Silane Modified Elastomeric Polymers

Patent metadata

Field	Value
Publication number	US-2016369015-A1
Application number	US-201315103111-A
Country	US
Kind code	A1
Filing date	Dec 9, 2013
Priority date	Dec 9, 2013
Publication date	Dec 22, 2016
Grant date	—

Abstract

The present invention relates to backbone-modified elastomeric polymers. The invention also relates to polymer compositions comprising such modified polymers, to the use of such compositions in the preparation of vulcanized polymer compositions, and to articles prepared from the same. The modified polymers are useful in the preparation of vulcanized, i.e. cross-linked, elastomeric compositions having relatively low hysteresis loss. Such vulcanized compositions are useful in many articles, including tire treads having low heat build-up, low rolling resistance, good wet grip and ice grip, in combination with a good balance of other desirable physical and chemical properties, for example, abrasion resistance and tensile strength. Moreover, the unvulcanized poly mer compositions exhibit excellent processability.

First claim

1 . A modified elastomeric polymer which is the reaction product of:
i) a copolymer of butadiene and one or more comonomers selected from conjugated dienes and aromatic vinyl compounds, wherein the copolymer contains at least 10 wt % of butadiene units and a total amount of at least 40 wt % of conjugated diene units and wherein the polybutadiene fraction of the copolymer has a vinyl group content of at least 30 wt %, and ii) a silane modifier represented by the following Formula 1:
(H) n Si(X) m (R 1 ) p   (Formula 1),

wherein
X is independently selected from Cl, —OR 2 , —SR 3 and —NR 4 R 5 ;
R 1 is independently selected from (C1-C6) alkyl and (C6-C18) aryl;
n is an integer selected from 1, 2 and 3; m and p are each independently an integer selected from 0, 1, 2 and 3; and n+m+p=4;
R 2 and R 3 are independently selected from hydrogen, (C1-C18) alkyl, (C6-C18) aryl, (C7-C18) alkylaryl and MR 6 R 7 R 8 ;
R 4 and R 5 are independently selected from (C1-C18) alkyl, (C6-C18) aryl, (C7-C18) alkylaryl and MR 9 R 10 R 11 ; R 4 and R 5 may be bonded together to form, together with the nitrogen atom, a ring structure which may additionally include within the ring one or more groups selected from —O—, —S—, >NH and >NR 12 ;
M is silicon or tin;
R 6 , R 7 , R 8 , R 9 , R 10 , R 11 and R 12 are independently selected from (C1-C6) alkyl.

2 . The modified elastomeric polymer according to claim 1 , wherein X is independently selected from —OR 2 and —NR 4 R 5 , R 1 is independently selected from methyl, ethyl, propyl, butyl and phenyl, n is 1, m is an integer selected from 1, 2 and 3 and p is an integer selected from 0, 1 and 2.

3 . The modified elastomeric polymer according to claim 1 , wherein the silane modifier of Formula 1 is selected from HSi(OMe) 3 , HSi(Me)(OMe) 2 , HSi(Me) 2 (OMe), HSi(Et)(OMe) 2 , HSi(Et) 2 (OMe), HSi(Pr)(OMe) 2 , HSi(Pr) 2 (OMe), HSi(Bu)(OMe) 2 , HSi(Bu) 2 (OMe), HSi(Ph)(OMe) 2 , HSi(Ph) 2 (OMe), HSi(OEt) 3 , HSi(Me)(OEt) 2 , HSi(Me) 2 (OEt), HSi(Et)(OEt) 2 , HSi(Et) 2 (OEt), HSi(Pr)(OEt) 2 , HSi(Pr) 2 (OEt), HSi(Bu)(OEt) 2 , HSi(Bu) 2 (OEt), HSi(Ph)(OEt) 2 , HSi(Ph) 2 (OEt), tris(trimethylsiloxy)silane, HSi(Cl) 3 , H 2 Si(Cl) 2 , HSi(Me)(Cl) 2 , HSi(Me) 2 (Cl), HSi(Et)(Cl) 2 , HSi(Et) 2 (Cl), HSi(Pr)(Cl) 2 , HSi(Pr) 2 (Cl), HSi(Bu)(Cl) 2 , HSi(Bu) 2 (Cl), HSi(Ph)(Cl) 2 , HSi(Ph) 2 (Cl 2 ), H 2 Si(Ph)(Cl), HSi(Ph)(Me)(Cl), 1,1,1,3,5,5,5-heptamethyltrisiloxane, (Me) 2 NSi(H)(Me) 2 , (Et) 2 NSi(H)(Me) 2 , (Pr) 2 NSi(H)(Me) 2 , (Bu) 2 NSi(H)(Me) 2 , ((Me) 2 N) 2 Si(H)(Me), ((Et) 2 N) 2 Si(H)(Me), ((Pr) 2 N) 2 Si(H)(Me), ((Bu) 2 N) 2 Si(H)(Me), ((Me) 2 N) 3 Si(H), ((Et) 2 N) 3 Si(H), ((Pr) 2 N) 3 Si(H), ((Bu) 2 N) 3 Si(H), (Me) 2 NSi(H)(Ph) 2 , (Et) 2 NSi(H)(Ph) 2 , (Pr) 2 NSi(H)(Ph) 2 , (Bu) 2 NSi(H)(Ph) 2 , ((Me) 2 N) 2 Si(H)(Ph), ((Et) 2 N) 2 Si(H)(Ph), ((Pr) 2 N) 2 Si(H)(Ph), ((Bu) 2 N) 2 Si(H)(Ph), (Me) 2 NSi(H)(Cl) 2 , (Et) 2 NSi(H)(Cl) 2 , (Pr) 2 NSi(H)(Cl) 2 , (Bu) 2 NSi(H)(Cl) 2 , ((Me) 2 N) 2 Si(H)(Cl), ((Et) 2 N) 2 Si(H)(Cl), ((Pr) 2 N) 2 Si(H)(Cl) and ((Bu) 2 N) 2 Si(H)(Cl).

4 . The modified elastomeric polymer according to claim 1 , wherein the conjugated diene is selected from isoprene, 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, 1,3-cyclohexadiene and 1,3-cyclooctadiene, preferably selected from isoprene and cyclopentadiene.

5 . The modified elastomeric polymer according to claim 1 , wherein the aromatic vinyl compound is selected from styrene, 2-methylstyrene, 3-methylstyrene, 4-methylstyrene, 2,4-dimethylstyrene, 2,4,6-trimethylstyrene, α-methylstyrene, 2,4-diisopropylstyrene, 4-tert-butylstyrene, stilbene, vinyl benzyl dimethylamine, (4-vinylbenzyl)dimethyl aminoethyl ether, N,N-dimethylaminoethyl styrene, tert-butoxystyrene, vinylpyridine, 1,2-divinylbenzene, 1,3-divinylbenzene and 1,4-divinylbenzene, preferably styrene.

6 . The modified elastomeric polymer according to claim 1 , wherein the aromatic vinyl compound(s) constitute(s) from 5 to 60 wt % of the total monomer content of the polymer.

7 . The modified elastomeric polymer according to claim 1 , wherein the copolymer is selected from styrene-butadiene rubber, butadiene-isoprene rubber and butadiene-isoprene-styrene rubber, preferably styrene-butadiene rubber with a styrene content of from 5 to 60% by weight of the total monomer content and even more preferably from 10 to 50% by weight of the total monomer content.

8 . The modified elastomeric polymer according to claim 1 , which contains a structural group of one or both of the following Formulas 11-a and 11-b:

wherein R 1 , X, n, m, p are as defined in claim 1 and R is independently selected from H and C1-C5 alkyl.

9 . The modified elastomeric polymer according to claim 1 , which contains a structural group of one or both of the following Formulas 11-c and 11-d:

wherein R 1 , X, n, m, p are as defined in claim 1 .

10 . The modified elastomeric polymer according to claim 1 , which is further modified with one or more chain end-modifying agents.

11 . A method of making a modified elastomeric polymer as defined in claim 1 , the method comprising the steps of reacting
i) a copolymer of butadiene and one or more comonomers selected from conjugated dienes and aromatic vinyl compounds, wherein the copolymer contains at least 10 wt % of butadiene units and at least 40 wt % of conjugated diene units and the polybutadiene fraction of the copolymer has a vinyl group content of at least 30 wt %, with ii) a silane modifier represented by Formula 1 as defined in claim 1 , 2 or 3 .

12 . The method of making a modified elastomeric polymer according to claim 11 , wherein the silane modifier of Formula 1 is added intermittently or continuously during the polymerization of butadiene and conjugated diene and aromatic vinyl compound.

13 . The method of making a modified elastomeric polymer according to claim 11 , wherein the silane modifier of Formula 1 is added at a time when the conversion rate of the polymerization has reached 80 wt % or more.

14 . The method of making a modified elastomeric polymer according to claim 11 , wherein the silane modifier of Formula 1 is used in a total amount of from 0.001 to 5 wt %, based on the weight of the copolymer.

15 . A non-cured polymer composition comprising the modified elastomeric polymer of the invention as defined in claim 1 and one or more further components selected from (i) components which are added to or formed as a result of the polymerization process and/or backbone modification process used for making the polymer, (ii) components which remain after solvent removal from the polymerization and/or backbone modification process, and (iii) components which are added to the polymer after completion of the polymerization and/or backbone modification process.

16 . The non-cured polymer composition according to claim 15 , which comprises one or more fillers.

17 . The non-cured polymer composition according to claim 15 , which comprises one or more extender oils.

18 . The non-cured polymer composition according to claim 15 , wherein the modified elastomeric polymer constitutes at least 15 wt % of the total polymer present, more preferably at least 25 wt %, even more preferably at least 35 wt %.

Assignees

• Trinseo Europe Gmbh

Inventors

• Doring Christian
• Thiele Sven
• Heidenreich Daniel

Classifications

• C08F2810/40

  taking place solely at one end or both ends of the polymer backbone, i.e. not in the side or lateral chains · CPC title

• C08F236/06

  Butadiene · CPC title

• C08L9/00

  Compositions of homopolymers or copolymers of conjugated diene hydrocarbons · CPC title

• C08F2500/17

  Viscosity · CPC title

• C08C19/25 Primary

  Incorporating silicon atoms into the molecule · CPC title