External electron donor for olefin polymerization catalyst, catalyst system and preparation method of polyolefin
An external electron donor and olefin polymerization technology, which is applied in the field of polyolefin preparation by olefin polymerization catalyst system, can solve the problems of high branching efficiency, large amount of monomer, and low efficiency of long-chain branching, and achieve increased melt elasticity, Effect of Long Chain Branching Efficiency Improvement
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[0041] The third aspect of the present invention provides a method for preparing polyolefin, wherein the method comprises: performing bulk polymerization, gas phase polymerization or slurry polymerization of olefin monomers in the presence of the above catalyst system.
[0042] In the present invention, the olefin may be, but not limited to: ethylene or propylene.
[0043] In the present invention, bulk polymerization refers to liquid phase bulk polymerization, for example, liquid propylene is subjected to bulk polymerization in the presence of the above-mentioned catalyst system.
[0044] In the present invention, gas-phase polymerization refers to the polymerization of olefin monomers in a gasified state, for example, the polymerization of gaseous propylene is catalyzed in the presence of the above-mentioned catalyst system.
[0045] In the present invention, slurry polymerization refers to the polymerization of olefin monomers catalyzed by the above-mentioned catalyst syste...
preparation example 1
[0057] (1) Preparation of two [3-(5-norbornenyl) propyl] diethoxysilane
[0058] Under the protection of nitrogen, 2.9g of magnesium chips were dispersed in 200ml of tetrahydrofuran solution, and 1-chloro-3(5-norbornene)propane (17.0g, 0.1mol) was dropped into the solution to prepare Grignard reagent 3(5- norbornene) propylmagnesium chloride.
[0059] 4.16g of tetraethoxysilane was dispersed in 500ml of tetrahydrofuran, and 0.042mol of 3(5-norbornene)propylmagnesium chloride in tetrahydrofuran was slowly added dropwise thereto, and reacted at room temperature for 24h. Product A was obtained by distillation under reduced pressure.
[0060] The hydrogen spectrum of A: 1 H NMR (300MHz, CDCl 3 ,ppm)δ:0.61(t,4H),1.21(m,16H),1.56(m,6H),1.75(m,2H),2.58(m,2H),2.84(m,2H),3.83(q ,4H),5.98(m,4H). The hydrogen spectrum is as follows figure 2 shown.
[0061] A carbon spectrum: 13 C NMR (300MHz, CDCl 3 , ppm) δ: 15.4, 33.6, 35.7, 47.2 (CH 2 ), 17.3 (SiCH 2 ), 18.4 (OCH 2 CH 3 )...
preparation example 2
[0064] (1) Preparation of two [3-(4-cyclohexenyl) propyl] diethoxysilane
[0065] Under the protection of nitrogen, 2.9g of magnesium chips were dispersed in 200ml of tetrahydrofuran solution, and 1-chloro-3(4-cyclohexenyl)propane (15.8g, 0.1mol) was dropped into the solution to prepare Grignard reagent 3(4 -cyclohexenyl)propylmagnesium chloride.
[0066] 2.08 g of tetraethoxysilane was dispersed in 500 ml of tetrahydrofuran, and 0.022 mol of 3(4-cyclohexenyl)propylmagnesium chloride in tetrahydrofuran was slowly added dropwise, and reacted at room temperature for 24 hours. Product B was obtained by distillation under reduced pressure.
[0067] The hydrogen spectrum of B: 1 H NMR (300MHz, CDCl 3 ,ppm)δ:0.61(t,4H),1.23(m,14H),1.35(m,2H),1,60(m,4H),2.11(m,8H),3.83(q,4H),5.65 (4H). The hydrogen spectrum is as follows Figure 4 shown.
[0068] Carbon spectrum of B: 13 C NMR (300MHz, CDCl 3 , ppm) δ: 15.1, 23.1, 29.3, 36.4, 38.2 (CH 2 ), 17.3 (SiCH 2 ), 18.4 (OCH 2 CH 3...
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