacting a saturated dibasic acid having 3 to 5 carbon atoms or an
anhydride thereof and a polyalkylene glycol monoalkyl ether, or
carrying out transesterification between a lower alkyl ester of a
saturated dibasic acid having 3 to 5 carbon atoms and a
polyalkylene glycol monoalkyl ether, in the presence of an acid
catalyst such as paratoluenesulfonic acid monohydrate or sulfuric
acid, or a metal catalyst such as dibutyltin oxide. Specifically,
for example, the carboxylic acid ester can be obtained by charging
a reaction vessel with a polyethylene glycol monoalkyl ether, a
saturated dibasic acid, and paratoluenesulfonic acid monohydrate as
a catalyst so as to have a proportion of polyethylene glycol
monoalkyl ether/saturated dibasic acid/paratoluenesulfonic acid
monohydrate (molar ratio) of 2-4/1/0.001-0.05, and subjecting the
mixture to dehydration at a temperature of from 100.degree. to
130.degree. C. under normal pressure or a reduced pressure, in the
presence or absence of a solvent such as toluene. A method of
carrying out the reaction under a reduced pressure without using a
solvent is preferred.
[0067] In addition, in a case where the carboxylic acid ester
usable in the present invention is a polyhydric alcohol ester, for
example, an alkylene oxide having from 2 to 3 carbon atoms is added
to glycerol using an autoclave at a temperature of from 120.degree.
to 160.degree. C. in an amount of from 3 to 9 mol per one mol of
glycerol, in the presence of an alkali metal catalyst. Based on one
mol of the alkylene oxide adduct of glycerol obtained is added
dropwise 3 mol of acetic acid anhydride at 110.degree. C., and
after the termination of the dropwise addition, the mixture is aged
at 110.degree. C. for 2 hours to carry out acetylation. The
reaction product is subjected to steam distillation under a reduced
pressure to distill away acetic acid and unreacted acetic acid
anhydride contained, whereby a carboxylic acid ester can be
obtained.
[0068] In addition, in a case where the carboxylic acid ester
usable in the present invention is a hydroxycarboxylic acid ether
ester, an alkylene oxide having from 2 to 3 carbon atoms is added
to a hydroxycarboxylic acid such as lactic acid in an amount of
from 2 to 5 mol per one mol of the hydroxycarboxylic acid using an
autoclave at a temperature of from 120.degree. to 160.degree. C.,
in the presence of an alkali metal catalyst. Based on one mol of
the alkylene oxide adduct of lactic acid obtained was added
dropwise 1 mol of acetic acid anhydride at 110.degree. C., and
after the termination of the dropwise addition, the mixture is aged
at 110.degree. C. for 2 hours to carry out acetylation. The
reaction product is subjected to steam distillation under a reduced
pressure to distill away acetic acid and unreacted acetic acid
anhydride contained. Next, a reaction vessel is charged with
materials so as to have a proportion of reaction product
obtained/polyalkylene glycol monoalkyl ether/paratoluenesulfonic
acid monohydrate (catalyst) (molar ratio) of 1/1-2/0.001-0.05, and
subjecting the mixture to dehydration at a temperature of from
100.degree. to 130.degree. C. under normal pressure or a reduced
pressure, in the presence or absence of a solvent such as toluene,
whereby a hydroxycarboxylic acid ether ester can be obtained.
[0069] Thus, the carboxylic acid ester usable in the step (1) is
obtained, and in the present invention, at least one member
selected from the group consisting of carboxylic acid esters formed
between succinic acid or adipic acid and a polyethylene glycol
monomethyl ether, and carboxylic acid esters formed between acetic
acid and ethylene oxide adduct of ethylene glycol is preferred, and
the carboxylic acid esters formed between succinic acid or adipic
acid and a polyethylene glycol monomethyl ether are more preferred,
from the viewpoint of fine pulverization of the organic crystal
nucleating agent, satisfaction of both strength and flexibility of
the polylactic acid resin composition, moldability, plasticization,
and bleeding resistance of the carboxylic acid ester.
[0070] In addition, more preferable are alkyl ether esters of
polyhydric alcohols, such as carboxylic acid esters formed between
acetic acid and an ethylene oxide adduct of glycerol, an ethylene
oxide moiety of which is added in an amount of from 3 to 9 mol in
average (1 to 3 mol per one hydroxyl group), carboxylic acid esters
formed between acetic acid and a propylene oxide adduct of
diglycerol, a propylene oxide moiety of which is added in an amount
of from 4 to 12 mol in average (1 to 3 mol per one hydroxyl group),
and carboxylic acid esters formed between acetic acid and an
ethylene oxide adduct of a polyethylene glycol, an ethylene oxide
moiety of which is added in an amount of from 4 to 9 mol in average
(1 to 3 mol per one hydroxyl group); and carboxylic acid esters
formed between polycarboxylic acids and a polyethylene glycol
monomethyl ether, such as carboxylic acid esters formed between
succinic acid and an ethylene oxide adduct of a polyethylene glycol
monomethyl ether, an ethylene oxide moiety of which is added in an
amount of from 2 to 4 mol in average, carboxylic acid esters formed
between adipic acid and an ethylene oxide adduct of a polyethylene
glycol monomethyl ether, an ethylene oxide moiety of which is added
in an amount of from 2 to 3 mol in average, and carboxylic acid
esters formed between 1,3,6-hexanetricarboxylic acid and an
ethylene oxide adduct of a polyethylene glycol monomethyl ether, an
ethylene oxide moiety of which is added in an amount of from 2 to 3
mol in average, from the viewpoint of finely pulverizing the
organic crystal nucleating agent, satisfying both strength and
flexibility of a molding article made of a polylactic acid resin
composition, and giving excellent moldability and impact resistance
to the polylactic acid resin composition.
[0071] Even more preferable are carboxylic acid esters formed
between acetic acid and an ethylene oxide adduct of glycerol, an
ethylene oxide moiety of which is added in an amount of from 3 to 6
mol in average (1 to 2 mol per one hydroxyl group), carboxylic acid
esters formed between acetic acid and an ethylene oxide adduct of a
polyethylene glycol, an ethylene oxide moiety of which is added in
an amount of from 4 to 6 mol in average, carboxylic acid esters
formed between succinic acid and an ethylene oxide adduct of a
polyethylene glycol monomethyl ether, an ethylene oxide moiety of
which is added in an amount of from 2 to 3 mol in average,
carboxylic acid esters formed between adipic acid and diethylene
glycol monomethyl ether, and carboxylic acid esters formed between
1,3,6-hexanetricarboxylic acid and diethylene glycol monomethyl
ether, from the viewpoint of finely pulverizing the organic crystal
nucleating agent, satisfying both strength and flexibility of a
molding article made of a polylactic acid resin composition, and
giving excellent moldability, impact resistance, and bleeding
resistance of the carboxylic acid ester. Even more preferable are
carboxylic cid esters formed between succinic acid and triethylene
glycol monomethyl ether, from the viewpoint of satisfying both
strength and flexibility of a molding article made of a polylactic
acid resin composition, and giving excellent moldability, impact
resistance, and bleeding resistance, volatile resistance, and
irritating odor resistance of the carboxylic acid ester.
[0072] In addition, a carboxylic acid ester formed between adipic
acid and a diethylene glycol monomethyl ether/benzyl alcohol
mixture (weight ratio: 1/1) is preferred, from the viewpoint of
volatile resistance.
[0073] (Phosphoric Ester Having Weight-Average Molecular Weight of
from 150 to 600 and Viscosity at 23.degree. C. of from 1 to 500
mPas)
[0074] The above-mentioned phosphoric ester has a weight-average
molecular weight of from 150 to 600. When the weight-average
molecular weight is 600 or less, its volume is large, so that the
fine pulverization of the organic crystal nucleating agent would
not be insufficient. On the other hand, when the phosphoric ester
has a weight-average molecular weight of 150 or more, the
plasticizing effect to the polylactic acid resin acts, so that a
polylactic acid resin composition having a sufficient
crystallization velocity can be obtained. The above-mentioned
phosphoric ester has a weight-average molecular weight of
preferably from 250 to 600, more preferably from 300 to 600, even
more preferably from 350 to 550, and even more preferably from 400
to 500, from the viewpoint of finely pulverizing the organic
crystal nucleating agent, and from the viewpoint of a plasticizing
effect to the polylactic acid resin.
[0075] The above-mentioned phosphoric ester has a viscosity at
23.degree. C. of from 1 to 500 mPas. When the phosphoric ester has
a viscosity of 500 mPs or less, there are no risk that the
viscosity is too high so that it is made difficult to finely
pulverize the organic crystal nucleating agent. On the other hand,
when the phosphoric ester has a viscosity of 1 mPs or more, a
plasticizing effect to the polylactic acid resin is favorable, so
that a polylactic acid resin composition having a sufficient
crystallization velocity can be obtained. The above-mentioned
phosphoric ester has a viscosity at 23.degree. C. of preferably
from 1 to 400 mPs, more preferably from 2 to 200 mPs, even more
preferably from 3 to 100 mPs, even more preferably from 3 to 50
mPs, from the viewpoint of finely pulverizing the organic crystal
nucleating agent, and from the viewpoint of a plasticizing effect
to the polylactic acid resin.
[0076] The phosphoric ester having a weight-average molecular
weight of from 150 to 600 and a viscosity at 23.degree. C. of from
1 to 500 mPs is obtained by polycondensation of an alcohol
component and a phosphoric acid component given below.
[0077] The alcohol component is exemplified by the alcohol
component usable in the preparation of the above-mentioned
carboxylic acid ester.
[0078] A phosphoric acid compound contained in the phosphoric acid
component includes known phosphoric acids, anhydrides thereof,
phosphorus oxyhalides, and alkyl(1 to 3 carbon atoms) esters of the
acids, and the like, and the phosphorus oxyhalides are preferred,
from the viewpoint of fine pulverization of the organic crystal
nucleating agent, compatibility with the polylactic acid resin,
plasticization, and volatile resistance of the phosphoric ester.
Specific examples thereof include phosphorus oxychloride,
phosphorus oxybromide, and phosphorus oxyfluoride. Among them,
phosphorus oxychloride is preferred, from the viewpoint of
compatibility between the ester obtained and the organic crystal
nucleating agent and the polylactic acid resin, plasticization, and
volatile resistance of the phosphoric ester. Here, phosphoric acid,
anhydrides thereof, phosphorus oxyhalides, and alkyl esters of the
acids are collectively referred to herein as phosphoric acid
compounds.
[0079] The polycondensation of the alcohol component and the
phosphoric acid component can be carried out in accordance with a
known method.
[0080] Thus, the phosphoric ester usable in the step (1) is
obtained, and in the present invention, a phosphoric triester is
preferred, from the viewpoint of increasing chemical stability with
the polylactic acid resin during kneading.
[0081] It is preferable that the phosphoric triester is a compound
represented by the formula (I):
##STR00001##
[0082] wherein each of R.sup.1, R.sup.2, and R.sup.3 is
independently an alkyl group having from 1 to 4 carbon atoms; each
of A.sup.1, A.sup.2, and A.sup.3 is independently an alkylene group
having 2 or 3 carbon atoms; and each of m, n, and p is
independently a positive number showing the number of average moles
of oxyalkylene groups added, wherein m+n+p satisfies the number
that exceeds 3 and is equal to or less than 12,
from the viewpoint of improving plasticization of the polylactic
acid resin and compatibility with the polylactic acid resin.
[0083] The compound represented by the formula (I) is a
polyether-form phosphoric triester, which may have a symmetric
structure or an asymmetric structure, and the phosphoric triester
having a symmetric structure is preferred, from the viewpoint of
simplicity in the production.
[0084] Each of R.sup.1, R.sup.2, and R.sup.3 is independently an
alkyl group having from 1 to 4 carbon atoms, which may be linear or
branched. Specific examples include a methyl group, an ethyl group,
a propyl group, an isopropyl group, a butyl group, and an isobutyl
group, and an ethyl group, a propyl group, and a butyl group are
preferred.
[0085] Each of A.sup.1, A.sup.2, and A.sup.3 is independently an
alkylene group having 2 or 3 carbon atoms, which may be linear or
branched. Specific examples include an ethylene group, an
n-propylene group, and an isopropylene group. Also, A.sup.1,
A.sup.2, and A.sup.3 form oxyalkylene groups (alkylene oxides) with
an adjoining oxygen atom to form a repeating structure in the
compound represented by the formula (I).
[0086] Each of m, n, and p is independently a positive number
showing the number of average moles of oxyalkylene groups added,
wherein m+n+p satisfies the number that exceeds 3 and is equal to
or less than 12. Among them, it is preferable that m, n, and p are
positive numbers, wherein m+n+p satisfies the number that exceeds 3
and is less than 12, and it is more preferable that m+n+p satisfies
the number that exceeds 4 and is less than 12, from the viewpoint
of improving plasticization of the polylactic acid resin and
compatibility with the polylactic acid resin.
[0087] Specific examples of the compound represented by the formula
(I) include symmetric polyether-form phosphoric triesters such as
tris(ethoxyethoxyethyl) phosphate represented by the formula
(II):
##STR00002##
wherein in the formula (I) all of R.sup.1, R.sup.2, and R.sup.3 are
ethyl groups, all of A.sup.1, A.sup.2, and A.sup.3 are ethylene
groups, all of m, n, and p are 2, and m+n+p=6,
tris(methoxyethoxyethyl) phosphate (m+n+p=6),
tris(propoxyethoxyethyl) phosphate (m+n+p=6),
tris(butoxyethoxyethyl) phosphate (m+n+p=6),
tris(methoxyethoxyethoxyethyl) phosphate (m+n+p=9), and
tris(ethoxyethoxyethoxyethyl) phosphate; and asymmetric
polyether-form phosphoric triesters such as
bis(ethoxyethoxyethyl)methoxyethoxyethoxyethyl phosphate (m+n+p=7)
and bis(methoxyethoxyethoxyethyl)ethoxyethoxyethyl phosphate
(m+n+p=8), or an asymmetric polyether-form phosphoric ester
obtained by triester-phosphorylating a mixture of a polyoxyethylene
adduct or polyoxypropylene adduct of an alcohol having 1 to 4
carbon atoms so as to satisfy the formula (I). Among them,
tris(ethoxyethoxyethyl) phosphate for which sufficient safety is
already confirmed is preferred.
[0088] The compound represented by the formula (I) may be a
commercially available product, or a compound synthesized by a
known production method, for example, a method described in
Japanese Patent Laid-Open No. Hei-10-17581 may be used.
[0089] Here, it is preferable that the carboxylic acid ester and
the phosphoric ester mentioned above are complete ester compounds
which are entirely esterified, from the viewpoint of finely
pulverizing the organic crystal nucleating agent, and from the
viewpoint of sufficiently exhibiting the function as a
plasticizer.
[0090] In addition, the carboxylic acid ester and the phosphoric
ester mentioned above can be used alone or in a combination of two
or more kinds. When plural number of each of the carboxylic acid
ester and the phosphoric ester are used, it is preferable that each
the weight-average molecular weight and the viscosity at 23.degree.
C. is such that a weighted average thereof is within the range
mentioned above.
[0091] The weight ratio of the organic crystal nucleating agent to
the carboxylic acid ester and/or the phosphoric ester mentioned
above (the pulverization aid ester) in the step (1), i.e. organic
crystal nucleating agent/pulverization aid ester, is preferably
from 1/99 to 50/50, more preferably from 2/98 to 40/60, and even
more preferably from 4/96 to 30/70, from the viewpoint of fine
pulverization of the organic crystal nucleating agent and from the
viewpoint of compatibility with the polylactic acid resin,
plasticization, and volatile resistance of the pulverization aid
ester. Here, the weight of the pulverization aid ester as referred
to herein means a total weight of the carboxylic acid ester and the
phosphoric ester used in the wet pulverization in the step (1), and
the weight ratio of the organic crystal nucleating agent to the
carboxylic acid ester and/or the phosphoric ester mentioned above
is expressed as a ratio of the weight of the organic crystal
nucleating agent and a total weight of the carboxylic acid ester
and the phosphoric ester mentioned above.
[0092] In addition, in the present invention, besides the
carboxylic acid ester and/or the phosphoric ester mentioned above,
other esters and the like can be used together in the fine
pulverization of the organic crystal nucleating agent, within the
range that would not impair the effects of the present
invention.
[0093] As pulverizers usable in the wet pulverization in the step
(1), known pulverizers such as media pulverizers and non-media
pulverizers can be used, and the media pulverizers are preferred,
from the viewpoint of pulverization efficiency. The non-media
pulverizers include high-pressure pulverizers such as jet mills.
The media pulverizers are classified into vessel driving
pulverizers and media agitating pulverizers. The vessel driving
pulverizers include tumbling mills, vibrating mills, planetary
mills, centrifugal fluidized bed mills, and the like. Among them,
the vibrating mills are preferred, from the viewpoint of high
pulverization efficiency and productivity. The media agitating
pulverizers include tower pulverizers such as Tower mills,
agitation tank-containing pulverizers such as Attritor, Aquamizer,
and Sand Grinder, flow tank-containing pulverizers such as Visco
mill and Pearl mill, flow tube-containing pulverizers, and annular
pulverizers such as Co-ball-mill; and continuous dynamic
pulverizers. Among them, the agitation tank-containing pulverizers
are preferred, from the viewpoint of high pulverization efficiency
and productivity. The peripheral speed of a tip end of agitation
blades in a case where a media agitating pulverizer is used is
preferably from 0.5 to 20 m/s, and more preferably from 1.0 to 15
m/s. Here, the kinds of the pulverizers can be referred to "Kagaku
Kogaku no Shinpo Dai 30 Shu Biryushi Seigyo (Advancement in
Chemical Engineering, vol. 30, Fine Particle Control)" (edited by
The Society of Chemical Engineers, Japan, Tokai Local Branch,
published Oct. 10, 1996, Maki Shoten). Also, the treatment method
therefor may be either in a batch method or a continuous
method.
[0094] The materials for the media of the media pulverizers are not
particularly limited, and the materials include, for example, iron,
stainless steel, alumina, zirconia, silicon carbide, silicon
nitride, glass, and the like, and zirconia is preferred from the
viewpoint of pulverization efficiency. The shapes of the media are
not particularly limited, and include, a ball, a rod, a tube, and
the like. Here, a rod refers to a rod-shaped medium, in which a
cross section of the rod of a polygonal form such as tetragonal or
hexagonal form, a circular form, an elliptic form or the like can
be used, and a ball is preferred from the viewpoint of
pulverization efficiency.
[0095] In a case of a pulverizer where a vessel driving pulverizer
is a vibrating mill and media are rod-shaped, the rod has an outer
diameter of preferably from 0.5 to 200 mm, more preferably from 1.0
to 100 mm, and even more preferably from 5 to 50 mm. So long as the
rod has a size within the range mentioned above, a desired
pulverization force is obtained, and at the same time the organic
crystal nucleating agent can be effectively finely pulverized
without allowing admixture of fragments of the rod to cause soiling
of the organic crystal nucleating agent.
[0096] Although a filling ratio of the rod differs in favorable
filling ratios depending upon the kinds of the vessel driving
pulverizers, a filling ratio is within the range of preferably from
10 to 70%, and more preferably from 15 to 60%. So long as the
filling ratio are within this range, the contact frequency of the
organic crystal nucleating agent and the above-mentioned
pulverization aid ester with the rod is improved, whereby the
pulverization efficiency can be improved.
[0097] Here, the filling ratio refers to an apparent volume of a
rod based on the volume of the agitating member of a vessel driving
pulverizer. In addition, it is preferable that the rods are used in
plurality, from the viewpoint of increasing contact frequency of
the organic crystal nucleating agent and the above-mentioned
pulverization aid ester with the rod, thereby improving
pulverization efficiency.
[0098] In addition, in a case of a pulverizer where a media
agitating pulverizer is an agitation tank-containing pulverizer and
media are a ball, the ball has an outer diameter within the range
of preferably from 0.01 to 5 mm, more preferably from 0.02 to 5 mm,
and even more preferably from 0.02 to 1 mm. So long as the ball has
a size within the range mentioned above, a desired pulverization
force is obtained, and at the same time the organic crystal
nucleating agent can be effectively finely pulverized without
allowing admixture of fragments of the ball to cause soiling of the
organic crystal nucleating agent.
[0099] Although a filling ratio of the ball differs in favorable
filling ratios depending upon the kinds of the agitation
tank-containing pulverizers, the filling ratio is within the range
of preferably from 10 to 97%, and more preferably from 15 to 95%.
So long as the filling ratio are within this range, the contact
frequency of the organic crystal nucleating agent and the
above-mentioned pulverization aid ester with the ball is improved,
and at the same time the pulverization efficiency can be improved
without hindering the movement of the media. Here, the filling
ratio refers to an apparent volume of a ball based on the volume of
the agitating member of the an agitation tank-containing
pulverizer.
[0100] The treatment time cannot be unconditionally determined
because the treatment time depends on the kinds of the pulverizers,
the kinds, the size and the filling ratio of the media, and the
like. The treatment time is preferably from 0.01 to 50 hr, more
preferably from 0.05 to 30 hr, even more preferably from 0.10 to 20
hr, and still even more preferably from 0.10 to 10 hr, from the
viewpoint of finely pulverizing the organic crystal nucleating
agent. The treatment temperature is not particularly limited, and
the treatment temperature is preferably from 5.degree. to
250.degree. C., and more preferably from 10.degree. to 200.degree.
C., from the viewpoint of avoidance of degradation by heat.
[0101] Specific embodiments for the wet pulverization in the step
(1) include embodiments, including, for example, adding
independently or concurrently each of an organic crystal nucleating
agent and the carboxylic acid ester and/or the phosphoric ester
mentioned above to a media pulverizer, and carry out a wet
pulverization.
[0102] Thus, an organic crystal nucleating agent composition that
is finely pulverized is obtained.
[0103] In the present invention, the organic crystal nucleating
agent composition that is finely pulverized (finely pulverized
organic crystal nucleating agent) has a volume-median particle size
(D.sub.50) of preferably from 50 to 700 nm, more preferably from 75
to 680 nm, even more preferably from 100 to 650 nm, even more
preferably from 100 to 600 nm, and even more preferably from 200 to
600 nm, from the viewpoint of enhancing crystallization of the
polylactic acid resin composition obtainable and heat resistance of
a molding article made of the polylactic acid resin composition.
For the same reasons, the volume-median particle size (D.sub.50) of
the organic crystal nucleating agent composition is preferably from
20 to 70%, more preferably from 25 to 65%, and even more preferably
from 30 to 60%, based on the volume-median particle size (D.sub.50)
of the organic crystal nucleating agent before the wet
pulverization.
[0104] In addition, the cumulative volume particle size (D.sub.90)
is preferably from 50 to 1400 nm, more preferably from 75 to 1200
nm, even more preferably from 100 to 1000 nm, and even more
preferably from 200 to 900 nm. Also, the cumulative volume particle
size (D.sub.10) is preferably from 10 to 600 nm, more preferably
from 20 to 500 nm, and even more preferably from 100 to 400 nm. In
addition, from the same viewpoint, a ratio of D.sub.10 to D.sub.50,
i.e. D.sub.10/D.sub.50, is preferably from 0.5 to 1.0, and more
preferably from 0.6 to 1.0, and a ratio of D.sub.90 to D.sub.50,
i.e. D.sub.90/D.sub.50, is preferably from 1.0 to 2.0, and more
preferably from 1.0 to 1.8.
[0105] In addition, from the same viewpoint, in one embodiment of
the organic crystal nucleating agent composition, it is preferable
that the volume-median particle size (D.sub.50) is from 100 to 600
nm, that the cumulative volume particle size (D.sub.90) is from 100
to 1000 nm, and that the cumulative volume particle size (D.sub.10)
is from 10 to 600 nm, and it is more preferable that the
volume-median particle size (D.sub.50) is from 200 to 600 nm, that
the cumulative volume particle size (D.sub.90) is from 200 to 900
nm, and that the cumulative volume particle size (D.sub.10) is from
100 to 400 nm. Here, in the present specification, the average
particle size of the organic crystal nucleating agent composition
means a volume-median particle size (D.sub.50), which can be
measured in accordance with the method described in Examples set
forth below. In addition, a cumulative volume particle size
(D.sub.X) refers to a particle size of particles having a
cumulative volume frequency x % counted from a smaller particle
size where the cumulative volume frequency is calculated in volume
percentage, which can be measured in accordance with the method
described in Examples set forth below.
[0106] [Step (2)]
[0107] The step (2) is a step of melt-kneading a raw material for a
polylactic acid resin composition containing the finely pulverized
organic crystal nucleating agent composition obtained in the step
(1) and a polylactic acid resin.
Raw Material for Polylactic Acid Resin Composition
[0108] The raw material for a polylactic acid resin composition
contains the finely pulverized organic crystal nucleating agent
composition obtained in the step (1) and a polylactic acid resin.
The finely pulverized organic crystal nucleating agent composition
obtained in the step (1) of the raw material for a polylactic acid
resin composition is contained in an amount of preferably from 1 to
50 parts by weight, more preferably from 5 to 40 parts by weight,
even more preferably from 7 to 30 parts by weight, and even more
preferably from 10 to 25 parts by weight, based on 100 parts by
weight of the polylactic acid resin, from the viewpoint of
crystallization velocity of the polylactic acid resin composition
obtainable, and heat resistance of the molded article made of the
polylactic acid resin composition. Here, the phrase "amount
contained" as used herein means "amount contained or amount
blended."
[0109] (Polylactic Acid Resin)
[0110] The polylactic acid resin in the present invention refers to
a polylactic acid, or a copolymer of a lactic acid and a
hydroxycarboxylic acid. The hydroxycarboxylic acid includes
glycolic acid, hydroxybutyric acid, hydroxyvaleric acid,
hydroxypentanoic acid, hydroxycaproic acid, and hydroxyheptanoic
acid, and glycolic acid and hydroxycaproic acid are preferred.
[0111] Preferred molecular structures of the polylactic acid are
those composed of from 80 to 100% by mol of either unit of L-lactic
acid (L-form) or D-lactic acid (D-form), and from 0 to 20% by mol
of a lactic acid unit in a symmetric form thereof. In addition, the
copolymer of a lactic acid and a hydroxycarboxylic acid is composed
of from 85 to 100% by mol of either unit of L-lactic acid or
D-lactic acid, and from 0 to 15% by mol of a hydroxycarboxylic acid
unit.
[0112] These polylactic acid resins can be obtained by selecting a
structure that is needed from L-lactic acid, D-lactic acid, and a
hydroxycarboxylic acid as raw materials, and subjecting the
components to dehydration polycondensation. Preferably, the
polylactic acid resin is obtained by selecting a structure that is
needed from as lactide, which is a cyclic lactic acid dimer, a
glycolide, which is a cyclic glycolic acid dimer, a caprolactone,
or the like, and subjecting the components to a ring-opening
polymerization. The lactides include the form of L-lactide, which
is a cyclic L-lactic acid dimer; D-lactide, which is a cyclic
D-lactic acid dimer; meso-lactide, which is a cyclic dimer of
D-lactic acid and L-lactic acid; and DL-lactide, which is a racemic
mixture of the D-lactide and the L-lactide. In the present
invention, any one of the lactides can be used, and the D-lactide
or the L-lactide is preferred as the main raw material.
[0113] In the present invention, it is preferable to use a
polylactic acid resin having a high optical purity of the lactic
acid component, from the viewpoint of moldability of the polylactic
acid resin composition. Specifically, L-form or D-form is contained
in an amount of preferably 80% or more, L-form or D-form is
contained in an amount of more preferably 90% or more, L-form or
D-form is contained in an amount of even more preferably 95% or
more, L-form or D-form is contained in an amount of even more
preferably 98% or more, and L-form or D-form is contained in an
amount of even more preferably 99% or more, of the entire lactic
acid component of the polylactic acid resin.
[0114] In addition, in the present invention, as the polylactic
acid, a stereocomplex polylactic acid, composed of two kinds of
polylactic acids, each obtained from a lactic acid component
containing an isomer different from one another as a main
component, may be used, from the viewpoint of moldability and
transparency of the polylactic acid resin composition, and
satisfaction of both strength and flexibility of the molded article
made of the polylactic acid resin composition, and heat resistance.
One polylactic acid constituting the stereocomplex polylactic acid
[hereinafter referred to as "polylactic acid (A)"] contains L-form
in an amount of from 90 to 100% by mol, and other component
including D-form in an amount of from 0 to 10% by mol. The other
polylactic acid [hereinafter referred to as "polylactic acid (B)"]
contains D-form in an amount of from 90 to 100% by mol, and other
component including L-form in an amount of from 0 to 10% by mol.
Other components besides L-form and the D-form include dicarboxylic
acids, polyhydric alcohols, hydroxycarboxylic acids, lactone, and
the like, each having a functional group capable of forming two or
more ester bonds. Also, other components may be a polyester, a
polyether, a polycarbonate, or the like, each having two or more
unreacted functional groups mentioned above in one molecule.
[0115] The polylactic acid (A) and the polylactic acid (B) in the
stereocomplex polylactic acid are in a weight ratio, i.e.
polylactic acid (A)/polylactic acid (B), of preferably from 10/90
to 90/10, more preferably from 20/80 to 80/20, and even more
preferably from 40/60 to 60/40.
[0116] The polylactic acid resin has a weight-average molecular
weight of preferably 100,000 or more, from the viewpoint of
mechanical properties of the molded article made of the polylactic
acid resin composition, and the polylactic acid resin has a
weight-average molecular weight of preferably 400,000 or less, from
the viewpoint of fluidity during the molding of the polylactic acid
resin composition. Here, the weight-average molecular weight of the
polylactic acid resin can be obtained by using gel permeation
chromatography (GPC), in which chloroform is used as a solvent, a
high-temperature SEC column (GMHHR-H Series) manufactured by Tosoh
Corporation as a column, a flow rate of 1.0 mL/min, a column
temperature of 40.degree. C., a differential refractive index
detector (RI) as a detector, and calculating using styrene having a
known molecular weight as a reference.
[0117] Here, the polylactic acid can be synthesized in accordance
with a known method, or commercially available manufactured
products can be used. Commercially available products include, for
example, trade name: LACEA (manufactured by Mitsui Chemicals,
Inc.), trade name: Ecoplastic U'z (manufactured by TOYOTA MOTOR
CORPORATION), trade name: Nature Works (manufactured by Nature
Works), trade name: REVODE (manufactured by Zhejiang Hisun
Biomaterials Co., Ltd.), and the like. In addition, among the
above-mentioned commercially available products, trade names LACEA
H-100, H-400, H-440 (manufactured by Mitsui Chemicals, Inc.), trade
names Ecoplastic U' z S-9, S-12, and S-17 (manufactured by TOYOTA
MOTOR CORPORATION), trade names Nature Works 4032D and 3001D
(manufactured by Nature Works) are preferred, from the viewpoint of
moldability.
[0118] The polylactic acid resin in the polylactic acid resin
composition of the present invention is contained in an amount of
preferably 50% by weight or more, and more preferably 70% by weight
or more, from the viewpoint of achieving the objectives of the
present invention.
[0119] The polylactic acid resin composition of the present
invention may further contain, in addition to the above-mentioned
finely pulverized organic crystal nucleating agent composition and
the above-mentioned polylactic acid resin, a crystal nucleating
agent, a plasticizer, a hydrolysis inhibitor, or the like in a
proper amount.
[0120] (Crystal Nucleating Agent)
[0121] In the present invention, the polylactic acid resin
composition may contain other crystal nucleating agent together
with the above-mentioned finely pulverized organic crystal
nucleating agent, from the viewpoint of further improving a
crystallization velocity of the polylactic acid resin composition
of the present invention, and improving heat resistance and
moldability of the molded article made of the polylactic acid resin
composition. It is preferable that other crystal nucleating agents
are compounds having hydroxyl group or groups and amide group or
groups in one molecule, from the viewpoint of a crystallization
velocity of the polylactic acid resin composition, and heat
resistance of the molded article made of the polylactic acid resin
composition. The above-mentioned crystal nucleating agent can
further improve a crystallization velocity and heat resistance of
the polylactic acid resin composition obtainable by dissolving the
crystal nucleating agent during the melt-kneading of the polylactic
acid resin to form a large number of crystal nuclei, and at the
same time interactions with the above-mentioned finely pulverized
organic crystal nucleating agent.
[0122] The compounds having hydroxyl group or groups and amide
group or groups in one molecule are preferably an aliphatic amide
having hydroxyl group or groups, and more preferably an aliphatic
amide having two or more hydroxyl groups and two or more amide
groups in one molecule, from the viewpoint of a crystallization
velocity of the polylactic acid resin composition, and
compatibility with the polylactic acid resin and impact resistance
and moldability of the polylactic acid resin composition.
[0123] The compounds having hydroxyl group or groups and amide
group or groups in one molecule have a melting point of preferably
65.degree. C. or higher, more preferably from 70.degree. to
220.degree. C., and even more preferably from 80.degree. to
190.degree. C., from the viewpoint of improving dispersibility of
the crystal nucleating agent during kneading, and improving a
crystallization velocity. The melting point of the crystal
nucleating agent as used herein is measured by a method described
in Examples described later.
[0124] Specific examples of the compounds having hydroxyl group or
groups and amide group or groups in one molecule include
hydroxyfatty acid monoamides such as 12-hydroxystearic acid
monoethanolamide; hydroxyfatty acid bisamides such as methylenebis
12-hydroxystearic amide, ethylenebis 12-hydroxystearic amide, and
hexamethylenebis 12-hydroxystearic amide; hydroxyfatty acid
triamides such as 12-hydroxystearic acid triglyceride; and the
like. The hydroxyfatty acid bisamides such as ethylenebis
12-hydroxystearic amide and hexamethylenebis 12-hydroxystearic
amide, and the 12-hydroxystearic acid triglyceride are preferred,
and ethylenebis 12-hydroxystearic amide is more preferred, from the
viewpoint of moldability of the polylactic acid resin composition,
heat resistance and impact resistance of the molded article made of
the polylactic acid resin composition, and anti-blooming property
of the crystal nucleating agent.
[0125] The compounds having hydroxyl group or groups and amide
group or groups in one molecule and the finely pulverized organic
crystal nucleating agent are in a weight ratio, i.e. the compounds
having hydroxyl group or groups and amide group or groups in one
molecule/the finely pulverized organic crystal nucleating agent, of
preferably from 0.5/99.5 to 20/80, more preferably from 0.5/99.5 to
17/83, even more preferably from 1.0/99.0 to 10/90, and still even
more preferably from 3/97 to 8/92, from the viewpoint of increasing
a crystallization velocity of the polylactic acid resin, and from
the viewpoint of increasing moldability of the polylactic acid
resin composition, and heat resistance of the molded article made
of the polylactic acid resin composition.
[0126] The crystal nucleating agent other than the finely
pulverized organic crystal nucleating agent in the polylactic acid
resin composition is contained in an amount of preferably from 0.1
to 5 parts by weight, more preferably from 0.5 to 3 parts by
weight, and even more preferably from 0.5 to 2 parts by weight,
based on 100 parts by weight of the polylactic acid resin, from the
viewpoint of heat resistance, impact resistance, and moldability of
the molded article made of the polylactic acid resin
composition.
[0127] (Plasticizer)
[0128] In the present invention, the polylactic acid resin
composition can contain a plasticizer, from the viewpoint of
further improving transparency and moldability of the polylactic
acid resin composition. In the present invention, the finely
pulverized organic crystal nucleating agent obtained by subjecting
an organic crystal nucleating agent to wet pulverization in the
presence of the above-mentioned pulverization aid ester in the step
(1) is melt-kneaded with a polylactic acid resin in the step (2),
so that the pulverization aid ester existing on the surface of the
finely pulverized organic crystal nucleating agent acts as a
plasticizer, whereby a polylactic acid resin composition having a
favorable crystallization velocity and heat resistance can be
obtained without separately adding a plasticizer in the
melt-kneading step.
[0129] As the plasticizer, the same ones as the pulverization aid
ester used in the step (1) can be used, and the plasticizer and the
pulverization aid ester are contained in a total amount of
preferably from 0.05 to 3 parts by weight, and more preferably from
0.10 to 2 parts by weight, based on 100 parts by weight of the
polylactic acid resin, from the viewpoint of heat resistance,
transparency, and moldability of the molded article made of the
polylactic acid resin composition.
[0130] (Hydrolysis Inhibitor)
[0131] The polylactic acid resin composition of the present
invention can further contain a hydrolysis inhibitor, from the
viewpoint of improving durability and hydrolysis resistance. The
hydrolysis inhibitor includes carbodiimide compounds such as
polycarbodiimide compounds and monocarbodiimide compounds, and the
polycarbodiimide compounds are preferred from the viewpoint of
durability and impact resistance of the polylactic acid resin
composition, and the monocarbodiimide compounds are preferred from
the viewpoint of durability and moldability (fluidity) of the
polylactic acid resin composition. It is preferable that the
monocarbodiimide compound and the polycarbodiimide compound are
used together, from the viewpoint of even more improving
durability, impact resistance, and moldability of the molded
article made of the polylactic acid resin composition.
[0132] The polycarbodiimide compound includes
poly(4,4'-diphenylmethanecarbodiimide),
poly(4,4'-dicyclohexylmethanecarbodiimide),
poly(1,3,5-triisopropylbenzene)polycarbodiimide,
poly(1,3,5-triisopropylbenzene and
1,5-diisopropylbenzene)polycarbodiimide, and the like. The
monocarbodiimide compound includes
N,N'-di-2,6-diisopropylphenylcarbodiimide, and the like.
[0133] In order to satisfy durability, impact resistance, and
moldability of the molded article made of the polylactic acid resin
composition, the above-mentioned carbodiimide compounds may be used
alone or in a combination of two or more kinds. In addition, as the
poly(4,4'-dicyclohexylmethanecarbodiimide), Carbodilite LA-1
(manufactured by Nisshin Boseki) can be purchased and used; as the
poly(1,3,5-triisopropylbenzene)polycarbodiimide and
poly(1,3,5-triisopropylbenzene and
1,5-diisopropylbenzene)polycarbodiimide, Stabaxol P and Stabaxol
P-100 (manufactured by Rhein Chemie) can be purchased and used; and
as N,N'-di-2,6-diisopropylphenylcarbodiimide, Stabaxol 1
(manufactured by Rhein Chemie) can be purchased and used,
respectively.
[0134] The hydrolysis inhibitor is contained in an amount of
preferably from 0.05 to 3 parts by weight, and more preferably from
0.10 to 2 parts by weight, based on 100 parts by weight of the
polylactic acid resin, from the viewpoint of transparency and
moldability of the molded article made of the polylactic acid resin
composition.
[0135] In addition, the polylactic acid resin composition of the
present invention contains, in addition to those mentioned above,
an inorganic filler, from the viewpoint of further improving the
physical properties such as rigidity.
[0136] (Inorganic Filler)
[0137] As the inorganic filler, the filler in the form of fibers,
plates, granules, or powders which are ordinarily usable in the
reinforcement of a thermoplastic resin can be used. Specific
examples include fibrous inorganic fillers such as glass fiber,
asbestos fiber, carbon fiber, graphite fiber, metal fiber,
potassium titanate whisker, aluminum borate whisker,
magnesium-based whisker, silicon-based whisker, wollastonite,
sepiolite, asbestos, slag fiber, xonotlite, ellestadite, gypsum
fiber, silica fiber, silica alumina fiber, zirconia fiber, boron
nitride fiber, silicon nitride fiber, and boron fiber; inorganic
fillers in the form of plates or granules, such as glass flake,
non-swellable mica, swellable mica, graphite, metal foil, ceramic
beads, talc, clay, mica, sericite, zeolite, bentonite, organic
modified bentonite, organic modified montmorillonite, dolomite,
kaolin, fine silicic acid powder, feldspar powder, potassium
titanate, silica balloon, calcium carbonate, magnesium carbonate,
barium sulfate, calcium oxide, aluminum oxide, titanium oxide,
aluminum silicate, silicon oxide, gypsum, novaculite, dawsonite,
and white clay. Among these inorganic fillers, carbon fiber, glass
fiber, wollastonite, mica, talc, and kaolin are preferred. In
addition, the fibrous filler has an aspect ratio of preferably 5 or
more, more preferably 10 or more, and even more preferably 20 or
more.
[0138] The above-mentioned inorganic filler may be subjected to a
coating or binding treatment with a thermoplastic resin such as an
ethylene/vinyl acetate copolymer, or with a thermosetting resin
such as an epoxy resin, or the inorganic filler may be treated with
a coupling agent such as amino silane or epoxy silane.
[0139] The inorganic filler is contained in an amount of preferably
from 1 to 100 parts by weight, and more preferably from 5 to 50
parts by weight, based on 100 parts by weight of the polylactic
acid resin.
[0140] (Organic Filler)
[0141] In addition, it is preferable that the polylactic acid resin
composition of the present invention further contains, in addition
to those mentioned above, an organic filler, from the viewpoint of
improving physical properties such as rigidity.
[0142] As the organic filler, the filler in the form of chips,
fibers, plates or powders that are ordinarily usable in
reinforcement of a thermoplastic resin can be used. Specific
examples thereof include those in the form of chips such as husks,
wood chips, bean-curd refuse, wastepaper-crushed material, and
clothing crushed material; those in the form of fibers, such as
plant fibers such as cotton fiber, flax fiber, bamboo fiber, wood
fiber, kenaf fiber, jute fiber, banana fiber, or coconut fiber, or
pulps or cellulose fiber processed from these plant fibers, and
animal fibers such as silk, wool, Angora, cashmere, or camel; those
in the form of powders such as pulp powder, paper powder, wood
powder, bamboo powder, cellulose powder, husk powder, fruit shell
powder, chitin powder, chitosan powder, protein, or starch. Those
in the form of powders such as paper powder, wood powder, bamboo
powder, cellulose powder, kenaf powder, husk powder, fruit shell
powder, chitin powder, chitosan powder, protein powder, or starch
powder are preferred, and paper powder, wood powder, bamboo powder,
cellulose powder, and kenaf powder are more preferred, from the
viewpoint of moldability. In addition, it is preferable to use an
organic filler in the form of a powder in which a cellulose is
amorphized with a vibrating rod mill, a beads mill or the like,
from the viewpoint of improving toughness.
[0143] The organic filler is contained in an amount of preferably
from 1 to 100 parts by weight, and more preferably from 5 to 50
parts by weight, based on 100 parts by weight of the polylactic
acid resin.
[0144] (Other Resins and Additives)
[0145] The polylactic acid resin composition of the present
invention can contain a high-strength organic synthetic fiber, from
the viewpoint of improving physical properties such as strength,
heat resistance, and impact resistance of the molded article made
of the polylactic acid resin composition. Specific examples of the
high-strength organic synthetic fiber include aramide fiber,
polyarylate fiber, PBO fiber, and the like, and the aramide fiber
is preferred, from the viewpoint of heat resistance. The
high-strength organic synthetic fiber is contained in an amount of
preferably from 3 to 20 parts by weight, and more preferably from 5
to 10 parts by weight, based on 100 parts by weight of the
polylactic acid resin.
[0146] The polylactic acid resin composition of the present
invention can contain other resins, from the viewpoint of improving
physical properties such as rigidity, flexibility, heat resistance,
and durability of the molded article made of the polylactic acid
resin composition. Specific examples of other resins include
thermoplastic resins such as polyethylene, polypropylene,
polystyrene, ABS resins, AS resins, acrylic resins, polyamides,
polyphenylene sulfide, polyether ether ketone, polyesters,
polyacetals, polysulfone, polyphenylene oxide, polyimide,
polyetherimide, and the like, or flexible thermoplastic resins such
as ethylene/glycidyl methacrylate copolymers, polyester elastomers,
polyamide elastomers, ethylene/propylene terpolymers,
ethylene/buten-1-e copolymers; thermosetting resins such as phenol
resins, melamine resins, unsaturated polyester resins, silicone
resins, and epoxy resins; and the like. Among them, a resin which
has a bond containing a carbonyl group, such as amide bond, an
ester bond, or carbonate bond is preferred, because the resin is
likely to have a structurally high affinity with a polylactic acid
resin, from the viewpoint of compatibility with the polylactic acid
resin.
[0147] The polylactic acid resin composition of the present
invention can further contain a flame retardant, from the viewpoint
of improving physical properties such as rigidity, flexibility,
heat resistance, and durability of the molded article made of the
polylactic acid resin composition. Specific examples of the flame
retardant include halogen-containing compounds, containing bromine
or chlorine, such as tetrabromobisphenol-A-epoxy oligomer,
tetrabromobisphenol-A-carbonate oligomer, and brominated epoxy
resin; inorganic flame retardants such as antimony trioxide and
zinc borate; silicone-based flame retardants such as silicone
resins and silicone oil; inorganic hydrates such as aluminum
hydroxide and magnesium hydroxide (preferably surface-treated with
a silane coupling agent, especially isocyanate silane, from the
viewpoint of physical properties); phosphorus-containing compounds
such as triarylisopropyl phosphate, condensed phosphoric ester,
melamine polyphosphoric acid, piperazine polyphosphoric acid, and
phosphazene compounds; and nitrogen-containing compounds such as
melamine cyanurate; and the like, and the inorganic hydrate or the
phosphorus-containing compound is preferred from the viewpoint of
safety, and a combined use of the inorganic hydrate and the
phosphorus-containing compound is preferred from the viewpoint of
physical properties. The flame retardant is contained in an amount
of preferably from 10 to 60 parts by weight, and more preferably
from 15 to 50 parts by weight, based on 100 parts by weight of the
polylactic acid resin.
[0148] The polylactic acid resin composition of the present
invention may contain a core-shell shaped rubber, from the
viewpoint of improving physical properties such as impact
resistance and toughness of the molded article made of the
polylactic acid resin composition. Specific examples thereof
include (core: silicone/acrylic polymer, shell: methyl methacrylate
polymer), (core: silicone/acrylic polymer, shell: methyl
methacrylate/glycidyl methacrylate polymer), (core:
butadiene/styrene polymer, shell: methyl methacrylate polymer),
(core: acrylic polymer, shell: methyl methacrylate polymer), and
the like. As a commercially available product, METABLEN S-2006,
S-2100, S-2200, manufactured by Mitsubishi Rayon, PARALOID BPM-500,
manufactured by Rohm and Haas are preferred, from the viewpoint of
transparency. The core-shell shaped rubber is contained in an
amount of preferably from 2 to 30 parts by weight, more preferably
from 3 to 20 parts by weight, based on 100 parts by weight of the
polylactic acid resin.
[0149] The polylactic acid resin composition of the present
invention can further contain, in addition to those mentioned
above, a hindered phenol-based or phosphite-based antioxidant, or a
lubricant such as an aliphatic amide, a metal salt of a fatty acid,
a hydrocarbon-based wax or an anionic surfactant. Each of the
antioxidant or lubricant is contained in an amount of preferably
from 0.05 to 3 parts by weight, and more preferably from 0.10 to 2
parts by weight, based on 100 parts by weight of a polylactic acid
resin.
[0150] The polylactic acid resin composition of the present
invention can further contain, as other components besides those
mentioned above, one or more of ordinary additives, including, for
example, ultraviolet absorbents such as benzophenone compounds,
benzotriazole compounds, aromatic benzoate compounds, oxalic acid
anilide compounds, cyanoacrylate compounds, and hindered amine
compounds, thermal stabilizers such as hindered phenol compounds,
phosphite compounds, and thioether compounds, antistatic agents,
anti-clouding agents, photostabilizers, blowing agents, mold
releasing agents, colorants including dyes and pigments,
mildewproof agents, and bactericidal agents, within the range that
would not impair the objective of the present invention.
[0151] The step (2) is a step of melt-kneading a raw material for a
polylactic acid resin composition containing the above-mentioned
finely pulverized organic crystal nucleating agent composition, the
polylactic acid resin, and optionally various additives, and
specifically, the step includes a step of melt-kneading the
components at 160.degree. to 250.degree. C. with a twin-screw
extruder or the like. In addition, the melt-kneading temperature is
preferably from 160.degree. to 250.degree. C., more preferably from
165.degree. to 230.degree. C., even more preferably from
170.degree. to 210.degree. C., and still even more preferably from
170.degree. to 200.degree. C., from the viewpoint of moldability
and degradation inhibition of the polylactic acid resin
composition.
[0152] Thus, the polylactic acid resin composition is obtained
according to the method of the present invention. Accordingly, the
present invention also provides a polylactic acid resin composition
obtainable by the method of the present invention. The polylactic
acid resin composition of the present invention has some advantages
that the polylactic acid resin composition has excellent
workability and can be worked at a low temperature of, for example,
200.degree. C. or lower, so that the degradation of the
pulverization aid ester and the plasticizer mentioned above are
less likely to take place, whereby the polylactic acid resin
composition can be used in various applications by molding into
films and sheets. Further, the polylactic acid resin composition
has an even higher crystallization velocity, so that molding can be
carried out at a low die temperature and in a short time period in
the injection molding.
Polylactic Acid Resin Molded Article and Production Method
Thereof
[0153] The molded article of the polylactic acid resin of the
present invention is obtainable by molding a polylactic acid resin
composition of the present invention. Specifically, the finely
pulverized organic nucleating agent composition and the polylactic
acid resin mentioned above are mixed using an extruder or the like,
and while melting the components, a plasticizer or a hydrolysis
inhibitor or the like is blended therewith as needed, and a molten
product obtained is subsequently filled in a die and molded with an
injection-molding machine or the like.
[0154] A preferred method for producing a molded article of a
polylactic acid resin of the present invention is a method
including the steps of subjecting an organic crystal nucleating
agent to a wet pulverization in the presence of the above-mentioned
pulverization aid ester, to give a finely pulverized organic
crystal nucleating agent composition [step (1)]; melt-kneading a
raw material for a polylactic acid resin composition containing the
finely pulverized organic crystal nucleating agent composition
obtained in the step (1) and a polylactic acid resin [step (2)];
and filling a molten product obtained in the step (2) in a die at
110.degree. C. or lower, and molding the molten product [step
(3)].
[0155] In the present invention, a method including the steps of,
subsequent to the step (2), cooling the product to make it in an
amorphous state, in other words, a state where a degree of
crystallinity as measured by a wide angle X-ray diffraction method
is 1% or less, and thereafter carrying out the step (3), or a
method including the steps of, subsequent to the step (2), cooling
the product and immediately carrying out the step (3) is preferred.
The method including the steps of, subsequent to the step (2),
cooling the product and immediately carrying out the step (3) is
more preferred, from the viewpoint of exhibiting an effect of
improving a crystallization velocity of the polylactic acid
resin.
[0156] Specific examples of the step (3) include, for example, a
step of filling a polylactic acid resin composition of the present
invention in a die at 110.degree. C. or lower, and molding the
composition with an injection-molding machine or the like. The die
temperature in the step (3) is preferably 110.degree. C. or lower,
more preferably 90.degree. C. or lower, and even more preferably
80.degree. C. or lower, from the viewpoint of improving a
crystallization velocity of the polylactic acid resin composition
and improving workability. Also, the die temperature is preferably
30.degree. C. or higher, more preferably 40.degree. C. or higher,
and even more preferably 60.degree. C. or higher. From the above
viewpoint, the die temperature is preferably from 30.degree. to
110.degree. C., more preferably from 40.degree. to 90.degree. C.,
and even more preferably from 60.degree. to 80.degree. C. The
polylactic acid resin composition of the present invention has an
excellent crystallization velocity and is capable of working at low
temperatures, a molded article having sufficient heat resistance
can be obtained even at the above-mentioned die temperature.
[0157] The retention time in the die in the step (3) is preferably
from 20 to 90 seconds, more preferably from 20 to 80 seconds, and
even more preferably 20 to 60 seconds, from the viewpoint of heat
resistance and productivity of the molded article made of the
polylactic acid resin composition. In other words, since the
polylactic acid resin composition obtained by the method of the
present invention has a high crystallization velocity, a molded
article having sufficient heat resistance, made of the polylactic
acid resin composition can be obtained even with a short retention
time as mentioned above.
[0158] The heat resistance of the molded article made of the
polylactic acid resin composition is proportional to the size of
the relative crystallinity. Here, the term relative crystallinity
as used herein refers to a crystallinity that is expressed by the
following formula:
Relative
Crystallinity(%)={(.DELTA.Hm-.DELTA.Hcc)/.DELTA.Hm.times.100}
Specifically, the relative crystallinity can be obtained with a DSC
apparatus (Diamond DSC, commercially available from Perkin-Elmer),
using .DELTA.Hcc, which is an absolute value of a cold
crystallization enthalpy of a polylactic acid resin observed in 1st
RUN and .DELTA.Hm, melt crystallization enthalpy observed in 2nd
RUN, wherein 1st RUN includes the steps of heating from 20.degree.
to 200.degree. C. at a heating rate of 20.degree. C./minute,
holding at 200.degree. C. for 5 minutes, cooling from 200.degree.
to 20.degree. C. at a cooling rate of -20.degree. C./minute,
holding at 20.degree. C. for 1 minute, and 2nd RUN includes, after
1st RUN, the step of heating from 20.degree. to 200.degree. C. at a
heating rate of 20.degree. C./minute.
EXAMPLES
[0159] The following examples further describe and demonstrate
embodiments of the present invention. The examples are given solely
for the purposes of illustration and are not to be construed as
limitations of the present invention. Parts in Examples are parts
by weight, unless specified otherwise.
[0160] [Weight-Average Molecular Weight (Mw) of Polylactic Acid
Resin]
[0161] The weight-average molecular weight (Mw) is measured in
accordance with GPC (gel permeation chromatography), under the
following measurement conditions.
Measurement Conditions
[0162] Column: GMHHR-H+GMHHR-H [0163] Column Temperature:
40.degree. C. [0164] Detector: RI [0165] Eluent: chloroform [0166]
Flow Rate: 1.0 mL/min [0167] Sample Concentration: 1 mg/mL [0168]
Amount Injected: 0.1 mL [0169] Calculation standard:
polystyrene
[0170] [Optical Purity of Polylactic Acid]
[0171] The optical purity of a polylactic acid is measured in
accordance with the measurement method for D-form content described
in "Poriorefin-toh Gosei-jushi-sei Shokuhin Youki Houso-toh ni
Kansuru Jishukijun (Self-Standards Concerning Food Containers and
Wrappings Made of Synthetic Resins Such as Polyolefins)," Revised
Third Edition, supplemented in June, 2004, Chapter 3 Eisei Shikenho
(Hygienic Test Method), p. 12-13'' under the following measurement
conditions. Specifically, 10 mL of 0.7 mol/L sodium hydroxide in
methanol is added to an accurately weighed polylactic acid (500
mg), and a mixture is set in a water bath shaking machine set at
65.degree. C., and allowed to be hydrolyzed until the resinous
components are formed into a homogeneous solution. Further, a
diluted hydrochloric acid (2 mol/L hydrochloric acid) is added to
an alkaline solution after hydrolysis is completed to neutralize,
and the hydrolyzed solution is diluted to a certain volume with
pure water. Thereafter, a given volume of the dilution is separated
in a volumetric flask, and the separated solution is diluted with a
mobile phase solution for high-performance liquid chromatography
(HPLC). The pH of the dilution is adjusted to a range of from 3 to
7, and the dilution in the volumetric flask is quantified, and
filtered with a membrane filter (0.45 .mu.m). The resulting
prepared solution is quantified for D-lactic acid and L-lactic acid
in accordance with HPLC, whereby optical purity of the polylactic
acid resin can be obtained.
Measurement Conditions for HPLC
[0172] Column: Optically Resolution Column [0173] SUMICHIRAL OA6100
(46 mm.phi..times.150 mm, 5 .mu.m), manufactured by Sumika Chemical
Analysis Service, Ltd. [0174] Pre-Column: Optically Resolution
Column [0175] SUMICHIRAL QA6100 (4 mm.phi..times.10 mm, 5 .mu.m),
manufactured by Sumika Chemical Analysis Service, Ltd. [0176]
Column Temperature: 25.degree. C. [0177] Mobile Phase: 2.5%
Methanol-containing 1.5 mM aqueous copper sulfate solution [0178]
Flow Rate of Mobile Phase: 1.0 mL/minute [0179] Detector:
Ultraviolet Detector (UV 254 nm) [0180] Amount of Injection: 20
.mu.L
[0181] [Melting Point of Crystal Nucleating Agent]
[0182] The melting point is measured with a DSC apparatus (Diamond
DSC, manufactured by Perkin-Elmer) by heating a sample from
20.degree. to 500.degree. C. at a heating rate of 10.degree.
C./minute.
[0183] [Particle Size of Crystal Nucleating Agent]
[0184] The particle size (nm) of the crystal nucleating agent is
measured by diluting a crystal nucleating agent so as to have a
concentration of 0.5% by weight with ethanol (Cica first grade,
manufactured by KANTO CHEMICAL CO., INC.), dispersing the dilution
with a ultrasonicator (device name: 1510J-MT, manufactured by
Yamato Kagaku) for 5 minutes, charging a glass cell (optical path
length 10 mm.times.width 10 mm.times.height 45 mm, glass 2-sided
transparent cell, manufactured by Sansyo Co., Ltd.) up to a height
of 10 mm from the bottom with a solution obtained, and carrying out
the measurement at 25.degree. C. using Zetasizer Nano-S
(manufactured by SYSMEX CORPORATION, dynamic light scattering
measurement instrument).
[0185] [Viscosity of Carboxylic Acid Ester and Phosphoric
Ester]
[0186] The viscosity is measured at 23.degree. C. with BII-type
viscometer BLII (manufactured by TOKI SANGYO CO., LTD.) on the
basis of the method for measuring viscosity according to S-method
as prescribed in JIS K7117 (rotational speed: 12 r/min).
[0187] [Weight-Average Molecular Weight of (Mw) of Carboxylic Acid
Ester and Phosphoric Ester]
[0188] The weight-average molecular weight (Mw) is measured in
accordance with GPC (gel permeation chromatography), under the
following measurement conditions.
Measurement Conditions
[0189] Column: TSKPWXL+G4000PWXL+G2500PWXL (all manufactured by
Tosoh Corporation) [0190] Column Temperature: 40.degree. C. [0191]
Detector: RI (210 nm) [0192] Eluent: 0.2 mol/L phosphate
buffer/acetonitrile (9/1) [0193] Flow Rate: 10 mL/min [0194] Sample
Concentration: 1 mg/mL [0195] Amount Injected: 0.1 mL [0196]
Standard: polyethylene glycol
Production Example 1 for Organic Crystal Nucleating Agent
Barium di(dimethyl 5-Sulfoisophthalate)
[0197] A reactor equipped with a stirrer was charged with 296 g of
sodium dimethyl 5-sulfoisophthalate and 2,000 g of ion-exchanged
water, and the contents were heated to 80.degree. C. while stirring
to dissolve. Thereto was gradually added dropwise a solution
prepared by dissolving 104 g barium chloride in 900 g of
ion-exchanged water under stirring. After cooling the mixture to
30.degree. C., the formed white particles were filtered, and the
white particles obtained were dispersed in 3,000 g of ion-exchanged
water. The dispersion was heated to 80.degree. C. and kept thereat
for 1 hour, and thereafter cooled to 30.degree. C., and a white
powder was separated by filtration and washed. Similar washing
procedures were carried out another time, and the white powder was
then dried at 120.degree. C. for 5 hours, to give 297 g of a white
powder of barium di(dimethyl 5-sulfoisophthalate).
Production Example 2 for Organic Crystal Nucleating Agent
p-Xylylenebis Rosin Acid Amide
[0198] A reaction vessel equipped with a condenser tube and a
stirring device was charged with 21.8 g (0.16 mol) of
p-xylylenediamine and 256.6 g of tetrahydrofuran to dissolve, and
thereto was added dropwise a solution prepared by mixing 26.1 g
(0.08 mol) of dehydroabietic acid chloride and 130.5 g of
tetrahydrofuran while stirring at room temperature over one and a
half hours. After stirring the contents overnight, a liquid
reaction mixture was filtered to remove by-products. About 40 g of
crude crystals obtained by distilling away the tetrahydrofuran from
the filtrate was dissolved in 1,200 g of methyl isobutyl ketone,
the solution was washed with a 10% hydrochloric acid, and then with
ion-exchanged water. After drying the solution with magnesium
sulfate, a liquid reaction mixture was concentrated to a total
weight of 430 g, and then allowed to recrystallize. Twenty-seven
grams of the crude crystals obtained were dissolved in 400 g of
methyl isobutyl ketone, concentrated to a total weight of 300 g,
and then allowed to recrystallize. The crude crystals were dried
under a reduced pressure at 100.degree. C. to provide 13.6 g of
p-xylylenebis rosin acid amide.
Production Example 1 of Carboxylic Acid Ester
Diester Formed Between Succinic Acid and Triethylene Glycol
Monomethyl Ether
[0199] A 3-L flask equipped with a stirrer, a thermometer, and a
dehydration tube was charged with 500 g of succinic anhydride, 2463
g of triethylene glycol monomethyl ether, and 9.5 g of
paratoluenesulfonic acid monohydrate, and the contents were reacted
at 110.degree. C. for 15 hours under a reduced pressure (4 to 10.7
kPa), while blowing nitrogen (500 mL/min) into a space portion. The
liquid reaction mixture had an acid value of 1.6 (KOH mg/g). To the
liquid reaction mixture was added 27 g of an adsorbent KYOWAAD
500SH (manufactured by Kyowa Chemical Industry Co., Ltd.), and the
mixture was stirred at 80.degree. C. and 2.7 kPa for 45 minutes,
and filtered. Thereafter, triethylene glycol monomethyl ether was
distilled off at a liquid temperature of from 115.degree. to
200.degree. C. and a pressure of 0.03 kPa, and after cooling to
80.degree. C., the residue was filtered in vacuo, to provide a
diester formed between succinic acid and triethylene glycol
monomethyl ether [(MeEO.sub.3).sub.2SA] as a filtrate. The diester
obtained had a weight-average molecular weight of 410, a viscosity
at 23.degree. C. of 27 mPas, an acid value of 0.2 KOH mg/g, a
saponification value of 274 KOH mg/g, a hydroxyl value of 1 KOH
mg/g or less, and a hue APHA of 200.
Production Example 2 of Carboxylic Acid Ester
Triester Compound Formed Between Acetic Acid and Ethylene Oxide
Adduct of Glycerol Added with 6 mol of Ethylene Oxide
[0200] An autoclave was charged with given amounts of a
concentrated glycerol for cosmetics manufactured by Kao Corporation
and ethylene oxide in a molar ratio of 6 mol of ethylene oxide per
one mol of the concentrated glycerol, and the contents were reacted
at 150.degree. C. with applying a constant pressure of a reaction
pressure of 0.3 MPa using 1% by mol KOH as a catalyst until the
pressure becomes constant. Thereafter, the reaction mixture was
cooled to 80.degree. C., to provide a catalyst-non-neutralized
product. To this product was added a catalyst which is an adsorbent
KYOWAAD 600S (manufactured by Kyowa Chemical Industry Co., Ltd.),
in an amount 8 times the weight of the catalyst to carry out an
adsorption treatment in the presence of nitrogen for 80.degree. C.
for 1 hour. Further, the adsorbent was filtered off from the liquid
mixture after the treatment with a Buchner funnel fitted with a No.
2 filter paper pre-coated with Radiolite #900, to provide an
ethylene oxide (6 mol) adduct of glycerol (hereinafter referred to
as POE(6) glycerol. A four-neck flask was charged with this
product, and the contents were heated to 105.degree. C., and
stirred at 300 r/min. Acetic acid anhydride was added dropwise over
about an hour in a given amount in a ratio of 7.2 mol of acetic
acid anhydride per one mol of POE(6) glycerol, and the components
were reacted. After the dropwise addition, the reaction mixture was
aged at 110.degree. C. for 2 hours, and further aged at 120.degree.
C. for 1 hour. After aging, unreacted acidic acid anhydride and a
by-product acetic acid were topped off under a reduced pressure,
and the residue was further steamed, to provide POE(6) glycerol
triacetate. The POE(6) glycerol triacetate obtained had a
weight-average molecular weight of 490 and a viscosity at
23.degree. C. of 79 mPas.
Production Example 3 of Carboxylic Acid Ester
Polyester-Polyol
[0201] A 1-liter glass reactor equipped with a reflux condenser, a
heating device, a thermometer, a pressure gauge and the like was
charged with 478 g of succinic acid and 668 g of triethylene
glycol, and a space portion of the reactor was replaced with a
nitrogen gas. Thereafter, the contents of the reactor were heated
to initiate the reaction. Thereafter, the internal temperature was
raised from 200.degree. to 210.degree. C. over 2 hours, and the
contents were kept at this temperature until the termination of the
reaction. On the other hand, the pressure inside the reactor was
maintained at 87 kPa at a degree of vacuum against a normal
pressure from a time point at which the internal temperature was
180.degree. C. up to a point where the internal temperature reached
200.degree. C. Thereafter, the reactor was charged with 0.05% by
weight of tetraisopropyl titanate (based on a total amount charged)
as a catalyst, and the pressure was gradually reduced to 4 kPa over
4 hours within the range in which the raw material alcohol was not
distilled off, and this pressure was kept until the reaction was
terminated. A part of the composition was taken out to measure an
acidic value. Having confirmed that the acidic value is less than
2.0 mg KOH/g, the reaction was terminated, to provide 1 kg of an
esterification reaction product. The esterified product had an acid
value of 0.9 mg KOH/g, a hydroxyl value of 51 mg KOH/g, a water
content of 0.04 g, a weight-average molecular weight of 2,200, and
a viscosity at 23.degree. C. of 21,000 mPas.
Production Example 4 of Carboxylic Acid Ester
Triester Formed Between 1,3,6-Hexanetricarboxylic Acid and
Triethylene Glycol Monomethyl Ether
[0202] A 1-L flask equipped with a stirrer, a thermometer, and a
dehydration tube was charged with 139 g of
1,3,6-hexanetricarboxylic acid, 376 g of triethylene glycol
monomethyl ether, and 1.59 g of dibutyltin oxide, and the contents
were reacted at 185.degree. C. for 12 hours. After the termination
of the reaction, 1.2 g of 85% phosphoric acid was added thereto,
and the mixture was heated at 70.degree. C. for 30 minutes while
stirring. Thereafter, KYOWAAD 600S (manufactured by Kyowa Chemical
Industry Co., Ltd.) was added thereto to carry out an adsorption
treatment, and the adsorbed mixture was filtered under pressure.
Further, excess triethylene glycol was distilled off under a
reduced pressure, and the residue was filtered under pressure, to
provide a triester formed between 1,3,6-hexanetricarboxylic acid
and triethylene glycol monomethyl ether. The triester obtained had
a weight-average molecular weight of 656 and a viscosity at
23.degree. C. of 40 mPas.
Production Example 5 of Carboxylic Acid Ester
Diester Formed Between Dimethyl Succinate and Diethylene Glycol
[0203] A four-neck flask (equipped with a stirrer, a thermometer, a
dropping funnel, a distillation tube, and a nitrogen gas inlet
tube) was charged with 999 g (9.41 mol) of diethylene glycol and
23.6 g of a methanol solution containing 28% by weight of sodium
methoxide (sodium methoxide: 0.122 mol) as a catalyst, and methanol
was distilled off at a normal pressure (101.3 kPa) and 120.degree.
C. for 0.5 hours, while stirring. Thereafter, 4125 g (28.2 mol) of
dimethyl succinate (manufactured by Wako Pure Chemical Industries,
Ltd.) was added dropwise thereto over 3 hours, and methanol formed
by the reaction was distilled off at a normal pressure and
120.degree. C. Next, the residue was cooled to 75.degree. C., and
the pressure was gradually reduced from a normal pressure to 6.7
kPa over 2 hours to distill off methanol. Thereafter, the pressure
was returned to a normal pressure, and further 4.4 g of a methanol
solution containing 28% by weight sodium methoxide (sodium
methoxide: 0.023 mol) was added as a catalyst. The pressure was
gradually reduced from a normal pressure to 2.9 kPa over 2 hours at
100.degree. C. to distill off methanol. Thereafter, the residue was
cooled to 80.degree. C., 41 g of KYOWAAD 600S (manufactured by
Kyowa Chemical Industry Co., Ltd.) was added thereto, and the
mixture was stirred at a pressure of 4.0 kPa and 80.degree. C. for
1 hour, and then filtered in vacuo. The filtrate was heated to a
temperature of from 70.degree. C. to 190.degree. C. over 4 hours at
a pressure of 0.3 kPa to distill off unreacted dimethyl succinate,
to provide a yellow liquid (ester compound A). The amount of the
catalyst used is 0.51 mol per 100 mol of the dicarboxylic acid
ester. The ester compound obtained had a weight-average molecular
weight of 450 and a viscosity at 23.degree. C. of 260 mPas.
Production Example 1 of Phosphoric Ester
Tris(ethoxyethoxyethyl) Phosphate
[0204] A 1-liter four-neck flask was charged with 600 g (4.47 mol)
of diethylene glycol monoethyl ether, and the content was stirred
under a reduced pressure (20 kPa), while blowing a dry nitrogen gas
at a flow rate of 50 mL per minute. Next, 114 g (0.745 mol) of
phosphorus oxychloride was slowly added dropwise while keeping the
internal of the reaction system at room temperature (15.degree.
C.), and the mixture was then aged at 40.degree. to 60.degree. C.
for 5 hours. Thereafter, 149 g of a 16% by weight aqueous sodium
hydroxide solution was added thereto to neutralize, and an excess
unreacted diethylene glycol monoethyl ether was distilled off in
vacuo under the temperature conditions of from 70.degree. to
120.degree. C. Further, the residue was contacted with steam, to
provide 367 g of a crude phosphoric triester. Further, to this
crude phosphoric triester was added 300 g of a 16% by weight
aqueous sodium chloride solution to wash the crude phosphoric
triester. Thereafter, a lower layer of the separated layers was
discarded, and the remaining upper layer was dehydrated at
75.degree. C. under a reduced pressure, and thereafter further
filtered to remove a solid content, to provide 266 g of an intended
tris(ethoxyethoxyethyl) phosphate (yield: 80%). This
tris(ethoxyethoxyethyl) phosphate was a colorless, transparent
homogeneous liquid, and was subjected to chlorine ion analysis. As
a result, the tris(ethoxyethoxyethyl) phosphate had a chlorine ion
content of 10 mg/kg or less.
[0205] Next, production examples for finely pulverized crystal
nucleating agent compositions are shown. In addition, the average
particle sizes of the crystal nucleating agent compositions
obtained in the following Production Examples are shown in Tables 1
to 9.
Production Example 1 of Crystal Nucleating Agent Composition
[0206] Seven-hundred and twenty grams of the carboxylic acid ester
[(MeEO.sub.3).sub.2SA] obtained in Production Example 1 of
Carboxylic Acid Ester and 36 g of a zinc salt of an unsubstituted
phenylphosphonic acid (manufactured by NISSAN CHEMICAL INDUSTRIES,
LTD.: "ECOPROMOTE") were supplied into a media pulverizer
(manufactured by Igarashi Kikai Seizo, "Sand Grinder TSG-6H":
pulverizer volume: 800 mL, filled with 720 g of zirconia beads
having sizes of 1 mm.phi., filling ratio: 30%, agitation blade
diameter: 70 mm) While allowing to flow cold water through a jacket
of the pulverizer, the mixture was subjected to a pulverization
treatment at a rotational speed of 2,000 r/min (agitation
peripheral speed: 7 m/s) for 9 hours, to provide a crystal
nucleating agent-1 (finely pulverized zinc salt of phenylphosphonic
acid). The temperature during the operation was in the range of
from 10.degree. to 90.degree. C.
Production Example 2 of Crystal Nucleating Agent Composition
[0207] The same procedures as in Production Example 1 were carried
out except that the kinds of a carboxylic acid ester was changed to
"DAIFATTY-101" (manufactured by DAIHACHI CHEMICAL INDUSTRY CO.,
LTD., diester formed between adipic acid and a 1/1 mixture of
diethylene glycol monomethyl ether and benzyl alcohol), to provide
a crystal nucleating agent-2 (finely pulverized zinc salt of
phenylphosphonic acid).
Production Example 3 of Crystal Nucleating Agent Composition
[0208] The same procedures as in Production Example 2 were carried
out except that the amount of the carboxylic acid ester
[(MeEO.sub.3).sub.2SA] supplied was changed to 360 g, and at the
same time 360 g of "DAIFATTY-101" was supplied, to provide a
crystal nucleating agent-3 (finely pulverized zinc salt of
phenylphosphonic acid).
Production Example 4 of Crystal Nucleating Agent Composition
[0209] The same procedures as in Production Example 1 were carried
out except that the amount of the zinc salt of an unsubstituted
phenylphosphonic acid supplied was changed to 72 g, to provide a
crystal nucleating agent-4 (finely pulverized zinc salt of
phenylphosphonic acid).
Production Example 5 of Crystal Nucleating Agent Composition
[0210] The same procedures as in Production Example 1 were carried
out except that the amount of the zinc salt of an unsubstituted
phenylphosphonic acid supplied was changed to 144 g, to provide a
crystal nucleating agent-5 (finely pulverized zinc salt of
phenylphosphonic acid).
Production Example 6 of Crystal Nucleating Agent Composition
[0211] The same procedures as in Production Example 1 were carried
out except that the amount of the zinc salt of an unsubstituted
phenylphosphonic acid supplied was changed to 216 g, to provide a
crystal nucleating agent-6 (finely pulverized zinc salt of
phenylphosphonic acid).
Production Example 7 of Crystal Nucleating Agent Composition
[0212] The same procedures as in Production Example 1 were carried
out except that the amount of the zinc salt of an unsubstituted
phenylphosphonic acid supplied was changed to 18 g, to provide a
crystal nucleating agent-7 (finely pulverized zinc salt of
phenylphosphonic acid).
Production Example 8 of Crystal Nucleating Agent Composition
[0213] The same procedures as in Production Example 1 were carried
out except that the kind of the carboxylic acid ester was changed
from (MeEO.sub.3).sub.2SA to a triester compound formed between
acetic acid and ethylene oxide adduct of glycerol added with 6 mol
of ethylene oxide obtained in Production Example 2 of Carboxylic
Acid Ester [(AcEO.sub.6).sub.3Gly], to provide a crystal nucleating
agent-8 (finely pulverized zinc salt of phenylphosphonic acid).
Production Example 9 of Crystal Nucleating Agent Composition
[0214] The same procedures as in Production Example 1 were carried
out except that the kind of the carboxylic acid ester was changed
from (MeEO.sub.3).sub.2SA to a polyester-polyol obtained in
Production Example 3 of Carboxylic Acid Ester, to provide a crystal
nucleating agent-9 (finely pulverized zinc salt of phenylphosphonic
acid).
Production Example 10 of Crystal Nucleating Agent Composition
[0215] The same procedures as in Production Example 1 were carried
out except that the kind of the carboxylic acid ester was changed
from (MeEO.sub.3).sub.2SA to a polyester-polyol obtained in
Production Example 3 of Carboxylic Acid Ester, and that 36 g of the
zinc salt of an unsubstituted phenylphosphonic acid was changed to
720 g of talc (manufactured by Nippon Talc, "MICRO ACE P-6," to
provide a crystal nucleating agent-10.
Production Example 11 of Crystal Nucleating Agent Composition
[0216] The same procedures as in Production Example 1 were carried
out except that the kind of the carboxylic acid ester was changed
from (MeEO.sub.3).sub.2SA to a triester compound formed between
1,3,6-hexanetricarboxylic acid and triethylene glycol monomethyl
ether obtained in Production Example 4 of Carboxylic Acid Ester
[(MeEO.sub.3).sub.3HTC], to provide a crystal nucleating
agent-11.
Production Example 12 of Crystal Nucleating Agent Composition
[0217] Fifty grams of a zinc salt of an unsubstituted
phenylphosphonic acid (manufactured by NISSAN CHEMICAL INDUSTRIES,
LTD.: "ECOPROMOTE") was supplied into a vibration mill ("MB-1"
manufactured by CHUO KAKOHKI CO., LTD, entire vessel volume 3.5 L),
and the vibration mill was filled with 11 rods (cross-sectional
shape: circular, diameter: 30 mm, length: 218 mm, material:
stainless) (filling ratio 48%), and the content was subjected to a
treatment at an amplitude of 8 mm and a rotational speed of 1,200
r/min for 60 minutes, to provide a crystal nucleating agent-12.
Production Examples 13 to 47 of Crystal Nucleating Agent
Compositions
[0218] With reference to Production Example 1, crystal nucleating
agents-13 to -47 were obtained with the apparatus and under the
conditions as shown in Tables 3 to 10, using the kinds and the
amounts of the crystal nucleating agents and the pulverization aid
esters used in the step (1) shown in Tables 3 to 10.
[0219] Here, the raw materials in Tables 1 to 10 are as
follows.
Crystal Nucleating Agents
(Organic Crystal Nucleating Agent (a))
[0220] PY109: a compound having an isoindolinone backbone
(manufactured by Ciba Fine Chemical Co., Ltd., IRGAZIN Yellow
2GLTE) PY110: a compound having an isoindolinone backbone
(manufactured by Ciba Fine Chemical Co., Ltd., CROMOPHTAL Yellow
2RLP) PR272: a compound having a diketo-pyrrolo-pyrrole backbone
(manufactured by Ciba Fine Chemical Co., Ltd., CROMOPHTAL DPP Flame
Red FP) PR254(1): a compound having a diketo-pyrrolo-pyrrole
backbone (manufactured by Ciba Fine Chemical Co., Ltd., CROMOPHTAL
DPP Red RP) PR254(2): a compound having a diketo-pyrrolo-pyrrole
backbone (manufactured by Ciba Fine Chemical Co., Ltd., IRGAZIN DPP
Red BTR) PV32: a compound having a benzimidazolone backbone
(manufactured by Clariant Japan, Graphtol Bordeaux HF3R) PR185: a
compound having a benzimidazolone backbone (manufactured by
Clariant Japan, Graphtol Cermine HF4C) PR208: a compound having a
benzimidazolone backbone (manufactured by Clariant Japan, Graphtol
Red HF2B) PB15:3: a compound having a phthalocyanine backbone
(manufactured by Ciba Fine Chemical Co., Ltd., IRGALITE Blue GBP)
PB15: a compound having a phthalocyanine backbone (manufactured by
Ciba Fine Chemical Co., Ltd., IRGALITE Blue BLPO) PB15:6: a
compound having a phthalocyanine backbone (manufactured by
DAINIPPON INK AND CHEMICALS, INCORPORATED, FASTROGEN Blue EP-7) Vat
Blue1: a compound having an indigo backbone (manufactured by KANTO
CHEMICAL CO., INC.)
(Organic Crystal Nucleating Agent (b))
[0221] T-1287: decamethylenedicarbonyldibenzoyl hydrazide
(manufactured by ADEKA) XyStUre: xylenebis stearylurea
(manufactured by Nippon Kasei Chemical Co., Ltd., Hakreen SX)
6-MeUra: 6-methylurasil (manufactured by Wako Pure Chemical
Industries, Ltd.) MC-6000: melamine cyanurate (manufactured by
NISSAN CHEMICAL INDUSTRIES, LTD.)
(Organic Crystal Nucleating Agent (c))
[0222] PPA-Zn: a zinc salt of an unsubstituted phenylphosphonic
acid (manufactured by NISSAN CHEMICAL INDUSTRIES, LTD.:
"ECOPROMOTE") SIP2MeBa: barium di(dimethyl 5-sulfoisophthalate)
obtained in Production Example 1 for Organic Crystal Nucleating
Agent mentioned above NA-21: a sodium salt of phosphoric ester
(manufactured by ADEKA, ADK STAB NA-21 KM-1500: a magnesium salt of
rosin acid (manufactured by Arakawa Chemical Industries, Ltd.,
PINECRYSTAL KM-1500) BTTCHA: tricyclohexyl
1,3,5-benzenetricarboxylic acid amide (manufactured by New Japan
Chemical Co., Ltd., NJSTAR TF-1) XBRA: p-xylylenebis rosin acid
amide produced in Production Example 2 for Organic Crystal
Nucleating Agent mentioned above
(Other Crystal Nucleating Agent)
[0223] Talc: MICRO ACE P-6 (manufactured by Nippon Talc, no melting
point)
Pulverization Aid Esters
[0224] (MeEO.sub.3).sub.2SA: a diester compound formed between
succinic acid and triethylene glycol monomethyl ether produced in
Production Example 1 of Carboxylic Acid Ester mentioned above
(weight-average molecular weight: 410, viscosity: 27 mPas)
DAIFATTY-101: a diester formed between adipic acid and a 1/1
mixture of diethylene glycol monomethyl ether/benzyl alcohol
(manufactured by DAIHACHI CHEMICAL INDUSTRY CO., LTD.,
weight-average molecular weight: 338, viscosity: 19 mPas)
(AcEO.sub.6).sub.3Gly: a triester compound formed between acetic
acid and ethylene oxide adduct of glycerol added with 6 mol of
ethylene oxide produced in Production Example 2 of Carboxylic Acid
Ester mentioned above (weight-average molecular weight: 490,
viscosity: 79 mPas) Polyester-Polyol: a polyester-polyol produced
in Production Example 3 of Carboxylic Acid Ester mentioned above
(weight-average molecular weight: 2,200, viscosity: 21,000 m Pas)
(MeEO.sub.3).sub.3HTC: a triester formed between
1,3,6-hexanetricarboxylic acid and triethylene glycol monomethyl
ether produced in Production Example 4 of Carboxylic Acid Ester
mentioned above (weight-average molecular weight: 656, viscosity:
40 mPas) TEP-2: tris(ethoxyethoxyethyl) phosphate produced in
Production Example 1 of Phosphoric Ester mentioned above
(weight-average molecular weight: 446, viscosity: 13 mPas)
MeSA-DEG: a diester formed between dimethyl succinate and
diethylene glycol produced in Production Example 5 of Carboxylic
Acid Ester mentioned above (weight-average molecular weight: 450,
viscosity: 260 mPas)
TABLE-US-00001 TABLE 1 Prod. Ex. 1 Prod. Ex. 2 Prod. Ex. 3 Prod.
Ex. 4 Prod. Ex. 5 Prod. Ex. 6 Crystal Crystal Crystal Crystal
Crystal Crystal Nucleating Nucleating Nucleating Nucleating
Nucleating Nucleating Agent-1 Agent-2 Agent-3 Agent-4 Agent-5
Agent-6 Pulverizing Step (step (1)) Crystal Kind PPA-Zn PPA-Zn
PPA-Zn PPA-Zn PPA-Zn PPA-Zn Nucleating Particle Size.sup.1)
D.sub.50 (nm) 1090 1090 1090 1090 1090 1090 Agent D.sub.90 (nm)
1350 1350 1350 1350 1350 1350 D.sub.10 (nm) 880 880 880 880 880 880
Amount (g) 36 36 36 72 144 216 Pulverization Kind
(MeEO.sub.3).sub.2SA DAIFATTY-101 (MeEO.sub.3).sub.2SA/
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA Aid
Ester DAIFATTY-101 Weight-Average Molecular 410 338 374 410 410 410
Weight.sup.2) Viscosity (23.degree. C., 27 19 23 27 27 27 mPa
s).sup.3) Amount (g) 720 720 360/360 720 720 720 Crystal Nucleating
Agent/Pulverization 1/20 1/20 1/20 1/10 1/5 3/10 Aid Ester.sup.4)
Pulverization Kind of Pulverizer Sand Grinder Sand Grinder Sand
Grinder Sand Grinder Sand Grinder Sand Grinder Conditions Material
of Media Zirconia Zirconia Zirconia Zirconia Zirconia Zirconia
Shape of Media (.phi.: Outer 1 mm beads 1 mm beads 1 mm beads 1 mm
beads 1 mm beads 1 mm beads Diameter) Rotational Speed (r/min) 2000
2000 2000 2000 2000 2000 Treatment Time (hours) 9 9 9 9 9 9
Physical Properties of D.sub.50 (nm) 490 590 535 530 561 598
Crystal Nucleating Agent D.sub.90 (nm) 716 801 780 761 810 830
after Pulverizing Step D.sub.10 (nm) 312 380 354 339 364 399
(Particle Size).sup.5) D.sub.10/D.sub.50 0.6 0.6 0.7 0.6 0.6 0.7
D.sub.90/D.sub.50 1.5 1.4 1.5 1.4 1.4 1.4 .sup.1)Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00002 TABLE 2 Prod. Ex. 7 Prod. Ex. 8 Prod. Ex. 9 Prod.
Ex. 10 Prod. Ex. 11 Prod. Ex. 12 Crystal Crystal Crystal Crystal
Crystal Crystal Nucleating Nucleating Nucleating Nucleating
Nucleating Nucleating Agent-7 Agent-8 Agent-9 Agent-10 Agent-11
Agent-12 Pulverizing Step (step (1)) Crystal Kind PPA-Zn PPA-Zn
PPA-Zn Talc PPA-Zn PPA-Zn Nucleating Particle Size.sup.1) D.sub.50
(nm) 1090 1090 1090 3240 1090 1090 Agent D.sub.90 (nm) 1350 1350
1350 4210 1350 1350 D.sub.10 (nm) 880 880 880 6230 880 880 Amount
(g) 18 36 36 720 36 50 Pulverization Kind (MeEO.sub.3).sub.2SA
(AcEO.sub.6).sub.3Gly Polyester-Polyol Polyester-Polyol
(MeEO.sub.3).sub.3HTC -- Aid Ester Weight-Average Molecular 410 490
2200 2200 656 -- Weight.sup.2) Viscosity (23.degree. C., mPa
s).sup.3) 27 79 21000 21000 40 -- Amount (g) 720 720 720 720 720 --
Crystal Nucleating Agent/Pulverization 1/40 1/20 1/20 1/1 1/20 --
Aid Ester.sup.4) Pulverization Kind of Pulverizer Sand Grinder Sand
Grinder Sand Grinder Sand Grinder Sand Grinder Vibration Mill
Conditions Material of Media Zirconia Zirconia Zirconia Zirconia
Zirconia Stainless Steel Shape of Media (.phi.: Outer 1 mm beads 1
mm beads 1 mm beads 1 mm beads 1 mm beads 30 mm rod Diameter)
Rotational Speed (r/min) 2000 2000 2000 2000 2000 1200 Treatment
Time (hours) 9 9 9 9 9 1 Physical Properties of D.sub.50 (nm) 479
650 ND ND 1010 1290 Crystal Nucleating Agent D.sub.90 (nm) 709 920
ND ND 1320 1830 after Pulverizing Step D.sub.10 (nm) 308 452 ND ND
860 807 (Particle Size).sup.5) D.sub.10 /D.sub.50 0.6 0.7 ND ND 0.9
0.6 D.sub.90/D.sub.50 1.5 1.4 ND ND 1.3 1.4 .sup.1)Particle size of
a crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to D.sub.50.
ND: not determined
TABLE-US-00003 TABLE 3 Prod. Ex. 13 Prod. Ex. 14 Crystal Crystal
Nucleating Nucleating Pulverizing Step (step (1)) Agent-13 Agent-14
Crystal Kind PPA-Zn PPA-Zn Nucleating Particle Size.sup.1) D.sub.50
(nm) 1090 1090 Agent D.sub.90 (nm) 1350 1350 D.sub.10 (nm) 880 880
Amount (g) 36 36 Pulverization Kind TEP-2 MeSA-DEG Aid Ester
Weight-Average Molecular Weight.sup.2) 446 450 Viscosity
(23.degree. C., mPa s).sup.3) 13 260 Amount (g) 720 720 Crystal
Nucleating Agent/Pulverization Aid Ester.sup.4) 1/20 1/20
Pulverization Kind of Pulverizer Sand Grinder Sand Grinder
Conditions Material of Media Zirconia Zirconia Shape of Media
(.phi.: Outer Diameter) 1 mm beads 1 mm beads Rotational Speed
(r/min) 2000 2000 Treatment Time (hours) 9 9 Physical Properties of
D.sub.50 (nm) 525 623 Crystal Nucleating Agent D.sub.90 (nm) 752
903 after Pulverizing Step D.sub.10 (nm) 341 423 (Particle
Size).sup.5) D.sub.10/D.sub.50 0.6 0.7 D.sub.90/D.sub.50 1.4 1.4
.sup.1)Particle size of a crystal nucleating agent to be subjected
to the pulverizing step, wherein D.sub.50 is a volume-median
particle size, D.sub.90 is a particle size at a cumulative volume
frequency of 90%, and D.sub.10 is a particle size at a cumulative
volume frequency of 10%. .sup.2)Weight-average molecular weight of
a pulverization aid ester, and is a weighted average when plural
kinds are used. .sup.3)Viscosity of the pulverization aid ester,
and is a weighted average when plural kinds are used. .sup.4)Ratio
of the weight of the crystal nucleating agent to a total weight of
the pulverization aid esters, i.e. crystal nucleating
agent/pulverization aid esters. .sup.5)Particle size of a crystal
nucleating agent after the pulverizing step, wherein D.sub.50 is a
volume-median particle size, D.sub.90 is a particle size at a
cumulative volume frequency of 90%, D.sub.10 is a particle size at
a cumulative volume frequency of 10%, and D.sub.10 /D.sub.50 is a
ratio of D.sub.10 to D.sub.50, and D.sub.90/D.sub.50 is a ratio of
D.sub.90 to D.sub.50.
TABLE-US-00004 TABLE 4 Prod. Ex. 15 Prod. Ex. 16 Prod. Ex. 17 Prod.
Ex. 18 Prod. Ex. 19 Prod. Ex. 20 Crystal Crystal Crystal Crystal
Crystal Crystal Nucleating Nucleating Nucleating Nucleating
Nucleating Nucleating Agent-15 Agent-16 Agent-17 Agent-18 Agent-19
Agent-20 Pulverizing Step (step (1)) Crystal Kind PY109 PY109 PY109
PY109 PY109 PY109 Nucleating Particle Size.sup.1) D.sub.50 (nm)
1130 1130 1130 1130 1130 1130 Agent D.sub.90 (nm) 2122 2122 2122
2122 2122 2122 D.sub.10 (nm) 654 654 654 654 654 654 Amount (g) 36
36 36 36 36 36 Pulverization Kind (MeEO.sub.3).sub.2SA DAIFATTY-101
(MeEO.sub.3).sub.2SA/ (AcEO.sub.6).sub.3Gly TEP-2 MeSA-DEG Aid
Ester DAIFATTY-101 Weight-Average Molecular Weight.sup.2) 410 338
374 490 446 450 Viscosity (23.degree. C., mPa s).sup.3) 27 19 23 79
13 260 Amount (g) 720 720 360/360 720 720 720 Crystal Nucleating
Agent/Pulverization Aid Ester.sup.4) 1/20 1/20 1/20 1/20 1/20 1/20
Pulverization Kind of Pulverizer Sand Grinder Sand Grinder Sand
Grinder Sand Grinder Sand Grinder Sand Grinder Conditions Material
of Media Zirconia Zirconia Zirconia Zirconia Zirconia Zirconia
Shape of Media (.phi.: Outer Diameter) mm beads 1 mm beads 1 mm
beads 1 mm beads 1 mm beads 1 mm beads Rotational Speed (r/min)
2000 2000 2000 2000 2000 2000 Treatment Time (hours) 9 9 9 9 9 9
Physical Properties of D.sub.50 (nm) 394 490 443 554 424 434
Crystal Nucleating Agent D.sub.90 (nm) 602 732 750 760 632 642
after Pulverizing Step D.sub.10 (nm) 230 335 287 390 260 270
(Particle Size).sup.5) D.sub.10/D.sub.50 0.6 0.7 0.6 0.7 0.6 0.6
D.sub.90/D.sub.50 1.5 1.5 1.7 1.4 1.5 1.5 .sup.1Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2Weight-average molecular weight of a pulverization aid ester,
and is a weighted average when plural kinds are used.
.sup.3Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00005 TABLE 5 Prod. Ex. 21 Prod. Ex. 22 Prod. Ex. 23 Prod.
Ex. 24 Crystal Crystal Crystal Crystal Nucleating Nucleating
Nucleating Nucleating Agent-21 Agent-22 Agent-23 Agent-24
Pulverizing Step (step (1)) Crystal Kind PY109 PY109 PY109 PY109
Nucleating Particle Size.sup.1) D.sub.50 (nm) 1130 1130 1130 1130
Agent D.sub.90 (nm) 2122 2122 2122 2122 D.sub.10 (nm) 654 654 654
654 Amount (g) 72 144 216 18 Pulverization Kind
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA Aid Ester Weight-Average Molecular
Weight.sup.2) 410 410 410 410 Viscosity (23.degree. C., mPa
s).sup.3) 27 27 27 27 Amount (g) 720 720 720 720 Crystal Nucleating
Agent/Pulverization Aid Ester.sup.4) 1/10 1/5 3/10 1/40
Pulverization Kind of Pulverizer Sand Grinder Sand Grinder Sand
Grinder Sand Grinder Conditions Material of Media Zirconia Zirconia
Zirconia Zirconia Shape of Media (.phi.: Outer Diameter) 1 mm beads
1 mm beads 1 mm beads 1 mm beads Rotational Speed (r/min) 2000 2000
2000 2000 Treatment Time (hours) 9 9 9 9 Physical Properties of
D.sub.50 (nm) 634 670 678 580 Crystal Nucleating Agent D.sub.90
(nm) 1045 1089 1143 980 after Pulverizing Step D.sub.10 (nm) 376
401 430 310 (Particle Size).sup.5) D.sub.10/D.sub.50 0.6 0.6 0.6
0.5 D.sub.90/D.sub.50 1.6 1.6 1.7 1.7 .sup.1)Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00006 TABLE 6 Prod. Ex. 25 Prod. Ex. 26 Prod. Ex. 27 Prod.
Ex. 28 Prod. Ex. 29 Prod. Ex. 30 Crystal Crystal Crystal Crystal
Crystal Crystal Nucleating Nucleating Nucleating Nucleating
Nucleating Nucleating Agent-25 Agent-26 Agent-27 Agent-28 Agent-29
Agent-30 Pulverizing Step (step (1)) Crystal Kind PY110 PR272
PR254(1) PR254(2) PV32 PR185 Nucleating Particle Size.sup.1)
D.sub.50 (nm) 811 1345 1201 756 1091 1233 Agent D.sub.90 (nm) 1156
1820 2155 1365 2071 2356 D.sub.10 (nm) 526 960 865 529 792 798
Amount (g) 36 36 36 36 36 36 Pulverization Kind
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA Aid
Ester Weight-Average Molecular Weight.sup.2) 410 410 410 410 410
410 Viscosity (23.degree. C., mPa s).sup.3) 27 27 27 27 27 27
Amount (g) 720 720 720 720 720 720 Crystal Nucleating
Agent/Pulverization Aid Ester.sup.4) 1/20 1/20 1/20 1/20 1/20 1/20
Pulverization Kind of Pulverizer Sand Grinder Sand Grinder Sand
Grinder Sand Grinder Sand Grinder Sand Grinder Conditions Material
of Media Zirconia Zirconia Zirconia Zirconia Zirconia Zirconia
Shape of Media (.phi.: Outer Diameter) 1 mm beads 1 mm beads 1 mm
beads 1 mm beads 1 mm beads 1 mm beads Rotational Speed (r/min)
2000 2000 2000 2000 2000 1200 Treatment Time (hours) 9 9 9 9 9 9
Physical Properties of D.sub.50 (nm) 356 672 616 396 534 630
Crystal Nucleating Agent D.sub.90 (nm) 578 1120 964 672 820 994
after Pulverizing Step D.sub.10 (nm) 209 492 440 264 396 396
(Particle Size).sup.5) D.sub.10/D.sub.50 0.6 0.7 0.7 0.7 0.7 0.6
D.sub.90/D.sub.50 1.6 1.7 1.6 1.7 1.5 1.6 .sup.1)Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00007 TABLE 7 Prod. Ex. 31 Prod. Ex. 32 Prod. Ex. 33 Prod.
Ex. 34 Prod. Ex. 35 Crystal Crystal Crystal Crystal Crystal
Nucleating Nucleating Nucleating Nucleating Nucleating Agent-31
Agent-32 Agent-33 Agent-34 Agent-35 Pulverizing Step (step (1))
Crystal Kind PR208 PB15:3 PB15 PB15:6 Vat Blue1 Nucleating Particle
Size.sup.1) D.sub.50 (nm) 792 1221 1154 1356 940 Agent D.sub.90
(nm) 1654 2200 2170 2321 1722 D.sub.10 (nm) 476 801 768 851 561
Amount (g) 36 36 36 36 36 Pulverization Kind (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA Aid Ester Weight-Average Molecular
Weight.sup.2) 410 410 410 410 410 Viscosity (23.degree. C., mPa
s).sup.3) 27 27 27 27 27 Amount (g) 720 720 720 720 720 Crystal
Nucleating Agent/Pulverization Aid Ester.sup.4) 1/20 1/20 1/20 1/20
1/20 Pulverization Kind of Pulverizer Sand Grinder Sand Grinder
Sand Grinder Sand Grinder Sand Grinder Conditions Material of Media
Zirconia Zirconia Zirconia Zirconia Zirconia Shape of Media (.phi.:
Outer Diameter) 1 mm beads 1 mm beads 1 mm beads 1 mm beads 1 mm
beads Rotational Speed (r/min) 2000 2000 2000 2000 1200 Treatment
Time (hours) 9 9 9 9 9 Physical Properties of D.sub.50 (nm) 396 612
588 660 468 Crystal Nucleating Agent D.sub.90 (nm) 670 898 880 964
840 after Pulverizing Step D.sub.10 (nm) 224 402 396 420 270
(Particle Size).sup.5) D.sub.10/D.sub.50 0.6 0.7 0.7 0.6 0.6
D.sub.90/D.sub.50 1.7 1.5 1.5 1.5 1.8 .sup.1)Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00008 TABLE 8 Prod. Ex. 36 Prod. Ex. 37 Prod. Ex. 38 Prod.
Ex. 39 Crystal Crystal Crystal Crystal Nucleating Nucleating
Nucleating Nucleating Agent-36 Agent-37 Agent-38 Agent-39
Pulverizing Step (step (1)) Crystal Kind T-1287 XyStUre 6-MeUra
MC-6000 Nucleating Particle Size.sup.1) D.sub.50 (nm) 986 990 1200
1123 Agent D.sub.90 (nm) 2121 2210 2107 2260 D.sub.10 (nm) 431 458
489 501 Amount (g) 36 36 36 36 Pulverization Kind
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA Aid Ester Weight-Average Molecular
Weight.sup.2) 410 410 410 410 Viscosity (23.degree. C., mPa
s).sup.3) 27 27 27 27 Amount (g) 720 720 720 720 Crystal Nucleating
Agent/Pulverization Aid Ester.sup.4) 1/20 1/20 1/20 1/20
Pulverization Kind of Pulverizer Sand Grinder Sand Grinder Sand
Grinder Sand Grinder Conditions Material of Media Zirconia Zirconia
Zirconia Zirconia Shape of Media (.phi.: Outer Diameter) 1 mm beads
1 mm beads 1 mm beads 1 mm beads Rotational Speed (r/min) 2000 2000
2000 2000 Treatment Time (hours) 9 9 9 9 Physical Properties of
D.sub.50 (nm) 513 523 532 564 Crystal Nucleating Agent D.sub.90
(nm) 790 809 980 890 after Pulverizing Step D.sub.10 (nm) 335 345
332 343 (Particle Size).sup.5) D.sub.10/D.sub.50 0.7 0.7 0.6 0.6
D.sub.90/D.sub.50 1.5 1.5 1.8 1.6 .sup.1)Particle size of a crystal
nucleating agent to be subjected to the pulverizing step, wherein
D.sub.50 is a volume-median particle size, D.sub.90 is a particle
size at a cumulative volume frequency of 90%, and D.sub.10 is a
particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00009 TABLE 9 Prod. Ex. 40 Prod. Ex. 41 Prod. Ex. 42 Prod.
Ex. 43 Prod. Ex. 44 Crystal Crystal Crystal Crystal Crystal
Nucleating Nucleating Nucleating Nucleating Nucleating Agent-40
Agent-41 Agent-42 Agent-43 Agent-44 Pulverizing Step (step (1))
Crystal Kind SIP2McBa NA-21 KM-1500 BTTCHA XBRA Nucleating Particle
Size.sup.1) D.sub.50 (nm) 986 990 1053 1064 1066 Agent D.sub.90
(nm) 2121 2125 2188 2199 2201 D.sub.10 (nm) 431 435 498 509 511
Amount (g) 36 36 36 36 36 Pulverization Kind (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA (MeEO.sub.3).sub.2SA
(MeEO.sub.3).sub.2SA Aid Ester Weight-Average Molecular
Weight.sup.2) 410 410 410 410 410 Viscosity (23.degree. C., mPa
s).sup.3) 27 27 27 27 27 Amount (g) 720 720 720 720 720 Crystal
Nucleating Agent/Pulverization Aid Ester.sup.4) 1/20 1/20 1/20 1/20
1/20 Pulverization Kind of Pulverizer Sand Grinder Sand Grinder
Sand Grinder Sand Grinder Sand Grinder Conditions Material of Media
Zirconia Zirconia Zirconia Zirconia Zirconia Shape of Media (.phi.:
Outer Diameter) 1 mm beads 1 mm beads 1 mm beads 1 mm beads 1 mm
beads Rotational Speed (r/min) 2000 2000 2000 2000 2000 Treatment
Time (hours) 9 9 9 9 9 Physical Properties of D.sub.50 (nm) 524 528
592 613 622 Crystal Nucleating Agent D.sub.90 (nm) 809 950 909 1009
1123 after Pulverizing Step D.sub.10 (nm) 346 350 414 435 444
(Particle Size).sup.5) D.sub.10/D.sub.50 0.7 0.7 0.7 0.7 0.7
D.sub.90/D.sub.50 1.5 1.8 1.5 1.6 1.8 .sup.1)Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to
D.sub.50.
TABLE-US-00010 TABLE 10 Prod. Ex. 45 Prod. Ex. 46 Prod. Ex. 47
Crystal Crystal Crystal Nucleating Nucleating Nucleating
Pulverizing Step (step (1)) Agent-45 Agent-46 Agent-47 Crystal Kind
PY109 PY109 PY109 Nucleating Particle Size.sup.1) D.sub.50 (nm)
1130 1130 1130 Agent D.sub.90 (nm) 2122 2122 2122 D.sub.10 (nm) 654
654 654 Amount (g) 36 36 50 Pulverization Kind Polyester-Polyol
(MeEO.sub.3).sub.3HTC -- Aid Ester Weight-Average Molecular
Weight.sup.2) 2200 656 -- Viscosity (23.degree. C., mPa s).sup.3)
21000 40 -- Amount (g) 720 720 -- Crystal Nucleating
Agent/Pulverization Aid Ester.sup.4) 1/20 1/20 -- Pulverization
Kind of Pulverizer Sand Grinder Sand Grinder Vibration Mill
Conditions Material of Media Zirconia Zirconia Stainless Steel
Shape of Media (.phi.: Outer Diameter) 1 mm beads 1 mm beads 30 mm
rod Rotational Speed (r/min) 2000 2000 1200 Treatment Time (hours)
9 9 1 Physical Properties of D.sub.50 (nm) ND 1002 1345 Crystal
Nucleating Agent D.sub.90 (nm) ND 1400 1989 after Pulverizing Step
D.sub.10 (nm) ND 789 806 (Particle Size).sup.5) D.sub.10/D.sub.50
ND 0.8 0.6 D.sub.90/D.sub.50 ND 1.4 1.5 .sup.1)Particle size of a
crystal nucleating agent to be subjected to the pulverizing step,
wherein D.sub.50 is a volume-median particle size, D.sub.90 is a
particle size at a cumulative volume frequency of 90%, and D.sub.10
is a particle size at a cumulative volume frequency of 10%.
.sup.2)Weight-average molecular weight of a pulverization aid
ester, and is a weighted average when plural kinds are used.
.sup.3)Viscosity of the pulverization aid ester, and is a weighted
average when plural kinds are used. .sup.4)Ratio of the weight of
the crystal nucleating agent to a total weight of the pulverization
aid esters, i.e. crystal nucleating agent/pulverization aid esters.
.sup.5)Particle size of a crystal nucleating agent after the
pulverizing step, wherein D.sub.50 is a volume-median particle
size, D.sub.90 is a particle size at a cumulative volume frequency
of 90%, D.sub.10 is a particle size at a cumulative volume
frequency of 10%, and D.sub.10/D.sub.50 is a ratio of D.sub.10 to
D.sub.50, and D.sub.90/D.sub.50 is a ratio of D.sub.90 to D.sub.50.
ND: not determined
[0225] It can be seen from Tables 1 to 3 that the zinc salt of
phenylphosphonic acid is finely pulverized by pulverizing the zinc
salt of phenylphosphonic acid in the presence of a carboxylic acid
ester or a phosphoric ester, having a specified weight-average
molecular weight and a specified viscosity. Incidentally, the
crystal nucleating agent composition obtained by pulverizing with a
polyester-polyol (Crystal Nucleating Agent-9, -10) had an
exceedingly high viscosity, so that the crystal nucleating agent
could not be dispersed in ethanol, whereby the particle size could
not be determined
[0226] It can be seen from Tables 4 to 10 that various kinds of the
organic crystal nucleating agent are finely dispersed by
pulverizing the organic nucleating agents in the presence of a
carboxylic acid ester or a phosphoric ester, having a specified
weight-average molecular weight and a specified viscosity.
Incidentally, the crystal nucleating agent composition obtained by
pulverizing with a polyester-polyol (Crystal Nucleating Agent-45)
had an exceedingly high viscosity, so that the crystal nucleating
agent could not be dispersed in ethanol, whereby the particle size
could not be determined
Examples 1 to 49 and Comparative Examples 1 to 36
[0227] Raw materials for a polylactic acid resin composition shown
in Tables 11 to 18 were melt-kneaded with a twin-screw extruder
(PCM-45, manufactured by Ikegai Ironworks Corp.) at a rotational
speed of 100 r/min and a kneading temperature of 190.degree. C.,
the kneaded mixture was strand-cut, to provide pellets of a
polylactic acid resin composition. The pellets obtained were dried
at 70.degree. C. under a reduced pressure for one day, so as to
have a water content of 500 ppm or less.
[0228] Here, the raw materials in Tables 11 to 18 are as
follows.
Polylactic Acid Resin
[0229] NW3001D: a polylactic acid resin (manufactured by Nature
Works LLC, Nature Works 3001D, optical purity: 98.5%,
weight-average molecular weight: 120,000)
Crystal Nucleating Agents
[0230] Crystal Nucleating Agent-1 to -47: crystal nucleating agent
compositions produced in Production Examples 1 to 47 of Crystal
Nucleating Agent Compositions mentioned above PPA-Zn: a zinc salt
of unsubstituted phenylphosphonic acid (manufactured by NISSAN
CHEMICAL INDUSTRIES, LTD., ECOPROMOTE, no melting point) OHC18EB:
ethylenebis-12-hydroxystearic amide (Nippon Kasei Chemical Co.,
Ltd., SLIPAX H, melting point: 145.degree. C.) PY109: a compound
having an isoindolinone backbone (manufactured by Ciba Fine
Chemical Co., Ltd., IRGAZIN Yellow 2GLTE)
Plasticizers
[0231] (MeEO.sub.3).sub.2SA: the same one as that used in the
production of the crystal nucleating agent composition mentioned
above. DAIFATTY-101: the same one as that used in the production of
the crystal nucleating agent composition mentioned above.
(AcEO.sub.6).sub.3Gly: the same one as that used in the production
of the crystal nucleating agent composition mentioned above.
Polyester-Polyol: the same one as that used in the production of
the crystal nucleating agent composition mentioned above.
(MeEO.sub.3).sub.3HTC: the same one as that used in the production
of the crystal nucleating agent composition mentioned above.
Examples 1 to 49 and Comparative Examples 1 to 36
Molded Articles of Polylactic Acid Resin Compositions
[0232] Next, the pellets of Examples and Comparative Examples were
injection-molded with an injection molding machine (manufactured by
The Japan Steel Works, Ltd., J75E-D) of which cylinder temperature
was 200.degree. C., into test pieces [flat plates (70 mm.times.40
mm.times.2 mm), rectangular test pieces (125 mm.times.12 mm.times.6
mm) and rectangular test pieces (63 mm.times.12 mm.times.5 mm)] at
a die temperature of 80.degree. C., 70.degree. C., or 60.degree.
C., to provide molded articles of polylactic acid resin
compositions.
[0233] Here, upon molding a molded article, a die retention time
necessary for demolding the test piece mentioned above was
evaluated by the following criteria. These results are shown in
Tables 11 to 18.
Evaluation of Crystallinity (Crystallization Velocity): Evaluation
Criteria of Die Retention Time Necessary for Releasing Mold
[0234] A time period in which a test piece could be easily demolded
without undergoing deformation at a die temperature shown in Tables
11 to 18 for all three kinds of test pieces is defined as a die
retention time necessary for demolding. The shorter the die
retention time, the faster the crystallization velocity of the test
piece at an internal portion and the runner portion of the die, and
the more excellent the moldability. Here, it is judged as "ND" when
a test piece could not be demolded, or even if a test piece could
be demolded, the deformation was caused.
TABLE-US-00011 TABLE 11 Examples 1 2 3 4 5 6 7 8 9 10 11 12 13 14
15 Components of Polylactic Acid Resin Composition Polylactic NW
3001D 100 100 100 100 100 100 100 100 100 100 100 100 100 100 100
Acid Resin Crystal Crystal Nucleating Agent-1 10.5 10.5 -- -- -- --
-- -- -- -- 21 -- -- -- -- Nucleating Crystal Nucleating Agent-2 --
-- 10.5 -- -- -- -- -- -- -- -- -- -- -- -- Agent Crystal
Nucleating Agent-3 -- -- -- 10.5 -- -- -- -- -- -- -- -- -- -- --
Crystal Nucleating Agent-4 -- -- -- -- 11.0 -- -- -- 5.5 -- -- 22
-- -- -- Crystal Nucleating Agent-5 -- -- -- -- -- 12.0 -- -- -- --
-- -- 18 -- -- Crystal Nucleating Agent-6 -- -- -- -- -- -- 13.0 --
-- -- -- -- -- -- -- Crystal Nucleating Agent-7 -- -- -- -- -- --
-- 20.5 -- -- -- -- -- -- -- Crystal Nucleating Agent-8 -- -- -- --
-- -- -- -- -- 10.5 -- -- -- -- -- Crystal Nucleating Agent-9 -- --
-- -- -- -- -- -- -- -- -- -- -- -- -- Crystal Nucleating -- -- --
-- -- -- -- -- -- -- -- -- -- -- -- Agent-10 Crystal Nucleating --
-- -- -- -- -- -- -- -- -- -- -- -- -- -- Agent-11 Crystal
Nucleating -- -- -- -- -- -- -- -- -- -- -- -- -- -- -- Agent-12
Crystal Nucleating -- -- -- -- -- -- -- -- -- -- -- -- -- 10.5 --
Agent-13 Crystal Nucleating -- -- -- -- -- -- -- -- -- -- -- -- --
-- 10.5 Agent-14 PPA-Zn -- -- -- -- -- -- -- -- -- -- -- -- -- --
-- OHC18EB 0.5 -- -- -- -- -- -- -- -- -- -- -- -- -- --
Plasticizer (MeEO.sub.3).sub.2SA -- -- -- -- -- -- -- -- -- -- --
-- -- -- -- DAIFATTY-101 -- -- -- -- -- -- -- -- -- -- -- -- -- --
-- (AcEO.sub.6).sub.3Gly -- -- -- -- -- -- -- -- -- -- -- -- -- --
-- Polyester-Polyol -- -- -- -- -- -- -- -- -- -- -- -- -- -- --
(MeEO.sub.3).sub.3HTC -- -- -- -- -- -- -- -- -- -- -- -- -- -- --
Evaluation Die Retention Time(s) 30 50 60 55 30 20 15 30 70 70 15
15 15 60 55 of Polylactic at Die Temperature of 80.degree. C. Acid
Resin Die Retention Time(s) 50 80 90 85 50 30 20 40 90 95 20 18 18
90 85 Composition at Die Temperature of 70.degree. C. Die Retention
Time(s) 60 90 110 100 70 40 25 50 120 120 22 20 20 110 100 at Die
Temperature of 60.degree. C. Note) Content of each of the raw
materials is expressed by parts by weight, based on 100 parts by
weight of the polylactic acid resin.
TABLE-US-00012 TABLE 12 Comparative Examples 1 2 3 4 5 6 7 8 9 10
11 12 Components of Polylactic Acid Resin Composition Polylactic
Acid NW 3001D 100 100 100 100 100 100 100 100 100 100 100 100 Resin
Crystal Crystal Nucleating Agent-1 -- -- -- -- -- -- -- -- -- -- --
-- Nucleating Crystal Nucleating Agent-2 -- -- -- -- -- -- -- -- --
-- -- -- Agent Crystal Nucleating Agent-3 -- -- -- -- -- -- -- --
-- -- -- -- Crystal Nucleating Agent-4 -- -- -- -- -- -- -- -- --
-- -- -- Crystal Nucleating Agent-5 -- -- -- -- -- -- -- -- -- --
-- -- Crystal Nucleating Agent-6 -- -- -- -- -- -- -- -- -- -- --
-- Crystal Nucleating Agent-7 -- -- -- -- -- -- -- -- -- -- -- --
Crystal Nucleating Agent-8 -- -- -- -- -- -- -- -- -- -- -- --
Crystal Nucleating Agent-9 -- -- -- 10.5 -- -- -- -- -- -- -- --
Crystal Nucleating Agent-10 -- -- -- -- 10.0 -- -- -- -- -- -- --
Crystal Nucleating Agent-11 -- -- -- -- -- -- 10.5 -- -- -- -- --
Crystal Nucleating Agent-12 -- -- -- -- -- -- -- 0.5 -- -- -- --
PPA-Zn 0.5 0.5 0.5 -- -- 0.5 -- -- 0.5 1.0 2.0 3.0 OHC18EB -- -- --
-- -- -- -- -- -- -- -- -- Plasticizer (MeEO.sub.3).sub.2SA 10.0 --
5.0 -- -- -- -- 10.0 -- 20.0 20.0 15.0 DAIFATTY-101 -- 10.0 5.0 --
-- -- -- -- -- -- -- -- (AcEO.sub.6).sub.3Gly -- -- -- -- -- 10.0
-- -- -- -- -- -- Polyester-Polyol -- -- -- -- -- -- -- -- -- -- --
-- (MeEO.sub.3).sub.3HTC -- -- -- -- -- -- -- -- 10.0 -- -- --
Evaluation of Die Retention Time(s) 90 100 95 130 150 110 100 100
140 80 80 80 Polylactic Acid at Die Temperature of 80.degree. C.
Resin Composition Die Retention Time(s) 120 130 125 ND ND 150 ND
130 ND 115 110 110 at Die Temperature of 70.degree. C. Die
Retention Time(s) ND ND ND ND ND ND ND ND ND ND ND ND at Die
Temperature of 60.degree. C. Note) Content of each of the raw
materials is expressed by parts by weight, based on 100 parts by
weight of the polylactic acid resin. ND: not determined
TABLE-US-00013 TABLE 13 Examples 16 17 18 19 20 21 22 23 24 25 26
27 28 29 Components of Polylactic Acid Resin Composition Polylactic
Acid NW 3001D 100 100 100 100 100 100 100 100 100 100 100 100 100
100 Resin Crystal Crystal Nucleating Agent-15 10.5 -- -- -- -- --
-- -- -- -- -- 21.0 -- -- Nucleating Crystal Nucleating Agent-16 --
10.5 -- -- -- -- -- -- -- -- -- -- -- -- Agent Crystal Nucleating
Agent-17 -- -- 10.5 -- -- -- -- -- -- -- -- -- -- -- Crystal
Nucleating Agent-18 -- -- -- 10.5 -- -- -- -- -- -- -- -- -- --
Crystal Nucleating Agent-19 -- -- -- -- 10.5 -- -- -- -- -- -- --
-- -- Crystal Nucleating Agent-20 -- -- -- -- -- 10.5 -- -- -- --
-- -- -- -- Crystal Nucleating Agent-21 -- -- -- -- -- -- 11.0 --
-- -- 5.5 -- 22.0 -- Crystal Nucleating Agent-22 -- -- -- -- -- --
-- 12.0 -- -- -- -- -- 18.0 Crystal Nucleating Agent-23 -- -- -- --
-- -- -- -- 13.0 -- -- -- -- -- Crystal Nucleating Agent-24 -- --
-- -- -- -- -- -- -- 20.5 -- -- -- -- Plasticizer
(MeEO.sub.3).sub.2SA -- -- -- -- -- -- -- -- -- -- -- -- -- --
Evaluation of Die Retention Time(s) 55 65 60 75 65 60 40 30 25 40
80 30 30 30 Polylactic Acid at Die Temperature of 80.degree. C.
Resin Die Retention Time(s) 85 90 90 100 90 90 65 50 40 60 115 40
35 35 Composition at Die Temperature of 70.degree. C. Die Retention
Time(s) 100 115 110 125 115 110 80 70 60 75 ND 55 50 50 at Die
Temperature of 60.degree. C. Note) Content of each of the raw
materials is expressed by parts by weight, based on 100 parts by
weight of the polylactic acid resin. ND: not determined
TABLE-US-00014 TABLE 14 Examples 30 31 32 33 34 35 36 37 38 39 40
Components of Polylactic Acid Resin Composition Polylactic Acid
Resin NW 3001D 100 100 100 100 100 100 100 100 100 100 100 Crystal
Crystal Nucleating Agent-25 10.5 -- -- -- -- -- -- -- -- -- --
Nucleating Crystal Nucleating Agent-26 -- 10.5 -- -- -- -- -- -- --
-- -- Agent Crystal Nucleating Agent-27 -- -- 10.5 -- -- -- -- --
-- -- -- Crystal Nucleating Agent-28 -- -- -- 10.5 -- -- -- -- --
-- -- Crystal Nucleating Agent-29 -- -- -- -- 10.5 -- -- -- -- --
-- Crystal Nucleating Agent-30 -- -- -- -- -- 10.5 -- -- -- -- --
Crystal Nucleating Agent-31 -- -- -- -- -- -- 10.5 -- -- -- --
Crystal Nucleating Agent-32 -- -- -- -- -- -- -- 10.5 -- -- --
Crystal Nucleating Agent-33 -- -- -- -- -- -- -- -- 10.5 -- --
Crystal Nucleating Agent-34 -- -- -- -- -- -- -- -- -- 10.5 --
Crystal Nucleating Agent-35 -- -- -- -- -- -- -- -- -- -- 10.5
Plasticizer (MeEO.sub.3).sub.2SA -- -- -- -- -- -- -- -- -- -- --
Evaluation of Die Retention Time(s) 85 70 80 70 80 90 90 55 65 60
90 Polylactic Acid at Die Temperature of 80.degree. C. Resin
Composition Die Retention Time(s) 120 95 115 95 115 120 120 85 90
90 120 at Die Temperature of 70.degree. C. Die Retention Time(s) ND
120 ND 120 ND ND ND 100 115 110 ND at Die Temperature of 60.degree.
C. Note) Content of each of the raw materials is expressed by parts
by weight, based on 100 parts by weight of the polylactic acid
resin. ND: not determined
TABLE-US-00015 TABLE 15 Comparative Examples 13 14 15 16 17 18 19
20 21 22 23 24 Components of Polylactic Acid Resin Composition
Polylactic Acid NW 3001D 100 100 100 100 100 100 100 100 100 100
100 100 Resin Crystal PY109 0.5 -- -- -- -- -- -- -- -- -- -- --
Nucleating PY110 -- 0.5 -- -- -- -- -- -- -- -- -- -- Agent PR272
-- -- 0.5 -- -- -- -- -- -- -- -- -- PR254(1) -- -- -- 0.5 -- -- --
-- -- -- -- -- PR254(2) -- -- -- -- 0.5 -- -- -- -- -- -- -- PV32
-- -- -- -- -- 0.5 -- -- -- -- -- -- PR185 -- -- -- -- -- -- 0.5 --
-- -- -- -- PR208 -- -- -- -- -- -- -- 0.5 -- -- -- -- PB15:3 -- --
-- -- -- -- -- -- 0.5 -- -- -- PB15 -- -- -- -- -- -- -- -- -- 0.5
-- -- PB15:6 -- -- -- -- -- -- -- -- -- -- 0.5 -- Vat Blue1 -- --
-- -- -- -- -- -- -- -- -- 0.5 Plasticizer (MeEO.sub.3).sub.2SA 10
10 10 10 10 10 10 10 10 10 10 10 Evaluation of Die Retention
Time(s) 100 125 110 120 110 120 130 130 95 105 100 130 Polylactic
Acid at Die Temperature of 80.degree. C. Resin Composition Die
Retention Time(s) 130 ND ND ND ND ND ND ND 125 130 130 ND at Die
Temperature of 70.degree. C. Die Retention Time(s) ND ND ND ND ND
ND ND ND ND ND ND ND at Die Temperature of 60.degree. C. Note)
Content of each of the raw materials is expressed by parts by
weight, based on 100 parts by weight of the polylactic acid resin.
ND: not determined
TABLE-US-00016 TABLE 16 Examples Comparative Examples 41 42 43 44
25 26 27 28 Components of Polylactic Acid Resin Composition
Polylactic Acid Resin NW 3001D 100 100 100 100 100 100 100 100
Crystal Crystal Nucleating Agent-36 10.5 -- -- -- -- -- -- --
Nucleating Crystal Nucleating Agent-37 -- 10.5 -- -- -- -- -- --
Agent Crystal Nucleating Agent-38 -- -- 10.5 -- -- -- -- -- Crystal
Nucleating Agent-39 -- -- -- 10.5 -- -- -- -- T-1287 -- -- -- --
0.5 -- -- -- XyStUre -- -- -- -- -- 0.5 -- -- 6-MeUra -- -- -- --
-- -- 0.5 -- MC-6000 -- -- -- -- -- -- -- 0.5 Plasticizer
(MeEO.sub.3).sub.2SA -- -- -- -- 10 10 10 10 Evaluation of Die
Retention Time(s) 75 85 85 90 115 125 125 130 Polylactic Acid at
Die Temperature of 80.degree. C. Resin Composition Die Retention
Time(s) 100 120 120 120 ND ND ND ND at Die Temperature of
70.degree. C. Die Retention Time(s) 125 ND ND ND ND ND ND ND at Die
Temperature of 60.degree. C. Note) Content of each of the raw
materials is expressed by parts by weight, based on 100 parts by
weight of the polylactic acid resin. ND: not determined
TABLE-US-00017 TABLE 17 Examples Comparative Examples 45 46 47 48
49 29 30 31 32 33 Components of Polylactic Acid Resin Composition
Polylactic Acid Resin NW 3001D 100 100 100 100 100 100 100 100 100
100 Crystal Crystal Nucleating Agent-40 10.5 -- -- -- -- -- -- --
-- -- Nucleating Crystal Nucleating Agent-41 -- 10.5 -- -- -- -- --
-- -- -- Agent Crystal Nucleating Agent-42 -- -- 10.5 -- -- -- --
-- -- -- Crystal Nucleating Agent-43 -- -- -- 10.5 -- -- -- -- --
-- Crystal Nucleating Agent-44 -- -- -- -- 10.5 -- -- -- -- --
SIP2MeBa -- -- -- -- -- 0.5 -- -- -- -- NA-21 -- -- -- -- -- -- 0.5
-- -- -- KM-1500 -- -- -- -- -- -- -- 0.5 -- -- BTTCHA -- -- -- --
-- -- -- -- 0.5 -- XBRA -- -- -- -- -- -- -- -- -- 0.5 Plasticizer
(MeEO.sub.3).sub.2SA -- -- -- -- -- 10 10 10 10 10 Evaluation of
Die Retention Time(s) 65 70 90 90 90 105 110 130 130 130 Polylactic
Acid at Die Temperature of 80.degree. C. Resin Composition Die
Retention Time(s) 90 95 120 120 120 130 ND ND ND ND at Die
Temperature of 70.degree. C. Die Retention Time(s) 115 120 ND ND ND
ND ND ND ND ND at Die Temperature of 60.degree. C. Note) Content of
each of the raw materials is expressed by parts by weight, based on
100 parts by weight of the polylactic acid resin. ND: not
determined
TABLE-US-00018 TABLE 18 Components of Polylactic Comparative
Examples Acid Resin Composition 34 35 36 Polylactic NW 3001D 100
100 100 Acid Resin Crystal Crystal Nucleating Agent-45 10.5 -- --
Nucleating Agent Crystal Nucleating Agent-46 -- 10.5 -- Crystal
Nucleating Agent-47 -- -- 0.5 Plasticizer (MeEO.sub.3).sub.2SA --
-- 10.0 Evaluation of Die Retention Time(s) 135 105 100 Polylactic
Acid at Die Temperature of 80.degree. C. Resin Die Retention
Time(s) ND 130 130 Composition at Die Temperature of 70.degree. C.
Die Retention Time(s) ND ND ND at Die Temperature of 60.degree. C.
Note) Content of each of the raw materials is expressed by parts by
weight, based on 100 parts by weight of the polylactic acid resin.
ND: not determined
[0235] It can be seen from the results of Tables 11 and 12 that the
polylactic acid resin compositions obtained according to the method
of the present invention (Examples 1 to 13, 14, and 15) are capable
of being molded in a short die retention time even at a die
temperature of 60.degree. C., so that the polylactic acid resin
compositions have excellent crystallization velocities. On the
other hand, the polylactic acid resin compositions of the
comparative examples obtained by methods other than the method of
the present invention were incapable of being molded within the
same die retention time as those of Examples at any of the die
temperatures of 60.degree., 70.degree. and 80.degree. C.
[0236] In addition, it can be seen from Tables 13 to 18 that the
polylactic acid resin compositions obtained according to the method
of the present invention (Examples 16 to 49) were capable of being
molded in a short die retention time at die temperatures of
60.degree. to 80.degree. C., so that the polylactic acid resin
compositions have excellent crystallization velocities. On the
other hand, the polylactic acid resin compositions of the
comparative examples obtained by methods other than the method of
the present invention (Comparative Examples 13 to 36) were
incapable of being molded within the same die retention time as
those of Examples at any of the die temperatures of 60.degree.,
70.degree. and 80.degree. C. It can be seen that even in polylactic
acid resin compositions containing the same crystal nucleating
agent, the crystallization velocities are remarkably improved by
making the crystal nucleating agent finer in the presence of a
carboxylic acid ester or a phosphoric ester in the present
invention.
[0237] Next, the pellets of Examples 11 to 13 and Comparative
Examples 10 to 12, and Example 27 and Comparative Example 37 were
injection-molded with an injection molding machine (manufactured by
The Japan Steel Works, Ltd., J75E-D) of which cylinder temperature
was 200.degree. C., into test pieces [flat plates (70 mm.times.40
mm.times.2 mm) and rectangular test pieces (125 mm.times.12
mm.times.6 mm)] in a die retention time of 30 seconds, to provide
molded articles of polylactic acid resin compositions. The physical
properties of the resulting molded articles were evaluated in
accordance with the methods of the following Test Examples 1 to 2.
The results are shown in Tables 19 and 20. Incidentally,
Comparative Example 37 was prepared in the same manner as in
Example 27 by blending 1.0 part by weight of PY109 and 20.0 parts
by weight of (MeEO.sub.3).sub.2SA, based on 100 parts by weight of
the polylactic acid resin.
Test Example 1
Evaluation of Heat Resistance: Thermal Deformation Temperature
[0238] A thermal deformation temperature (.degree. C.) at which a
rectangular test piece (125 mm.times.12 mm.times.6 mm) was bowed
for 0.25 mm at a load of 0.45 MPa was measured with a thermal
deformation temperature measurement instrument (manufactured by
Toyo Seiki, B-32) as prescribed in JIS-K7191. The higher this
temperature, the more excellent the heat resistance.
Test Example 2
Evaluation of Crystallinity: Relative Crystallinity
[0239] A 7.5 mg sample was taken from a central portion of a flat
plate (70 mm.times.40 mm.times.2 mm) Using a DSC apparatus (Diamond
DSC, manufactured by Perkin-Elmer), the 1st RUN includes heating
from 20.degree. to 200.degree. C. at a heating rate of 20.degree.
C./minute, keeping at 200.degree. C. for 5 minutes, cooling from
200.degree. to 20.degree. C. at a cooling rate of -20.degree.
C./minute, and keeping at 20.degree. C. for 1 minute, and further,
the 2nd RUN includes heating from 20.degree. to 200.degree. C. at a
heating rate of 20.degree. C./minute. Using .DELTA.Hcc, which is an
absolute value of a cold crystallization enthalpy of a polylactic
acid resin observed in 1st RUN, and .DELTA.Hm, a melt
crystallization enthalpy observed in 2nd RUN, the relative
crystallinity can be calculated by the following formula:
Relative
Crystallinity(%)=(.DELTA.Hm-.DELTA.Hcc)/.DELTA.Hm.times.100
The higher this numerical value, the more excellent the
crystallinity.
TABLE-US-00019 TABLE 19 Comparative Examples Examples 11 12 13 10
11 12 Components of Polylactic Acid Resin Composition Polylactic
Acid Resin NW 3001D 100 100 100 100 100 100 Crystal Crystal
Nucleating Agent-1 21 -- -- -- -- -- Nucleating Crystal Nucleating
Agent-2 -- -- -- -- -- -- Agent Crystal Nucleating Agent-3 -- -- --
-- -- -- Crystal Nucleating Agcnt-4 -- 22 -- -- -- -- Crystal
Nucleating Agent-5 -- -- 18 -- -- -- Crystal Nucleating Agent-6 --
-- -- -- -- -- Crystal Nucleating Agent-7 -- -- -- -- -- -- Crystal
Nucleating Agent-8 -- -- -- -- -- -- Crystal Nucleating Agent-9 --
-- -- -- -- -- Crystal Nucleating Agent-10 -- -- -- -- -- --
Crystal Nucleating Agent-11 -- -- -- -- -- -- Crystal Nucleating
Agent-12 -- -- -- -- -- -- PPA-Zn -- -- -- 1.0 2.0 3.0 OHC18EB --
-- -- -- -- -- Plasticizer (MeEO.sub.3).sub.2SA -- -- -- 20.0 20.0
15.0 DAIFATTY-101 -- -- -- -- -- -- (AcEO.sub.6).sub.3Gly -- -- --
-- -- -- Polyester-Polyol -- -- -- -- -- -- (MeEO.sub.3).sub.3HTC
-- -- -- -- -- -- Evaluation of Thermal Deformation 87 90 95 39 40
42 Polylactic Acid Temperature (.degree. C.) Resin Composition
Relative Crystallinity (%) 93 96 100 51 55 60 Note) Content of each
of the raw materials is expressed by parts by weight, based on 100
parts by weight of the polylactic acid resin.
TABLE-US-00020 TABLE 20 Exam- Comparative Components of Polylactic
ples Examples Acid Resin Composition 27 37 Polylactic Acid Resin NW
3001D 100 100 Crystal Nucleating Crystal Nucleating 21 -- Agent
Agent-15 PY109 -- 1.0 Plasticizer (MeEO.sub.3).sub.2SA -- 20.0
Evaluation of Polylactic Thermal Deformation 90 38 Acid Resin
Composition Temperature (.degree. C.) Relative 90 50 Crystallinity
(%) Note) Content of each of the raw materials is expressed by
parts by weight, based on 100 parts by weight of the polylactic
acid resin.
[0240] From the results of Tables 19 and 20, the molded articles of
the polylactic acid resin compositions of Examples molded at a die
temperature of 30.degree. C. and a die retention time of 30 seconds
had a relative crystallinity of 90% or more and heat resistance of
80.degree. C. or more. From the above, it is considered that the
polylactic acid resin compositions of Examples 1 to 49 would have a
relative crystallinity of 90% or more and heat resistance of
80.degree. C. or more in the same test. On the other hand, the
molded articles of the polylactic acid resin compositions of
comparative examples obtained according to the methods other than
the present invention were able to be demolded from the die, but
had a low relative crystallinity of 60% or less, and had heat
resistance of lower than 50.degree. C.
INDUSTRIAL APPLICABILITY
[0241] The polylactic acid resin composition obtainable by the
method of the present invention can be suitably used in various
industrial applications, such as daily sundries, household electric
appliance parts, packaging materials for household electric
appliance parts, and automobile parts.
* * * * *