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

Process for selective hydrogenation of styrene-conjugated diene block polymer

A conjugated diene block and block polymer technology, which is applied in the field of selective hydrogenation of styrene-conjugated diene block polymers, can solve the problem of complex catalyst preparation, difficult hydrogenation degree, good process reproducibility, etc. question

Active Publication Date: 2006-10-11
CHINA PETROCHEMICAL CORP +1
View PDF7 Cites 13 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

USA6,040,390 catalyst system for selective hydrogenation of unsaturated bonds in block copolymers consists of dicyclopentadiene dithienyl (which can be thienyl, 4-methylthienyl, 3-methylthienyl, 2,4 -Dimethylthienyl, 4-ethylthienyl, 3-ethylthienyl, 2,4-diethylthienyl) titanium composition, its structure is shown in (b), wherein: R 1 , R 2 , R 3 It is hydrogen or low-carbon alkane group, which can be the same or different; the catalyst does not need to add a reducing agent, the process reproducibility is good, the catalyst system has a strong ability to resist interference from impurities, and when a small amount of impurities exist, it will not affect the catalytic activity of the catalyst , the reaction condition of this method is that the amount of catalyst is 0.1mmol / 100g活性聚合物 ~2mmol / 100g活性聚合物 , The polymer molecular weight ranges from 500 to 1,000,000, the polymer concentration is 5wt% to 25wt%, the reaction temperature is 50°C to 140°C, and the reaction pressure is 2kgf / cm 2 ~30kgf / cm 2 , The reaction time is several minutes to 100 hours, but the hydrogenation degree of SEBS in this method is difficult to guarantee, and the preparation of the catalyst is complicated

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
  • Process for selective hydrogenation of styrene-conjugated diene block polymer
  • Process for selective hydrogenation of styrene-conjugated diene block polymer
  • Process for selective hydrogenation of styrene-conjugated diene block polymer

Examples

Experimental program
Comparison scheme
Effect test

Embodiment Construction

[0024] The following examples will further illustrate the present invention, but do not thereby limit the scope of the present invention.

[0025] In a 5L autoclave purified by pure nitrogen, add 3500ml of cyclohexane, 57ml of styrene, 0.159mmol of butyllithium, and the calculated amount of a microstructure regulator (tetrahydrofuran or ethylene glycol diethyl ether is used as the microstructure regulator) at 40 After 30 minutes of reaction at ℃~60℃, 395ml of butadiene was added to react for 35 minutes, and finally 57ml of styrene was added, and the reaction was carried out for 25 minutes to obtain a glue solution of styrene-conjugated diene triblock polymer. Under the protection of pure nitrogen, it was introduced into a nitrogen-purified 5L hydrogenation kettle, and different co-catalysts were added to investigate the influence of different co-catalysts on the hydrogenation reaction and the color of the SEBS product. The conditions of the hydrogenation reaction were: the main...

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 is selection hydrogenization method of phenylethene-conjugated diene block copolymer. In the hydrogenization, catalyst promoter could be added in the proportion of 1:1- 1:5 with compound like phenyl phthalate. catalyst promoter's structure is as followings: R1 means C1-C3 acroleic acid, R2,R3,R4,R5 represent H or C1-C3 acroleic acid respectively. This invention is advantageous in short hydrogenization time (60 minutes), high product efficiency (>=98%)and high white content.

Description

technical field [0001] The present invention relates to a method for selective hydrogenation of a styrene-conjugated diene block polymer. Background technique [0002] The earliest method used for the selective hydrogenation of styrene-conjugated diene block polymers is iron, cobalt, nickel carboxylates (general formula [R(CO) 2 M]) or the reaction product of an alkoxy compound (such as alcohol, etc.) and an organometallic compound as the main catalyst, organometallic compounds such as lithium, magnesium, aluminum, such as n-, sec-butyllithium, triisobutylaluminum, diisobutyl Hydrogenation reaction such as US3,333,024, US3,431,323 is carried out by using base or diethylaluminum chloride etc. as co-catalyst. [0003] In 1980, Japanese scientist Kishiomot first applied for the application of metallocene catalytic hydrogenation, such as US4,501,857. With the progress of metal-organic chemistry, coordination chemistry and synthesis technology, various metallocene catalysts hav...

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): C08F297/04C08F8/04
Inventor 张志斌陈海龙李望明梁红文姜西平彭小寒康铮
Owner CHINA PETROCHEMICAL 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