IP Library Granted Patent US 12,497,499
Granted Patent B2
US 12,497,499 · App. 17/782,943 · Granted Dec 16, 2025

Polymer composition production method

Inventor: Yusuke Amano (Tokyo, JP)
Assignee: ENEOS MATERIALS CORPORATION
C08K13/02
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Quick Facts
Patent No.
US 12,497,499
App. No.
17/782,943
Granted
Dec 16, 2025
Kind
B2
Abstract

A method of producing a polymer composition is provided, including: kneading (A) a conjugated diene-based polymer that is a polymer of a conjugated diene compound or a copolymer of a conjugated diene compound and an aromatic vinyl compound, and is a reaction product between an active polymerization end and a compound represented by any one of the general formulae (1) to (3), and (B) a basic compound having an acid dissociation constant of 8.0 or more; and kneading a kneaded product from (A) and a crosslinking agent.

Claims (12)

1 . A method of producing a polymer composition, comprising:

a first step of kneading (A) a conjugated diene-based polymer that is a polymer of a conjugated diene compound or a copolymer of a conjugated diene compound and an aromatic vinyl compound, and is a reaction product of an active polymerization end and a compound represented by any one of the following general formulae (1) to (2), and (B) a basic compound having an acid dissociation constant of 8.0 or more; and

a second step of kneading a kneaded product obtained in the first step and a crosslinking agent:

in the formula (1), A 2 represents a monovalent group bonded to L 2 via an imino group, an amide group, a (thio)carbonyl group, a (thio)carbonyloxy group, a sulfide, or a polysulfide, or represents a protected primary amino group, a protected secondary amino group, a tertiary amino group, a nitrile group, a pyridyl group, a (thio)epoxy group, a (thio)isocyanate group, a (thio)formyl group, a (thio)carboxylic acid ester, a metal salt of a (thio)carboxylic acid ester, a carboxylic halide, or an imidazolyl group, L 2 and L 3 each independently represent a single bond or a hydrocarbylene group having 1 to 20 carbon atoms, R 3 and R 4 each independently represent a hydrocarbyl group having 1 to 4 carbon atoms, n2 represents from 0 to 3, and m1 represents 1;

in the formula (2), A 3 s each independently represent an imino group, an amide group, a (thio)carbonyl group, a (thio)carbonyloxy group, a secondary amino group, or a tertiary amino group, Z represents a nitrogen atom-containing or -free t-valent group having 1 to 20 carbon atoms, L 4 represents a single bond or a hydrocarbylene group having 1 to 20 carbon atoms, L 5 represents a hydrocarbylene group having 1 to 20 carbon atoms, R 5 and R 6 each independently represent a hydrocarbyl group having 1 to 4 carbon atoms, n3 represents 0 or 1, and “t” represents 2 or 3.

2 . The method of producing a polymer composition according to claim 1 , wherein the basic compound having an acid dissociation constant of 8.0 or more is an amine compound.

3 . The method of producing a polymer composition according to claim 1 , wherein the basic compound having an acid dissociation constant of 8.0 or more is a guanidine-based compound.

4 . The method of producing a polymer composition according to claim 1 , wherein the second step comprises kneading an acidic compound together with the kneaded product and the crosslinking agent.

5 . The method of producing a polymer composition according to claim 4 , wherein the acidic compound is a saturated fatty acid having 12 to 24 carbon atoms.

6 . The method of producing a polymer composition according to claim 1 , wherein the first step comprises kneading silica together with the conjugated diene-based polymer and the basic compound having an acid dissociation constant of 8.0 or more.

7 . The method of producing a polymer composition according to claim 6 , wherein the first step comprises kneading the conjugated diene-based polymer, the basic compound having an acid dissociation constant of 8.0 or more, and the silica, followed by addition of a silane coupling agent and further kneading.

8 . The method of producing a polymer composition according to claim 1 , wherein the crosslinking agent is sulfur.

Assignments (2)
CHANGE OF ADDRESS Recorded Oct 3, 2024
From: ENEOS MATERIALS CORPORATION
To: ENEOS MATERIALS CORPORATION
Reel/Frame 069105/0903 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 6, 2022
From: AMANO, YUSUKE
To: ENEOS MATERIALS CORPORATION
Reel/Frame 060113/0881 →
Priority Claims (1)
JP 2019-221071 · Dec 6, 2019 · national
Continuity (1)
Related Publication 20230033703A1 · Feb 2, 2023
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