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deNO_x Performance and Reaction Mechanism of the Di-Air System

机译:空气系统的deNO_x性能和反应机理

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The detailed reaction mechanism of Di-Air, which showed the unprecedented high deNO_x performance at high temperature conditions, was studied in this work. Since the Di-Air phenomenon occurs with continuous short pulse injections of hydrocarbons over NSR (NOx storage and reduction) catalyst, this study focused on the specific function of HC as an effective reductant for NO_x reduction reaction. As a first step, the deNO_x performance was compared with three different reductant gases including CO, H2 and C3H6 in a modified synthetic gas bench equipped with a gas injector which enables continuous small amount of injections. At inlet gas temperature of 450 °C C3H6 showed the best deNO_x performance whereas H2 was the best at 150 °C. Moreover the result of temperature programmed desorption showed that intermediate species represented by-NCO (isocyanates) produced from C3H6 was thermally more stable than that produced from CO. These results confirmed that the injected HC reacts with adsorbed NO_x on NSR catalyst generating thermally stable intermediates, which could contribute the high deNO_x performance at high temperature conditions.
机译:在这项工作中,研究了Di-Air的详细反应机理,该机理在高温条件下显示出前所未有的高deNO_x性能。由于Di-Air现象是通过在NSR(NOx存储和还原)催化剂上连续短脉冲注入烃而发生的,因此本研究着重于HC作为NO_x还原反应有效还原剂的特殊功能。第一步,在配备有可连续进行少量喷射的气体喷射器的改良型合成气工作台中,将deNO_x性能与包括CO,H2和C3H6在内的三种不同的还原性气体进行了比较。在进气温度为450°C时,C3H6表现出最佳的deNO_x性能,而H2在150°C时表现最佳。此外,程序升温解吸的结果表明,由C3H6生成的以NCO(异氰酸酯)为代表的中间体比从CO生成的中间体更热稳定。这些结果证实,注入的HC与NSR催化剂上吸附的NO_x反应,生成热稳定的中间体,这可以在高温条件下提供较高的deNO_x性能。

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