Ultrahigh molecular weight functionalized isotactic polypropylene and preparation method thereof
An ultra-high molecular weight, isotactic polypropylene technology, applied in the production of bulk chemicals, etc., can solve the problems of inability to achieve high isotacticity and harsh polymerization conditions, and achieve the effect of easy industrialization and simple process
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[0030] The present invention also provides a preparation method of ultra-high molecular weight functionalized isotactic polypropylene, comprising:
[0031] Under anhydrous and oxygen-free conditions, a solvent and a polar monomer of formula II structure are added into the reactor, the solvent is preferably toluene, then propylene gas is introduced, and after stirring and mixing evenly, a catalyst and a co-catalyst are added to react , the reaction temperature is preferably room temperature, and the reaction time is preferably 20-720 min. After the polymerization reaction is completed, the polymer is precipitated in the solvent, the solvent is preferably a hydrochloric acid / ethanol mixture, and then dried, the drying temperature is preferably 60°C, and the reaction time is preferably 24h, to obtain ultra-high molecular weight functionalization, etc. Regular polypropylene; the catalyst is a front transition metal alkyl compound; the equivalent of the polar monomer of the formula...
Embodiment 1
[0048] Under anhydrous and anaerobic conditions, feed 1 equivalent of phenol, 1.5 equivalents of 6-bromo-1-hexene, 3 equivalents of K to the reaction flask 2 CO 3 , 300 ml of N,N-dimethylformamide, reacted at 80 degrees Celsius for 12 hours, quenched with a saturated aqueous solution of ammonium chloride, extracted with dichloromethane to obtain an organic phase, spin-dried, and distilled under reduced pressure to obtain Purified polar monomer 4 (X=O).
[0049] Under anhydrous and oxygen-free conditions, put 145 ml of toluene solution into the reaction kettle, and add 100 equivalents of polar monomer 4 (X=O), then connect 1 atmosphere of propylene gas, and after magnetic stirring and mixing, put into the system 1 equivalent of catalyst and 1.05 equivalents of Ph 3 CB(C 6 F 5 ) 4 5 ml of mixed toluene solution. The polymerization was completed after 2 hours of magnetic stirring, the polymer was precipitated in the hydrochloric acid / ethanol mixed solution, and the polymer ...
Embodiment 2
[0051] Under anhydrous and anaerobic conditions, feed 1 equivalent of phenol, 1.5 equivalents of 6-bromo-1-hexene, 3 equivalents of K to the reaction flask 2 CO 3 , 300 ml of N,N-dimethylformamide, reacted at 80 degrees Celsius for 12 hours, quenched with a saturated aqueous solution of ammonium chloride, extracted with dichloromethane to obtain an organic phase, spin-dried, and distilled under reduced pressure to obtain Purified polar monomer 4 (X=O).
[0052] Under anhydrous and oxygen-free conditions, put 145 ml of toluene solution into the reactor, and add 500 equivalents of polar monomer 4 (X=O), then connect 1 atmosphere of propylene gas, and after magnetic stirring and mixing, put into the system 1 equivalent of catalyst and 1.05 equivalents of Ph 3 CB(C 6 F 5 ) 4 5 ml of mixed toluene solution. The polymerization was completed after 12 hours of magnetic stirring, the polymer was precipitated in the hydrochloric acid / ethanol mixed solution, and the polymer was dri...
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