Rare earth catalyst and controllable polymerization method for conjugated diene in arene medium
A technology of rare earth catalysts and conjugated diolefins, applied in the field of rare earth catalysts, can solve the problems of reducing catalyst activity and stereoselectivity, and achieve high catalytic activity and high directional selectivity
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Embodiment 1
[0026] Under the protection of nitrogen, with hexane as solvent medium, add 0.80mmol neodymium 2-ethylhexanoate, 0.16mmol 2-ethylhexanoate, 6.4mmol chloroform, 0.17mmol ethanol, 15.9mmol triisobutylaluminum Al (i-Bu) 3 and 0.1 mmol of diisobutylaluminum hydride, mixed uniformly and then reacted at 40°C for 2 hours to form a homogeneous catalyst system.
[0027] Under the protection of nitrogen, add 27mL of butadiene / styrene solution ([Bd]=3.1mol / L) to a 100mL dry polymerization reactor, and then add the above catalyst, wherein the moles of component A and butadiene monomer The ratio is 1.6×10 -3 After mixing evenly, polymerize at 10°C for 4.5h, terminate the reaction with an ethanol solution containing antioxidant-264 (1%), remove the solvent and unreacted monomers, and dry in a vacuum oven at 50°C until constant weight . Polybutadiene yield is 85%, polybutadiene weight-average molecular weight (M w ) is 4.1×10 5 , molecular weight distribution index (M w / M n ) is 3.8,...
Embodiment 2
[0029] Under nitrogen protection, with hexane as the solvent medium, add 0.8mmol neodymium 2-ethylhexanoate, 1.3mmol 2-ethylhexanoate, 2.4mmol 1,1,1-trichloroethane, 0.07mmol ethanol, 12.6 mmol Triisobutylaluminum Al(i-Bu) 3 and 0.2mmol diisobutylaluminum hydride and 1.6mmol butadiene, mixed for 1 evenly and then reacted at 50°C for 5h to form a homogeneous catalyst system.
[0030] Under the protection of nitrogen, add 27mL of butadiene / styrene solution ([Bd]=3.1mol / L) to a 100mL dry polymerization reactor, and then add the above catalyst, wherein the moles of component A and butadiene monomer The ratio is 4.3×10 -4 , After mixing evenly, polymerize at 20°C for 4.5h. The termination reaction and aftertreatment are the same as in Example 1. Polymer yield was 76%, M w 3.2×10 5 ,M w / M n 3.1, the cis-1,4 structure content is 98.2%, and the polymer basically does not contain styrene units.
Embodiment 3
[0032] Under nitrogen protection, with hexane as solvent medium, add 0.80mmol neodymium 2-ethylhexanoate, 0.16mmol 2-ethylhexanoate, 6.4mmol chloroform, 0.005mmol methyl trichlorobenzoate, 0.51mmol Ethanol, 15.9mmol triisobutylaluminum Al(i-Bu) 3 and 0.1 mmol of diisobutylaluminum hydride, mixed uniformly and then reacted at 40°C for 2 hours to form a homogeneous catalyst system.
[0033] Under the protection of nitrogen, add 27mL of butadiene / α-methylstyrene solution ([Bd]=3.1mol / L) to a 100mL dry polymerization reactor, and then add the above catalyst, wherein component A and butadiene The molar ratio of monomers is 1.6×10 -3 , After mixing evenly, polymerize at 10°C for 4.5h. The termination reaction and aftertreatment are the same as in Example 1. Polymer yield was 97%, M w 2.9×10 5 ,M w / M n 3.2, the cis-1,4 structure content is 99.4%, and the polymer basically does not contain α-methylstyrene units.
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