Manufacturing method of solid catalyst for propylene polymerization
Disclosed is a method for preparing a solid catalyst for propylene polymerization, specifically to a method for preparing a solid catalyst for propylene polymerization which can produce a polypropylene having high melt flow rate, a wide molecular distribution and excellent stereoregularity with a high production yield.
1. A method for preparing a solid catalyst comprising the following steps:
(1) reacting dialkoxymagnesium and a titanium halide, in the presence of an organic solvent;
(2) adding an internal electron donor selected from the compounds represented by the following formula (II) together with another internal electron donor selected from the compounds represented by the following formula (III) to the resulted product from the above step (1), and mixing them together, while elevating the temperature to the range of 80-130° C.,
wherein, R 1 , R 2 , R 3 and R 4 are independently a linear, branched or cyclic C1-10 alkyl group or hydrogen;
wherein, R 1 and R 2 are independently a linear, branched or cyclic C1-10 alkyl group or hydrogen; and R 3 and R 4 are independently a linear, branched or cyclic C1-10 alkyl group; and
(3) reacting titanium halide with the resulted product from the above step (2) at the temperature range of 80-130° C. and washing the resulted product.
2. The method according to claim 1 , wherein the solid catalyst comprises magnesium 5-40 wt %, titanium 0.5-10 wt %, halogen 50-85 wt % and the internal electron donor mixture 2.5-30 wt %, calculated based on a total weight of the weight of the solid catalyst.
3. The method according to claim 1 , wherein the internal electron donor is selected from the following compounds: diethyl-2,3-dimethylsuccinate, diethyl-2,3-diethylsuccinate, diethyl-2,3-dipropylsuccinate, diethyl-2,3-diisopropylsuccinate, diethyl-2,3-dibutylsuccinate, diethyl-2,3-diisobutylsuccinate, diethyl-2,3-dipentylsuccinate, diethyl-2,3-dihexylsuccinate, diethyl-2,3-dicyclopentylsuccinate, diethyl-2,3-dicyclohexylsuccinate, diethyl-2-cyclopentyl-3-methylsuccinate, diethyl-2-cyclohexyl-3-methylsuccinate, diethyl-2-isopropyl-3-methylsuccinate, diethyl-2-isobutyl-3-methylsuccinate, diethyl-2-cyclopentyl-3-ethylsuccinate, diethyl-2-cyclohexyl-3-ethylsuccinate, diethyl-2-isopropyl-3-ethylsuccinate, diethyl-2-isobutyl-3-ethylsuccinate, diethyl-2-cyclopentyl-3-propylsuccinate, diethyl-2-cyclohexyl-3-propylsuccinate, diethyl-2-isopropyl-3-propylsuccinate, diethyl-2-isobutyl-3-propylsuccinate, diethyl-2-cyclopentyl-3-isopropylsuccinate, diethyl-2-cyclohexyl-3-isopropylsuccinate, diethyl-2-isobutyl-3-isopropylsuccinate, diethyl-2-cyclopentyl-3-isobutylsuccinate, diethyl-2-cyclohexyl-3-isobutylsuccinate, diethyl-2,3-dimethylidenesuccinate, diethyl-2,3-diethylidenesuccinate, diethyl-2,3-dipropylidenesuccinate, diethyl-2,3-diisopropylidenesuccinate, diethyl-2,3-dibutylidenesuccinate, diethyl-2,3-diisobutylidenesuccinate, diethyl-2,3-dipentylidenesuccinate, diethyl-2,3-dihexylidenesuccinate, diethyl-2,3-dicyclopentylidenesuccinate, and diethyl-2,3-dicyclohexylidenesuccinate.
4. The method according to claim 1 , wherein the amount of the internal electron donor used is 0.1-1.0 mole based on 1 mole of the dialkoxymagnesium.
5. The method according to claim 2 , wherein the amount of the internal electron donor used is 0.1-1.0 mole based on 1 mole of the dialkoxymagnesium.
6. The method according to claim 3 , wherein the amount of the internal electron donor used is 0.1-1.0 mole based on 1 mole of the dialkoxymagnesium.