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Experimental and kinetic study of oxidative steam reforming of ethanol over fresh and spent bimetallic catalysts

机译:新鲜乙醇对新鲜和废弃双金属催化剂氧化蒸汽重整的实验动力学研究

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Two bimetallic catalysts (Pt-Co and Ni-Co), supported on a CeO2-SiO2 mixed oxide and prepared by wet impregnation, were tested for oxidative steam reforming of ethanol in a fixed bed and compared with a previously investigated Pt-Ni sample. The Ni-Co catalyst displayed an improved performance compared to the Pt-Co one, in terms of both activity and stability: a mean conversion below 80% was reached over the noble metal-based catalyst after 70 h of time-on-stream at 500 degrees C while the same value, with a higher H-2 yield, was recorded over the Ni-Co sample after 260 h. A kinetic investigation was also performed and the model assuring the best agreement with experimental data involved ethanol decomposition, methane oxidation, methane steam reforming and water gas shift reactions. The activation energies (E-a) of the above reactions over the Ni-Co catalyst were shown to be lower than those measured for the noble-metal based sample, demonstrating that a higher activity can be reached by combining nickel and cobalt: for example, in the case of methane reforming, E-a = 77.1 kJ.mol(-1) was predicted against a value of 231.7 kJ.mol(-1) found for the Pt-Co sample. A further kinetic study was performed over the spent catalysts and the extent of deactivation was found to be more pronounced over the Pt-Co/CeO2-SiO2 catalyst.
机译:在CeO2-SiO 2的混合氧化物上负载并通过湿浸渍制备的两种双金属催化剂(Pt-Co和Ni-Co)用于乙醇在固定床中氧化蒸汽重整,并与先前研究的Pt-Ni样品进行比较。与活性和稳定性相比,Ni-Co催化剂与PT-CO相比显示出改善的性能:在70小时后,在70小时后,在贵金属基催化剂上达到50%以下的平均转化率在260小时后,在Ni-Co样品中记录了500℃而具有较高的H-2产量的相同值。还进行了动力学调查,模型确保了与实验数据的最佳协议涉及乙醇分解,甲烷氧化,甲烷蒸汽重整和水煤气变换反应。在Ni-Co催化剂上的上述反应的活化能量(EA)被显示为低于测量的贵金属基物样品的活化能量(EA),表明通过组合镍和钴可以达到更高的活性:例如,甲烷重整的情况,EA = 77.1kJ.mol(-1)预测为PT-CO样品的231.7kJ.mol(-1)的值。在废催化剂上进行进一步的动力学研究,发现失活的程度在Pt-Co / CeO 2-SiO 2催化剂上更加明显。

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