A kind of catalyst component and catalyst for propylene polymerization
A technology of propylene polymerization and catalyst, which is applied in the field of olefin polymerization catalysts, can solve the problems that other properties have not been studied in depth, and the molecular weight distribution of catalysts is not very satisfactory, etc., and achieve the effects of facilitating processing and application, easy control, and less fine powder content
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Embodiment 1
[0030] Embodiment 1 (2, the preparation of 4-pentanediol dibenzoate)
[0031] 1. Preparation of 2,4-pentanediol
[0032] A mixture of 10g of 2,4-pentanedione and 30ml of methanol was added dropwise to a mixed solution of 2.5g of sodium borohydride, 0.1g of sodium hydroxide and 25ml of water at 0-10°C. After the addition, the solvent was removed under reduced pressure and extracted continuously with 40ml of ethyl acetate for 15h. The solvent was removed and column chromatography was used to obtain 2,4-pentanediol as a colorless liquid with a yield of 90%.
[0033] 2.2, Preparation of 4-pentanediol dibenzoate
[0034] Add 30ml tetrahydrofuran and 0.09mol pyridine to 0.03mol 2,4-pentanediol, add 0.075mol benzoyl chloride under stirring, and heat to reflux for 4h. After cooling, add 20ml of saturated brine, extract with ethyl acetate, anhydrous Na 2 SO 4 Dry and remove solvent. The colorless liquid 2,4-pentanediol dibenzoate was obtained by column chromatography or vacuum di...
Embodiment 2
[0036] Embodiment 2 (4-ethyl-3, the preparation of 5-heptanediol dibenzoate)
[0037] 1. Preparation of 4-ethyl-3,5-heptanedione
[0038] A mixture of 10.2 g of 3,5-heptanedione, ethyl iodide and 80 ml of THF was added in batches to 4.8 g of 50% sodium hydride oil under stirring. After the addition, the reaction was heated to reflux under stirring for 8h. Removal of the solvent yielded 4-ethyl-3,5-heptanedione.
[0039] 2. Preparation of 4-ethyl-3,5-heptanediol
[0040] A mixture of 14.6g of 3,5-heptanedione and 30ml of methanol was added dropwise to a mixed solution of 3.1g of sodium borohydride, 0.06g of sodium hydroxide and 25ml of water at 0-10°C. After the addition, the solvent was removed under reduced pressure and extracted continuously with 40ml of ethyl acetate for 15h. The solvent was removed to obtain the product with a yield of 90%. IR spectrum at 3400cm -1 There is a strong absorption peak at 1700cm -1 There are no absorption peaks on the left and right, wh...
Embodiment 3
[0045] 1. Preparation of Mg / Ti Solids
[0046] Add 6.5kg of magnesium chloride, 132.7L of toluene, 5.4L of epichlorohydrin, and 16.9L of tributyl phosphate into the reactor, and react for 2.5 hours at a stirring speed of 130rpm and a temperature of 60°C, and add 4.5mol 2, 4-Pentanediol dibenzoate, continue to react for 1.0h, cool down to -28°C, add 56L of titanium tetrachloride dropwise, gradually raise the temperature to 85°C, keep the temperature for 1.0h after reaching the temperature, filter off the mother liquor, and inertly dilute The solids containing magnesium / titanium were obtained after being washed several times with toluene and hexane and then dried.
[0047] 2. Preparation of solid titanium catalyst components
[0048] Add 1.4L ethanol and 96L toluene to the solid prepared above at -10°C, keep the temperature for 0.5h, slowly add 64L titanium tetrachloride, gradually raise the temperature to 110°C, add 2.0mol 2,4-pentanediol diol at 80°C Benzoic acid ester, 110°...
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