Water gas shift reaction The water-gas shift reaction (WGS) is a chemical reaction in which carbon monoxide

reacts with water vapor to form carbon dioxide and hydrogen: CO(g) + H2O(v) → CO2(g) + H2(g) The water-gas shift reaction is an important industrial reaction. It is often used in conjunction with steam reforming of methane or other hydrocarbons,[1] which is important for the production of high purity hydrogen for use in ammonia synthesis. The water-gas shift reaction was discovered by Italian physicist Felice Fontana in 1780. The reaction is slightly exothermic, yielding 41.1 kJ (10 kcal) per mole.[1] The carbon monoxide can also be generated by bogs or other waste regenerative means by physical/chemical processes such as bog and landfill fires. Applications This reaction has been used as a CO removal method from the reformate for fuel cell applications. The reverse water gas shift reaction has recently found a possible application in In-Situ Resource Utilization on Mars to provide oxygen for fuel for the Mars Direct mission concept. Reaction conditions The water gas shift reaction is sensitive to temperature, with the tendency to shift towards reactants as temperature increases due to Le Chatelier's principle. In fuel-rich hydrocarbon combustion processes, the water gas reaction at equilibrium state is often employed as a means to provide estimates for molar concentrations of burnt gas constituents. The process is often used in two stages, stage one a high temperature shift (HTS) at 350 °C (662 °F) and stage two a low temperature shift (LTS) at 190–210 °C (374–410 °F).[2] Standard industrial catalysts for this process are iron oxide promoted with chromium oxide for the HTS step and copper on a mixed support composed of zinc oxide and aluminum oxide for the LTS shift step.[3]

The water gas shift reaction may be an undesired side reaction in processes which use water and carbon monoxide are present. which suppresses this reaction. The iridium-based Cativa process uses less water. . which decarboxylates to give a metal hydride ([M]-H−). the rhodium-based Monsanto process. Reaction with hydronium from water and carbon monoxide regenerates the metal carbonyl complex. it may involve β-hydride elimination. [5] The mechanism of decarboxylation is debated.Catalysts Attempts to lower the reaction temperature of this reaction have been done primarily with a catalyst such as Fe3O4 (magnetite). e. Another catalyst is the Raney copper catalyst. or it may require the action of an external base.[4] The mechanism for the transition metal-catalyzed reaction can be generally understood as follows: a metal carbonyl complex ([M]-CO) reacts with hydroxide to give a metallacarboxylic acid ([M]-COOH−).g. or other transition metals and transition metal oxides.

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