Method for manufacturing rubber composition

Patent metadata

Field	Value
Publication number	US-9464174-B2
Application number	US-201113877028-A
Country	US
Kind code	B2
Filing date	Oct 3, 2011
Priority date	Oct 1, 2010
Publication date	Oct 11, 2016
Grant date	Oct 11, 2016

Abstract

The present invention provides a method for producing a rubber composition containing a rubber component (A) of at least one selected from natural rubbers and synthetic dienic rubbers, an inorganic filler (B), a silane coupling agent (C) and an acidic compound (D), wherein the rubber composition is kneaded in multiple stages, and in the final stage of kneading, the acidic compound (D) is added, and the highest temperature of the rubber composition in the final stage of kneading is from 60 to 120° C. The production method enables production of a rubber composition having a low-heat-generation property while successfully preventing the coupling function activity of the silane coupling agent from lowering.

First claim

The invention claimed is:

1. A method for producing a rubber composition containing a rubber component (A) of at least one selected from natural rubbers and synthetic dienic rubbers, an inorganic filler (B), a silane coupling agent (C) and an acidic compound (D),
wherein the rubber composition is kneaded in multiple stages, and in the final stage of kneading, the acidic compound (D) is added, and the highest temperature of the rubber composition in the final stage of kneading is from 60 to 120° C.,
wherein the highest temperature of the rubber composition in the first stage of kneading is from 140 to 190° C., and
wherein the rubber component (A), all or a part of the inorganic filler (B) and all or a part of the silane coupling agent (C) are kneaded in the first stage of kneading, and on the way of the first stage, a vulcanization promoter (E) is added after an elapsed time of 60 to 90 seconds from adding the silane coupling agent (C) and further kneaded.

2. The method for producing a rubber composition according to claim 1 , wherein the highest temperature of the rubber composition in the final stage of kneading is from 100 to 120° C.

3. The method for producing a rubber composition according to claim 1 , wherein the acidic compound (D) is a fatty acid.

4. The method for producing a rubber composition according to claim 3 , wherein the fatty acid is stearic acid.

5. The method for producing a rubber composition according to claim 1 , wherein in the stage before the final stage of kneading, at least one vulcanization promoter (E) selected from guanidines, sulfenamides, thiazoles, thiurams, dithiocarbamate salts, thioureas and xanthate salts is added.

6. The method for producing a rubber composition according to claim 1 , wherein the silane coupling agent (C) is at least one compound selected from a group of compounds represented by the following general formulae (I) to (IV):
(R 1 O) 3-p (R 2 ) p Si—R 3 —S a —R 3 —Si(OR 1 ) 3-r (R 2 ) r   (I)

(wherein multiple R 1 's may be the same or different, each representing a linear, cyclic or branched alkyl group having from 1 to 8 carbon atoms, a linear or branched alkoxylalkyl group having from 2 to 8 carbon atoms, or a hydrogen atom; multiple R 2 's may be the same or different, each representing a linear, cyclic or branched alkyl group having from 1 to 8 carbon atoms; multiple R 3 's may be the same or different, each representing a linear or branched alkylene group having from 1 to 8 carbon atoms; a indicates from 2 to 6 as a mean value; p and r may be the same or different, each indicating from 0 to 3 as a mean value, provided that both p and r are not 3 at the same time);

(wherein R 4 represents a monovalent group selected from —Cl, —Br, R 9 O—, R 9 C(—O)O—, R 9 R 10 C—NO—, R 9 R 10 CNO—, R 9 R 10 N—, and —(OSi R 9 R 10 ) h (OSi R 9 R 10 R 11 ) (where R 9 , R 10 and R 11 each represents a hydrogen atom or a monovalent hydrocarbon group having from 1 to 18 carbon atoms; and h indicates from 1 to 4 as a mean value); R 5 represents R 4 , a hydrogen atom, or a hydrocarbon group having from 1 to 18 carbon atoms; R 6 represents R 4 , R 5 , a hydrogen atom, or a group —[O(R 12 O) j ] 0.5 (where R 12 represents an alkylene group having from 1 to 18 carbon atoms; and j indicates an integer of from 1 to 4); R 7 represents a divalent hydrocarbon group having from 1 to 18 carbon atoms; R 8 represents a monovalent hydrocarbon group having from 1 to 18 carbon atoms; x, y and z each indicates a number satisfying the relationship of x+y+2z=3, 0≦x≦3, 0≦y≦2, 0≦z≦1);
(R 13 O) 3-s (R 14 ) s Si—R 15 —S k —R 16 —S k —R 15 —Si(OR 13 ) 3-t (R 14 ) t   (III)

(wherein multiple R 13 's may be the same or different, each representing a linear, cyclic or branched alkyl group having from 1 to 8 carbon atoms, a linear or branched alkoxylalkyl group having from 2 to 8 carbon atoms, or a hydrogen atom; multiple R 14 's may be the same or different, each representing a linear, cyclic or branched alkyl group having from 1 to 8 carbon atoms; multiple R 15 's may be the same or different, each representing a linear or branched alkylene group having from 1 to 8 carbon atoms; R 16 represents a divalent group of a general formula (—S—R 17 —S—), (—R 18 —S m1 —R 19 —) or (—R 20 —S m2 —R 21 —S m3 —R 22 —) (where R 17 to R 22 each represents a divalent hydrocarbon group, a divalent aromatic group or a divalent organic group containing a hetero element except sulfur and oxygen, having from 1 to 20 carbon atoms; m1, m2 and m3 may be the same or different, each indicating from 1 to less than 4 as a mean value); multiple k's may be the same or different, each indicating from 1 to 6 as a mean value; s and t each indicates from 0 to 3 as a mean value, provided that both s and t are not 3 at the same time);

(wherein R 23 represents a linear, branched or cyclic alkyl group having from 1 to 20 carbon atoms; multiple G's may be the same or different, each representing an alkanediyl group or an alkenediyl group having from 1 to 9 carbon atoms; multiple Z a 's may be the same or different, each representing a functional group capable of bonding to the two silicon atoms and selected from [—O—] 0.5 , [—O-G-] 0.5 and [—O-G-O—] 0.5 ; multiple Z b 's may be the same or different, each representing a functional group capable of bonding to the two silicon atoms and represented by [—O-G-O-] 0.5 ; multiple Z c 's may be the same or different, each representing a functional group selected from —Cl, —Br, —OR a , R a C(═O)O—, R a R b C═NO—, R a R b N—, R a — and HO-G-O— (where G is the same as above); R a and R b each represents a linear, branched or cyclic alkyl group having from 1 to 20 carbon atoms; m, n, u, v and w each are 1≦m≦20, 0≦n≦20, 0≦u≦3, 0≦v≦2, 0≦w≦1, and (u/2)+v+2w is 2 or 3; in case where the formula has multiple A's, then Z a u , Z b v and Z c w may be the same or different in those multiple A's; in case where the formula has multiple B's, then Z a u , Z b v and Z c w may be the same or different in those multiple B's).

7. The method for producing a rubber composition according to claim 5 , wherein the guanidine is at least one compound selected from 1,3-diphenylguanidine, 1,3-di-o-tolylguanidine and 1-o-tolylbiguanide.

8. The method for producing a rubber composition according to claim 5 , wherein the sulfenamide is N-cyclohexyl-2-benzothiazolylsulfenamide and/or N-tert-butyl-2-benzothiazolylsulfenamide.

9. The method for producing a rubber composition according to claim 5 , wherein the thiazol is at least one compound selected from 2-mercaptobenzothiazole and di-2-benzothiazolyl disulfide.

10. The method for producing a rubber composition according to claim 5 , wherein the thiuram is at least one compound selected from tetrakis(2-ethylhexyl)thiuram disulfide and tetrabenzylthiuram disulfide.

11. The method for producing a rubber composition according to claim 5 , wherein the thiourea is at least one compound selected from N,N′-diethylthiourea, trimethylthiourea, N,N′-diphenylthiourea and N,N′-dimethylthiourea.

12. The method for producing a rubber composition according to claim 5 , wherein the dithiocarbamate salt is at least one compound selected from zinc dibenzyldithiocarbamate, zinc N-ethyl-N-phenyldithiocarbamate, zinc dimethyldithiocarbamate and copper dimethyldithiocarbamate.

13. The method for producing a rubber composition according to claim 5 , wherein the xanthate salt is zinc isopropylxanthate.

Assignees

• Katou Seiichi
• Horie Satoshi
• Bridgestone Corp

Inventors

• Katou Seiichi
• Horie Satoshi

Classifications

• B29B7/183

  having a casing closely surrounding the rotors, e.g. of Banbury type (with single shaft B29B7/125) · CPC title

• B29B7/48

  with intermeshing devices, e.g. screws · CPC title

• B60C1/0016

  Compositions of the tread · CPC title

• B29C48/40

  using two or more parallel screws {or at least two parallel non-intermeshing screws}, e.g. twin screw extruders · CPC title

• B29C48/57

  provided with kneading disc-like elements, e.g. with oval-shaped elements · CPC title