U.S. patent application number 14/364482 was filed with the patent office on 2014-10-30 for functionalized block composite and crystalline block composite compositions.
This patent application is currently assigned to Dow Global Technologies LLC. The applicant listed for this patent is DOW GLOBAL TECHNOLOGIES LLC. Invention is credited to Yushan Hu, Gary R. Marchand, Michael D. Read, H. C. Silvis, Kim L. Walton.
Application Number | 20140323656 14/364482 |
Document ID | / |
Family ID | 47520261 |
Filed Date | 2014-10-30 |
United States Patent
Application |
20140323656 |
Kind Code |
A1 |
Hu; Yushan ; et al. |
October 30, 2014 |
FUNCTIONALIZED BLOCK COMPOSITE AND CRYSTALLINE BLOCK COMPOSITE
COMPOSITIONS
Abstract
The invention provides functionalized block composites and
crystalline block composites. In particular, the invention provides
a functionalized olefin-based polymer formed from at least (A) and
(B): (A) a crystalline block composite comprising: a block
copolymer comprising a propylene-based crystalline block and
crystalline ethylene-based block; a propylene-based crystalline
polymer; and, a crystalline ethylene-based polymer; and (B) at
least one functionalization agent or a functionalized olefin-based
polymer formed from at least (A) and (B): (A) a crystalline block
composite comprising: a block copolymer comprising a
propylene-based crystalline block and crystalline ethylene-based
block; a propylene-based crystalline polymer; and, a crystalline
ethylene-based polymer; and (B) at least one functionalization
agent.
Inventors: |
Hu; Yushan; (Pearland,
TX) ; Walton; Kim L.; (Lake Jackson, TX) ;
Marchand; Gary R.; (Gonzales, LA) ; Read; Michael
D.; (Midland, MI) ; Silvis; H. C.; (Midland,
MI) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
DOW GLOBAL TECHNOLOGIES LLC |
Midland |
MI |
US |
|
|
Assignee: |
Dow Global Technologies LLC
Midland
MI
|
Family ID: |
47520261 |
Appl. No.: |
14/364482 |
Filed: |
December 12, 2012 |
PCT Filed: |
December 12, 2012 |
PCT NO: |
PCT/US2012/069194 |
371 Date: |
June 11, 2014 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
61570340 |
Dec 14, 2011 |
|
|
|
Current U.S.
Class: |
525/88 |
Current CPC
Class: |
C08L 53/00 20130101;
C08L 51/06 20130101; C08L 51/003 20130101; C08L 51/06 20130101;
C08F 287/00 20130101; C08L 23/08 20130101; C08F 222/06 20130101;
C08F 287/00 20130101; C08L 23/142 20130101 |
Class at
Publication: |
525/88 |
International
Class: |
C08L 53/00 20060101
C08L053/00; C08L 51/00 20060101 C08L051/00 |
Claims
1. A composition comprising a functionalized olefin-based polymer
formed from at least (A) and (B): (A) a block composite comprising:
i) a block copolymer comprising a crystalline propylene-based block
and an ethylene/.alpha.-olefin block; ii) a crystalline
propylene-based polymer; and, iii) an ethylene/.alpha.-olefin
polymer; and (B) at least one functionalization agent.
2. A composition comprising a functionalized olefin-based polymer
formed from at least (A) and (B): (A) a crystalline block composite
comprising: i) a block copolymer comprising a crystalline
propylene-based block and an crystalline ethylene-based block; ii)
a crystalline propylene-based polymer; and, iii) an crystalline
ethylene-based polymer; and (B) at least one functionalization
agent.
3. The composition of claim 1 wherein the functionalization agent
is selected from silane, maleic anhydride, peroxide, and amine.
4. The composition of claim 2 wherein the functionalization agent
is selected from silane, maleic anhydride, peroxide, and amine.
5. The composition of claim 1 wherein the crystalline
propylene-based block comprises an amount greater than 90 mol % of
propylene, the ethylene/.alpha.-olefin block comprises an amount of
10 mol % to 90 mol % of ethylene, and the functionalization agent
is a silane for grafting onto polymers in the block composite and
having the formula
CH.sub.2.dbd.CR--(COO).sub.x(C.sub.nH.sub.2n).sub.ySiR'.sub.3,
where R is a hydrogen atom or methyl group; x and y are 0 or 1,
with the proviso that when x is 1, y is 1; n is an integer from 1
to 12 inclusive, and each R' independently is an organic group.
6. The composition of claim 2 wherein the crystalline
propylene-based block comprises an amount greater than 90 mol % of
propylene, the crystalline ethylene/.alpha.-olefin block comprises
an amount of 10 mol % to 90 mol % of ethylene, and the
functionalization agent is a silane for grafting onto polymers in
the crystalline block composite and having the formula
CH.sub.2.dbd.CR--(COO).sub.x(C.sub.nH.sub.2n).sub.ySiR'.sub.3,
where R is a hydrogen atom or methyl group; x and y are 0 or 1,
with the proviso that when x is 1, y is 1; n is an integer from 1
to 12 inclusive, and each R' independently is an organic group.
7. The composition of claim 1 wherein the crystalline
propylene-based block comprises an amount greater than 90 mol % of
propylene, the ethylene/.alpha.-olefin block comprises an amount of
10 mol % to 90 mol % of ethylene, and the functionalization agent
is maleic anhydride for grafting onto polymers in the block
composite.
8. The composition of claim 2 wherein the crystalline
propylene-based block comprises an amount greater than 90 mol % of
propylene, the crystalline ethylene/.alpha.-olefin block comprises
an amount of 10 mol % to 90 mol % of ethylene, and the
functionalization agent is maleic anhydride for grafting onto
polymers in the crystalline block composite.
9. The composition of claim 1 wherein the crystalline
propylene-based block comprises an amount greater than 90 mol % of
propylene, the ethylene/.alpha.-olefin block comprises an amount of
10 mol % to 90 mol % of ethylene, and the functionalization agent
is amine for grafting onto polymers in the block composite.
10. The composition of claim 2 wherein the crystalline
propylene-based block comprises an amount greater than 90 mol % of
propylene, the crystalline ethylene/.alpha.-olefin block comprises
an amount of 10 mol % to 90 mol % of ethylene, and the
functionalization agent is amine for grafting onto polymers in the
crystalline block composite.
Description
FIELD OF THE INVENTION
[0001] This invention relates to functionalized block composites
and functionalized crystalline block composites.
BACKGROUND OF THE INVENTION
[0002] Despite advances in the polyolefin industry, there remains a
need to develop compatibilizing agents for compatibilizing
incompatible polymer blends; and thus, which can be used to develop
new polymer alloys. Many consumer and industrial products are
formed from multiple thermoplastic materials. Some commonly used
polymers include non polar polyolefins, such as polypropylene (PP)
and polyethylene (PE) and polar polymers such polyamides,
polyesters, polyurethanes and polycarbonates. Maleated polymers are
a useful class of compatibilizing agents for thermoplastic
polymers. Such polymers include maleic anhydride-grafted PP, PE and
ethylene copolymers. However, such maleated polyolefins are
typically used as compatibilizers for PP/polar polymer systems or
PE/polar polymer systems; they have not been used in PP/PE/polar
polymer systems due to the inherent incompatibility of PP/PE/polar
polymer.
[0003] In addition, there is a need to develop polyolefins for use
in coatings, adhesive and tie layer applications, where such
polyolefins provide strong adhesion to polar and/or non-polar
substrates, improve paintability and/or printability, provide good
flexibility, and provide structural and chemical stability over a
broad service temperature range.
[0004] U.S. Pat. No. 7,897,689 relates to functionalized
interpolymers derived from base olefin interpolymers, which are
prepared by polymerizing one or more monomers or mixtures of
monomers, such as ethylene and one or more comonomers, to form an
interpolymer product having unique physical properties. The
functionalized olefin interpolymers contain two or more differing
regions or segments (blocks), resulting in unique processing and
physical properties.
[0005] US Patent Application Publication No. US2010-0093942 relates
to polyolefin blend compositions of polar and/or non-polar
polymers, with at least one functionalized polyolefin polymer
selected from the group consisting of: amine functionalized,
hydroxyl functionalized, imide functionalized, anhydride
functionalized, or carboxylic acid functionalized polyolefin
polymers. Also disclosed are methods for making the functionalized
polyolefin polymer and materials and articles containing at least
one component prepared from such compositions
[0006] U.S. Pat. No. 7,622,529 relates to olefin interpolymers as
compatiblizers, which are prepared by polymerizing one or more
monomers or mixtures of monomers, such as ethylene and one or more
comonomers, to form an interpolymer product having unique physical
properties. The olefin interpolymers contain two or more differing
regions or segments (blocks), resulting in unique processing and
physical properties.
[0007] WO/2011/041696 relates to block composites and their use as
impact modifiers; WO/2011/041698 relates to block composites in
soft compounds; and WO/2011/041699 relates to block composites in
thermoplastic vulcanisates.
SUMMARY
[0008] The invention provides a composition comprising a
functionalized olefin-based polymer formed from at least (A) and
(B):
[0009] (A) a block composite comprising: [0010] i) a block
copolymer comprising a propylene-based crystalline block and an
ethylene/.alpha.-olefin block; [0011] ii) a propylene-based
crystalline polymer; and, [0012] iii) an ethylene/.alpha.-olefin
polymer; and
[0013] (B) at least one functionalization agent.
The invention also provides a composition comprising a
functionalized olefin-based polymer formed from at least (A) and
(B):
[0014] (A) a crystalline block composite comprising: [0015] i) a
block copolymer comprising a crystalline propylene-based block and
an crystalline ethylene-based block; [0016] ii) a crystalline
propylene-based polymer; and, [0017] iii) an crystalline
ethylene-based polymer; and
[0018] (B) at least one functionalization agent.
BRIEF DESCRIPTION OF THE DRAWINGS
[0019] FIG. 1 shows the DSC profile for CBC2.
[0020] FIG. 2 shows the TREF analysis of CBC2
[0021] FIG. 3 shows HTLC analysis of CBC2.
[0022] FIG. 4 shows the IR spectrum for MAH-g-CBC2-4.
[0023] FIG. 5 shows the DSC profile for MAH-g-CBC2-4.
[0024] FIG. 6 shows HTLC analysis of MAH-g-CBC2-4.
[0025] FIG. 7 shows TEM for CBC5, MAH-g-CBC2 (Ex. 5) and
MAH-g-(EP1/iPP1 50/50 Blend) (Ex. C).
[0026] FIG. 8 shows the IR spectrum for Imide-g-CBC2-4.
DETAILED DESCRIPTION
[0027] All references to the Periodic Table of the Elements herein
shall refer to the Periodic Table of the Elements, published and
copyrighted by CRC Press, Inc., 2003. Also, any references to a
Group or Groups shall be to the Group or Groups reflected in this
Periodic Table of the Elements using the IUPAC system for numbering
groups. Unless stated to the contrary, implicit from the context,
or customary in the art, all parts and percents are based on
weight. For purposes of United States patent practice, the contents
of any patent, patent application, or publication referenced herein
are hereby incorporated by reference in their entirety (or the
equivalent US version thereof is so incorporated by reference)
especially with respect to the disclosure of synthetic techniques,
definitions (to the extent not inconsistent with any definitions
provided herein) and general knowledge in the art.
[0028] The invention provides functionalized derivatives of block
composites (BC) and crystalline block composites (CBC), as
described herein, and provides for compositions comprising the
same. The functionalized BCs and CBCs of this invention often
exhibit improved grafting efficiency and minimal molecular weight
change as a result of the functionalization process. The invention
also provides methods of using these functionalized BCs and CBCs in
applications requiring unique combinations of processing elements
and unique physical properties in the final product. In still
another aspect, the invention provides the articles prepared from
these functionalized BCs and CBCs.
[0029] The term "polyethylene" includes homopolymers of ethylene
and copolymers of ethylene and one or more C.sub.3-8
.alpha.-olefins in which ethylene comprises at least 50 mole
percent.
[0030] The term "polypropylene" includes homopolymers of propylene
such as isotactic polypropylene, syndiotactic polypropylene, and
copolymers of propylene and one or more C.sub.2,4-8 .alpha.-olefins
in which propylene comprises at least 50 mole percent.
[0031] The term "crystalline" refers to a polymer or polymer block
that possesses a first order transition or crystalline melting
point (Tm) as determined by differential scanning calorimetry (DSC)
or equivalent technique. The term may be used interchangeably with
the term "semicrystalline".
[0032] The term "crystallizable" refers to a monomer that can
polymerize such that the resulting polymer is crystalline.
Crystalline ethylene polymers typically have, but are not limited
to, densities of 0.89 g/cc to 0.97 g/cc and melting points of
75.degree. C. to 140.degree. C. Crystalline propylene polymers
typically have, but are not limited to, densities of 0.88 g/cc to
0.91 g/cc and melting points of 100.degree. C. to 170.degree.
C.
[0033] The term "amorphous" refers to a polymer lacking a
crystalline melting point.
[0034] The term "isotactic" is defined as polymer repeat units
having at least 70 percent isotactic pentads as determined by
.sup.13C-NMR analysis. "Highly isotactic" is defined as polymers
having at least 90 percent isotactic pentads.
[0035] The term "block copolymer" or "segmented copolymer" refers
to a polymer comprising two or more chemically distinct regions or
segments (referred to as "blocks") joined in a linear manner, that
is, a polymer comprising chemically differentiated units which are
joined (covalently bonded) end-to-end with respect to polymerized
functionality, rather than in pendent or grafted fashion. In a
preferred embodiment, the blocks differ in the amount or type of
comonomer incorporated therein, the density, the amount of
crystallinity, the type of crystallinity (e.g. polyethylene versus
polypropylene), the crystallite size attributable to a polymer of
such composition, the type or degree of tacticity (isotactic or
syndiotactic), regio-regularity or regio-irregularity, the amount
of branching, including long chain branching or hyper-branching,
the homogeneity, or any other chemical or physical property. The
block copolymers of the invention are characterized by unique
distributions of both polymer polydispersity (PDI or Mw/Mn) and
block length distribution, due, in a preferred embodiment, to the
effect of a shuttling agent(s) in combination with the
catalyst(s).
[0036] The term "block composite" refers to polymers comprising a
soft copolymer, polymerized units in which the comonomer content is
greater than 10 mol % and less than 90 mol % and preferably greater
than 20 mol % and less than 80 mol %, and most preferably greater
than 33 mol % and less than 75 mol %, a hard polymer, in which the
monomer is present in an amount greater than 90 mol % and up to 100
mol %, and preferably greater than 93 mol % and up to 100 mol %,
and more preferably greater than 95 mol % and up to 100 mol %, and
most preferably greater than 98 mol % and up to mol %, and a block
copolymer, preferably a diblock, having a soft segment and a hard
segment, wherein the hard segment of the block copolymer is
essentially the same composition as the hard polymer in the block
composite and the soft segment of the block copolymer is
essentially the same composition as the soft copolymer of the block
composite. The block copolymers can be linear or branched. More
specifically, when produced in a continuous process, the block
composites desirably possess PDI from 1.7 to 15, preferably from
1.8 to 3.5, more preferably from 1.8 to 2.2, and most preferably
from 1.8 to 2.1. When produced in a batch or semi-batch process,
the block composites desirably possess PDI from 1.0 to 2.9,
preferably from 1.3 to 2.5, more preferably from 1.4 to 2.0, and
most preferably from 1.4 to 1.8. Such block composites are
described in, for example, US Patent Application Publication Nos
US2011-0082257, US2011-0082258 and US2011-0082249, all published on
Apr. 7, 2011 and incorporated herein by reference with respect to
descriptions of the block composites, processes to make them and
methods of analyzing them.
[0037] The term "crystalline block composite" (CBC) refers to
polymers comprising a crystalline ethylene based polymer (CEP), a
crystalline alpha-olefin based polymer (CAOP), and a block
copolymer having a crystalline ethylene block (CEB) and a
crystalline alpha-olefin block (CAOB), wherein the CEB of the block
copolymer is essentially the same composition as the CEP in the
block composite and the CAOB of the block copolymer is essentially
the same composition as the CAOP of the block composite.
Additionally, the compositional split between the amount of CEP and
CAOP will be essentially the same as that between the corresponding
blocks in the block copolymer. The block copolymers can be linear
or branched. More specifically, each of the respective block
segments can contain long chain branches, but the block copolymer
segment is substantially linear as opposed to containing grafted or
branched blocks. When produced in a continuous process, the
crystalline block composites desirably possess PDI from 1.7 to 15,
preferably 1.8 to 10, preferably from 1.8 to 5, more preferably
from 1.8 to 3.5. Such crystalline block composites are described
in, for example, U.S. Provisional Application Ser. Nos. 61/356,978,
61/356,957 and 61/356,990, all filed on Jun. 21, 2010 and
incorporated herein by reference with respect to descriptions of
the block composites, processes to make them and methods of
analyzing them.
[0038] CAOB refers to highly crystalline blocks of polymerized
alpha olefin units in which the monomer is present in an amount
greater than 90 mol %, preferably greater than 93 mol percent, more
preferably greater than 95 mol percent, and preferably greater than
96 mol percent. In other words, the comonomer content in the CAOBs
is less than 10 mol percent, and preferably less than 7 mol
percent, and more preferably less than 5 mol percent, and most
preferably less than 4 mol %. CAOBs with propylene crystallinity
have corresponding melting points that are 80.degree. C. and above,
preferably 100.degree. C. and above, more preferably 115.degree. C.
and above, and most preferably 120.degree. C. and above. In some
embodiments, the CAOB comprise all or substantially all propylene
units. CEB, on the other hand, refers to blocks of polymerized
ethylene units in which the comonomer content is 10 mol % or less,
preferably between 0 mol % and 10 mol %, more preferably between 0
mol % and 7 mol % and most preferably between 0 mol % and 5 mol %.
Such CEB have corresponding melting points that are preferably
75.degree. C. and above, more preferably 90.degree. C., and
100.degree. C. and above.
[0039] "Hard" segments refer to highly crystalline blocks of
polymerized units in which the monomer is present in an amount
greater than 90 mol percent, and preferably greater than 93 mol
percent, and more preferably greater than 95 mol percent, and most
preferably greater than 98 mol percent. In other words, the
comonomer content in the hard segments is most preferably less than
2 mol percent, and more preferably less than 5 mol percent, and
preferably less than 7 mol percent, and less than 10 mol percent.
In some embodiments, the hard segments comprise all or
substantially all propylene units. "Soft" segments, on the other
hand, refer to amorphous, substantially amorphous or elastomeric
blocks of polymerized units in which the comonomer content is
greater than 10 mol % and less than 90 mol % and preferably greater
than 20 mol % and less than 80 mol %, and most preferably greater
than 33 mol % and less than 75 mol %.
[0040] The block composite and crystalline block composite polymers
are preferably prepared by a process comprising contacting an
addition polymerizable monomer or mixture of monomers under
addition polymerization conditions with a composition comprising at
least one addition polymerization catalyst, a cocatalyst and a
chain shuttling agent, said process being characterized by
formation of at least some of the growing polymer chains under
differentiated process conditions in two or more reactors operating
under steady state polymerization conditions or in two or more
zones of a reactor operating under plug flow polymerization
conditions. In a preferred embodiment, the block composites of the
invention comprise a fraction of block polymer which possesses a
most probable distribution of block lengths.
[0041] Suitable processes useful in producing the block composites
and crystalline block composites may be found, for example, in US
Patent Application Publication No. 2008/0269412, published on Oct.
30, 2008, which is herein incorporated by reference. In particular,
the polymerization is desirably carried out as a continuous
polymerization, preferably a continuous, solution polymerization,
in which catalyst components, monomers, and optionally solvent,
adjuvants, scavengers, and polymerization aids are continuously
supplied to one or more reactors or zones and polymer product
continuously removed therefrom. Within the scope of the terms
"continuous" and "continuously" as used in this context are those
processes in which there are intermittent additions of reactants
and removal of products at small regular or irregular intervals, so
that, over time, the overall process is substantially continuous.
Moreover, as previously explained, the chain shuttling agent(s) may
be added at any point during the polymerization including in the
first reactor or zone, at the exit or slightly before the exit of
the first reactor, or between the first reactor or zone and the
second or any subsequent reactor or zone. Due to the difference in
monomers, temperatures, pressures or other difference in
polymerization conditions between at least two of the reactors or
zones connected in series, polymer segments of differing
composition such as comonomer content, crystallinity, density,
tacticity, regio-regularity, or other chemical or physical
difference, within the same molecule are formed in the different
reactors or zones. The size of each segment or block is determined
by continuous polymer reaction conditions, and preferably is a most
probable distribution of polymer sizes.
[0042] When producing a block polymer having a crystalline ethylene
block (CEB) and a crystalline alpha-olefin block (CAOB) in two
reactors or zones it is possible to produce the CEB in the first
reactor or zone and the CAOB in the second reactor or zone or to
produce the CAOB in the first reactor or zone and the CEB in the
second reactor or zone. It is more advantageous to produce CEB in
the first reactor or zone with fresh chain shuttling agent added.
The presence of increased levels of ethylene in the reactor or zone
producing CEB will typically lead to much higher molecular weight
in that reactor or zone than in the zone or reactor producing CAOB.
The fresh chain shuttling agent will reduce the MW of polymer in
the reactor or zone producing CEB thus leading to better overall
balance between the length of the CEB and CAOB segments.
[0043] When operating reactors or zones in series it is necessary
to maintain diverse reaction conditions such that one reactor
produces CEB and the other reactor produces CAOB. Carryover of
ethylene from the first reactor to the second reactor (in series)
or from the second reactor back to the first reactor through a
solvent and monomer recycle system is preferably minimized. There
are many possible unit operations to remove this ethylene, but
because ethylene is more volatile than higher alpha olefins one
simple way is to remove much of the unreacted ethylene through a
flash step by reducing the pressure of the effluent of the reactor
producing CEB and flashing off the ethylene. A more preferable
approach is to avoid additional unit operations and to utilize the
much greater reactivity of ethylene versus higher alpha olefins
such that the conversion of ethylene across the CEB reactor
approaches 100%. The overall conversion of monomers across the
reactors can be controlled by maintaining the alpha olefin
conversion at a high level (90 to 95%).
[0044] Suitable catalysts and catalyst precursors for use in the
present invention include metal complexes such as disclosed in
WO2005/090426, in particular, those disclosed starting on page 20,
line 30 through page 53, line 20, which is herein incorporated by
reference. Suitable catalysts are also disclosed in US
2006/0199930; US 2007/0167578; US 2008/0311812; U.S. Pat. No.
7,355,089 B2; or WO 2009/012215, which are herein incorporated by
reference with respect to catalysts.
[0045] Particularly preferred catalysts are those of the following
formula:
##STR00001##
where: R.sup.20 is an aromatic or inertly substituted aromatic
group containing from 5 to 20 atoms not counting hydrogen, or a
polyvalent derivative thereof; T.sup.3 is a hydrocarbylene or
silane group having from 1 to 20 atoms not counting hydrogen, or an
inertly substituted derivative thereof; M.sup.3 is a Group 4 metal,
preferably zirconium or hafnium; G is an anionic, neutral or
dianionic ligand group; preferably a halide, hydrocarbyl or
dihydrocarbylamide group having up to 20 atoms not counting
hydrogen; g is a number from 1 to 5 indicating the number of such G
groups; and bonds and electron donative interactions are
represented by lines and arrows respectively.
[0046] Preferably, such complexes correspond to the formula:
##STR00002##
wherein: T.sup.3 is a divalent bridging group of from 2 to 20 atoms
not counting hydrogen, preferably a substituted or unsubstituted,
C.sub.3-6 alkylene group; and Ar.sup.2 independently each
occurrence is an arylene or an alkyl- or aryl-substituted arylene
group of from 6 to 20 atoms not counting hydrogen; M.sup.3 is a
Group 4 metal, preferably hafnium or zirconium; G independently
each occurrence is an anionic, neutral or dianionic ligand group; g
is a number from 1 to 5 indicating the number of such X groups; and
electron donative interactions are represented by arrows.
[0047] Preferred examples of metal complexes of foregoing formula
include the following compounds:
##STR00003##
where M.sup.3 is Hf or Zr; Ar.sup.4 is C.sub.6-20 aryl or inertly
substituted derivatives thereof, especially
3,5-di(isopropyl)phenyl, 3,5-di(isobutyl)phenyl,
dibenzo-1H-pyrrole-1-yl, or anthracen-5-yl, and T.sup.4
independently each occurrence comprises a C.sub.3-6 alkylene group,
a C.sub.3-6 cycloalkylene group, or an inertly substituted
derivative thereof;
[0048] R.sup.21 independently each occurrence is hydrogen, halo,
hydrocarbyl, trihydrocarbylsilyl, or trihydrocarbylsilylhydrocarbyl
of up to 50 atoms not counting hydrogen; and
G, independently each occurrence is halo or a hydrocarbyl or
trihydrocarbylsilyl group of up to 20 atoms not counting hydrogen,
or 2 G groups together are a divalent derivative of the foregoing
hydrocarbyl or trihydrocarbylsilyl groups.
[0049] Especially preferred are compounds of the formula:
##STR00004##
wherein Ar.sup.4 is 3,5-di(isopropyl)phenyl,
3,5-di(isobutyl)phenyl, dibenzo-1H-pyrrole-1-yl, or anthracen-5-yl,
R.sup.21 is hydrogen, halo, or C.sub.1-4 alkyl, especially methyl
T.sup.4 is propan-1,3-diyl or butan-1,4-diyl, and G is chloro,
methyl or benzyl.
[0050] Other suitable metal complexes are those of the formula:
##STR00005##
[0051] The foregoing polyvalent Lewis base complexes are
conveniently prepared by standard metallation and ligand exchange
procedures involving a source of the Group 4 metal and the neutral
polyfunctional ligand source. In addition, the complexes may also
be prepared by means of an amide elimination and hydrocarbylation
process starting from the corresponding Group 4 metal tetraamide
and a hydrocarbylating agent, such as trimethylaluminum. Other
techniques may be used as well. These complexes are known from the
disclosures of, among others, U.S. Pat. Nos. 6,320,005, 6,103,657,
6,953,764 and International Publication Nos WO 02/38628 and WO
03/40195.
[0052] Suitable co-catalysts are those disclosed in WO2005/090426,
in particular, those disclosed on page 54, line 1 to page 60, line
12, which is herein incorporated by reference.
[0053] Suitable chain shuttling agents are those disclosed in
WO2005/090426, in particular, those disclosed on page 19, line 21
through page 20 line 12, which is herein incorporated by reference.
Particularly preferred chain shuttling agents are dialkyl zinc
compounds.
[0054] Preferably, the block composite polymers comprise propylene,
1-butene or 4-methyl-1-pentene and one or more comonomers.
Preferably, the block polymers of the block composites comprise in
polymerized form propylene and ethylene and/or one or more
C.sub.4-20 .alpha.-olefin comonomers, and/or one or more additional
copolymerizable comonomers or they comprise 4-methyl-1-pentene and
ethylene and/or one or more C.sub.4-20 .alpha.-olefin comonomers,
or they comprise 1-butene and ethylene, propylene and/or one or
more C.sub.5-C.sub.20 .alpha.-olefin comonomers and/or one or more
additional copolymerizable comonomers. Additional suitable
comonomers are selected from diolefins, cyclic olefins, and cyclic
diolefins, halogenated vinyl compounds, and vinylidene aromatic
compounds. Preferably, the monomer is propylene and the comonomer
is ethylene.
[0055] Comonomer content in the resulting block composite polymers
may be measured using any suitable technique, with techniques based
on nuclear magnetic resonance (NMR) spectroscopy preferred. It is
highly desirable that some or all of the polymer blocks comprise
amorphous or relatively amorphous polymers such as copolymers of
propylene, 1-butene or 4-methyl-1-pentene and a comonomer,
especially random copolymers of propylene, 1-butene or
4-methyl-1-pentene with ethylene, and any remaining polymer blocks
(hard segments), if any, predominantly comprise propylene, 1-butene
or 4-methyl-1-pentene in polymerized form. Preferably such segments
are highly crystalline or stereospecific polypropylene, polybutene
or poly-4-methyl-1-pentene, especially isotactic homopolymers.
Additional suitable comonomers are selected from diolefins, cyclic
olefins, and cyclic diolefins, halogenated vinyl compounds, and
vinylidene aromatic compounds.
[0056] In the case wherein the comonomer is ethylene, it is
preferably present in an amount of 10 mol % to 90 mol %, more
preferably from 20 mol % to 80 mol %, and most preferably from 33
mol % to 75 mol % percent. Preferably, the copolymers comprise hard
segments that are 90 mol % to 100 mol % propylene. The hard
segments can be greater than 90 mol % preferably greater than 93
mol % and more preferably greater than 95 mol % propylene, and most
preferably greater than 98 mol % propylene. Such hard segments have
corresponding melting points that are 80.degree. C. and above,
preferably 100.degree. C. and above, more preferably 115.degree. C.
and above, and most preferably 120.degree. C. and above.
[0057] In some embodiments, the block composites of the invention
have a Block Composite Index (BCI), as defined below, that is
greater than zero but less than about 0.4 or from about 0.1 to
about 0.3. In other embodiments, BCI is greater than about 0.4 and
up to about 1.0. Additionally, the BCI can be in the range of from
about 0.4 to about 0.7, from about 0.5 to about 0.7, or from about
0.6 to about 0.9. In some embodiments, BCI is in the range of from
about 0.3 to about 0.9, from about 0.3 to about 0.8, or from about
0.3 to about 0.7, from about 0.3 to about 0.6, from about 0.3 to
about 0.5, or from about 0.3 to about 0.4. In other embodiments,
BCI is in the range of from about 0.4 to about 1.0, from about 0.5
to about 1.0, or from about 0.6 to about 1.0, from about 0.7 to
about 1.0, from about 0.8 to about 1.0, or from about 0.9 to about
1.0.
[0058] The block composites and crystalline block composites
preferably have a Tm greater than 100.degree. C., preferably
greater than 120.degree. C., and more preferably greater than
125.degree. C. Preferably the Tm is in the range of from
100.degree. C. to 250.degree. C., more preferably from 120.degree.
C. to 220.degree. C. and also preferably in the range of from
125.degree. C. to 220.degree. C. Preferably the MFR of the block
composites and crystalline block composites is from 0.1 to 1000
dg/min, more preferably from 0.1 to 50 dg/min and more preferably
from 0.1 to 30 dg/min.
[0059] Further preferably, the block composites and crystalline
block composites have a weight average molecular weight (Mw) from
10,000 to about 2,500,000, preferably from 35,000 to about
1,000,000 and more preferably from 50,000 to about 300,000,
preferably from 50,000 to about 200,000.
[0060] Comonomer content in the resulting block composite polymers
may be measured using any suitable technique, with techniques based
on nuclear magnetic resonance (NMR) spectroscopy preferred.
[0061] Preferably the block composite polymers of the invention
comprise from 0.5 to 95 wt % soft copolymer, from 0.5 to 95 wt %
hard polymer and from 5 to 99 wt % block copolymer. More
preferably, the block composite polymers comprise from 0.5 to 79 wt
% soft copolymer, from 0.5 to 79 wt % hard polymer and from 20 to
99 wt % block copolymer and more preferably from 0.5 to 49 wt %
soft copolymer, from 0.5 to 49 wt % hard polymer and from 50 to 99
wt % block copolymer. Weight percents are based on total weight of
block composite. The sum of the weight percents of soft copolymer,
hard polymer and block copolymer equals 100%.
[0062] Preferably the crystalline block composite polymers of the
invention comprise from 0.5 to 95 wt % CEP, from 0.5 to 95 wt %
CAOP and from 5 to 99 wt % block copolymer. More preferably, the
crystalline block composite polymers comprise from 0.5 to 79 wt %
CEP, from 0.5 to 79 wt % CAOP and from 20 to 99 wt % block
copolymer and more preferably from 0.5 to 49 wt % CEP, from 0.5 to
49 wt % CAOP and from 50 to 99 wt % block copolymer. Weight
percents are based on total weight of crystalline block composite.
The sum of the weight percents of CEP, CAOP and block copolymer
equals 100%.
[0063] Preferably, the block copolymers of the block composite
comprise from 5 to 95 weight percent soft blocks and 95 to 5 wt
percent hard blocks. They may comprise 10 wt % to 90 wt % soft
blocks and 90 wt % to 10 wt % hard blocks. More preferably, the
block copolymers comprise 25 to 75 wt % soft blocks and 75 to 25 wt
% hard blocks, and even more preferably they comprise 30 to 70 wt %
soft blocks and 70 to 30 wt % hard blocks.
[0064] Preferably, the block copolymers of the crystalline block
composite comprise from 5 to 95 weight percent crystalline ethylene
blocks (CEB) and 95 to 5 wt percent crystalline alpha-olefin blocks
(CAOB). They may comprise 10 wt % to 90 wt % CEB and 90 wt % to 10
wt % CAOB. More preferably, the block copolymers comprise 25 to 75
wt % CEB and 75 to 25 wt % CAOB, and even more preferably they
comprise 30 to 70 wt % CEB and 70 to 30 wt % CAOB.
[0065] In some embodiments, the crystalline block composites have a
Crystalline Block Composite Index (CBCI), as defined below, that is
greater than zero but less than about 0.4 or from about 0.1 to
about 0.3. In other embodiments, CBCI is greater than about 0.4 and
up to about 1.0. In some embodiments, the CBCI is in the range of
from about 0.1 to about 0.9, from about 0.1 to about 0.8, from
about 0.1 to about 0.7 or from about 0.1 to about 0.6.
Additionally, the CBCI can be in the range of from about 0.4 to
about 0.7, from about 0.5 to about 0.7, or from about 0.6 to about
0.9. In some embodiments, CBCI is in the range of from about 0.3 to
about 0.9, from about 0.3 to about 0.8, or from about 0.3 to about
0.7, from about 0.3 to about 0.6, from about 0.3 to about 0.5, or
from about 0.3 to about 0.4. In other embodiments, CBCI is in the
range of from about 0.4 to about 1.0, from about 0.5 to about 1.0,
or from about 0.6 to about 1.0, from about 0.7 to about 1.0, from
about 0.8 to about 1.0, or from about 0.9 to about 1.0.
[0066] Some embodiments of the present invention comprise
compositions comprising from 98 to 0.5 wt % crystalline block
composite and/or block composite with the remainder being
polyethylene, polyalpha-olefin, and combinations thereof.
Preferably, the compositions comprise 50 to 0.5 wt % CBC and/or BC
and more preferably 15 to 0.5 wt % CBC and/or BC.
[0067] Preferred suitable BC and/or CBC resin(s) will have heat of
fusion values at least about 50 Joules per gram (J/g), more
preferably at least about 75 J/g, still more preferably at least
about 85 J/g, and most preferably at least about 90 J/g, as
measured by DSC.
[0068] The block composites and crystalline block composites may be
modified by, for example, grafting, hydrogenation, nitrene
insertion reactions, or other functionalization reactions using
functionalization agents such as those known to those skilled in
the art. Preferred functionalizations are grafting reactions using
a free radical mechanism.
[0069] A variety of radically graftable species as
functionalization agents may be attached to the polymer, either
individually, or as relatively short grafts. These species include
unsaturated molecules, each containing at least one heteroatom.
These species include, but are not limited to, maleic anhydride,
dibutyl maleate, dicyclohexyl maleate, diisobutyl maleate,
dioctadecyl maleate, N-phenylmaleimide, citraconic anhydride,
tetrahydrophthalic anhydride, bromomaleic anhydride, chloromaleic
anhydride, nadic anhydride, methylnadic anhydride, alkenylsuccinic
anhydride, maleic acid, fumaric acid, diethyl fumarate, itaconic
acid, citraconic acid, crotonic acid, and the respective esters,
imides, salts, and Diels-Alder adducts of these compounds. These
species also include silane compounds.
[0070] Radically graftable species of the silane class of materials
may be attached to the polymer, either individually, or as
relatively short grafts. These species include, but are not limited
to, vinylalkoxysilanes, vinyltrimethoxysilane,
vinyltriethoxysilane, vinyltriacetoxysilane, vinyltrichlorosilane,
and the like. Generally, materials of this class include, but are
not limited to, hydrolyzable groups, such as alkoxy, acyloxy, or
halide groups, attached to silicon. Materials of this class also
include non-hydrolyzable groups, such as alkyl and siloxy groups,
attached to silicon.
[0071] Other radically graftable species may be attached to the
polymer, individually, or as short-to-longer grafts. These species
include, but are not limited to, methacrylic acid; acrylic acid;
Diels-Alder adducts of acrylic acid; methacrylates including
methyl, ethyl, butyl, isobutyl, ethylhexyl, lauryl, stearyl,
hydroxyethyl, and dimethylaminoethyl; acrylates including methyl,
ethyl, butyl, isobutyl, ethylhexyl, lauryl, stearyl, and
hydroxyethyl; glycidyl methacrylate; trialkoxysilane methacrylates,
such as 3-(methacryloxy)propyltrimethoxysilane and
3-(methacryloxy)propyl-triethoxysilane,
methacryloxymethyltrimethoxysilane,
methacryloxymethyltriethoxysilane; acrylonitrile;
2-isopropenyl-2-oxazoline; styrene; .alpha.-methylstyrene;
vinyltoluene; dichlorostyrene; N-vinylpyrrolidinone, vinyl acetate,
methacryloxypropyltrialkoxysilanes,
methacryloxymethyltrialkoxysilanes and vinyl chloride.
[0072] Mixtures of radically graftable species that comprise at
least one of the above species may be used, with styrene/maleic
anhydride and styrene/acrylonitrile as illustrative examples.
[0073] A thermal grafting process is one method for reaction,
however, other grafting processes may be used, such as photo
initiation, including different forms of radiation, e-beam, or
redox radical generation.
[0074] The functionalized interpolymers disclosed herein may also
be modified by various chain extending or cross-linking processes,
including, but not limited to peroxide-, silane-, sulfur-,
radiation-, or azide-based cure systems. A full description of the
various cross-linking technologies is described in U.S. Pat. No.
5,869,591 and U.S. Pat. No. 5,977,271, both of which are herein
incorporated by reference in their entirety.
[0075] Suitable curing agents may include peroxides, phenols,
azides, aldehyde-amine reaction products, substituted ureas,
substituted guanidines; substituted xanthates; substituted
dithiocarbamates; sulfur-containing compounds, such as thiazoles,
imidazoles, sulfenamides, thiuramidisulfides, paraquinonedioxime,
dibenzoparaquinonedioxime, sulfur; and combinations thereof.
Elemental sulfur may be used as a crosslinking agent for diene
containing polymers.
[0076] In some systems, for example, in silane grafted systems,
crosslinking may be promoted with a crosslinking catalyst, and any
catalyst that will provide this function can be used in this
invention. These catalysts generally include acids and bases,
especially organic bases, carboxylic acids and sulfonic acids, and
organometallic compounds including organic titanates, organic
zirconates, and complexes or carboxylates of lead, cobalt, iron,
nickel, zinc and tin. Dibutyltin dilaurate, dioctyltin maleate,
dibutyltin diacetate, dibutyltin dioctoate, stannous acetate,
stannous octoate, lead naphthenate, zinc caprylate, cobalt
naphthenate, and the like, are examples of suitable crosslinking
catalysts.
[0077] Rather than employing a chemical crosslinking agent,
crosslinking may be effected by use of radiation or by the use of
electron beam. Useful radiation types include ultraviolet (UV) or
visible radiation, beta ray, gamma rays, X-rays, or neutron rays.
Radiation is believed to effect crosslinking by generating polymer
radicals which may combine and crosslink
[0078] Dual cure systems, which use a combination of heat, moisture
cure, and radiation steps, may be effectively employed. Dual cure
systems are disclosed in U.S. Pat. No. 5,911,940 and U.S. Pat. No.
6,124,370, which are incorporated herein by reference in their
entirety. For example, it may be desirable to employ peroxide
crosslinking agents in conjunction with silane crosslinking agents;
peroxide crosslinking agents in conjunction with radiation; or
sulfur-containing crosslinking agents in conjunction with silane
crosslinking agents.
[0079] The functionalization may also occur at the terminal
unsaturated group (e.g., vinyl group) or an internal unsaturation
group, when such groups are present in the polymer. Such
functionalization includes, but is not limited to, hydrogenation,
halogenation (such as chlorination), ozonation, hydroxylation,
sulfonation, carboxylation, epoxidation, and grafting reactions.
Any functional groups, such as halogen, amine, amide, ester,
carboxylic acid, ether, silane, siloxane, and so on, or functional
unsaturated compounds, such as maleic anhydride, can be added
across a terminal or internal unsaturation via known chemistry.
Other functionalization methods include those disclosed in the
following U.S. Pat. No. 5,849,828, entitled, "Metalation and
Functionalization of Polymers and Copolymers;" U.S. Pat. No.
5,814,708, entitled, "Process for Oxidative Functionalization of
Polymers Containing Alkylstyrene;" and U.S. Pat. No. 5,717,039,
entitled, "Functionalization of Polymers Based on Koch Chemistry
and Derivatives Thereof." Each of these patents is incorporated by
reference, herein, in its entirety.
[0080] There are several types of compounds that can initiate
grafting reactions by decomposing to form free radicals, including
azo-containing compounds, carboxylic peroxyacids and peroxyesters,
alkyl hydroperoxides, and dialkyl and diacyl peroxides, among
others. Many of these compounds and their properties have been
described (Reference: J. Branderup, E. Immergut, E. Grulke, eds.
"Polymer Handbook," 4th ed., Wiley, New York, 1999, Section II, pp.
1-76.). It is preferable for the species that is formed by the
decomposition of the initiator to be an oxygen-based free radical.
It is more preferable for the initiator to be selected from
carboxylic peroxyesters, peroxyketals, dialkyl peroxides, and
diacyl peroxides. Some of the more preferable initiators, commonly
used to modify the structure of polymers, are listed in U.S. Pat.
No. 7,897,689, in the table spanning Col. 48 line 13-Col. 49 line
29, which is hereby incorporated by reference.
[0081] The amount of maleic anhydride used in the grafting reaction
is less than, or equal to, 10 phr (parts per hundred, based on the
weight of the olefin interpolymer), preferably less than 5 phr, and
more preferably from 0.5 to 10 phr, and even more preferably from
0.5 to 5 phr.
[0082] The amount of initiator used in the grafting reaction is
less than, or equal to, 10 millimoles radicals per 100 grams olefin
interpolymer, preferably, less than, or equal to, 6 millimoles
radicals per 100 grams olefin interpolymer, and more preferably,
less than, or equal to, 3 millimoles radicals per 100 grams olefin
interpolymer.
[0083] The amount of maleic anhydride constituent grafted onto the
polyolefin chain is greater than 0.05 weight percent to 2.0 wt
percent (based on the weight of the olefin interpolymer), as
determined by titration analysis, FTIR analysis, or any other
appropriate method. More preferably, this amount is greater than
0.25 weight percent to 2.0 weight percent, and in yet a further
embodiment, this amount is greater than 0.3 weight percent to 2.0
weight percent. In a preferred embodiment, 0.5 weight percent to
2.0 weight percent of maleic anhydride is grafted.
[0084] The grafted resins have an MFR from 0.1 to 300 MFR
(230.degree. C. @ 2.16 kg), more preferred, 0.2 to 200, more
preferred 0.5 to 100.
[0085] The CBCI of the grafted resins have a crystalline block
composite index of at least about 0.10, preferably at least about
0.35, preferably at least about 0.57 and more preferably at least
about 0.97.
[0086] The heat of fusion, or melt enthalpy, values of the grafted
CBC are at least about 75 Joules per gram (J/g), more preferably at
least about 80 J/g, still more preferably at least about 85 J/g and
most preferably at least about 90 J/g, as measured by DSC. The heat
of fusion values are also from 75 J/g to 250 J/g, preferably from
80 J/g to 200 J/g and also from 85 J/g to 150 J/g. All individual
values and subranges from 75 J/g to 200 J/g are included herein and
disclosed herein.
[0087] For silane grafting, the amount of silane used in the
grafting reaction is greater than, or equal to, 0.05 phr (based on
the amount of the olefin interpolymer), more preferably, from 0.5
phr to 6 phr, and even more preferably, from 0.5 phr to 4 phr. All
individual values and subranges from 0.05 phr to 6 phr are included
herein and disclosed herein.
[0088] In another embodiment, the amount of amount of initiator
used in the silane grafting reaction is less than, or equal to, 4
millimoles radicals per 100 grams olefin interpolymer, preferably,
from 0.01 millimoles to 2 millimoles radicals per 100 grams olefin
interpolymer, and more preferably from 0.02 millimoles to 2
millimoles radicals per 100 grams olefin interpolymer. All
individual values and subranges from 0.01 millimoles to 4
millimoles radicals per 100 grams olefin interpolymer are included
herein and disclosed herein.
[0089] In another embodiment, the amount of silane constituent
grafted on the polyolefin chain is greater than, or equal to, 0.05
weight percent (based on the weight of the olefin interpolymer), as
determined by FTIR analysis, Si elemental analysis using neutron
activation analysis, or other appropriate method. In a further
embodiment, this amount is greater than, or equal to, 0.5 weight
percent, and in yet a further embodiment, this amount is greater
than, or equal to, 1.2 weight percent. In a preferred embodiment,
the amount silane constituent grafted on the olefin interpolymer is
from 0.5 weight percent to 4.0 weight percent. All individual
values and subranges from 0.05 weight percent to 4.0 weight percent
are considered within the scope of this invention, and are
disclosed herein.
[0090] Suitable silanes include, but are not limited to, those of
the general formula (I):
CH.sub.2.dbd.CR--(COO).sub.x(C.sub.nH.sub.2n).sub.ySiR'.sub.3
(I).
[0091] In this formula, R is a hydrogen atom or methyl group; x and
y are 0 or 1, with the proviso that when x is 1, y is 1; n is an
integer from 1 to 12 inclusive, preferably 1 to 4, and each R'
independently is an organic group, including, but not limited to,
an alkoxy group having from 1 to 12 carbon atoms (e.g. methoxy,
ethoxy, butoxy), an aryloxy group (e.g. phenoxy), an araloxy group
(e.g. benzyloxy), an aliphatic or aromatic siloxy group, an
aromatic acyloxyl group, an aliphatic acyloxy group having from 1
to 12 carbon atoms (e.g. formyloxy, acetyloxy, propanoyloxy), amino
or substituted amino groups (alkylamino, arylamino), or a lower
alkyl group having 1 to 6 carbon atoms.
[0092] In one embodiment, the silane compound is selected from
vinyltrialkoxysilanes, vinyltriacyloxysilanes or
vinyltrichlorosilane. In addition, any silane, or mixtures of
silanes, which will effectively graft to, and/or crosslink, the
olefin interpolymers can be used in the practice of this invention.
Suitable silanes include unsaturated silanes that comprise both an
ethylenically unsaturated hydrocarbyl group, such as a vinyl,
allyl, isopropenyl, butenyl, cyclohexenyl or .gamma.-(meth)acryloxy
allyl group, and a hydrolyzable group, such as, a hydrocarbyloxy,
hydrocarbonyloxy, or hydrocarbylamino group, or a halide. Examples
of hydrolyzable groups include methoxy, ethoxy, formyloxy, acetoxy,
proprionyloxy, chloro, and alkyl or arylamino groups. Preferred
silanes are the unsaturated alkoxy silanes which can be grafted
onto the polymer. These silanes and their method of preparation are
more fully described in U.S. Pat. No. 5,266,627 to Meverden, et
al., which is incorporated herein, in its entirety, by reference.
Preferred silanes include vinyltrimethoxysilane,
vinyltriethoxysilane, 3-(trimethoxysilyl)propyl methacrylate
(.gamma.-(meth)acryloxypropyl trimethoxysilane), and mixtures
thereof.
[0093] In certain embodiments of the claimed invention, dual
crosslinking systems, which use a combination of radiation, heat,
moisture and crosslinking steps, may be effectively employed. For
instance, it may be desirable to employ peroxide crosslinking
agents in conjunction with silane crosslinking agents, peroxide
crosslinking agents in conjunction with radiation, or
sulfur-containing crosslinking agents in conjunction with silane
crosslinking agents. Dual crosslinking systems are disclosed, and
claimed in, U.S. Pat. Nos. 5,911,940 and 6,124,370, the entire
contents of both are herein incorporated by reference.
[0094] The block composites and crystalline block composites may
also be modified by azide modification. Compounds having at least
two sulfonyl azide groups capable of C--H insertion under reaction
conditions are referred to herein as coupling agents. For the
purpose of the invention, the poly(sulfonyl azide) is any compound
having at least two sulfonyl azide groups reactive with a
polyolefin under reaction conditions. Preferably the poly(sulfonyl
azide)s have a structure X--R--X wherein each X is SO.sub.2 N.sub.3
and R represents an unsubstituted or inertly substituted
hydrocarbyl, hydrocarbyl ether or silicon-containing group,
preferably having sufficient carbon, oxygen or silicon, preferably
carbon, atoms to separate the sulfonyl azide groups sufficiently to
permit a facile reaction between the polyolefin and the sulfonyl
azide, more preferably at least 1, more preferably at least 2, most
preferably at least 3 carbon, oxygen or silicon, preferably carbon,
atoms between functional groups. While there is no critical limit
to the length of R, each R advantageously has at least one carbon
or silicon atom between X's and preferably has less than about 50,
more preferably less than about 30, most preferably less than about
20 carbon, oxygen or silicon atoms. Within these limits, larger is
better for reasons including thermal and shock stability. When R is
straight-chain alkyl hydrocarbon, there are preferably less than 4
carbon atoms between the sulfonyl azide groups to reduce the
propensity of the nitrene to bend back and react with itself.
Silicon containing groups include silanes and siloxanes, preferably
siloxanes. The term inertly substituted refers to substitution with
atoms or groups which do not undesirably interfere with the desired
reaction(s) or desired properties of the resulting coupled
polymers. Such groups include fluorine, aliphatic or aromatic
ether, siloxane as well as sulfonyl azide groups when more than two
polyolefin chains are to be joined. Suitable structures include R
as aryl, alkyl, aryl alkaryl, arylalkyl silane, siloxane or
heterocyclic, groups and other groups which are inert and separate
the sulfonyl azide groups as described. More preferably R includes
at least one aryl group between the sulfonyl groups, most
preferably at least two aryl groups (such as when R is 4,4'
diphenylether or 4,4'-biphenyl). When R is one aryl group, it is
preferred that the group have more than one ring, as in the case of
naphthylene bis(sulfonyl azides). Poly(sulfonyl)azides include such
compounds as 1,5-pentane bis(sulfonyl azide), 1,8-octane
bis(sulfonyl azide), 1,10-decane bis(sulfonyl azide),
1,10-octadecane bis(sulfonyl azide), 1-octyl-2,4,6-benzene
tris(sulfonyl azide), 4,4'-diphenyl ether bis(sulfonyl azide),
1,6-bis(4'-sulfonazidophenyl)hexane, 2,7-naphthalene bis(sulfonyl
azide), and mixed sulfonyl azides of chlorinated aliphatic
hydrocarbons containing an average of from 1 to 8 chlorine atoms
and from about 2 to 5 sulfonyl azide groups per molecule, and
mixtures thereof. Preferred poly(sulfonyl azide)s include
oxy-bis(4-sulfonylazidobenzene), 2,7-naphthalene bis(sulfonyl
azido), 4,4'-bis(sulfonyl azido)biphenyl, 4,4'-diphenyl ether
bis(sulfonyl azide) and bis(4-sulfonyl azidophenyl)methane, and
mixtures thereof.
[0095] Polyfunctional compounds capable of insertions into C--H
bonds also include carbene-forming compounds such as salts of alkyl
and aryl hydrazones and diazo compounds, and nitrene-forming
compounds such as alkyl and aryl azides (R--N3), acyl azides
(R--C(O)N3), azidoformates (R--O--C(O)--N3), sulfonyl azides
(R--SO2-N3), phosphoryl azides ((RO)2-(PO)--N3), phosphinic azides
(R2-P(O)--N3) and silyl azides (R3-S1-N3).
[0096] To modify rheology, also referred to herein as "to couple,"
an azide, peroxide or other crosslinking agent is used in a
rheology modifying amount, that is an amount effective to increase
the low-shear viscosity (at 0.1 rad/sec) of the polymer preferably
at least about 5 percent as compared with the starting material
polymer, but less than a crosslinking amount, that is an amount
sufficient to result in at least about 10 weight percent gel as
measured by ASTM D2765-procedure A.
[0097] The functionalized polymers may also contain additives such
as, but not limited to, antioxidants, slip agents, UV absorbers or
stabilizers, antiblock agents, inorganic or organic fillers, color
pigments or dyes and processing agents.
Test Methods
[0098] MFR: Melt Flow Rate is measured in accordance with ASTM
D1238, Condition 230.degree. C./2.16 kg.
[0099] DSC: Differential Scanning calorimetry is used to measure,
among other things, the heats of fusion of the crystalline block
and block composites and is performed on a TA Instruments Q1000 DSC
equipped with an RCS cooling accessory and an auto sampler. A
nitrogen purge gas flow of 50 ml/min is used. The sample is pressed
into a thin film and melted in the press at about 190.degree. C.
and then air-cooled to room temperature (25.degree. C.). About 3-10
mg of material is then cut, accurately weighed, and placed in a
light aluminum pan (ca 50 mg) which is later crimped shut. The
thermal behavior of the sample is investigated with the following
temperature profile: the sample is rapidly heated to 190.degree. C.
and held isothermal for 3 minutes in order to remove any previous
thermal history. The sample is then cooled to -90.degree. C. at
10.degree. C./min cooling rate and held at -90.degree. C. for 3
minutes. The sample is then heated to 190.degree. C. at 10.degree.
C./min heating rate. The cooling and second heating curves are
recorded. For the heat of fusion measurements for the CBC and
specified BC resins, as known and routinely performed by skilled
practitioners in this area, the baseline for the calculation is was
drawn from the flat initial section prior to the onset of melting
(typically in the range of from about -10 to about 20.degree. C.
for these types of materials) and extends to the end of melting for
the second heating curve. MAH grafting level
[0100] The polymer pellets are dried in a vacuum oven at
150.degree. C. for 1.5 hr. The pellets are molded into film using a
Carver hydraulic press at 190.degree. C. for 30 sec under 3000 lb
pressure at ambient atmosphere. The films of 3 mil thickness are
cooled by transferring the plates to the lower level platens set at
ambient temperature. IR spectra are collected using Nicolet 6700
FTIR. FTIR spectra were used for determining the level of g-MAH in
each sample using a method that has been calibrated against the
tetrabutylammonium Hydroxide (TBAOH) titration. The wt % of g-MAH
was determined from the ratio of the height of the peak at ca. 1790
cm.sup.-1 corresponding to the carbonyl stretch of the anhydride,
to the height of the 2751 cm.sup.-1, as follows
wt % MAH = 0.0344 .times. ( peak height @ ca . 1790 cm - 1 ) ( peak
height @ ca . 2751 cm - 1 ) + 0.1925 .times. ( peak height @ ca .
1790 cm - 1 ) ( peak height @ ca . 2751 cm - 1 ) + 0.767
##EQU00001##
[0101] As for the TBAOH titration, 1-2 g of the dried resin was
dissolved in 150 ml xylene by heating the sample to 100 deg. C. on
a stirred hot plate. Upon dissolution, the sample was titrated,
while hot, with 0.025N TBAOH in 1:1 toluene/methanol using 10 drops
of Bromothymol blue as indicator. The endpoint is recorded when
solution turns blue.
Silane Grafting Level Analysis
[0102] Duplicate samples were prepared by transferring
approximately 3.0 grams of the pellets into pre-cleaned 2-dram
polyethylene vials. Samples are vacuum stripped at 140.degree. C.
for 20 minutes in a vacuum oven to remove any residual, volatile,
or surface silane. Duplicate Si standards are prepared from their
NIST traceable standard solution into similar vials. The standards
are diluted to a similar volume as the samples using pure water. A
blank sample of the water is also prepared. The samples, standards
and a blank are then analyzed for Si. Specifically, irradiation is
done for 3 minutes at 250 kW reactor power. The waiting time is 9
minutes and the counting time was 270 seconds using an HPGe
detector set. The Si concentrations are calculated in ppm using
Canberra software and comparative technique. Typical uncertainty
ranges from 2% to 5% relative and the detection limit is less than
100 ppm. The vinyltrimethoxysilane content is back calculated using
stoichiometry, assuming that the grafting is done using
vinyltrimethoxysilane only.
Gel Fraction Analysis
[0103] Gel fractions of crosslinked silane grafted samples are
measured using a Soxhlet extractor and xylene as solvent.
Crosslinked samples are extracted under reflux for a minimum of 19
hours. The extracted samples are dried in a vacuum oven at
90.degree. C. for 3 hours. The samples are crosslinked at 85%
relative humidity and 85.degree. C. for 3 weeks on a 4 mil
compression molded film. Triple specimens are tested and the
average was reported.
Tensile Properties
[0104] For tensile property measurements, samples are compression
molded into 70 mil thick plaque (5 inch.times.5 inch) with a Carver
hydraulic press at 190.degree. C. for 6 min at 6000 lb at ambient
atmosphere. The plaques are then cooled to 50.degree. C. at
15.degree. C./min in the press under 30000 lb force. Stress-strain
behavior in uniaxial tension is measured using ASTM D1708
microtensile specimens. Specimens are die-cut from the plaques in
conformation of the dimensions specified in ASTM D1708. The gauge
length of samples is 22 mm and samples are stretched with an
Instron at 554% of (initial gauge length) min.sup.-1 at 23.degree.
C. Tensile properties are reported from an average of 5
specimens.
Transmission Electron Microscopy
[0105] The compression molded plaques used for microtensile test
are examined by TEM. The samples are trimmed so that sections could
be collected near the core of thickness of the sample. The trimmed
samples are cryopolished at -60.degree. C. to prevent smearing
using a diamond knife on a Leica UCT microtome prior to staining.
The cryo-polished blocks are stained with the vapor phase of a 2%
aqueous ruthenium tetraoxide solution for 3 hrs at ambient
temperature. The staining solution is prepared by weighing 0.2 gm
of ruthenium (III) chloride hydrate (RuCl3.times.H2O) into a glass
bottle with a screw lid and adding 10 ml of 5.25% aqueous sodium
hypochlorite to the jar. The samples are attached to a glass slide
using double sided tape. The slide is placed in the jar in order to
suspend the blocks about 1 inch above the staining solution for 3
hr. Sections of approximately 100 nanometers in thickness are
collected from the stained sample at ambient temperature using a
diamond knife on a Leica EM UC6 microtome and placed on 600 mesh
virgin TEM grids for observation. TEM images are collected using a
JEOL JEM-1230 operated at 100 kV accelerating voltage and
photographed using a Gatan-791 and 794 digital cameras.
.sup.13C NMR Spectroscopy Method for .sup.13C-Labeled Maleic
Anhydride Grafted Polyolefin
[0106] The sample was prepared by adding approximately 2.7 g of
TCE-d.sub.2 with 0.025M chromium acetylacetonate (relaxation agent)
to 0.2 g sample in a 10 mm NMR tube, and then purging in a N.sub.2
box for 2 h. The sample was dissolved and homogenized by heating
the tube and its contents at 140-150.degree. C.
[0107] For .sup.13C NMR, the data were collected using a Bruker 400
MHz spectrometer equipped with a Bruker Dual DUL high-temperature
CryoProbe. This method is described in, for example, Z. Zhou, R.
Kuemmerle, J. C. Stevens, D. Redwine, Y. He, X. Qiu, R. Cong, J.
Klosin, N. Montanez, G. Roof, Journal of Magnetic Resonance, 2009,
200, 328-333 and Z. Zhou, J. C. Stevens, J. Klosin, R. Kummerle, X.
Qiu, D. Redwine, R. Cong, A. Taha, J. Mason, B. Winniford, P.
Chauvel and N. Montanez, Macromolecules, 2009, 42, 2291-2294.
[0108] The data were acquired using 320 transients per data file, a
7.3 sec pulse repetition delay (6 sec delay+1.3 sec acq. time), 90
degree flip angles, and a modified inverse gated decoupling with a
sample temperature of 120.degree. C. All measurements were made on
non spinning samples in locked mode. Samples were homogenized
immediately prior to insertion into the heated (125.degree. C.) NMR
Sample changer, and were allowed to thermally equilibrate in the
probe for 7 minutes prior to data acquisition.
Gel Permeation Chromatography (GPC)
[0109] The gel permeation chromatographic system consists of either
a Polymer Laboratories Model PL-210 or a Polymer Laboratories Model
PL-220 instrument. The column and carousel compartments are
operated at 140.degree. C. Three Polymer Laboratories 10-micron
Mixed-B columns are used. The solvent is 1,2,4 trichlorobenzene.
The samples are prepared at a concentration of 0.1 grams of polymer
in 50 milliliters of solvent containing 200 ppm of butylated
hydroxytoluene (BHT). Samples are prepared by agitating lightly for
2 hours at 160.degree. C. The injection volume used is 100
microliters and the flow rate is 1.0 ml/minute. Calibration of the
GPC column set is performed with 21 narrow molecular weight
distribution polystyrene standards with molecular weights ranging
from 580 to 8,400,000, arranged in 6 "cocktail" mixtures with at
least a decade of separation between individual molecular weights.
The standards are purchased from Polymer Laboratories (Shropshire,
UK). The polystyrene standards are prepared at 0.025 grams in 50
milliliters of solvent for molecular weights equal to or greater
than 1,000,000, and 0.05 grams in 50 milliliters of solvent for
molecular weights less than 1,000,000. The polystyrene standards
are dissolved at 80.degree. C. with gentle agitation for 30
minutes. The narrow standards mixtures are run first and in order
of decreasing highest molecular weight component to minimize
degradation. The polystyrene standard peak molecular weights are
converted to polyethylene molecular weights using the following
equation (as described in Williams and Ward, J. Polym. Sci., Polym.
Let., 6, 621 (1968)): M.sub.polypropylene=0.645
(M.sub.polystyrene). Polypropylene equivalent molecular weight
calculations are performed using Viscotek TriSEC software Version
3.0.
Fast-Temperature Rising Elution Fractionation (F-TREF)
[0110] In F-TREF analysis, the composition to be analyzed is
dissolved in ortho-dichlorobenzene and allowed to crystallize in a
column containing an inert support (stainless steel shot) by slowly
reducing the temperature to 30.degree. C. (at a preferred rate of
0.4.degree. C./min). The column is equipped with an infra-red
detector. An F-TREF chromatogram curve is then generated by eluting
the crystallized polymer sample from the column by slowly
increasing the temperature of the eluting solvent
(o-dichlorobenzene) from 30 to 140.degree. C. (at a preferred rate
of 1.5.degree. C./min).
High Temperature Liquid Chromatography (HTLC)
[0111] HTLC is performed according to the methods disclosed in U.S.
Pat. No. 8,076,147 and US Patent Application Publication No.
2011-152499, both of which are herein incorporated by reference.
Samples are analyzed by the methodology described below.
[0112] A Waters GPCV2000 high temperature SEC chromatograph was
reconfigured to build the HT-2DLC instrumentation. Two Shimadzu
LC-20AD pumps were connected to the injector valve in GPCV2000
through a binary mixer. The first dimension (D1) HPLC column was
connected between the injector and a 10-port switch valve (Valco
Inc). The second dimension (D2) SEC column was connected between
the 10-port valve and LS (Varian Inc.), IR (concentration and
composition), RI (refractive index), and IV (intrinsic viscosity)
detectors. RI and IV were built-in detector in GPCV2000. The IR5
detector was provided by PolymerChar, Valencia, Spain.
Columns: The D1 column was a high temperature Hypercarb graphite
column (2.1.times.100 mm) purchased from Thermo Scientific. The D2
column was a PLRapid-H column purchased from Varian (10.times.100
mm). Reagents: HPLC grade trichlorobenzene (TCB) was purchased from
Fisher Scientific. 1-Decanol and decane were from Aldrich.
2,6-Di-tert-butyl-4-methylphenol (Ionol) was also purchased from
Aldrich. Sample Preparation: 0.01-0.15 g of polyolefin sample was
placed in a 10-mL Waters autosampler vial. 7-mL of either 1-decanol
or decane with 200 ppm Ionol was added to the vial afterwards.
After sparging helium to the sample vial for about 1 min, the
sample vial was put on a heated shaker with temperature set at
160.degree. C. The dissolution was done by shaking the vial at the
temperature for 2 hr. The vial was then transferred to the
autosampler for injection. Please note that the actual volume of
the solution was more than 7 mL due to the thermal expansion of the
solvent. HT-2DLC: The D1 flow rate was at 0.01 mL/min. The
composition of the mobile phase was 100% of the weak eluent
(1-decanol or decane) for the first 10 min of the run. The
composition was then increased to 60% of strong eluent (TCB) in 489
min. The data were collected for 489 min as the duration of the raw
chromatogram. The 10-port valve switched every three minutes
yielding 489/3=163 SEC chromatograms. A post-run gradient was used
after the 489 min data acquisition time to clean and equilibrate
the column for the next run:
Clean Step:
[0113] 1. 490 min: flow=0.01 min;//Maintain the constant flow rate
of 0.01 mL/min from 0-490 min.
[0114] 2. 491 min: flow=0.20 min;//Increase the flow rate to 0.20
mL/min.
[0115] 3. 492 min: % B=100;//Increase the mobile phase composition
to 100% TCB
[0116] 4. 502 min: % B=100;//Wash the column using 2 mL of TCB
Equilibrium Step:
[0117] 5. 503 min: % B=0;//Change the mobile phase composition to
100% of 1-decanol or decane
[0118] 6. 513 min: % B=0;//Equilibrate the column using 2 mL of
weak eluent
[0119] 7. 514 min: flow=0.2 mL/min;//Maintain the constant flow of
0.2 mL/min from 491-514 min
[0120] 8. 515 min: flow=0.01 mL/min;//Lower the flow rate to 0.01
mL/min.
After step 8, the flow rate and mobile phase composition were the
same as the initial conditions of the run gradient. The D2 flow
rate was at 2.51 mL/min. Two 60 .mu.L loops were installed on the
10-port switch valve. 30-.mu.L of the eluent from D1 column was
loaded onto the SEC column with every switch of the valve. The IR,
LS15 (light scattering signal at 15.degree.), LS90 (light
scattering signal at 90.degree.), and IV (intrinsic viscosity)
signals were collected by EZChrom through a SS420X
analogue-to-digital conversion box. The chromatograms were exported
in ASCII format and imported into a home-written MATLAB software
for data reduction. Using an appropriate calibration curve of
polymer composition and retention volume, of polymers that are of
similar nature of the hard block and soft block contained in the
block composite being analyzed. Calibration polymers should be
narrow in composition (both molecular weight and chemical
composition) and span a reasonable molecular weight range to cover
the composition of interest during the analysis. Analysis of the
raw data was calculated as follows, the first dimension HPLC
chromatogram was reconstructed by plotting the IR signal of every
cut (from total IR SEC chromatogram of the cut) as a function of
the elution volume. The IR vs. D1 elution volume was normalized by
total IR signal to obtain weight fraction vs. D1 elution volume
plot. The IR methyl/measure ratio was obtained from the
reconstructed IR measure and IR methyl chromatograms. The ratio was
converted to composition using a calibration curve of PP wt. % (by
NMR) vs. methyl/measure obtained from SEC experiments. The MW was
obtained from the reconstructed IR measure and LS chromatograms.
The ratio was converted to MW after calibration of both IR and LS
detectors using a PE standard.
[0121] The weight % of isolated PP is measured as the area that
corresponds to the hard block composition based on the isolated
peak and the retention volume as determined by a composition
calibration curve.
Xylene Soluble Fractionation Analysis
[0122] A weighed amount of resin is dissolved in 200 ml o-xylene
under reflux conditions for 2 hours. The solution is then cooled in
a temperature controlled water bath to 25.degree. C. to allow the
crystallization of the xylene insoluble (XI) fraction. Once the
solution is cooled and the insoluble fraction precipitates from the
solution, the separation of the xylene soluble (XS) fraction from
the xylene insoluble fraction is done by filtration through a
filter paper. The remaining o-xylene solution is evaporated from
the filtrate. Both XS and XI fractions are dried in a vacuum oven
at 100.degree. C. for 60 min and then weighed.
[0123] If the solution crystallization temperature of the soft
block polymer is above room temperature, the fractionation step can
be carried out at a temperature 10-20.degree. C. above the soft
blocks crystallization temperature but below the hard blocks
crystallization temperature. The temperature of separation can be
determined by TREF or CRYSTAF measurement as described by
reference, TREF and CRYSTAF technologies for Polymer
Characterization, Encyclopedia of Analytical Chemistry. 2000 Issue,
Pages 8074-8094. This fractionation can be carried out in a
laboratory heated dissolution and filtration apparatus or a
fractionation instrument such as the Preparatory mc.sup.2
(available from Polymer Char, Valencia, Spain).
Estimating the Block Composite Index
[0124] For a block composite derived from ethylene and propylene,
the insoluble fractions will contain an appreciable amount of
ethylene that would not otherwise be present if the polymer was
simply a blend of iPP homopolymer and EP copolymer. To account for
this "extra ethylene", a mass balance calculation can be performed
to estimate a block composite index from the amount of xylene
insoluble and soluble fractions and the weight % ethylene present
in each of the fractions.
[0125] A summation of the weight % ethylene from each fraction
according to equation 1 results in an overall weight % ethylene (in
the polymer). This mass balance equation can also be used to
quantify the amount of each component in a binary blend or extended
to a ternary, or n-component blend.
Wt % C.sub.2.sub.Overall=w.sub.Insoluble(wt %
C.sub.2.sub.Insoluble)+w.sub.soluble(wt % C.sub.2.sub.soluble) Eq.
1
[0126] Applying equations 2 through 4, the amount of the soft block
(providing the source of the extra ethylene) present in the
insoluble fraction is calculated. By substituting the weight %
C.sub.2 of the insoluble fraction in the left hand side of equation
2, the weight % iPP hard and weight % EP soft can be calculated
using equations 3 and 4. Note that the weight % of ethylene in the
EP soft is set to be equal to the weight % ethylene in the xylene
soluble fraction. The weight % ethylene in the iPP block is set to
zero or if otherwise known from its DSC melting point or other
composition measurement, the value can be put into its place.
Wt % C 2 Overall or xylene in soluble = w iPPHard ( wt % C 2 iPP )
+ w EP soft ( wt % C 2 EPsoft ) Eq . 2 w iPPhard = wt % C 2 overall
or xylene insoluble - wt % C 2 EPsoft wt % C 2 ipphard - wt % C 2
EPsoft Eq . 3 w EPsoft = 1 - w iPPHard 25 Eq . 4 ##EQU00002##
[0127] After accounting for the `additional` ethylene present in
the insoluble fraction, the only way to have an EP copolymer
present in the insoluble fraction, the EP polymer chain must be
connected to an iPP polymer block (or else it would have been
extracted into the xylene soluble fraction). Thus, when the iPP
block crystallizes, it prevents the EP block from solubilizing.
[0128] To estimate the block composite index, the relative amount
of each block must be taken into account. To approximate this, the
ratio between the EP soft and iPP hard is used. The ratio of the EP
soft polymer and iPP hard polymer can be calculated using Equation
2 from the mass balance of the total ethylene measured in the
polymer. Alternatively it could also be estimated from a mass
balance of the monomer and comonomer consumption during the
polymerization. The weight fraction of iPP hard and weight fraction
of EP soft is calculated using Equation 2 and assumes the iPP hard
contains no ethylene. The weight % ethylene of the EP soft is the
amount of ethylene present in the xylene soluble fraction.
[0129] For example, if an iPP-EP block composite contains an
overall ethylene content of 47 wt % C.sub.2 and is made under
conditions to produce an EP soft polymer with 67 wt % C.sub.2 and
an iPP homopolymer containing zero ethylene, the amount of EP soft
and iPP hard is 70 wt % and 30 wt %, respectively (as calculated
using Equations 3 and 4). If the percent of EP is 70 wt % and the
iPP is 30 wt %, the relative ratio of the EP:iPP blocks could be
expressed as 2.33:1.
[0130] Hence, if one skilled in the art carries out a xylene
extraction of the polymer and recovers 40 wt % insoluble and 60 wt
% soluble, this would be an unexpected result and this would lead
to the conclusion that a fraction of block copolymer was present.
If the ethylene content of the insoluble fraction is subsequently
measured to be 25 wt % C.sub.2, Equations 2 thru 4 can be solved to
account for this additional ethylene and result in 37.3 wt % EP
soft polymer and 62.7 wt % iPP hard polymer present in the
insoluble fraction.
[0131] Since the insoluble fraction contains 37.3 wt % EP
copolymer, it should be attached to an additional 16 wt % of iPP
polymer based on the EP:iPP block ratio of 2.33:1. This brings the
estimated amount of diblock in the insoluble fraction to be 53.3 wt
%. For the entire polymer (unfractionated), the composition is
described as 21.3 wt % iPP-EP Diblock, 18.7 wt % iPP polymer, and
60 wt % EP polymer. The term block composite index (BCI) is herein
defined to equal the weight percentage of diblock divided by 100%
(i.e. weight fraction). The value of the block composite index can
range from 0 to 1, wherein 1 would be equal to 100% diblock and
zero would be for a material such as a traditional blend or random
copolymer. For the example described above, the block composite
index for the block composite is 0.213. For the insoluble fraction,
the BCI is 0.533, and for the soluble fraction the BCI is assigned
a value of zero.
[0132] Depending on the estimations made of the total polymer
composition and the error in the analytical measurements which are
used to estimate the composition of the hard and soft blocks,
between 5 to 10% relative error is possible in the computed value
of the block composite index. Such estimations include the wt % C2
in the iPP hard block as measured from the DSC melting point, NMR
analysis, or process conditions; the average wt % C2 in the soft
block as estimated from the composition of the xylene solubles, or
by NMR, or by DSC melting point of the soft block (if detected).
But overall, the block composite index calculation reasonably
accounts for the unexpected amount of `additional` ethylene present
in the insoluble fraction, the only way to have an EP copolymer
present in the insoluble fraction, the EP polymer chain must be
connected to an iPP polymer block (or else it would have been
extracted into the xylene soluble fraction).
Estimating the Crystalline Block Composite Index (CBCI)
[0133] Cyrstalline block composites having CAOP and CAOB composed
of crystalline polypropylene and a CEP and CEB composed of
crystalline polyethylene cannot be fractionated by conventional
means. Techniques based on solvent or temperature fractionation,
for example, using xylene fractionation, solvent/non-solvent
separation, temperature rising elution fractionation, or
crystallization elution fractionation are not capable of resolving
the block copolymer since the CEB and CAOB cocrystallize with the
CEP and CAOP, respectively. However, using a method such as high
temperature liquid chromatography which separates polymer chains
using a combination of a mixed solvent/non-solvent and a graphitic
column, crystalline polymer species such as polypropylene and
polyethylene can be separated from each other and from the block
copolymer.
[0134] For crystalline block composites, the amount of isolated PP
is less than if the polymer was a simple blend of iPP homopolymer
(in this example the CAOP) and polyethylene (in this case the CEP).
Consequently, the polyethylene fraction contains an appreciable
amount of propylene that would not otherwise be present if the
polymer was simply a blend of iPP and polyethylene. To account for
this "extra propylene", a mass balance calculation can be performed
to estimate a crystalline block composite index from the amount of
the polypropylene and polyethylene fractions and the weight %
propylene present in each of the fractions that are separated by
HTLC. The polymers contained within the crystalline block composite
include iPP-PE diblock, unbound iPP, and unbound PE where the
individual PP or PE components can contain a minor amount of
ethylene or propylene respectively.
Composition of the Crystalline Block Composite
[0135] A summation of the weight % propylene from each component in
the polymer according to equation 1 results in the overall weight %
propylene (of the whole polymer). This mass balance equation can be
used to quantify the amount of the iPP and PE present in the
diblock copolymer. This mass balance equation can also be used to
quantify the amount of iPP and PE in a binary blend or extended to
a ternary, or n-component blend. For the crystalline block
composite, the overall amount of iPP or PE is contained within the
blocks present in the diblock and the unbound iPP and PE
polymers.
Wt % C3.sub.Overall=w.sub.PP(wt % C3.sub.PP)+w.sub.PE(wt %
C3.sub.PE) Eq. 1
where w.sub.PP=weight fraction of PP in the polymer w.sub.PE=weight
fraction of PE in the polymer wt % C3.sub.pp=weight percent of
propylene in PP component or block wt % C3.sub.PE=weight percent of
propylene in PE component or block.
[0136] Note that the overall weight % of propylene (C3) is
preferably measured from C13 NMR or some other composition
measurement that represents the total amount of C3 present in the
whole polymer. The weight % propylene in the iPP block (wt %
C3.sub.PP) is set to 100 or if otherwise known from its DSC melting
point, NMR measurement, or other composition estimate, that value
can be put into its place. Similarly, the weight % propylene in the
PE block (wt % C3.sub.PE) is set to 100 or if otherwise known from
its DSC melting point, NMR measurement, or other composition
estimate, that value can be put into its place.
Calculating the Ratio of PP to PE in the Crystalline Block
Composite
[0137] Based on equation 1, the overall weight fraction of PP
present in the polymer can be calculated using Equation 2 from the
mass balance of the total C3 measured in the polymer.
Alternatively, it could also be estimated from a mass balance of
the monomer and comonomer consumption during the polymerization.
Overall, this represents the amount of PP and PE present in the
polymer regardless of whether it is present in the unbound
components or in the diblock copolymer. For a conventional blend,
the weight fraction of PP and weight fraction of PE corresponds to
the individual amount of PP and PE polymer present. For the
crystalline block composite, it is assumed that the ratio of the
weight fraction of PP to PE also corresponds to the average block
ratio between PP and PE present in this statistical block
copolymer.
w PP = wt % C 3 Overall - wt % C 3 PE wt % C 3 PP - wt % C 3 PE Eq
. 2 ##EQU00003##
where w.sub.PP=weight fraction of PP present in the whole polymer
wt % C3.sub.PP=weight percent of propylene in PP component or block
wt % C3.sub.PE=weight percent of propylene in PE component or
block
Estimating the Amount of the Diblock in the Crystalline Block
Composite
[0138] Applying equations 3 through 5, the amount of the isolated
PP that is measured by HTLC analysis is used to determine the
amount of polypropylene present in the diblock copolymer. The
amount isolated or separated first in the HTLC analysis represents
the `unbound PP` and its composition is representative of the PP
hard block present in the diblock copolymer. By substituting the
overall weight % C3 of the whole polymer in the left hand side of
equation 3, and the weight fraction of PP (isolated from HTLC) and
the weight fraction of PE (separated by HTLC) into the right hand
side of equation 3, the weight % of C3 in the PE fraction can be
calculated using equations 4 and 5. The PE fraction is described as
the fraction separated from the unbound PP and contains the diblock
and unbound PE. The composition of the isolated PP is assumed to be
the same as the weight % propylene in the iPP block as described
previously.
wt % C 3 Overall = w PP isolated ( wt % C 3 PP ) + w PE - fraction
( wt % C 3 PE - fraction ) Eq . 3 wt % C 3 PE - fraction = wt % C 3
Overall - w PPisolated ( wt % C 3 PP ) w PE - fraction Eq . 4 w PE
fraction = 1 - w PPisolated 10 Eq . 5 ##EQU00004##
where w.sub.PPisolated=weight fraction of isolated PP from HTLC
w.sub.PE-fraction=weight fraction of PE separated from HTLC,
containing the diblock and unbound PE wt % C3.sub.PP=weight % of
propylene in the PP; which is also the same amount of propylene
present in the PP block and in the unbound PP Wt %
C3.sub.PE-fraction=weight % of propylene in the PE-fraction that
was separated by HTLC wt % C3.sub.Overall=overall weight %
propylene in the whole polymer
[0139] The amount of wt % C3 in the polyethylene fraction from HTLC
represents the amount of propylene present in the block copolymer
fraction that is above the amount present in the `unbound
polyethylene`.
[0140] To account for the `additional` propylene present in the
polyethylene fraction, the only way to have PP present in this
fraction, is that the PP polymer chain must be connected to a PE
polymer chain (or else it would have been isolated with the PP
fraction separated by HTLC). Thus, the PP block remains adsorbed
with the PE block until the PE fraction is separated.
The amount of PP present in the diblock is calculated using
Equation 6.
w PP - diblock = wt % C 3 PE - fraction - wt % C 3 PE wt % C 3 PP -
wt % C 3 PE Eq . 6 ##EQU00005##
Where
[0141] Wt % C3.sub.PE-fraction=weight % of propylene in the
PE-fraction that was separated by HTLC (Equation 4) wt %
C3.sub.PP=weight % of propylene in the PP component or block
(defined previously) wt % C3.sub.PE=weight % of propylene in the PE
component or block (defined previously) w.sub.PP-diblock=weight
fraction of PP in the diblock separated with PE-fraction by
HTLC
[0142] The amount of the diblock present in this PE fraction can be
estimated by assuming that the ratio of the PP block to PE block is
the same as the overall ratio of PP to PE present in the whole
polymer. For example, if the overall ratio of PP to PE is 1:1 in
the whole polymer, then it assumed that the ratio of PP to PE in
the diblock is also 1:1. Thus the weight fraction of diblock
present in the PE fraction would be weight fraction of PP in the
diblock (w.sub.PP-diblock) multiplied by two. Another way to
calculate this is by dividing the weight fraction of PP in the
diblock (w.sub.PP-diblock) by the weight fraction of PP in the
whole polymer (equation 2).
To further estimate the amount of diblock present in the whole
polymer, the estimated amount of diblock in the PE fraction is
multiplied by the weight fraction of the PE fraction measured from
HTLC.
[0143] To estimate the crystalline block composite index, the
amount of block copolymer is determined by equation 7. To estimate
the CBCI, the weight fraction of diblock in the PE fraction
calculated using equation 6 is divided by the overall weight
fraction of PP (as calculated in equation 2) and then multiplied by
the weight fraction of the PE fraction. The value of the CBCI can
range from 0 to 1, wherein 1 would be equal to 100% diblock and
zero would be for a material such as a traditional blend or random
copolymer.
CBCI = w PP - diblock w PP w PE - fraction Eq . 7 ##EQU00006##
Where
[0144] w.sub.PP-diblock=weight fraction of PP in the diblock
separated with the PE-fraction by HTLC (Equation 6) w.sub.PP=weight
fraction of PP in the polymer w.sub.PE-fraction=weight fraction of
PE separated from HTLC, containing the diblock and unbound PE
(Equation 5)
[0145] For example, if an iPP-PE polymer contains a total of 62.5
wt % C3 and is made under the conditions to produce an PE polymer
with 10 wt % C3 and an iPP polymer containing 97.5 wt % C3, the
weight fractions of PE and PP are 0.400 and 0.600, respectively (as
calculated using Equation 2). Since the percent of PE is 40.0 wt %
and the iPP is 60.0 wt %, the relative ratio of the PE:PP blocks is
expressed as 1:1.5.
[0146] Hence, if one skilled in the art, carries out an HTLC
separation of the polymer and isolates 28 wt % PP and 72 wt % of
the PE fraction, this would be an unexpected result and this would
lead to the conclusion that a fraction of block copolymer was
present. If the C3 content of the PE fraction (wt %
C.sub.3PE-fraction) is subsequently calculated to be 48.9 wt % C3
from equations 4 and 5, the PE fraction containing the additional
propylene has 0.556 wt fraction of PE polymer and 0.444 weight
fraction of PP polymer (w.sub.PP-diblock, calculated using Equation
6).
[0147] Since the PE fraction contains 0.444 weight fraction of PP,
it should be attached to an additional 0.293 weight fraction of PE
polymer based on the iPP:PE block ratio of 1.5:1. Thus, the weight
fraction of diblock present in the PE fraction is 0.741; further
calculation of the weight fraction of diblock present in the whole
polymer is 0.533. For the entire polymer, the composition is
described as 53.3 wt % iPP-PE diblock, 28 wt % PP polymer, and 18.7
wt % PE polymer. The crystalline block composite index (CBCI) is
the estimated weight fraction of diblock present in the whole
polymer. For the example described above, the CBCI for the
crystalline block composite is 0.533.
[0148] The Crystalline Block Composite Index (CBCI) provides an
estimate of the quantity of block copolymer within the crystalline
block composite under the assumption that the ratio of CEB to CAOB
within the diblock is the same as the ratio of crystalline ethylene
to crystalline alpha-olefin in the overall crystalline block
composite. This assumption is valid for these statistical olefin
block copolymers based on the understanding of the individual
catalyst kinetics and the polymerization mechanism for the
formation of the diblocks via chain shuttling catalysis as
described in the specification.
[0149] The calculation of CBCI is based on the analytical
observation that the amount of free CAOP is lower than the total
amount of CAOP that was produced in the polymerization. The
remainder of the CAOP is bound to CEB to form the diblock
copolymer. Because the PE fraction separated by HTLC contains both
the CEP and the diblock polymer, the observed amount of propylene
for this fraction is above that of the CEP. This difference can be
used to calculate the CBCI.
[0150] Based solely on the analytical observations without prior
knowledge of the polymerization statistics, the minimum and maximum
quantities of block copolymer present in a polymer can be
calculated, thus distinguishing a crystalline block composite from
a simple copolymer or copolymer blend.
[0151] The upper bound on the amount of block copolymer present
within a crystalline block composite, w.sub.DB.sub.max, is obtained
by subtracting the fraction of unbound PP measured by HTLC from one
as in Equation 8. This maximum assumes that the PE fraction from
HTLC is entirely diblock and that all crystalline ethylene is bound
to crystalline PP with no unbound PE. The only material in the CBC
that is not diblock is that portion of PP separated via HTLC.
w.sub.DB.sub.Max=1-w.sub.PP.sub.isolated Eq. 8
[0152] The lower bound on the amount of block copolymer present
within a crystalline block composite, w.sub.DB.sub.Min, corresponds
to the situation where little to no PE is bound to PP. This lower
limit is obtained by subtracting the amount of unbound PP as
measured by HTLC from the total amount of PP in the sample as shown
in Equation 9.
w.sub.DB.sub.Min=w.sub.PP-w.sub.PP.sub.isolated Eq. 9
[0153] Furthermore, the crystalline block composite index will fall
between these two values:
w.sub.DB.sub.Min<CBCI.ltoreq.w.sub.DB.sub.Max.
[0154] Based on the polymerization mechanism for production of the
crystalline block composites, the CBCI represents the best estimate
of the actual fraction of diblock copolymer in the composite. For
unknown polymer samples, w.sub.DB.sub.Min can be used to determine
if a material is a crystalline block composite. Consider the
application of this analysis to homopolymers, copolymers or blends.
For a physical blend of PE and PP, the overall weight fraction of
PP should be equal to that of the wt % PP from HTLC and the lower
bound on diblock content, Equation 9, is zero. If this analysis is
applied to a sample of PP that does not contain PE both the weight
fraction of PP and amount of PP obtained from HTLC are 100% and
again the lower bound on diblock content, Equation 9, is zero.
Finally if this analysis is applied to a sample of PE that does not
contain PP then both the weight fraction of PP and weight fraction
PP recovered via HTLC are zero and the lower bound on diblock,
Equation 9, is zero. Because the lower bound on diblock content is
not greater than zero in any of these three cases, these materials
are not crystalline block composites.
EXAMPLES
TABLE-US-00001 [0155] TABLE 1 Description of materials Material
Description CBC1 50/50 EP/iPP, 90 wt % C2 in EP, 30 MFR CBC2 50/50
EP/iPP, 90 wt % C2 in EP, 3.6 MFR CBC3 30/70 EP/iPP, 90 wt % C2 in
EP, 20 MFR CBC4 30/70 EP/iPP, 90 wt % C2 in EP, 3 MFR CBC5 50/50
EP/iPP, 90 wt % C2 in EP, 7.5 MFR CBC6 30/70 EP/iPP, 90 wt % C2 in
EP, 4.9 MFR OBC1 INFUSE .TM. 9807; ethylene octene block copolymer,
Density = 0.866 g/cc, MI = 15 g/10 min (@190.degree. C.) (The Dow
Chemical Company) OBC2 INFUSE .TM. 9500; ethylene octene block
copolymer, Density = 0.877 g/cc, MI = 5 g/10 min (@190.degree. C.)
(The Dow Chemical Company) EP1 EP single reactor product, 90 wt %
C2, 6.3 MFR iPP1 iPP single reactor product, 7.7 MFR BC1 50/50
EP/iPP, 65 wt % C2 in EP, 4.1 MFR BC2 50/50 EP/iPP, 40 wt % C2 in
EP, 6.0 MFR POX 2,5-Dimethyl-2,5-di(t-butylperoxy) hexane, CAS#
78-63-7, LUPEROX 101 dialkyl peroxide, supplied by Aldrich MAH
Maleic anhydride CAS# 108-31-6, 98+% from Alfa Aesar MEK Methyl
ethyl ketone (CAS# 78-93-3, 2-Butanone from Sigma- Aldrich) VTMOS
Vinyltrimethoxysilane (VTMOS), CAS# 2768-02-7, XIAMETER OFS-6300
Silane from Dow Corning DEDA 2-ethylaminoethylamine (CAS# 110-72-5,
from Sigma- Aldrich) .sup.13C-MAH Maleic anhydride(2,3-13C2), CAS#
41403-35-4, supplied by Cambridge Isotope Laboratories, Inc.
Synthesis of Crystalline Block Composites
General
[0156] Catalyst-1
([[rel-2',2'''-[(1R,2R)-1,2-cylcohexanediylbis(methyleneoxy-.kappa.O)]bis-
[3-(9H-carbazol-9-yl)-5-methyl[1,1'-biphenyl]-2-olato-.kappa.
O]](2-)]dimethyl-hafnium) and cocatalyst-1, a mixture of
methyldi(C.sub.14-18alkyl)ammonium salts of
tetrakis(pentafluorophenyl)borate, prepared by reaction of a long
chain trialkylamine (Armeen.TM. M2HT, available from Akzo-Nobel,
Inc.), HCl and Li[B(C.sub.6F.sub.5).sub.4], substantially as
disclosed in U.S. Pat. No. 5,919,983, Ex. 2., are purchased from
Boulder Scientific and used without further purification.
[0157] CSA-1 (diethylzinc or DEZ) and cocatalyst-2 (modified
methylalumoxane (MMAO)) were purchased from Akzo Nobel and used
without further purification. The solvent for the polymerization
reactions is a hydrocarbon mixture (ISOPAR.RTM.E) obtainable from
ExxonMobil Chemical Company and purified through beds of 13-X
molecular sieves prior to use.
[0158] The crystalline block composites of the present Examples are
designated CBC1-CBC6. They are prepared using two continuous
stirred tank reactors (CSTR) connected in series. The first reactor
was approximately 12 gallons in volume while the second reactor was
approximately 26 gallons. Each reactor is hydraulically full and
set to operate at steady state conditions. Monomers, solvent,
hydrogen, catalyst-1, cocatalyst-1, cocatalyst-2 and CSA-1 are fed
to the first reactor according to the process conditions outlined
in Table 2. The first reactor contents as described in Table 2 flow
to a second reactor in series. Additional monomers, solvent,
hydrogen, catalyst-1, cocatalyst-1, and optionally, cocatalyst-2,
are added to the second reactor. Table 3 shows the analytical
characteristics of CBC1-CBC6.
TABLE-US-00002 TABLE 2 Reactor process conditions to produce
crystalline block composites CBC1-CBC6 Material CBC1 CBC2 CBC3
Reactor 1st Reactor 2nd Reactor 1st Reactor 2nd Reactor 1st Reactor
2nd Reactor Reactor Control 130 115 118 110 120 115 Temp. (.degree.
C.) Solvent Feed 228 185 145 145 130 292 (lb/hr) Propylene Feed
4.34 34.88 1.98 31.03 2.92 58.66 (lb/hr) Ethylene Feed 32.9 0.0
27.8 0.0 24.5 0.0 (lb/hr) Hydrogen Feed 9.7 9.3 9.6 9.2 9.7 9.8
(SCCM) Reactor Propylene 1.64 2.27 1.06 2.00 1.98 1.93 Conc. (g/L)
Catalyst Efficiency 0.877 0.238 5.166 0.167 0.738 0.081 (gPoly/gM)
*1.0E6 Catalyst Flow 0.68 0.38 1.16 0.95 0.89 1.79 (lb/hr) Catalyst
Conc. 60 385 5 196 40 400 (ppm) Cocatalyst-1 Flow 0.91 0.20 1.48
0.93 0.80 0.96 (lb/hr) Cocatalyst-1 Conc. 600 6000 50 2000 600 6000
(ppm) Cocat.-2 Flow 0.57 0.00 0.91 0.00 0.51 0.00 (lb/hr) Cocat.-2
Conc. 3995 0 1494 0 3995 0 (ppm) DEZ Flow 1.24 0.00 1.10 0.00 1.65
0.00 (lb/hr) DEZ Conc. 50000 0 30000 0 30000 0 (ppm) Production
Rate 35.6 35.0 29.2 31.1 26.3 58.4 (lb/hr) Material CBC4 CBC5 CBC6
Reactor 1st Reactor 2nd Reactor 1st Reactor 2nd Reactor 1st Reactor
2nd Reactor Reactor Control 96 116 141 135 140 115 Temp. (.degree.
C.) Solvent Feed 167 253 242 245 144 360 (lb/hr) Propylene Feed
3.48 50.99 5.44 48.76 3.42 69.17 (lb/hr) Ethylene Feed 28.2 0.0
47.0 0.0 28.0 0.0 (lb/hr) Hydrogen Feed 9.7 9.6 9.5 0.0 9.6 9.6
(SCCM) Reactor Propylene 2.20 2.67 3.57 2.26 1.99 2.03 Conc. (g/L)
Catalyst Efficiency 2.434 0.028 0.706 0.075 0.581 0.146 (gPoly/gM)
*1.0E6 Catalyst Flow 0.42 3.00 0.47 1.78 0.36 0.93 (lb/hr) Catalyst
Conc. 30 600 150 500 150 500 (ppm) Cocatalyst-1 Flow 0.57 2.08 1.41
1.12 0.36 0.58 (lb/hr) Cocatalyst-1 Conc. 300 7800 500 8000 2000
8000 (ppm) Cocat.-2 Flow 0.60 0.00 1.18 9.98 0.75 15.02 (lb/hr)
Cocat.-2 Conc. 1993 0 1993 1993 1993 1797 (ppm) DEZ Flow 0.97 0.00
1.89 0.00 1.20 0.00 (lb/hr) DEZ Conc. 30000 0 30000 0 30000 0 (ppm)
Production Rate 30.9 50.4 49.5 56.1 31.0 68.1 (lb/hr)
TABLE-US-00003 TABLE 3 Crystalline block composite physical
properties MFR Wt % PP Total Tm (.degree. C.) Melt (230.degree. C./
from HTLC Mw Mw/ Wt % Peak 1 Tc Enthalpy Example 2.16 kg)
Separation Kg/mol Mn C.sub.2 (Peak 2) (.degree. C.) (J/g) CBC1 30.9
16.3 69.7 3.18 47.5 120 (106) 89 90 CBC2 3.6 13.2 146 2.76 46.7 130
(114) 97 126 CBC3 23.5 27.1 127 4.26 28.8 136 (105) 94 100 CBC4 3.5
34.0 180 3.63 28.9 136 (101) 97 97 CBC5 7.5 19.4 109 2.83 48.3 129
(108) 91 91 CBC6 4.9 35.8 160 2.84 29.4 139 (104) 102 89
Table 4 shows the ratio of iPP to EP as well as the estimated
crystalline block composite index for CBC1-CBC6.
TABLE-US-00004 TABLE 4 Crystalline Block Composite Index Estimation
wt % wt % Crystalline Block Sample iPP EP Wt % C.sub.2 in EP
Composite Index CBC1 48 52 90 0.634 CBC2 49 51 90 0.729 CBC3 69 31
90 0.605 CBC4 70 30 90 0.702 CBC5 50 50 90 0.583 CBC6 70 30 90
0.473
[0159] FIG. 1 shows the DSC profile for CBC2. The DSC profile shows
a melting peak at 129.degree. C. which is representative of the
CAOP and CAOB and 113.degree. C. which corresponds to the CEP and
CEB. The observed melt enthalpy was 115 J/g and glass transition
temperature was observed at -11.degree. C.
[0160] FIG. 2 shows the TREF analysis of CBC2. The TREF elution
profile shows that CBC2 is highly crystalline and in contrast to
the DSC melting profile, shows little or no separation of the CEP
and CAOP or the block copolymer. Only 2.4 wt % purge was measured
which also indicates the very high crystallinity of components in
CBC2.
[0161] FIG. 3 shows HTLC analysis of CBC2. The elution profile of
CBC2 by HTLC showed that 13.2 wt % of an early eluting peak between
1-2 mL and 86.8 wt % of a later eluting peak between 3-5 mL was
eluted. From the concentration and composition measurement, it is
determined that the early eluting peak was isolated PP which is
CAOP and representative of the CAOB. This is shown by the
composition profile of the wt % of C3 present. The second peak and
later eluting peak is rich in C2 and shows a gradient of C3. It can
be interpreted that this peak is the PE phase and contains the
block copolymer and CEP. The composition gradient shows that the
block copolymer is eluted earlier and the CEP is eluted last.
Synthesis of Block Composites
[0162] The Block Composite samples are synthesized in dual reactors
in series in a similar fashion to the Crystalline Block Composite
samples. The first reactor in each case was approximately 12
gallons in volume while the second reactor was approximately 26
gallons. The process conditions are contained in Table 5.
TABLE-US-00005 TABLE 5 Reactor process conditions to produce block
composites Material BC1 BC2 1st 2nd 1st 2nd Reactor reactor reactor
reactor reactor Reactor Control Temp. (.degree. C.) 95 105 96 109
Solvent Feed (lb/hr) 145 145 145 145 Propylene Feed (lb/hr) 11 30
19 29 Ethylene Feed (lb/hr) 20 0 12 0 Reactor Propylene Conc. 1.72
2.08 2.14 2.08 (g/L) Hydrogen Feed (SCCM) 15 19 10 11 Catalyst
Efficiency 4.55 0.20 5.42 0.15 (gPoly/gM) * 106 Catalyst Flow
(lb/hr) 0.15 0.74 0.38 1.02 Catalyst Conc. (ppm) 45 196 15 196
Cocatalyst-1 Flow (lb/hr) 0.3 0.73 0.38 1.99 Cocatalyst-1 Conc.
(ppm) 300 2000 199 1000 Cocat.-2 Flow (lb/hr) 1.01 0 0.61 0
Cocat.-2 Conc. (ppm) 1494 0 1494 0 DEZ Flow (lb/hr) 0.81 0 .72 0
DEZ Concentration (ppm) 30000 0 30000 0 Production Rate (lb/hr) 30
30 31 29
TABLE-US-00006 TABLE 6 Block composite physical properties MFR Wt %
PP Total Tm (.degree. C.) Melt (230.degree. C./ from HTLC Mw Mw/ Wt
% Peak 1 Tc Enthalpy Example 2.16 kg) Separation Kg/mol Mn C.sub.2
(Peak 2) (.degree. C.) (J/g) BC1 4.1 21.5 133 2.35 33.8 139 (40) 93
66 BC2 6.0 21.6 176 3.69 20.5 138 (na) 96 56
TABLE-US-00007 TABLE 7 Block Composite Index Estimations Wt % Wt %
(Crystalline) Block Sample iPP EP Wt % C2 in EP Composite Index BC1
49 51 65 0.413 BC2 50 50 40 0.368
Synthesis of EP1 and iPP1
[0163] Samples EP1 and iPP1 were produced using the same catalyst
and cocatalysts as the Crystalline Block Composites and Block
Composites but each were produced in a single reactor. For sample
EP1 the final product MFR was regulated by manipulating the DEZ
flow. Sample iPP1 was produced at higher propylene concentration in
the reactor and hydrogen was used to regulate the final product MFR
rather than DEZ. Sample EP1 was produced in a 12 gallon reactor and
iPP1 was produced in a 52 gallon reactor.
TABLE-US-00008 TABLE 8 Reactor process conditions to produce EP1
and iPP1 Material EP1 iPP1 Reactor Control Temp. (.degree. C.) 146
155 Solvent Feed (lb/hr) 290 1208.3 Propylene Feed (lb/hr) 7.4
322.2 Ethylene Feed (lb/hr) 57.8 2.5 Hydrogen Feed (SCCM) 0 171
Reactor Propylene Conc. (g/L) 4.13 46.56 Catalyst Efficiency
(gPoly/gM) * 106 1.12 0.794 Catalyst Flow (lb/hr) 0.85 2.45
Catalyst Conc. (ppm) 64.9 120 Cocatalyst-1 Flow (lb/hr) 0.55 1.55
Cocatalyst-1 Conc. (ppm) 1000 1397 Cocat.-2 Flow (lb/hr) 1.40 1.11
Cocat.-2 Conc. (ppm) 3995 1397 DEZ Flow (lb Zn/hr) 1.68 0 DEZ
Concentration (ppm) 40,000 0 Production Rate (lb/hr) 63.4 233
TABLE-US-00009 TABLE 9 Single reactor product physical properties
MFR Total Melt (230.degree. C./ Mw Mw/ Wt % Tm Tc Enthalpy Example
2.16 kg) Kg/mol Mn C.sub.2 (.degree. C.) (.degree. C.) (J/g) EP1
6.2 70.6 2.06 92 108 92 115 iPP1 7.7 248 2.64 0.9 131 99 75
Preparation of MAH Grafted OBC1 (MAH-g-OBC1)
[0164] A ZSK-92 Megacompounder with 11 barrels (45 L/D) is used to
graft MAH on INFUSE.TM. 9807 (OBC1). The OBC1 resin is fed with
K-Tron T-60 feeder. MAH is injected at barrel 3, port 1 using a
Lewa pump. The peroxide/oil mixture (50/50 wt/wt) was injected at
barrel 3, port 2 using a Prominent Sigma plunger pump. The barrel
temperature is set at 80.degree. C. for zone 1 and 225.degree. C.
for zone 2 to 11. A vacuum pump system is used for devolatilization
at barrel 9. A minimum of 20 inches Hg is used. The screw RPM is at
200 to 230, the torque ranges from 56% to 61%. The feed rate for
OBC1 is set at 1500 lb/hr. The feed formulation is 1.70% MAH, 0.20%
peroxide/mineral oil (50/50, wt/wt) mixture. The final MAH grafting
level is 0.95% and melt index of MAH-g-OBC1 is 8.0 (2.16 kg,
190.degree. C.).
Preparation of MAH Grafted Polymers (MAH Grafted CBC, EP1, iPP1 and
Blends of EP1 and iPP1)
[0165] A Coperion ZSK-25MC twin screw extruder is used for the
reactive extrusion process to functionalize the base plastic
resins. The 25-mm diameter extruder was equipped with 12 barrel
segments for a total length to diameter ratio of 48. There are 11
independently controlled barrel sections with electric heating and
water cooling. Polymer pellets are fed to the main extruder hopper
in barrel 1 using a K-tron Model KCLQX3 loss-in-weight feeder. The
liquid reactants were injected into the third barrel section of the
extruder using a HPLC precision metering pump (Alltech Model 627
HPLC pump). A dialkyl organic peroxide (Luperox 101, CAS#78-63-7)
is used as the initiator. The liquid feed to the extruder included
a solvent blend containing both the maleic anhydride monomer and
the organic peroxide. In order to improve the accuracy of the
feeding, both the peroxide and maleic anhydride powder were
dissolved in methylethylketone (MEK) solvent. 300 grams of maleic
anhydride crystals were weighted out and placed into a 2-liter
plastic container with a sealable lid. An equal weight of MEK
solvent was weighted out on a scale, and added to the container
with the maleic anhydride. The blend was left in the laboratory
hood with a magnetic stir bar to assist in dissolving the maleic
anhydride into the solvent. The ratio of maleic anhydride to
peroxide was held constant for the experimental samples at 0.02
parts peroxide and 0.9 parts maleic anhydride. In order to minimize
the time when the peroxide and monomer are mixed together, the
peroxide were dissolved in the previously made MEK/maleic anhydride
solution immediately before moving the blend to the inlet of the
positive displacement pump. The HPLC injection rate was 9.07 g/min.
Typical injection pressures for the liquids were 115-160 psi. The
MEK solvent, unreacted maleic anhydride and volatile compounds were
removed via the vacuum line-trap system at the devolatilization
port in barrel 11. The vacuum system was operated at 508 mm Hg
vacuum. The melt was pelletized using a GALA LPU underwater
pelletization system. A two-hole die was used with 7.2.degree. C.
water temperature and a cutter speed of 1700 rpm. The polymer feed
rate to the process was 6.80 kg/h with a fixed extruder screw speed
of 500 rpm and a motor torque load of 55-65%.
[0166] The formulations used for grafting maleic anhydride (MAH) to
CBC1-CBC4 are shown in Table 10. Process conditions for production
of MAH grafted CBC2 are shown in Table 11. Similar conditions were
used for CBC1 and CBC3-CBC6.
[0167] An IR spectrum for MAH-g-CBC2-4 is shown in FIG. 4. The
anhydride peak can be seen at 1785 cm.sup.-1. A typical thermogram
for MAH-g-CBC2-4 is shown in FIG. 5. The DSC profile shows a
melting peak at 131.degree. C. which is representative of the CAOP
and CAOB and 113.degree. C. which corresponds to the CEP and CEB.
The observed melt enthalpy is 103 J/g. The thermal properties of
the grafted CBC2 are comparable to the original CBC2 before
grafting. A typical HTLC for MAH-g-CBC2-4 is shown in FIG. 6. The
elution profile of CBC2 by HTLC shows that 29 wt % of an early
eluting peak between 1.6-2.2 mL and 71 wt % of a later eluting peak
between 3-5 mL is eluted. From the concentration and composition
measurement, it is determined that the early eluting peak was
isolated PP which is CAOP and representative of the CAOB. This is
shown by the composition profile of the wt % of C.sub.3 present.
The second peak and later eluting peak is rich in C.sub.2 and shows
a gradient of C.sub.3. It can be interpreted that this peak is the
PE phase and contains the block copolymer and CEP. The composition
gradient shows that the block copolymer is eluted earlier and the
CEP is eluted last.
[0168] The characterizations of MAH-g-CBC and MAH-g-OBC1 are shown
in Table 12. Compared to Example A, inventive Examples 1, 2 and 5-8
have higher melting temperatures. All inventive examples in Table
12 have higher melt enthalpy than Example A, which translates to a
high crystallinity. The tensile properties of MAH-g-CBC and
MAH-g-OBC1 are shown in Table 13. The inventive examples in Table
12 have higher tensile modulus, toughness and ultimate tensile
strength.
TABLE-US-00010 TABLE 10 MAH grafting formulation and resin
properties Feed (wt %) Example Description Polymer MAH POX MEK 1
MAH-g-CBC2-2 96.36 1.80 0.04 1.80 2 MAH-g-CBC2-4 92.72 3.60 0.08
3.60 3 MAH-g-CBC1-1 92.72 3.60 0.08 3.60 4 MAH-g-CBC1-2 92.68 3.60
0.12 3.60 5 MAH-g-CBC3-1 92.68 3.60 0.12 3.60 6 MAH-g-CBC3-2 92.60
3.60 0.20 3.60 7 MAH-g-CBC4-1 92.68 3.60 0.12 3.60 8 MAH-g-CBC4-2
92.60 3.60 0.20 3.60
TABLE-US-00011 TABLE 11 Process Conditions for Production of MAH
grafted Polymer Samples Sample No. MAH-g- MAH-g- CBC2-2 CBC2-4 #1
Pellet Feed 6.80 6.80 Rate [kg/h] HPLC [g/min] 4.29 9.07 Screw RPM
500 500 SP Actual SP Actual Zone #1 [.degree. C.] 120 112 120 112
Zone #2 [.degree. C.] 200 200 200 200 Zone #3 [.degree. C.] 200 200
200 200 Zone #4 [.degree. C.] 200 200 200 200 Zone #5 [.degree. C.]
200 200 200 200 Zone #6 [.degree. C.] 200 198 200 200 Zone #7
[.degree. C.] 200 200 200 200 Zone #8 [.degree. C.] 200 200 200 200
Zone #9 [.degree. C.] 200 200 200 200 Zone #10 [.degree. C.] 200
200 200 200 Zone #11 [.degree. C.] 200 200 200 200 Divert Valve [C]
200 200 200 200 Gala Die [.degree. C.] 185 185 185 185 Gala RPM
1700 1700 Gala water temp 7.2 7.2 (.degree. C.) Torque % 56 62 Die
pressure 3.25 3.31 (MPa)
TABLE-US-00012 TABLE 12 Characterizations of MAH-g-CBC MFR Grafting
Wt % PP Tm (.degree. C.) Melt (230.degree. C./ level From HTLC Peak
1 Tc Enthalpy Example Description 2.16 kg) MAH wt % Separation
(Peak 2) (.degree. C.) (J/g) 1 MAH-g-CBC2-2 2.7 0.28 24.0 131 (113)
97 105 2 MAH-g-CBC2-4 0.71 0.64 29.0 131 (113) 95 103 3
MAH-g-CBC1-1 13.0 0.47 23.9 120 (104) 87 98 4 MAH-g-CBC1-2 8.8 0.76
26.8 119 (103) 86 95 5 MAH-g-CBC3-1 87.6 0.46 38.3 136 (103) 94 105
6 MAH-g-CBC3-2 87.1 0.88 41.3 137 (102) 95 96 7 MAH-g-CBC4-1 24.1
0.54 49.6 135 (97) 96 95 8 MAH-g-CBC4-2 31.9 0.87 56.3 136 (97) 98
83 A MAH-g-OBC1 8.0* 0.98 n/a 121 111 32 *Measured at 2.16 kg,
190.degree. C.
TABLE-US-00013 TABLE 13 Tensile properties of MAH-g-CBC and
MAH-g-OBC1 2% Secant Ult. Ult Modulus Elongation Toughness Tensile
Example Description (psi) (%) (in * lbf) (psi) 1 MAH-g-CBC2- 34057
660 170 3135 2 2 MAH-g-CBC2- 35700 697 188 3259 4 3 MAH-g-CBC1-
32600 619 111 2226 1 4 MAH-g-CBC1- 30550 645 125 2341 2 5
MAH-g-CBC3- 43602 357 76 2880 1 6 MAH-g-CBC3- 45819 391 85 2886 2 7
MAH-g-CBC4- 40924 601 156 3646 1 8 MAH-g-CBC4- 41958 601 158 3646 2
A MAH-g-OBC1 1735 1456 104 1073
Comparison of MAH-g-CBC and MAH-g-iPP1/EP1 Blends
[0169] The process of grafting iPP1/EP1 blends is the same as
described for the CBCs above. The iPP1 and EP1 are dry blended
prior to grafting. The formulations used for grafting MAH to
iPP1/EP1 blends and CBC5 and CBC6 are shown in Table 14.
Characterizations of MAH grafted iPP1/EP1 blends and CBC5 and CBC6
are shown in Table 15. Tensile properties of MAH grafted iPP1/EP1
blends and CBC5 and CBC6 are shown in Table 16.
[0170] At total C2 content of 46-48 wt %, compared to Example D
[MAH-g-(EP1/iPP1 50/50 blend)], Example 9 (MAH-g-CBC5) has higher
grafting level. Similarly at total C2 content of 28-29 wt %,
Example 10 (MAH-g-CBC6) has higher grafting level than Example E
[MAH-g-(EP1/iPP1 30/70 blend)]. More distinctively, the tensile
properties of Examples 9 and 10 show significantly better
elongation and toughness, whereas Examples D and E are brittle in
nature.
[0171] FIG. 7 shows the TEM images for CBC5, Example 9 (MAH-g-CBC5)
and Example D [MAH-g-(EP1/iPP1 50/50 blend)] at 2 .mu.m resolution
and 0.2 .mu.m resolution. Based on the staining applied, the darker
domains are PE and the lighter domains are PP. The very small PE
domain size of CBC5 and Example 9 (MAH-g-CBC5) strongly suggests
the presence of high levels of block copolymers which acted to
compatibilize the PP and PE phases. The nano-scale nature indicates
that the block copolymer is effective in reducing the PE domains.
In contrast, Example D [MAH-g-(EP1/iPP1 50/50 blend)] exhibits
coarse and phase separated morphologies with more than an order of
magnitude higher domain size.
TABLE-US-00014 TABLE 14 MAH grafting formulation and resin
properties Feed (wt %) Example Description Polymer MAH POX MEK 9
MAH-g-CBC5 95.8 2.00 0.20 2.00 10 MAH-g-CBC6 95.8 2.00 0.20 2.00 B
MAH-g-EP1 95.8 2.00 0.20 2.00 C MAH-g-iPP1 95.8 2.00 0.20 2.00 D
MAH-g-(EP1/iPP1 50/50 95.8 2.00 0.20 2.00 blend) E MAH-g-(EP1/iPP1
30/70 95.8 2.00 0.20 2.00 blend)
TABLE-US-00015 TABLE 15 Characterizations of MAH-g-CBC and
MAH-g-iPP1/EP1 blends MFR before grafting MFR Grafting Wt % PP
Total Tm (.degree. C.) Melt (2.16 kg, (2.16 kg, level From HTLC Wt
% Peak 1 Tc Enthalpy Oligomer Example Description 230.degree. C.)
230.degree. C.) MAH wt % Separation C.sub.2 (Peak 2) (.degree. C.)
(J/g) (ppm) 9 MAH-g-CBC5 7.5 3.1 0.98 32.4 48.3 128 (104) 90 90 264
10 MAH-g-CBC6 4.9 39.1 0.90 49.1 29.4 136 (101) 102 90 91 B
MAH-g-EP1 6.2 1.2 1.24 0 92 105 92 113 135 C MAH-g-iPP1 7.7 195
0.45 100 0.9 131 95 78 117 D MAH-g-(EP1/iPP1 6.9* 8.6 0.94 57.3
46.2 131 (104) 93 99 124 50/50 blend) E MAH-g-(EP1/iPP1 7.2* 33.7
0.74 78.1 28.2 131 (103) 94 88 141 30/70 blend) *Calculated
according to logarithmic additivity rule.
TABLE-US-00016 TABLE 16 Tensile properties of MAH-g-CBC and
MAH-g-iPP1/EP1 blends 2% Secant Ult. Ult Modulus Elongation
Toughness Tensile Example Description (psi) (%) (in * lbf) (psi) 9
MAH-g-CBC5 30672 604 119 2157 10 MAH-g-CBC6 47848 495 130 3007 B
MAH-g-EP1 28413 588 121 1906 C MAH-g-iPP1 79019 184 49 4149 D
MAH-g- 45068 58 15 2405 (EP1/iPP1 50/50 blend) E MAH-g- 50693 17 5
3008 (EP1/iPP1 30/70 blend)
Preparation of MAH-g-BC
[0172] The process of grafting iPP1/EP1 blends is the same as
described for the CBCs above. The formulations used for grafting
MAH to BC are shown in Table 17. Characterizations of MAH-g-BC are
shown in Table 18. Compared to Example A, inventive Examples 11 and
12 have higher melting temperatures and higher melt enthalpy than
Example A.
TABLE-US-00017 TABLE 17 MAH grafting formulation and resin
properties Feed (wt %) Example ID Description Polymer MAH POX MEK
11 12022-38587 MAH-g-BC1 95.8 2.00 0.20 2.00 12 12022-38588
MAH-g-BC2 95.8 2.00 0.20 2.00
TABLE-US-00018 TABLE 18 Characterizations of MAH-g-CBC and
MAH-g-iPP1/EP1 blends MFR Grafting Wt % PP Total Tm (.degree. C.)
Melt (2.16 kg, level From HTLC Wt % Peak 1 Tc Enthalpy Oligomer
Example Description 230.degree. C.) MAH wt % Separation C.sub.2
(Peak 2) (.degree. C.) (J/g) (ppm) 11 MAH-g-BC1 15.9 1.01 34.9 33.8
140 (42) 98 62 198 12 MAH-g-BC2 52.6 0.78 33.0 20.5 138 98 43 196 A
MAH-g-OBC1 8.0* 0.98 n/a 57.4 121 111 32 n/m
Grafting .sup.13C labeled Maleic Anhydride
[0173] The unit used to graft .sup.13C-labeled maleic anhydride to
the polyolefin resin was a Thermo Haake MiniLab Rheomex model CTW5
with synchronous rotating screws. The temperature set point was
180.degree. C. and screw rotation speed was 150 RPM. Polyolefin
resin (CBC5, CBC6, EP1, iPP1, EP1/iPP1 50/50 blend, or EP1/iPP1
30/70 blend) was added to the mixer and allowed to melt for 5 min.
For EP1/iPP1 blend experiments, the pellets were dry-blended before
adding to the mixer. Subsequently, 2,3-.sup.13C.sub.2-maleic
anhydride was added and allowed to mix for 2 min. Afterwards,
2,5-di-t-butylperoxy-2,5-dimethylhexane was added as a 10 wt %
mixture in mineral oil and mixing was continued for 6 min. The
amount of each component is listed in Table 19. After reaction the
collected product was dissolved in boiling xylene to give a 5 wt %
solution and then precipitated into five volumes of methanol. The
solids were collected by vacuum filtration and dried in a vacuum
oven at 145.degree. C. The products and base resins were analyzed
by .sup.13C NMR spectroscopy.
[0174] The total C2 wt % of CBC5, CBC6, EP1 and iPP1 used for MAH
grafting is determined by .sup.13C NMR and the results are listed
in Table 19. The total C2 wt % of EP1/iPP1 50/50 blend and EP1/iPP1
30/70 blend is calculated based on the blend ratio and total C2 wt
% of EP1 and iPP1 determined by .sup.13C NMR. The
ethylene/propylene (E/P) molar ratio is calculated from the total
C2 wt % and shown in Table 19.
[0175] .sup.13C NMR spectroscopy is used to determine the location
of the graft site of the .sup.13C-MAH, whether at an ethylene site
or a propylene site. The E-graft/P-graft mol ratio determined by
.sup.13C NMR is shown in Table 19. Since the molar ratios of
E-graft/P-graft in the grafted resins are considerably larger than
the corresponding molar ratios of E/P sites in the base resins,
this indicates that there is a preference for grafting at an
ethylene site. The E/P graft selectivity is calculated by dividing
E-graft/P-graft mol ratio with E/P mol ratio. The E/P graft
selectivity being greater than 1 indicates that there is a
preference for grafting at an ethylene site. Although the tertiary
C--H bond at a propylene site would be expected to react with the
peroxide faster than a secondary C--H bond at an ethylene site, it
is hypothesized that the tertiary free radical intermediate formed
at a propylene site exhibits a greater preference for chain
scission rather than grafting, whereas the secondary free radical
intermediate exhibits a greater preference for grafting.
Surprisingly, the E/P graft selectivity for CBC is greater than
that for corresponding EP1/iPP1 blends. This contrast in graft
selectivity is hypothesized to be caused by the unique morphology
of the CBC.
TABLE-US-00019 TABLE 19 Results of analysis by .sup.13C NMR
spectroscopy Total C2 E/P E-graft/ E/P Haake Feed composition, g wt
% by mol P-graft graft Example Description Resin .sup.13C-MAH
Peroxide .sup.13C NMR ratio mol ratio selectivity 13
.sup.13C-MAH-g-CBC-5 5.0 0.10 0.01 48.3 1.40 Infinite** Infinite 14
.sup.13C-MAH-g-CBC-6 5.0 0.10 0.01 29.1 0.62 1.8 2.9 F
.sup.13C-MAH-g-EP1 5.0 0.07 0.01 91.8 16.86 n/a n/a G
.sup.13C-MAH-g-iPP1 5.0 0.10 0.01 1.4 0.02 n/a n/a H
.sup.13C-MAH-g-EP1/iPP1 5.0 0.10 0.01 46.6* 1.31 3.1 2.4 50/50
blend I .sup.13C-MAH-g-EP1/iPP1 5.0 0.09 0.01 28.5* 0.60 1.1 1.8
30/70 blend *Calculated value; **zero P-graft as determined by
.sup.13C-MAH
Converting MAH- to Imide-g-CBC2 (Representative preparation of
Imide-g-CBC2)
##STR00006##
[0176] MAH-g-CBC.sub.2-2 and MAH-g-CBC2-4 are converted to
imide-g-CBC.sub.2-2 and imide-g-CBC2-4, respectively. Imide-g-CBC
describes the preparation of a secondary amine pendant functional
group with an imide group. An imide is a functional group having
two carbonyl groups bound to nitrogen. The unit used to convert
MAH-g-CBC2 to DEDA grafted version is a Thermo Haake Polylab, Model
557-9301 (the drive unit) and Haake Rheomix 3000p, Model 557-1306
(with roller mixing rotors). Control is from a Dell Pentium 4
computer (Model DHM, S/N 9D56K21) running Windows 2002 with
proprietary Haake software that controls automated operation of
Polylab drive unit and Rheomix mixing bowls and acquires data.
[0177] For Imide-g-CBC2-4, 195 g of maleated resin (MAH-g-CBC2-4)
is weighed into 16 oz., wide mouthed glass jars then warmed in an
oven at 50.degree. C. temperature for 30 minutes. Three molar
equivalents of DEDA (2-ethylaminoethylamine) per mol of anhydride
is added by gas-tight syringe into the jars. Specifically, 6.3 ml
of DEDA (5.23 g) is added. Jars are shaken to distribute the amine,
capped lightly with Teflon lined lids and returned to the oven for
1 hr. The jars are removed, shaken again, lids secured with
electrical tape and placed inside a 1-gallon wide mouthed HDPE jug
as a secondary container. The glass bottles are padded with brown
crepe paper to keep them from rolling within the secondary jars.
Lids of the secondary containers are sealed with electrical tape
then put on a Stovall low profile powered roller unit set to
maximum rolling speed. Jars are rolled for 2 days. When checked the
next day there was still some visible "loose" liquid on the sides
so returned the jars to the 50.degree. C. oven for 2 hours. Samples
are again put in 50.degree. C. oven for at least 3 hours before
running
[0178] Haake unit is set to 170.degree. C., allowed to equilibrate
and the rotors are calibrated at 100 RPM rotor speed. Imbibed
pellets are added to mix bowl and ran for 10 minutes after feed ram
secured in closed position. The bowl is opened; sample removed and
allowed to cool on Teflon sheet. Films of raw samples (about 3 mil
thick) are pressed at 160.degree. C. using Carver hydraulic press
and checked by FTIR (Perkin-Elmer Spectrum One) for conversion.
Samples are then dried under vacuum at 120.degree. C. for
overnight. An IR spectrum for Imide-g-CBC2-4 is shown in FIG. 7.
The anhydride (1785-1790 cm.sup.-1) band is transformed to the
imide band at 1700-1710 cm.sup.-1 after reaction with the diamine.
The disappearance of the anhydride band and formation of imide band
indicate the reaction is complete.
Converting MAH-g-OBC1 to Imide-g-OBC1
[0179] For converting MAH-g-OBC1 to Imide-g-OBC1, 190 g of
MAH-g-OBC is weighed into 16 oz., wide mouthed glass jars then
warmed in an oven at 50.degree. C. temperature for 30 minutes. 6.1
ml of DEDA (5.12 g) is added by gastight syringe into the jars. The
rest follows the same procedure as converting MAH-g-CBC2 to
Imide-g-CBC2.
[0180] The characterizations of Imide-g-CBC and Imide-g-OBC1 are
shown in Table 20. Compared to Example J (Imide-g-OBC1), inventive
Examples 15 and 16 have higher melting temperatures and higher melt
enthalpy. The inventive examples in Table 20 have higher tensile
modulus, toughness and ultimate tensile strength.
TABLE-US-00020 TABLE 20 Characterizations and tensile properties of
imide grafted polymers MFR Tm (.degree. C.) Melt 2% Secant Ult. Ult
(2.16 kg, Peak 1 Tc Enthalpy Modulus Elongation Toughness Tensile
Example Description 230.degree. C.) (Peak 2) (.degree. C.) (J/g)
(psi) (%) (in*lbf) (psi) 15 Imide-g-CBC2-2 0.79 132 (114) 101 102
48156 436 113 2893 16 Imide-g-CBC2-4 n/m 133 (113) 99 92 43580 663
172 3433 J Imide-g-OBC1 0.33 121 111 29 1214 964 62 565
Preparation of Silane Grated OBC2 (VTMOS-g-OBC2)
[0181] A ZSK-92 Megacompounder with 11 barrels (45 L/D) is used to
graft VTMOS on INFUSE.TM. 9500 (OBC2). The OBC2 resin is fed with
K-Tron T-60 feeder. The barrel temperature is set at 25.degree. C.
for zone 1 and zone 2 and 190.degree. C. for zone 3 and zone 4,
230.degree. C. for zone 5 to 8, and 190.degree. C. for zone 9 to
11. The die temperature is set at 190.degree. C. A vacuum pump
system is used for devolatilization at barrel 9. A minimum of 20
inches Hg is used. The VTMOS/peroxide mixture (20/1, wt/wt) is
injected using an American Lewa, Inc. type EH-1 pump with a
micromotion flow meter model CMP025 to measure flow. The injection
point is at barrel #4. A vacuum pump system is used for
devolatilization at barrel 9 and a vacuum of 20 inches Hg is used
on order to minimize the concentration of volatile components and
residual silane in the melt. The screw RPM is at 250 RPM and feed
rate of OBC2 is 1800 lb/hr. The feed formulation is 1.90% VTMOS and
0.095% peroxide. The final VTMOS grafting level is 1.47% and melt
index of VTMOS-g-OBC2 is 4.9 (2.16 kg, 190.degree. C.).
Silane Grafting of CBC and BC
[0182] The same equipment was used for the preparation of the
silane grafted polymer samples as discussed previously for the
maleic anhydride grafting examples (1-8). A Coperion ZSK-25MC twin
screw extruder is used for the reactive extrusion process to
functionalize the base plastic resins. Polymer pellets are fed to
the main extruder hopper in barrel 1 using a K-tron Model KCLQX3
loss-in-weight feeder. The liquid reactants were injected into the
third barrel section of the extruder using a HPLC precision
metering pump (Alltech Model 627 HPLC pump). A dialkyl organic
peroxide (Luperox 101, CAS#78-63-7) is used as the initiator. The
liquid feed to the extruder included a blend containing both the
vinyltrimethoxysilane monomer and the organic peroxide. In order to
minimize the time when the peroxide and monomer are mixed together,
the peroxide was dissolved in the vinyltrimethoxysilane immediately
before moving the blend to the inlet of the positive displacement
pump. The HPLC injection rate was 4.0 ml/min. Typical injection
pressures for the liquids were 2.56-2.78 MPa. The unreacted
vinyltrimethoxysilane and volatile compounds were removed via the
vacuum line-trap system at the devolatilization port in barrel 11.
The vacuum system was operated at 508 mm Hg vacuum. The melt was
pelletized using a GALA LPU underwater pelletization system. A
two-hole die was used with 7.2.degree. C. water temperature and a
cutter speed of 3400 rpm. The polymer feed rate to the process was
11.36 kg/h with a fixed extruder screw speed of 450 rpm and a motor
torque load of 63-73%.
[0183] The formulations used for grafting VTMOS to CBC and BC are
shown in Table 21. The process conditions are shown in Table 22.
Characterizations of Silane grafted CBC and BC are shown in Table
23. Gel fraction of crosslinked VTMS-g-CBC, VTMS-g-BC and
VTMS-g-OBC2 is shown in Table 24. Compared to Example K
(VTMOS-g-OBC2), inventive Examples 17 to 19 have higher melting
temperatures and higher melt enthalpy. The inventive examples in
Table 23 also have higher tensile modulus and ultimate tensile
strength. Significant crosslinking is developed for examples 17 and
18 as manifested by high gel fraction after cure.
TABLE-US-00021 TABLE 21 Silane grafting formulation and resin
properties Feed (wt %) Example Description Polymer VTMOS POX 17
VTMOS-g-CBC5 98.00 1.90 0.10 18 VTMOS-g-CBC6 98.00 1.90 0.10 19
VTMOS-g-BC1 98.00 1.90 0.10
TABLE-US-00022 TABLE 22 Process Conditions for Production of VTMOS
grafted Polymer Samples Sample No. VTMOS- VTMOS- g-CBC5 g-CBC6 #1
Pellet Feed 11.36 11.36 Rate [kg/h] HPLC [ml/min] 4.0 4.0 Screw RPM
450 450 SP Actual SP Actual Zone #1 [.degree. C.] 50 50 50 50 Zone
#2 [.degree. C.] 180 180 180 180 Zone #3 [.degree. C.] 240 240 240
240 Zone #4 [.degree. C.] 240 240 240 240 Zone #5 [.degree. C.] 240
240 240 240 Zone #6 [.degree. C.] 240 240 240 240 Zone #7 [.degree.
C.] 240 240 240 240 Zone #8 [.degree. C.] 200 200 200 200 Zone #9
[.degree. C.] 200 200 200 200 Zone #10 [.degree. C.] 200 200 200
200 Zone #11 [.degree. C.] 200 200 200 200 Divert Valve [C] 175 175
175 175 Gala Die [.degree. C.] 150 150 150 150 Gala RPM 3400 3400
Gala water temp 7.2 7.2 (.degree. C.) Torque % 63 68 Die pressure
2.23 2.78 (MPa)
TABLE-US-00023 TABLE 23 Characterizations of VTMOS-g-CBC,
VTMOS-g-BC and VTMOS-g-OBC2 MFR Grafting Tm (.degree. C.) Melt 2%
Secant Ult. Ult (2.16 kg, level Peak 1 Tc Enthalpy Modulus
Elongation Toughness Tensile Example Description 230.degree. C.)
VTMOS wt % (Peak 2) (.degree. C.) (J/g) (psi) (%) (in*lbf) (psi) 17
VTMOS-g-CBC5 11.7 1.19 128 (107) 93 98 38698 554 100 2103 18
VTMOS-g-CBC6 35.0 1.06 139 (102) 101 97 69214 329 73 3097 19
VTMOS-g-BC1 8.5 1.27 141 (44) 100 50 25687 186 27 1449 K
VTMOS-g-OBC2 4.9* 1.47 122** 102** 52** 2606** 1767** 146** 1281**
*Measured at 2.16 kg, 190.degree. C. **Measured on ungrafted
OBC2
TABLE-US-00024 TABLE 24 Gel fraction of crosslinked VTMS-g-CBC,
VTMS-g-BC and VTMS-g-OBC2 Example Description Gel fraction (%) 17
VTMS-g-CBC5 49 18 VTMS-g-CBC6 39 19 VTMS-g-BC1 16 K VTMS-g-OBC2
>60
* * * * *