Anionic copolymerization of DGEBA with two bicyclic bis(γ-lactone) derivatives using tertiary amines as initiators

被引:12
作者
Arasa, Merce [1 ]
Ramis, Xavier [2 ]
Salla, Josep Maria [2 ]
Mantecon, Ana [1 ]
Serra, Angels [1 ]
机构
[1] Univ Rovira & Virgili, Dept Quim Analit & Quim Organ, Tarragona 43007, Spain
[2] Univ Politecn Cataluna, Lab Termodinam, ETSEIB, E-08028 Barcelona, Spain
关键词
Anionic polymerization; Thermosets; DSC; CROSS-LINKABLE POLYMERS; SPIROCYCLIC BIS(GAMMA-LACTONE)S; ALTERNATING COPOLYMERIZATION; THERMOSETS; SHRINKAGE; KINETICS; EPOXIDE;
D O I
10.1016/j.polymer.2009.03.030
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The anionic copolymerization, to form thermosets, of diglycidylether of bisphenol A (DGEBA) with two condensed bis(gamma-lactone)s (bisMe and bisPhe) using 4-(N,N-dimethylamino)pyridine (DMAP), 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU), and 1-methylimidazole (1MI) as initiators was studied by differential scanning calorimetry (DSC). The kinetics was evaluated by isoconversional procedures. The evolution of the typical functional groups that form or disappear during curing was followed by Fourier transform infrared in the attenuated-total-reflection mode (FTIR/ATR) to clarify the reactive processes that takes place. Unexpected processes, which lead to the formation of five-membered lactones, were detected when non-stoichiometric proportions of monomers were used. The stoichiometric DGEBA/bislactone ratio produces the expected alternate poly(ester-ketone) network. The thermal degradability of the materials obtained was evaluated by TGA, and their reworkable character was confirmed. Materials obtained from stoichiometric mixtures were completely soluble in ethanolic KOH. (C) 2009 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2228 / 2236
页数:9
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