SOLID CATALYST FOR PROPYLENE POLYMERIZATION AND A METHOD FOR PREPARATION OF POLYPROPYLENE
Provided are a solid catalyst which includes an internal electron donor mixture including at least one selected from bicycloalkane dicarboxylates and bicycloalkene dicarboxylates, and benzene 1,2-dicarboxylic acid ester, and can produce a polypropylene having excellent stereoregularity and melt flowability with a high catalytic activity, and a method for preparing polypropylene using the catalyst.
1 . A solid catalyst for propylene polymerization comprising titanium, magnesium, halogen and an internal electron donor mixture, wherein the internal electron donor mixture comprises at least one selected from the bicycloalkane dicarboxylates and bicycloalkene dicarboxylates represented by the following formula (II), formula (III), formula (IV) and formula (V), and benzene-1,2-dicarboxylic acid ester:
wherein, R1 and R2, which may be same or different, are a linear, branched or cyclic C1-20 alkyl, alkenyl, aryl, arylalkyl or alkylaryl group, respectively; R3, R4, R5 and R6, which may be same or different, are hydrogen, a linear, branched or cyclic C1-20 alkyl, alkenyl, aryl, arylalkyl or alkylaryl group, respectively.
2 . The solid catalyst for propylene polymerization according to claim 1 , comprising magnesium 5-40 wt %, titanium 0.5-10 wt %, halogen 50-85 wt % and the internal electron donor mixture 2.5-30 wt %.
3 . Method for preparing polypropylene comprising polymerizing propylene or copolymerizing propylene with other alpha-olefins, in the presence of a solid catalyst according to claim 1 , AlR3, wherein R is C1-8 alkyl group as a cocatalyst and R1mR2nSi(OR3)(4−m−n), wherein R1 and R2, which are same or different, linear, branched or cyclic C1-12 alkyl or aryl group; R3 is linear or branched C1-6 alkyl group; m and n are 0 or 1, respectively, provided that m+n is 1 or 2, as an external electron donor.
4 . Method for preparing polypropylene comprising polymerizing propylene or copolymerizing propylene with other alpha-olefins, in the presence of a solid catalyst according to claim 2 , AlR3, wherein R is C1-8 alkyl group as a cocatalyst and R1mR2nSi(OR3)(4−m−n), wherein R1 and R2, which are same or different, linear, branched or cyclic C1-12 alkyl or aryl group; R3 is linear or branched C1-6 alkyl group; m and n are 0 or 1, respectively, provided that m+n is 1 or 2, as an external electron donor.