Vulcanizable epoxy group-containing elastomer composition

This invention relates to a vulcanizable epoxy group-containing elastomer composition. More specifically, it relates to a vulcanizable epoxy group-containing elastomer composition which has excellent processing safety and storage stability for premature vulcanization, and gives vulcanizates having excellent mechanical properties, heat aging resistance and compression set.
It has been the usual practice to use polyamines, diamine carbamates, ammonium salts of organic carboxylic acids, and dithiocarbamic acid salts as vulcanization systems for epoxy group-containing elastomers. The use of polyamines or diamine carbamates, however, has the defect that because the rate of vulcanization is fast, the elastomers are liable to undergo scorching in the mixing and processing steps. When the ammonium salts of organic carboxylic acids or dithiocarbamic acid salts are used, elastomer stocks having stability to scorching can be obtained because the rate of vulcanization is relatively slow. But long post-vulcanization must be performed in order to obtain good compression sets.
Various vulcanization methods have been suggested in an attempt to remove these defects. For example, the specification of Japanese Laid-Open Patent Publication No. 145727/1980 discloses a vulcanization system comprising a phthalic acid anhydride and a specific imidazole compound for epoxy group-containing elastomers. The specifications of Japanese Laid-Open Patent Publications Nos. 177044/1982 and 177045/1982 disclose vulcanization systems comprising a guanidine compound and sulfur or a sulfur donor compound for epoxy group-containing elastomers. These vulcanization systems are stable to scorching, but have the defect of requiring post-vulcanization for long periods of time in order to obtain good compression sets.
It is an object of this invention to remedy these defects of the prior art.
The present inventors have made extensive investigations on various vulcanization systems in order to achieve this object, and consequently found that by using a polycarboxylic acid having at least 2 carboxyl groups in the molecule and a quaternary ammonium salt or a quaternary phosphonium salt as a vulcanizing agent for an epoxy group-containing elastomer, there can be obtained a vulcanizable composition which has excellent processing safety and storage stability for premature vulcanization and gives a vulcanizate having excellent mechanical properties, heat aging resistance and compression set.
According to this invention, there is provided a vulcanizable epoxy group-containing elastomer composition comprising an elastomer containing epoxy groups, a polycarboxylic acid having at least 2 carboxyl groups in the molecule, and either a quaternary ammonium salt or a quaternary phosphonium salt.
The epoxy group-containing elastomer used in this invention is an elastomer having epoxy groups as a vulcanization site, and includes epoxidized elastomers obtained by epoxidizing elastomers containing no epoxy group, and elastomers obtained by copolymerizing usually 0.1 to 10% by weight, preferably 0.3 to 3% by weight, of an epoxy group-containing monomer as a vulcanization site with 90 to 99.9% by weight, preferably 97 to 99.7% by weight, of at least one monomer containing a copolymerizable terminal vinyl or vinylidene group by known polymerization methods such as emulsion, suspension, solution or bulk polymerization.
Examples of the epoxy group-containing monomer used as a crosslinking site include glycidyl acrylate, glycidyl methacrylate, vinyl glycidyl ether, allyl glycidyl ether, and methallyl glycidyl ether. Of these, glycidyl acrylate and glycidyl methacrylate are preferred.
Examples of the monomers having a terminal vinyl or vinylidene group copolymerizable with the epoxy group-containing monomer are alkyl acrylates having 1 to 8 carbon atoms in the alkyl moiety such as methyl acrylate, ethyl acrylate, propyl acrylate, n-butyl acrylate, 2-ethylhexyl acrylate and n-octyl acrylate, and the corresponding methacrylates; alkoxyalklyl acrylates having 1 to 4 carbon atoms in each of the alkoxy and alkyl moieties such as methoxymethyl acrylate, methoxyethyl acrylate, ethoxyethyl acrylate, butoxyethyl acrylate and methoxyethoxyethyl acrylate; vinyl esters such as vinyl acetate, vinyl propionate and vinyl butyrate; vinyl ketones such as methyl vinyl ketone and ethyl vinyl ketone; vinyl aromatic compounds such as styrene, alphamethylstyrene and vinyltoluene; conjugated dienes such as butadiene and isoprene; alpha-monolefins such as ethylene, propylene and 1-butene; vinyl monomers having a hydroxyl group such as beta-hydroxyethyl acrylate and 4-hydroxybutyl acrylate; vinyl and vinylidene monomers having a nitrile group such as acrylonitrile, methacrylonitrile and beta-cyanoethyl acrylate; and unsaturated amide monomers such as acrylamide and N-methyl methacrylamide. These monomers may be used singly or in combination.
Specific examples of the epoxy group-containing elastomer include epoxy group-containing acrylate copolymer elastomers, epoxy group-containing ethylene/vinyl acetate copolymer elastomers, epoxy group-containing ethylene/acrylate copolymer elastomers, epoxy group-containing ethylene/vinyl acetate/acrylate copolymer elastomers, epoxy group-containing ethylene/propylene copolymer elastomers, epoxy group-containing acrylate/acrylonitrile copolymer elastomers, epoxy group-containing butadiene/acrylonitrile copolymer elastomers, epoxy group-containing butadiene/styrene copolymer elastomers, and epoxy group-containing butadiene/acrylonitrile/acrylate copolymer elastomers.
These epoxy group-containing elastomers are vulcanized by using a vulcanization system comprising a polycarboxylic acid having at least 2 carboxyl groups in the molecule and either a quaternary ammonium salt or a quaternary phosphonium salt.
The polycarboxylic acid having at least 2 carboxyl groups in the molecule is usually selected from saturated and unsaturated aliphatic compounds, alicylic compounds, aromatic compounds and low-molecular-weight polymers. The polycarboxylic acid used in this invention also includes a polycarboxylic acid anhydride.
The following are typical examples of carboxyl group-containing compounds which can be used in this invention.
Examples of the aliphatic compounds include malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, azelaic acid, sebacic acid, octanedioic acid, dodecanedioic acid, tridecanedioic acid, tetradecanedioic acid, hexadecanedioic acid, octadecanediocic acid, tartronic acid, methyltartronic acid, methylmalonic acid, ethylmalonic acid, tetramethylsuccinic acid, 2,2'-dimethylsuccinic acid, malic acid, alpha-methylmalic acid, alpha-hydroxyglutaric acid, alpha-hydroxyadipic acid, oxosuccinic acid, 2-oxoadipic acid, acetylmalonic acid, 2-acetylglutaric acid, beta-hydroxyglutaric acid, maleic acid, citraconic acid, glutaconic acid, muconic acid, citric acid, tartaric acid, 1,2,3-propanetricarboxylic acid, 1,2,3-propenetricarboxylic acid, 1,3,5-pentanetricarboxylic acid, cystine, aspartic acid, glutamic acid, beta-hydroxyglutamic acid, iminodiacetic acid, nitrilotriacetic acid and ethylenediaminetetraacetic acid.
Examples of the alicyclic compound include cis-1,3-cyclopentanedicarboxylic acid, cis-1,4-cyclohexanedicarboxylic acid, 1,5-cyclooctanedicarboxylic acid and hexahydroterephthalic acid.
Examples of the aromatic compounds include phthalic acid, 3-methylphthalic acid, terephthalic acid, phthalonic acid, hydroxyterephthalic acid, hemipinic acid, benzophenonedicarboxylic acid, phenylsuccinic acid, trimellitic acid, pyromellitic acid and 7,8-diphenyltetradecanedicarboxylic acid.
Examples of the low-molecular-weight polymers include carboxyl-terminated-liquid polybutadiene, carboxyl-terminated liquid butadiene/acrylonitrile copolymer, and liquid butadiene/acrylonitrile copolymer having carboxyl groups in the molecular chain.
Examples of the polycarboxylic acid anhydride are malonic anhydride, succinic anhydride, glutaric anhydride, maleic anhydride, phthalic anhydride, trimellitic anhydride, pyrophosphoric anhydride, 1,2-cyclohexanedicarboxylic anhydride, and long-chain dibasic acid anhydrides such as octadecyldioic acid condensate. These examples are not limitative, however, and anhydrides of the above-exemplified polycarboxylic acids can all be used in this invention.
For good compression sets and low-temperature properties, aliphatic dicarboxylic acids and the anhydrides thereof are especially preferred among the polycarboxylic acids used in this invention.
The polycarboxylic acid may be added during or after the polymerization reaction for producing the elastomer, or may be added to the elastomer together with other compounding chemicals such as a filler by a kneader normally used in the rubber industry.
The polycarboxylic acid can be used in an amount of usually 0.1 to 30 parts by weight per 100 parts by weight of the epoxy group-containing elastomer. The proportion of the polycarboxylic acid relative to the epoxy group-containing elastomer specified above has been selected in view of the speed of vulcanization and the mechanical properties, compression set, etc. of the vulcanizates. If it is below the specified lower limit, the speed of vulcanization is drasticaly reduced, and a practical vulcanizate cannot be obtained. On the other hand, if it exceeds the specified upper limit, the speed of vulcanization becomes very small, and a practical vulcanizate cannot be obtained. The preferred proportion of the polycarboxylic acid is 0.1 to 20 parts by weight.
The quaternary ammonium salt and the quaternary phosphonium salt used in this invention are compounds represented by the following formula ##STR1##
In the above general formula, Y is a nitrogen or phosphorus atom; R.sub.1 to R.sub.4 each represent a hydrocarbon group having about 1 to 25 carbon atoms such as an alkyl, aryl or alkylaryl group, or two or three of the groups R.sub.1 to R.sub.4 may form together with Y a heterocyclic ring wherein at least two ring atoms are carbon atoms and the remainder are oxygen, nitrogen, phosphorus or sulfur atoms; and X is an anion derived from an inorganic or organic acid in which acidic hydrogen is bonded to halogen or oxygen, preferably Cl, Br, I, HSO.sub.4, H.sub.2 PO.sub.4, R.sub.3 COO, R.sub.5 OSO.sub.3, R.sub.5 SO or R.sub.5 OPO.sub.3 H (R.sub.5 is the same hydrocarbon group as R.sub.1 to R.sub.4).
Specific examples of the quaternary ammonium salt include tetraethyl ammonium bromide, tetrabutyl ammonium chloride, tetrabutyl ammonium bromide, tetrabutyl ammonium iodide, n-dodecyltrimethyl ammonium bromide, cetyldimethylbenzyl ammonium chloride, methylcetyldibenzyl ammonium bromide, cetyldimethylethyl ammonium bromide, octadecyltrimethyl ammonium bromide, cetylpyridinium chloride, cetyl pyridinium bromide, 1,8-diaza-bicyclo(5,4,0)undecene-7-methyl ammonium methosulfate, 1,8-diazabicyclo(5,4,0)undecene-7-benzyl ammonium chloride, cetyltrimethyl ammonium alkylphenoxypoly(ethyleneoxy)ethyl phosphate, cetyl pyridinium sulfate, tetraethyl ammonium acetate, trimethylbenzyl ammonium benzoate, trimethylbenzylammonium p-toluenesulfonate and trimethylbenzyl ammonium borate.
Specific examples of the quaternary phosphonium salts include triphenylbenzyl phosphonium chloride, triphenylbenzyl phosphonium bromide, triphenylbenzyl phosphonium iodide, triphenylmethoxymethyl phosphonium chloride, triethylbenzylphosphonium chloride, tricyclohexylbenzyl phosphonium chloride, trioctylmethyl phosphonium dimethyl phosphate, tetrabutyl phosphonium, bromide, and trioctylmethyl phosphonium acetate.
These quaternary ammonium salts or quaternary phosphonium salts may be used singly or as a mixture of two or more. The amount of the quaternary ammonium or phosphonium salt is usually 0.1 to 10 parts by weight per 100 parts by weight of the epoxy group-containing elastomer. This range has been selected for the high vulcanization speeds and excellent processing stability and storage stability of the vulcanizable composition and the excellent mechanical properties and compression sets of vulcanizates. If it is below the specified lower limit, vulcanization hardly proceeds. On the other hand, if it exceeds the specified upper limit, the speed of vulcaniztion becomes extremely fast, and the processing stability and storage stability of the vulcanizable composition are reduced. The preferred range is 0.1 to 5 parts by weight.
The vulcanizable composition of this invention is prepared by mixing the epoxy group-containing elastomer with the aforesaid vulcanization agent and compounding chemicals normally used in the rubber industry, such as a reinforcing agent, a filler, a plasticizer, a stabilizer, and a processing aid, by an ordinary kneader such as a roll mill or a Banbury mixer. The composition is molded into a desired shape, and then vulcanized to form a final product. The vulcanization is carried out usually at a temperature of at least 120.degree. C., preferably about 150.degree. to 220.degree. C., for about 1 to 60 minutes. Post-vulcanization can be carried out at a temperature of about 150.degree. to 200.degree. C. for about 1 to 24 hours.
The vulcanizable epoxy group-containing elastomer composition of this invention is a novel and efficient composition which has excellent processing safety and storage stability for early vulcanization, and gives vulcanizates having excellent mechanical properties, heat aging resistance and compression sets. It has been thought that vulcanizable epoxy group-containing elastomer compositions require a relatively long period of post-vulcanization in order to obtain a good compression set. With the vulcanizable composition of this invention, however, a good compression set can be obtained even when it is press-cured for a short period of time. Accordingly, the post-vulcanization can be greatly shortened, or omitted.
Since vulcanizates of epoxy group-containing elastomers obtained from the vulcanizable composition of this invention have excellent heat aging resistance, weatherability, water resistance and compression sets, they can find wide applications in various sealing materials (gaskets, O-rings, packings, oil seals), various hoses, diaphragms, and various belts or rolls.
The present invention will be more specifically illustrated by the following Referential Example, Examples and the accompanying drawing.
In these examples, all parts are by weight.

In the accompanying drawings,
FIGS. 1 and 2 show cure curves of the compositions in Example 1 measured by an oscillating disk rheometer;
FIGS. 3 and 4 show cure curves of the compositions in Example 3;
FIG. 5 shows cure curves of the compositions in Example 4; and
FIG. 6 shows cure curves of the compositions in Example 5.

The numerals shown in these figures are run numbers.
REFERENTIAL EXAMPLE
Synthesis of epoxy group-containing elastomers:
In each run, each of the monomeric mixtures indicated in Table 1 was copolymerized in a 2-liter separable flask in accordance with the following polymerization recipes (I) and (II). First, the substances shown in (I) were charged into the flask, and the pH of the mixture in the flask was adjusted to 7. With stirring, the temperature of the mixture was adjusted to 5.degree. C. Deaeration and nitrogen purging were repeated to remove oxygen from the flask sufficiently. Then, the substances shown in (II) were added, and the polymerization was started. The polymerization was terminated in about 10 hours. The polymerization conversion was 97 to 99%. After the polymerization, the polymerization product was salted out, fully washed with water, and dried under reduced pressure to obtain an epoxy group-containing acrylic elastomer.
The Mooney viscosities of the elastomers obtained are also shown in Table 1.
______________________________________Polymerization Recipe (I)Water 1000 gSodium dodecylbenzenesulfonate 20 gSodium naphthalenesulfonate 10 gSodium sulfate 3 gTetrasodium ethylenediamine- 0.2 gtetraacetateFerric sodium ethylenediamine- 0.005 gacetateMonomeric mixture (Table 1) 1000 gPolymerization Recipe (II)Na.sub.2 SO.sub.4 0.2 gSodium formaldehyde sulfoxylate 0.2 gp-Menthane hydroperoxide 0.1 g______________________________________
TABLE 1______________________________________ Acrylic elastomerMonomers (parts) A B C______________________________________Ethyl acrylate 97.5 98 48Butyl acrylate -- -- 30Methoxyethyl -- -- 20acrylateGlycidyl meth- 2.5 -- 2acrylateGlycidyl acrylate -- 2 --Mooney viscosity 48 52 36(ML.sub.1+4, 100.degree. C.)______________________________________
EXAMPLE 1
In each run, 100 parts of the epoxy group-containing acrylic elastomer A, 1 part of stearic acid, 50 parts of MAF carbon black (Seast 116, a trade name for a product of Tokai Carbon Co., Ltd.), and the various vulcanization agents shown in Table 2 in the amounts indicated were kneaded on a 6-inch roll mill to prepare a compound.
TABLE 2__________________________________________________________________________ AmountRun No. Vulcanizing agent (parts)__________________________________________________________________________Invention 1 Succinic acid/Cetyltrimethyl ammonium bromide 0.75/2 2 Glutaric acid/Cetyltrimethyl ammonium bromide 0.85/2 3 Pimelic acid/Cetyltrimethyl ammonium bromide 1.0/2 4 Azelaic acid/Cetyltrimethyl ammonium bromide 1.2/2 5 Tetradecanedioic acid/Cetyltrimethyl ammonium bromide 1.7/2 6 1,3,5-Pentanetricarboxylic acid/Cetyltrimethyl ammonium 0.9/2de 7 7,8-Diphenyltetradecanedioic acid/Cetyltrimethyl ammonium bromide 2.5/2 8 cis-1,4-Cyclohexanedicarboxylic acid/Cetyltrimethyl ammonium bromide 1.1/2 9 Phthalic acid/Cetyltrimethyl ammonium bromide 1.0/2 10 C-1000 (*1)/Cetyltrimethyl ammonium bromide 10/3 11 CTBN (*2)/Cetyltrimethyl ammonium bromide 12/3 12 DN-601 (*3)/Cetyltrimethyl ammonium bromide 10/3 13 Phthalic anhydride/Cetyltrimethyl ammonium bromide 0.9/2 14 SL-2OAH (*4)/Cetyltrimethyl ammonium bromide 2.6/2 15 SL-2PAH (*5)/Cetyltrimethyl ammonium bromide 2.6/2Comparison 16 2-Methylimidazole/hexahydrophthalic anhydride 0.2/1.0 17 Ammonium benzoate 1.3__________________________________________________________________________ (*1): Carboxylterminated liquid polybutadiene (NISSO PB C1000, a product of Nippon Soda Co., Ltd.). (*2): Carboxylterminated liquid butadiene/acrylonitrile copolymer (Hycar CTBN, a product of B. F. Goodrich Co., Ltd.). (*3): Liquid butadiene/acrylonitrile copolymer containing carboxyl groups in the molecular chain (Nipol DN601, a product of Nippon Zeon Co., Ltd.). (*4): Octadecyldioic acid condensate (acid anhydride) (a product of Okamura Seiyu K.K.). (*5): 7,8diphenyl-tetradecanedicarboxylic acid condensate (acid anhydride (a product of Okamura Seiyu K.K.).
The Mooney scorch time was measured on the resulting compound, and then it was press-cured at 170.degree. C. for 20 minutes. Thereafter, it was post-cured in a Geer's oven at 150.degree. C. for 16 hours. The various properties of the cured products were measured in accordance with JIS K-6301. To judge the storage stability of the compound, its Mooney scorch time on standing for 2 weeks at room temperature was also measured. The results are shown in Table 3. FIGS. 1 and 2 show cure curves of the compounds measured by an Oscillating Disc Rheometer (made by Toyo Seiki K.K.; to be abbreviated as ODR hereinafter) at 170.degree. C.
TABLE 3__________________________________________________________________________ Run No. Com- Invention parisonTest Item 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17__________________________________________________________________________Mooney scorch time (125.degree. C.)t.sub.5 (minutes) 16 18 13 14 16 36 19 17 28 12 13 11 12 13 14 12 8t.sub.35 (minutes) 36 41 34 36 43 125 63 40 -- 26 30 23 33 38 39 22 17Minimum viscosity 46 50 50 51 46 44 45 47 43 40 36 38 51 48 47 47 52Mooney scorch time (125.degree. C.) after standing for 2 weeks at roomtemperaturet.sub.5 (minutes) 17 19 14 14 17 38 20 19 30 13 15 13 18 15 15 8 7t.sub.35 (minutes) 39 44 37 35 45 -- 66 45 -- 28 37 25 46 42 45 16 14Minimum viscosity 47 50 51 52 47 45 46 50 43 41 36 38 49 47 46 56 53Properties after press-curing at 170.degree. C. for 20 minutesTensile strength 112 114 117 115 114 119 116 113 83 121 106 105 111 120 119 113 107(kg/cm.sup.2)Elongation (%) 340 320 310 320 330 280 330 310 540 300 470 400 380 290 320 280 360100% Tensile stress 42 46 47 45 46 55 41 45 21 38 23 33 36 51 50 49 36(kg/cm.sup.2)Hardness (JIS) 68 68 69 68 69 68 67 68 63 62 56 59 67 71 70 69 68Properties after post-vulcanization at 150.degree. C. for 16 hoursTensile strength 135 140 143 145 142 148 149 138 128 153 144 146 135 133 136 159 138(kg/cm.sup.2)Elongation (%) 220 210 210 220 220 170 230 220 260 160 170 180 230 200 210 150 270100% Tensile stress 71 78 72 71 70 95 73 74 64 81 67 74 74 71 72 113 54(kg/cm.sup.2)Hardness (JIS) 69 70 71 70 70 72 68 71 69 72 67 69 72 72 71 77 73Properties after heat-aging at 175.degree. C. for 70 hours (vulcanizateobtained by press curing at 170.degree. C. for 20 minutes)Tensile strength 148 152 156 157 150 153 151 151 153 149 151 149 151 147 141(kg/cm.sup.2)Elongation (%) 130 120 120 120 130 110 140 110 110 100 120 130 130 110 150Hardness (JIS) 76 77 76 75 76 78 75 77 79 79 76 76 76 81 79Compression set (150.degree. C. .times. 70 hours; 25% compression)Vulcanizate obtained 41 34 36 38 34 40 35 34 59 53 61 60 49 35 34 69 78by press-curing at170.degree. C. for 20 min. (%)Vulcanizate obtained 28 22 26 24 21 31 23 22 40 37 39 39 28 22 21 63 52by post-curing at150.degree. C. for 16 hours (%)__________________________________________________________________________
These results show that the vulcanization systems in accordance with this invention have better scorch stability and vulcanization snappy property (the behavior whereby in a cure curve, the torque rises within a short time after vulcanization begins, and reaches a plateau value) than the vulcanization systems used heretofore (Comparative Examples 16 and 17). Even after standing for 2 weeks at room temperature, the compound shows a vulcanization behavior not much different from that of the compound immediately after preparation, and therefore, it has excellent storage stability. The conventional vulcanization systems give poor compression sets upon press curing at 170.degree. C. for 20 minutes, and a good compression set cannot be obtained unless post-curing is performed for a long period of time. In contrast, the vulcanization systems in accordance with this invention give good compression set values even by press curing at 170.degree. C. for as short as 20 minutes. This can allow omission of post-curing.
EXAMPLE 2
In each run, 100 parts of each of the epoxy group-containing acrylic elastomers shown in Table 4, 1 part of stearic acid, 50 parts of MAF carbon black and each of the vulcanization agents shown in Table 4 in the amounts indicated were kneaded on a 6-inch roll mill to prepare a compound.
TABLE 4______________________________________ AmountsRun Elastomer Vulcanization agents (parts)______________________________________21 B Tetradecanedioic acid/ 1.7/2 Cetyltrimethyl ammonium bromide22 C Tetradecanedioic acid/ 1.7/2 Cetyltrimethyl ammonium bromide23 C 2-Methylimidazole/ 0.2/1 Hexahydrophthalic anhydride______________________________________
Runs Nos. 21 and 22 are within the scope of the invention, and Run 23 is a comparison.
The compound was press-cured at 170.degree. C. for 20 minutes, and then post-cured in Geer's oven at 150.degree. C. for 16 hours. The properties of the cured product were measured in the same way as in Example 1, and the results are shown in Table 5.
TABLE 5______________________________________ Run No. Com- Invention parisonTest Item 21 22 23______________________________________Properties after press-curing at 170.degree. C. for 20 minutesTensile strength (kg/cm.sup.2) 112 101 83Elongation (%) 370 280 320100% Tensile stress (kg/cm.sup.2) 35 29 24Hardness (JIS) 68 63 65Properties after post-curing at 150.degree. C. for 16 hoursTensile strength (kg/cm.sup.2) 138 121 132Elongation (%) 240 180 180100% Tensile stress (kg/cm.sup.2) 57 45 80Hardness (JIS) 69 66 73Compression set (150.degree. C. .times. 70 hours; 25% compressionVulcanizate obtained 38 41 78by press-curing at 170.degree. C.for 20 minutes (%)Vulcanizate obtained 26 23 42by post-curing at 150.degree. C.for 16 hours (%)______________________________________
EXAMPLE 3
One hundred parts of the epoxy group-containing acrylic elastomer, 1 part of stearic acid, 50 parts of MAF carbon black and each of the vulcanization agents indicated in Table 6 in the amounts indicated were kneaded on a 6-inch roll mill to prepare a compound. The compound was press-cured at 170.degree. C. for 20 minutes, and then post-cured in a Geer's oven at 150.degree. C. for 16 hours. The properties of the cured product were measured in the same way as in Example 1. The results are shown in Table 7. The cure curves of the compositions at 170.degree. C. were measured by ODR, and are shown in FIGS. 3 and 4.
TABLE 6__________________________________________________________________________ AmountRun No. Vulcanization agent (parts)__________________________________________________________________________Invention 31 Cetyl pyridinium bromide/Tetradecanedioic acid 1/1.7 32 " 2/1.7 33 " 4/1.7 34 " 2/5Comparison 35 " 2/0 36 " 0/1.7Invention 37 Cetyltrimethyl ammonium iodide/Tetradecanedioic 1.5/1.7 38 Triphenylbenzyl phosphonium chloride/Tetradecanedioic 3/1.7 39 Tetrabutyl phosphonium bromide/Tetradecanedioic 1.5/1.7 40 Triphenylbenzyl phosphonium iodide/Tetradecanedioic 1.5/1.7__________________________________________________________________________
TABLE 7__________________________________________________________________________ Run No. Invention Comparison InventionTest Item 31 32 33 34 35 36 37 38 39 40__________________________________________________________________________Properties after press-curing at 170.degree. C. for 20 minutesTensile strength (kg/cm.sup.2) 91 113 110 73 Vulcanization Vulcanization 122 93 118 120Elongation (%) 430 350 360 630 insufficient* insufficient* 290 450 320 290100% Tensile stress (kg/cm.sup.2) 23 40 38 21 52 25 40 45Hardness (JIS) 64 68 67 59 69 65 64 68Properties after post-curing at 150.degree. C. for 16 hoursTensile strength (kg/cm.sup.2) 149 140 137 115 146 141 137 146Elongation (%) 220 230 220 350 200 250 190 180100% Tensile stress (kg/cm.sup.2) 72 67 67 32 82 59 80 83Hardness (JIS) 70 69 67 65 71 69 71 72Properties after heat-aging at 175.degree. C. for 70 hours (vulcanizateobtainedby press-curing at 170.degree. C. for 20 minutes)Tensile strength (kg/cm.sup.2) 152 147 148 144 152 137 142 154Elongation (%) 140 140 130 120 130 210 130 120Hardness (JIS) 76 75 74 78 76 74 76 76Compression set (150.degree. C. .times. 70 hours; 25% compression)Vulcanizate obtained 82 35 37 78 34 61 39 37by press-curing at 170.degree. C.for 20 minutes (%)Vulcanizate obtained 25 23 27 45 20 26 29 28by post-curing at 150.degree. C.for 16 hours (%)__________________________________________________________________________ *Since the compounds were not practical, vulcanizate were not prepared from them.
These results demonstrate that the increasing of the amount of the quaternary ammonium salt increases the speed of curing; the addition of an excessive amount of the polycarboxylic acid retards the speed of vulcanization and impairs the various properties of the resulting vulcanizate; and that if either one of the quaternary ammonium salt or the polycarboxylic acid is lacking (Comparative Runs Nos. 35 and 36), the degree of vulcanization did not rise, and the compositions were not practical.
It is also seen that the various quaternary ammonium salts and quaternary phosphonium salts can be used as the vulcanization system in accordance with this invention, and they are excellent in regard to vulcanization snappy property, vulcanizate properties and compression set.
EXAMPLE 4
One hundred parts of an ethylene/vinyl acetate/butyl acrylate/glycidyl methacrylate four-component copolymer synthesized by a known polymerization method [the composition (% by weight) determined from chemical shifts in .sup.13 C-NMR was 18 ethylene, 39 vinyl aceteate, 42 butyl acrylate and 1 glycidyl methacrylate], 1 part of stearic acid, 50 parts of MAF carbon black, and each of the vulcanization agents shown in Table 8 in the amounts indicated were kneaded on a 6-inch roll mill to prepare a compound.
The Mooney scorch time of the compound was measured, and it was cured in the same way as in Example 1. The various properties of the vulcanizate were measured.
The results are shown in Table 9. The cure curves of the compositions at 170.degree. C. measured by ODR are shown in FIG. 5.
TABLE 8______________________________________ AmountRun No. Vulcanization agent (parts)______________________________________41 Cetyltrimethyl ammonium 1/1.5 bromide/Tetradecanedioic acid42 Tetrabutyl phosphonium 1.5/1.5 bromide/Tetradecanedioic acid43 2-Methylimidazole/Hexahydro- 0.2/0.5 phthalic anhydride______________________________________
Runs Nos. 41 and 42 are within the scope of the invention, and Run No. 43 is a comparison.
TABLE 9______________________________________ Run No. Com- Invention parisonTest Item 41 42 43______________________________________Mooney scorch time (125.degree. C.)t5 (minutes) 19 13 12t35 (minutes) 36 23 27Minimum viscosity 45 47 46Properties after press-curing at 170.degree. C. for 20 minutesTensile strength (kg/cm.sup.2) 118 113 100Elongation (%) 450 320 430100% Tensile stress (kg/cm.sup.2) 33 37 30Hardness (JIS) 68 64 68Properties after post-curing at 150.degree. C. for 16 hoursTensile strength (kg/cm.sup.2) 141 135 138Elongation (%) 320 190 250100% Tensile stress (kg/cm.sup.2) 45 80 55Hardness (JIS) 71 70 72Permanent compression set (150.degree. C. .times. 70 hours,25% compression)Tensile strength (kg/cm.sup.2) 147 144 146Elongation (%) 230 120 190100% Tensile stress (kg/cm.sup.2) 61 96 73Hardness (JIS) 75 76 76Compression set (150.degree. C. .times. 70 hours, 25% compressionVulcanizate obtained 39 42 68by press-curing at 170.degree. C.for 20 minutes (%)Vulcanizate obtained 23 32 36by post-curing at 150.degree. C.for 16 hours (%)______________________________________
EXAMPLE 5
One hundred parts of a butadiene/acrylonitrile/glycidyl methacrylate terpolymer elastomer synthesized by a known polymerization method (composition by weight percent: butadiene 65, acrylonitrile 33, glycidyl methacrylate 2), 1 part of stearic acid, 40 parts of MAF carbon black, and each of the vulcanization agents shown in Table 10 in the amounts indicated were kneaded on a 6-inch roll to prepare a compound. The compound was press-cured at 160.degree. C. for 20 minutes, and the properties of the vulcanizate were measured in the same way as in Example 1.
The results are shown in Table 11. The cure curves of the compounds at 170.degree. C. measured by ODR are shown in FIG. 6.
TABLE 10______________________________________ AmountRun No. Vulcanization agent (parts)______________________________________51 Cetyltrimethyl ammonium 2/2.2 bromide/Tetradecanedioic acid52 Tetrabutyl phosphonium 1.5/2.2 bromide/Tetradecanedioic acid______________________________________
TABLE 11______________________________________ Run No. InventionTest item 51 52______________________________________Properties after press curing at 160.degree. C. for 20 min.Tensile strength (kg/cm.sup.2) 143 142Elongation (%) 340 360100% Tensile stress (kg/cm.sup.2) 45 42Hardness (JIS) 69 68Compression set (120.degree. C. .times. 70 hours, 25% compression)Vulcanizate obtained by press 12 13curing at 60.degree. C. for 20 min. (%)______________________________________

Vulcanizable epoxy group-containing elastomer composition

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (1)

US Referenced Citations (1)