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首页> 外文期刊>Polymer Degradation and Stability >A study of the degradation of ester-modified epoxy resins obtained by cationic copolymerization of DGEBA with γ-lactones initiated by rare earth triflates
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A study of the degradation of ester-modified epoxy resins obtained by cationic copolymerization of DGEBA with γ-lactones initiated by rare earth triflates

机译:稀土三氟甲磺酸酯引发的DGEBA与γ-内酯的阳离子共聚得到的酯改性环氧树脂的降解研究

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摘要

The thermal degradation of new thermosetting materials prepared by cationic copolymerization of mixtures with different proportions of diglycidylether of bisphenol A (DGEBA) with γ-valerolactone (γ-VL) or α-methyl-γ-butyrolactone (γ-MBL) initiated by scandium, ytterbium or lanthanum triflate and a complex of boron trifluoride was investigated. To study the thermal degradation thermogravimetry (TGA) was used. The materials are more degradable than conventional epoxy resins due to the presence of ester groups in the polymer chain, which are broken at the beginning of degradation. The degradability increased with the proportion of linear ester groups and the Lewis acidity of the initiator used in the polymerization and when the proportion of lactone in the initial mixture increased. The kinetic parameters of the degradation were calculated from TGA data by applying isoconversional procedures.
机译:通过scan引发不同比例的双酚A二缩水甘油醚(DGEBA)的混合物与γ-戊内酯(γ-VL)或α-甲基-γ-丁内酯(γ-MBL)的阳离子共聚制备的新型热固性材料的热降解,研究了tri或三氟甲磺酸镧与三氟化硼的配合物。为了研究热降解热重法(TGA)。由于在聚合物链中存在酯基,该酯比常规环氧树脂更易降解,而酯基在降解开始时会断裂。随着线性酯基的比例和聚合反应中所用引发剂的路易斯酸度的增加,以及当初始混合物中内酯的比例增加时,可降解性增加。降解的动力学参数通过应用等转换程序从TGA数据计算得出。

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