Catalyst component used for olefin polymerization reaction and its catalyst

A technology for olefin polymerization and catalyst, applied in the field of solid catalyst components

Active Publication Date: 2008-01-16
CHINA PETROLEUM & CHEM CORP +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] However, the catalyst disclosed above still has some unsatisfactory defects in the practical application of olefin polymerization. The compound can be used as an electron donor to obtain a catalyst with excellent comprehensive performance. When used in the po

Method used

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  • Catalyst component used for olefin polymerization reaction and its catalyst
  • Catalyst component used for olefin polymerization reaction and its catalyst
  • Catalyst component used for olefin polymerization reaction and its catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0074] Example 1 Synthesis of 1-benzamido-3-benzoyloxybutane

[0075] Add 1-amino-3-butanol (5.2g), sodium bicarbonate (6.4g), tetrahydrofuran (50ml) into a reaction flask equipped with a stirring device and a reflux condenser, add benzoyl chloride (7ml) dropwise under stirring ) and tetrahydrofuran (30ml). After the addition, react at room temperature for 1 hour, then heat to reflux for 4 hours. After the reaction was completed, the temperature was lowered, diluted with water, extracted three times with ether, and the organic phases were combined. Wash with water at 40°C and then with saturated sodium chloride solution, and dry the organic phase over anhydrous magnesium sulfate overnight. The product was obtained by column chromatography after removing the solvent.

[0076] 1 H-NMR (δ, ppm, TMS, CDCl 3 ): 7.3~8.0 (10H, m, ArH), 4.0 (1H, m, OCH), 2.5~2.7 (2H, m, NCH 2 ), 1.2 (2H, m, CH 3 ), 0.9 (3H, d, CH 3 ).

Embodiment 2

[0077] Example 2 Synthesis of 1-benzoyloxy-3-benzamidopropane

[0078] Add 3-aminopropanol (4.6g), sodium bicarbonate (9.6g), tetrahydrofuran (50ml) into a reaction flask equipped with a stirring device and a reflux condenser, and add benzoyl chloride (14ml) and tetrahydrofuran dropwise under stirring (30ml). After the addition, react at room temperature for 1 hour, then heat to reflux for 4 hours. After the reaction was completed, the temperature was lowered, diluted with water, extracted three times with ether, and the organic phases were combined. Wash with water at 40°C and then with saturated sodium chloride solution, and dry the organic phase over anhydrous magnesium sulfate overnight. The product was obtained by column chromatography after removing the solvent.

[0079] 1 H-NMR (δ, ppm, TMS, CDCl 3 ): 7.3~8.1 (10H, m, ArH), 3.9 (2H, t, OCH 2 ), 2.4~2.6 (2H, m, NCH 2 ), 1.0 (2H, m, CH 2 ).

Embodiment 3

[0080] Example 3 Synthesis of 1-dimethylamino-2-benzoyloxypropane

[0081] Add 1-dimethylamino-2-propanol (5.7g), sodium bicarbonate (6.4g), tetrahydrofuran (50ml) in a reaction flask equipped with a stirring device and a reflux condenser, add benzoyl chloride ( 7ml) and tetrahydrofuran (25ml). After the addition, react at room temperature for 1 hour, then heat to reflux for 4 hours. After the reaction was completed, the temperature was lowered, diluted with water, extracted three times with ether, and the organic phases were combined. Wash with water at 40°C and then with saturated sodium chloride solution, and dry the organic phase over anhydrous magnesium sulfate overnight. The product was obtained by column chromatography after removing the solvent.

[0082] 1 H-NMR (δ, ppm, TMS, CDCl 3 ): 7.3~8.0 (5H, m, ArH), 4.3 (1H, m, OCH), 2.8~2.9 (2H, m, NCH 2 ), 2.4 (6H, s, CH 3 ), 0.9 (3H, t, CH 3 ).

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Abstract

The invention provides catalyst components used for CH2=CH olefin polymerization reaction and a catalyst, wherein R is alkyl or aryl of hydrogen or C1-C6. The catalyst components comprise magnesium, titanium, halogen and electron donors. The electron donors are at least one of amine ester compounds presented as the following general formula (I), wherein, R1 is the aryl or alkaryl of C6-C20; R2 and R3 can be the same or different, which are the alkyl of the hydrogen or a straight chain or a branched chain of the C1-6, and the aryl, aralkyl, ester group or acyl of the C6-C20, but R2 and R3 can not be the hydrogen at the same time. A is a divalent linking group whose chain length is 1 to 15 carbon atoms. Hydrogen atoms on the divalent linking group can be substituted by the alkyl, amino-alkane or the acyl. When the catalyst is used in propylene polymerization, a satisfied polymerization yield can be obtained, and the polymer is in higher stereospecificity and is helpful to develop the different grades of the polymers.

Description

technical field [0001] The invention relates to a solid catalyst component containing a urethane compound of a special structure, a catalyst containing the solid catalyst component and the catalyst in CH 2 = Application in CHR olefin polymerization, where R is hydrogen or C 1 -C 6 The alkyl or aryl group, especially in the application of propylene polymerization reaction, can obtain the polymer with higher yield and higher isotacticity. technical background [0002] It is well known that solid titanium catalyst components based on magnesium, titanium, halogen and electron donors can be used for CH 2 = CHR Olefin polymerization, especially in the polymerization of α-olefins with 3 or more carbon atoms, polymers with higher yield and higher stereoregularity can be obtained, wherein the electron donor compound is in the catalyst component One of the essential ingredients, and with the development of internal electron donor compounds, polyolefin catalysts are constantly updat...

Claims

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Application Information

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IPC IPC(8): C08F10/00C08F4/645
Inventor 高明智刘海涛王军李昌秀丁春敏李葳莅蔡晓霞陈建华
Owner CHINA PETROLEUM & CHEM CORP
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