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首页> 外文期刊>Journal of Catalysis >The reactions of nitroalkanes over Cu-MFI and Fe-MFI catalysts under hydrocarbon-selective catalytic reduction conditions
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The reactions of nitroalkanes over Cu-MFI and Fe-MFI catalysts under hydrocarbon-selective catalytic reduction conditions

机译:烃选择性催化还原条件下硝基烷烃在Cu-MFI和Fe-MFI催化剂上的反应

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The reactions of 2-nitropropane (2NP) and 2-methyl-2-nitropropane (2M2NP),typical of secondary and tertiary nitroalkanes,respectively,have been investigated over Cu-MFI and Fe-MFI catalysts under conditions relevant to the selective catalytic reduction (SCR) of NO with the use of alkanes.With both catalysts the primary reaction is decomposition to form NO and the alkene,propene from 2NP,and isobutene from 2M2NP.If O_2 is present,then some N2 is formed by the subsequent SCR reaction between the alkene and NO_x.Production of N_2 is greater when the feed contains NO,but this is largely due to enhancement of the alkene SCR reaction rather than a direct reaction between the nitroalkane and NO_x.The alkene also reacts partly through deposition of carbonaceous material,which causes deactivation.In the absence of O_2 propene is also formed,through cracking of the oligomers derived from isobutene produced by 2M2NP decomposition.The reduction of NO/O_2 by propene and isobutene over Fe-MFI proceeds in a manner similar to that of the reduction with propane and isobutane,except for a lower production of HCN.With mixed alkane/alkene feeds,the alkene reacts in preference to the alkane.Overall the data show that secondary and tertiary nitroalkanes are less reactive than primary nitroalkanes over transition-metal zeolites because of the absence of the two alpha-hydrogens necessary for tautomerism to an aci form and its subsequent dehydration to a reactive isocyanate.Thus secondary and tertiary nitroalkanes are unlikely to be a major source of N_2 during alkane SCR over these catalysts but could play a part through the generation of alkenes that are more reactive than alkanes.
机译:在与选择性催化还原有关的条件下,分别在Cu-MFI和Fe-MFI催化剂上研究了典型的仲硝基和叔硝基烷烃2-硝基丙烷(2NP)和2-甲基-2-硝基丙烷(2M2NP)的反应用两种烷烃进行催化反应(SCR)。两种催化剂的主要反应是分解生成NO,然后由2NP生成烯烃,丙烯,由2M2NP生成异丁烯。如果存在O_2,则随后的SCR反应会生成一些N2。进料中含有NO时,N_2的生成量更大,但这主要是由于SCR催化反应的增强,而不是硝基烷与NO_x之间的直接反应。烯烃也通过碳质物质的沉积而部分反应在不存在O_2丙烯的情况下,通过2M2NP分解产生的异丁烯衍生的低聚物的裂解也形成了丙烯。Fe-MFI流程上丙烯和异丁烯还原NO / O_2 ds的反应方式与丙烷和异丁烷的还原反应类似,只是降低了HCN的产量。在混合的烷烃/烯烃进料中,烯烃优先于烷烃反应。总体数据显示仲和叔硝基烷烃较少由于不存在互变异构体转变为aci形式和随后脱水成反应性异氰酸酯所必需的两个α氢,因此它们比过渡金属沸石具有更高的反应活性,因此仲和叔硝基烷烃不太可能是N_2的主要来源在这些催化剂上使用烷烃SCR,但可以通过产生比烷烃更具反应性的烯烃发挥作用。

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