Cold flow reduced polymers with good processing behaviour

Patent metadata

Field	Value
Publication number	US-9969833-B2
Application number	US-201414786692-A
Country	US
Kind code	B2
Filing date	Apr 11, 2014
Priority date	Apr 24, 2013
Publication date	May 15, 2018
Grant date	May 15, 2018

Abstract

Cold flow-reduced polymers having good processing characteristics have, at the ends of the polymer chains, a silane-containing carboxyl group of the formula (I)

where R 1 and R 2 are the same or different and are each an H, alkyl, alkoxy, cycloalkyl, cycloalkoxy, aryl, aryloxy, alkaryl, alkaryloxy, aralkyl or aralkoxy; R 3 and R 4 are the same or different and are each an H, alkyl, cycloalkyl, aryl, alkaryl or aralkyl radical; A is a divalent organic radical.

First claim

What is claimed is:

1. A polymer mixture comprising:
a) cold-flow reduced, end group functionalized polymers comprising a polymer chain terminated by at least one sane-containing carboxyl group of the formula (I)

where
R 1 , R 2 are the same or different and are each an H, alkyl, alkoxy, cycloalkyl, cycloalkoxy, aryl, aryloxy, alkaryl, alkaryloxy, aralkyl, or aralkoxy radical,
R 3 , R 4 are the same or different and are each an H, alkyl, cycloalkyl, aryl, alkaryl or aralkyl radical, and
A is a divalent organic radical wherein the polymers are diene polymers or diene copolymers; and

b) dimers having one or more structural elements derived from silalactones of the formula (III),

2. The polymer mixture according to claim 1 , wherein the polymer is obtained by reaction of reactive ends of the polymer chain with one or more silalactone functionalizing reagents wherein the silalactones are compounds of the formula (III)

3. The polymer mixture according to claim 1 , wherein:
the polymer is obtained by reaction of reactive ends of the polymer chain with one or more silalactones of the formula (III)

the polymers comprise at least one of polybutadiene, polyisoprene, butadiene-isoprene copolymer, butadiene-styrene copolymer, isoprene-styrene copolymer, and butadiene-isoprene-styrene terpolymer;
R 1 and R 2 are the same or different and are each an H, (C 1 -C 24 )-alkyl, (C 1 -C 24 )-alkoxy, (C 3 -C 24 )-cycloalkyl, (C 3 -C 24 )-cycloalkoxy, (C 6 -C 24 )-aryl, (C 6 -C 24 )-aryloxy, (C 6 -C 24 -alkaryl, (C 6 -C 24 )-alkaryloxy, (C 6 -C 24 )-aralkyl or (C 6 -C 24 )-aralkoxy radical; and
R 3 and R 4 are the same or different and are each an H, (C 1 -C 24 )-alkyl, (C 3 -C 24 )cycloalkyl, (C 6 -C 4 )-aryl, (C 6 -C 24 )-alkaryl or (C 6 -C 24 )-aralkyl radical.

4. The polymer mixture according to claim 3 , wherein any alkyl, alkoxy, cycloalkyl, cycloalkoxy, aryl, aryloxy, alkaryl, alkaryloxy, aralkyl, aralkoxy, or divalent organic radical may contain one or more heteroatoms selected from the group consisting of O, N, S and Si.

5. The polymer mixture according to claim 4 , wherein:
the silalactones comprise one or more of 2,2-dimethyl-1-oxa-2-silacyclohexan-6-one, 2,2,4-trimethyl-1-oxa-2-silacyclohexan-6-one, 2,2,5-trimethyl-1-oxa-2-silacyclohexan-6-one, 2,2,4,5-tetramethyl-1-oxa-2-silacyclohexan-6-one, 2,2-diethyl-1-oxa-2-silacyclohexan-6-one, 2,2-diethoxy-1-oxa-2-silacyclohexan-6-one, 2,2-dimethyl-1,4-dioxa-2-silacyclohexan-6-one, 2,2,5-trimethyl-1,4-dioxa-2-silacyclohexan-6-one, 2,2,3,3-tetramethyl-1,4-dioxa-2-silacyclohexan-6-one, 2,2-dimethyl-1-oxa-4-thia-2-silacyclohexan-6-one, 2,2-diethyl-1-oxa-4-thia-2-silacyclohexan-6-one, 2,2-dphenyl-1-oxa-4-thia-2-silacyclohexan-6-one, 2-methyl-2-ethenyl-1-oxa-4-thia-2-silacyclohexan-6-one, 2,2,5-trimethyl-1-oxa-4-thia-2-silacyclohexan-6-one, 2,2-dimethyl-1-oxa-4-aza-2-silacyclohexan-6-one, 2,2,4-trimethyl-1-oxa-4-aza-2-silacyclohexan-6-one, 2,4-dimethyl-2-phenyl-1-oxa-4-aza-2-silacyclohexan-6-one, 2,2-dimethyl-4 trimethylsilyl-1-oxa-4-aza-2-silacyclohexan-6-one, 2,2-diethoxy-4-methy-1-oxa-4-aza-2-silacyclohexan-6-one, 2,2,4,4-tetramethyl-1-oxa-2,4-disilacyclohexan-6-one, 3,4-dihydro-3,3-dimethyl-1H-2,3-benzoxasilin-1-one, 2,2-dimethyl-1-oxa-2-silacyclopentan-5-one, 2,2,3-trimethyl-1-oxa-2-silacyclopentan-5-one, 2,2-dimethyl-4-phenyl-1-oxa-2-silacyclopentan-5-one, 2,2-di(tert-butyl)-1-oxa-2-silacyclopentan-5-one, 2-methyl-2-(2-propen-1-yl)-1-oxa-2-silacyclopentan-5-one, 1,1-dimethyl-2,1-benzoxasilol-3(1H)-one, and 2,2-dimethyl-1-oxa-2-silacyclohexan-7-one; and
the polymer is at least one of 1,3-butadiene, isoprene, a copolymer of 1,3-butadiene and styrene, and a copolymer of isoprene and styrene, and the polymers have n mean molar masses of 100,000 to 1,000,000 g/mol, and glass transition temperatures of −110° C. to 0° C.

6. The polymer mixture according to claim 1 , wherein the one or more structural elements derived from silalactones is a structural element of the formula (IV)

interconnecting two polymers via chain ends of the polymers.

7. The polymer mixtures according to claim 1 , wherein the polymers have mean molar masses of 10,000 to 2,000,000 g/mol.

8. The polymer mixtures according to claim 7 , wherein the polymers have glass transition temperatures of −110° C. to +20° C.

9. A process for preparing end group-functionalized polymers comprising a polymer chain terminated by at least one silane-containing carboxyl group of the formula (I)

where
R 1 , R 2 are the same or different and are each an H, alkyl, alkoxy, cycloalkyl, cycloalkoxy, aryl, aryloxy, alkaryl, alkaryloxy, aralkyl, or aralkoxy radical,
R 3 , R 4 are the same or different and are each an H, alkyl, cycloalkyl, aryl, alkaryl or aralkyl radical, and

A is a divalent organic radical;

the process comprising contacting polymers with 0.005 to 2% by weight of one or more silalactones based on the amount of the polymer, to produce end group-functionalized polymers.

10. Vulcanizable rubber compositions comprising:
a) a polymer mixture according to claim 1 ; and
b) ageing stabilizers, oils, fillers, rubbers and/or further rubber auxiliaries.

11. Mouldings produced from vulcanizable rubber compositions according to claim 10 .

Assignees

• Lanxess Deutschland Gmbh
• Arlanxeo Deutschland Gmbh

Inventors

• Steinhauser Norbert
• Gross Thomas

Classifications

• C08C19/25

  Incorporating silicon atoms into the molecule · CPC title

• C07F7/1804

  Compounds having Si-O-C linkages (Si-O-acyl linkages C07F7/1896) · CPC title

• C08F236/14 Primary

  containing elements other than carbon and hydrogen · CPC title

• C08K5/18

  with aromatically bound amino groups · CPC title

• C08C19/36

  with carboxy radicals · CPC title