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Synthesis of two novolac type epoxy resin curing agents and their application

机译:两种酚醛清漆型环氧树脂固化剂的合成及其应用

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Two novolac resins were synthesized by the reaction between bisphenol A and benzaldehyde (bis-BENR) or bisphenol A and p-hydroxybenzaldehyde (bis-PHNR). Fourier Transform Infrared Spectroscopy (FTIR) and nuclear magnetic resonance (NMR) were applied to characterize the molecular structure of bis-BENR (or bis-PHNR). Then the two novolac resins were used as curing agent for bisphenol A type epoxy resin (DGEBA). The curing reaction and curing kinetics were studied by Dynamic FTIR and Differential Scanning Calorimetry (DSC). Dynamic FTIR showed that the two novolac resins reacted with epoxy resins and formed a crosslinking network structure. DSC results show that the optimum mass ratio between DGEBA and bis-BENR (or bis-PHNR) was 7:3, under which the curing reaction processed completely. The mechanical properties and sulfide resistance of DGEBA/bis-BENR (or bis-PHNR) system were also investigated. The results showed that when the mass ratio between DGEBA and bis-BENR (or bis-PHNR) was 7:3, the curing coatings had optimum mechanical properties and sulfide resistance.
机译:通过双酚A和苯甲醛(BIS-BENR)或双酚A和p-羟基苯甲醛(BIS-PHNR)之间的反应合成了两种酚醛清漆树脂。傅里叶变换红外光谱(FTIR)和核磁共振(NMR)施用以表征双Benr(或双-PHNR)的分子结构。然后将两种酚醛清漆树脂用作双酚A型环氧树脂(DGEBA)的固化剂。通过动态FTIR和差示扫描量热法(DSC)研究了固化反应和固化动力学。动态FTIR显示两种酚醛清漆树脂与环氧树脂反应并形成交联网络结构。 DSC结果表明,DGEBA和BIS-BENR(或BIS-PHNR)之间的最佳质量比为7:3,固化反应完全加工。还研究了DGEBA / BIS-BENR(或BIS-PHNR)系统的机械性能和硫化物抗性。结果表明,当DGEBA和BIS-BENR(或BIS-PHNR)之间的质量比为7:3时,固化涂层具有最佳的机械性能和硫化物抗性。

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