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Preparation of a Carbon-Based Solid Acid Catalyst by Sulfonating Activated Carbon in a Chemical Reduction Process

机译:化学还原法磺化活性炭制备碳基固体酸催化剂

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Sulfonated (SO3H-bearing) activated carbon (AC-SO3H) was synthesized by an aryl diazonium salt reduction process. The obtained material had a SO3H density of 0.64 mmol·g-1 and a specific surface area of 602 m2·g-1. The catalytic properties of AC-SO3H were compared with that of two commercial solid acid catalysts, Nafion NR50 and Amberlyst-15. In a 10-h esterification reaction of acetic acid with ethanol, the acid conversion with AC-SO3H (78%) was lower than that of Amberlyst-15 (86%), which could be attributed to the fact that the SO3H density of the sulfonated carbon was lower than that of Amberlyst-15 (4.60 mmol·g-1). However, AC-SO3H exhibited comparable and even much higher catalytic activities than the commercial catalysts in the esterification of aliphatic acids with longer carbon chains such as hexanoic acid and decanoic acid, which may be due to the large specific surface area and mesoporous structures of the activated carbon. The disadvantage of AC-SO3H is the leaching of SO3H group during the reactions.
机译:通过芳基重氮盐还原法合成了磺化(SO 3 H)活性炭(AC-SO 3 H)。所得材料的SO 3 H密度为0.64 mmol·g -1 ,比表面积为602 m 2 ·g -1 。将AC-SO 3 H的催化性能与两种商用固体酸催化剂Nafion NR50和Amberlyst-15进行了比较。在乙酸与乙醇的10小时酯化反应中,AC-SO 3 H的酸转化率(78%)低于Amberlyst-15(86%)的酸转化率。磺化碳的SO 3 H密度低于Amberlyst-15(4.60 mmol·g -1 )。但是,AC-SO 3 H在具有较长碳链的脂肪酸(己酸和癸酸)的酯化中表现出与商业催化剂相当甚至更高的催化活性,这可能是由于大比表面积和活性炭的介孔结构。 AC-SO 3 H的缺点是反应过程中SO 3 H基团的浸出。

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    《Molecules》 |2010年第10期|共9页
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  • 中图分类 有机化学;
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