Branched functionalized solution polymerized styrene-butadiene rubber and preparation method thereof
A solution-polymerized styrene-butadiene rubber and functionalization technology, which is applied in the field of siloxane branched modified solution-polymerized styrene-butadiene rubber and its synthesis, can solve the problem of difficult industrialization of functionalized solution-polymerized styrene-butadiene rubber and the high price of comonomers, etc. problems, to achieve good anti-wet skid performance, excellent physical and mechanical properties, and the effect of regular product structure
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
Embodiment 1
[0029] In a jacketed 10L polymerization kettle, the system was replaced 3 times with nitrogen gas. Add 5109g of hexane, 200g of styrene, 600g of butadiene, and 0.62g of tetrahydrofuran into the polymerization kettle, raise the temperature to 40°C, add 5.3mmol of n-butyllithium, and naturally raise the temperature to 90-100°C. After 2 hours of polymerization, the conversion rate Reach 100%, obtain number-average molecular weight and be 150,000, the linear polymer that molecular weight distribution is 1.2, add 106mmol H-Si-(OC 8 h 17 )(C 12 h 25 ) 2 , 1.24mmol Karstedt catalyst (platinum complex) and 0.8mmol methanol, the temperature was raised to 100°C, the reaction was continued for 1 hour, the reaction was terminated, the anti-aging agent was added, the material was discharged, the glue was coagulated by wet method, and dried. The nuclear magnetic test results show that the branched siloxane content accounts for 0.7wt% of the weight of the solution-polymerized styrene-but...
Embodiment 2
[0033] In a jacketed 10L polymerization kettle, the system was replaced 3 times with nitrogen gas. Add 5109g of cyclopentane, 200g of styrene, 600g of butadiene, and 0.31g of tetrahydrofurfuryl ether into the polymerization kettle, raise the temperature to 50°C, add 4.0mmol of n-butyllithium, naturally raise the temperature to 90-100°C, and polymerize for 1 hour Afterwards, conversion ratio reaches 100%, obtains number-average molecular weight and is 200,000, and the linear polymer of molecular weight distribution is 1.25, adds 80mmol H-Si-(OC 12 h 25 ) 3 , 0.12mmol Wilkinson catalyst (rhodium complex) and 0.11mmol phenothiazine, maintain the temperature at 90-100°C, continue the reaction for 1 hour, terminate the reaction, add anti-aging agent, discharge, the glue is condensed by wet method, and dried . The nuclear magnetic test results show that the branched siloxane content accounts for 1.3 wt% of the weight of the solution-polymerized styrene-butadiene rubber.
Embodiment 3
[0037] In a jacketed 10L polymerization kettle, the system was replaced 3 times with nitrogen gas. Add 5097g of cyclohexane, 120g of styrene, 680g of butadiene, 0.54g of tetramethyldivinyldiamine into the polymerization kettle, raise the temperature to 50°C, add 3.2mmol of n-butyl lithium, and naturally raise the temperature to 60-70°C , After 1.5 hours of polymerization, the conversion rate reached 100%. Adding 0.96mmol of tin tetrachloride coupling agent, the number average molecular weight obtained was 300,000, and the molecular weight distribution was a star-shaped polymer of 1.4. Adding 64mmol of H-Si-(OC 10 h 21 ) 3 , 0.75mmol Wilkinson catalyst (rhodium complex) and 0.15mmol aniline, maintain the temperature at 60-70°C, continue the reaction for 1.5 hours, terminate the reaction, add anti-aging agent, discharge, the glue is coagulated by wet method, and dried. The nuclear magnetic test results show that the branched siloxane content accounts for 2.1% by weight of the ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
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