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Melamine formaldehyde: curing studies and reaction mechanism

固化(化学) 傅里叶变换红外光谱 热重分析 差示扫描量热法 三聚氰胺树脂 高分子化学 三聚氰胺 热稳定性 甲醛 化学 材料科学 反应机理 化学工程 有机化学 催化作用 涂层 物理 工程类 热力学
作者
Dyana J Merline,Sulafudin Vukusic,Ahmed Abdala
出处
期刊:Polymer Journal [Springer Nature]
卷期号:45 (4): 413-419 被引量:405
标识
DOI:10.1038/pj.2012.162
摘要

Melamine formaldehyde (MF) resin was synthesized by the reaction between melamine and formaldehyde under alkaline condition in tetrohydrofuran medium with 1:3 melamine to formaldehyde molar ratio. The synthesized resins were characterized by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR) and thermal gravimetric analysis (TGA). Curing and reaction mechanism was studied by thermal and spectroscopic analysis. Two exothermic peaks were observed in the DSC analysis indicating a two-step crosslinking reaction process was correlated to TGA analysis. FTIR studies at different temperatures explained the two-stage curing mechanism which is concurring with the DSC data. At a temperature range of 140–160 °C, reversible demethylolation is dominating to the crosslinking reaction. At temperature >160 °C, the crosslinking reaction dominates. On the basis of DSC and FTIR data, a possible crosslinking reaction route was derived and explained. The first stage of curing is the conversion of methylol groups to primary amine and the second stage is the crosslinking of methylol groups to the final product, methylene bridges. The thermal stability of the methylol groups, methylene bridges and the triazine ring, as well as the evaporation of effluents at different stages of curing, are also discussed based on combined TGA and DSC results. Curing studies and reaction mechanism of MF resin was studied by thermal and spectroscopic tools comparing DSC and FTIR studies explains the two-stage thermal curing mechanism. The first step of thermal curing at temperature range of 140–160 °C is the reverse reaction of methylol groups to melamine and second step occurring at temperature >160 °C is the crosslinking of methylol groups to the final product, methylene bridge. Hence, by the mutual agreement of DSC and FTIR studies, a possible reaction route was derived for the thermal curing process. The DSC–TGA thermogram supports the two-step process of the cure reaction by exhibiting two peaks in the same temperature region.
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