Process for preparing a catalyst component for polymerization of olefins
US-2015368381-A1 · Dec 24, 2015 · US
US9593171B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9593171-B2 |
| Application number | US-201214111144-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 29, 2012 |
| Priority date | Apr 12, 2011 |
| Publication date | Mar 14, 2017 |
| Grant date | Mar 14, 2017 |
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A porous solid catalyst component comprising a magnesium halide, a titanium compound having at least a Ti-halogen bond and at least two electron donor compounds one of which being selected from 1,3-diethers and the other being selected from succinates, characterized by the fact that the molar ratio ID/Ti is from 0.30 to 0.90, where ID is the total molar amount of succinate and 1,3-diether, the molar ratio of the 1,3-diether donor to the succinate donor is higher than, or equal to, 0.60.
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What is claimed is: 1. A catalyst system comprising: (A) a solid catalyst component comprising: (i) a magnesium halide, (ii) TiCl 4 , (iii) a first internal electron donor, and (iii) a second internal electron donor, wherein the first internal electron donor compound is a 1,3-diether, and wherein the second internal electron donor is a succinate; wherein the first internal electron donor and the second internal electron donor have an internal electron donor molar ratio from 0.80-1.80, and the ratio of the total amount of the first and second internal electron donors to Ti is from 0.45-0.75; and wherein the solid catalyst component has a porosity of greater than 0.40 cm 3 /g, based upon pores with a radius equal to or less than 1 μm present in the solid catalyst component; (B) an alkylaluminum cocatalyst compound; and (C) an external electron donor compound selected from silicon compounds of formula R a 5 R b 6 Si(OR 7 ) c , where a and b are integers from 0 to 2, c is an integer from 1 to 4 and the sum (a+b+c) is 4; R 5 , R 6 and R 7 are alkyl, cycloalkyl or aryl radicals with 1-18 carbon atoms optionally containing heteroatoms. 2. The catalyst system according to claim 1 , wherein the succinate is selected from formula (I): wherein the radicals R 1 and R 2 , equal to or different from each other, are a C 1 -C 20 linear or branched alkyl, alkenyl, cycloalkyl, aryl, arylalkyl or alkylaryl group, optionally containing heteroatoms; the radicals R 3 to R 6 equal to or different from each other, are hydrogen or a C 1 -C 20 linear or branched alkyl, alkenyl, cycloalkyl, aryl, arylalkyl or alkylaryl group, optionally containing heteroatoms, and the radicals R 3 to R 6 which are joined to the same carbon atom of the succinate chain can be linked together to form a cycle. 3. The catalyst system according to claim 1 , wherein the 1,3-diether has a formula (III): wherein R I and R II are the same or different and are hydrogen or linear or branched C 1 -C 18 hydrocarbon groups which can also form one or more cyclic structures;R III groups, equal or different from each other, are hydrogen or C 1 -C 18 hydrocarbon groups; R IV groups equal or different from each other, have the same meaning of R III except that they cannot be hydrogen; each of R I to R IV groups can contain heteroatoms selected from halogens, N, O, S and Si. 4. The catalyst system according to claim 1 , wherein the solid catalyst component is supported on a Mg halide in active form.
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