U.S. patent application number 17/694859 was filed with the patent office on 2022-06-30 for nucleating agent, polyolefin-based resin composition containing same, and molded article thereof.
This patent application is currently assigned to ADEKA CORPORATION. The applicant listed for this patent is ADEKA CORPORATION. Invention is credited to Takuya FUKUDA, Hiroaki MIZUSHIMA, Yuri YOKOTA.
Application Number | 20220204724 17/694859 |
Document ID | / |
Family ID | 1000006196645 |
Filed Date | 2022-06-30 |
United States Patent
Application |
20220204724 |
Kind Code |
A1 |
FUKUDA; Takuya ; et
al. |
June 30, 2022 |
NUCLEATING AGENT, POLYOLEFIN-BASED RESIN COMPOSITION CONTAINING
SAME, AND MOLDED ARTICLE THEREOF
Abstract
Provided are: a nucleating agent capable of simultaneously
improving the thermal stability and the transparency of a
polyolefin resin; a polyolefin-based resin composition containing
the same; and a molded article of the composition. The nucleating
agent contains a compound represented by Formula (1) below where
R.sup.1 to R.sup.4 each independently represent a hydrogen atom or
a linear or branched alkyl group having 1 to 9 carbon atoms;
R.sup.5 represents an alkanediyl group having 1 to 4 carbon atoms;
and M represents a hydrogen atom or a sodium atom. In this
nucleating agent, the mass ratio of phosphorus atoms and sodium
atoms, P/Na, is in a range of 1.200 to 1.500. ##STR00001##
Inventors: |
FUKUDA; Takuya;
(Saitama-shi, JP) ; MIZUSHIMA; Hiroaki;
(Saitama-shi, JP) ; YOKOTA; Yuri; (Saitama-shi,
JP) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
ADEKA CORPORATION |
Tokyo |
|
JP |
|
|
Assignee: |
ADEKA CORPORATION
Tokyo
JP
|
Family ID: |
1000006196645 |
Appl. No.: |
17/694859 |
Filed: |
March 15, 2022 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
16969404 |
Aug 12, 2020 |
11306194 |
|
|
PCT/JP2019/003907 |
Feb 4, 2019 |
|
|
|
17694859 |
|
|
|
|
Current U.S.
Class: |
1/1 |
Current CPC
Class: |
C08L 23/12 20130101;
C08K 5/527 20130101; C08K 5/0083 20130101; C08L 2205/24
20130101 |
International
Class: |
C08K 5/00 20060101
C08K005/00; C08K 5/527 20060101 C08K005/527; C08L 23/12 20060101
C08L023/12 |
Foreign Application Data
Date |
Code |
Application Number |
Feb 13, 2018 |
CN |
201810150606.1 |
Claims
1. A nucleating agent, comprising: a compound represented by the
following Formula (1): ##STR00004## wherein in Formula (1), R.sup.1
to R.sup.4 each independently represents a hydrogen atom or a
linear or branched alkyl group having 1 to 9 carbon atoms; R.sup.5
represents an alkanediyl group having 1 to 4 carbon atoms; and M
represents a sodium atom, and a compound represented by the
following Formula (1'): ##STR00005## wherein in Formula (1'),
R.sup.1 to R.sup.4 each independently represents a hydrogen atom or
a linear or branched alkyl group having 1 to 9 carbon atoms;
R.sup.5 represents an alkanediyl group having 1 to 4 carbon atoms;
and M represents a hydrogen atom, wherein a mass ratio of
phosphorus atoms and sodium atoms in the nucleating agent, P/Na, is
in a range of 1.350 to 1.500.
2. The nucleating agent according to claim 1, wherein the mass
ratio of phosphorus atoms and sodium atoms in the nucleating agent,
P/Na, is in a range of 1.350 to 1.450.
Description
CROSS REFERENCE TO RELATED APPLICATIONS
[0001] This application is a Continuation of copending U.S.
application Ser. No. 16/969,404, filed on Aug. 12, 2020, which is
the National Phase under 35 U.S.C. .sctn. 371 of International
Application No. PCT/JP2019/003907, filed on Feb. 4, 2019, and under
35 U.S.C. .sctn. 119(a) to Patent Application No. 201810150606.1,
filed in China on Feb.13, 2018, all of which are hereby expressly
incorporated by reference into the present application.
TECHNICAL FIELD
[0002] The present invention relates to a nucleating agent, a
polyolefin-based resin composition containing the same, and a
molded article of the composition. More particularly, the present
invention relates to: a nucleating agent capable of simultaneously
improving the thermal stability and the transparency of a
polyolefin resin; a polyolefin-based resin composition containing
the same; and a molded article of the composition.
BACKGROUND ART
[0003] Olefin resins, such as polyethylene, polypropylene and
polybutene-1, advantageously have excellent moldability, heat
resistance, mechanical characteristics, low specific gravity and
the like; therefore, they are widely utilized in films, sheets, and
various molded articles (e.g., structural components). However,
olefin-based resins have problems of, for example, requiring a long
molding cycle in processing due to slow crystallization after being
heat-molded, and there are cases where their molded articles are
deformed due to crystallization that progresses even after molding.
Moreover, since olefin resins generate large crystals when
heat-molded, there are such drawbacks that the resulting molded
articles have insufficient strength and poor transparency.
[0004] It is known that these drawbacks are attributed to the
crystallinity of olefin resins and can be overcome by allowing each
olefin resin to rapidly generate fine crystals. In order to achieve
rapid generation of fine crystals, a method of adding a nucleating
agent, a crystallization accelerator and/or the like is
employed.
[0005] As such nucleating agents, conventionally, for example,
metal carboxylates, such as sodium benzoate, 4-tert-butylbenzoate
aluminum salt, sodium adipate, and disodium
bicyclo[2.2.1]heptane-2,3-dicarboxylate; metal phosphates, such as
sodium bis(4-tert-butylphenyl) phosphate, sodium
2,2'-methylene-bis(4,6-di-tert-butylphenyl) phosphate, and lithium
2,2'-methylene-bis(4,6-di-tert-butylphenyl) phosphate; and
compounds having an acetal skeleton, such as dibenzylidene
sorbitol, bis(methylbenzylidene)sorbitol and
bis(dimethylbenzylidene)sorbitol, are used as disclosed in, for
example, Patent Documents 1 to 8.
RELATED ART DOCUMENTS
Patent Documents
[0006] [Patent Document 1] JPS58-1736A
[0007] [Patent Document 2] JPS59-184252A
[0008] [Patent Document 3] JPH06-340786
[0009] [Patent Document 4] JPH07-11075A
[0010] [Patent Document 5] JPH07-48473A
[0011] [Patent Document 6] JPH08-3364A
[0012] [Patent Document 7] JPH09-118776A
[0013] [Patent Document 8] JPH10-25295A
SUMMARY OF THE INVENTION
Problems to be Solved by the Invention
[0014] Among these nucleating agents, sodium
2,2'-methylene-bis(4,6-di-tert-butylphenyl) phosphate not only
markedly improves the rigidity, the thermal deformation temperature
and the crystallization temperature of polyolefin resins, but also
exhibits excellent effects of improving the heat resistance and the
transparency. However, even sodium
2,2'-methylene-bis(4,6-di-tert-butylphenyl) phosphate does not
necessarily improve the heat resistance and the transparency of a
polyolefin resin. In other words, even sodium
2,2'-methylene-bis(4,6-di-tert-butylphenyl) phosphate is
inconsistent in its effect of improving the heat resistance and the
transparency of a polyolefin resin and has problems of, for
example, not being able to simultaneously improve these properties;
therefore, an improvement is desired at present.
[0015] In view of the above, an object of the present invention is
to provide: a nucleating agent which can solve the above-described
problems and improve simultaneously the thermal stability and the
transparency of a polyolefin resin; a polyolefin-based resin
composition containing the same; and a molded article of the
composition.
Means for Solving the Problems
[0016] The present inventors intensively studied to solve the
above-described problems and consequently found that the
above-described problems occur even with the use of a nucleating
agent containing sodium 2,2'-methylene-bis(4,6-di-tert-butylphenyl)
phosphate when the ratio P/Na is outside a specific range in its
relationship with other components that are impurities. Based on
this finding, the present inventors further intensively studied to
discover that the above-described problems can be solved by
adopting the below-described constitution, thereby completing the
present invention.
[0017] That is, the nucleating agent of the present invention is a
nucleating agent containing a compound represented by the following
Formula (1):
##STR00002##
[0018] where R.sup.1 to R.sup.4 each independently represent a
hydrogen atom or a linear or branched alkyl group having 1 to 9
carbon atoms; R.sup.5 represents an alkanediyl group having 1 to 4
carbon atoms; and M represents a hydrogen atom or a sodium
atom,
[0019] the nucleating agent being characterized in that a mass
ratio of phosphorus atoms and sodium atoms therein, P/Na, is in a
range of 1.200 to 1.500.
[0020] In the nucleating agent of the present invention, the mass
ratio of phosphorus atoms and sodium atoms, P/Na, is preferably in
a range of 1.350 to 1.450.
[0021] A polyolefin-based resin composition of the present
invention is characterized by containing the nucleating agent of
the present invention in an amount of 0.001 to 10 parts by mass
with respect to 100 parts by mass of a polyolefin-based resin.
[0022] A molded article of the present invention is characterized
in that it is obtained by molding the polyolefin-based resin
composition of the present invention.
Effects of the Invention
[0023] According to the present invention, a nucleating agent
capable of simultaneously improving the thermal stability and the
transparency of a polyolefin resin, a polyolefin-based resin
composition containing the same, and a molded article of the
composition can be provided.
Mode for Carrying Out the Invention
[0024] The nucleating agent of the present invention, the
polyolefin-based resin composition containing the same, and the
molded article of the composition will now be described in
detail.
[0025] The nucleating agent of the present invention is a
nucleating agent containing a compound represented by the following
Formula (1):
##STR00003##
[0026] where R.sup.1 to R.sup.4 each independently represent a
hydrogen atom or a linear or branched alkyl group having 1 to 9
carbon atoms, R.sup.5 represents an alkanediyl group having 1 to 4
carbon atoms, and M represents a hydrogen atom or a sodium
atom.
[0027] Examples of the alkyl group having 1 to 9 carbon atoms that
is represented by R.sup.1, R.sup.2, R.sup.3 and R.sup.4 in Formula
(1) include a methyl group, an ethyl group, a propyl group, an
isopropyl group, a butyl group, a sec-butyl group, a tert-butyl
group, an isobutyl group, an amyl group, an isoamyl group, a
tert-amyl group, a hexyl group, a cyclohexyl group, a heptyl group,
an isoheptyl group, and a tert-heptyl group, among which a
tert-butyl group is particularly preferred.
[0028] Examples of the alkanediyl group having 1 to 4 carbon atoms
that is represented by R.sup.5 in Formula (1) include methylene,
ethylene, propane-1,3-diyl, propane-1,2-diyl, butane-1,4-diyl, and
butane-1,3-diyl. The alkanediyl group is preferably methylene.
[0029] In the nucleating agent of the present invention, the mass
ratio of phosphorus atoms and sodium atoms, P/Na, is in a range of
1.200 to 1.500. By controlling this ratio P/Na in this range, the
nucleating agent can simultaneously improve the thermal stability
and the transparency. When the ratio P/Na is lower than 1.200, the
nucleating agent contains a large amount of sodium salt other than
the compound represented by Formula (1), and this makes the
nucleating agent alkaline, as a result of which yellowing caused by
a phenolic antioxidant occurs in a composition and a molded article
thereof. Meanwhile, when the ratio P/Na is higher than 1.500, the
proportion of a compound wherein M is a hydrogen atom is high in
compounds represented by Formula (1) that are contained in the
nucleating agent, as a result of which sufficient
transparentization performance and sufficient thermal stability
cannot be ensured. The ratio P/Na is preferably 1.350 to 1.450.
[0030] A method of producing the compound represented by Formula
(1) according to the nucleating agent of the present invention is
not particularly restricted, and a compound represented by Formula
(1) according to the nucleating agent of the present invention
wherein M is a sodium atom can be obtained by, for example,
allowing phosphorus trichloride (or phosphorus oxychloride) and
2,2'-alkylidenebisphenol to react with each other, subsequently
hydrolyzing the resultant as required to obtain a cyclic acidic
phosphate, allowing the thus obtained cyclic acidic phosphate to
react with sodium hydroxide, and then filtering and drying the
resulting compound.
[0031] When a compound represented by Formula (1) according to the
nucleating agent of the present invention wherein M is a sodium
atom is synthesized by the above-described method, the theoretical
value of P/Na is 1.347. However, usually, when a compound
represented by Formula (1) wherein M is a sodium atom is
synthesized by this production method, a compound wherein M is a
hydrogen atom remains as an impurity in a case where neutralization
is imperfect, or excess sodium hydroxide remains in a case where
neutralization is excessive. This causes the ratio P/Na to be
outside the above-described range, making the nucleating agent
unable to impart sufficient heat resistance and transparency to a
polyolefin resin composition. Therefore, by controlling the ratio
P/Na to be in the above-described range using a known purification
means or the like, excellent heat resistance and transparency can
be imparted to a polyolefin-based resin.
[0032] The nucleating agent of the present invention may be
produced by, as described above, allowing a cyclic acidic
phosphoric acid ester to react with sodium hydroxide and adjusting
the ratio P/Na to be in the above-described range using a known
purification means or the like in the process of producing a
compound represented by Formula (1) wherein M is a sodium atom, or
by mixing a compound of Formula (1) wherein M is a sodium atom,
which is obtained by the above-described procedure, with a compound
of Formula (1) wherein M is a hydrogen atom such that the
above-described ratio is attained; however, the method of producing
the nucleating agent is not necessarily restricted thereto.
[0033] The nucleating agent of the present invention may consist of
only a compound represented by Formula (1) or may contain a known
additive(s) in addition to a compound represented by Formula (1).
The content of the compound represented by Formula (1) is
preferably 1 to 100% by mass, more preferably 10 to 100% by
mass.
[0034] Next, the polyolefin-based resin composition of the present
invention will be described.
[0035] The polyolefin-based resin composition of the present
invention contains the nucleating agent of the present invention in
an amount of 0.001 to 10 parts by mass with respect to 100 parts by
mass of a polyolefin-based resin. When this amount is less than
0.001 parts by mass, the effects of the nucleating agent are not
sufficiently exerted, whereas when the amount is greater than 10
parts by mass, the nucleating agent may bleed out on the surface of
a molded article obtained by molding the polyolefin-based resin
composition. The nucleating agent is incorporated in an amount of
preferably 0.005 to 8 parts by mass, more preferably 0.01 to 5
parts by mass.
[0036] Examples of the polyolefin-based resin used in the
polyolefin-based resin composition of the present invention include
a-olefin polymers, such as low-density polyethylenes, linear
low-density polyethylenes, high-density polyethylenes, isotactic
polypropylenes, syndiotactic polypropylenes, hemi-isotactic
polypropylenes, cycloolefin polymers, stereo block polypropylenes,
poly-3-methyl-1-butenes, poly-3-methyl-1-pentenes, and
poly-4-methyl-1-pentenes; and .alpha.-olefin copolymers, such as
ethylene-propylene block or random copolymers. Among these
polyolefin-based resins, polypropylene-based resins for which the
nucleating agent of the present invention exhibits a prominent
effect of use are preferred and, for example, polypropylenes,
ethylene-propylene block or random copolymers, block or random
copolymers of an .alpha.-olefin other than ethylene and propylene,
and mixtures of any of these propylene-based polymers and other
.alpha.-olefin polymer can be used as well.
[0037] Further, among these polyolefin-based resins, ones having a
melt flow rate in a range of 1 to 100 g/10 min can be preferably
used since the effects of the present invention are thereby
obtained in a favorable manner, and those polyolefin-based resins
having a melt flow rate in a range of 2 to 60 g/10 min are
particularly preferred.
[0038] As for a method of producing the polyolefin-based resin, in
a variety of polymerization methods such as vapor-phase
polymerization, solution polymerization, emulsion polymerization
and bulk polymerization that include the use of various
polymerization catalysts (e.g., Ziegler catalysts, Ziegler-Natta
catalysts, and metallocene catalysts), co-catalysts, catalyst
carriers and chain transfer agents, the polyolefin-based resin can
be produced by appropriately selecting the polymerization
conditions (e.g., temperature, pressure, concentration, flow rate,
and removal of catalyst residue) that yield a resin having physical
properties suitable for a packaging material or a resin having
physical properties suitable for molding of a packaging material.
Other properties of the polyolefin-based resin, such as
number-average molecular weight, weight-average molecular weight,
molecular weight distribution, melt flow rate, melting point,
melting peak temperature, stereoregularity (e.g., isotacticity or
syndiotacticity), presence/absence and degree of branching,
specific gravity, ratio of a component(s) dissolving in various
solvents, haze, gloss, impact strength, bending elastic modulus and
Olsen rigidity, as well as whether or not the respective property
values satisfy a specific formula, can be selected as appropriate
in accordance with the desired properties.
[0039] In the polyolefin-based resin composition of the present
invention, as required, conventionally known other additives that
are generally used may be incorporated within a range that does not
impair the effects of the present invention. These other additives
may be added to the nucleating agent of the present invention to
prepare an additive composition, and this composition may then be
added to a polyolefin-based resin.
[0040] Examples of such other additives that can be used include:
plasticizers, such as neopentyl glycol derivatives, polyalkylene
glycols and derivatives thereof, and epoxy compounds of polyhydric
alcohols and derivatives thereof; antioxidants, such as phenolic,
phosphorus-based, and sulfur-based antioxidants; light stabilizers,
such as hindered amine-based light stabilizers and ultraviolet
absorbers; lubricants, such as hydrocarbon compounds, fatty acid
compounds, aliphatic alcohol compounds, aliphatic ester compounds,
aliphatic amide compounds, aliphatic carboxylic acid metal salt
compounds, and other metallic soaps; heavy metal deactivators;
antistatic agents, such as cationic surfactants, anionic
surfactants, nonionic surfactants, and amphoteric surfactants;
halogen compounds; phosphoric acid ester compounds; phosphoric acid
amide compounds; melamine compounds; fluorocarbon resins or metal
oxides; flame retardants, such as melamine (poly)phosphate and
piperazine (poly)phosphate; fillers, such as glass fibers and
calcium carbonate; silicate-based inorganic additives, such as
hydrotalcite, fumed silica, fine particle silica, silica rock,
diatomites, clay, kaolin, diatomaceous earth, silica gel, calcium
silicate, sericite, kaolinite, flint, feldspar powder, vermiculite,
attapulgite, talc, mica, minnesotaite, pyrophyllite, and silica;
nucleating agents other than the one used in the polyolefin-based
resin composition of the present invention; colorants; pigments;
anti-fogging agents; various fillers; mold release agents;
fragrants; foaming agents; antibacterial agents; and antifungal
agents. Particularly, a phenolic or phosphorus-based antioxidant is
preferably used since it also exhibits an effect as an
anti-coloring agent of a polyolefin-based resin composition.
[0041] Examples of the phenolic antioxidants include
2,6-di-tert-butyl-p-cresol, 2,6-diphenyl-4-octadecyloxyphenol,
stearyl(3,5-di-tert-butyl-4-hydroxyphenyl)propionate, [0042]
distearyl(3,5-di-tert-butyl-4-hydroxybenzyl)phosphonate, [0043]
tridecyl-3,5-di-tert-butyl-4-hydroxybenzyl thioacetate, [0044]
thiodiethylene-bis[(3,5-di-tert-butyl-4-hydroxyphenyl)propionate],
[0045] 4,4'-thiobis(6-tert-butyl-m-cresol), [0046]
2-octylthio-4,6-di(3,5-di-tert-butyl-4-hydroxyphenoxy)-s-triazine,
[0047] 2,2'-methylene-bis(4-methyl-6-tert-butylphenol), [0048]
bis[3,3-bis(4-hydroxy-3-tert-butylphenyl)butyric acid]glycol ester,
[0049] 4,4'-butylidene-bis(2,6-di-tert-butylphenol),
4,4'-butylidene-bis(6-tert-butyl-3-methylphenol), [0050]
2,2'-ethylidene-bis(4,6-di-tert-butylphenol), [0051]
1,1,3-tris(2-methyl-4-hydroxy-5-tert-butylphenyl)butane, [0052]
bis[2-tert-butyl-4-methyl-6-(2-hydroxy-3-tert-butyl-5-methylbenzyl)phenyl-
]terephthalate, [0053]
1,3,5-tris(2,6-dimethyl-3-hydroxy-4-tert-butylbenzyl)isocyanurate,
[0054] 1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)isocyanurate,
[0055]
1,3,5-tris(3,5-di-tert-butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene,
[0056]
1,3,5-tris[(3,5-di-tert-butyl-4-hydroxyphenyl)propionyloxyethyl]is-
ocyanurate, [0057]
tetrakis[methylene-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)propionate]met-
hane, [0058]
2-tert-butyl-4-methyl-6-(2-acryloyloxy-3-tert-butyl-5-methylbenzyl)phenol-
, [0059]
3,9-bis[2-(3-tert-butyl-4-hydroxy-5-methylhydrocinnamoyloxy)-1,1--
dimethylethyl]-2,4,8,10-tetraoxaspiro[5.5]undecane, and triethylene
glycol-bis[.beta.-(3-tert-butyl-4-hydroxy-5-methylphenyl)propionate].
The amount of a phenolic antioxidant to be used is preferably 0.001
to 10 parts by mass, more preferably 0.01 to 5 parts by mass, with
respect to 100 parts by mass of the polyolefin-based resin.
[0060] Examples of the phosphorus-based antioxidants include
triphenyl phosphite, tris(2,4-di-tert-butylphenyl)phosphite,
tris(2,5-di-tert-butylphenyl)phosphite, tris(nonylphenyl)phosphite,
tris(dinonylphenyl)phosphite, tris(mono- or di-mixed
nonylphenyl)phosphite, diphenyl acid phosphite, [0061]
2,2'-methylene-bis(4,6-di-tert-butylphenyl)octyl phosphite,
diphenyldecyl phosphite, diphenyloctyl phosphite,
di(nonylphenyl)pentaerythritol diphosphite, phenyldiisodecyl
phosphite, tributyl phosphite, tris(2-ethylhexyl)phosphite,
tridecyl phosphite, trilauryl phosphite, dibutyl acid phosphite,
dilauryl acid phosphite, trilauryl trithiophosphite, bis(neopentyl
glycol)-1,4-cyclohexane dimethyl diphosphite,
bis(2,4-di-tert-butylphenyl)pentaerythritol diphosphite,
bis(2,5-di-tert-butylphenyl)pentaerythritol diphosphite, [0062]
bis(2,6-di-tert-butyl-4-methylphenyl)pentaerythritol diphosphite,
[0063] bis(2,4-dicumylphenyl)pentaerythritol diphosphite, distearyl
pentaerythritol diphosphite, [0064] tetra(C12-15 mixed
alkyl)-4,4'-isopropylidene diphenyl phosphite, [0065]
bis[2,2'-methylene-bis(4,6-diamylphenyl)]-isopropylidene diphenyl
phosphite, [0066]
tetratridecyl-4,4'-butylidenebis(2-tert-butyl-5-methylphenol)diphosphite,
[0067]
hexa(tridecyl)-1,1,3-tris(2-methyl-5-tert-butyl-4-hydroxyphenyl)bu-
tane triphosphite, tetrakis(2,4-di-tert-butylphenyl)biphenylene
diphosphonite, [0068]
tris(2-[(2,4,7,9-tetrakis-tert-butyldibenzo[d,f][1,3,2]dioxaphosphepin-6--
yl)oxy]ethyl)amine,
9,10-dihydro-9-oxa-10-phosphaphenanthrene-10-oxide, and [0069]
2-butyl-2-ethylpropanediol-2,4,6-tri-tert-butylphenol
monophosphite. The amount of a phosphorus-based antioxidant to be
used is preferably 0.001 to 10 parts by mass, more preferably 0.01
to 5 parts by mass, with respect to 100 parts by mass of the
polyolefin-based resin.
[0070] Examples of the sulfur-based antioxidants include: dialkyl
thiodipropionates, such as dilauryl thiodipropionate, dimyristyl
thiodipropionate, myristylstearyl thiodipropionate, and distearyl
thiodipropionate; and .beta.-alkylmercaptopropionates of polyols,
such as pentaerythritol-tetra(.beta.-dodecylmercaptopropionate).
The amount of a sulfur-based antioxidant to be used is preferably
0.001 to 10 parts by mass, more preferably 0.01 to 5 parts by mass,
with respect to 100 parts by mass of the polyolefin-based
resin.
[0071] Examples of the hindered amine-based light stabilizers
include [0072] 2,2,6,6-tetramethyl-4-piperidyl stearate,
1,2,2,6,6-pentamethyl-4-piperidyl stearate, [0073]
2,2,6,6-tetramethyl-4-piperidyl benzoate,
bis(2,2,6,6-tetramethyl-4-piperidyl)sebacate, [0074]
tetrakis(2,2,6,6-tetramethyl-4-piperidyl)-1,2,3,4-butanetetracarboxylate,
[0075]
tetrakis(1,2,2,6,6-pentamethyl-4-piperidyl)-1,2,3,4-butanetetracar-
boxylate, [0076]
bis(2,2,6,6-tetramethyl-4-piperidyl).di(tridecyl)-1,2,3,4-butanetetracarb-
oxylate, [0077]
bis(1,2,2,6,6-pentamethyl-4-piperidyl).di(tridecyl)-1,2,3,4-butanetetraca-
rboxylate, [0078]
bis(1,2,2,4,4-pentamethyl-4-piperidyl)-2-butyl-2-(3,5-di-tert-butyl-4-hyd-
roxybenzyl)malonate, [0079]
1-(2-hydroxyethyl)-2,2,6,6-tetramethyl-4-piperidinol/diethyl
succinate polycondensate, [0080]
1,6-bis(2,2,6,6-tetramethyl-4-piperidylamino)hexane/2,4-dichloro-6-morpho-
lino-s-triazine polycondensate, [0081]
1,6-bis(2,2,6,6-tetramethyl-4-piperidylamino)hexane/2,4-dichloro-6-tert-o-
ctylamino-s-triazine polycondensate, [0082]
1,5,8,12-tetrakis[2,4-bis(N-butyl-N-(2,2,6,
6-tetramethyl-4-piperidyl)amino)-s-triazine-6-yl]-1,5,8,12-tetraazadodeca-
ne, [0083]
1,5,8,12-tetrakis[2,4-bis(N-butyl-N-(1,2,2,6,6-pentamethyl-4-pi-
peridyl)amino)-s-triazine-6-yl]-1,5,8,12-tetraazadodecane, [0084]
1,6,11-tris[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-s-t-
riazine-6-yl]aminoundecane, [0085]
1,6,11-tris[2,4-bis(N-butyl-N-(1,2,2,6,6-pentamethyl-4-piperidyl)amino)-s-
-triazine-6-yl]aminoundecane, [0086]
bis{4-(1-octyloxy-2,2,6,6-tetramethyl)piperidyl}decanedionate,
[0087] bis{4-(2,2,6,6-tetramethyl-1-undecyloxy)piperidyl)carbonate,
and TINUVIN NOR 371 manufactured by Ciba Specialty Chemicals K.K.
The amount of a hindered amine-based light stabilizer to be used is
preferably 0.001 to 5 parts by mass, more preferably 0.005 to 0.5
parts by mass, with respect to 100 parts by mass of the
polyolefin-based resin
[0088] Examples of the ultraviolet absorbers include
2-hydroxybenzophenones, such as [0089] 2,4-dihydroxybenzophenone,
2-hydroxy-4-methoxybenzophenone, [0090]
2-hydroxy-4-octoxybenzophenone, and [0091]
5,5'-methylene-bis(2-hydroxy-4-methoxybenzophenone);
2-(2-hydroxyphenyl)benzotriazoles, such as
2-(2-hydroxy-5-methylphenyl)benzotriazole, [0092]
2-(2-hydroxy-5-tert-octylphenyl)benzotriazole, [0093]
2-(2-hydroxy-3,5-di-tert-butylphenyl)-5-chlorobenzotriazole, [0094]
2-(2-hydroxy-3-tert-butyl-5-methylphenyl)-5-chlorobenzotriazole,
[0095] 2-(2-hydroxy-3,5-dicumylphenyl)benzotriazole, [0096]
2,2'-methylene-bis(4-tert-octyl-6-benzotriazolylphenol),
polyethylene glycol esters of [0097]
2-(2-hydroxy-3-tert-butyl-5-carboxyphenyl)benzotriazole, [0098]
2-[2-hydroxy-3-(2-acryloyloxyethyl)-5-methylphenyl]benzotriazole,
[0099]
2-[2-hydroxy-3-(2-methacryloyloxyethyl)-5-tert-butylphenyl]benzotriazole,
[0100]
2-[2-hydroxy-3-(2-methacryloyloxyethyl)-5-tert-octylphenyl]benzotr-
iazole, [0101]
2-[2-hydroxy-3-(2-methacryloyloxyethyl)-5-tert-butylphenyl]-5-chlorobenzo-
triazole, [0102]
2-[2-hydroxy-5-(2-methacryloyloxyethyl)phenyl]benzotriazole, [0103]
2-[2-hydroxy-3-tert-butyl-5-(2-methacryloyloxyethyl)phenyl]benzotriazole,
[0104]
2-[2hydroxy-3-tert-amyl-5-(2-methacryloyloxyethyl)phenyl]benzotria-
zole, [0105]
2-[2-hydroxy-3-tert-butyl-5-(3-methacryloyloxypropyl)phenyl]-5-chlorobenz-
otriazole, [0106]
2-[2-hydroxy-4-(2-methacryloyloxymethyl)phenyl]benzotriazole,
[0107]
2-[2-hydroxy-4-(3-methacryloyloxy-2-hydroxypropyl)phenyl]benzotriazole,
and [0108]
2-[2-hydroxy-4-(3-methacryloyloxypropyl)phenyl]benzotriazole;
[0109] 2-(2-hydroxyphenyl)-4,6-diaryl-1,3,5-triazines, such as
[0110] 2-(2-hydroxy-4-methoxyphenyl)-4,6-diphenyl-1,3,5-triazine,
[0111] 2-(2-hydroxy-4-hexyloxyphenyl)-4,6-diphenyl-1,3,5-triazine,
[0112]
2-(2-hydroxy-4-octoxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazine,
[0113] 2-[2-hydroxy-4-(3-C12 to 13 mixed
alkoxy-2-hydroxypropoxy)phenyl]-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-
e, [0114]
2-[2-hydroxy-4-(2-acryloyloxyethoxy)phenyl]-4,6-bis(4-methylphen-
yl)-1,3,5-triazine, [0115]
2-(2,4-dihydroxy-3-allylphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin-
e and [0116]
2,4,6-tris(2-hydroxy-3-methyl-4-hexyloxyphenyl)-1,3,5-triazine;
benzoates, such as phenyl salicylate, resorcinol monobenzoate,
2,4-di-tert-butylphenyl-3,5-di-tert-butyl-4-hydroxybenzoate,
octyl(3,5-di-tert-butyl-4-hydroxy)benzoate,
dodecyl(3,5-di-tert-butyl-4-hydroxy)benzoate,
tetradecyl(3,5-di-tert-butyl-4-hydroxy)benzoate,
hexadecyl(3,5-di-tert-butyl-4-hydroxy)benzoate,
octadecyl(3,5-di-tert-butyl-4-hydroxy)benzoate, and [0117]
behenyl(3,5-di-tert-butyl-4-hydroxy)benzoate; substituted
oxanilides, such as 2-ethyl-2'-ethoxyoxanilide and
2-ethoxy-4'-dodecyloxanilide; cyanoacrylates, such as
ethyl-.alpha.-cyano-.beta.,.beta.-diphenylacrylate and
methyl-2-cyano-3-methyl-3-(p-methoxyphenyl)acrylate; and a variety
of metal salts and metal chelates, particularly salts and chelates
of nickel and chromium. The amount of an ultraviolet absorber to be
used preferably 0.001 to 10 parts by mass, more preferably 0.01 to
5 parts by mass, with respect to 100 parts by mass of the
polyolefin-based resin.
[0118] Examples of the aliphatic amide compounds used as lubricants
include mono-fatty acid amides, such as lauric acid amide, stearic
acid amide, oleic acid amide, erucic acid amide, ricinoleic acid
amide, and 12-hydroxystearic acid amide; N,N'-bis-fatty acid
amides, such as [0119] N,N'-ethylene-bis-lauric acid amide,
N,N'-methylene-bis-stearic acid amide, [0120]
N,N'-ethylene-bis-stearic acid amide, N,N'-ethylene-bis-oleic acid
amide, [0121] N,N'-ethylene-bis-behenic acid amide,
N,N'-ethylene-bis-12-hydroxystearic acid amide, [0122]
N,N'-butylene-bis-stearic acid amide,
N,N'-hexamethylene-bis-stearic acid amide, [0123]
N,N'-hexamethylene-bis-oleic acid amide, and
N,N'-xylylene-bis-stearic acid amide; alkylol amides, such as
stearic acid monomethylol amide, coconut oil fatty acid monoethanol
amide, and stearic acid diethanol amide; N-substituted fatty acid
amides, such as N-oleyl stearic acid amide, N-oleyl oleic acid
amide, N-stearyl stearic acid amide, N-stearyl oleic acid amide,
N-oleyl palmitic acid amide, and N-stearyl erucic acid amide; and
N,N'-substituted dicarboxylic acid amides, such as N,N'-dioleyl
adipic acid amide, N,N'-distearyl adipic acid amide, N,N'-dioleyl
sebacic acid amide, N,N'-distearyl sebacic acid amide,
N,N'-distearyl terephthalic acid amide, and N,N'-distearyl
isophthalic acid amide. These lubricants may be used individually,
or two or more thereof may be used in the form of a mixture. The
amount of the lubricant(s) to be used is preferably 0.01 to 30
parts by mass, more preferably 0.1 to 20 parts by mass, with
respect to 100 parts by mass of the polyolefin-based resin.
[0124] Examples of other nucleating agents include metal
carboxylates, such as sodium benzoate, 4-tert-butylbenzoate
aluminum salt, sodium adipate, and disodium [0125]
bicyclo[2.2.1]heptane-2,3-dicarboxylate; metal phosphates, such as
sodium [0126] bis(4-tert-butylphenyl) phosphate, hydroxyaluminum
[0127] bis[2,2'-methylene-bis(4,6-di-tert-butylphenyl) phosphate],
and lithium [0128] 2,2'-methylene-bis(4,6-di-tert-butylphenyl)
phosphate; polyhydric alcohol derivatives, such as dibenzylidene
sorbitol, bis(methylbenzylidene)sorbitol,
bis(p-ethylbenzylidene)sorbitol, and
bis(dimethylbenzylidene)sorbitol; and amide compounds, such as
[0129]
N,N',N''-tris[2-methylcyclohexyl]-1,2,3-propanetricarboxamide
(RIKACLEAR PC1), [0130]
N,N',N''-tricyclohexyl-1,3,5-benzenetricarboxamide, [0131]
N,N'-dicyclohexyl-naphthalenedicarboxamide, and
1,3,5-tri(dimethylisopropoylamino)benzene. The amount of the
above-described other nucleating agent(s) to be used is preferably
0.001 to 10 parts by mass, more preferably 0.005 to 5 parts by
mass, with respect to 100 parts by mass of the polyolefin-based
resin.
[0132] In the polyolefin-based resin composition of the present
invention, a method of blending the nucleating agent of the present
invention into the polyolefin-based resin is not particularly
restricted, and any conventionally known method can be employed.
For example, the polyolefin-based resin in a powder or pellet form
may be mixed with the nucleating agent of the present invention by
dry blending, or the nucleating agent of the present invention may
be partially pre-blended and then dry-blended along with remaining
components. After the dry blending, for example, the resultant may
be mixed using a mill roll, a Banbury mixer, a super mixer or the
like, and kneaded using a uniaxial or biaxial extruder or the like.
The mixing and kneading are usually performed at a temperature of
about 120 to 250.degree. C. For example, a method in which the
nucleating agent of the present invention is added in the stage of
polymerizing the polyolefin-based resin; a method in which, after
mixing the nucleating agent of the present invention in advance
with, for example, a granulation aid such as a binder, a wax, a
solvent, or silica at a desired ratio, the resulting mixture is
granulated to prepare a one-pack composite additive and this
one-pack composite additive is added to the polyolefin-based resin;
or a method in which a masterbatch containing the nucleating agent
of the present invention at a high concentration is prepared and
then added to the polyolefin-based resin, can be employed.
[0133] The molded article of the present invention is obtained by
molding the polyolefin-based resin composition of the present
invention. The polyolefin-based resin composition of the present
invention can be molded in the same manner as general plastics by,
for example, extrusion molding, injection molding, blow molding,
vacuum molding, rotational molding, inflation molding, calender
molding, slush molding, dip molding, or foam molding, and among
these molding methods, injection molding, extrusion molding or blow
molding is preferred. Examples of the molded article of the present
invention include injection-molded articles, fibers, flat yarns,
biaxially stretched films, uniaxially stretched films, unstretched
films, sheets, thermoformed articles, extrusion blow-molded
articles, injection blow-molded articles, injection stretch
blow-molded articles, profile extrusion-molded articles, and
rotationally molded articles. Thereamong, the molded article of the
present invention is preferably an injection-molded article, a
film, a sheet, or a thermoformed article.
[0134] The polyolefin-based resin composition of the present
invention can be used in various applications, such as building
materials, agricultural materials, components for vehicles (e.g.,
automobiles, trains, ships, and airplanes), packaging materials,
miscellaneous goods, toys, home electric appliances, and medical
supplies. Specific examples of these applications include
automobile components, such as bumpers, dashboards, instrument
panels, battery casings, luggage cases, door panels, door trims,
and fender liners; resin components for home electric appliances,
such as refrigerators, laundry machines, and vacuum cleaners;
household articles, such as tableware, buckets, and bath goods;
resin components for connection, such as connectors; miscellaneous
goods, such as toys, storage containers, and synthetic paper;
medical molded articles, such as medical packages, syringes,
catheters, medical tubes, syringe preparations, infusion solution
bags, reagent containers, medicine containers, and medicine
individual packagings; building materials, such as wall materials,
flooring materials, window frames, wall papers, windows; wire
coating materials; agricultural materials, such as greenhouses
tunnels, and flat yarn mesh bags; industrial materials, such as
pallets, pail cans, backgrind tapes, tapes for liquid crystal
protection, pipes, and modified silicone polymers for sealing
materials; food packaging materials, such as wraps, trays, cups,
films, bottles, caps, and storage containers; 3D printer materials;
and battery separator films. The polyolefin-based resin composition
of the present invention can also be used in those applications
where various post-treatments are performed, for example,
applications where sterilization by radiation is performed, such as
medical applications and food packaging applications, as well as
applications where a low-temperature plasma treatment and the like
are performed after molding so as to improve the surface properties
such as coating properties. Among these applications, the
polyolefin-based resin composition of the present invention is
preferably used in automobile components, household articles, and
food packaging materials. Moreover, the polyolefin-based resin
composition of the present invention may be blended with glass
fibers, carbon fibers or the like to produce fiber-reinforced
plastics.
[0135] The above-described molding is affected by the melt
viscosity of the resin, and the molding temperature is preferably
in a range of 120 to 250.degree. C., more preferably in a range of
130 to 240.degree. C. When the molding temperature is lower than
120.degree. C., the polyolefin-based resin itself cannot be
sufficiently melted, and this may lead to irregularities on the
resulting molded article, whereas when the molding temperature is
250.degree. C. or higher, the effects of the present invention may
not be attained.
EXAMPLES
[0136] The present invention will now be described more concretely
by way of Examples and Comparative Examples. It is noted here that,
in Examples and Comparative Examples, "part(s)" means "parts by
mass".
Examples 1 to 5 and Comparative Examples 1 and 2
[0137] To a homopolypropylene (trade name "H700" manufactured by
Prime Polymer Co., Ltd., melt flow rate=8 g/10 min (2.16
kg.times.230.degree. C. according to ISO Standard 1133)) in an
amount of 100 parts by mass, 0.05 parts by mass of a phenolic
antioxidant
(tetrakis[methylene-3-(3',5'-di-tert-butyl-4'-hydroxyphenyl)propionate]me-
thane), 0.1 parts by mass of a phosphorus-based antioxidant
(tris(2,4-di-tert-butylphenyl)phosphite), 0.05 parts by mass of
calcium stearate and 0.1 parts by mass of each organic phosphate
compound (nucleating agent) shown in Table 2 were added, and these
materials were mixed at 1,000 rpm for 1 minute using a Henschel
mixer (FM100, manufactured by Mitsui Mining Co., Ltd.) and
subsequently kneaded using a biaxial extruder (TEX28V, manufactured
by The Japan Steel Works, Ltd.) at an extrusion temperature of
230.degree. C., a screw rotation speed of 150 rpm and a feed rate
of 7.5 kg/h, whereby a pellet was produced. For the thus obtained
resin composition, the yellowness (Y.I.), the haze, the bending
elastic modulus, and the heat resistance in storage at 150.degree.
C. were evaluated in accordance with the below-described
procedures. The production of nucleating agents and the measurement
of P/Na were performed by the following procedures.
Synthesis of Nucleating Agent 1
[0138] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1.000 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 19 g (0.039 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate was added to the
resultant, which was mixed for 30 minutes, dried under reduced
pressure, and then pulverized to obtain a nucleating agent 1 in the
form of white powder.
Synthesis of Nucleating Agent 2
[0139] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1.000 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 14 g (0.350 mol) of sodium
hydroxide was added to the resultant, which was mixed for 30
minutes, dried under reduced pressure, and then pulverized to
obtain a nucleating agent 2 in the form of white powder.
Synthesis of Nucleating Agent 3
[0140] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1.000 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 199 g (0.409 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate was added to the
resultant, which was mixed for 30 minutes, dried under reduced
pressure, and then pulverized to obtain a nucleating agent 3 in the
form of white powder.
Synthesis of Nucleating Agent 4
[0141] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1.000 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 1 g (0.002 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate was added to the
resultant, which was mixed for 30 minutes, dried under reduced
pressure, and then pulverized to obtain a nucleating agent 4 in the
form of white powder.
Synthesis of Nucleating Agent 5
[0142] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1.000 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 37 g (0.076 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate was added to the
resultant, which was mixed for 30 minutes, dried under reduced
pressure, and then pulverized to obtain a nucleating agent 5 in the
form of white powder.
Synthesis of Nucleating Agent 6
[0143] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1.000 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 1.48 g (0.037 mol) of sodium
hydroxide was added to the resultant, which was dried under reduced
pressure and then pulverized to obtain a nucleating agent 6 in the
form of white powder.
Synthesis of Nucleating Agent 7
[0144] To a kneader, 486 g (1.000 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate, a solution of
40 g (1 mol) of sodium hydroxide in 100 g of water, and 97 g of
methanol were added, and these materials were kneaded for 1 hour at
room temperature. Subsequently, 55 g (0.113 mol) of
2,2'-methylene-bis(4,6-di-t-butylphenyl) phosphate was added to the
resultant, which was mixed for 30 minutes, dried under reduced
pressure, and then pulverized to obtain a nucleating agent 7 in the
form of white powder.
Measurement of P/Na
[0145] The thus obtained nucleating agents were each weighed in an
amount of 100 mg, and 10 ml of 61% nitric acid was added thereto,
and the resultant was decomposed in a microwave sample
decomposition apparatus (TOPwave, manufactured by Analytik Jena
AG). The resulting decomposition solution was diluted to 100 ml in
a measuring flask and then further diluted 10-fold, after which the
diluted solution was filtered through a disposable membrane filter
having a pore size of 0.45 .mu.m to prepare a measurement sample
solution. Thereafter, P and Na in this measurement sample solution
were quantified under the following conditions using an ICP
emission spectrophotometer (SPS3500, manufactured by SII
NanoTechnology Inc.), and the ratio P/Na in an NA-11 sample was
calculated from the thus obtained results.
TABLE-US-00001 TABLE 1 P Na Phosphorus ICP Multielement Standard
Solution Standard IV Standard solution (Merck Millipore Ltd.)
(Merck Millipore Ltd.) Chamber gas absent absent Purge gas present
absent
Y.I.
[0146] Each pellet obtained above was injection-molded at
200.degree. C. using an injection molding machine (EC100-2A,
manufactured by Toshiba Machine Co., Ltd.) to prepare a test piece
having dimensions of 60 mm.times.60 mm.times.2 mm. Immediately
thereafter, the test piece was left to stand in a 23.degree. C.
incubator for 48 hours, and the test piece was subsequently taken
out and the Y.I. thereof was measured a spectrocolorimeter
(COLOR-EYE 7000A, manufactured by X-Rite Inc.). The results thereof
are shown together in Table 2.
Haze
[0147] Each pellet obtained above was injection-molded at an
injection temperature of 200.degree. C. and a mold temperature of
50.degree. C. using an injection molding machine (EC100-2A,
manufactured by Toshiba Machine Co., Ltd.) to prepare a test piece
having dimensions of 60 mm.times.60 mm.times.2 mm. Immediately
thereafter, the test piece was left to stand in a 23.degree. C.
incubator for 48 hours, and the test piece was subsequently taken
out and the haze thereof was measured in accordance with ISO-14782.
The results thereof are shown together in Table 2.
Flexural Modulus
[0148] Each pellet obtained above was injection-molded at an
injection temperature of 200.degree. C. and a mold temperature of
50.degree. C. using an injection molding machine (EC100-2A,
manufactured by Toshiba Machine Co., Ltd.) to prepare a test piece
having dimensions of 80 mm.times.10 mm.times.4 mm. Immediately
thereafter, the test piece was left to stand in a 23.degree. C.
incubator for 48 hours, and the test piece was subsequently taken
out and the flexural modulus (MPa) thereof was measured in
accordance with ISO-178. The results thereof are shown together in
Table 2.
Heat Resistance in Storage at 150.degree. C.
[0149] Each test piece obtained above was placed in a 150.degree.
C. gear oven. Thereafter, the test piece was taken out every 24
hours, and the presence or absence of a crack was checked by
observation under a microscope and the Y.I. was measured. An
evaluation of o was given when the endurance time until the crack
generation and an increase in Y.I. was 550 hours to 600 hours,
while an evaluation of .DELTA. was given when the endurance time
was 500 hours to 550 hours. The results thereof are shown together
in Table 2.
TABLE-US-00002 TABLE 2 Comparative Comparative Example 1 Example 1
Example 2 Example 2 Example 3 Example 4 Example 5 Nucleating agent
1 2 3 4 5 6 7 P/Na 1.400 1.000 1.900 1.350 1.450 1.300 1.500 Y.I.
of 2-mm test 6.6 9.0 7.0 6.8 6.7 7.6 6.8 piece Haze, 2 mm (%) 51.2
51.5 54.4 51.2 51.6 51.9 52.3 Flexural modulus 1,935 1,935 1,926
1,934 1,933 1,931 1,930 (MPa) Heat resistance in .smallcircle.
.DELTA. .DELTA. .smallcircle. .smallcircle. .smallcircle.
.smallcircle. storage at 150.degree. C.
[0150] From Table 2, it was confirmed that the nucleating agent of
the present invention is capable of improving the transparency and
the heat resistance of a molded article composed of a polyolefin
resin composition. Particularly, it is seen that the Y.I. value was
in the 6 range, the haze value was in the 51 rage, and the storage
stability at 150.degree. C. was favorable in those cases where the
ratio P/Na was 1.350, 1.400 or 1.450.
* * * * *