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Role of accelerator in curing of epoxy-anhydride pressure impregnant

机译:促进剂在环氧酸酐压力浸渍固化中的作用

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In the present paper, Differential Scanning Calorimetry (DSC) has been applied to bring out the role of zinc naphthenate accelerator in the curing of epoxy-anhydride pressure impregnant used for impregnation of electrical machines. Effect of concentration of zinc naphthenate on curing behavior of bisphenol-A epoxy resin and methylhexahydrophthalic anhydride hardener has been studied by obtaining dynamic DSC thermograms for uncatalysed, and catalysed system with various concentration of zinc naphthenate. The investigations reveal that the un-catalyzed purified epoxyanhydride mix exhibits an endothermic peak at temperature around 260 u000b0;C in place of cure exothermic peak in the DSC curve. The analysis of DSC and TGA data of individual resin, hardener and their mix indicate that the endothermic peak is attributed to the evaporation of resin and hardener implying that the hardener does not react with resin in absence of accelerator. The addition of zinc naphthenate accelerator at concentration of 1 pph (parts of zinc naphthenate per hundred parts of resin- hardener mix) causes two exothermic peaks in the DSC thermogram. The position and area under these peaks vary with the accelerator content resulting in the variation in the processing parameters and the performance properties of the cured material. The first peak from esterification reaction appears between 90 and 200 u000b0;C and second peak from etherification reaction appears in the temperature range of 180 to 330 u000b0;C. The area under the first exothermic peak appearing at low temperature increases with increase of accelerator content and predominates at concentration of ʧE; 1.5 pph. The area under the second exothermic peak appearing at high temperature increases with the decrease of accelerator content and predominates at concentration of ʧD; 0.5 pph. The accelerator concentration of 2 pph provides maximum reactivity.
机译:在本文中,差示扫描量热法(DSC)已被应用来揭示环烷酸锌促进剂在用于电机浸渍的环氧酐压力浸渍剂的固化中的作用。通过获得各种浓度的环烷酸锌的未催化和催化体系的动态DSC热谱图,研究了环烷酸锌的浓度对双酚A环氧树脂和甲基六氢邻苯二甲酸酐硬化剂固化行为的影响。研究表明,未催化的纯化环氧酸酐混合物在260 u000b0; C左右的温度下显示出吸热峰,而不是DSC曲线中的固化放热峰。对单个树脂,固化剂及其混合物的DSC和TGA数据的分析表明,吸热峰归因于树脂和固化剂的蒸发,这意味着在没有促进剂的情况下,固化剂不会与树脂反应。添加浓度为1 pph的环烷酸锌促进剂(每100份树脂-硬化剂混合物中的环烷酸锌含量)会在DSC热谱图中产生两个放热峰。这些峰下的位置和面积随促进剂含量而变化,从而导致加工参数和固化材料的性能特性发生变化。酯化反应的第一个峰出现在90至200 u000b0; C之间,醚化反应的第二个峰出现在180至330 u000b0; C的温度范围内。低温下出现的第一个放热峰下的面积随促进剂含量的增加而增加,并在ʧE浓度下占优势。 1.5 pph。高温下出现的第二个放热峰下的面积随促进剂含量的减少而增加,在ʧD浓度下占优势。 0.5 pph。 2pph的促进剂浓度可提供最大的反应性。

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