期刊文献+

Epoxidation of Styrene-Isoprene-Styrene Block Copolymer and Research on Its Reaction Mechanism 被引量:2

Epoxidation of Styrene-Isoprene-Styrene Block Copolymer and Research on Its Reaction Mechanism
下载PDF
导出
摘要 Styrene-isoprene-styrene(SIS) block copolymer was modified into epoxidized styrene-isoprene-styrene(ESIS) block copolymer with performic acid generated in situ from hydrogen peroxide and formic acid.The structure and property of ESIS were characterized by Fourier transform infrared(FT-IR) spectroscopy,gel permeation chromatography(GPC),thermogravimetric/differential thermogravimetric(TG/DTG),melt flow rate(MFR) and dynamic mechanical analysis(DMA),and the reaction mechanism in the process of epoxidation was analyzed.The results showed that C=C double bonds of 1,4-structure were more active than that of 3,4-structure in polyisoprene chains.With epoxidation reaction proceeding,the whole tendency of molecular weight increased and molecular weight distribution widened,and MFR firstly increased and latterly decreased.The heat resistance of ESIS was superior to that of SIS.When SIS was changed into ESIS with 15.3% of mass fraction of epoxide groups,Tg of polyisoprene chains increased from-45.3 ℃ to 10.9 ℃.In the earlier period of epoxidation,some molecular chains ruptured and new substances with low molecular weight formed.However,in the latter period,crosslinking reaction between molecular chains which was initiated by epoxide groups or C=C double bonds occurred and crosslinked insoluble substances came into being. Styrene-isoprene-styrene(SIS) block copolymer was modified into epoxidized styrene-isoprene-styrene(ESIS) block copolymer with performic acid generated in situ from hydrogen peroxide and formic acid.The structure and property of ESIS were characterized by Fourier transform infrared(FT-IR) spectroscopy,gel permeation chromatography(GPC),thermogravimetric/differential thermogravimetric(TG/DTG),melt flow rate(MFR) and dynamic mechanical analysis(DMA),and the reaction mechanism in the process of epoxidation was analyzed.The results showed that C=C double bonds of 1,4-structure were more active than that of 3,4-structure in polyisoprene chains.With epoxidation reaction proceeding,the whole tendency of molecular weight increased and molecular weight distribution widened,and MFR firstly increased and latterly decreased.The heat resistance of ESIS was superior to that of SIS.When SIS was changed into ESIS with 15.3% of mass fraction of epoxide groups,Tg of polyisoprene chains increased from-45.3 ℃ to 10.9 ℃.In the earlier period of epoxidation,some molecular chains ruptured and new substances with low molecular weight formed.However,in the latter period,crosslinking reaction between molecular chains which was initiated by epoxide groups or C=C double bonds occurred and crosslinked insoluble substances came into being.
出处 《Journal of Wuhan University of Technology(Materials Science)》 SCIE EI CAS 2010年第3期403-407,共5页 武汉理工大学学报(材料科学英文版)
关键词 styrene-isoprene-styrene block copolymer EPOXIDATION ring-open reaction mechanism styrene-isoprene-styrene block copolymer epoxidation ring-open reaction mechanism
  • 相关文献

参考文献19

  • 1S N Nazhat, S Parker, M P Parel, et al. Isoprene-Styrene Copolymer Elastomer and Tetrahydrofurfuryl Methacrylate Mixtures for Soft Prosthetic Applications[J]. Biomaterials, 2001, 22 (17): 2 411-2 416.
  • 2D J Kim, H J Kim, G H Yoon. Effect of Substrate and Tackifier on Peel Strength of SIS (Styrene-Isoprene-Styrene)-Based HMPSAs[J]. Int. J. ~Adhes" Adhes., 2005, 25(4): 288-295.
  • 3J Sun, H Y Tian, Y P Bai. Graft Polymerization of Acrylic Acid and Acrylamide onto BOPET Corona Films[J]. J. Wuhan University of Technology-Mater. Sci. Ed., 2004, 19(2): 90-93.
  • 4C D Dordella, N S M Cardozo, R B Neto, et al. Functionalization of Styrene-Butadiene-Styrene (SBS) Triblock Copolymer with Glycidyl Methacrylate (GMA)[J]. J. AppL Polym. Sci., 2003, 87(13): 2 074-2 079.
  • 5H Q Xie, D G Liu, D Xie. Preparation, Characterization, and Some Properties of Ionomers from a Sulfonated Styrene-Butadiene-Styrene Triblock Copolymer without Gelation[J]. J. Appl. Polym. Sci., 2005, 96(4): 1 398-1 404.
  • 6R Resendes, G Kaszas. Method of Halogenating Butyl Rubber without Acid Neutralization Agents [P]. EP 1820808, 2007-08-22.
  • 7W K Huang, G H Hsiue, W H Hou. Epoxidation of Polybutadiene and Styrene-Butadiene Triblock Copolymers with Monoperoxyphthalic Acid: Kinetic and Conformation Study[J]. J. Polyrn. Sci. Pol. Chem., 1988, 26(7): 1 867-1 883.
  • 8E Serrano, M Larranaga, P M Remiro, et al, Synthesis and Characterization of Epoxidized Styrene-Butadiene Block Copolymer as Templates for Nanostructured Thermosets[J]. Macromol. Chem. Phys., 2004, 205(7): 987-996.
  • 9K Udipi. Epoxidation of Styrene-Butadiene Block Polymers II [J]. J. Appl. Polym. Sci., 1979, 23(11): 3 311-3 321.
  • 10G H Hsiue, J M Yang. Epoxidation of Styrene-Butadiene-Styrene Block Copolymer and Use for Gas Permeation[J]. J. Polym. Sci. PoL Chem., 1990, 28(13): 3 761-3 773.

二级参考文献1

  • 1JAY R R.Direct titration of epoxy compounds and aziridines[].Analytical Chemistry.1964

共引文献2

同被引文献17

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部