IP Library Granted Patent US 10,344,147
Granted Patent B2
US 10,344,147 · App. 15/551,629 · Granted Jul 9, 2019

Functionalized polymer blend for a tire

Inventors: Evemarie Hamann (Halle, DE); Daniel Heidenreich (Halle, DE); Sven Thiele (Halle, DE)
Assignee: TRINSEO EUROPE GMBH
C08L9/06B60C1/0016B60C1/0025C08C19/20C08C19/22C08C19/25C08C19/44
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Quick Facts
Patent No.
US 10,344,147
App. No.
15/551,629
Granted
Jul 9, 2019
Kind
B2
Abstract

A polymer blend consisting of (a) 60-96 percent by weight of a high molecular weight first elastomeric polymer, (b) 4-35 percent by weight of a low molecular weight second polymer, and optionally (c) 0-13 percent by weight of an extender oil, wherein the amounts of the components (a), (b) and (c) are based on the total weight of the polymer blend.

Claims (55)

1. A polymer blend, comprising:

(a) 60 to 96 percent by weight of a first elastomeric polymer,

(b) 4 to 35 percent by weight of a second polymer, and optionally

(c) 0 to 13 percent by weight of one or more extender oil(s);

wherein the first elastomeric polymer is produced by

(I) anionic polymerization of at least one conjugated diene monomer and optionally one or more α-olefin monomer(s) in the presence of a polymerization initiator in an organic solvent, and optionally

(II) modification of the polymer chain ends obtained in (I) by addition and reaction of at least one compound represented by any of formula (1) to (3) or formula (11) to (15), as defined below;

wherein the second polymer is produced by

(i) anionic polymerization in the presence of a polymerization initiator in an organic solvent of (i-1) at least one conjugated diene monomer, or (i-2) at least one conjugated diene monomer and one or more α-olefin monomer(s), or (i-3) at least one or more α-olefin monomer(s), and

(ii) modification of the polymer chain ends obtained in (i) by addition and reaction of at least one compound represented by any of formula (1), formula (3), or formula (11) to (15), as defined below, provided that, in the corresponding formula, x, x 1′ , r 4 , t 1 , and v are each selected from 1 and 2;

wherein the first elastomeric polymer (a) has a number average molecular weight (M n ) of 400,000 to 2,000,000 g/mol, and a weight-average molecular weight (M w ) of 500,000 to 3,000,000 g/mol;

wherein the second polymer (b) has a number average molecular weight (M n ) of 500 to 80,000 g/mol, and a weight-average molecular weight (M w ) of 500 to 100,000 g/mol; and

wherein the amounts of the components (a), (b) and (c) are based on the total weight of the polymer blend;

(R***O) X (R**) y Si-A-S—SiR** 3   formula(1),

wherein each of R** is independently selected from C 1 -C 16 alkyl or alkylaryl; R*** is independently selected from C 1 -C 4 alkyl; A is selected from C 6 -C 18 aryl, C 7 -C 50 alkylaryl, C 1 -C 50 alkyl and C 2 -C 50 dialkylether; and optionally R**, R***, or A may independently be substituted with one or more groups, selected from C 1 -C 4 alkyl, C 1 -C 4 alkoxy, C 6 -C 12 aryl, C 7 -C 16 alkylaryl, di(C 1 -C 7 hydrocarbyl)amino, bis(tri(C 1 -C 12 alkyl)silyl)amino, tris(C 1 -C 7 hydrocarbyl)silyl and C 1 -C 12 thioalkyl; x is an integer selected from 1, 2 and 3; y is an integer selected from 0, 1 and 2; provided that x+y=3;

((R 1 O) x2′ (R 2 ) y2′ Si—R 3 —S) s2′ M*(R 4 ) t2′ (X*) u2′   formula (2),

wherein M* is silicon or tin; x 2′ is an integer selected from 1, 2 and 3; y2′ is an integer selected from 0, 1, and 2; wherein x2′+y2′=3; s2′ is an integer selected from 2, 3 and 4; t2′ is an integer selected from 0, 1 and 2; u2′ is an integer selected from 0, 1 and 2; wherein s2′+t2′+u2′=4; R 1 is independently selected from hydrogen and (C 1 -C 6 ) alkyl; R 2 is independently selected from (C 1 -C 16 ) alkyl, (C 7 -C 16 ) alkylaryl and (C 7 -C 16 ) arylalkyl; R 3 is at least divalent and is independently selected from (C 1 -C 16 ) alkyl, (C 8 -C 16 ) alkylarylalkyl, (C 7 -C 16 ) arylalkyl and (C 7 -C 16 ) alkylaryl, and each group may be substituted with one or more of the following groups: tertiary amine group, silyl group, (C 7 -C 18 ) aralkyl group and (C 6 -C 18 ) aryl group; R 4 is independently selected from (C 1 -C 16 ) alkyl and (C 7 -C 16 ) alkylaryl; X* is independently selected from chloride, bromide and —OR 5 *; wherein R 5 * is selected from (C 1 -C 16 ) alkyl and (C 7 -C 16 ) arylalkyl;

(R I O) x1′ (R II ) y1′ Si—R IV —S-E  formula (3),

wherein R I and R II are independently selected from C 1 -C 8 alkyl or C 1 -C 4 alkoxy, provided that at least one of R I and R II are C 1 -C 4 alkoxy; x1′ is an integer selected from 1, 2, and 3; y1′ is an integer selected from 0, 1 and 2;

R IV is selected from C 1 -C 8 alkyl; and E is R V or of formula (3a):

wherein R V is C 1 -C 6 alkyl, C 6 -C 12 aryl, C 7 -C 16 alkylaryl, or C 7 -C 16 arylalkyl;

wherein each R 1d is independently selected from (C 1 -C 16 ) alkyl; each R 2d is independently selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) aralkyl; R 3d is independently selected from divalent (C 1 -C 16 ) alkyl, divalent (C 6 -C 18 ) aryl, divalent (C 7 -C 18 ) aralkyl and —R 4d —O—R 5d —, wherein R 4d and R 5d are independently selected from divalent (C 1 -C 6 ) alkyl; and Z d is independently selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl, (C 7 -C 18 ) aralkyl, (C═S)—S—R 6d , wherein R 6d is selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) aralkyl, and -M 1d (R 7d ) c4 (R 8d ) d4 , wherein M 1d is silicon or tin, each R 7d is independently selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) aralkyl; each R 8d is independently selected from —S—R 3d —Si(OR 1d ) r4 (R 2d ) s4 , wherein R 1d , R 2d and R 3d are as defined above, r 4 is an integer independently selected from 1, 2 and 3 and s 4 is an integer independently selected from 0, 1 and 2, with r 4 +s 4 =3; c 4 is an integer independently selected from 2 and 3; d 4 is an integer independently selected from 0 and 1; and c 4 +d 4 =3;

wherein R 9e , R 10e , R 11e and R 12e are independently selected from hydrogen, (C 1 -C 16 ) alkyl, (C 6 -C 16 ) aryl and (C 7 -C 16 ) aralkyl;

wherein each R 13a , R 14a , R 18a and R 19a is independently selected from (C 1 -C 16 ) alkyl; R 15a and R 20a are independently selected from divalent (C 1 -C 16 ) alkyl, divalent (C 6 -C 18 ) aryl, divalent (C 7 -C 18 ) aralkyl and —R 24a —O—R 25a —, wherein R 24a and R 25a are independently selected from divalent (C 1 -C 6 ) alkyl; R 16a and R 17a are independently selected from (C 1 -C 16 ) alkyl and —SiR 26a R 27a R 28a , wherein R 26a , R 27a and R 28a are independently selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) alkylaryl; each R 21a and R 22a is independently selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) alkylaryl; each R 23a is independently selected from hydrogen and (C 1 -C 6 ) alkyl; t 1 and v are integers independently selected from 1, 2 and 3; u 1 and w are integers independently selected from 0, 1 and 2; t 1 +u 1 =3; and v+w=3;

wherein each R 29 and R 30 is independently selected from (C 1 -C 16 ) alkyl, (C 6 -C 18 ) aryl, (C 7 -C 18 ) alkylaryl and vinyl; and x 10 is an integer selected from 1 to 6.

2. The polymer blend according to claim 1 , wherein the modification (II) for component (a) is carried out by addition and reaction of at least one compound represented by any of formula (1), formula (2), or formula (11).

3. The polymer blend according to claim 1 , wherein the modification (ii) for component (b) is carried out by addition and reaction of at least one compound represented by any of formula (1), or formula (11), provided that x, and r 4 are each selected from 1 and 2.

4. The polymer blend according to claim 1 , wherein the polymerization initiator is selected from the group consisting of n-BuLi, sec-BuLi, tert-BuLi, a compound represented by the following formula (6) to formula (10), as defined below, or Lewis base adducts thereof, and/or mixtures thereof

wherein R 3a is independently selected from —N(R 28 )R 29 , C 1 -C 18 alkyl, C 6 -C 18 aryl and (C 7 -C 18 ) aralkyl; R 4a is independently selected from —N(R 30a )R 31a , (C 1 -C 18 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) aralkyl; R 5 and R 6 are each independently selected from hydrogen, C 1 -C 18 alkyl, C 6 -C 18 aryl and C 7 -C 18 aralkyl; M 2 is lithium; R 12 , R 13 , R 14 , R 15 , R 16 , R 17 , R 18 , R 19 , R 20 , R 21 , R 22 , R 23 , R 24 and R 25 are each independently selected from hydrogen, C 1 -C 18 alkyl, C 6 -C 18 aryl and C 7 -C 18 aralkyl; R 26 , R 27 , R 28 , R 29 , R 30a and R 31a are each independently selected from C 1 -C 18 alkyl, C 6 -C 18 aryl and C 7 -C 18 aralkyl; q is selected from an integer of 1, 2, 3, 4 and 5; r is selected from an integer of 1, 2 and 3; and a1′ is selected from an integer of 0 or 1;

wherein each R 0 is independently selected from C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 7 -C 10 alkylaryl and C 6 -C 10 aryl; R 1′ is an optionally substituted methylene group; each R 1b is independently selected from C 1 -C 10 alkyl, C 7 -C 10 alkylaryl and C 6 -C 10 aryl; each R 2b is independently selected from C 1 -C 10 alkyl, C 7 -C 10 alkylaryl and C 6 -C 10 aryl, wherein the R 2b groups may be connected to each other to form a ring together with the Si-bonded nitrogen atom; R 3b and R 4b are each independently selected from hydrogen, methyl, ethyl, propyl, butyl and vinyl; each R 5b is independently selected from C 1 -C 5 alkyl, C 7 -C 12 alkylaryl and C 6 -C 12 aryl; R 6b is selected from C 1 -C 6 alkyl, phenyl and benzyl; M is lithium; a 1 ≥1; b1≥0; a 1 +b1≤10; m 1 =0 or 1; n 1 =0 to 12; x 1 =0, 1 or 2; y 1 =1, 2 or 3; z 1 =0, 1 or 2; x 1 +y 1 +z 1 =3; or x 1 +y 1 +z 1 =2 when the silicon atom of the aminosilyl group is bonded twice to the benzene rings via groups R 1′ or single bonds; provided that when m 1 =1, then n 1 =1 to 12, and when m 1 =0, then n 1 =0 and x 1 =1 or 2; wherein the aminosilyl group(s) may be bonded to any of the two benzene rings, plural aminosilyl groups may be different from each other, and the R 5b group(s) may be bonded to any of the two benzene rings;

wherein each M 1c is lithium; each R 1c is independently selected from C 1 -C 100 alkyl and C 2 -C 100 alkenyl, optionally substituted with one or more C 6 -C 12 aryl groups and optionally linked to the carbon atom C by up to 25 monomer units selected from conjugated diene monomers and aromatic vinyl compounds, especially butadiene, isoprene and styrene; each R 12c is independently selected from hydrogen, (C 1 -C 10 ) alkyl, (C 6 -C 12 ) aryl and (C 7 -C 18 ) alkylaryl; each Y 1c is independently selected from a nitrogen atom, a sulfur atom and a silicon atom; R 3c , R 4c and R 5c are each independently selected from (C 1 -C 18 ) alkyl, di(C 1 -C 6 ) alkyl amine (only when Y 1c is a silicon atom), (C 6 -C 18 ) aryl, (C 7 -C 18 ) alkylaryl and, when Y 1c is not a silicon atom, —SiR 14c R 15c R 16c , wherein R 14c , R 15c and R 16c are each independently selected from (C 1 -C 18 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) alkylaryl; n 3 and o 3 are each an integer selected from 0 and 1; and n 3 +o 3 =1 when Y 1c ═N, n 3 =o 3 =0 when Y 1c ═S, and n 3 +o 3 =2 when Y 1c ═Si; m 3 is an integer selected from 0, 1, 2 and 3; K is selected from nitrogen and >C—H; each E 3 is independently selected from (C 1 -C 18 ) alkyl, (C 6 -C 18 ) aryl, (C 7 -C 18 ) alkylaryl, and —Y 3c (R 9c )(R 10c ) t3 (R 11c ) u3 , wherein Y 3c is selected from a nitrogen atom, a sulfur atom and a silicon atom; R 9c , R 10c and R 11c are each independently selected from (C 1 -C 18 ) alkyl, di(C 1 -C 6 ) alkyl amine (only when Y 3c is a silicon atom), (C 6 -C 18 ) aryl, (C 7 -C 18 ) alkylaryl, and, when Y 3c is not a silicon atom, —SiR 20c R 21c R 22c , wherein R 20c , R 21c and R 22c are each independently selected from (C 1 -C 18 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) alkylaryl; t 3 and u 3 are each an integer selected from 0 and 1; and t 3 +u 3 =1 when Y 3c ═N, t 3 =u 3 =0 when Y 3c ═S, and t 3 +u 3 =2 when Y 3c ═Si; s 3 is an integer selected from 0, 1 and 2; each F 3 is independently selected from (C 1 -C 18 ) alkyl, (C 6 -C 18 ) aryl, (C 7 -C 18 ) alkylaryl, and —Y 2c (R 6c )(R 7c ) q3 (R 8c ) r3 , wherein Y 2c is selected from a nitrogen atom, a sulfur atom and a silicon atom; R 6c , R 7c and R 8c are each independently selected from (C 1 -C 18 ) alkyl, di(C 1 -C 6 ) alkyl amine (only when Y 2c is a silicon atom), (C 6 -C 18 ) aryl, (C 7 -C 18 ) alkylaryl and, when Y 2c is not a silicon atom, —SiR 17c R 18c R 19c , wherein R 17c , R 18c and R 19c are each independently selected from (C 1 -C 18 ) alkyl, (C 6 -C 18 ) aryl and (C 7 -C 18 ) alkylaryl; q 3 and r 3 are each an integer selected from 0 and 1; and q 3 +r 3 =1 when Y 2c ═N, q 3 =q 3 =r 3 =0 when Y 2c ═S, and q 3 +r 3 =2 when Y 2c ═Si; p 3 is an integer selected from 0, 1, 2 and 3;

 wherein each R 31 is independently selected from hydrogen, (C 1 -C 10 ) alkyl, (C 6 -C 12 ) aryl and (C 7 -C 18 ) aralkyl; each R 32 , R 33 and R 34 is independently selected from hydrogen, (C 1 -C 18 ) alkyl and (C 1 -C 18 ) alkoxy; each R 41 is independently selected from (C 1 -C 100 ) alkyl and (C 2 -C 100 ) alkenyl, wherein each R 41 is optionally substituted with one to three (C 6 -C 12 ) aryl groups and is optionally bonded to the skeleton of formula (10 via an oligomer chain composed of up to 25 monomer units selected from conjugated dienes, especially 1,3-butadiene and isoprene, and aromatic vinyl compounds, especially styrene and divinylbenzene; M 2 is lithium; and k, l and q are integers independently selected from 0, 1, 2 and 3.

5. The polymer blend according to claim 1 , wherein

(5.a) the conjugated diene monomer is selected from 1,3-butadiene, 2-alkyl-1,3-butadiene, 2-methyl-1,3-butadiene, 2,3-dimethyl-1,3-butadiene, 1,3-pentadiene, 2,4-hexadiene, 1,3-hexadiene, 1,3-heptadiene, 1,3-octadiene, 2-methyl-2,4-pentadiene, cyclopentadiene, 2,4-hexadiene and/or 1,3-cyclooctadiene; and/or

(5.b) the α-olefin monomer is selected from styrene, 2-methylstyrene, 3-methylstyrene, 4-methylstyrene, 2,4-dimethylstyrene, 2,4,6-trimethylstyrene, α-methylstyrene, stilbene, 2,4-diisopropylstyrene, 4-tert-butylstyrene, vinyl benzyl dimethylamine, (4-vinylbenzyl)dimethyl aminoethyl ether, N,N-dimethylaminoethyl styrene, N,N-bis-(trialkylsilyl)aminostyrene, tert-butoxystyrene, vinylpyridine, divinylbenzene, a vinylsilane compound of the following formula (4) or formula (5), and/or mixtures thereof;

wherein R d is independently selected from C 1 -C 18 hydrocarbyl; R″ is selected from C 1 -C 6 hydrocarbyl; R a , R b and R c are independently selected from hydrogen, methyl, ethyl and vinyl; x4 and y4 are independently integers selected from 1 and 2; z4 is an integer selected from 0 and 1; and x4+y4+z4=3; R′ is independently selected from C 1 -C 12 alkyl, C 2 -C 12 alkenyl, C 6 -C 18 aryl, C 7 -C 18 alkylaryl, and tri(C 1 -C 6 alkyl, C 6 -C 12 aryl or C 7 -C 18 (alkylaryl)silyl, wherein the two R′ groups may be connected to form a ring and the ring may contain, further to the Si-bonded nitrogen atom, one or more of an oxygen atom, a nitrogen atom, an >N(C 1 -C 6 alkyl) group and a sulfur atom; and one R′ may be —Si(CR c ═CR a R b )(OSiR 3 ) y4 (R″) z4 , wherein R a , R b , R c , R, R″, y4 and z4 are independently as defined above and y4+z4=2;

(A 1 )-B n1   formula (5),

wherein A 1 is an organic group having at least two amino groups; each B is independently selected from a group —Si(R 51 )(R 52 )(R 53 ), wherein R 51 , R 52 and R 53 are each independently selected from vinyl, butadienyl, methyl, ethyl, propyl, butyl and phenyl, provided that at least one of R 51 , R 52 and R 53 is selected from vinyl and butadienyl, wherein each group B is a substituent of an amino group of group A 1 , at least two of the amino groups of group A 1 are each substituted with at least one group B; and n 1 is an integer of at least 2; and all amino groups in group A 1 are tertiary amino groups; or

(5.c) the first elastomeric polymer (a) obtained in step (I) is a styrene-butadiene-polymer; and/or

(5.d) the second polymer (b) obtained in step (i) is an elastomeric polymer.

6. The polymer blend according to claim 1 , wherein

(6.a) in formula (1), each of R*** are independently selected from methyl, ethyl, iso-propyl, n-propyl, n-butyl, iso-butyl, or tert-butyl; each of R** are independently selected from C 1 -C 6 alkyl, C 6 -C 12 aryl, or C 7 -C 10 aralkyl; and A is —(CH 2 ) N —, wherein N is an integer selected from 1, 2, 3, 4, 5 or 6; and/or

(6.b) in formula (2), M* is a silicon atom; R 3 is divalent and is (C 1 -C 16 ) alkyl; X* is —OR 5 *, wherein R 5 * is selected from (C 1 -C 4 ) alkyl; R 1 , R 2 , and R 4 are independently selected from (C 1 -C 4 ) alkyl; s2′ and t2′ are each 2 and u2′ is 0; and x2′ is 2 and y2′ is 1; and/or

(6.c) in formula (3), each of R I and R II are independently C 1 -C 4 alkoxy; R IV is selected from C 1 -C 4 alkyl; and E is of formula (3a).

7. A polymer composition, comprising the polymer blend according to claim 1 .

8. The polymer composition according to claim 7 , further comprising one or more filler(s) and optionally one or more vulcanizing agent(s).

9. The polymer composition according to claim 7 , further comprising up to 13 percent by weight of one or more extender oil(s), based on the total weight of the high molecular polymer components in the polymer composition.

10. A method for the preparation of a crosslinked elastomeric polymer, said method comprising the following steps:

(1) providing the polymer blend according to claim 1 or the polymer composition according to claim 7 ;

(2) adding one or more filler(s) and optionally one or more silane coupling agent(s); and compounding said mixture; and

(3) adding one or more vulcanizing agent(s) and optionally one or more vulcanizing accelerator(s) to the mixture of step (2); and cross-linking said mixture.

11. A crosslinked elastomeric polymer produced according claim 10 .

12. An article, comprising the polymer composition according to claim 7 or the crosslinked elastomeric polymer according to claim 11 .

13. The article according to claim 12 , wherein the article is a tire, a tire tread, a tire side wall, a conveyer belt, a seal or a hose.

14. A polymer kit, comprising (II.1) the polymer blend according to claim 1 , or (II.2) the polymer composition according to claim 7 .

Assignments (3)
CHANGE OF NAME Recorded May 15, 2025
From: SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA SPOLKA JAWNA (CURRENTLY SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA)
To: SYNTHOS DWORY 7 SPOLKA Z OGRANICZONA ODPOWIEDZIALNOSCIA
Reel/Frame 071281/0339 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 4, 2025
From: TRINSEO EUROPE GMBH
To: SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA SPOLKA JAWNA (CURRENTLY SYNTHOS DWORY 7 SPOLKA Z ORGANICZONA ODPOWIEDZIALNOSCIA)
Reel/Frame 070743/0153 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2017
From: HAMANN, EVEMARIE; HEIDENREICH, DANIEL; THIELE, SVEN
To: TRINSEO EUROPE GMBH
Reel/Frame 043316/0631 →
Priority Claims (1)
EP 15155546 · Feb 18, 2015 · regional
Continuity (1)
Related Publication 20180016424A1 · Jan 18, 2018
Cited By (10)
US 12,215,231 US 12,251,965 US 12,325,797 US 12,365,202 US 12,365,787 US 12,370,830 US 12,370,831 US 12,371,552 US 12,371,553 US 12,466,214