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Viscoelastic changes of epoxy resin–acid anhydride system during curing

机译:环氧树脂-酸酐体系固化过程中的粘弹性变化

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AbstractThe changed viscoelastic properties of the epoxy resin‐acid anhydride system, Epikote 834‐HHPA, are followed to the gel point at 130, 140, and 150°C with a dynamic viscoelastometer. The viscosity increases with curing time through two inflections designated A and B. The point A is interpreted (from the reference to the chemical changes reported in the previous paper) as the termination of the initial stage of this curring reaction, and point B coincides with the gel point determined by the torsion method. The resonance frequency remains constant value up to the point B, followed by a rapid increase. The extents of reaction for epoxide, anhydride, and initial OH are 15, 45.8, and 100 at the point A; 27.8, 63.7, and 100 at the point B, respectively. The apparent activation energies for viscosity are 7.5 kcal/mole for the resin mixture before curing, 10.5 kcal/mole for point A, 48.8 kcal/mole for point B (gel point). The overall apparent activation energies of this curing reaction are obtained from the Arrhenius plots for the curing time required for the resin mixture to reach the state of the points A and B; these values were 8.9 kcal/mole for point A and 16.2 kcal/mole for poi
机译:摘要 在130°C、140°C和150°C下,用动态粘弹性仪跟踪环氧树脂酸酐体系Epikote 834-HHPA的粘弹性变化。粘度随着固化时间的增加而增加,通过两个变化分别命名为 A 和 B。A点被解释为(来自上一篇论文中报道的化学变化的参考)为该固化反应初始阶段的终止,B点与扭转法确定的凝胶点重合。谐振频率在B点之前保持恒定值,然后迅速增加。环氧化物、酸酐和初始 OH 的反应范围在 A 点分别为 15%、45.8% 和 100%;B点分别为27.8%、63.7%和100%。固化前树脂混合物的粘度表观活化能为7.5 kcal/mole,A点为10.5 kcal/mole,B点(凝胶点)为48.8 kcal/mole。该固化反应的总表观活化能是从树脂混合物达到 A 点和 B 点状态所需的固化时间的 Arrhenius 图中获得的;这些值为 A 点的 8.9 kcal/mole 和 poi 的 16.2 kcal/mole

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