Method for low temperature bonding of elastomers

Abstract

A method of bonding a vulcanized elastomer is provided comprising the steps of; providing an adhesive comprising a primary acrylate monomer, a reactive flexibilizing monomer, and further optionally comprising a toughener, an adhesion promoter and a free radical initiator, then depositing the adhesive on at least one surface of an elastomer or a second substrate, wherein the elastomer is a vulcanized elastomer, then bringing the elastomer substrate and second substrate together with the adhesive disposed therebetween, and allowing the adhesive to cure and bond the elastomer and second substrate together at a temperature of less than about 100° C. to produce a bonded structure.

Claims

1. A method of bonding a vulcanized elastomer comprising the steps of: a) providing an adhesive comprising two parts, wherein the first part comprises: 30 to 60 weight percent primary acrylate monomer comprising at least one of methyl methacrylate or tetrahydrofurfuryl methacrylate, 5 to 15 weight percent reactive flexibilizing monomer comprising at least one of 2-ethylhexyl methacrylate, hexyl methacrylate, or octyl methacrylate, 5 to 15 weight percent of a substrate dependent reactive monomer comprising iso-butyl methacrylate, 10 to 30 weight percent of a toughener, 0.5 to 5 weight percent of a reducing agent, and the second part comprises: 30 to 60 weight percent of an epoxy resin, and 20 to 40 weight percent of an organic peroxide; b) depositing the adhesive on at least one surface of an elastomer or a second substrate, wherein the elastomer is a vulcanized elastomer; c) bringing the elastomer and second substrate together with the adhesive disposed therebetween; and, d) allowing the adhesive to cure and bond the elastomer and second substrate together at a temperature of less than about 100° C. to produce a bonded structure.

2. The method of claim 1, wherein step d) is performed at a temperature of less than about 50° C.

3. The method of claim 1, wherein the second substrate comprises at least one of an elastomer substrate, a thermoplastic substrate, or a metallic substrate.

4. The method of claim 1, wherein the toughener comprises at least one of poly(styrene:butadiene:styrene), poly(styrene:acrylonitrile:butadiene), or styrene:isoprene:styrene.

5. The method of claim 1, wherein the adhesive is free of halogenated compounds, isocyanate compounds, or solvents.

6. The method of claim 1, wherein the 2-part adhesive is mixed immediately prior to the step of depositing the adhesive.

7. The method of claim 1, wherein there is no elastomer chlorination step.

8. The method of claim 1, wherein there is no metal degreasing step.

9. The method of claim 1, where the adhesive comprises the sole chemical composition applied to either the elastomer or second substrate prior to bonding, and the elastomer and second substrate are absent any metal primer, tack coating, or elastomer pre-treatment.

10. The method of claim 1, wherein the cured adhesive has an adhesion as measured by pull value of greater than 25pli as measured by ASTM D429 Method D at a peel rate of 2.0in/min.

11. The method of claim 1, wherein the adhesive is deposited by providing the first part on one of the elastomer or second substrate and providing the second part on the other of the elastomer or second substrate, and wherein when the elastomer and second substrate are brought together an initiator cures the acrylate monomer.

Description

DETAILED DESCRIPTION OF THE INVENTION

(1) In a first embodiment of the present invention, a method of bonding a vulcanized elastomer is provided comprising the steps of; providing an adhesive comprising a primary acrylate monomer, a reactive flexibilizing monomer, and further optionally comprising a toughener, an adhesion promoter and a free radical initiator, then depositing the adhesive on at least one surface of an elastomer or a second substrate, wherein the elastomer is a vulcanized elastomer, then bringing the elastomer substrate and second substrate together with the adhesive disposed therebetween, and allowing the adhesive to cure and bond the elastomer and second substrate together at a temperature of less than about 100° C. to produce a bonded structure. This method allows for bonding vulcanized elastomers to other substrates at low, preferably near room, temperatures without the use of multi-layered adhesives or adhesives with undesirable compounds such as halogens, isocyanates, solvents, and the like.

(2) In a first aspect of the present invention, a primary acrylate monomer is provided comprising at least one free radical-polymerizable monomer in a major amount of the composition. Representative monomers include esters of (meth)acrylic add such as methyl methacrylate, ethyl methacrylate, butyl methacrylate, methyl acrylate, butyl acrylate, cyclohexyl acrylate, hexyl acrylate, 2-ethylhexyl acrylate, lauryl acrylate, ethyl acrylate, diethylene glycol dimethacrylate, dicyclopentadienyloxyethyl methacrylate, cyclohexyl methacrylate, lauryl methacrylate, glycidyl methacrylate and tetrahydrofurfuryl methacrylate (THFMA). The preferred monomer(s) contributes rigidity in the cured polymer and is selected from methacrylic esters exhibiting a homopolymer Tg of at least 50° C., preferably 60° C., and some as much as 105° C. In a preferred embodiment of the present invent, the acrylate monomer comprises at least 50 weight percent tetrahydrofurfuryl methacrylate and a minority amount of methylmethacrylate.

(3) In an embodiment of the present invention, the primary acrylate monomer is present in the composition in an amount of between about 10 and about 90 weight percent, more preferably between about 30 and about 70 weight percent, and most preferably between about 40 and about 60 weight percent, based on the total weight of the composition.

(4) In a further embodiment of the present invention a reactive flexibilizing monomer is provided. The reactive flexibilizing monomer is reactive with the primary acrylate monomer and provides flexibility to the backbone of the resulting acrylic polymer. In one embodiment of the present invention, the reactive flexibilizing monomer comprises an acrylate comprising an olefinic group having at least 6 carbon atoms. This olefininc group provides the desired flexibility while the acrylate moiety allows for compatibility with the primary acrylate monomer. In one embodiment of the present invention, the reactive flexibilizing monomer can be represented by the formula H2C═CHCO2R, where R is a linear or branched hydrocarbon chain and the homopolymer has a Tg<0° C. In a preferred embodiment of the present invention, the reactive flexibilizing monomer comprises at least one of hexyl methacrylate, 2-ethylhexyl methacrylate, octyl methacrylate, or dodecyl (lauryl) methacrylate.

(5) In an embodiment of the present invention, the reactive flexibilizing monomer is present in the composition in an amount of between about 0 and about 50 weight percent, more preferably between about 5 and about 25 weight percent, and most preferably between about 10 and about 15 weight percent, based on the total weight of the composition.

(6) In a further embodiment of the present invention, a substrate dependent reactive monomer is optionally provided. It is believed that an acrylate monomer that is substantially compatible with an elastomeric substrate aids in forming a robust bond with the substrate. For example, in an embodiment wherein the substrate comprises natural rubber, a substrate dependent reactive monomer comprising isobutylmethacrylate substantially improves bonding to the natural rubber. The substrate dependent reactive monomer is selected such that its Hildebrand solubility parameter is compatible with the Hildebrand solubility parameter of the elastomeric substrate. In particular, it is chosen in such a way that its solubility parameter does not differ by more than 10% from the Hildebrand solubility parameter of the elastomeric substrate.

(7) The Hildebrand solubility parameter is well known and calculated by the square root of the cohesive energy density of the compound. The Hildebrand solubility parameter is directly related to the dispersion forces (Van der Waals forces) that are exerted between the molecules of a chemical substance. In particular, the Hildebrand solubility parameter is generally expressed in cal.sup.1/2cm.sup.−3/2.

(8) Another method for determining compatibility is through a swell test. A selection of monomers is chosen to cover a wide range of Hildebrand solubility parameters. For each selected monomer, a rectangular piece of rubber of mass ˜2g is weighed and then submerged in monomer. The rubber is allowed to soak in the monomer for 24 hours with mass being measured beginning at 1 hour and then at regular intervals up to 24 hours. Those monomers which swell the rubber to the greatest extent on a per mole monomer basis are judged to be most compatible with the elastomeric substrate. These are then tested as candidates for the compatibilizing monomer within the adhesive formulation.

(9) In an embodiment of the present invention, the substrate dependent reactive monomer is present in the composition in an amount of between about 0 and about 50 weight percent, more preferably between about 0 and about 25 weight percent, and most preferably between about 0 and about 10 weight percent, based on the total weight of the composition.

(10) In one embodiment of the present invention, the adhesive composition further comprises a toughener. The toughener improves impact resistance of the cured adhesive and provides flexibility to reduce cohesive failure of the adhesive. The toughener examples include various solid and liquid elastomeric polymeric materials, and in particular liquid olefinic-terminated elastomers as described in U.S. Pat. Nos. 4,223,115; 4,452,944 4,769,419; 5,641,834 and 5,710,235, the entire disclosure of each which is hereby incorporated by reference.

(11) A-B-A or A-B-C triblock block copolymers are useful tougheners. In one example the A block is polystyrene, alpha-methyl styrene, t-butyl styrene, or other ring alkylated styrenes as well as mixtures of some or all of the above and the B block is an elastomeric segment having a Tg of 0° C. or less, such as that derived from a conjugated diene; isobutylene or other olefin, like ethylene-propylene monomer, and the C block, if present, is acrylonitrile.

(12) In one embodiment of the present invention, a preferred toughener comprises a terblock polymer of styrene-butadiene-styrene with a polystyrene content of about 23% by weight. In another preferred embodiment of the present invention, a preferred toughener comprises styrene-butadiene-acrylonitrile,

(13) In another embodiment of the present invention, other high molecular weight tougheners include, for example, block copolymers and random copolymers including but not limited to polyethylene, polypropylene, styrene-butadiene, polychloroprene, EPDM, chlorinated rubber, butyl rubber, styrene/butadiene/acrylonitrile rubber and chlorosulfonated polyethylene.

(14) In another embodiment of the present invention an auxiliary toughener is provided. Preferred auxiliary tougheners comprise urethane modified olefinic -terminated liquid elastomers include those disclosed in U.S. Pat. No. 4,769,419 comprising the reaction product of an olefinic monoepoxide compound with a polycarboxylic homopolymer of conjugated dienes, and most specifically, the glycidyl methacrylate/carboxyl terminated butadiene (GMA/CTB) adduct as described in U.S. Pat. No. 4,769,419, Example 1.

(15) In an embodiment of the present invention, the combined tougheners are present in the composition in an amount of between about 0 and about 50 weight percent, more preferably between about 10 and about 30 weight percent, and most preferably between about 20 and about 30 weight percent, based on the total weight of the composition.

(16) In a further embodiment of the present invention, an adhesion promoter is provided to enhance the adhesion between the adhesive and metallic substrate. Adhesion promoters useful herein are the known phosphorus-containing compounds with mono-esters of phosphinic, mono- and diesters of phosphonic and phosphoric acids having one unit of vinyl or aliylic unsaturation present. Vinylic unsaturation is preferred. Representative of the phoshorus-containing adhesion promoters are, without limitation, phosphoric acid; 2-methacryloyloxyethyl phosphate; bis-(2-methacryloxyloxyethyl)phosphate; 2-acryloyloxyethyl phosphate; bis-(2-acryloyloxyethyl)phosphate; methyl-(2-methacryloyloxyethyl)phosphate; ethyl methacryloyloxyethyl phosphate; methyl acryloyloxyethyl phosphate; ethyl acryloyloxyethyl phosphate; propyl acryloyloxyethyl phosphate, isobutyl acryloyloxyethyl phosphate, ethylhexyl acryloyloxyethyl phosphate, halopropyl acryloyloxyethyl phosphate, haloisobutyl acryloyloxyethyl phosphate or haloethylhexyl acryloyloxyethyl phosphate; vinyl phosphonic acid; cyclohexene-3-phosphonic acid; (α-hydroxybutene-2 phosphonic acid; 1-hydroxy-1-phenylmethane-1,1-diphosphonic acid; 1-hydroxy-1-methyl-1-disphosphonic acid; 1-amino-1-phenyl-1,1-diphosphonic acid; 3-amino-3-hydroxypropane-1,1-disphosphonic acid; amino-tris(methylenephosphonic acid); gamma-amino-propylphosphonic acid; gamma-glycidoxypropylphosphonic acid; phosphoric acid-mono-2-aminoethyl ester; allyl phosphonic acid; allyl phosphinic acid; β-methacryloyloxyethyl phosphinic acid; diallylphosphinic acid; β-methacryloyloxyethyl)phosphinic acid and allyl methacryloyloxyethyl phosphinic acid. A preferred adhesion promoter: is 2-hydroxyethylmethacrylate phosphate.

(17) Further adhesion promoters useful herein are the known alkenyl functional silanes, having an unsaturated organic moiety bonded to the silicone atom, for example an unsaturated acrylic, vinyl, allyl, methallyl, propenyl, hexenyl, ethynyl, butadienyl, hexadienyl, cyclopentenyl, cyclopentadienyl, cyclohexenyl, vinylcyclohexylethyl, divinylcyclohexylethyl, norbornenyl, vinylphenyl or styryl groups. Other alkenyl functional organometallics include titanates, such as vinylalkyl titanates, zirconates, zinc diacrylate, and zinc dimethacrylates.

(18) Additionally carboxylic acids are good adhesion promoters, including methacrylic acid, itaconic acid, maleic acid, formic acid, mono-2-(methacryloyloxy)ethylsuccinate.

(19) In an embodiment of the present invention, the adhesion promoter is present in the composition in an amount of between about 0 and about 20 weight percent, more preferably between about 0 and about 10 weight percent, and most preferably between about 0 and about 5 weight percent, based on the total weight of the composition.

(20) In an additional embodiment of the present invention, a free-radical cure system is employed to cure the adhesive. A preferred system comprises known redox couple systems and need not be discussed herein in detail. Basically, such systems comprise at least one oxidizing agent and at least one reducing agent which are co-reactive at room temperature to generate free radicals effective to initiate addition polymerization reactions and cure the adhesive.

(21) Substantially any of the known oxidizing and reducing agents which are so co-reactive can be employed. Representative oxidizing agents include, without limitation, organic peroxides, such as benzoyl peroxide and other diacyl peroxides, hydroperoxides such as cumene hydroperoxide, peresters such as β-butylperoxybenzoate; ketone hydroperoxides such as methyl ethyl ketone hydroperoxide, organic salts of transition metals such as cobalt naphthenate, and compounds containing a labile chlorine such as sulfonyl chloride.

(22) Representative reducing agents include, without limitation, sulfinic acids; azo compounds such as azoisobutyric acid dinitrile; alpha-aminosulfones such as bis(tolysulfonmethyl)-benzyl amine; tertiary amines such as diisopropanol-p-toluidine (DIIPT), dimethyl aniline, p-halogenated aniline derivatives and dimethyl-p-toluidine; and aminealdehyde condensation products, for example, the condensation products of aliphatic aldehydes such as butyraldehyde with primary amines such as aniline or butylamine. The use of known accelerators and promoters with the redox couple catalyst systems can be advantageous.

(23) In a further embodiment of the present invention, the acrylic adhesive composition comprises a co-accelerator. The co-accelerator will not cure the acrylic adhesive by itself but serves to increase the rate at which the redox system cures the adhesive. In a preferred embodiment of the present invention, the co-accelerator comprises a bicyclic diaza compound wherein the nitrogen atoms are present in the rings. In a most preferred embodiment of the present invention, the co-accelerator comprises 1,4-diazabicyclo[2.2.2]octane. In a further embodiment of the present invention, the co-accelerator comprises dimethylpiperazine. In an embodiment of the present invention, the co-accelerator is present in an amount from 0.10 to 3.0 weight percent based on the total weight of the composition.

(24) Preferably, the oxidizing agent will be present in an amount in the range from about 1.0 to about 20, preferably about 5.0 to about 10 percent by weight of the adhesive composition, with the amount of reducing agent being in the range from about 0.1 to about 20, preferably about 1.0 to about 10 percent by weight of the adhesive composition. DIIPT is the most preferred reducing agent. The most preferred oxidizing agent is benzoyl peroxide.

(25) In an additional embodiment of the present invention, the free-radical cure system comprises an initiator such as a triethylborane-hexamethylenediamine complex.

(26) In a further embodiment of the present invention, the adhesive comprises an epoxy compound. Epoxy compounds are thought to provide post-bake resistance and an acid-scavenging functionality to prevent acid formed in the cure reaction from reacting with the metallic substrate. The epoxy compound of embodiments of the present invention comprises any material that contains an epoxy (oxirane) group. Included epoxy resins are epoxy cresol novolacs, epoxy phenol novolacs and blends of either of these with bisphenol A epoxy resins. Monomeric epoxy compounds and epoxides of the polymeric type can be aliphatic, cycloaliphatic, aromatic or heterocyclic.

(27) Epoxy resins based on bisphenol A, either solids, and capable of dissolution in a carrier, or liquid, are preferred as these are relatively inexpensive. There are a myriad of available epoxy materials, collectively referred to as epoxy resins whether resinous or simple compounds. In particular, simple epoxy compounds which are readily available include octadecylene oxide, glycidylmethacrylate, diglycidyl ether of bisphenol A.

(28) In an embodiment of the present invention comprising an epoxy resin, the epoxy resin is present at no more than about 20 weight percent, based on the final weight of the adhesive formulation. In a preferred embodiment of the present invention, the epoxy resin is present in an amount of no more than about 15 weight percent, and in a most preferred embodiment of the present invention, the epoxy resin is present from about 2.5 to about 10 weight percent, based on the total weight of the adhesive formulation.

(29) Other optional additives which are typically considered in fully formulated adhesives include antioxidants, inhibitors, anti-sag additives, thixotropes, processing aids, waxes, UV stabilizers, arc suppressants, and drip suppressants. Examples of typical additives are silicas, fumed silica, zirconium silicate, alumina, hindered phenols, substituted hydroquinone, silane-treated talc, mica, feldspar, and wollastonite.

(30) Although the adhesive of the present invention may take many forms, the most preferred adhesive systems are provided as multipack or two-part adhesive systems where one package or part contains the free radical-polymerizable monomer component and the reducing agent and a second part or package contains the oxidizing agent. The two parts are mixed together at the time of use in order to initiate the reactive cure. After mixing the individual parts, one or both surfaces to be joined are coated with the mixed adhesive system and the surfaces are placed in contact with each other. Typical mixing ratios range from 1:1, to 4:1, to 10:1 with the acrylic monomers typically in the “A” side and oxidizing agents in the “B” side with other components balanced between the two.

(31) In one embodiment of the resent invention, the adhesive is provided in a two-part system with a first part comprising 30 to 60 weight percent of a primary acrylate monomer, 5 to 15 weight percent of a reactive flexibilizing monomer, 5 to 15 weight percent of a substrate dependent reactive monomer, 10 to 30 weight percent of a toughener, and 0.5 to 5 weight percent of a reducing agent, all based on the total weight of the first part. Similarly, the second part comprises 30 to 60 weight percent of an epoxy resin and 20 to 40 weight percent of an organic peroxide, all based on the weight of the second side. In a further preferred embodiment of the present invention, both sides optionally comprise fillers and additives.

(32) The adhesives described in the embodiments of the present invention are useful in a number of elastomer to metal bonding applications. In a preferred embodiment of the present invention the adhesives are employed in a low-temperature bonding application of post-vulcanized rubber. “Low-temperature” refers to bonding without the application of external pressure or heat such as in an autoclave or through induction. In one embodiment of the present invention, this bonding operation takes place at a temperature of less than about 100° C. In a preferred embodiment of the present invention, the bonding process takes place at ambient conditions of less than about 70° C., and most preferably less than about 50° C.

(33) In one embodiment of the present invention, some elastomer formulations (commonly natural rubber) have additives such as free-radical inhibitors, waxes, and other compounds which can interfere with bonding. For these elastomers, a solvent wipe is often employed to remove any of these materials that have migrated to the surface of the rubber. Prior to bonding, a rag is moistened with applicable solvent (i.e. IPA, heptanes, etc) and used to wipe the elastomer surface several times to remove impurities. The bonding surface is then allowed to dry completely (5-10 minutes) before mating the pieces together.

(34) In another embodiment of the present invention, the adhesive is deposited on at least one surface of a vulcanized elastomeric substrate or a second substrate, and then the elastomeric substrate is brought into contact with the second substrate such that the adhesive is disposed there between. The adhesive is then allowed to cure thereby bonding the vulcanized substrate to the second substrate. In a preferred embodiment of the present invention the second substrate comprises a metallic substrate. In another preferred embodiment of the present invention, the elastomeric substrate comprises a rubber for use in tank lining applications.

EXAMPLES

(35) In a first example, the following formulation was prepared to demonstrate the effectiveness of employing an acrylic-based adhesive to bond vulcanized rubber at or near room temperature.

(36) A-Side:

(37) TABLE-US-00001 Functional Role Constituent Weight Percent Primary Acrylate Monomer(s) MMA 44 Reactive Flexibilizing Monomer (see below) 12 Substrate Dependent Monomer (see below) 10 Rubbery Toughener Core/Shell and 23 GMA/CTB Reducing Agent DIIPT 0.7 Additives various 8.3
B-Side:

(38) TABLE-US-00002 Functional Role Constituent Weight Percent Initiator 57% di-benzoyl peroxide in 50 surfactant Epoxy resin Bisphenol-A Epoxy 45 Thickeners and pigments TiO2 and Fumed silica 5

(39) Adhesive samples were prepared according to ASTM 429D method for testing rubber to metal bonded samples in pull mode. Blasted CRS steel substrates were taped off to give a 1×1 inch bonding area. Adhesive was applied using a mixing cartridge (10:1 volume ratio) equipped with a mixer tip to the bonding area. 10 mil glass bead were applied to the wet adhesive and the elastomer (1×4 inch, ¼ inch thick) was then pressed on to the adhesive bead to give a 1×1 inch bonded area ˜10 mil in thickness. The bonded samples were allowed to cure at ˜20-25° C. overnight (˜10-15 hrs).

(40) The samples were then pulled at 2.0 in/min at an angle of 90 degrees for elastomer-to-metal bonded samples, and 180 degrees for elastomer-to-elastomer bonded samples. The maximum value of force was recorded as the value of strength (pli) and the amount of rubber retention (% R-R) was recorded as percentage of the disbonded 1×1 inch area. Peel strength defining a “successful” adhesive is typically defined as a strength at which the elastomer begins to tear apart rather than the adhesive delaminating. While peel strength values will therefore vary depending upon the internal strength of the elastomer, a “successful” bond will typically exhibit at least 15-20 pli for a soft elastomer such as unfilled natural rubber, however more preferably peel values comprise 25 pli to 50 pli. Further, adhesives are typically judged to be sufficient if the bond holds past the breaking point of the elastomer and therefore the percent rubber retention is the more important measure with 100% being the goal and indicating a robust adhesive bond.

(41) The following table provides the result of peel tests of an adhesive according to the above-formulation wherein the primary acrylic monomer comprises methyl methacrylate, and the reactive flexibilizing monomer comprises the constituent listed in the table. The mix of reactive flexibilizing monomers was varied to include hexyl methacrylate, octyl methacrylate, lauryl methacrylate, and 2-ethylhexyl methacrylate. Additionally, in some formulations the optional substrate dependent monomer isobutyl methacrylate was added to the formulation.

(42) TABLE-US-00003 Maximum Peel Force Rubber Type Monomer Mix (lbs) % R-R Natural Rubber MMA, 2-EHMA, Iso-BMA 35  2% Natural Rubber MMA, 2-EHMA 28  2% Natural Rubber MMA, Iso-BMA 30  0% Natural Rubber MMA, Hexyl MA 33  0% Natural Rubber MMA, Octyl MA 28  0% Natural Rubber MMA, Lauryl MA 39  5% EPDM MMA, 2-EHMA, Iso-BMA 80 80% EPDM MMA, 2-EHMA 70 90% EPDM MMA, Iso-BMA 72 100%  EPDM MMA, Hexyl MA 65 67% EPDM MMA, Octyl MA 64 87% EPDM MMA, Lauryl MA 65 100%  Chloroprene MMA, 2-EHMA, Iso-BMA 93 50% Chloroprene MMA, 2-EHMA 87 80% Chloroprene MMA, Iso-BMA 97 100%  Chloroprene MMA, Hexyl MA 104 97% Chloroprene MMA, Octyl MA 100 100%  Chloroprene MMA, Lauryl MA 98 94%

(43) The following table provides the result of peel tests of a THFMA-based adhesive formulation according to an embodiment of the present invention with variation in accompanying monomers.

(44) TABLE-US-00004 Maximum Peel Force Rubber Type Monomer mix (lbs) % R-R Natural Rubber THFMA 64  22% Natural Rubber THFMA, 2-EHMA 45  50% Natural Rubber THFMA, Iso-BMA 55  60% Natural Rubber THFMA, Iso-BMA, 2-EHMA 68  90% EPDM THFMA 68 100% EPDM THFMA, 2-EHMA 70 100% EPDM THFMA, Iso-BMA 73 100% EPDM THFMA, Iso-BMA, 2-EHMA 71 100% Chloroprene THFMA 81  67% Chloroprene THFMA, 2-EHMA 94 100% Chloroprene THFMA, Iso-BMA 100 100% Chloroprene THFMA, Iso-BMA, 2-EHMA 93 100%

(45) In a further example, a non-peroxide based initiation system was demonstrated to be effective in conjuction with an embodiment of the present invention. A two part adhesive based on a borane-amine complex was prepared as follows:

(46) A-Side:

(47) TABLE-US-00005 Functional Role Component Weight Percent Primary Acrylic Tetrahydrofurfuryl Methacrylate 53 Monomer (THFMA) Reactive 2-Ethylhexyl methacrylate (2-EHMA) 17 Flexibilizing Monomer Accellerator/ Mono-2-(methyacryloxyloxy) ethyl 6 activator succinate Toughener Poly(styrene:acrylonitrile:butandiene) 14 HPSEC, MW of 45,300 Filler Silica 10 Total 100
B-Side:

(48) TABLE-US-00006 Functional Role Component Weight Percent Carrier Polypropylene glycol adipate) 43 Initiator Hexamethylenediamine/triethylborane 24 Acid scavenger Trimethylolpropanetris(2-methyl-1- 27 aziridine propionate) Filler Silica 6 Total 100

(49) This adhesive was applied and tested in accordance with the procedures outlined above on a variety of different rubber types:

(50) TABLE-US-00007 Peel Force Rubber Type (lbs) % R-R Natural Rubber 57 77% Natural Rubber (with IPA wipe) 60 72% EPDM 67 67% Chloroprene 48  0%

(51) The following examples demonstrate the heat aging and environmental resistance of adhesives of certain embodiments of the present invention. In these examples, the adhesives were prepared and applied to the substrates as indicated. After the aging/environmental conditions were applied, the samples were pulled at 2.0 in/min at an angle of 90 or 180 degrees as noted above. The maximum value of force was recorded as the value of strength (pli) and the amount of rubber retention (% R-R) was recorded as percentage of the disbonded 1×1 inch area.

(52) A-Side:

(53) TABLE-US-00008 Functional Role Component Weight Percent Acrylate Monomer THFMA 36 Acrylate Monomer MMA 3.0 Reactive Flexibilizing 2-EHMA 12 Monomer Substrate Dependent iso-BMA 10 Monomer Reducing Agent DIIPT 0.7 Toughener (various) 25 Additives (various) 13 Total 100
B Side:

(54) TABLE-US-00009 Functional Role Component Weight Percent Epoxy Bis-A epoxy resin 46.6 Initiator 57% di-BPO in surfactant 48 Pigment Titanium dioxide 3.0 Thickener Fumed silica 2.4 Total 100

(55) In this example, a polychloroprene elastomer was bonded using the adhesive described above to either another polychloroprene elastomer or a grit-blasted cold rolled steel coupon. The sample was exposed to the listed conditions and tested to determine peel strength and rubber retention:

(56) Heat Aging Conditions of 100° C. for 24 and 48 Hours. (Rubber-to-metal)

(57) TABLE-US-00010 Time 110 C. (hours) Peel (pli) % R-R 0 89.4 100 24 98.7 100 48 107 100
10%, Brine Soaking at 100° C. (Rubber-to-rubber Bonding)

(58) TABLE-US-00011 Time 100 C. (days) Peel (pli) % R-R 0 74.6 100 3 81.0 100 7 79.8 100
Thermal Cycling at −40° C. to 110° C. (42 Cycles in 7 Days) (Rubber-to-metal Bonding)

(59) TABLE-US-00012 Time (weeks) Peel (pli) % R-R 0 89.4 100 1 96.6 100
High Humidity Treatment (14 Days at 85% RH and 85° C.) (Rubber-to-metal Bonding)

(60) TABLE-US-00013 Time (weeks) Peel (pli) % R-R 0 89.4 100 2 100 100

(61) In this example, a polychloroprene elastomer was bonded using the adhesive described above to either another polychloroprene elastomer or a grit-blasted cold rolled steel coupon. The sample was exposed to the listed conditions and tested to determine peel strength and rubber retention:

(62) Chemical Resistance for 7 days (Rubber-to-rubber)

(63) TABLE-US-00014 Chemical Test Sample Peel (pli) % R-R 10% Brine at 1 57.9 80 100° C. 2 67.8 90 3 73.1 90 85% 1 97.5 100  Phosphoric Acid 2 72.1 100  at 100° C. 3 72.2 100  60% Sulfuric 1 100 100  Acid at 52° C. 2 103 90 3 70.3 100* 37% HCl at 1 136 90 52° C. 2 150 100  3 121 90 15% Bleach 1 102 90 (NaClO) at 52° C. 2 90.8 100  3 75.8 90 *This sample experienced “stock break” which indicates a potential issue or defect with the rubber sample.