WO2005082960A1 - アクリルゴム及び架橋性アクリルゴム組成物 - Google Patents
アクリルゴム及び架橋性アクリルゴム組成物 Download PDFInfo
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- WO2005082960A1 WO2005082960A1 PCT/JP2005/002996 JP2005002996W WO2005082960A1 WO 2005082960 A1 WO2005082960 A1 WO 2005082960A1 JP 2005002996 W JP2005002996 W JP 2005002996W WO 2005082960 A1 WO2005082960 A1 WO 2005082960A1
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- acrylic rubber
- monomer unit
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- crosslinkable
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/0025—Crosslinking or vulcanising agents; including accelerators
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/281—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/26—Esters containing oxygen in addition to the carboxy oxygen
- C08F220/28—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
- C08F220/285—Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing a polyether chain in the alcohol moiety
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/42—Nitriles
Definitions
- the present invention relates to an acrylic rubber, a crosslinkable acrylic rubber composition containing the acrylic rubber and a crosslinking agent, and a crosslinked product thereof, and more particularly to heat resistance, cold resistance and fuel oil resistance.
- the present invention relates to a crosslinkable acrylic rubber composition excellent in water resistance, a crosslinked product thereof, and an acrylic rubber suitable for the crosslinkable acrylic rubber composition.
- Acrylic rubber is excellent in heat resistance and oil resistance, and is used as a material for rubber parts used in contact with oil, such as seals, hoses, tubes, and belts, in the field of automobiles and the like. Widely used. Acrylic rubber imparts rubber elasticity by being cross-linked so that it can be used as these rubber parts.
- a cross-linkable monomer having an active cross-linking point is usually copolymerized at about 115% by weight. ing.
- Such cross-linkable acrylic rubber is required to have excellent heat resistance and cold resistance as well as low compression set, excellent fuel oil resistance, and excellent scorch stability. It has become desired.
- the selection of the crosslinkable monomer to be copolymerized with the acrylic rubber determines the crosslinking reaction rate together with the crosslinking agent used in combination with the acrylic rubber, so that storage stability, mechanical properties, compression set and heat resistance are determined. Affects gender.
- a chlorine monomer such as 2-chloroethyl vinyl ether or vinyl chloride acetate
- an epoxy monomer such as arinoleglycidinoleatene is used. Have been.
- cross-linking monomer monoesters of butenedioic acids such as maleic acid Ya fumaric acid, specifically has also been studied monobutyl ester of butenedionic acid, among them, 0.1 one 10 weight 0/0
- a crosslinked product of an acrylic rubber composition containing an aromatic diamine cross-linking agent and a guadin ligating compound cross-linking auxiliary agent in an acrylic rubber copolymerized with a mono-lower alkyl fumarate is useful for heat resistance and cold resistance.
- Patent Document 1 Patent Document 1 .
- these acrylic rubber compositions have particularly insufficient scorch stability.
- composition comprising a carboxyl group-containing acryl rubber containing a specific structural unit derived from a metallized mouth-tolyl and a specific cross-linking agent and a specific amine conjugate is added to a metal surface. It has been reported that it does not stick and does not generate scorch during processing, and that the obtained crosslinked product has excellent heat resistance, cold resistance, and oil resistance to deterioration (Patent Document 3). However, this composition has insufficient cold resistance and fuel oil resistance.
- Patent document 1 JP-A-11-92614
- Patent Document 2 Japanese Patent Application Laid-Open No. 2001-146540
- Patent Document 3 Japanese Patent Application Laid-Open No. 2003-342437
- An object of the present invention is to provide a crosslinkable acrylic rubber composition in which the obtained crosslinked product has an excellent balance of heat resistance, cold resistance and fuel oil resistance, and also has excellent scorch stability.
- the present inventors have conducted intensive studies to achieve the above object, and as a result, they have specified amounts of alkoxyalkyl (meth) atalylate units and methallyl-tolyl units, and further have a monoalkyl butenedionate.
- Acrylic rubber obtained by copolymerizing a specific amount of styrene as a crosslinkable monomer does not cause scorch during processing with a crosslinking agent added, and the obtained crosslinked product has heat resistance, cold resistance and fuel oil resistance. It was found that the present invention was excellent, and based on this knowledge, the present invention was completed.
- Mouth - Tolyl monomer unit 0. 1-9 9 wt% and butenedionic acid monoester monomer unit of 0. 1- 20 weight 0/0 and power made acrylic rubber.
- a crosslinkable acrylic rubber composition comprising the acrylic rubber according to any one of the above items 1 to 4 and a crosslinking agent.
- alkoxyalkyl (meth) acrylate ester monomer unit means an alkoxyalkyl acrylate polymer unit or an alkoxyalkyl methacrylate monomer unit.
- an atalyl rubber composition having excellent scorch stability when compounding and processing a crosslinking agent. Furthermore, by crosslinking the acrylic rubber composition, a crosslinked product having excellent heat resistance, cold resistance and fuel oil resistance is provided. Therefore, by virtue of these properties, it can be suitably used as a material for rubber parts such as seals, hoses, vibration-proof materials, tubes, belts, boots, etc., which are used after crosslinking after molding.
- alkoxyalkyl acrylate polymer unit or an alkoxyalkyl methacrylate monomer unit hereinafter abbreviated as an alkoxyalkyl (meth) acrylate polymer monomer 70.1 to 99.8% by weight
- alkoxyalkyl (meth) acrylate monomer an ester compound of an alkoxyalkyl alcohol having 2 to 8 carbon atoms and (meth) acrylic acid is preferred! /.
- methoxymethyl (meth) acrylate methoxymethyl (meth) acrylate, ethoxymethyl (meth) acrylate, 2-ethoxyhexyl (meth) acrylate, 2-butoxyshethyl (meth) acrylate, 2-methoxyethyl (meth) acrylate, ) 2-propoxyshetyl acrylate, 3-methoxypropyl (meth) acrylate, 4-methoxybutyl (meth) acrylate and the like.
- 2-methoxyethyl (meth) acrylate and 2-methoxyxyl (meth) acrylate are particularly preferable.
- Acrylic rubber of the present invention including Yuryou alkoxyalkyl (meth) Atari Rate monomer units is preferably 80 - 95 weight 0/0, more preferably 85 to 95 wt%. If the content of the alkoxyalkyl (meth) acrylate monomer unit in the acrylic rubber is too small, the cold resistance and the fuel oil resistance of the crosslinked product may decrease.
- Acrylic rubber of the present invention Metatari port - content tolyl monomer units is preferably 1 one 9 wt 0/0, more preferably 2-6 wt 0/0. If the content of the metallized-tolyl monomer unit in the acrylic rubber is too large, the heat resistance and cold resistance of the crosslinked product may be reduced. On the other hand, if the content is too small, the fuel oil resistance of the crosslinked product may decrease.
- the butenedioic acid monoester monomer is a compound having a monoester structure obtained by reacting butenedioic acid, ie, one carboxyl group of fumaric acid or maleic acid with an alcohol.
- the butenedionic acid monoester monomer functions as a crosslinkable monomer.
- a butenedionic acid monoester monomer having an alicyclic structure is preferred.
- the alicyclic structure has 3 to 20 carbon atoms, preferably 4 to 10 carbon atoms, and may be a saturated or unsaturated ring, and may be a monocyclic or polycyclic ring. Specific examples include a monocycloalkane structure, a monocycloalkene structure, a norbornane ring structure, a norbornene ring structure, and the like, and a combination thereof may be used.
- a butenedioic acid monoester monomer having an alicyclic structure As the alcohol to be reacted with the carboxyl group of the acid, it is preferable to use an alcohol having an alicyclic structure.
- the alcohol having such an alicyclic structure any of cycloalkyl alcohol, cycloalkyl alcohol, and an alcohol having the above alicyclic structure in a part or a side chain of a main chain can be used.
- cycloalkyl alcohol which is preferably a cycloalkyl alcohol / cycloalkyl alcohol, is more preferable. That is, the butenedionic acid monoester monomer unit is most preferably a butenedionic acid monocycloalkyl ester monomer unit.
- butenedioic acid monoester monomer having an alicyclic structure examples include monocyclopentynole fumarate, monocyclohexinole fumanate, monocycloheptinole fumanolate, monocyclooctyl fumarate, and fumaric acid monocyclooctyl.
- Monocycloalkyl fumarate monomers such as monomethylcyclohexyl, mono-3,5-dimethyl fumarate, dicyclopentyl fumarate and isobol fumarate; monocyclopentyl fumarate, fumarate Monocycloalkenyl ester of fumaric acid, such as monocyclohexenyl acid, monocyclohepturic fumarate, monocyclooctatyl fumarate, and monodicyclopentagel fumarate; monocyclopentyl maleate, monocyclomaleate Hexyl, monocycloheptyl maleate, maleic acid Monocycloalkyl maleate monomers such as monocyclooctyl, monomethylcyclohexyl maleate, mono-3,5-dimethylcyclohexyl maleate, monodicyclopentyl maleate, and monoisobo-maleate; Monocyclomaleic acid maleic esters such as monocyclopentyl maleate, monocyclohe
- monocyclohexyl fumarate and monocyclohexyl maleate are preferred.
- the content of the butenedionic acid monoester monomer unit in the acrylic rubber of the present invention is preferably 0.5 to 10% by weight, more preferably 115 to 5% by weight. If the amount of the butenedionic acid monoester monomer unit is too small, the crosslinked product will not have sufficient crosslink density and will not have good mechanical properties. On the other hand, if the amount is too large, the elongation of the crosslinked product decreases. Also, the compression set may increase.
- the acrylic rubber of the present invention per carboxyl group content force hundred rubber grams, preferably 5 X 10- 4 - 4 X 10- 1 equivalents, more preferably 2 X 10- 3 - 2 X 10- 1 eq, a 1 X 10- 1 equivalent - particularly preferably 4 X 10- 3. If the content of the carboxyl group in the acrylic rubber is too small, cross-linking will not proceed sufficiently, and the shape of the cross-linked product may not be maintained. On the other hand, if the amount is too large, the crosslinked product becomes hard and may lose rubber elasticity.
- the acrylic rubber of the present invention can be used, if necessary, in the above-mentioned alkoxyalkyl (meth) acrylate polymer, methacrylo-tolyl monomer and butenedioic acid monoester monomer. It can be obtained by radical polymerization of a monomer mixture comprising a monomer and a copolymerizable monomer.
- any of an emulsion polymerization method, a suspension polymerization method, a bulk polymerization method, and a solution polymerization method can be used.However, because of the ease of control of the polymerization reaction, the production of a conventionally known acrylic rubber can be performed. It is preferable to use an emulsion polymerization method under normal pressure, which is generally used as the method.
- the acrylic rubber of the present invention has a viscosity of one to one (ML)
- (1 +4, 100 ° C) is preferably 10-80, more preferably 20-70, and particularly preferably 30-70. If the viscosity is too small, the moldability and the mechanical strength of the crosslinked product may be poor, and if too large, the moldability may be poor.
- the acrylic rubber of the present invention can be used in various rubber parts by compounding a crosslinking agent to form a crosslinkable acrylic rubber composition, and converting the crosslinkable acrylic rubber composition into a crosslinked product by a crosslinking reaction. .
- the crosslinkable acrylic rubber composition of the present invention contains the above acrylic rubber and a crosslinking agent described below.
- the cross-linking agent used in the cross-linkable acrylic rubber composition of the present invention is generally used as a cross-linking agent for an acrylic rubber.
- a crosslinked structure can be formed relatively easily with the carboxyl group of the body unit, etc.
- the polyvalent amine conjugates which are preferred by the amine conjugates, are most preferred.
- an amine conjugate examples include an aliphatic polyamine crosslinker and an aromatic polyamine crosslinker.
- compounds having a non-conjugated nitrogen-carbon double bond such as guanidine compounds are not included.
- Examples of the aliphatic polyamine cross-linking agent include hexamethylene diamine, hexamethylene diamine carbamate, N, N, dicinnamylidene 1,6-hexanediamine and the like.
- Examples of the aromatic polyamine crosslinking agent include 4,4-methylenediamine, m-phenylenediamine, 4,4, diaminodiphenyl ether, 3,4, diaminodiphenyl ether, 4,4, — (M-Phenylenediisopropylidene) dialine, 4,4,1- (p-Phenylenediisopropylidene) dialine, 2,2,1-bis [4- (4-aminophenoxy) phenyl ] Propane, 4,4, diaminobenzalide, 4,4'bis (4aminophenoxy) biphenyl, m-xylylenediamine, p-xylylenediamine, 1,3,5 benzenetriamine, 1,3 5 Benzen
- the amount of the crosslinking agent in the crosslinkable acrylic rubber composition is preferably 0.05 to 20 parts by weight, more preferably 0.1 to 10 parts by weight, and still more preferably 100 parts by weight of the acrylic rubber. Or 0.2 to 7 parts by weight, particularly preferably 0.3 to 5 parts by weight. If the amount of the cross-linking agent is too small, the cross-linking is not performed sufficiently, and it becomes difficult to maintain the shape of the cross-linked product. On the other hand, if the content is too large, the crosslinked product becomes too hard, and the elasticity of the crosslinked rubber is impaired.
- crosslinkable acrylic rubber composition of the present invention a crosslinking accelerator may be further blended and used in combination with the above crosslinking agent.
- the crosslinking accelerator is also not limited, but is preferably a crosslinking accelerator that can be used in combination with the polyvalent amine crosslinking agent.
- the base dissociation constant at 25 ° C. in water is 10_. It is preferably 12 to 10 6 .
- Examples of such a cross-linking accelerator include guanidine compounds, imidazole compounds, quaternary onium salts, tertiary phosphine compounds, and alkali metal salts of weak acids.
- Examples of the guanidine compound include 1,3-diphenyl-guanidine, 1,3-diortolylguanidine and the like.
- Examples of the imidazole compound include 2-methylimidazole, 2-phenylimidazole and the like.
- Examples of the quaternary potassium salt include tetra n-butylammonium-prombromide, octadecyl tri-n-butylammonium-pambromide and the like.
- polyvalent tertiary amine disulfide examples include triethylenediamine, 1,8 diazabicyclo [5.4.0] indene7, and the like.
- tertiary phosphine compound examples include triphenylphosphine and tri-p-tolylphosphine.
- alkali metal salt of a weak acid examples include inorganic weak salts such as sodium or potassium phosphates and carbonates and organic weak salts such as stearates and laurates.
- the amount of the crosslinking accelerator used in the crosslinkable acrylic rubber composition is preferably 0.1 to 20 parts by weight, more preferably 0.2 to 15 parts by weight, and particularly preferably 100 parts by weight of the acrylic rubber. Preferably, it is 0.3 to 10 parts by weight. If the amount of the cross-linking accelerator is too large, the cross-linking speed may be too high during cross-linking, the cross-linking accelerator may bloom on the cross-linked product surface, or the cross-linked product may be too hard. If the amount of the crosslinking accelerator is too small, the tensile strength of the crosslinked product may be remarkably reduced, or the change in elongation or change in tensile strength after heat load may be too large.
- the crosslinkable rubber composition of the present invention preferably further contains a monoamine conjugate.
- the composition is less likely to adhere to the metal in the processing of the roll force before crosslinking and the processability is improved.
- Examples of such a monoamine conjugate include an aromatic monoamine conjugate and an aliphatic monoamine compound. These may be any of a primary amine diary, a secondary amine diary, and a tertiary amine diary. In the present invention, these monoamine conjugates can be used alone or in combination of two or more. When used alone, a mono-grade aminy conjugate is preferred. When two or more kinds are used in combination, it is preferable to use a combination of an aliphatic mono-secondary amine conjugate and an aliphatic mono-tertiary amine conjugate.
- the blending amount of the above monoamine conjugate to 100 parts by weight of the acrylic rubber is 0.05-2. 0 parts by weight, preferably 0.1-10 parts by weight.
- the amount is preferably 0.1 to 10 parts by weight, more preferably 0.2 to 5 parts by weight.
- the total amount is preferably 0.2 to 10 parts by weight, more preferably 0.5 to 7 parts by weight. If the amount of the monoamine compound is too small, the adhesion of the acrylic rubber composition to metal becomes large, resulting in inferior caloric properties. On the other hand, if the amount is too large, the monoamine conjugate may bloom on the surface of the crosslinked product, the strength of the crosslinked product may be significantly reduced, or the compression set may be increased.
- the crosslinkable acrylic rubber composition of the present invention may contain a reinforcing material, a filler, an antioxidant, a light stabilizer, a plasticizer, a lubricant, an adhesive, a lubricant, a flame retardant, Fungicides, antistatic agents
- an additive such as a coloring agent.
- the acrylic rubber composition may further contain, if necessary, a rubber other than the acrylic rubber of the present invention, an elastomer, a resin, or the like.
- Examples of the rubber that can be blended include natural rubber, acrylic rubber having a composition other than the acrylic rubber of the present invention, polybutadiene rubber, polyisoprene rubber, styrene butadiene rubber, Atariguchi-trilubutadiene rubber, and the like.
- Examples of the elastomer that can be blended include an olefin elastomer, a styrene elastomer, a butyl chloride elastomer, a polyester elastomer, a polyamide elastomer, a polyurethane elastomer, and a polysiloxane elastomer.
- Examples of resins that can be blended include polyolefin resin, polystyrene resin, polyacrylic resin, polyphenylene ether resin, polyester resin, polycarbonate resin, polyamide resin, and the like. Is mentioned.
- the crosslinkable acrylic rubber composition of the present invention In preparing the crosslinkable acrylic rubber composition of the present invention, an appropriate mixing method such as roll mixing, Banbury mixing, screw mixing, and solution mixing can be adopted.
- the order of blending is not particularly limited, but after sufficiently mixing components that are hard to react or decompose by heat, a component that reacts or decomposes by heat, such as a cross-linking agent, is used at a temperature at which no reaction or decomposition occurs. Mix in a short time.
- the method for molding the crosslinkable acrylic rubber composition is not particularly limited! Any method such as compression molding, injection molding, transfer molding or extrusion molding can be used.
- the crosslinking method may be selected according to the shape of the crosslinked product, etc., and may be a method of performing molding and crosslinking at the same time, or a method of performing crosslinking after molding!
- the crosslinkable acrylic rubber composition of the present invention can be made into a crosslinked product by heating.
- the heating temperature is preferably from 130 to 220 ° C, more preferably from 140 to 200 ° C, and the bridge time is preferably from 30 seconds to 5 hours.
- a heating method a method used for rubber crosslinking such as press heating, steam heating, oven heating, and hot air heating may be appropriately selected.
- post-crosslinking may be performed in order to surely crosslink the inside of the crosslinked product.
- Post-crosslinking varies depending on the heating method, crosslinking temperature, shape and the like, but is preferably performed for 1 to 48 hours.
- a heating method and a heating temperature for performing post-crosslinking may be appropriately selected.
- the crosslinkable acrylic rubber composition of the present invention is excellent in scorch stability during processing, and is excellent in heat resistance after compression and compression set characteristics. Therefore, a cross-linked product obtained by cross-linking the acrylic rubber composition makes use of these properties and can be used as a material for rubber parts such as seals, hoses, vibration-proof materials, tubes, belts, and boots in a wide range. It can be suitably used.
- the M-I viscosity ML of the acrylic rubber at a measurement temperature of 100 ° C was measured.
- the Mooney scorch time (t5) of the crosslinkable acrylic rubber composition was measured at 125 ° C. according to JIS K6300. The greater the value of the Mooney scorch time (t5), the better the scorch stability.
- T 1 in Gehman torsion test First, the crosslinkable acrylic rubber composition was heated at 170 ° C for 20 minutes by press molding to form a sheet having a thickness of 2 mm, and the sheet-shaped sample was left at 170 ° C for 4 hours to form a secondary sheet. After the bridge, it was punched into a rectangle of 40mm X 30mm and used as a test piece. The temperature (Gehman T) at which the specific modulus RM was 10 was measured for the obtained test piece according to the low-temperature torsion test of JIS K 6261.
- Fuel oil-resistant matter body ratio in fuel oil refining tests and tests
- the cross-linkable acrylic rubber composition was molded and cross-linked by pressing at 170 ° C for 20 minutes, sized to 15 cm x 15 cm x 2 mm, and left at 170 ° C for 4 hours for post-crosslinking. Then, a test piece was prepared by punching into a predetermined shape. The following measurements were performed using the obtained test pieces.
- hardness as a physical property in a normal state was measured according to a hardness test of JIS K6253.
- air aging was performed for 336 hours in an environment of 175 ° C, and the hardness was measured again. From these results, the hardness change (point) before and after heat aging was determined. The closer to this variation force, the better the heat resistance.
- the acrylic rubber A obtained by the above reaction (methoxyethyl acrylate unit content 93%, Tacrylo-tolyl unit content 5%, monocyclohexyl fumarate unit content 2%, mu-viscosity 47.5 (ML, 100.C)) 100 parts, carbon black (according to ASTM D1765)
- Acrylic rubber B was produced in the same manner as in the production of acrylic rubber A in Example 1, except that 53 parts of methoxyethyl acrylate, 40 parts of ethoxyl acrylate, 5 parts of metall-tolyl and 2 parts of monocyclohexyl fumarate were used. Got. Then, a crosslinkable acrylic rubber composition was prepared in the same manner as in Example 1 except that acrylic rubber B was used.
- An acrylic rubber C was obtained in the same manner as in the production of the acrylic rubber A in Example 1, except that 95 parts of methoxyethyl acrylate, 3 parts of metallitol-tolyl, and 2 parts of monocyclohexyl fumarate were used. Then, a crosslinkable acrylic rubber composition was prepared in the same manner as in Example 1 except that acrylic rubber C was used.
- Acrylic rubber D was obtained in the same manner as in the production of acrylic rubber A in Example 1, except that 95 parts of methoxyethyl acrylate, 3 parts of metall-tolyl and 2 parts of mono-n-butyl fumarate were used. Then, a crosslinkable acrylic rubber composition was prepared in the same manner as in Example 1 except that acrylic rubber D was used.
- An acrylic rubber G was obtained in the same manner as in the production of the acrylic rubber A in Example 1, except that 83 parts of methoxyethyl acrylate, 15 parts of acrylonitrile and 2 parts of monocyclohexyl fumarate were used.
- the acrylic rubber containing the metallized mouth-tolyl unit in 10 parts or more as specified in the present invention (Comparative Example 3) has a remarkably low cold resistance when used as a crosslinkable acrylic rubber composition.
- the acrylic rubber and the acrylic rubber composition of the present invention are excellent in scorch stability, and excellent in cold resistance, heat resistance and fuel oil resistance of the crosslinked product (Examples 14 to 14).
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Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05710647A EP1719783B1 (en) | 2004-02-27 | 2005-02-24 | Acrylic rubber and crosslinkable acrylic rubber composition |
| DE602005007186T DE602005007186D1 (de) | 2004-02-27 | 2005-02-24 | Acrylkautschuk und vernetzbare acrylkautschukzusammensetzung |
| JP2006510439A JP4807255B2 (ja) | 2004-02-27 | 2005-02-24 | アクリルゴム及び架橋性アクリルゴム組成物 |
| US10/590,732 US7402631B2 (en) | 2004-02-27 | 2005-02-24 | Acrylic rubber and cross-linkable acrylic rubber composition |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004-052911 | 2004-02-27 | ||
| JP2004052911 | 2004-02-27 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2005082960A1 true WO2005082960A1 (ja) | 2005-09-09 |
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| Application Number | Title | Priority Date | Filing Date |
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| PCT/JP2005/002996 Ceased WO2005082960A1 (ja) | 2004-02-27 | 2005-02-24 | アクリルゴム及び架橋性アクリルゴム組成物 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US7402631B2 (ja) |
| EP (1) | EP1719783B1 (ja) |
| JP (1) | JP4807255B2 (ja) |
| DE (1) | DE602005007186D1 (ja) |
| WO (1) | WO2005082960A1 (ja) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007114108A1 (ja) * | 2006-03-31 | 2007-10-11 | Zeon Corporation | アクリルゴムおよびその製造方法 |
| JP2008163114A (ja) * | 2006-12-27 | 2008-07-17 | Nippon Zeon Co Ltd | 架橋性ゴム組成物およびゴム架橋物 |
| JP2009275204A (ja) * | 2008-04-18 | 2009-11-26 | Nok Corp | 架橋剤マスターバッチ及びその製造方法並びにアクリルゴム組成物 |
| WO2018168395A1 (ja) * | 2017-03-17 | 2018-09-20 | 日本ゼオン株式会社 | ニトリル基含有共重合体ゴム |
| JPWO2021149443A1 (ja) * | 2020-01-24 | 2021-07-29 | ||
| JP2021143278A (ja) * | 2020-03-12 | 2021-09-24 | 株式会社フコク | ゴム組成物およびそれを用いたゴム部材 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8791180B2 (en) | 2011-06-21 | 2014-07-29 | E I Du Pont De Nemours And Company | Process for production of a heat-stabilized acrylate polymer |
| US8921460B2 (en) * | 2011-06-21 | 2014-12-30 | E. I. Du Pont De Nemours And Company | Heat-stabilized acrylate elastomer composition and process for its production |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0586137A (ja) * | 1991-09-25 | 1993-04-06 | Tosoh Corp | アクリル系共重合体ゴムの製造方法 |
| JPH0680735A (ja) * | 1992-07-13 | 1994-03-22 | Nippon Shokubai Co Ltd | 高分子量アクリル系重合体およびその用途と製造方法 |
| JP2003342437A (ja) * | 2002-05-27 | 2003-12-03 | Nippon Zeon Co Ltd | アクリルゴム組成物及び架橋物 |
| JP2004018567A (ja) * | 2002-06-12 | 2004-01-22 | Nippon Zeon Co Ltd | アクリルゴム及び架橋性アクリルゴム組成物 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2842931B2 (ja) * | 1990-06-05 | 1999-01-06 | 日本メクトロン株式会社 | 加硫可能なアクリルエラストマー配合物 |
| JPH0733410B2 (ja) * | 1990-08-03 | 1995-04-12 | 東洋シール工業株式会社 | 架橋可能なアクリルゴムの製造方法 |
| EP0578498B1 (en) * | 1992-07-10 | 1997-04-16 | Nippon Shokubai Co., Ltd. | Acrylic polymer, its use and process for producing it |
| JP2001146540A (ja) * | 1999-11-22 | 2001-05-29 | Tokai Rubber Ind Ltd | ゴム組成物及び自動車用燃料輸送ホース |
| JP4505913B2 (ja) * | 1999-12-24 | 2010-07-21 | ユニマテック株式会社 | アクリル系エラストマー組成物およびその架橋性組成物 |
| JP4075389B2 (ja) * | 2002-01-30 | 2008-04-16 | 日本ゼオン株式会社 | 加硫性アクリルゴム組成物および加硫物 |
| US20050250913A1 (en) * | 2002-06-12 | 2005-11-10 | Zeon Corporation | Acrylic rubber, crosslinkable acrylic rubber composition and moldings |
-
2005
- 2005-02-24 US US10/590,732 patent/US7402631B2/en not_active Expired - Fee Related
- 2005-02-24 WO PCT/JP2005/002996 patent/WO2005082960A1/ja not_active Ceased
- 2005-02-24 EP EP05710647A patent/EP1719783B1/en not_active Expired - Lifetime
- 2005-02-24 JP JP2006510439A patent/JP4807255B2/ja not_active Expired - Fee Related
- 2005-02-24 DE DE602005007186T patent/DE602005007186D1/de not_active Expired - Fee Related
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0586137A (ja) * | 1991-09-25 | 1993-04-06 | Tosoh Corp | アクリル系共重合体ゴムの製造方法 |
| JPH0680735A (ja) * | 1992-07-13 | 1994-03-22 | Nippon Shokubai Co Ltd | 高分子量アクリル系重合体およびその用途と製造方法 |
| JP2003342437A (ja) * | 2002-05-27 | 2003-12-03 | Nippon Zeon Co Ltd | アクリルゴム組成物及び架橋物 |
| JP2004018567A (ja) * | 2002-06-12 | 2004-01-22 | Nippon Zeon Co Ltd | アクリルゴム及び架橋性アクリルゴム組成物 |
Non-Patent Citations (1)
| Title |
|---|
| See also references of EP1719783A4 * |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007114108A1 (ja) * | 2006-03-31 | 2007-10-11 | Zeon Corporation | アクリルゴムおよびその製造方法 |
| JP2008163114A (ja) * | 2006-12-27 | 2008-07-17 | Nippon Zeon Co Ltd | 架橋性ゴム組成物およびゴム架橋物 |
| JP2009275204A (ja) * | 2008-04-18 | 2009-11-26 | Nok Corp | 架橋剤マスターバッチ及びその製造方法並びにアクリルゴム組成物 |
| WO2018168395A1 (ja) * | 2017-03-17 | 2018-09-20 | 日本ゼオン株式会社 | ニトリル基含有共重合体ゴム |
| JPWO2018168395A1 (ja) * | 2017-03-17 | 2020-01-16 | 日本ゼオン株式会社 | ニトリル基含有共重合体ゴム |
| JP7063320B2 (ja) | 2017-03-17 | 2022-05-09 | 日本ゼオン株式会社 | ニトリル基含有共重合体ゴム |
| JPWO2021149443A1 (ja) * | 2020-01-24 | 2021-07-29 | ||
| WO2021149443A1 (ja) * | 2020-01-24 | 2021-07-29 | Nok株式会社 | アクリルゴム組成物 |
| JP7352661B2 (ja) | 2020-01-24 | 2023-09-28 | Nok株式会社 | アクリルゴム組成物 |
| JP2021143278A (ja) * | 2020-03-12 | 2021-09-24 | 株式会社フコク | ゴム組成物およびそれを用いたゴム部材 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1719783A1 (en) | 2006-11-08 |
| JP4807255B2 (ja) | 2011-11-02 |
| EP1719783A4 (en) | 2007-04-18 |
| EP1719783B1 (en) | 2008-05-28 |
| US7402631B2 (en) | 2008-07-22 |
| JPWO2005082960A1 (ja) | 2007-11-15 |
| DE602005007186D1 (de) | 2008-07-10 |
| US20070173621A1 (en) | 2007-07-26 |
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