Process for producing polypropylene impact block copolymers
A process for producing a polypropylene impact copolymer by polymerizing propylene and optionally a monomer selected from the group consisting of ethylene, butene-1, pentene-1, and hexene-1 in a first reactor in the presence of a titanium, magnesium, halogen, and a inside electron donor catalyst, an organoaluminum cocatalyst, and an outside electron donor, R.sup.1.sub.2 Si(OR.sup.2).sub.2, to produce a first polymer which enters a second reactor where it is reacted with propylene and another monomer in the absence of additional catalyst and in the presence of a third electron donor, Si(OR.sup.3).sub.4 is provided.
Claims
1. A process for producing polypropylene, impact, block copolymers, which process comprises the steps of
- 1) polymerizing propylene and optionally less than 3 mol % of a comonomer selected from the group consisting of ethylene, butene-1, pentene-1, and hexene-1, in a first polymerization reactor under polymerization conditions in the presence of a catalyst system of:
- i) a solid catalyst precursor consisting essentially of magnesium, titanium, halogen, and an inside electron donor,
- ii) an organoaluminum cocatalyst,
- iii) an outside electron donor of the formula
- 2) polymerizing in a second reactor the first polymer obtained in step 1 with propylene and a monomer selected from the group consisting of ethylene, butene-1, pentene-1, and hexene-1 in the absence of an additional catalyst system and in the presence of tetraethoxysilane.
2. The process of claim 1 wherein the solid catalyst precursor is magnesium, titanium, halide and a polycarboxylic acid ester containing two coplanar ester groups attached to adjacent carbon atoms, said catalyst component being obtained by halogenating a magnesium compound of the formula MgR'R", wherein R' and R are alkoxide groups containing from 1 to 8 carbon atoms, with titanium tetrachloride, in the presence of (1) an aromatic halohydrocarbon containing from 6 to 12 carbon atoms and from 1 to 2 halogen atoms and (2) a polycarboxylic acid ester derived from (i) a branched or unbranched monohydric alcohol containing from 1 to 12 carbon atoms and (ii) a monocyclic or polycyclic aromatic compound containing from 8 to 20 carbon atoms and two carboxyl groups which are attached to ortho carbon atoms of the ring structure.
3. The process of claim 2 wherein the catalyst contains an atomic ratio of aluminum in the organoaluminum cocatalyst to silicon in the electron donor of from 0.5:1 to 100:1, and an atomic ratio of aluminum in the organoaluminum cocatalyst to titanium in the solid catalyst component of from 5:1 to 300:1 and a rubber phase of the copolymer product has a Sequence Index greater than 1.3.
4. A process as in claim 3 wherein the magnesium compound is magnesium diethoxide or magnesium ethyl carbonate.
5. A process as in claim 4 wherein the halohydrocarbon is chlorobenzene.
6. A process as in claim 5 wherein the polycarboxylic acid ester is diisobutyl phthalate.
7. A process as in claim 6 wherein the halogenated product is treated twice with additional titanium tetrachloride and the second treatment is effected in the presence of a polycarboxylic acid halide containing two coplanar acid halide groups attached to adjacent carbon atoms.
8. A process as in claim 7 wherein the polycarboxylic acid halide is phthaloyl dichloride.
9. A process as in claim 8 wherein propylene is copolymerized with up to 40 mole percent ethylene in a second polymerization reactor in the presence of the product of the first polymerization reactor.
10. A process as in claim 6 wherein the outside electron donor is dicyclopentyldimethoxysilane.
11. A process as in claim 8 wherein the outside electron donor is dicyclopentyldimethoxysilane.
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Type: Grant
Filed: May 5, 1995
Date of Patent: Apr 7, 1998
Inventors: Mark Gregory Goode (Hurricane, WV), Kersten Anne Erickson (Dunbar, WV), James Douglas McCullough, Jr. (Houston, TX)
Primary Examiner: Charles T. Jordan
Assistant Examiner: Meena Chelliah
Attorney: Andrew R. Reiskind
Application Number: 8/436,808
International Classification: C08F 4649;