Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Cocatalyst composition and application thereof

A co-catalyst and composition technology, applied in the field of copolymerization of alkenes and cyclic olefins, can solve the problem of unsatisfactory glass transition temperature of copolymers

Active Publication Date: 2016-03-09
CHINA PETROLEUM & CHEM CORP +1
View PDF5 Cites 32 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, when using aluminoxane alone as a cocatalyst, the glass transition temperature of the resulting copolymer is still not satisfactory

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Cocatalyst composition and application thereof
  • Cocatalyst composition and application thereof
  • Cocatalyst composition and application thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment

[0210] The following examples will be used to illustrate the present invention in further detail, but the present invention is not limited to these examples.

[0211] The various performance parameters involved in the following examples and comparative examples were measured according to the following methods.

[0212] (1) Polymerization activity

[0213] Catalyst polymerization activity (unit is g(P)·(mol(M)·h) -1 , where P refers to the copolymer, M refers to the metal element M such as Ti) is calculated according to the following formula:

[0214] Polymerization activity = m 1 ×4×Mw / m 2

[0215] in,

[0216] m 1 The amount (g) of copolymer obtained for 15 minutes of polymerization time;

[0217] Mw is the molecular weight of catalyst;

[0218] m 2 is the amount of catalyst added (g).

[0219] (2) Molecular weight Mη of polymer

[0220] The viscosity-average molecular weight Mη of polymer is calculated according to the following method:

[0221] According to the ...

manufacture Embodiment 1

[0228] In a dry 500ml three-necked flask, add 2-aminoanisole sulfide (0.2mol), absolute ethanol (160ml), 3,5-di-tert-butyl salicylaldehyde (0.2mol), acetic acid (0.3ml) successively , heated up to reflux temperature and reacted for 2hr, cooled to room temperature, filtered, washed three times with absolute ethanol, and dried in vacuum to obtain 49.7g of 2-aminoanisole sulfide 3,5-di-tert-butyl salicylaldehyde, called Ligand L1,

[0229]

[0230] L1.

[0231] Elemental analysis: C74.57% (theoretical value 74.32%); H8.35% (theoretical value 8.22%); N4.07% (theoretical value 3.94%). 1 H NMR δ=13.4(OH), 8.6(CHN), 7.5-7.1(Ar-H), 3.25(SCH 3 ), 1.45 (C (CH 3 ) 3 ), 1.35 (C (CH 3 ) 3 ).

manufacture Embodiment 2

[0233] In a dry 500ml three-necked flask, add 2-aminophenylpropyl sulfide (0.2mol), absolute ethanol (160ml), 3,5-di-tert-butyl salicylaldehyde (0.2mol), acetic acid (0.3ml) successively , heated up to reflux temperature and reacted for 2hr, cooled to room temperature, filtered, washed three times with absolute ethanol, and dried in vacuum to obtain 49.7g of 2-aminophenylpropyl sulfide 3,5-di-tert-butyl salicylaldehyde, called Ligand L2,

[0234]

[0235] L2.

[0236] Elemental analysis: C74.57% (theoretical value 75.15%); H8.35% (theoretical value 8.67%); N3.95% (theoretical value 3.65%). 1 H NMR δ=13.4(OH), 8.55(CHN), 7.5-7.1(Ar-H), 2.10(CH 2 CH 3 ), 1.47 (C (CH 3 ) 3 ), 1.35 (C (CH 3 ) 3 ), 1.17 (CH 2 CH 3 ).

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The present invention relates to a cocatalyst composition and application thereof, in particular to a cocatalyst composition. The cocatalyst is characterized by comprising a reaction product of alkylaluminium and water, and alkyl aluminum, wherein based on A1, the molar ratio of the reaction product of the alkylaluminium and the water to the alkyl aluminum is 0.5: 1 to smaller than 4: 1. The present invention further relates to a catalyst system containing the cocatalyst composition, and application of the cocatalyst composition in non-metallocene complexe catalyzed chain alkene-cycloalkene copolymerization. Compared with the alkyl aluminum, the cost of the cocatalyst composition disclosed by the present invention is lower.

Description

technical field [0001] The invention relates to a cocatalyst composition, which is especially suitable for the copolymerization reaction of alkenes and cycloalkenes catalyzed by non-metallocene complexes. The present invention also relates to the catalyst system comprising the cocatalyst composition, the application of the cocatalyst composition in non-metallocene complex-catalyzed alkene-cycloolefin copolymerization and the alkene and cycloolefin co-catalyzed by the cocatalyst composition Copolymerization of olefins. Background technique [0002] With the continuous progress of society and the rapid development of science and technology, the demand for high-performance materials is also increasing. Olefin-cycloolefin copolymers, especially ethylene-cycloolefin copolymers, are excellent amorphous thermoplastic polymer materials with high transparency, low water absorption, high heat resistance and high refractive index. As one of the high-end products of C5 series comprehe...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): C08F4/642C08F232/08C08F210/02
Inventor 郭峰汪文睿易玉明李传峰任鸿平汪开秀魏金花杨爱武陈韶辉柏基业
Owner CHINA PETROLEUM & CHEM CORP
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products