Catalyst component and catalyst for olefin polymerization
A technology of olefin polymerization and catalyst, which is applied in the field of catalysts and can solve problems such as low melt index, low activity, and wide molecular weight distribution
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Embodiment 1
[0088] 1. Synthesis of internal electron donor compound (compound 1: 2-n-pentyl carbonate acetophenone)
[0089] 300g of 2-hydroxyacetophenone, 226.3g of anhydrous pyridine, and 10g of 4-dimethylaminopyridine were added to a mixed solvent of 300mL of dry tetrahydrofuran and 200mL of chloroform. 397.6g of n-pentyl chloroformate was added to 200mL of chloroform, and then added dropwise into the reaction system, and the temperature was kept stable between 10-20°C during the dropwise addition. After the dropwise addition, the temperature was raised to 50°C and stirred for 3-4 hours, and then reacted at 80°C for 8-10 hours. End the reaction, cool, filter to remove solid salt, spin dry the solvent, add 200mL ethyl acetate, 400mL water, use 10% hydrochloric acid to adjust to pH=5-6, separate liquid, ethyl acetate extract the aqueous phase twice (100mL, 80 mL), the organic phases were combined, dried over anhydrous magnesium sulfate, filtered, and the solvent was spin-dried to obtain...
Embodiment 2
[0097] 1. Synthesis of internal electron donor compound (compound 2: 2-n-butyl carbonate acetophenone)
[0098] Using a synthesis method similar to compound 1, n-pentyl chloroformate was replaced by n-butyl chloroformate to prepare 383.5 g of 2-n-butyl carbonate acetophenone with a yield of 73.6% and a purity of 98.81% (GC).
[0099] 1 H NMR (CDCl 3 / TMS,300MHz)δ(ppm):0.94-0.99(t,-O(CH 2 ) 3 CH 3 ),1.42-1.50(m,-OCH 2 CH 2 CH 2 CH 3 ),1.72-1.77(m,-OCH 2 CH 2 CH 2 CH 3 ),2.56(s,-C(O)CH 3 ),4.26-4.30(m,-OCH 2 CH 2 CH 2 CH 3 ),7.19-7.53(m,-C 6 h 4 ).
[0100] Two, the preparation method of catalyst component is with embodiment 1, and difference is, in step (2), compound 1 is replaced by compound 2 (the mol ratio of compound 2 and magnesium compound is 0.088 with compound 2: magnesium), Catalyst component 2 was obtained.
[0101] 3. The method for propylene polymerization is the same as in Example 1, except that catalyst component 1 is replaced by catalyst comp...
Embodiment 3
[0103] 1. Synthesis of internal electron donor compound (compound 3: 2-isobutyl carbonate acetophenone)
[0104] Using a synthesis method similar to compound 1, n-pentyl chloroformate was replaced by isobutyl chloroformate to prepare 282.6 g of 2-isobutyl carbonate acetophenone with a yield of 55.6% and a purity of 98.7% (GC).
[0105] 1 H NMR (CDCl 3 / TMS,300MHz)δ(ppm):0.98-1.00(t,-OCH 2 CH(CH 3 ) 2 ),(m,-OCH 2 CH(CH 3 ) 2 ),2.53(s,-C(O)CH 3 ),4.04-4.06(d,-OCH 2 CH(CH 3 ) 2 ),7.17-7.80(m,-C 6 h 4 ).
[0106] Two, the preparation method of catalyst component is the same as embodiment 1, and difference is that compound 1 is replaced by compound 3 (the molar ratio of compound 3 and magnesium compound is calculated as 0.088 with compound 3:magnesium), obtains catalyst component 3.
[0107] 3. The method of propylene polymerization is the same as in Example 1, except that the catalyst component 1 is replaced by the catalyst component 3, and the polymerization results...
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