Patent Application
20220363793
The present invention relates to an acrylic rubber, a crosslinkable rubber composition and cured rubber products.
Acrylic rubber is known as a rubber material having excellent heat and oil resistance, and a cured product obtained by curing a rubber composition containing acrylic rubber is suitably used for various applications such as automotive parts (for example, Patent Documents 1 and 2).
[Patent Document 1] Japanese Unexamined Patent Application Publication No. 2002-265737
[Patent Document 2] Japanese Unexamined Patent Application Publication No. 2010-70713
In recent years, further heat resistance has been required for automotive rubber member due to exhaust gas regulation measures, higher engine output, and the like. In particular, there is a need for a rubber material that can maintain its properties even when held in a high temperature environment for a long time.
An object of the present invention is to provide a cured rubber product that can maintain a high tensile strength even when held in a high temperature environment for a long time. Another object of the present invention is to provide an acrylic rubber that can realize the cured rubber product described above, and a crosslinked rubber composition containing the acrylic rubber.
An aspect of the present invention relates to an acrylic rubber comprising: an alkyl acrylate unit; a crosslinking monomer unit; a unit of a bifunctional monomer represented by the following formula (A-1):
wherein n represents 1 to 9, R1 represents a hydrogen atom or a methyl group, and R2 represents an alkanediyl group having 2 to 4 carbon atoms; and an ethylene unit, wherein the acrylic rubber has a toluene insoluble content of 4 to 40% by mass.
In an aspect, the alkyl acrylate unit may comprise a first alkyl acrylate unit having an alkyl group having 1 to 3 carbon atoms and a second alkyl acrylate unit having an alkyl group having 4 to 8 carbon atoms.
In an aspect, a content of the first alkyl acrylate unit may be 60 to 95% by mass and a content of the second alkyl acrylate may be 5 to 40% by mass, based on the total amount of the alkyl acrylate unit.
In an aspect, a content of the unit of the bifunctional monomer may be 0.1 to 5 parts by mass with respect to 100 parts by mass of the alkyl acrylate unit.
In an aspect, a content of the crosslinking monomer unit may 0.5 to 10 parts by mass with respect to 100 parts by mass of the alkyl acrylate unit.
In an aspect, a content of the ethylene unit is 0.1 to 10 parts by mass with respect to 100 parts by mass of the alkyl acrylate unit.
Another aspect of the present invention relates to a crosslinkable rubber composition comprising: the above acrylic rubber; a crosslinking agent; and a filler.
In an aspect, the filler may comprise a carbon black.
Another aspect of the present invention relates to a cured rubber product that is a cured product of the above crosslinkable rubber composition.
The present also relates to a hose member, a seal member and a vibration-proofing rubber member which comprise the above cured rubber product.
According to the present invention, a cured rubber product that can maintain a high tensile strength even when held in a high temperature environment for a long time can be provided. In addition, according to the present invention, an acrylic rubber that can realize the cured rubber product described above, and a crosslinked rubber composition containing the acrylic rubber can be provided.
Embodiments of the present invention will be described in detail.
The acrylic rubber according to the present embodiment contain an alkyl acrylate unit, a crosslinking monomer unit, a unit of a bifunctional monomer represented by the following formula (A-1) (hereinafter also referred to as “bifunctional monomer unit”), and an ethylene unit.
In the formula (A-1), n represents 1 to 9, R1 represents a hydrogen atom or a methyl group, and R2 represents an alkanediyl group having 2 to 4 carbon atoms.
The acrylic rubber according to the present embodiment has a structural unit derived from the bifunctional monomer in which two (meth)acryloyl groups are bonded by the specific linking chain. Since the bifunctional monomer forms a specific crosslinked structure containing a polyether chain having high mobility in the acrylic rubber, the acrylic rubber according to the present embodiment can realize a cured rubber product that can maintain a high tensile strength even when held in a high temperature environment for a long time.
The alkyl acrylate unit is a structural unit derived from an alkyl acrylate. The alkyl acrylate may be, for example, an alkyl acrylate having an alkyl group having 1 to 12 carbon atoms, and is preferably an alkyl acrylate having an alkyl group having 1 to 8 carbon atoms.
The alkyl acrylate unit may contain a structural unit derived from a first alkyl acrylate having an alkyl group having 1 to 3 carbon atoms (first alkyl acrylate unit), and a structural unit derived from a second alkyl acrylate having an alkyl group having 4 to 8 carbon atoms (second alkyl acrylate unit).
Examples of the first alkyl acrylate include methyl acrylate, ethyl acrylate, n-propyl acrylate, isopropyl acrylate and the like.
Examples of the second alkyl acrylate include n-butyl acrylate, isobutyl acrylate, n-pentyl acrylate, isoamyl acrylate, n-hexyl acrylate, 2-methylpentyl acrylate, n-octyl acrylate, 2-ethylhexyl acrylate and the like.
The content of the first alkyl acrylate unit is preferably 60% by mass or more, more preferably 70% by mass or more, and still more preferably 80% by mass or more, based on the total amount of the alkyl acrylate unit. This further improves the oil resistance of the cured rubber product. The content of the first alkyl acrylate unit is preferably 95% by mass or less, more preferably 93% by mass or less, and still more preferably 90% by mass or less, based on the total amount of the alkyl acrylate unit. This improves the cold resistance of the cured rubber product.
The content of the second alkyl acrylate unit is preferably 5% by mass or more, more preferably 7% by mass or more, and still more preferably 10% by mass or more, based on the total amount of the alkyl acrylate unit. This improves the cold resistance of the cured rubber product. The content of the second alkyl acrylate unit is preferably 40% by mass or less, more preferably 30% by mass or less, and still more preferably 20% by mass or less, based on the total amount of the alkyl acrylate unit. This further improves the oil resistance of the cured rubber product.
The content of alkyl acrylate unit in the acrylic rubber may be, for example, 80% by mass or more, preferably 90% by mass or more, and more preferably 93% by mass or more, based on the total amount of the acrylic rubber. The content of the alkyl acrylate unit in the acrylic rubber may be, for example, 99% by mass or less, preferably 97% by mass or less, and more preferably 95% by mass or less, based on the total amount of the acrylic rubber.
The crosslinking monomer unit is a structural unit derived from a crosslinking monomer. The crosslinking monomer means a monomer having a functional group forming a crosslinking site (crosslinking point). Examples of the functional group forming the crosslinking site include a halogeno group, an epoxy group, and a carboxyl group.
Examples of the crosslinking monomer having a halogeno group include 2-chloroethyl vinyl ether, 2-chloroethyl acrylate, vinyl benzyl chloride, vinyl chloroacetate, allyl chloroacetate and the like.
Examples of the crosslinking monomer having an epoxy group include glycidyl acrylate, glycidyl methacrylate, allyl glycidyl ether, and metaallyl glycidyl ether.
Examples of the crosslinking monomer having a carboxyl group include acrylic acid, methacrylic acid, crotonic acid, 2-pentenoic acid, maleic acid, fumaric acid, itaconic acid, butenedioic acid monobutyl ester, cinnamic acid and the like.
The content of the crosslinking monomer unit may be, for example, 0.3 parts by mass or more, preferably 0.5 parts by mass or more, more preferably 1.0 parts by mass or more, and still more preferably 1.5 parts by mass or more, with respect to 100 parts by mass of the alkyl acrylate unit. This tends to improve the tensile strength of the cured rubber product. The content of the crosslinking monomer unit may be, for example, 15 parts by mass or less, preferably 10 parts by mass or less, more preferably 5 parts by mass or less, and still more preferably 3 parts by mass or less, with respect to 100 parts by mass of the alkyl acrylate unit. This tends to make the cured rubber product more resilient to rubber.
The bifunctional monomer unit is a structural unit derived from a bifunctional monomer represented by the following formula (A-1).
n is an integer of 1 to 9. From the viewpoint of further suppressing a decrease in elongation when held under a high temperature environment for a long time, n is preferably an integer of 1 to 6, and more preferably an integer of 1 to 4.
R1 represents a hydrogen atom or a methyl group, preferably a methyl group.
R2 represents an alkanediyl group having 2 to 4 carbon atoms, and preferably an alkanediyl group having 2 to 3 carbon atoms. Examples of the alkanediyl group include an ethylene group, a 1,2-propanediyl group, a 1,3-propanediyl group, and the like. R2 is preferably an ethylene group or a 1,2-propanediyl group.
The content of the bifunctional monomer unit may be, for example, 0.05 parts by mass or more, preferably 0.1 parts by mass or more, more preferably 0.5 parts by mass or more, and still more preferably 0.7 parts by mass or more, with respect to 100 parts by mass of the alkyl acrylate unit. This tends to result in a shorter scorch time of the crosslinkable rubber composition. The content of the bifunctional monomer unit may be, for example, 10 parts by mass or less, preferably 5 parts by mass or less, more preferably 3 parts by mass or less, and still more preferably 2.5 parts by mass or less, with respect to 100 parts by mass of the alkyl acrylate unit. This tends to maintain good elongation characteristics even when held in a high temperature environment for a long time.
The ethylene unit is a structural unit derived from ethylene. Since the acrylic rubber contains ethylene units, the cold resistance of cured rubber products is improved.
The content of the ethylene unit may be, for example, 0.1 parts by mass or more, preferably 0.5 parts by mass or more, and more preferably 1.0 parts by mass or more, with respect to 100 parts by mass of the alkyl acrylate unit. This improves the cold resistance of the cured rubber product. The content of the ethylene unit may be, for example, 10 parts by mass or less, preferably 8 parts by mass or less, and more preferably 5 parts by mass or less, with respect to 100 parts by mass of the alkyl acrylate unit. This further improves the oil resistance of the cured rubber product.
The acrylic rubber may further contain a structural unit derived from a monomer other than the above-mentioned monomers. Other monomers include, for example, alkyl vinyl ketones such as methyl vinyl ketone; vinyl ethers such as vinyl ethyl ether; allyl ethers such as allyl methyl ether; vinyl aromatic compounds such as styrene, a-methyl styrene, chlorostyrene, vinyl toluene, vinyl naphthalene; vinyl nitriles such as acrylonitrile, methacrylonitrile; and ethylenically unsaturated compounds such as acrylamide, propylene, butadiene, isoprene, pentadiene, vinyl acetate, vinyl chloride, vinylidene chloride, vinyl fluoride, vinylidene fluoride, ethylene, vinyl propionate and the like.
The content of the other monomer units may be 10 parts by mass or less, preferably 5 parts by mass or less, more preferably 1 parts by mass or less, and may be 0 parts by mass (that is, acrylic rubber may not contain other monomer units), with respect to 100 parts by mass of the alkyl acrylate unit.
The total content of the alkyl acrylate unit, the crosslinking monomer unit, the bifunctional monomer unit and the ethylene unit may be, for example, 80% by mass or more, 85% by mass or more, 90% by mass or more, 95% by mass or more, or 99% by mass or more, based the total amount of the acrylic rubber, and may be 100% by mass or more (that is, the acrylic rubber may consist of the above-mentioned units).
The toluene insoluble content of the acrylic rubber may be, for example, 4% by mass or more, preferably 10% by mass or more, and more preferably 20% by mass or more. When the toluene insoluble content is less than 4% by mass, the heat resistance improvement effect of the bifunctional monomer may not be sufficiently obtained. The toluene insoluble content of the acrylic rubber may be, for example, 40% by mass or less, preferably 38% by mass or less, and more preferably 35% by mass or less. When the toluene insoluble content exceeds 40% by mass, the extrusion processability of the acrylic rubber tends to deteriorate. The toluene insoluble content is calculated from the following equation:
toluene insoluble content (% by mass)=(x/0.2)×100
wherein x (g) is the dried solid content (toluene insoluble content) which is weighed by immersing 0.2 g of the acrylic rubber in toluene in 100 ml, leaving it at 23° C. for 24 hours, filtering it using a 200 mesh wire netting, and drying the filter cake at 120° C. for 1 hour.
The acrylic rubber can be obtained by polymerizing a monomer corresponding to each of the above-mentioned monomer units. The polymerization method and conditions are not particularly limited, and a known method may be appropriately selected. For example, the acrylic rubber may be obtained by copolymerizing the above-mentioned monomers by a known method such as a emulsion polymerization, a suspension polymerization, a solution polymerization, and a bulk polymerization.
The crosslinkable rubber composition according to this embodiment contains the above-described acrylic rubber, a crosslinking agent, and a filler.
The crosslinking agent may be any crosslinking agent capable of crosslinking the acrylic rubber. As the crosslinking agent, a known crosslinking agent capable of crosslinking by using the functional group of the crosslinking monomer unit as a crosslinking point can be used without any particular limitation.
For example, when a monomer having a carboxyl group is used as the crosslinking monomer, a polyamine compound (more preferably a crosslinking system to which a guanidine compound is added) is preferably used as the crosslinking agent. When a monomer having an epoxy group is used as the crosslinking monomer, an imidazole compound is preferably used as the crosslinking agent.
Examples of the polyamine compound include aromatic polyamine compounds such as 4,4′-bis(4-aminophenoxy) biphenyl, 4,4′-diaminodiphenyl sulfide, 1,3-bis(4-aminophenoxy)-2,2-dimethylpropane, 1,3-bis(4-aminophenoxy) benzene, 1,4-bis(4-aminophenoxy) benzene, 1,4-bis(4-aminophenoxy) pentane, 2,2-bis[4-(4-aminophenoxy)phenyl] propane, 2,2-bis[4-(4-aminophenoxy)phenyl] sulfone, 4,4′-diaminodiphenyl sulfone, bis(4-3-aminophenoxy) phenyl sulfone, 2,2-bis[4-(4-aminophenoxy) phenyl] hexafluoropropane, 3,4′-diaminodiphenyl ether, 4,4′-diaminodiphenyl ether, 4,4′-diaminobenzanilide, bis[4-(4-aminophenoxy) phenyl] sulfone, and the like; aliphatic polyamine compounds such as hexamethylenediamine, hexamethylenediamine carbamate, N,N′-dicinnamylidene-1,6-hexanediamine, diethylenetriamine, triethylenetetramine, tetraethylenepentamine, and the like.
Examples of the guanidine compound include guanidine, tetramethylguanidine, dibutylguanidine, diphenylguanidine, di-o-tolylguanidine, and the like.
Examples of the imidazole compounds include 1-methylimidazole, 1,2-dimethylimidazole, 1-methyl-2-ethylimidazole, 1-benzyl-2-methylimidazole, 1-benzyl-2-ethylimidazole, 1-benzyl-2-ethyl-5-methylimidazole, 1-benzyl-2-phenylimidazole, 1-benzyl-2-phenylimidazole trimellitic acid salt, 1-aminoethylimidazole, 1-aminoethyl-2-methylimidazole, 1-aminoethyl-2-ethylimidazole, 1-cyanoethyl-2-methylimidazole, 1-cyanoethyl-2-phenylimidazole, 1-cyanoethyl-2-ethyl-4-methylimidazole, 1-cyanoethyl-2-undecylimidazole, 1-cyanoethyl-2-methylimidazole trimellitate, 1-cyanoethyl-2-phenylimidazole trimellitate, 1-cyanoethyl-2-ethyl-4-methylimidazole trimellitate, 1-cyanoethyl-2-undecyl-imidazole trimellitate, 2,4-diamino-6-[2′-methylimidazolyl-(1)′] ethyl-s-triazine isocyanuric acid adduct, 1-cyanoethyl-2-phenyl-4,5-di-(cyanoethoxy methyl) imidazole, N-(2-methyl imidazolyl-1-ethyl) urea, N,N′-bis-(2-methyl imidazolyl-1-ethyl) urea, 1-(cyanoethyl aminoethyl)-2-methyl imidazole, N,N′-[2-methyl imidazolyl-(1)-ethyl]-adipoyl diamide, N,N′-[2-methyl imidazolyl-(1)-ethyl]-dodecane dioyl diamide, N,N′-[2-methyl imidazolyl-(1)-ethyl]-eicosane dioyl diamide, 2,4-diamino-6-[2′-methyl imidazolyl-(1)′]-ethyl-s-triazine, 2,4-diamino-6-[2′-undecyl imidazolyl-(1)′]-ethyl-s-triazine, 1-dodecyl-2-methyl-3-benzyl imidazolium chloride, 1,3-dibenzyl-2-methyl imidazolium chloride, and the like.
The content of the crosslinking agent may be, for example, 0.1 parts by mass or more, preferably 0.2 parts by mass or more, and more preferably 0.3 parts by mass or more, with respect to 100 parts by mass of the acrylic rubber. This tends to increase the crosslinking density and further improve the tensile strength of the cured rubber product. The content of the crosslinking agent may be, for example, 10 parts by mass or less, preferably 5 parts by mass or less, and more preferably 1 part by mass or less, with respect to 100 parts by mass of the acrylic rubber. This tends to improve the elongation at break of the cured rubber product.
The filler may have a function as a reinforcing material, for example. Examples of the filler include a carbon black, a silica, a clay, a talc and calcium carbonate. The filler is preferably a carbon black. Examples of the carbon black include an acetylene black, a ketchen black, a thermal black, a channel black, a furnace black, a lamp black, a graphitized carbon black, and the like.
The filler content may be, for example, 20 parts by mass or more, preferably 30 parts by mass or more, and more preferably 40 parts by mass or more, with respect to 100 parts by mass of the acrylic rubber. This tends to further improve the tensile strength and hardness of the cured rubber product. The content of carbon black may be, for example, 100 parts by mass or less, preferably 80 parts by mass or less, and more preferably 60 parts by mass or less, with respect to 100 parts by mass of the acrylic rubber. This tends to further improve the elongation at break and heat resistance of the cured rubber product.
The crosslinkable rubber composition may further contain other components than those described above. Examples of other components include, for example, lubricants, crosslinking accelerators, anti-aging agents, plasticizers, stabilizers, silane coupling agents, and the like.
Examples of the lubricant include a liquid paraffin, stearic acid, stearylamine, a process oil and the like.
The content of the lubricant maybe, for example, 0.1 parts by mass or more, preferably 0.3 parts by mass or more, and more preferably 0.5 parts by mass or more, with respect to 100 parts by mass of the acrylic rubber. As a result, the crosslinkable rubber composition tends to be easily released from a molding machine, a mold, or the like. The content of the lubricant may be, for example, 10 parts by mass or less, preferably 5 parts by mass or less, and more preferably 3 parts by mass or less, with respect to 100 parts by mass of the acrylic rubber. This tends to improve the oil resistance and heat resistance of cured rubber products.
As the crosslinking accelerator, a known crosslinking accelerator can be appropriately selected according to the type of the crosslinking agent and the like. As the crosslinking accelerator, for example, a curing agent for an epoxy resin may be used. Examples of the crosslinking accelerator include pyrolyzed ammonium salts, organic acids, acid anhydrides, amines, sulfur, sulfur compounds and the like.
The content of the crosslinking accelerator may be, for example, 0.4 parts by mass or more, preferably 0.5 parts by mass or more, and more preferably 0.6 parts by mass or more, with respect to 100 parts by mass of the acrylic rubber. This tends to reduce the scorch time of the crosslinkable rubber composition. The content of the crosslinking accelerator may be, for example, 5 parts by mass or less, preferably 4 parts by mass or less, and more preferably 3 parts by mass or less, with respect to 100 parts by mass of the acrylic rubber. This tends to reduce the bridging torque at the same time.
As the anti-aging agent, a known anti-aging agent blended in an acrylic rubber-based rubber composition can be appropriately selected and used. Examples of the anti-aging agent include an amine-based anti-aging agent, an imidazole-based anti-aging agent, a carbamic acid metal salt, a phenol-based anti-aging agent, a wax, and the like.
The content of the anti-aging agent may be, for example, 0.1 parts by mass or more, preferably 0.3 parts by mass or more, and more preferably 0.5 parts by mass or more, with respect to 100 parts by mass of the acrylic rubber. This tends to improve the heat resistance. The content of the anti-aging agent may be, for example, 20 parts by mass or less, preferably 10 parts by mass or less, and more preferably 5 parts by mass or less, with respect to 100 parts by mass of the acrylic rubber. This tends to improve oil resistance.
The cured rubber product according to the present embodiment can be obtained by heat-curing the crosslinkable rubber composition described above.
The curing conditions of the crosslinkable rubber composition are not particularly limited. The curing temperature may be, for example, 150 to 200° C., and preferably 170 to 190° C. The curing time may be, for example, 5 minutes to 1 hour, and preferably 10 minutes to 30 minutes.
The cured rubber product according to the present embodiment maintains the high tensile strength even when held in a high temperature (for example, 175° C.) for a long time (for example, 500 hours or more). Therefore, the cured rubber product according to the present embodiment can be preferably used as a rubber member exposed to a high temperature for a long time.
The cured rubber product according to the present embodiment can be suitably used for applications such as, for example, a hose member; a seal member such as a gasket and a packing; and a vibration-proofing member.
Examples of the hose member include a transmission oil cooler hose for automobiles, construction machines, hydraulic equipment or the like, an engine oil cooler hose, an air duct hose, a turbo intercooler hose, a hot air hose, a radiator hose, a power steering hose, a fuel system hose, a drain system hose, and the like.
The hose member may be a single-layer hose composed of the cured rubber product, and may be a multi-layer hose in which a layer composed of the cured rubber product is combined with an inner layer, an intermediate layer, or an outer layer which is composed of, for example, a fluororubber, a fluorine-modified acrylic rubber, a hydrin rubber, a nitrile rubber, a hydrogenated nitrile rubber, a chloroprene rubber, an ethylene-propylene rubber, a silicone rubber, a chlorosulfonated polyethylene rubber or the like. As is commonly practiced, the hose member may have reinforcing threads or wires provided in the intermediate or outermost layer of the rubber hose.
Examples of the seal member include an engine head cover gasket, an oil pan gasket, an oil seal, lip seal packing, an 0-ring, a transmission seal gasket, a crankshaft, a camshaft seal gasket, a valve stem, a power steering seal belt cover seal, a boot material for a constant-velocity joint, a rack-and-pinion boot material and the like.
Examples of the vibration-proofing rubber member include a damper pulley, a center support cushion, a suspension bush and the like.
Embodiments of the present invention are described above, but the present invention is not limited to the above-described embodiments.
Hereinafter, the present invention will be described in more detail with reference to examples, but the present invention is not limited to these examples.
An acrylic rubber was produced by the following method.
17 kg of an aqueous solution of a partially saponified polyvinyl alcohol (concentration: 4% by mass) and 22 g of sodium acetate were charged into a pressure-resistant reactor having an internal volume of 40 liters, and thoroughly mixed with a stirrer in advance to prepare a uniform slurry. After air in the upper part of the reactor was replaced with nitrogen, ethylene was injected into the upper part of the reactor to adjust the pressure at 50 kg/cm2. After the inside of the reactor was maintained at 55° C., 9.0 kg of ethyl acrylate, 2.2 kg of n-butyl acrylate, 445 g of monobutyl butenedioate, 82 g of polyethylene glycol dimethacrylate (manufactured by Tokyo Chemical Industry Co., Ltd.), which is a bifunctional monomer, and 2.0 kg of an aqueous solution of t-butylhydroperoxide (concentration: 0.25% by mass) were charged from the charging port to initiate polymerization. During the reaction, the temperature in the reactor was maintained at 55° C., and the reaction was completed in 6 hours. 20 kg of an aqueous solution of sodium borate (concentration: 0.3% by mass) was added to the reacted polymerization liquid to solidify the polymer, which was dehydrated and dried to obtain an acrylic rubber. The acrylic rubber had a copolymer composition of 2 parts by mass of an ethylene unit, 1.8 parts by mass of a monobutyl butenedioate unit (MBM unit, crosslinking monomer unit), 78 parts by mass of an ethyl acrylate unit (EA unit), 16 parts by mass of an n-butyl acrylate unit (BA unit), and 0.7 parts by mass of a polyethylene glycol dimethacrylate unit (bifunctional monomer unit), and had a toluene insoluble content of 7.6% by mass.
100 parts by mass of the acrylic rubber obtained by the above method, 50 parts by mass of a carbon black (trade name “Seast SO” manufactured by Tokai Carbon Co., Ltd.), 1 part by mass of a liquid paraffin (lubricant, trade name “Hycol K-230” manufactured by Kaneda Ltd.), 0.5 parts by mass of stearic acid (lubricant, trade name “Tsubaki stearate” manufactured by NOF Corporation), 1 part by mass of stearylamine (trade name “Furamine #80” manufactured by Kao Corporation), 1.6 parts by mass of an amine-based anti-aging agent (trade name “Nocrac CD” manufactured by Ouchi Shinko Chemical Industrial Co., Ltd.), 0.3 parts by mass of an imidazole-based anti-aging agent (trade name “Nocrac 810NA” manufactured by Ouchi Shinko Chemical Co., Ltd.), 0.4 parts by mass of a crosslinking agent (hexamethylenediamine carbide, trade name “Diak #1” manufactured by Dupont), and 1.6 parts by mass of a crosslinking accelerator (trade name “Rhenogran XLA-60” manufactured by Lanxess) were kneaded with an 8-inch open roll to obtain a crosslinkable rubber composition.
The resulting crosslinkable rubber composition was evaluated in the following manner. The results are shown in Table 1.
Measurement of Scorch Time
Using a test piece cut out from the crosslinkable rubber composition, the scorch time (t5) was measured in accordance with JIS K6300. The measurement was performed at 125° C.
Measurement of Δtorque
Using a test piece cut out from the crosslinkable rubber composition, a curve (crosslinking curve) showing the relationship between crosslinking time and torque was obtained in accordance with JIS K6300. Next, Atorque was obtained by calculating (maximum torque value)-(minimum torque value) from the crosslinking curve. The measurement was performed at 170° C.
The crosslinkable rubber composition obtained by the above method was heat-treated in a hot press at 180° C. for 20 minutes to obtain a primary crosslinked product, and then heat-treated in hot air (gear oven) at 185° C. for 3 hours to obtain a cured rubber product.
The resulting cured rubber product was evaluated in the following manner. The results are shown in Table 2.
Measurement of 100% modulus, tensile strength, and elongation at break
The 100% modulus, tensile strength, and elongation at break were measured in accordance with JIS K6251.
Measurement of Hardness
The hardness was measured using a durometer hardness tester in accordance with JIS K6253.
Heat Resistance Test (1)
Heat treatment was performed at 175° C. for 504 hours in accordance with JIS K6257, and then the tensile strength, elongation at break, and hardness were measured in accordance with JIS K6251. From the tensile strength and elongation at break of the test piece before the heat treatment and the tensile strength and elongation at break of the test piece after the heat treatment, the retention of tensile strength and the retention of elongation at break were determined by the following equations:
Retention ratio (%)=100 ×(measured value after heat treatment)/(measured value before heat treatment)
Heat Resistance Test (2)
Heat treatment was performed at 190° C. for 94 hours in accordance with JIS K6257, and then the tensile strength, elongation at break, and hardness were measured in accordance with JIS K6251. From the tensile strength and elongation at break of the test piece before the heat treatment and the tensile strength and elongation at break of the test piece after the heat treatment, the retention ratio of the tensile strength and the retention ratio of the elongation at break were determined by the above formula.
Cold Resistance Test
In accordance with JIS K6261, torsional rigidity was determined by twisting a test piece via a torsion wire over a temperature range from a freezing temperature to room temperature and measuring a torsion angle. The specific modulus is a value with respect to the modulus at 23±2° C., and was calculated by the following equation:
Specific modulus (−)=((180-torsion angle at measurement temperature)/torsion angle at measurement temperature)/((180-torsion angle at 23±2° C.)/torsion angle at 23±2° C.)
The temperature at which the specific modulus becomes 10 can be obtained from the temperature and temperature-torsion angle curve with respect to the value of the specific modulus. An angle corresponding to a specific modulus of 10 was selected, and the temperature corresponding to this angle from the temperature-torsion angle curve obtained in the test was taken as the T10.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were produced in the same manner as in Example A-1 except that the amount of the bifunctional monomer added was changed to 164 g. In addition, the crosslinkable rubber composition and the cured rubber product were evaluated in the same manner as in Example A-1. The results are shown in Tables 1 and 2. The acrylic rubber of Example A-2 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.8 parts by mass of a monobutyl butenedioate unit, 78 parts by mass of an ethyl acrylate unit, 16 parts by mass of an n-butyl acrylate unit, and 1.5 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Example A-2 was 12.8% by mass.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were produced in the same manner as in Example A-1 except that the amount of the bifunctional monomer added was changed to 329 g. In addition, the crosslinkable rubber composition and the cured rubber product were evaluated in the same manner as in Example A-1. The results are shown in Tables 1 and 2. The acrylic rubber of Example A-3 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.8 parts by mass of a monobutyl butenedioate unit, 78 parts by mass of an ethyl acrylate unit, 16 parts by mass of an n-butyl acrylate unit, and 2.9 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Example A-3 was 33.1% by mass.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were produced in the same manner as in Example A-1 except that the bifunctional monomer was not used. In addition, the crosslinkable rubber composition and the cured rubber product were evaluated in the same manner as in Example A-1. The results are shown in Tables 1 and 2. The acrylic rubber of Comparative Example a-1 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.8 parts by mass of a monobutyl butenedioate unit, 79 parts by mass of an ethyl acrylate unit, and 17 parts by mass of an n-butyl acrylate unit. The toluene insoluble content of the acrylic rubber of Comparative Example a-1 was 1.0% by mass.
An acrylic rubber and a crosslinkable rubber composition were produced in the same manner as in Example A-1 except that the amount of the bifunctional monomer added was changed to 768 g. The results are shown in Tables 1 and 2. The acrylic rubber of Comparative Example a-2 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.8 parts by mass of a monobutyl butenedioate unit, 75 parts by mass of an ethyl acrylate unit, 14 parts by mass of an n-butyl acrylate unit, and 7 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the polymer obtained in Comparative Example a-2 was 65.3% by mass. In Comparative Example a-2, since it was difficult to obtain an acrylic rubber through an extrusion process, evaluation of a crosslinkable rubber composition and preparation of a cured rubber product were impossible.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were prepared in the same manner as in Example A-1, except that the amount of the bifunctional monomer added was changed to 5.5 g. The results are shown in Tables 1 and 2. The acrylic rubber of Comparative Example a-3 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.8 parts by mass of a monobutyl butenedioate unit, 79 parts by mass of an ethyl acrylate unit, 17 parts by mass of an n-butyl acrylate unit, and 1.8 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Comparative Example a-3 was 1.8% by mass.
An acrylic rubber was produced by the following method.
17 kg of an aqueous solution of a partially saponified polyvinyl alcohol (concentration: 4% by mass) and 22 g of sodium acetate were charged into a pressure-resistant reactor having an internal volume of 40 liters, and thoroughly mixed with a stirrer in advance to prepare a uniform slurry. After air in the upper part of the reactor was replaced with nitrogen, ethylene was injected into the upper part of the reactor to adjust the pressure at 50 kg/cm2. After the inside of the reactor was maintained at 55° C., 9.0 kg of ethyl acrylate, 2.2 kg of n-butyl acrylate, 390 g of monobutyl butenedioate, 98 g of ethylene glycol dimethacrylate (EGDMA) that is a bifunctional monomer, and 2.0 kg of an aqueous solution of t-butylhydroperoxide (concentration: 0.25% by mass) were charged from the charging port to initiate polymerization. During the reaction, the temperature in the reactor was maintained at 55° C., and the reaction was completed in 6 hours. 20 kg of an aqueous solution of sodium borate (concentration: 0.3% by mass) was added to the reacted polymerization liquid to solidify the polymer, which was dehydrated and dried to obtain an acrylic rubber. The acrylic rubber had a copolymer composition of 2 parts by mass of an ethylene unit, 1.5 parts by mass of a monobutyl butenedioate unit (MBM unit, crosslinking monomer unit), 78 parts by mass of an ethyl acrylate unit (EA unit), 16 parts by mass of an n-butyl acrylate unit (BA unit), and 1.2 parts by mass of a ethylene glycol dimethacrylate unit (bifunctional monomer unit), and had a toluene insoluble content of 24.3% by mass.
100 parts by mass of the acrylic rubber obtained by the above method, 50 parts by mass of a carbon black (trade name “Seast SO” manufactured by Tokai Carbon Co., Ltd.), 1 part by mass of a liquid paraffin (lubricant, trade name “Hycol K-230” manufactured by Kaneda Ltd.), 1 part by mass of stearic acid (lubricant, trade name “Tsubaki stearate” manufactured by NOF Corporation), 0.3 parts by mass of stearylamine (trade name “Furamine #80” manufactured by Kao Corporation), 0.5 parts by mass of an amine-based anti-aging agent (trade name “Nocrac CD” manufactured by Ouchi Shinko Chemical Industrial Co., Ltd.), 1.6 parts by mass of an imidazole-based anti-aging agent (trade name “Nocrac 810NA” manufactured by Ouchi Shinko Chemical Co., Ltd.), 0.4 parts by mass of a crosslinking agent (hexamethylenediamine carbide, trade name “Diak #1” manufactured by Dupont), and 0.8 parts by mass of a crosslinking accelerator (trade name “Rhenogran XLA-60” manufactured by Lanxess) were kneaded with an 8-inch open roll to obtain a crosslinkable rubber composition. The obtained crosslinkable rubber composition was evaluated in the same manner as in Example A-1. The results are shown in Table 3.
The crosslinkable rubber composition obtained by the above method was heat-treated in a hot press at 180° C. for 20 minutes to obtain a primary crosslinked product, and then heat-treated in hot air (gear oven) at 185° C. for 3 hours to obtain a cured rubber product. The obtained cured rubber product was evaluated in the same manner as in Example A-1. The results are shown in Table 4.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were produced in the same manner as in Example B-1 except that 120 g of diethylene glycol dimethacrylate (DEGDM) was charged instead of 164 g of ethylene glycol dimethacrylate (EGDMA) as the bifunctional monomer. In addition, the crosslinkable rubber composition and the cured rubber product were evaluated in the same manner as in Example B-1. The acrylic rubber of Example B-2 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.5 parts by mass of a monobutyl butenedioate unit, 78 parts by mass of an ethyl acrylate unit, 16 parts by mass of an n-butyl acrylate unit, and 1.4 parts by mass of a diethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Example B-2 was 17.3% by mass.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were produced in the same manner as in Example B-1 except that 164 g of polyethylene glycol dimethacrylate (PEGDM) (manufactured by Tokyo Kasei Kogyo Co., Ltd., n is about 4) was charged instead of ethylene glycol dimethacrylate (EGDMA) as the bifunctional monomer. In addition, the crosslinkable rubber composition and the cured rubber product were evaluated in the same manner as in Example B-1. The acrylic rubber of Example B-3 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.5 parts by mass of a monobutyl butenedioate unit, 78 parts by mass of an ethyl acrylate unit, 16 parts by mass of an n-butyl acrylate unit, and 2 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Example B-3 was 28.8% by mass.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were produced in the same manner as in Example B-1 except that 273 g of polyethylene glycol dimethacrylate (PEGDM) (manufactured by ALDRICH CO., n is about 9) was charged instead of ethylene glycol dimethacrylate (EGDMA) as the bifunctional monomer. In addition, the crosslinkable rubber composition and the cured rubber product were evaluated in the same manner as in Example B-1. The acrylic rubber of Example B-4 had a copolymer composition of 2 parts by mass of an ethylene unit, 1.5 parts by mass of a monobutyl butenedioate unit, 78 parts by mass of an ethyl acrylate unit, 16 parts by mass of an n-butyl acrylate unit, and 3.3 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Example B-4 was 33.4% by mass.
An acrylic rubber and a crosslinkable rubber composition were produced in the same manner as in Example B-3 except that ethylene was not charged. The acrylic rubber of Comparative Example b-1 had a copolymer composition of 1.5 parts by mass of a monobutyl butenedioate unit, 79 parts by mass of an ethyl acrylate unit, 17 parts by mass of an n-butyl acrylate unit, and 2 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Comparative Example b-1 was 20.4% by mass.
An acrylic rubber, a crosslinkable rubber composition, and a cured rubber product were prepared in the same manner as in Example B-3, except that monobutyl butenedioate was not charged. In addition, the crosslinkable rubber composition was evaluated in the same manner as in Example B-1. The acrylic rubber of Comparative Example b-2 had a copolymer composition of 2 parts by mass of an ethylene unit, 79 parts by mass of an ethyl acrylate unit, 17 parts by mass of an n-butyl acrylate unit, and 2 parts by mass of a polyethylene glycol dimethacrylate unit. The toluene insoluble content of the acrylic rubber of Comparative Example b-2 was 24.7% by mass. It was difficult to evaluate the crosslinkable rubber composition of Comparative Example b-2 and produce a cured rubber product thereof, since the vulcanization torque did not increase and crosslinking did not occur.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2019-178882 | Sep 2019 | JP | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/JP2020/036021 | 9/24/2020 | WO |
