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氢化萜烯酯型环氧树脂固化反应表征与机械性能研究 被引量:3

Study on Curing Reaction and Mechanical Properties of Epoxy Resin from Hydrogenated Terpinene-maleic Anhydride
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摘要 氢化萜烯酯型环氧树脂(HTME)是以萜烯-马来酸酐加成物的氢化产物与环氧氯丙烷反应合成的环氧树脂。通过DSC热分析、凝胶时间的测定及其影响因素分析,研究了HTME与甲基六氢苯酐(MeHHPA)的固化反应活性;通过FT-IR光谱法定性分析与固化度测定法定量分析,表征了HTME/MeHHPA体系的固化反应行为及完成固化反应的条件;并比较了HTME、TME及环氧树脂6101与Me-HHPA固化产物的机械性能。结果表明,HTME/M eHHPA体系的固化反应属于放热反应,反应热焓为153.5 J/g,峰顶温度为157.9℃;在0.5%BDMA促进剂条件下,110℃经8 h可完全固化,且HTME与MeHHPA按化学计量配比时固化效果最好,固化产物的机械性能与环氧树脂6101固化物的性能相似。 Hydrogenated terpinene-maleic ester type epoxy resin(HTME) is a type of epoxy resin synthesized from hydrogenated terpinene-maleic anhydride. The activity of curing reaction of HTME/methyl hexahydrophthalic anhydride (MeHHPA) system was investigated by means of DSC and gelation time determination. The curing behaviors of HTME/MeHHPA system were studied by qualitative analysis of FT-IR spectrum and quantitative analysis of curing degree determination. The mechanical properties of HTME cured with MeHHPA were compared with those of terpinene-maleic ester type epoxy resin (TME) and epoxy resin 6101 under the same condition. The results show that the reaction between HTME and MeHHPA was an exothermic one with reaction heat of 153.5 J/g and peak temperature at 157.9 ℃, and the HTME/MeHHPA system could be cured completely at 110 ℃ for 8 h with 0.5 % benzyldimethylamine (BDMA) by weight of HTME as aecelerant. The mechanic properties of the three kinds of cured epoxy products were about the same.
出处 《林产化学与工业》 EI CAS CSCD 2007年第4期21-26,共6页 Chemistry and Industry of Forest Products
基金 国家杰出青年基金资助项目(30325031) 国家林业局"948"创新项目资助(2006-4-C03)
关键词 氢化萜烯马来酸酐 环氧树脂 固化反应 机械性能 hydrogenated terpinene-maleic anhydride epoxy resin curing reaction mechanical property
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  • 1孔振武,黄焕,周浩.改性松香脂环基环氧树脂的固化反应特性[J].林产化学与工业,2004,24(B08):29-32. 被引量:8
  • 2陆占国,小林直,笠井博子.α-松油烯为原料的单萜衍生物合成及其构造解析[J].化学试剂,2005,27(10):585-588. 被引量:13
  • 3杜郢,龚建贤,高国生.环保型透明双组分改性聚氨酯胶黏剂的研究[J].化工进展,2006,25(4):436-438. 被引量:13
  • 4吴国民,孔振武,储富祥.氢化萜烯马来酸酐合成环氧树脂的研究[J].林产化学与工业,2007,27(3):57-62. 被引量:14
  • 5WONG K H ,ZINKE-ALLMANG M ,WAN W K. Low energy oxygen ion beam modification of the surface morphology and chemical structure of polyurethane fibers[ J]. Nuclear Instruments and Methods in Physics Research,2006,234( 1 ) :63-74.
  • 6SONG Hao-jie, ZHANG Zhao-zhu, MEN Xue-hu. Surface-modified carbon nanotubes and the effect of their addition on the tribological behavior of a polyurethane coating[ J]. European Polymer Journal,2007,43(10) :4092-4102.
  • 7ASWINI K, MISHRA D K, CHATTOPADHYAY B, et al. FT-IR and XPS studies of polyurethane-urea-imide coatings [ J ]. Progress in Organic Coatings,2006,55 ( 1 ) :231-243.
  • 8GIULIO M, ALDO P, FRANCO F. Polyurethane resin-based adhesives: curing reaction and properties of cured systems [ J ]. International Journal of Adhesion and Adhesives,2005,25 ( 1 ) :87-91.
  • 9Zeno W威克斯 Frank N琼斯 Peter S柏巴斯.有机涂料科学和技术[M].北京:化学工业出版社,2002.3..
  • 10李桂林.环氧树脂与酸酐类固化反应的促进剂[J].热固性树脂,1988(3):44-48.

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