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A 'Smart' Hollandite DeNO_x Catalyst: Self-Protection against Alkali Poisoning

机译:一种“智能”的荷兰沸石DeNO_x催化剂:防止碱中毒的自我保护

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摘要

Global warming, caused by an increase in atmospheric CO2 concentrations, and limited fossil-fuel resources have stimulated the search for environmentally sustainable energy sources with zero or low CO2 emission. The use of biomass as a CO2-neutral fuel has drawn widespread attention, since biomass as part of the global carbon ecocycle is an increasingly important energy resource. An associated issue, which is often encountered in the control of NO_x emissions from the alkali-rich stack gas of power plants (co-)fuelled by biomass, is the severe deactivation of conventional V2O5-WO3/TiO2 catalysts in the selective catalytic reduction of NO by NH3 (NH3-SCR). This deactivation is predominately caused by the strong interaction of alkali-metal ions with catalytically active sites. For example, Zheng et al. proposed a deactivation mechanism by proton exchange at catalytically active Br0nsted acid sites with alkali-metal ions. The exchange reactions occur readily at normal NH3-SCR operating temperatures because alkali species, such as KC1 and K2SO4, are mobile in view of their low Tamman temperatures (T_(Tam)).
机译:由大气中二氧化碳浓度增加引起的全球变暖和有限的化石燃料资源促使人们寻求二氧化碳排放量为零或低的环境可持续能源。由于生物质作为全球碳生态循环的一部分已成为越来越重要的能源,因此将其用作二氧化碳中和燃料已引起广泛关注。在控制以生物质为燃料的电厂(共)发电厂的富碱烟囱气中NO_x排放时经常遇到的一个相关问题是,传统的V2O5-WO3 / TiO2催化剂在选择性催化还原三氧化二钒中会严重失活NH3(NH3-SCR)生成的NO。这种失活主要是由于碱金属离子与催化活性位点的强相互作用引起的。例如,Zheng等。提出了通过质子交换在具有碱金属离子的催化活性布朗斯台德酸位上的失活机理。由于碱性物质(例如KCl和K2SO4)由于其较低的塔曼温度(T_(Tam))而可移动,因此在正常的NH3-SCR操作温度下很容易发生交换反应。

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