赵地顺, 任红威, 周二鹏, 李 乐. 季铵盐相转移催化氧化噻吩的研究[J]. 燃料化学学报(中英文), 2007, 35(01): 47-50.
引用本文: 赵地顺, 任红威, 周二鹏, 李 乐. 季铵盐相转移催化氧化噻吩的研究[J]. 燃料化学学报(中英文), 2007, 35(01): 47-50.
ZHAO Dishun, REN Hongwei, ZHOU Erpeng, LI Le. 季铵盐相转移催化氧化噻吩的研究[J]. Journal of Fuel Chemistry and Technology, 2007, 35(01): 47-50.
Citation: ZHAO Dishun, REN Hongwei, ZHOU Erpeng, LI Le. 季铵盐相转移催化氧化噻吩的研究[J]. Journal of Fuel Chemistry and Technology, 2007, 35(01): 47-50.

季铵盐相转移催化氧化噻吩的研究

季铵盐相转移催化氧化噻吩的研究

  • 摘要: 以噻吩的正庚烷溶液模拟轻质油品,研究了H2O2—HCOOH氧化条件下,相转移催化氧化噻吩脱硫。实验结果表明,四丁基溴化铵用量0.10g,反应1.5h,反应温度45℃,脱硫率最高可达86.36%。动力学研究表明,以四丁基溴化铵作为相转移催化剂,过氧化氢甲酸氧化噻吩脱硫为表观一级反应,反应速率常数 K30℃=0.6152h-1、K40℃=1.2672h-1、K50℃=0.8581h-1;相转移催化在H2O2—有机酸体系氧化噻吩脱硫反应中的作用为相转移催化剂阳离子Q+对氧化剂活性组分HCOOO-的转移作用。并建立了相转移催化氧化噻吩脱硫反应的循环模型。

     

    Abstract: Oxidative desulfurization of thiophene by phase transfer catalysis has been investigated with hydrogen peroxideformic acid as the oxidant, thiophene in nheptane as model compound of light oil. It was shown that the desulfurization rate of thiophene was 86.36%, under the conditions of water/oil ratio being 1∶1, after1.5h at temperature of 45℃ by TBAB. From the kinetics investigation, it was shown that when the model compound was oxidized by hydrogen peroxideformic acid with TBAB as phase transfer catalyst, the reaction was pseudo firstorder reaction with rate constants of K30℃=0.6152h-1, K40℃=1.2672h-1, and K50℃=0.8581h-1. The essential process of catalytic oxidation is the transfer of oxidizing active ingredients RCOOO- from water phase to oil phase by Q+, and the cycling models of oxidative desulfurization of thiophene by phase transfer catalysis(Q+X-) is builted.

     

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