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The Catalytic Oxidation of p-Xylene to Terephthalic Acid in ScCO{sub}2

机译:在SCCO {Sub} 2中对苯二甲酸对苯二甲酸的催化氧化

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The feasibility of synthesizing terephthalic acid (TA) has been demonstrated via the oxidation of p-xylene (PX) in supercritical carbon dioxide (scCO{sub}2) at 150°C in our paper. Reactions were carried out in a 150 ml vessel. Oxygen served as the oxidant and CoBr{sub}2 or Co(OAc)2·4H{sub}2O as the catalysts. The effects of reaction time, metal ion and different catalysts on the conversion of PX and the selectivity of TA and the product distribution were investigated. Results showed that when the iron ion, especially Fe{sup}(2+), reduced the oxidation ability by reacting with Co{sup}(3+). The conversions of PX with CoBr{sub}2 as the catalysts at 1 hour and 6 hour were 74.45% and 84.80% respectively, and the corresponding molar selectivities of PT, TA and 4-CBA were 0.57, 0.21, 0.17 and 0.49, 0.31 0.16 separately. However, longer reaction time resulted in the degradation of target products. The experimental results provided some insight into the reaction mechanism.
机译:通过在150℃下在150℃下,通过在150℃下在超临界二氧化碳(SCCO {Sub} 2)中来证明合成对苯二甲酸(Ta)的可行性。反应在150ml容器中进行。氧气用作氧化剂和COBR {亚} 2或CO(OAC)2·4H {亚} 2O作为催化剂。研究了反应时间,金属离子和不同催化剂对PX转化的影响及TA的选择性及产物分布。结果表明,当铁离子,尤其是Fe {sup}(2+)时,通过与Co {sup}(3+)反应来降低氧化能力。用COBR {Sub} 2的PX转化为1小时和6小时的催化剂分别为74.45%和84.80%,相应的Pt,Ta和4-CBA的摩尔选择性为0.57,0.21,0.17和0.49,0.31 0.16分开。然而,更长的反应时间导致目标产品的降解。实验结果提供了一些洞察反应机制。

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