期刊文献+

红外光谱对室温固化聚氨酯/乙烯基酯树脂的动力学研究(英文)

DYNAMICS OF PU/VER SINS CURED AT ROOM TEMPERATURE BY FT-IR
下载PDF
导出
摘要 利用"同步互穿"工艺室温固化制备了一系列聚氨酯/乙烯基酯树脂互穿聚合物网络(PU/VER SINs),采用傅立叶变换红外光谱(FT-IR)对SINs体系的聚合过程进行了动态跟踪及半定量分析,研究了固化体系对SINs的影响及两组分间的相互作用.结果表明:BPO和DBTDL的用量直接影响到两个网络的相对聚合速率;当BPO用量为VER树脂的0.75%,DBTDL用量为PU的0.6%时,PU的加聚反应首先进行并与VER的转化率近似.两个网络的最终转化率高于90%,基本实现了同步互穿工艺. Polyurethane/vinyl ester resin SINs (PU/VER SINs) were synthesized at room temperature by simultaneous interpenetrating process. Polymerization processes of PU/VER SINs were determined by the dynamic tracing and the half quantitative analysis of FT-IR, the interreaction of the two polymers and the effects of curing system on reaction of SINs were investigated. Results indicated the ratio of BPO and DBTDL directly impacted the conversion of two networks,and the reactions of PU and VER in the system had effects on each other. When the dosage of BPO was 0. 75%(w/w) of VER and the amount of DBTDL was 0. 6% (w/w) of PU, the polyaddition reactions of PU took place at the first and the conservations of two polymers were similar during the reaction. Both of ultimate conversations were higher than 90%, and the reaction realized interpenetrating polymer networks basically.
出处 《陕西科技大学学报(自然科学版)》 2008年第6期39-44,共6页 Journal of Shaanxi University of Science & Technology
关键词 聚氨酯/乙烯基酯树脂 同步互穿网络聚合物 动力学 傅立叶红外光谱 室温固化 PU/VER SINs dynamics FT-IR, curing at room temperature
  • 相关文献

参考文献9

  • 1Cascaval C N,Rou D, Rosu L. Advanced materials based on epoxy resins-2. Interpenetrating polymer networks[J].Materiale Plas tiee,2005,42(1) : 41-46.
  • 2Bhuniya S,Adhikari B. Toughening of epoxy resins by hydroxy-terminated, silicon-modified polyurethane oligomers[J]. Journal of Applied Polymer Science, 2003,90(6) : 1 497-1 506.
  • 3Frisch H L, Klempner D, Frisch K C. Recent advances in interpenetrating polymer networks[J]. Polymer engineering Science, 1982, 22(17): 1 143-1 152.
  • 4Pernice R,Frisch K C, Navare R. RIM Systems from interpenetrating polymer networks[J].Journal of Cellular Plastics, 1982, 18 (2) : 121-128.
  • 5Rokhade A P,Shelke N B,Patil S A, etal. Novel interpenetrating polymer network microspheres of chitosan and methylcellulose for controlled release of theophylline[J].Carbohy-drate Polymers,2007,69(4): 678-687.
  • 6Hua F J,Hu C P. Interpenetrating polymer networks of epoxy resin and urethane acrylate resin: 1. Kinetics of network formation [J]. European Polymer Journal, 1999,35 (1) : 103 112.
  • 7Widmaier J M,Drillieres S. Relationships between polymerization activating systems and viscoelastic properties of the subsequent polyurethane/poly(tertbutyl acrylate) interpenetrating polymer networks[J]. Journal of Applied Polymer Science, 1997,63(7) :951-958.
  • 8Hsu J T, Lee J L. Reaction kinetics of polyurethane-polyester interpenetrating polymer network in the bulk polymerization[J]. Polymer Engineering and Scienee, 1985,25(15) : 951-958.
  • 9Dean K,Cook W D,Zipper M D, etal. Curing behaviour of IPNs formed from model VERs and epoxy systems I amine cured epoxy [J]. Polymer, 2001,42 (4) : 1 345-1 363.

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