Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.chemrev.2c00439
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dc.titleMethane Oxidation to Methanol
dc.contributor.authorDummer, Nicholas F
dc.contributor.authorWillock, David J
dc.contributor.authorQian He
dc.contributor.authorHoward, Mark J
dc.contributor.authorLewis, Richard J
dc.contributor.authorQi, Guodong
dc.contributor.authorTaylor, Stuart H
dc.contributor.authorXu, Jun
dc.contributor.authorBethell, Don
dc.contributor.authorKiely, Christopher J
dc.contributor.authorHutchings, Graham J
dc.date.accessioned2022-12-23T01:47:42Z
dc.date.available2022-12-23T01:47:42Z
dc.date.issued2022-12-02
dc.identifier.citationDummer, Nicholas F, Willock, David J, Qian He, Howard, Mark J, Lewis, Richard J, Qi, Guodong, Taylor, Stuart H, Xu, Jun, Bethell, Don, Kiely, Christopher J, Hutchings, Graham J (2022-12-02). Methane Oxidation to Methanol. CHEMICAL REVIEWS. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.chemrev.2c00439
dc.identifier.issn0009-2665
dc.identifier.issn1520-6890
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/235657
dc.description.abstractThe direct transformation of methane to methanol remains a significant challenge for operation at a larger scale. Central to this challenge is the low reactivity of methane at conditions that can facilitate product recovery. This review discusses the issue through examination of several promising routes to methanol and an evaluation of performance targets that are required to develop the process at scale. We explore the methods currently used, the emergence of active heterogeneous catalysts and their design and reaction mechanisms and provide a critical perspective on future operation. Initial experiments are discussed where identification of gas phase radical chemistry limited further development by this approach. Subsequently, a new class of catalytic materials based on natural systems such as iron or copper containing zeolites were explored at milder conditions. The key issues of these technologies are low methane conversion and often significant overoxidation of products. Despite this, interest remains high in this reaction and the wider appeal of an effective route to key products from C-H activation, particularly with the need to transition to net carbon zero with new routes from renewable methane sources is exciting.
dc.language.isoen
dc.publisherAMER CHEMICAL SOC
dc.sourceElements
dc.subjectScience & Technology
dc.subjectPhysical Sciences
dc.subjectChemistry, Multidisciplinary
dc.subjectChemistry
dc.subjectTEMPERATURE SELECTIVE OXIDATION
dc.subjectNITROUS-OXIDE DECOMPOSITION
dc.subjectMETAL-ORGANIC FRAMEWORKS
dc.subjectC-H ACTIVATION
dc.subjectDIRECT CATALYTIC CONVERSION
dc.subjectCOPPER-EXCHANGED ZEOLITES
dc.subjectDENSITY-FUNCTIONAL THEORY
dc.subjectPHASE PARTIAL OXIDATION
dc.subjectSTATE ION-EXCHANGE
dc.subjectN2O DECOMPOSITION
dc.typeReview
dc.date.updated2022-12-23T00:59:22Z
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.description.doi10.1021/acs.chemrev.2c00439
dc.description.sourcetitleCHEMICAL REVIEWS
dc.published.statePublished
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