Catalyst for polymerization of propylene and method for polymerization of propylene using the same
Provided are a catalyst for polymerization of propylene and a method for polymerization of propylene using the same. Specifically, provided are a catalyst for propylene polymerization which comprises titanium tetrachloride, an internal electron donor, and dialkoxy magnesium particles, as a carrier, obtained from the reaction of a halogen compound or nitrogen-halogen compound as a reaction initiator, metal magnesium and an alcohol, and a method for propylene polymerization using the same.
1. A method for preparing a catalyst for propylene polymerization, wherein the method comprises:
obtaining a dialkoxy magnesium carrier by reacting metal magnesium with 5-50 parts by weight of an alcohol, based on 1 part by weight of metal magnesium, at 60-110° C. in the presence of 0.001-0.2 parts by weight of a nitrogen-based halogen compound as a reaction initiator, based on 1 part by weight of metal magnesium, selected from the following (1)-(4):
(1) N-halide succinimides represented by the general formula
wherein, X is a halogen atom, and R 1 , R 2 , R 3 and R 4 are independently hydrogen, or C 1-12 alkyl or C 1-12 aryl;
(2) trihaloisocyanuric acid compounds represented by the general formula
wherein, X is a halogen atom;
(3) N-halophthalimide compounds represented by the general formula
wherein, X is a halogen atom, and R 1 , R 2 , R 3 and R 4 are independently, hydrogen, or C 1-12 alkyl or C 1-12 aryl; and
(4) hydantoin compounds represented by the general formula
wherein, X is a halogen atom, and R 1 and R 2 are independently hydrogen, or C 1-12 alkyl or C 1-12 aryl;
reacting the above obtained dialkoxy magnesium carrier with titanium tetrachloride; and
reacting the resultant product with titanium tetrachloride and an internal electron donor.
2. The method according to claim 1 , wherein the average particle diameter of the metal magnesium is 10-300 μm.
3. The method according to claim 1 , wherein the alcohol is one or more selected from aliphatic alcohols represented by ROH, wherein R is a C1-6 alkyl group, and aromatic alcohols.
4. The method according to claim 1 , wherein the internal electron donor is one or more selected from phthalic acid diesters and derivatives thereof, and benzoates and derivatives thereof.