期刊文献+

端异氰酸酯基聚丁二烯/纳米二氧化硅弹性体的制备及其力学性能研究 被引量:2

Synthesis and mechanical properties of isocyanate block polybutadiene/nano silica elastomer
下载PDF
导出
摘要 以自制的端异氰酸酯基聚丁二烯(ITPB)为基体,纳米二氧化硅(SiO_2)为固化剂,制备了ITPB型聚氨酯/纳米SiO_2弹性体。阐述了ITPB/SiO_2弹性体的制备机理,研究了溶剂的种类、SiO_2加入量和固化条件对ITPB/SiO_2弹性体力学性能的影响。结果表明,以环己酮为溶剂制备的ITPB/SiO_2弹性体力学性能最佳;随着SiO_2加入量的增加,弹性体的拉伸强度、断裂伸长率、断裂强度及硬度均有明显提高,SiO_2加入量为6%时,弹性体的断裂伸长率达到最大值220.14%,当SiO_2加入量为8%时,弹性体的拉伸强度达到最大值7.11 MPa;提高固化温度和延长固化时间,有助于提高ITPB/SiO_2弹性体的力学性能。 With homemade isocyanate block polybutadiene (ITPB) as the matrix and the nano silica as the curing agent, the ITPB/Nanosilica elastomer was prepared.This paper illustrated the preparation mechanism of ITPB/silica elastomer,and studied the effects of types of solvent, silica content and curing conditions on the mechanical properties of ITPB/silica elastomer.The results showed that the mechanical property of ITPB/silica elastomer were the best using cyclohexanone as the solvent; increasing silica amount, the tensile strength, elongation at break, fracture strength and hardness were of the ITPB/silica elastomer increased significantly; when the silica content was 6%, the elongation at break of ITPB/silica elastomer reached a maximum value of 220.14%; when the silica content was 8%, the tensile strength of ITPB/silica elastomer reached a maximum value of 7.11 MPa; increasing the curing temperature and curing time can improve the mechanical properties ofITPB/silica elastomer.
出处 《粘接》 CAS 2015年第10期60-63,共4页 Adhesion
关键词 SIO2 ITPB纳米 弹性体 力学性能 nano silica polybutadiene elastomer mechanical properties
  • 相关文献

参考文献11

  • 1Seil J T,Webster T J.Decreased astroglial cell adhesion and proliferation on zinc oxide nanoparticle polyurethane composites[J].Interriational Journal of Nanomedicine,2008,3(4) :523- 531.
  • 2Guo C Q,Zheng Z,Zhu Q R,et al. Preparation and characterization of polyurethane/ZnO nanoparticle composites [J] .Polymer-Plastics Technology and Engineering,2007,46(12): 1161- 1166.
  • 3Nanda G S,Yong C J Hye J Y, et al.Influence of carbon nanotubes and polypyrrole on the thenml,mechanical and eleetroactive shape-memory properties of polyurethane nanocompositesLl].Composites Science and Technology,2007,67 (9): 1920-1929.
  • 4Xiong Jiawen,Zheng Zhen,Qin Xiumin,et al.Thethermal and mechanical properties of a polyurethane/multi-walled carbon nanotube composite [J]. Carbon, 2006,44 (13) :2701 - 2707.
  • 5Kuan Hsuchiang,Chenchi M Ma,Chang Weiping,et al .Synthesis,thermal,mechanical and theological properties ofmultiwall carbon nanotube/waterborne polyurethane nanocomposite[J].Composites Science and Technology, 2005,65 (11 - 12) : 1703-1710.
  • 6张永成,赵雨花,亢茂青,王心葵.聚氨酯基层状硅酸盐纳米复合物研究进展[J].化学进展,2006,18(1):59-65. 被引量:6
  • 7Salahudin N,Abo-E1-Enein S A,et al. Synthesis and characterization of polyurethane-urea clay nanocomposites using nmotmorillonite modified by oxyethylene- oxypropylene copolymer[J].Polymers for Advanced Technologier,2010,21(8) :533-542.
  • 8Schwab J J,Reinergth W A,LichtenhanJ D,et al.POSS(TM) Nanostructured(TM)chemicals:Tr ue multifunctional polymer additives. [J].Abstracts of Papers of the American Chemical Society,2001,222:285.
  • 9Fu B X,Hsiao B S,Pagola S,et al.Structural development during deformation of polyurethane containing polyhedral oligomeric silsesquioxanes (POSS) molecules [J]. Polymer, 2001,42 (2) :599-611.
  • 10Petrovic Z S,Javni I,Waddon A,et al.Structure and properties of polyyurthane- lilica nanocomposites[J].Journal of Applied Poly Science,2000,76(2) : 133-151.

二级参考文献58

  • 1Hall B, Cheng A M, Ji G D. J. Appl. Polym. Sci., 2004, 91:2536-2542.
  • 2Wang W J, Chin W K, Wang W J. J. Polym. Sei. Part B:Polym. Phys., 2002, 40:1690-1703.
  • 3Tien Y I, Wei K H. Macromolecules, 2001, 34:9045-9052.
  • 4Dai X H, Xu J, Guo X L, et al. Macromolecules, 2004, 37:5615-5623.
  • 5Devaux E, Rochery M, Bourbigot S. Fire Mater., 2002, 26:149-154.
  • 6Chen T K, Tien Y I, Wei K H.J. Polym. Sci. Part A: Polym.Chem., 1999, 37:2225-2233.
  • 7Ma X Y, Lu H J, Liang G Z, et al. J. Appl. Polym. Sci.,2004, 93:608-614.
  • 8Kim J Y, Jung W C, Park K Y, et al. J. Appl. Polym. Sci.,2003, 89:3130-3136.
  • 9Kim B K, Jang W S, Hart M J. Europ. Polym. J., 2003, 39:85-91.
  • 10Blumstein R, Blumstein A, Parikh K K. Appl. Polym. Symp.,1994, 25:81-89.

共引文献5

同被引文献29

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