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

Catalyst component for olefinic polymerization and its catalyst

A technology for olefin polymerization and catalysts, which is applied in the field of catalyst components and catalysts, and can solve problems such as reduced catalyst activity and unsatisfactory results

Active Publication Date: 2007-09-19
CHINA PETROLEUM & CHEM CORP +1
View PDF29 Cites 6 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

But the results are not yet satisfactory
Generally, after using two or more internal electron donor compounds, although the molecular weight distribution of the obtained polymer can be broadened, the activity of the catalyst is reduced

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
  • Catalyst component for olefinic polymerization and its catalyst
  • Catalyst component for olefinic polymerization and its catalyst
  • Catalyst component for olefinic polymerization and its catalyst

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1、9

[0047] Embodiment 1,9, the synthesis of 9-two (benzyl carboxymethyl) fluorene

[0048] (1) Synthesis of 9,9-dimethylolfluorene (see CN1141285A for the preparation method)

[0049] 9g (0.3mol) paraformaldehyde (vacuum dehydration 8h) was added 60ml dimethyl sulfoxide (DMSO, with CaH 2 Remove water) and the sodium ethylate solution after the reaction of 0.4gNa and 8ml absolute ethanol, and ice will be cooled. Under stirring, 100 ml of DMSO solution containing 16.6 g of fluorene (0.1 mol, dehydrated in vacuum for 8 h) was added within 30 seconds, and reacted for 10 min.

[0050] Add hydrochloric acid to terminate the reaction, and make the solution neutral, pour it into 300ml saturated brine, extract with ethyl acetate, separate the organic phase, wash twice with saturated brine, and dry over anhydrous sodium sulfate. The solvent was removed, and toluene was recrystallized to obtain 9,9-dimethylolfluorene as a white solid with a yield of 72%, m.p.142-145°C.

[0051] 1 H NMR (...

Embodiment 2

[0056] Embodiment 2, the synthesis of 2-isopropyl-2-isoamyl-1,3-propanediol benzhydryl carboxylate

[0057] (1) Synthesis of 2-isopropyl-5-methyl-2-hexenal (see CN1036846C for the preparation method).

[0058] 207 g of isovaleraldehyde and 26 ml of OH-form Amberlite IRA910 resin (manufactured by Rohm & Hass) were heated to reflux. Remove the generated water with a water separator, stop the reaction after collecting about 26ml of water, and filter out the resin. Distill under reduced pressure and collect fractions at 85-90°C / 20mmHg.

[0059] (2) Synthesis of 2-isopropyl-5-methylhexanal

[0060] Add 70ml of ethanol, 1ml of saturated NaHCO to the 10g of 2-isopropyl-5-methyl-2-hexenal synthesized above 3 solution and 0.25 g of 10% Pd on carbon support. Access to N 2 , then pass into H 2 , means filled with graduated H 2 connected to the burette. The reaction was stirred at normal temperature and pressure until H 2 The absorption reaches the calculated value. Filter and u...

Embodiment 3、2

[0067] Embodiment 3,2, the preparation of 4-pentanediol dibenzoate

[0068] (1) Preparation of 2,4-pentanediol

[0069] 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%.

[0070] (2) Preparation of 2,4-pentanediol dibenzoate

[0071] 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. Column chromatography or distillation under reduced pressure gave 2,4-pentanediol dibenzoate as a ...

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

This invention relates to a catalyst component for olefinic polymerization and its catalyst, said catalyst component comprises titanium compoumd with at least one Ti- halogen bond loaded on MgCl2nROH adduct and reaction product of two electronic doner compounds,wherein electronic doner compound A is chosen from poly alcohol ester compounds, and electronic doner compound B is chosen from ester,ether, ketone, amine and silicane compounds except compound A.The invented catalyst has high catalytic activity for olefinic polymerization ,in particular propylene polymerization, and wider molecular weight distribution.

Description

technical field [0001] The present invention relates to a kind of catalyst component and catalyst for olefin polymerization, and it in alpha-olefin CH 2 = Use in polymerization of CHR and mixtures thereof, wherein R is hydrogen or an alkyl group of 1 to 12 carbon atoms. More particularly, it relates to a catalyst component and catalyst containing at least two electron donor compounds and their use. technical background [0002] Catalysts comprising titanium compounds and electron donor compounds supported on active magnesium halides are well known in the art. [0003] US Patent No. 4,544,717 discloses that the stereospecificity of a catalyst can be improved by adding an electron donor compound (ie, an internal electron donor compound) to a solid component containing a titanium compound. So far, many patents have disclosed various internal electron donor compounds suitable for the preparation of Ziegler-Natta catalysts, and catalysts for olefin polymerization containing the...

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
Patent Type & Authority Patents(China)
IPC IPC(8): C08F10/00C08F4/645
Inventor 杜宏斌夏先知王新生张天一王军李昌秀高平尹茂平乔素珍王晓东王音
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

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com