IE894191L

IE894191L - Vulcanizate activator system for rubber compositions

Info

Publication number: IE894191L
Application number: IE894191A
Authority: IE
Inventors: Carl Ramsey Parks; Sidocky Richard Michael D; Martin Paul Cohen
Original assignee: Merck Patent Gmbh
Priority date: 1988-12-28
Filing date: 1989-12-28
Publication date: 1990-06-28
Also published as: CN1043726A; MA21696A1; PT92754A; FI99134B; CN1277210A; AR247219A1; BR8906667A; CN1062574C; ZA899579B; FI99134C; NO179951C; KR900009701A; FI896047A0; IE66562B1; ATE105001T1; CA1340497C; DK668089D0; NO895244L; DK668089A; PT92754B

Abstract

A method is disclosed for increasing the rate of vulcanization of a rubber composition comprising adding to a sulfur vulcanizable rubber a methyl trialkyl ammonium salt of the formula: (see fig. I) wherein R1, R2, and R3 are independently alkyl radicals having 8 to 10 carbon atoms and M is selected from the group consisting of Cl, Br, CH3SO4 and HSO4. Addition of a methyl trialkyl ammonium salt of the above formula significantly increases the rate of vulcanization of the rubber. [CA1340497C]

Description

The preserve Invention relates co the vulcanisation of a sulfur curable rubber composition. More • particularly,, the present invention relates co a method for increasing the rate of cure of a sulfur vulcanizable rubber by the addition of a methyl trialkyl ammonium salt.

The "rata of cure'9 Is defined as the rate at which crosslinking and the development of the stiffness (modulus) of a rubber compound occurs. As the rubber compound is heated, the properties of the rubber compound change from a soft plastic to a tough elastic material.. During the curing step, crosslinks are introduced, which connect the long polymer chains of the rubber. As more cross links are introduced, the polymer chains become more firmly connected and the stiffness or modulus of the compound increases. The rate of cure is an Important vulcanization parameter since it in part determines the time the compound must be cured, i.e. , the "cure time". In the manufacture of vulcanised rubber articles, significant cost savings can be realized through a reduction of cure tine. Through enhanced rates of cure, the cure time required to meet minimum states of cure can be reduced. Given the above, extensive research has been conducted In order to shorten the cure times of rubbers. Therefore, there exists a need for improved methods which enhance the rate of cure in the absence of imparting undesirable properties to the vulcanizate.

The present invention relates to a method for enhancing the race of vulcanization of a, rubber composition comprising adding to a sulfur vulcanizable rubber a methyl trialkyl ammonium salt of the formula: E2 © R^-N-R3 M © ch3 i 2 3 wherein R", R , and R are independently alkyl radicals having 8 to 10 carbon atoms and H is selected from the group consisting of CI, Br, CH^SO^ and HSO^. In addition, there is disclosed a sulfur vulcanizable rubber composition comprising an elastomer containing olefinic unsaturation, a sulfur vulcanizing agent, an accelerator and a methyl trialkyl ammonium salt selected from the above formula.

The present invention relates to the use of a methyl trialkyl ammonium salt as an activator for sulfur curable rubber compositions. A particularly preferred methyl trialkyl ammonium salt is methyl trialkyl(Cg-C-jg) ammonium chloride which is commercially available under the trademark Adogen® 464 froe Sherex Chemical Company of Dublin, Ohio and from Henkel Corporation, Minneapolis, Minnesota, under the trademark Aliquot© 336. Methyl trialkyl ammonium salts are generally known as phase-transfer catalysts and are described in U.S. Patent 3,992,432 which is incorporated by reference in its entirety™ For ease in handling, the methyl trialkyl ammonium salt may be deposited on suitable carriers. Examples of carriers which may be used in the present invention include silica, carbon black, alumina, kieselguhr, silica gel and calcium silicate* Use of a methyl trialkyl ammonium salt does not 5 appear co affect crosslink distribution when used in combination with primary and optionally secondary accelerators., However, along with increased cure rate, there is usually seen an Increased curative efficiency in the form of increased state or degree of cure. 10 The present invention may be used to cure sulfur vulcanizable rubbers or elastomers containing oleflnic unsaturation. The phrase "rubber or elascomer containing oleflnic unsaturation80 Is intended to Include both natural rubber and its various ra» and 13 reclaim forms as well as various synthetic rubbers. Representative synthetic polymers are the homopolyraerization products of butadiene and Its homologues and derivatives, for example, methylbutadiene» dimethylbutadiene and pentadiene as 20 well as copolymers such as those formed from butadiene or its homologues or derivatives with other unsaturated monomers. Among the latter are acetylenes „ for example, vinyl acetylene; olefins, for example, isobutylene, which copolymerizes with isoprene to form 25 butyl rubber; vinyl compounds, for example, acrylic acid, acrylonitrile (which polymerize with butadiene to form NBR), methacrylic acid and styrene „ the latter compound polymerizing with butadiene to form SBR, as well as vinyl esters and various unsaturated aldehydes. 30 ketones and ethers, e.g., acrolein, methyl isopropenyl ketone and vinylethyl ether., Specific examples of synthetic rubbers include neoprene (polychloroprene), polybutadiene (including cis-lf4-polybutadiene) „ polyisoprene (including els-l „4-polyIsoprene)butyl rubber, copolymers of 1,3-butadiene or isoprene with monomers such as scyrene, acrylonitrile and methyl methacrylate, as well as ethylene/propylene terpolymers, also known as ethylene/propylene/diene 5 monomer (EPDM) , and in particular, ethylene/propylene/ dicyclopentadiene cerpolymers.

The activator used in che present invention may be added co the rubber by .any conventional technique such as on a mill or in a Banbury. The amount of methyl 10 trialkyl ammonium salt may vary widely depending on the type of rubber and other compounds present in che vulcanizable composition. Generally, the amount of methyl trialkyl ammonium salt is used in a range of from about .05 to about 5.0 phr with a range of . 1 to 15 about 1.5 phr being preferred.

Vulcanization of the rubber is generally carried out at temperatures of between about 100°C and 200°C. Preferably, the vulcanization is conducted at temperatures ranging from about 110°C to 180°C. Any of 20 the usual vulcanization processes may be used such as heating in a press or mold, heating with superheated steam or hot air or in a salt bath.

In addition to the methyl trialkyl asmnonium salt, other rubber additives may also be incorporated in the 25 sulfur vulcanizable material. The additives commonly used in rubber vulcanizates are, for example, extenders, fillers, pigments, plasticizers, zinc oxide, stearic acid, antioxidants antiozonants.

The. vulcanisation is conducted In che presence of a 30 sulfur vulcanizing agent. Examples of suitable sulfur vulcanizing agents include elemental sulfur (free sulfur) or sulfur donating vulcanizing agents, for example, an amine disulfide, polymeric polysulfide or sulfur olefin adducts. Preferably, the sulfur 35 vulcanising agent is elemental sulfur.

Accelerators are used co control the time and/or temperature required for vulcanization and co improve che properties of the vulcanizate. In one embodiment, a single accelerator system may be -ased, i.e.. primary accelerator™ In another embodiment,, combinations of two or more accelerators may be used which may consist of a primary accelerator which Is generally used In the larger amount,,, and a, secondary accelerator which is generally used in smaller amounts In order to activate and co improve the properties of the vulcanizate. Combinations of these accelerators have been known to produce a synergistic effect of the final properties and are somewhat better than chose produced by use of either accelerator alone. In addition, delayed action accelerators may be used which are not effected by normal processing temperatures but produce satisfactory cures at ordinary vulcanisation temperatures. Suitable types of accelerators that may be used in che present Invention are .amines, disulfides, gmanidines, thioureas, thiazoles, thiurams, sulfenaraides, dithiocarbamates and xanthates.

Claims

-6- CIAIMS

1. A method for increasing the rate of vulcanization of a rubber composition comprising adding to a sulfur vulcanizable rubber a methyl trialkyl 5 ammonium salt of the formulas R2 0 Ri-N-R3 M ® i ch3 19 3 wherein E*% R", and R are independently alkyl radicals having 8 to 10 carbon atoms and M is selected from the group consisting of CI, Br, CH^S0& and HSO^. 10

2. The method of claim 1 wherein at least 0.5 parts by weight per 100 parts by weight of rnbber of said methyl trialkyl ammonium salt is added.

3. The method of claim 2 wherein the methyl trialkyl ammonium salt is added in an amount ranging from 0.05 to 5.0 parts by weight 15 per 100 parts by weight of rubber.

4. The method of claim 1 wherein M is CI or CH3S04.

5. The method of claim 4 wherein M Is CI.

6. The method of claim 4 wherein M is CH^SO^,, 20

7. The method of claim 2 wherein said sulfur vulcanizable rubber contains &n elastomer containing oleflnic unsaturation and is selected from che group consisting of natural rubber, neoprene, polyisoprene, butyl rubber,, polvbutadiene, styrene-butadiene copolymer, methyl raethacrylace-butadiene copolymer, isoprene-styrene copolymer, methyl otechacrylace-isoprene copolymer, acrylonitrile-isoprene copolymer, acrylonitrile- butadiene copolymer, EPDM or aixtures thereof.

8. The method of claim 7 wherein said sulfur vulcanizable rubber is selected from the group consisting of natural rubber, SBR, polyisoprene, or mixtures thereof.

9. A sulfur vulcanizable rubber composition comprising an elastomer containing olefinic unsaturation, a vulcanizing agent,, an accelerator and a methyl trialkyl ammonium salt of the formula: R* 0 E^-N-R3 M © 8 CH3 1 9 3 wherein R „ R*"» and R are independently alkyl radicals having 8 Co 10 carbon atoms and M is selected from the group consisting of CI, Br, CH^SO^ and HSO^.

10. The sulfur vulcanizable rubber composition of claim 9 wherein said methyl trialkyl ammonium salt is present In an amount of at least 0,05 parts by weight per 100 parts by weight of rubber.

11. The sulfur vulcanizable rubber composition of claim 10 wherein said methyl trialkly ammonium salt is present in an amount ranging from 0.05 to 5.0 parts by weight per 100 parts by weight o rubber.

12. Tne sulfur vulcanizable rubber compos it:ion of claim 9 wherein M is CI or CH^SO^.

13. The sulfur curable rubber composition of claim 9 wherein said elastomer is selected from che group consisting of natural rubber, neoprene, polyisoprene, butyl rubber, polybutadiene, styrene-butadiene copolymer, methyl cathacrylate- butadiene copolymer, isoprene-styrene copolymer, nethyl raethacrylate-isoprene copolyner, acrylonitrile-isoprene copolymer, acrylonitrile-butadiene copolymer, EPDM or mixtures thereof.

14. The sulfur curable rubber composition of claim 9 wherein the sulfur vulcanizing agent is selected from. the group consisting of elenental sulfur, amine disulfide, polymeric polysulfide or sulfur olefin adduces.

15. The sulfur vulcanizable composition of claim 9 wherein the accelerator is selected from the group consisting of amines, disulfides, guanidines, thioureas, thiazoles, thiurams, sulfenamides, ditniocarbamates, xar.thates or mixtures thereof.

16. A method substantially as hereinbefore described with reference to the Exacoles.

17. A comoosition substantially as hereinbefore described with reference to the Exacples. Dated this 28th day of December 1989 CMJICKSHANK & CO. „ Agents for the Applicant 1 s, Holies Streets Dublin 2. IRISH PATENT APPLICATION NO. 419l\89 '! ' 3 R--N-R 8 © H©