Examining the nature of network formation during epoxy polymerisation initiated with ionic liquids

被引:11
作者
Binks, Fiona C. [1 ,4 ]
Cavalli, Gabriel [1 ,5 ]
Henningsen, Michael [2 ]
Howlin, Brendan J. [1 ]
Hamerton, Ian [3 ]
机构
[1] Univ Surrey, Fac Engn & Phys Sci, Dept Chem, Surrey GU2 7XH, England
[2] BASF AG, Intermediates Div, Carl Bosch Str 38, D-67056 Ludwigshafen, Germany
[3] Univ Bristol, Bristol Composites Inst ACCIS, Dept Aerosp Engn, Sch Civil Aerosp & Mech Engn,Univ Walk, Queens Bldg, Bristol BS8 1TR, Avon, England
[4] Hexcel Composites, Cambridge CB22 4QD, England
[5] Queen Mary Univ London, Sch Engn & Mat Sci, 327 Mile End Rd, London E1 4NS, England
关键词
Epoxy resins; Ionic liquids; Initiators; Network formation; Physico-mechanical properties; DIGLYCIDYL ETHER; BISPHENOL-A; MECHANISM; RESINS;
D O I
10.1016/j.polymer.2018.07.046
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A commercial diglycidyl ether of bisphenol A monomer (Baxxores (TM) ER 2200, eew 182 g/mole, DGEBA) is thermally polymerized in the presence of an ionic liquid, 1-ethyl-3-methylimidazolium acetate at a variety of loadings (5-45 wt %). The loss modulus data for cured samples, containing 5 wt % initiator, display at least two thermal transitions and the highest storage modulus occurs in the sample that has been cured for the shortest time at the lowest temperature. Samples that are exposed to higher temperatures (140, 150 degrees C) yield more heterogenous networks, whereas following exposure to a much shorter/lower temperature cure schedule (80 degrees C) exhibits a considerably higher damping ability than the other samples, coupled with a lower glass transition temperature. Differential scanning calorimetry reveals that the latter sample achieves a conversion of 95%, while crosslink densities for the DGEBA samples containing 5 wt % and 15 wt % are respectively 9.5 x 10(-3)mol. dm(-3) and 1.2 x 10(-3)mol. dm(-3 )(when cured to 80 degrees C) and 2.0 x 10(-2)mol. dm(-3) and 2.4 x 10(-3)mol. dm(-3) (when cured to 140 degrees C). (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:318 / 325
页数:8
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