Catalytic system for preparing polar group-containing polyolefin and preparation method of the polyolefin
A catalytic system and polar group technology, applied in the field of polyolefin materials, can solve the problems of reduced copolymerization activity, catalyst deactivation, and low molecular weight of polymers
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Embodiment 1
[0057] Fully dry the polymerization device, then vacuumize it and flush it with nitrogen, repeat three times. The polymerization device is vacuumized again, controlled by a solenoid valve, charged with ethylene, 25.8 milliliters of toluene is added at 25° C., 0.1 milliliters of 9-decen-1-alcohol is added, 0.6 milliliters of triisobutylaluminum toluene solution (1.1 mol / mL), stirred for 10 minutes. Add 3 mL of MAO toluene solution (1.67 mol / ml) and 1 ml of transition metal compound (X=Cl) solution (10 micromol / ml) described in formula I, and start timing. After 20 minutes, turn off ethylene, add acidified ethanol to the reaction solution, stir for more than 6 hours, filter to obtain the polymer, vacuum dry the obtained polymer at 60° C. for 24 hours, and weigh to obtain 0.49 g of the polymer. The specific reaction conditions and results are listed in Table 1. The CPC test curve, DSC curve and the compound that present embodiment makes 13 C-NMR test results are as follows ...
Embodiment 2
[0059] Fully dry the polymerization device, then vacuumize it and flush it with nitrogen, repeat three times. The polymerization device is vacuumized again, controlled by a solenoid valve, charged with ethylene, 25.1 milliliters of toluene is added at 25° C., 0.2 milliliters of 9-decen-1-ol is added, 1.2 milliliters of triisobutylaluminum toluene solution (1.1 mol / mL), stirred for 10 minutes. Add 3 mL of MAO toluene solution (1.67 mol / ml) and 1 ml of transition metal compound (X=Cl) solution (10 micromol / ml) described in formula I, and start timing. After 20 minutes, turn off ethylene, add acidified ethanol to the reaction solution, stir for more than 6 hours, filter to obtain the polymer, vacuum dry at 60° C. for 24 hours, and weigh to obtain 0.61 g of the polymer. The specific reaction conditions and results are listed in Table 1.
Embodiment 3
[0061] Fully dry the polymerization device, then vacuumize it and flush it with nitrogen, repeat three times. The polymerization device is vacuumized again, controlled by a solenoid valve, charged with ethylene, 24.4 milliliters of toluene is added at 25° C., 0.3 milliliters of 9-decen-1-alcohol is added, 1.8 milliliters of triisobutylaluminum toluene solution (1.1 mol / mL), stirred for 10 minutes. Add 3 mL of MAO toluene solution (1.67 mol / ml) and 1 ml of transition metal compound (X=Cl) solution (10 micromol / ml) described in formula I, and start timing. After 20 minutes, turn off the ethylene, add acidified ethanol to the reaction solution, stir for more than 6 hours, filter to obtain the polymer, vacuum dry at 60° C. for 24 hours, and weigh to obtain 0.43 g of the polymer. The specific reaction conditions and results are listed in Table 1.
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