欢迎登录材料期刊网

材料期刊网

高级检索

用自制的γ-(2,3-环氧丙氧)丙基倍半硅氧烷为改性剂,对双酚A缩水甘油醚型环氧树脂E-51进行改性,两者配比为60/40(质量比),选用等当量的4,4'-二氨基二苯砜(DDS)为固化剂,形成环氧-倍半硅氧烷杂化材料.通过凝胶特性曲线、傅立叶变换红外光谱(FTIR)以及差示扫描量热方法(DSC)研究了该体系的固化反应特性及动力学问题;初步研究了固化体系的力学性能以及热性能.结果表明,该体系具有较好的工艺性,其固化反应的活化能是 48.7 kJ/mol,体系的热变形温度(HDT)达到200℃,热分解温度达到442℃,玻璃化转变温度(Tg)达到245℃,比相同条件下的E-51/DDS体系分别高出了31,58,20℃,体系在800℃时热残余量为25%,同时其弯曲强度和冲击强度基本保持不变.

参考文献

[1] Ronald H. Baney;Maki Itoh;Akihito Sakakibara;Toshio Suzuki .Silsesquioxanes[J].Chemical Reviews,1995(5):1409-1430.
[2] JANG J;BAE J;KANG D .Synthesis and characterization of thebiodegradable copolymers from succinic acid and adipic acid with 1,4-butanediol[J].Journal of Applied Polymer Science,2002,82:2310-2318.
[3] FEHER F J;WELLER K J .Polyhedral aluminosilsesquioxanes as models for aluminosilicates:unique synthesis of anionic aluminum/silicon/oxygen frameworks[J].Organometallics,1990,9:2638-2640.
[4] Daniel Schmidt;Deepak Shah;Emmanuel P. Giannelis .New advances in polymer/layered silicate nanocomposites[J].Current opinion in solid state & materials science,2002(3):205-212.
[5] Paolo P.Pescarmona;Anthony F.Masters;Jan C.van der Waal;Thomas Maschmeyer .Osmium silsesquioxane as model compound and homogeneous catalyst for the dihydroxylation of alkenes[J].Journal of molecular catalysis, A. Chemical,2004(1):37-42.
[6] MURUGAVEL R;VOIGT A .Hetero-and metallasiloxanes derived from silanediols,disilanols,silanetriols,and trisilanols[J].Chemical Reviews,1996,96:2205-2236.
[7] E. Tegou;V. Bellas;E. Gogolides;P. Argitis .Polyhedral oligomeric silsesquioxane (POSS) acrylate copolymers for microfabrication: properties and formulation of resist materials[J].Microelectronic engineering,2004(1):238-243.
[8] LICHTENHAN J D;YOSHIKO A OTONARI .Linear hybrid polymer building blocks:methacrylate-functionalized polyhedral oligomeric silsesquioxane monomers and polymers[J].Macromolecules,1995,28:8435-8437.
上一张 下一张
上一张 下一张
计量
  • 下载量()
  • 访问量()
文章评分
  • 您的评分:
  • 1
    0%
  • 2
    0%
  • 3
    0%
  • 4
    0%
  • 5
    0%