External electron donor composition, olefin polymerization catalyst and application thereof, and polyolefin and preparation method thereof
An external electron donor and olefin polymerization technology, applied in the field of olefin polymerization, can solve the problems of narrow molecular weight distribution of polypropylene and achieve the effects of wide relative molecular weight distribution, high isotactic index, and high MFR
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[0044] According to a preferred embodiment of the present invention, the first external electron donor compound is selected from the group consisting of the compound represented by formula I-1, the compound represented by formula I-2 and the compound represented by formula I-3 At least one of:
[0045]
[0046] In some embodiments of the present invention, the molar ratio of the first external electron donor compound and the second external electron donor compound is 1-10:1. Preferably, the molar ratio of the first external electron donor compound and the second external electron donor compound is 2.5-9:1, more preferably 3-8:1, further preferably 3-5:1. In the present invention, the new active center formed by the coordination between the first external electron donor compound and the active center of the catalyst can induce polymerization to obtain a polymer with both high activity and high regularity; The new active center formed by the coordination of the active center...
preparation example 1
[0120] Preparation Example 1 is used to prepare the first external electron donor compound A represented by formula I-1:
[0121]
[0122] (1) Preparation of Grignard reagent
[0123] Take a 500 ml three-necked flask with a magnetron, a spherical condenser and a constant pressure dropping funnel, add magnesium powder (28.8 g, 1.2 mol) and a little iodine under nitrogen protection; add ortho-bromine to the constant pressure dropping funnel Anisole (1.0 mol) and tetrahydrofuran (200 ml), then 5 ml of o-bromoanisole in tetrahydrofuran was added dropwise to the flask, stirred for 3-5 minutes to initiate the reaction; then o-bromoanisole was added dropwise tetrahydrofuran solution; after the dropwise addition is completed, heat under reflux for 1 hour to complete the preparation of Grignard reagent.
[0124] (2) Synthesis of Silane
[0125] Take a 2.5-liter three-necked flask with a magnetron and a spherical condenser, add diphenyldichlorosilane (253 g, 1.0 mol) and 500 mL of ...
preparation example 2
[0127] Preparation Example 2 is used to prepare the first external electron donor compound B represented by formula I-2:
[0128]
[0129] According to the method of Preparation Example 1, the difference is that in step (1), an equal amount of 1-bromo-2-methoxy-3-methylbenzene is used In place of o-bromoanisole, the obtained product was identified as the first external electron donor compound B represented by formula I-2 (the yield was 75% by weight) through hydrogen nuclear magnetic resonance spectroscopy.
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