Nikafshar Saeid, Zabihi Omid, Moradi Yousef, Ahmadi Mojtaba, Amiri Saba, Naebe Minoo
Department of Applied Chemistry, Faculty of Chemistry, University of Tabriz, Tabriz 51666, Iran.
Institute for Frontier Materials, Deakin University, Geelong VIC 3216, Victoria, Australia.
Polymers (Basel). 2017 Jul 4;9(7):266. doi: 10.3390/polym9070266.
In this study, lignin, an aromatic compound from the forestry industry, was used as a renewable material to synthesize a new aromatic amine curing agent for epoxy resin. Firstly, lignin was separated from black liquor and hydroxyl groups were converted to tosyl groups as leaving groups. Then, primary amination was conducted using an ammonia solution at high pressure and temperature, in the presence of a nano-alumina-based catalyst. The structure of the nanocatalyst was confirmed by FT-IR, ICP, SEM, and XPS analyses. According to the FT-IR spectra, a demethylation reaction, the substitution of hydroxyl groups with tosyl groups, and then an amination reaction were successfully performed on lignin, which was further confirmed by the C NMR and CHNS analyses. The active hydrogen equivalent of aminated lignin was determined and three samples with 9.9 wt %, 12.9 wt %, and 15.9 wt % of aminated lignin, as curing agents, were prepared for curing the diglycidyl ether of bisphenol A (DGEBA). The thermal characteristics of the curing process of these epoxy samples were determined by DSC and TGA analyses. Moreover, the mechanical performance of the cured epoxy systems, e.g., the tensile strength and Izod impact strength, were measured, showing that in the presence of 12.9 wt % aminated lignin, the mechanical properties of the aminated lignin-epoxy system exhibited the best performance, which was competitive, compared to the epoxy systems cured by commercial aromatic curing agents.
在本研究中,木质素这种来自林业工业的芳香族化合物被用作可再生材料,以合成一种用于环氧树脂的新型芳香胺固化剂。首先,从黑液中分离出木质素,并将羟基转化为甲苯磺酰基作为离去基团。然后,在基于纳米氧化铝的催化剂存在下,使用氨水溶液在高压和高温下进行伯胺化反应。通过傅里叶变换红外光谱(FT-IR)、电感耦合等离子体质谱(ICP)、扫描电子显微镜(SEM)和X射线光电子能谱(XPS)分析对纳米催化剂的结构进行了确认。根据FT-IR光谱,在木质素上成功进行了脱甲基反应、羟基被甲苯磺酰基取代反应,然后是胺化反应,这通过碳核磁共振(C NMR)和元素分析(CHNS)进一步得到证实。测定了胺化木质素的活性氢当量,并制备了三种分别含有9.9 wt%、12.9 wt%和15.9 wt%胺化木质素的样品作为固化剂,用于固化双酚A二缩水甘油醚(DGEBA)。通过差示扫描量热法(DSC)和热重分析法(TGA)分析测定了这些环氧样品固化过程的热特性。此外,还测量了固化环氧体系的力学性能,如拉伸强度和悬臂梁冲击强度,结果表明,在含有12.9 wt%胺化木质素的情况下,胺化木质素-环氧体系的力学性能表现最佳,与由商业芳香族固化剂固化的环氧体系相比具有竞争力。