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首页> 外文期刊>Iranian polymer journal >Rheokinetics in curing process of polyfurfuryl alcohol: effect of homologous acid catalysts
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Rheokinetics in curing process of polyfurfuryl alcohol: effect of homologous acid catalysts

机译:聚糠醇固化过程中的流变动力学:同源酸催化剂的作用

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Curing reaction of polyfurfuryl alcohol (PFA) resin was investigated using rheological measurements in the presence of different acid catalysts. A homologous series of dicarboxylic acid catalysts with even number of carbons of 2, 4 and 6 were chosen, i.e., oxalic acid (OX, 2 carbon), succinic acid (SU, 4 carbon) and adipic acid (AD, 6 carbon). Acidity of these catalysts in terms of pK(a) was in the range of 1.25-4.43. Firstly, non-isothermal curing kinetics were investigated, and then, isothermal studies were performed at three different temperatures using 3 and 5 wt% of each acid catalyst. Isothermal cure behavior was best described by an empirical Arrhenius model of viscosity. An isoconversional method was applied to compute the changes in the effective activation energy as a function of degree of conversion. The change in activation energy at 50-10 kJ mol(-1) was observed for PFA/3 wt% OX system due to the vitrification and diffusion-controlled processes. Gel time, t(gel), was determined as a function of curing temperature, acid catalyst type and its concentration. The gelation time was consistent for all the formulations with an extent of conversion of about 0.7. Significant differences were observed in the curing behavior of resins in the presence of different acid catalysts. Increasing of the curing temperature significantly accelerated the curing process and increased curing rate constant of the PFA resin.
机译:在不同酸催化剂存在下,使用流变学方法研究了聚糠醇(PFA)树脂的固化反应。选择具有偶数个碳的2、4和6的同源系列的二羧酸催化剂,即草酸(OX,2个碳),琥珀酸(SU,4个碳)和己二酸(AD,6个碳)。以pK(a)计,这些催化剂的酸度为1.25-4.43。首先,研究了非等温固化动力学,然后,分别使用3和5 wt%的每种酸催化剂在三个不同的温度下进行了等温研究。等温固化行为最好通过经验的Arrhenius粘度模型来描述。应用了等转化方法来计算有效活化能随转化度的变化。对于PFA / 3 wt%OX系统,由于玻璃化和扩散控制过程,在50-10 kJ mol(-1)处观察到活化能的变化。测定胶凝时间t(gel)与固化温度,酸催化剂类型及其浓度的关系。所有制剂的胶凝时间是一致的,转化率约为0.7。在存在不同酸催化剂的情况下,在树脂的固化行为中观察到了显着差异。固化温度的升高显着加速了固化过程并提高了PFA树脂的固化速率常数。

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