CA1246770A

CA1246770A - Crosslinking composition for butyl rubber or halobutyl rubber and epihalohydrin rubber blends

Info

Publication number: CA1246770A
Application number: CA000498649A
Authority: CA
Inventors: Dominic A. Berta
Original assignee: Hercules LLC
Current assignee: Hercules LLC
Priority date: 1985-01-14
Filing date: 1985-12-24
Publication date: 1988-12-13
Also published as: JP2714372B2; EP0191299B1; JPH09132005A; US4616686A; JPS61163948A; JPH09118715A; ES8707561A1; US4591617A; JP2793572B2; KR940006462B1; EP0191299A3; DE3686491D1; DE3686491T2; ES550820A0; KR860005852A; EP0191299A2; ATE79891T1; JP2608545B2

Abstract

CROSS-LINKING COMPOSITION FOR BUTYL RUBBER OR
HALOBUTYL RUBBER AND EPIHALOHYDRIN RUBBER BLENDS

Abstract of the Disclosure Disclosed are cross-linking compositions having both sul-fur and nonsulfur curative systems which are particularly adapted for cross-linking rubber blends of (a) from about 35%
to about 85% halobutyl rubber or a mixture of butyl rubber and halobutyl rubber wherein the halobutyl rubber is at least 50%
by weight of the mixture and (b) from about 15% to about 65%
of an epihalohydrin rubber, and to the rubber materials cross-linked therewith. The rubber materials cross-linked with these cross-linking compositions have an excellent balance of cure rate, cure state and scorch safety; have improved tire carcass adhesion and good impermeability to gases; and are useful in tire inner tubes and inner liners.

Description

0322p ~6770 This invention relates to a cross-linking composition used for cross-linking blends of an epihalohydrin rubber and (i) halobutyl rubber or (ii) a mixture of butyl rubber and halobutyl rubber wherein the halobutyl rubber is at least 50 by weight of the mixture.
Tire liners based on cross-linked blends of halobutyl rubber and butyl rubber experience difficulty due to sensitiv-ity to entraument of gases, particularly air. In the past, epichlorohydrin rubber has been cross-linked with the afore-mentioned blends to improve impermeability (See, e.g., U.S.Patent 3,586,087). However, while these improved tire liner compositions have yood air impermeability, they do not have a good balance of cure rate, scorch safety and physical proper-ties, and do not adhere well to the tire carcasses, which are lS primarily natural rubber.
According to the invention a cross-linking composition for cross-linking a blend of (A) halobutyl rubber or a mix-ture of butyl rubber and halobutyl rubber and (B) an epihalo-hydrin rubber is characterized in that the cross-linking com-position consists of, for each 100 parts by weight of the rub-ber blend: (a) from about 1.0 part to about 20 parts of a sulfur curative system consisting of (i) from about 0.1 part to about 5 parts sulfur, (ii) from about about 0.1 part to about S parts sulfur accelerator selected from the group con-sisting of mercaptobenzothiazole, mercaptobenzothiazole deriv-atives, sulfenamides, thiurams, and dithiocarbamate salts, and (iii) from about 0.5 part to about 10 parts zinc oxide promot-er; and (b) from about 0.3 part to about 10 parts of a non-sulfur curative system consisting of (i) from about 0.1 part to about 5 parts nonsulfur curative compound selected from the group consisting of di- and tri-functional mercapto compound~

-` i Z~j770 and derivatives thereof; and (ii) from about 0.2 part to about 10 parts metal compound promoter selected from the group con-sisting of oxides, hydroxides, and carbonates of metals in Groups Ia and IIa of the Periodic Table.
The rubber blends cured with the cross-linking composi-tion of this invention have an excellent balance of cure rate, cure state, scorch safety and physical properties and have im-proved tire carcass adhesion while exhibiting good imperme-ability to gases, ecpecially air. The cured blends are use-ful in tire inner tubes and inner liners for pneumatic tires, where sensitivity to gas entrapment is imyortant.
Sulfur curative systems cure through the unsaturation present in halobutyl rubber or mixtures thereof with butyl rubber. The nonsulfur curative systems cure through the halo-gen functionally of the halogen-containing rubbers of the blend.
Preferable sulfur accelerators are mercaptobenzothiazole and its derivatives, such as mercaptobenzothiazole disulfide,

2,2'-dithiobis(benzothiazole) and its salts, tetramethyl-thiuram, cadmium diethyl dithiocarbamate, N-cyclohexyl-2-benzothiazyl-sulfenamide, and N,N-diisopropyl-2-benzothiazyl-sulfenamide.
Preferable nonsulfur curatives are 2,5-dimercapto-1,3,4-thiadiazole, 2-mercapto-1,3,4-thiadiazole-5-benzoate, trithio-cyanuric acid, dithiohydantoins, dimercaptotriazoles, dithiol-triazene, and their ester derivatives, alone or together with an appropriate organic base activator as set forth in U.S.
4,128,510 and U.S. 4,288,576.
Preferable metal compound promoters selected from ox-ides, hydroxides and carbonates of the metals in Groups Iaand IIa of the Periodic Table of the Elements are magnesium oxide and barium carbonate.
The optimum amounts of the cross-linking compositions will depend upon the degree of cross-linking desired, the de-gree of scorch safety desired, and the rate of cure desired.The determination of the amounts to be used is well within 12~6770 the skill of those in the art.
Preferably the sulfur curative system is present in the cross-linking compositions of this invention in an amount, for each 100 parts by weight of the rubber blend, from about 1.7 parts to about 9 parts, and more preferably about 3.0 parts to about 7 parts. Preferably the nonsulfur curative system is present in the compositions of this invention in an amount from about 0.5 part to about 7 parts, and more pref-erably 0.7 part to about S parts.
Preferably the sulfur curative system consists of, for each 100 parts by weight of the rubber blend, from about 0.2 part to about 1 part sulfur; from about 0.5 part to about 3 parts useful accelerator; and from about 1.0 part to about 5 parts, more preferably from about 1.5 parts to about 3.0 parts, zinc oxide promoter.
Preferably the nonsulfur curative system consists of, for each 100 parts by weight of the rubber blend, from about 0.2 part to about 2 parts nonsulfur curative compound, and from about 0.3 part to about 5 parts, more preferably from about 0.5 part to about 3.0 parts, Group Ia or IIa metal compound promoter. The Group Ia or IIa metal compound promoter also functions as an acid acceptor.
The cross-linking composition of this invention is used to cross-link or vulcanize rubber blends of, by weight, (a) from about 35% to about 85% of halobutyl rubber or a mixture of butyl rubber and halobutyl rubber wherein the halobutyl rubber is at least 50% by weight of the mixture, and (b) from about 15% to about 65~ of epihalohydrin rubber.
The rubber blends can be prepared by blending the rubber compounds together with all desired ingredients, except the cross-linking composition of this invention, in any desired fashion that allows intimate mixing; for example, in a Ban-bury mixer or two roll differential speed mill.
The cross-linking composition of this invention can then be incorporated or mixed with the blended ingredients in any desired fashion, such as by simply milling the blended ingre-dients and the cross-linking composition on a conventional rubber mill. Preferably the milling is conducted at 50C to about 90C; Other methods of mixing the cross-linking compo-sition with the polymer will be apparent to those skilled in the art.
Cross-linking is effected at elevated temperatures. In general the cross-linking temperature will be from about 140C
to about 260C, preferably from about 150C to about 225C, and most preferably from about 150C to about 205C. The time will vary inversely with the temperature and will range from about 5 seconds to 10 hours. The cross-linking tempera-tures and times are within the skill of those versed in the art.
As is well known in the art, butyl rubber is a copolymer of from about 95.5 to about 99.5 mole % isobutylene and from about 0.5 to about 4.5 mole ~ isoprene.
~ alobutyl rubbers are halogenated butyl rubbers. The halogen is present as a result of post-treatment of the butyl rubber by reacting chlorine or bromine with the butyl rubber 2~ by methods known in the art. Halobutyl rubbers include chlorobutyl, bromobutyl or mixtures of chloro and bromobutyl rubbers.
Such materials include chlorobutyl and bromobutyl rubbers prepared by reacting chlorine or bromine with butyl rubber wherein the original unsaturation ~usually from about 0.5 to

3.0 mole ~ isoprene residues) is largely tnaintained. A suit-able commercially available chlorobutyl rubber contains from about 1.1~ to about 1.35% by weight of chlorine frotn about 0.5 to 2 mole ~ unsaturation, and has a Mooney viscosity after 8 30 minutes at 212F using the large (4-inch) rotor of 40 to 89 ML. A satisfactory bromobutyl rubber prepared from a highly unsaturated butyl rubber contains from 2.1 to 3.0% by weight of bromine, a density at 25C of about 0.96, and evidences a Mooney viscosity at 212F of 40 to 70 ML.
Generally, the halobutyl rubber or the mixture of butyl rubber and halobutyl rubber is present in an amount of from about 35% to about 85~ by weight of the rubber content, pref-24~770 erably from about 40% to about 75~. Halobutyl rubber is preferred.
Epihalohydrin rubber includes (1) homopolymers of an epihalohydrin, such as epichlorohydrin, epibromohydrin and others, (2) copolymers of an epihalohydrin with less than 30% of saturated epoxy monomers or with an unsaturated epoxy monomer, and (3) terpolymers of an epihalohydrin with (a) less than 30% of a saturated epoxy monomer or mixtures thereof, (b) an unsaturated epoxy monomer or mixtures thereof, or (c) mixtures of (a) and (b).
The epihalohydrin polymers are prepared by polymerizing a monomeric epihalohydrin alone or together with one or more of the aforementioned epoxy monomers with a suitable catalyst, such as an organometallic catalyst. For example, a reaction product of water with an alkyl aluminum compound is a suitable organometallic catalyst. Such homopolymers are believed to have a repeating structure:

wherein X is a halogen, derived by a polymerization involving the epoxide linkages. Suitable halogenq include chlorine and bromine.
Typical saturated epoxy monomers include alkylene oxides, such as ethylene oxide, and typical unsaturated epoxy monomers include allylglycidyl ether.
The epihalohydrin polymers are strong, rubbery materials sometimes evidencing more or less crystallinity, having high molecular weight, a density in the range of from about 1.35 to about 1.38, and after 4 min. at 212F, a Mooney viscosity of from about 40 to about 80ML. The properties and the preparation of "~
.~

epihalohydrin polymers suitable for use in the practice of this invention are more fully disclosed in U.S. Patent 3,158,500.
Copolymers and terpolymers of an epihalohydrin with greater than 30% of saturated epoxy monomers, especially with alkylene oxide monomers, such as ethylene oxide, do not have the required air impermeability and are not useful in tire inner liners and inner tubes.

-5a-~L2~6~7~

Copolymers or terpolymers of epihalohydrin with un-saturated epoxy monomers, such as allylglycidyl ether, tend to cocure with the unsaturation of the halobutyl rubber or mixtures thereof in the rubber blend and the natural rubber in the carcass. Preferably, from about 1% to about 30~ of an unsaturated epoxy monomer is used. Copolymers and terpolymers of epihalohydrin with a saturated epoxy monomer preferably contain less than about 10~ of the saturated epoxy monomer, and most preferably less than about 5~.
; lO Preferably the epihalohydrin rubber is present in an amount of from about 15~ to about 65~ by weight of the total rubber blend, preferably from about 25% to about 55~.
The amount of (a) halobutyl rubber or mixtures thereof with butyl rubber and (b) epichlorohydrin rubber present in the rubber blend totals 100%.
In addition to the cross-linking composition of this invention, the rubber blend may contain other ingredients commonly used in rubber vulcanization. For example, extend-ers, fillers, pigments, stabilizers, antioxidants, tacki-fiers, plasticizers, and softeners may be added. The pres-ence of a filler, particularly carbon black, while not neces-sary, is beneficial. The particle size of the filler is not critical.
Other additives such as polychloroprene rubber, mineral rubber (blown asphalt), and chlorinated hydrocarbon polymers, such as chlorinated polyisoprene rubber and chlorinated poly-olefins, may be present in an amount from about 1~ to about 10~ by weight of the rubber blend.
Typically the chlorinated hydrocarbon polymers have a chlorine content of from about 30~ to about 70~, by weight, preferably 40~ to about 66~, and a molecular weight of about 50,000 to about 1,000,000 as determined by size exclusion chromatography. Chlorinated polyisoprene having from about 63~ to about 66~ by weight chlorine is the preferred chlori-nated hydrocarbon polymer.
The polychloroprene improves green strength, the mineralrubber improves aged adhesion, and the chlorinated hydrocarbon ~246770 ..-- --...

polymers generally tend to improve the impermeability to air and other gases.
The following examples set forth in Table 1 illustrate the invention. The controls or comparative examples are set forth in Table 2. The examples and the controls are prepared by the same procedure as set forth above. The properties of the examples and controls are set forth in Tables 3 and 4, respectively.
All parts and percentages in this s~ecification are by weight unless otherwise indicated.

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Adhesion to the tire carcass of at least 25 T-Peel lbs./-in.-pli is acceptable: however, preferably it is greater than 30 T-Peel lbs./in.-pli.
A Mooney scorch of 16 minutes or better is good for the 3 point rise, and 20 minutes or better is good for the 5 point rise.
Tensile strength of at least 900 psi is acceptable, pref-erably greater than 900 psi.
Control 1 shows that a rubber blend containing a large particle size carbon black and oil when cross-linked with mag-nesium oxide and ethylene thiourea conventional cross-linking system does not provide an acceptable tensile strength, where-as the same rubber-based composition (Example 1) when it is cured with the cross-linking composition of this invention lS does provide acceptable tensile strength.
Control 2 shows that the same rubber blend containing small particle size carbon black and no oil when cross-linked with a conventional cross-linking system likewise does not provide an acceptable tensile strength or scorch safety, whereas the same composition (Example 2) when it is cured with the cross-linking composition of this invention does provide acceptable tensile strength and scorch safety.
Control 3 shows that a rubber blend containing smaller amounts of chlorobutyl rubber ~25%) when cross-linked with the cross-linking system of this invention does not provide a material having acceptable scorch or adhesion properties.
Control 4 shows that the sulfur curative system alone and Control 5 shows that the nonsulfur curative system alone, when used to cross-link a respresentative rubber blend, do not provide materials having acceptable scorch properties.
Further, nonsulfur curative system alone (Control 5), does not provide a material having acceptable tensile strength properties.
Usually oil makes rubber compositions more permeable to gases. While the composition of Example 1 is more permeable to gases than the composition of Example 2, it still has im-proved scorch safety, cure rate and physical properties.

The tire carcass is typically natural rubber with other rubbers, such as styrene-butadiene, added in lesser amounts and cured with a conventional sulfur cure system.
Thus, this invention provides a sulfur and nonsulfur cross-linking composition especially adapted for cross-link-ing blends of (a) halobutyl rubber or a mixture of butyl rub-ber and halobutyl rubber wherein the halobutyl rubber is at least 50~ by weight of the mixture, and (b) an epihalohydrin rubber. Rubber blends cured with the compositions of this invention have a better balance of cure rate, cure state, scorch safety and physical properties and have improved ad-hesion to the tire carcasses and good impermeability to gases.
The cured rubber material is especially useful in tire inner tubes and tire inner liners, particularly in a pneumatic tire having cured rubber liner ply overlying all internal tire sur-faces exposed in service to pressurized gas.
The expressions "consists essentially of" and "consist-ing essentially of" as used in this specification excludes any unrecited substance at a concentration sufficient to substantially adversely affect the essential properties and characteristics of the composition of matter being defined, while permitting the presence of one or more unrecited sub-stances at concentrations insufficient to substantially ad-versely affect said essential properties and characteristics.
Features, advantages and other specific embodiments of this invention will become readily apparent to those exercis-ing ordinary skill in the art after reading the foregoing dis-closures. In this regard, while specific embodiments of this invention have been described in considerable detail, variations and modifications of these embodiments can be effected without departing from the spirit and scope of the invention as disclosed and claimed.

Claims

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows:

1. A cross-linking composition for cross-linking a blend of (A) halobutyl rubber or a mixture of butyl rubber and halobutyl rubber and (B) an epihalohydrin rubber, charac-terized in that the cross-linking composition consists of, for each 100 parts by weight of the rubber blend: (a) from about 1.0 part to about 20 parts of a sulfur curative system con-sisting of (i) from about 0.1 part to about 5 parts sulfur, (ii) from about 0.1 part to about 5 parts sulfur accelerator selected from the group consisting of mercaptobenzothiazole, mercaptobenzothiazole derivatives, sulfenamides, thiurams, and dithiocarbamate salts, and (iii) from about 0.5 part to about 10 parts zinc oxide promoter; and (b) from about 0.3 part to about 10 parts of a nonsulfur curative system con-sisting of (i) from about 0.1 part to about 5 parts nonsulfur curative compound selected from the group consisting of di-and tri-functional mercapto compounds and derivatives there-of; and (ii) from about 0.2 part to about 10 parts metal com-pound promoter selected from the group consisting of oxides, hydroxides, and carbonates of metals in Groups Ia and IIa of the Periodic Table.

2. The composition of claim 1, further characterized in that the sulfur accelerator is mercaptobenzothiazole disulfide.

3. The composition of claim 1, further characterized in that the nonsulfur curative compound is a 2-mercapto-1,3,4-thiadiazole-5-benzoate.

4. The compositon of claim 1, further characterized in that the metal compound promoter is barium carbonate.

5, The composition of claim 1, further characterized in that the metal compound promoter is magnesium oxide.

6. The composition of claim 1 wherein (a)(i) is pres-ent in an amount from about 0.2 part to about 1 part; (a)(ii) is present in an amount from about 0.5 part to about 3 parts;
(a)(iii) is present in an amount from about 1.0 part to about 5 parts; (b)(i) is present in an amount from about 0.2 part to about 2 parts; and (b)(ii) is present in an amount from about 0.3 part to about 5 parts.

7. A cross-linkable rubber composition containing (I) a rubber blend of (a) halobutyl rubber or a mixture of butyl rubber and halobutyl rubber and (b) epihalohydrin rubber and (II) a cross-linking composition, characterized in that the rubber blend contains from about 35% to about 85%, by weight of the rubber blend, (i) halobutyl rubber or (ii) a mixture of butyl rubber and halobutyl rubber wherein halobutyl rubber is present in an amount of at least 50% by weight of the mix-ture and (b) from about 15% to about 65%, by weight of the rubber blend, epihalohydrin rubber, and the cross-linking com-position consists of the cross-linking composition of claim 1.

8. A process for cross-linking comprising heating to a temperature sufficient to effect cross-linking in the pres-ence of a cross-linking composition a rubber blend of (A) halobutyl rubber or a mixture of butyl rubber and halobutyl rubber and (B) epihalohydrin rubber, characterized in that the rubber blend contains from about 35% to about 85%, by weight of the rubber blend, (i) halobutyl rubber or (ii) a mixture of halobutyl rubber and butyl rubber wherein at least 50% by weight of the mixture is halobutyl rubber and from about 15%, to about 65% by weight of the rubber blend, epihalohydrin rub-ber, and the cross-linking composition consists of the cross-linking composition of claim 1.

9. A pneumatic tire containing a liner ply overlying all internal tire surfaces exposed in service to pressurized gas, said liner ply containing a cross-linked blend of (A) halobutyl rubber or a mixture of butyl rubber and halobutyl rubber and (B) epihalohydrin rubber, characterized in that the blend is cross-linked according to the process of claim 8.

10. The method of use of a cross-linked blend of (A) halobutyl rubber or a mixture of halobutyl rubber and butyl rubber and (B) epihalohydrin rubber in a pneumatic tire liner ply that overlies all internal tire surfaces exposed to gas, character-ized in that the blend is cross-linked according to claim 8.