Hydrogen purification over lanthanum-doped iron oxides by WGSR

赤铁矿 无机化学 催化作用 化学 程序升温还原 煅烧 水煤气变换反应 氧化镧 材料科学 矿物学 有机化学
作者
María do Carmo Rangel,Peterson Santos Querino,Sarah Maria Santana Borges,S. G. Marchetti,José Mansur Assaf,Doris Polett Ruiz Vásquez,Cristiane B. Rodella,Tatiana de Freitas Silva,Alisson H. M. da Silva,Adriana P. Ramón
出处
期刊:Catalysis Today [Elsevier]
卷期号:296: 262-271 被引量:12
标识
DOI:10.1016/j.cattod.2017.05.058
摘要

Hydrogen technology has been greatly increased in last decades as a promising solution to protect the environment. When carbon-based feedstocks are used, such as natural gas, biomass and biogas, the water gas shift reaction (WGSR) plays an important step in the production of high pure hydrogen for several purposes. By this reaction, the residual carbon monoxide in the gaseous stream (coming from steam reforming of carbon-based feedstocks) can be converted to carbon dioxide and then removed from the stream, avoiding the poisoning of industrial metallic catalysts as well as of electrocatalysts in fuel cells. Aiming to obtain no toxic catalysts that can replace the commercial chromium-doped hematite catalysts, lanthanum-doped hematite was studied in this work. Iron oxide-based samples with different amounts of lanthanum (La/Fe (molar) = 0.02; 0.08 and 0.2) were obtained by sol-gel method and calcined at 600 °C. The catalysts were characterized by X-ray diffraction, specific surface area measurements, temperature programmed reduction, Raman spectroscopy, Mössbauer spectroscopy, transmission electron microscopy and X-ray photoelectron spectroscopy. It was found that lanthanum affected the textural and reducing properties of hematite, depending on the amount. Moreover, lanthanum oxide increased the activity of hematite by decreasing the size of hematite crystals and then increasing the number of exposed active sites. In addition, lanthanum favored hematite reduction to produce magnetite (active phase). The activity increased with the amount of lanthanum in solids, the lanthanum-richest sample being the most active catalyst.
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