Efficiently and Directly Produce Triacetylglycerol from Oils and Fats Over Mesoporous Polymer Solid Acid Catalysts

Lijuan Su, Xiaojie Shao, L. Chai, H. Ge, Hongliang Wang, Xiao-jing Cui, Tiansheng Deng, Xianglin Hou
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Abstract

A series of mesoporous solid acid catalysts (PDS-x) with large BET surface area, superior thermal stability, strong sulfonic acid groups and tunable Brönsted acidity were synthesized by copolymerization of divinylbenzene (DVB) and p-styrenesulfonate hydrate (SPSS). The PDS-x catalysts showed high activity on the direct and efficient production of triacetylglycerol (TAG) by acyl exchange reaction of oils (fats) and acetic acid. The highest TAG yield of 92.2 mol% was obtained on the PDS-x catalysts at a mild condition of 200 o C. By combining SEM, TEM, FT-IR/DRIFT, BET, XRD, and TG-DTG, the key factors that affected the TAG yield were clarified on the PDS-x catalysts. Moreover, the origin of the slow deactivation on these catalysts was elucidated. The large BET surface area and abundant mesopores allowed the contact of large-sized glycerol tristearate with the strong sulfonic acid groups, accounting for the high TAG yield.
介孔聚合物固体酸催化剂催化油脂高效直接制备三乙酰甘油
以二乙烯基苯(DVB)和对苯乙烯磺酸盐(SPSS)为共聚材料,合成了一系列具有BET比表面积大、热稳定性好、强磺酸基和Brönsted酸度可调的介孔固体酸催化剂(PDS-x)。PDS-x催化剂对油(脂肪)与乙酸的酰基交换反应直接高效生产三乙酰甘油(TAG)具有较高的催化活性。通过SEM、TEM、FT-IR/DRIFT、BET、XRD和TG-DTG的综合分析,明确了影响PDS-x催化剂上TAG产率的关键因素。此外,还阐明了这些催化剂缓慢失活的原因。大的BET表面积和丰富的介孔允许大尺寸的三硬脂酸甘油与强磺酸基团接触,这是TAG产率高的原因。
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