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The water‐gas shift reaction: from conventional catalytic systems to Pd‐based membrane reactors—a review

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TLDR
In this article, the most relevant topics of water-gas shift (WGS) reaction in hydrogen perm-selective membrane reactors (MRs) are reviewed and the most used catalysts and relevant progress achieved so far are described and critically reviewed.
Abstract
The water-gas shift (WGS) reaction is a well-known step for upgrading carbon monoxide to hydrogen in the production of synthesis gas. For more than 90 years after its first industrial application, many issues in respect of the catalyst, process configuration, reactor design, reaction mechanisms and kinetics have been investigated. More recently, a renewed interest in the WGS reaction carried out in hydrogen perm-selective membrane reactors (MRs) has been observed because of the growing use of polymeric electrolyte membrane (PEM) fuel cells that operate using high-purity hydrogen. Moreover, MRs are viewed as an interesting technology in order to overcome the equilibrium conversion limitations in traditional reactors. This article reviews the most relevant topics of WGS MR technology—catalysis and membrane science. The most used catalysts and relevant progress achieved so far are described and critically reviewed. The effects of the most important parameters affecting the WGS in MRs are detailed. In addition, an overview on the most used membranes in MRs is also presented and discussed. Copyright © 2009 Curtin University of Technology and John Wiley & Sons, Ltd.

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Hydrogen production with CO2 capture

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Noble-Metal Nanocrystals with Controlled Shapes for Catalytic and Electrocatalytic Applications.

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References
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Journal ArticleDOI

Materials for fuel-cell technologies

TL;DR: Recent progress in the search and development of innovative alternative materials in the development of fuel-cell stack is summarized.
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Catalytic Properties of Ceria and CeO2-Containing Materials

TL;DR: A survey of the use of cerium oxide and CeO2-containing materials as oxidation and reduction catalysts is presented in this paper, with a special focus on catalytic interaction with small molecules such as hydrogen, carbon monoxide, oxygen, and nitric oxide.
Journal ArticleDOI

Gold catalysts prepared by coprecipitation for low-temperature oxidation of hydrogen and of carbon monoxide

TL;DR: In this paper, gold catalysts were prepared by coprecipitation from an aqueous solution of HAuCl4 and the nitrates of various transition metals, including Auα-Fe2O3, AuCo3O4, and AuNiO.
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Active Nonmetallic Au and Pt Species on Ceria-Based Water-Gas Shift Catalysts

TL;DR: It is reported here that for the class of nanostructured gold– or platinum–cerium oxide catalysts, which are active for the water-gas shift reaction, metal nanoparticles do not participate in the reaction.
Journal ArticleDOI

Low-Temperature Oxidation of CO over Gold Supported on TiO2, α-Fe2O3, and Co3O4

TL;DR: In this paper, the authors proposed a mechanism in which CO adsorbed on gold particles migrates toward the perimeter on support oxides and there it reacts with oxygen to form bidentate carbonate species.
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