A kind of stereoregular styrene thermoplastic elastomer and preparation method thereof
A thermoplastic elastomer and stereoregular technology, which is applied in the preparation of the thermoplastic elastomer by coordination polymerization, the stereoregular styrene thermoplastic elastomer and the preparation field thereof, can solve the problem that the stereoregularity of polystyrene is difficult to improve. Polybutadiene cis structure content, difficult to improve polystyrene tacticity, difficult to coordinate efficient block copolymerization and other problems, to achieve the effect of improving stereoregularity, good elasticity and wear resistance, and increasing service temperature
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Embodiment 1
[0028] During the synthesis, all operations were carried out under the protection of nitrogen.
[0029] The catalyst is composed of neodymium (A) 2-ethylhexanoate, triisobutylaluminum, trichloroethane, 2-ethylhexanoic acid and styrene, and the molar ratio of each component is A:B:C:D:E = 1:16:3:3:2.
[0030] (1) In a reaction flask, mix 10 mL of styrene with the above catalyst so that the molar ratio of A / total monomer is 5×10 -3 , polymerized at 35°C for 6.5h to produce stereoregular polystyrene active chains (S s ) solution;
[0031] (2) In (1) system, add 37mL butadiene (Bd) / n-hexane (HEX) / cyclohexane (CHX) solution ([Bd]=2.4M, V CHX :V HEX =1:1), polymerized at 18°C for 8 hours, and obtained active chains of butadiene-styrene diblock copolymers rich in syndiotactic polystyrene and high cis-polybutadiene (S s B cis ) solution.
[0032] (3) Further polymerize styrene at 40°C for 10 h to obtain active chains of styrene-butadiene triblock copolymers rich in syndiotact...
Embodiment 2
[0037] Experimental operation method is the same as embodiment 1.
[0038] The catalyst consists of 2,5-dimethyl-2-ethyl-hexanoic acid neodymium (A), triisobutylaluminum, trichloroethane and 2,5-dimethyl-2-ethyl-hexanoic acid, Wherein the molar ratio of each component is A:B:C:D=1:14:2.4:0.4.
[0039] (1) In a reaction flask, mix a small amount of styrene (A / St=1 / 1.5, molar ratio) with the above-mentioned catalyst, pre-react at 30°C for 0.5h, and then mix with 20mL styrene / cyclohexane solution ([St ]=6M) mixed so that the molar ratio of A / total monomer is 2.5×10 -3 , polymerized at 40°C for 5h to obtain S s active chain solution;
[0040] (2) In (1) system, add 48mL butadiene / n-hexane / cyclohexane solution ([Bd]=2.5M, V CHX :V HEX =1:1), continued polymerization at 15°C for 10h, and obtained S s B ci active chain solution;
[0041] (3) Further polymerize styrene at 55°C for 7 hours to obtain S s B cis S s active chain system.
[0042] (4) termination reaction and af...
Embodiment 3
[0046] Experimental operation method is the same as embodiment 1.
[0047] The catalyst is composed of neodymium (A) 2-ethylhexanoate, triisobutylaluminum, trichloroethane, 2-ethylhexanoic acid and styrene, and the molar ratio of each component is A:B:C:D:E =1:16:2:1.5:1.
[0048] (1) In a reaction flask, mix 20 mL of styrene cyclohexane solution ([St]=6.0 M) with the above catalyst so that the molar ratio of A / total monomer is 1×10 -3 , polymerized at 45°C for 5h to obtain S s active chain solution;
[0049] (2) In the system (1), add 25mL of butadiene / cyclohexane solution ([Bd]=2.4M), polymerize at 23°C for 4.5h, and obtain S s B cis active chain solution;
[0050] (3) Further polymerize styrene at 60°C for 5 hours to obtain S s B cis S s active chain system.
[0051] (4) termination reaction and aftertreatment mode are the same as embodiment 1, obtain S s B cis S s Tri-block copolymer system with a block efficiency of 93%.
[0052] S s B cis S s Number avera...
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