Ir/SiO2上甲烷部分氧化制合成气反应的原位时间分辨红外和原位Raman光谱表征

采用原位时间分辨红外光谱和原位显微Raman光谱技术对Ir/SiO₂上甲烷部分氧化(POM)制合成气反应的初级产物和反应条件下催化剂表面物种进行了跟踪考察,实验结果表明,在H₂预还原的新鲜Ir/SiO₂表面,CO是V(CH₄):V(O₂):V(Ar)=2:1:45混合气反应的初级产物,因而甲烷的直接氧化过程是CO生成的主要途径;而在稳态反应条件下,CO生成的途径可能主要来自CO₂和H₂O与催化剂表面积碳物种(CHx)和/或CH₄的反应.催化剂上生成的积碳可能是导致稳态条件下Ir/SiO₂上POM反应机理不同于H₂预还原的新鲜催化剂的主要原因.

In situ Time-resolved FTIR and Raman Characterizations of the Partial Oxidation of Methane to Synthesis Gas over Ir/SiO2 Catalyst

In situ time-resolved FTIR and in situ microprobe Raman spectroscopies were used to follow the primary products as well as the surface and gas phase species formed during the reaction of partial oxidation of methane (POM) to synthesis gas over Ir/SiO 2 catalyst. The results suggested that direct oxidation of CH 4 to CO is the dominant pathway of POM reaction over the freshly reduced Ir/SiO 2 catalyst, while the dominant schemes of CO formation over the catalyst under the steady state reaction condition are probably via the reactions of CO 2 and H 2O with the deposited carbon species (CH x) and/or CH 4. The mechanistic difference between the POM to synthesis gas over freshly reduced Ir/SiO 2 catalyst and the catalyst under the steady state reaction may have resulted from the formation of significant amount of deposited carbon species in the latter system.