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首页> 外文期刊>Journal of industrial and engineering chemistry >Preparation of gadolinia doped ceria via metal complex decomposition method: Its application as catalyst for the steam reforming of ethane
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Preparation of gadolinia doped ceria via metal complex decomposition method: Its application as catalyst for the steam reforming of ethane

机译:金属配合物分解法制备氧化ado掺杂二氧化铈:在乙烷蒸汽重整中的应用

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摘要

The ceria (CeO2) and gadolinia doped ceria (GDC; Ce_(1-x)Gd_xO_(2-δ)with x = 0.10,0.15, and 0.20) catalysts were successfully prepared via metal complex decomposition method at 900 °C for 2 h. The synthesized CeO2 and GDC were found to have useful activity to convert ethane to syngas via the steam reforming reaction at the temperature range of 800-900 °C. The catalytic activity was improved with increasing Gd doping amount from 0 to 0.1 and 0.15; nevertheless, at higher Gd doping content (0.2), the improvement becomes less pronounced. Among all catalysts, Ce_(0.85)Gd_(0.15)O_(2-δ) showed the best steam reforming activity; furthermore, the amount of carbon formation over this catalyst was relatively low. These enhancements are mainly due to the high specific surface area and the good oxygen storage capacity (OSC) of the material. During the steam reforming process, the gas-solid reactions between the gaseous components presented in the system (C2H6, C2H4, and CH4) and the lattice oxygen (O_x) on the surface CeO2 or GDC occurs. The reactions of hydrocarbons adsorbed on the surface with O_x (C_nH_m + O_x → nCO + m/2(H2) + O_(x-n)) can prevent the formation of carbon species from hydrocarbons decomposition reaction (C_nH_m <=> nC + m/2H2). Moreover, the formation of carbon via Boudouard reaction (2CO<= >CO2 + C) is also reduced by the gas-solid reaction of CO with the lattice oxygen (CO + O_x <=> CO2 + O_(x-1)).
机译:通过金属络合物分解法在900°C下成功制备了二氧化铈(CeO2)和氧化ado掺杂的二氧化铈(GDC; Ce_(1-x)Gd_xO_(2-δ)x = 0.10,0.15和0.20)催化剂。 。发现合成的CeO2和GDC具有有用的活性,可在800-900°C的温度范围内通过蒸汽重整反应将乙烷转化为合成气。随着Gd掺杂量从0增加到0.1和0.15,催化活性得到改善。然而,在较高的Gd掺杂含量(0.2)下,改进变得不那么明显。在所有催化剂中,Ce_(0.85)Gd_(0.15)O_(2-δ)表现出最佳的蒸汽重整活性。此外,在该催化剂上形成的碳量较低。这些增强主要是由于材料的高比表面积和良好的储氧能力(OSC)。在蒸汽重整过程中,系统中存在的气态组分(C2H6,C2H4和CH4)与表面CeO2或GDC上的晶格氧(O_x)之间发生气固反应。 O_x(C_nH_m + O_x→nCO + m / 2(H2)+ O_(xn))吸附在表面的碳氢化合物的反应可以防止碳氢化合物分解反应形成碳物质(C_nH_m <=> nC + m / 2H2 )。此外,通过Boudouard反应(2CO = CO 2 + C)形成的碳还通过CO与晶格氧的气固反应(CO +O_x≤CO2 + O_(x-1))而减少。

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