WO2010119708A1 - チオール含有液状ゴム組成物 - Google Patents
チオール含有液状ゴム組成物 Download PDFInfo
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- WO2010119708A1 WO2010119708A1 PCT/JP2010/002794 JP2010002794W WO2010119708A1 WO 2010119708 A1 WO2010119708 A1 WO 2010119708A1 JP 2010002794 W JP2010002794 W JP 2010002794W WO 2010119708 A1 WO2010119708 A1 WO 2010119708A1
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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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
Definitions
- the present invention relates to a thiol-containing liquid rubber composition excellent in curability in which a liquid styrene-butadiene copolymer and a specific polythiol are blended.
- rollers such as developing rollers, charging rollers, and transfer rollers used in printers and copiers, blades such as developing blades and cleaning blades, gasket members, display sealing materials, and architectural sealing materials.
- a rubber composition using a rubber-based resin such as a styrene-butadiene copolymer is employed.
- a curing treatment is performed by adding a thiol-based crosslinking agent such as a triazine thiol compound (see Patent Document 1).
- thiol-based crosslinking agents have polarity, they are not compatible with rubber-based resins such as styrene-butadiene copolymers, and when photocured or thermally cured due to poor solution uniformity. There is a possibility that an uncured portion may be formed or phase separation may occur, resulting in poor storage stability. Since such a phenomenon may cause the composition to become opaque, in particular, in the case of photocuring, there is a possibility that the light transmittance is deteriorated and the internal curing becomes insufficient.
- an object of the present invention is to provide a rubber composition having improved curability by improving compatibility with a thiol-based crosslinking agent while employing such a styrene-butadiene copolymer.
- the present inventors have found a thiol-containing liquid rubber composition containing a specific styrene-butadiene copolymer and polythiol, and have completed the present invention.
- the thiol-containing liquid rubber composition of the present invention is A styrene-butadiene copolymer (A) which is liquid at 25 ° C .; And a polythiol (B) derived from mercaptocarboxylic acid.
- the styrene-butadiene copolymer (A) preferably has a bound styrene content of 20 to 90% by mass, and is preferably a random copolymer.
- the polythiol (B) includes tetraethylene glycol bis (3-mercaptopropionate), trimethylolpropane tris (3-mercaptopropionate), tris [(3-mercaptopropionyloxy) -ethyl] isocyanurate, penta Erythritol tetrakis (3-mercaptopropionate), dipentaerythritol hexakis (3-mercaptopropionate), 1,4-bis (3-mercaptobutyryloxy) butane, pentaerythritol tetrakis (3-mercaptobutyrate) And at least one selected from the group consisting of 1,3,5-tris (3-mercaptobutyloxyethyl) -1,3,5-triazine-2,4,6 (1H, 3H, 5H) -trione Preferably there is.
- the content of the polythiol (B) may be 40 parts by mass or less with respect to 100 parts by weight of the styrene-butadiene copolymer (A).
- the number average molecular weight (Mn) of the styrene-butadiene copolymer (A) is preferably 1200 to 40000.
- the compatibility between the styrene-butadiene copolymer as a rubber resin and the polythiol (B) as a crosslinking agent is extremely excellent, and due to the nonuniformity of the solution.
- production of an unhardened part can be avoided.
- production of an unhardened part can be reduced effectively, even if it is any of photocurability and thermosetting, favorable sclerosis
- rollers such as developing rollers, charging rollers, and transfer rollers used in printers and copying machines, blades such as developing blades and cleaning blades, and gaskets. It is useful in a wide range of applications such as members, sealing materials for displays, and sealing materials for buildings.
- the thiol-containing liquid rubber composition of the present invention is A styrene-butadiene copolymer (A) which is liquid at 25 ° C .; It contains polythiol (B) derived from mercaptocarboxylic acid, and an initiator or the like used for photocuring or thermosetting can be added as necessary.
- the styrene-butadiene copolymer (A) used in the thiol-containing liquid rubber composition of the present invention is liquid at 25 ° C. (room temperature).
- diene rubbers such as butadiene rubber and isoprene rubber are non-polar, and thus have poor compatibility with polar compounds such as thiol cross-linking agents.
- polar compounds such as thiol cross-linking agents.
- the styrene-butadiene copolymer is similarly nonpolar. In spite of this, the compatibility becomes good and the mixing operation of these components becomes easy.
- the method for producing the styrene-butadiene copolymer (A) is not particularly limited, and can be obtained by copolymerizing a monomer that is 1,3-butadiene and a styrene monomer.
- a lithium-based polymerization initiator can be used for the copolymerization, and a randomizer or the like may be used as necessary.
- anionic polymerization is performed using a lithium-based polymerization initiator, it is also possible to optionally modify the living terminal of the polymer chain with various modifiers. For example, by using an alkylene oxide such as ethylene oxide or propylene oxide as a modifier, a diene polymer having hydroxyl groups at both ends or one end can be obtained.
- the arrangement of the monomers in the copolymer in the styrene-butadiene copolymer (A) is not particularly limited, and is a random copolymer, an alternating copolymer, a block copolymer, or a graft copolymer. Any of them may be used, but a random copolymer is preferable. If it is a random copolymer, unsaturated groups will be arranged more randomly in the copolymer, which can contribute to improved compatibility with polythiol (B) and further to improved heat resistance of the cured product. .
- an ether such as tetrahydrofuran or a randomizer such as 2,2-bis (tetrahydrofuryl) propane may be added for polymerization.
- the styrene-butadiene copolymer (A) has a number average molecular weight (Mn) of 1200 to 40000, preferably 3000 to 30000.
- Mn number average molecular weight
- the physical properties such as the strength and elongation are good, and when it is 40000 or less, the compatibility with the polythiol, or the viscosity Due to this problem, the processability at the time of molding is also good.
- the styrene-butadiene copolymer (A) has a bound styrene content of 90% by mass or less, preferably 25 to 65% by mass.
- the vinyl bond content of the butadiene moiety is 20 to 85%, preferably 25 to 80%.
- the styrene-butadiene copolymer (A) preferably has hydroxyl groups at both ends or one end.
- the compatibility with polythiol is further improved.
- the polythiol (B) used in the thiol-containing liquid rubber composition of the present invention is a polythiol derived from mercaptocarboxylic acid, and preferably a polythiol derived from 3-mercaptopropionic acid.
- the polythiol (B) preferably has a plurality of mercaptoacyloxy groups in the molecule, more preferably 2-6.
- the mercaptoacyloxy group specifically, 3-mercaptopropionyloxy group [HS— (CH 2 ) 2 —COO—], 3-mercaptobutyloxy group [HS—CH (CH 3 ) —CH 2- COO-] and the like, and a 3-mercaptopropionyloxy group is preferable.
- the mercaptocarboxylic acid-derived polythiol (B) is blended with, for example, a thermal radical generator, a thiyl radical is generated by the radical derived from the thermal radical generator, and the thiyl radical is converted into the styrene-butadiene copolymer (A). Adding to the unsaturated bond promotes the curing (crosslinking) reaction.
- polythiol (B) examples include tetraethylene glycol bis (3-mercaptopropionate) represented by the following chemical formula (I) and trimethylolpropane tris (3-mercaptoprote represented by the following chemical formula (II).
- the polythiol (B) has a high compatibility with the styrene-butadiene copolymer (A), and a uniform and stable composition can be obtained.
- these polythiol (B) may be used individually by 1 type, and may be used in combination of 2 or more type.
- the blending amount of the polythiol (B) is not particularly limited, but is preferably in the range of 40 parts by mass or less with respect to 100 parts by mass of the styrene-butadiene copolymer (A), and 3 to 35 parts by mass. The range of 5 to 30 parts by mass is even more preferable. If the blending amount of the polythiol (B) is 40 parts by mass or less, good compatibility with the liquid rubber can be maintained, and if it is 3 parts by mass or more, the light or thermosetting property of the composition is sufficiently improved. This is desirable.
- the thiol-containing liquid rubber composition of the present invention contains a so-called diene polymer other than the above styrene-butadiene copolymer (A) as long as it does not impair the object of the present invention. May be.
- diene polymer examples include natural rubber, polyisoprene, polybutadiene, butadiene-isoprene copolymer, isobutylene-isoprene copolymer, butadiene-acrylonitrile copolymer, styrene-isoprene copolymer, and polychloroprene. It is done.
- the terminal of these diene polymers may be modified or may not be modified.
- a photopolymerization initiator may be blended.
- photopolymerization initiators include benzoin derivatives and benzyl ketals [for example, Ciba Specialty Chemicals, trade name: Irgacure 651], ⁇ -hydroxyacetophenones, as intramolecular cleavage types.
- Ciba Specialty Chemicals, Inc. trade names: Darocur 1173, Irgacure 184, Irgacure 127], ⁇ -aminoacetophenones [for example, Ciba Specialty Chemicals, Inc., trade names: Irgacure 907, Irgacure 369], a combination of ⁇ -aminoacetophenones and thioxanthones (for example, isopropylthioxanthone, diethylthioxanthone), acylphosphine oxides [for example, manufactured by Ciba Specialty Chemicals Co., Ltd.
- oligomerized ⁇ -hydroxyacetophenone and acrylated benzophenones are preferable. More specifically, oligo [2-hydroxy-2-methyl-1- [4- (1-methylvinyl) phenyl] propanone] [for example, Lamberti S., et al. p.
- the blending amount of the photopolymerization initiator is preferably in the range of 0.01 to 20 parts by mass with respect to 100 parts by mass in total of the styrene-butadiene copolymer (A) and the polythiol (B), and 0.05 to The range of 15 parts by mass is further preferable, and the range of 0.1 to 10 parts by mass is even more preferable.
- thermosetting the thiol-containing liquid rubber composition of the present invention a radical generator that generates radicals by heat and initiates (accelerates) thermosetting of the composition may be blended.
- a thermal radical generator organic peroxides and azobis compounds are preferred. These thermal radical generators may be used individually by 1 type, and may be used in combination of 2 or more type.
- organic peroxide examples include 1,1-di (t-hexylperoxy) -3,3,5-trimethylcyclohexane, t-amylperoxy-2-ethylhexanoate, di (2-t -Butylperoxyisopropyl) benzene, benzoyl peroxide, 1,1'-di (t-butylperoxy) cyclohexane, di (3,5,5-trimethylhexanoyl) peroxide, t-butylperoxyneodecano And t-hexylperoxyneodecanoate, dicumyl peroxide and the like.
- azobis compounds examples include 2,2′-azobis (2-methylpropionitrile), 2,2′-azobis (2-methylbutyronitrile), 2,2′-azobis (2,4- Dimethylvaleronitrile), 2,2'-azobis (4-methoxy-2,4-dimethylvaleronitrile), 2-phenylazo-4-methoxy-2,4-dimethylvaleronitrile, dimethyl 2,2'-azobis (2 -Methyl propionate) and the like.
- the amount of the radical generator is not particularly limited, but is preferably in the range of 0.05 to 30 parts by mass with respect to 100 parts by mass of the styrene-butadiene copolymer (A), and 0.2. The range of ⁇ 20 parts by mass is further preferred, and the range of 0.5 to 15 parts by mass is even more preferred. If the amount of the radical generator is 0.05 parts by mass or more, the thermosetting reaction of the composition can be started, and if it is 30 parts by mass or less, gas generation due to the radical generator, residual radicals Bleeding out and outgas generation of the generating agent can be suppressed.
- thiol-containing liquid rubber composition of the present invention is excellent in both photocurability and thermosetting properties, various applications, in particular, rollers such as developing rollers, charging rollers, and transfer rollers used in printers and copiers, etc. It is useful in blades such as developing blades and cleaning blades, gasket members, display sealing materials, architectural sealing materials, and the like.
- Styrene-butadiene copolymer is also referred to as “SB copolymer”.
- Polymerization was carried out for 1.5 hours while raising the temperature of the polymerization reactor to 50 ° C., 254 ml of a 1 mol / liter ethylene oxide cyclohexane solution was added, and the mixture was further stirred for 2 hours, and then 50 ml of isopropyl alcohol was added. A hexane solution of the polymer was precipitated in isopropyl alcohol and sufficiently dried to obtain a liquid rubber at 25 ° C. in which both ends are hydroxyl groups.
- the liquid rubber thus obtained is a hydroxyl-terminated styrene-butadiene copolymer (SB copolymer A) having a terminal styrene content of 35% by mass and a vinyl bond content of the butadiene portion of 65%. Met. Further, the number average molecular weight was 5,200, the weight average molecular weight was 6,700, and the molecular weight distribution was 1.28.
- Polymerization was carried out for 1.5 hours while raising the temperature of the polymerization reactor to 50 ° C., 254 ml of a 1 mol / liter ethylene oxide cyclohexane solution was added, and further stirred for 2 hours, and then 50 ml of isopropyl alcohol was added. A hexane solution of the polymer was precipitated in isopropyl alcohol and sufficiently dried to obtain a liquid rubber at 25 ° C. in which both ends are hydroxyl groups.
- the liquid rubber obtained as described above is a hydroxyl-terminated styrene-butadiene copolymer (SB copolymer B) having a terminal styrene content of 55% by mass and a vinyl bond content of the butadiene portion of 65%.
- SB copolymer B hydroxyl-terminated styrene-butadiene copolymer having a terminal styrene content of 55% by mass and a vinyl bond content of the butadiene portion of 65%.
- the number average molecular weight was 4000, the weight average molecular weight was 4800, and the molecular weight distribution was 1.20.
- Polymerization was carried out for 1.5 hours while raising the temperature of the polymerization reactor to 50 ° C., 254 ml of a 1 mol / liter ethylene oxide cyclohexane solution was added, and the mixture was further stirred for 2 hours, and then 50 ml of isopropyl alcohol was added. A hexane solution of the polymer was precipitated in isopropyl alcohol and sufficiently dried to obtain a liquid rubber at 25 ° C. in which both ends are hydroxyl groups.
- the liquid rubber thus obtained is a hydroxyl-terminated styrene-butadiene copolymer (SB copolymer C) with a terminal styrene content of 23% by mass and a vinyl bond content of the butadiene portion of 65%.
- SB copolymer C hydroxyl-terminated styrene-butadiene copolymer
- Met The number average molecular weight was 4,900, the weight average molecular weight was 6,200, and the molecular weight distribution was 1.26.
- Polymerization was carried out for 1.5 hours while raising the temperature of the polymerization reactor to 50 ° C., 254 ml of a 1 mol / liter ethylene oxide cyclohexane solution was added, and the mixture was further stirred for 2 hours, and then 50 ml of isopropyl alcohol was added. A hexane solution of the polymer was precipitated in isopropyl alcohol and sufficiently dried to obtain a liquid rubber at 25 ° C. in which both ends are hydroxyl groups.
- the liquid rubber thus obtained is a hydroxyl-terminated styrene-butadiene copolymer (SB copolymer D) with a terminal styrene content of 35% by mass and a vinyl bond content of the butadiene portion of 78%. Met.
- the number average molecular weight was 4,400, the weight average molecular weight was 5,300, and the molecular weight distribution was 1.20.
- Polymerization is carried out for 1.5 hours while raising the temperature of the polymerization reactor to 50 ° C., 108.0 ml of a 1 mol / liter ethylene oxide cyclohexane solution is added, and further stirred for 2 hours, and then 50 ml of isopropyl alcohol is added. did. A hexane solution of the polymer was precipitated in isopropyl alcohol and sufficiently dried to obtain a liquid rubber at 25 ° C. in which both ends are hydroxyl groups.
- the photocurable liquid rubber thus obtained is a hydroxyl-terminated styrene-butadiene copolymer (SB copolymer E) having a terminal styrene content of 29% by mass and a vinyl bond content in the butadiene portion.
- SB copolymer E hydroxyl-terminated styrene-butadiene copolymer having a terminal styrene content of 29% by mass and a vinyl bond content in the butadiene portion.
- the number average molecular weight was 12,500, the weight average molecular weight was 16,000, and the molecular weight distribution was 1.26.
- Polymerization was carried out for 1.5 hours while raising the temperature of the polymerization reactor to 50 ° C., then 70 ml of a 1 mol / liter ethylene oxide cyclohexane solution was added, and after further stirring for 2 hours, 50 ml of isopropyl alcohol was added. A hexane solution of the polymer was precipitated in isopropyl alcohol and sufficiently dried to obtain a liquid rubber at 25 ° C. in which both ends are hydroxyl groups.
- the photocurable liquid rubber thus obtained is a hydroxyl-terminated styrene-butadiene copolymer (SB copolymer F) having a terminal styrene content of 35% by mass, and a vinyl bond content in the butadiene portion.
- SB copolymer F hydroxyl-terminated styrene-butadiene copolymer having a terminal styrene content of 35% by mass, and a vinyl bond content in the butadiene portion.
- the number average molecular weight was 17,200, the weight average molecular weight was 21,500, and the molecular weight distribution was 1.25.
- Irgacure 184D manufactured by Ciba Specialty Chemicals, 1-hydroxycyclohexyl phenyl ketone
- Irgacure 184D is blended in an amount of 1 part by mass with respect to 100 parts by mass of liquid rubber, irradiated with 7000 mJ / cm 2 of ultraviolet rays, and then cured at 23 ° C. Sex was assessed by palpation. The case where it was hardened completely as a solid as compared with the solution was indicated as ⁇ , the case where it was slightly cured as ⁇ , and the case where it was not cured at all as ⁇ . The results are shown in Tables 1-5.
- Trigonox 121 manufactured by Akzo, t-amylperoxy-2-ethylhexanoate was blended in an amount of 5 parts by mass with respect to 100 parts by mass of the liquid rubber and cured at 150 ° C. for 10 minutes. The curability of the composition at this time was evaluated by palpation. The case where it was completely cured as compared with the solution was evaluated as ⁇ , the case where it was slightly cured as ⁇ , and the case where it did not at all as ⁇ . The results are shown in Tables 1-5.
- SB copolymer B synthesized by the above method
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Abstract
Description
すなわち、本発明のチオール含有液状ゴム組成物は、
25℃において液状であるスチレン-ブタジエン共重合体(A)と、
メルカプトカルボン酸由来のポリチオール(B)と
を含むことを特徴とする。
また、前記スチレン-ブタジエン共重合体(A)の結合スチレン含有量は、20~90質量%であるのが好ましく、ランダム共重合体であるのが望ましい。
前記スチレン-ブタジエン共重合体(A)の数平均分子量(Mn)は、1200~40000であるのが望ましい。
本発明のチオール含有液状ゴム組成物は、
25℃において液状であるスチレン-ブタジエン共重合体(A)と、
メルカプトカルボン酸由来のポリチオール(B)と
を含むことを特徴とし、必要に応じて光硬化或いは熱硬化させる際に用いる開始剤等を添加することができる。
本発明のチオール含有液状ゴム組成物に用いるスチレン-ブタジエン共重合体(A)は、25℃(室温)において液状である。一般に、ブタジエンゴムやイソプレンゴムなどのジエン系ゴムは非極性であるため、チオール系架橋剤のような極性を有する化合物との相溶性が芳しくない。しかしながら、本発明のように、このような液状のスチレン-ブタジエン共重合体(A)を採用しつつ、後述する特定のチオール系架橋剤を用いると、スチレン-ブタジエン共重合体も同様に非極性であるにも関わらず相溶性が良好となり、これら各成分の混合作業が容易となる。
本発明のチオール含有液状ゴム組成物に用いるポリチオール(B)は、メルカプトカルボン酸由来のポリチオールであり、好ましくは3-メルカプトプロピオン酸由来のポリチオールである。該ポリチオール(B)は、好ましくは分子中にメルカプトアシロキシ基を複数有し、より好ましくは2~6個有する。ここで、メルカプトアシロキシ基として、具体的には、3-メルカプトプロピオニロキシ基[HS-(CH2)2-COO-]、3-メルカプトブチルオキシ基[HS-CH(CH3)-CH2-COO-]等が挙げられ、3-メルカプトプロピオニロキシ基が好ましい。該メルカプトカルボン酸由来のポリチオール(B)は、例えば熱ラジカル発生剤などを配合した場合、該熱ラジカル発生剤由来のラジカルによってチイルラジカルを発生し、該チイルラジカルがスチレン-ブタジエン共重合体(A)の不飽和結合に付加して、硬化(架橋)反応を促進することとなる。
本発明のチオール含有液状ゴム組成物には、上記成分のほか、本発明の目的を阻害しない範囲内であれば、上記スチレン-ブタジエン共重合体(A)以外の、いわゆるジエン系ポリマーを含有させてもよい。
充分に脱水精製したシクロヘキサン溶媒中に、1,3-(ジイソプロペニル)ベンゼン 1モルを添加した後、トリエチルアミン 2モル、sec-ブチルリチウム 2モルを順次添加し、50℃で2時間撹拌して、ジリチウム系重合開始剤を調製した。
充分に脱水精製したシクロヘキサン溶媒中に、1,3-(ジイソプロペニル)ベンゼン 1モルを添加した後、トリエチルアミン 2モル、sec-ブチルリチウム 2モルを順次添加し、50℃で2時間撹拌して、ジリチウム系重合開始剤を調製した。
充分に脱水精製したシクロヘキサン溶媒中に、1,3-(ジイソプロペニル)ベンゼン 1モルを添加した後、トリエチルアミン 2モル、sec-ブチルリチウム 2モルを順次添加し、50℃で2時間撹拌して、ジリチウム系重合開始剤を調製した。
充分に脱水精製したシクロヘキサン溶媒中に、1,3-(ジイソプロペニル)ベンゼン1モルを添加した後、トリエチルアミン2モル、sec-ブチルリチウム2モルを順次添加し、50℃で2時間攪拌して、ジリチウム系重合開始剤を調製した。
充分に脱水精製したシクロヘキサン溶媒中に、1,3-(ジイソプロペニル)ベンゼン1モルを添加した後、トリエチルアミン2モル、sec-ブチルリチウム2モルを順次添加し、50℃で2時間攪拌して、ジリチウム系重合開始剤を調製した。
充分に脱水精製したシクロヘキサン溶媒中に、1,3-(ジイソプロペニル)ベンゼン1モルを添加した後、トリエチルアミン2モル、sec-ブチルリチウム2モルを順次添加し、50℃で2時間攪拌して、ジリチウム系重合開始剤を調製した。
上記のようにして合成したスチレン-ブタジエン共重合体又は市販のジエン系ポリマーを用いて、表1~5に示す配合のゴム組成物を調製し、下記の方法で、硬化性及び相溶性を評価した。
イルガキュア184D(チバスペシャルティーケミカルズ社製、1-ヒドロキシシクロヘキシルフェニルケトン)を液状ゴム100質量部に対して1質量部配合し、紫外線を7000mJ/cm2照射した後、23℃において、組成物の硬化性を触診により評価した。溶液時と比較して完全に固体として硬化した場合を○、若干硬化した場合を△、全くしなかった場合を×とした。結果を表1~5に示す。
トリゴノックス121(アクゾ社製、t-アミルパーオキシ-2-エチルヘキサノエート)を液状ゴム100質量部に対して5質量部配合し、150℃で10分間硬化させた。この際における組成物の硬化性を触診により評価し、溶液時と比較して完全に固体として硬化した場合を○、若干硬化した場合を△、全くしなかった場合を×とした。結果を表1~5に示す。
各成分を配合した後、得られた組成物を透明ガラス基板上に塗布し、目視にて評価した。評価基準を以下に示す。
○ :透明
○△:若干白濁
△ :白濁
△×:やや相分離
× :完全に相分離或いは溶解せず
結果を表1~5に示す。
※2:Ricon181、サートマー社製、数平均分子量=3200、結合スチレン含量=25質量%、ブタジエン部分のビニル結合含量=30%、末端官能基:無し、25℃において液状
※3:SB共重合体A、上記の方法で合成、数平均分子量=5200、結合スチレン含量=35質量%、ブタジエン部分のビニル結合含量=65%、末端官能基:OH、25℃において液状
※4:SB共重合体B、上記の方法で合成、数平均分子量=4000、結合スチレン含量=55質量%、ブタジエン部分のビニル結合含量=65%、末端官能基:OH、25℃において液状
※5:SB共重合体C、上記の方法で合成、数平均分子量=4900、結合スチレン含量=23質量%、ブタジエン部分のビニル結合含量=65%、末端官能基:OH、25℃において液状
※6:SB共重合体D、数平均分子量=4400、結合スチレン含量=35質量%、ブタジエン部分のビニル結合含量=78%、末端官能基:OH、25℃において液状
※7:SB共重合体E、数平均分子量=12500、結合スチレン含量=29質量%、ブタジエン部分のビニル結合含量=65%、末端官能基:OH、25℃において液状
※8:SB共重合体F、数平均分子量=17200、結合スチレン含量=35質量%、ブタジエン部分のビニル結合含量=60%、末端官能基:OH、25℃において液状
※9:Poly-IP(イソプレンゴム、ホモポリマー)、出光興産製、数平均分子量=2500、末端官能基:OH、25℃において液状のポリイソプレン
※10:Poly-bd R-15HT(ブタジエンゴム、1,4-ポリブタジエン構造)、出光興産製、数平均分子量=1200、末端官能基:OH
※11:LIR-30(イソプレンゴム、ホモポリマー)、(株)クラレ製、数平均分子量=28000、末端官能基:なし
※12:LIR-50(イソプレンゴム、ホモポリマー)、(株)クラレ製、数平均分子量=54000、末端官能基:なし
※13:LIR-300(ブタジエンゴム、1,4-ポリブタジエン構造)、(株)クラレ製、数平均分子量=44000、末端官能基:なし
※14:LIR-403(イソプレンゴム、官能基含有ホモポリマー)、(株)クラレ製、数平均分子量=34000、末端官能基:無水マレイン酸
※15:Ricon142(ブタジエンゴム、1,4-ポリブタジエン構造)、サートマー社製、数平均分子量=3900、結合スチレン含量=0質量%、ブタジエン部分のビニル結合含量=55%、末端官能基:なし、25℃において液状のポリブタジエン
※16:Ricon150(ブタジエンゴム、1,4-ポリブタジエン構造)、サートマー社製、数平均分子量=3900、ブタジエン部分のビニル結合含量=70%、末端官能基:なし
※17:Ricon134(ブタジエンゴム、1,4-ポリブタジエン構造)、サートマー社製、数平均分子量=8000、ブタジエン部分のビニル結合含量=28%、末端官能基:なし
※18:Ricon154(ブタジエンゴム、1,3-ブタジエンホモポリマー)、サートマー社製、数平均分子量=5200、末端官能基:なし
※19:TMMP、トリメチロールプロパントリス(3-メルカプトプロピオネート)
※20:TEMPIC、トリス[(3-メルカプトプロピオニロキシ)-エチル]イソシアヌレート
※21:PEMP、ペンタエリスリトールテトラキス(3-メルカプトプロピオネート)
※22:DPMP、ジペンタエリスリトールヘキサキス(3-メルカプトプロピオネート)
※23:PE1、ペンタエリスリトールテトラキス(3-メルカプトブチレート)
※24:EGMP-4、テトラエチレングリコールビス(3-メルカプトプロピオネート)
※25:ジスネットF、三協化成(株)製
Claims (6)
- 25℃において液状であるスチレン-ブタジエン共重合体(A)と、
メルカプトカルボン酸由来のポリチオール(B)と
を含むことを特徴とするチオール含有液状ゴム組成物。 - 前記スチレン-ブタジエン共重合体(A)の結合スチレン含有量が、20~90質量%であることを特徴とする請求項1に記載のチオール含有液状ゴム組成物。
- 前記スチレン-ブタジエン共重合体(A)がランダム共重合体であることを特徴とする請求項1または2に記載のチオール含有液状ゴム組成物。
- 前記ポリチオール(B)が、テトラエチレングリコールビス(3-メルカプトプロピオネート)、トリメチロールプロパントリス(3-メルカプトプロピオネート)、トリス[(3-メルカプトプロピオニロキシ)-エチル]イソシアヌレート、ペンタエリスリトールテトラキス(3-メルカプトプロピオネート)、ジペンタエリスリトールヘキサキス(3-メルカプトプロピオネート)、1,4-ビス(3-メルカプトブチリルオキシ)ブタン、ペンタエリスリトールテトラキス(3-メルカプトブチレート)、及び1,3,5-トリス(3-メルカプトブチルオキシエチル)-1,3,5-トリアジン-2,4,6(1H,3H,5H)-トリオンからなる群から選択される少なくとも一種であることを特徴とする請求項1~3のいずれかに記載のチオール含有液状ゴム組成物。
- 前記ポリチオール(B)の含有量が、スチレン-ブタジエン共重合体(A)100重量部に対して、40質量部以下であることを特徴とする請求項1~4のいずれかに記載のチオール含有液状ゴム組成物。
- 前記スチレン-ブタジエン共重合体(A)の数平均分子量(Mn)が、1200~40000であることを特徴とする請求項1~5のいずれかに記載のチオール含有液状ゴム組成物。
Priority Applications (4)
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EP10764294.4A EP2420535A4 (en) | 2009-04-16 | 2010-04-16 | THIOLIC LIQUID RUBBER COMPOSITION |
CN201080027163.9A CN102459447B (zh) | 2009-04-16 | 2010-04-16 | 含硫醇的液态橡胶组合物 |
JP2011509228A JP5653344B2 (ja) | 2009-04-16 | 2010-04-16 | チオール含有液状ゴム組成物 |
US13/264,666 US8865841B2 (en) | 2009-04-16 | 2010-04-16 | Thiol-containing liquid rubber composition |
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JP2009-100152 | 2009-04-16 | ||
JP2009100152 | 2009-04-16 |
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WO2010119708A1 true WO2010119708A1 (ja) | 2010-10-21 |
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PCT/JP2010/002794 WO2010119708A1 (ja) | 2009-04-16 | 2010-04-16 | チオール含有液状ゴム組成物 |
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US (1) | US8865841B2 (ja) |
EP (1) | EP2420535A4 (ja) |
JP (1) | JP5653344B2 (ja) |
CN (1) | CN102459447B (ja) |
WO (1) | WO2010119708A1 (ja) |
Cited By (5)
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JP2014506951A (ja) * | 2011-03-04 | 2014-03-20 | スティロン ヨーロッパ ゲゼルシャフト ミット ベシュレンクテル ハフツング | 高スチレン高ビニルスチレン−ブタジエンゴムおよびそれらの調製方法 |
JP2015063648A (ja) * | 2013-08-26 | 2015-04-09 | 横浜ゴム株式会社 | ゴム組成物およびこれを用いる空気入りタイヤ |
JP2015524492A (ja) * | 2012-07-09 | 2015-08-24 | ランクセス・ドイチュランド・ゲーエムベーハー | 多価アルコールのω−メルカプトカルボン酸エステルを含むシリカ含有ゴム混合物 |
WO2021235678A1 (ko) * | 2020-05-22 | 2021-11-25 | 주식회사 엘지화학 | 액상 고무 제조방법 및 이로부터 제조된 액상 고무 |
KR20230106748A (ko) * | 2017-06-06 | 2023-07-13 | 탑 글로브 글로벌 에스디엔 비에이치디 | 가교된 스타이렌계 블록 공중합체 |
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JP5887274B2 (ja) * | 2010-10-29 | 2016-03-16 | 株式会社カネカ | イソブチレン系ブロック共重合体組成物 |
TWI580720B (zh) * | 2015-12-10 | 2017-05-01 | 奇美實業股份有限公司 | 熱可塑性樹脂組成物及其所形成的成型品 |
CN111434705B (zh) * | 2019-01-14 | 2022-03-15 | 中国石油化工股份有限公司 | 改性液体橡胶及其制备方法和应用 |
US11214676B2 (en) * | 2019-04-05 | 2022-01-04 | Fina Technology, Inc. | Polyenes for curable liquid rubber-based compositions |
EP3907256A1 (en) * | 2020-05-04 | 2021-11-10 | Evonik Operations GmbH | Rubber mixtures with improved properties |
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- 2010-04-16 JP JP2011509228A patent/JP5653344B2/ja not_active Expired - Fee Related
- 2010-04-16 EP EP10764294.4A patent/EP2420535A4/en not_active Withdrawn
- 2010-04-16 CN CN201080027163.9A patent/CN102459447B/zh not_active Expired - Fee Related
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JP2014506951A (ja) * | 2011-03-04 | 2014-03-20 | スティロン ヨーロッパ ゲゼルシャフト ミット ベシュレンクテル ハフツング | 高スチレン高ビニルスチレン−ブタジエンゴムおよびそれらの調製方法 |
JP2015524492A (ja) * | 2012-07-09 | 2015-08-24 | ランクセス・ドイチュランド・ゲーエムベーハー | 多価アルコールのω−メルカプトカルボン酸エステルを含むシリカ含有ゴム混合物 |
JP2015063648A (ja) * | 2013-08-26 | 2015-04-09 | 横浜ゴム株式会社 | ゴム組成物およびこれを用いる空気入りタイヤ |
KR20230106748A (ko) * | 2017-06-06 | 2023-07-13 | 탑 글로브 글로벌 에스디엔 비에이치디 | 가교된 스타이렌계 블록 공중합체 |
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WO2021235678A1 (ko) * | 2020-05-22 | 2021-11-25 | 주식회사 엘지화학 | 액상 고무 제조방법 및 이로부터 제조된 액상 고무 |
JP2022537911A (ja) * | 2020-05-22 | 2022-08-31 | エルジー・ケム・リミテッド | 液状ゴムの製造方法およびそれから製造された液状ゴム |
EP3981803A4 (en) * | 2020-05-22 | 2023-04-19 | LG Chem, Ltd. | LIQUID RUBBER MANUFACTURING PROCESS AND LIQUID RUBBER MANUFACTURED THEREFORE |
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JPWO2010119708A1 (ja) | 2012-10-22 |
CN102459447A (zh) | 2012-05-16 |
US8865841B2 (en) | 2014-10-21 |
US20120041154A1 (en) | 2012-02-16 |
CN102459447B (zh) | 2014-07-02 |
JP5653344B2 (ja) | 2015-01-14 |
EP2420535A4 (en) | 2015-02-18 |
EP2420535A1 (en) | 2012-02-22 |
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