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Chemical interactions at the interface between a carbon fiber and a boron trifluoride‐catalyzed epoxy matrix

机译:碳纤维与三氟化硼催化环氧基体界面的化学相互作用

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AbstractThe cure of a tetrafunctional epoxy resin (largely tetraglycidyldiaminodiphenylmethane, TGDDM), cross‐linked with diaminodiphenylsulphone (DDS) and boron trifluoride/ethylamine (BF3EA) catalyst, is affected in a complex fashion by the presence of an oxidized carbon fiber surface. If the fiber is aged in a humid environment (25°C, 95 humidity) before coating with the matrix, the affinity of the oxidized fiber surface for water leads to destruction of the catalyst and retardation of the cure. This retardation is noticeable at lower humidities if the polymer content of the composite is reduced to>20. For oxidized fibers that are stored under ambient conditions (40 humidity), the retarding effect of water is overwhelmed by the catalytic effect of the acidic fiber surface. This activates the latent catalyst, increasing the rate of epoxy consumption and the proportion of the epoxy–epoxy reaction relative to the epoxy–amine reaction. For the low‐humidity case, even though the rate of chemical reaction is increased, vitrification of the matrix is retarded, implying that there is less cross‐linking and more extended epoxy–epoxy sequences in the network. The proposed chemical changes in epoxy/carbon fiber composites were confirmed by analysis of model reactions in solution. © 1992 John Wi
机译:摘要与二氨基二苯砜(DDS)和三氟化硼/乙胺(BF3EA)催化剂交联的四官能团环氧树脂(主要是四缩水甘油基二氨基二苯甲烷,TGDDM)的固化受到氧化碳纤维表面的复杂影响。如果纤维在涂覆基体之前在潮湿环境(25°C,95%湿度)中老化,氧化纤维表面对水的亲和力会导致催化剂的破坏和固化的延迟。如果将复合材料的聚合物含量降低到>20%,则在较低的湿度下,这种延迟是明显的。对于在环境条件(40%湿度)下储存的氧化纤维,水的缓缓作用被酸性纤维表面的催化作用所淹没。这激活了潜伏催化剂,增加了环氧树脂消耗的速率以及环氧-环氧反应相对于环氧-胺反应的比例。对于低湿度情况,即使化学反应速率增加,基质的玻璃化也会延迟,这意味着网络中的交联更少,环氧-环氧序列更长。通过对溶液中模型反应的分析,证实了所提出的环氧/碳纤维复合材料的化学变化。© 1992 约翰·威

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