dc.creatorANGELUCCI, Camilo A.
dc.creatorDEINER, L. Jay
dc.creatorNART, Francisco C.
dc.date.accessioned2012-10-20T05:30:12Z
dc.date.accessioned2018-07-04T15:50:55Z
dc.date.available2012-10-20T05:30:12Z
dc.date.available2018-07-04T15:50:55Z
dc.date.created2012-10-20T05:30:12Z
dc.date.issued2008
dc.identifierJOURNAL OF SOLID STATE ELECTROCHEMISTRY, v.12, n.12, p.1599-1603, 2008
dc.identifier1432-8488
dc.identifierhttp://producao.usp.br/handle/BDPI/31590
dc.identifier10.1007/s10008-007-0495-x
dc.identifierhttp://dx.doi.org/10.1007/s10008-007-0495-x
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1628228
dc.description.abstractThe electro-oxidation of methanol at supported tungsten carbide (WC) nanoparticles in sulfuric acid solution was studied using cyclic voltammetry, potentiostatic measurements, and differential electrochemical mass spectroscopy (DEMS). The catalyst was prepared by a sonochemical method and characterized by X-ray diffraction. Over the WC catalyst, the oxidation of methanol (1 M in a sulfuric acid electrolyte) begins at a potential below 0.5 V/RHE during the anodic sweep. During potentiostatic measurements, a maximum current of 0.8 mA mg(-1) was obtained at 0.4 V. Measurements of DEMS showed that the methanol oxidation reaction over tungsten carbide produces CO2 (m/z=44); no methylformate (m/z=60) was detected. These results are discussed in the context of the continued search for alternative materials for the anode catalyst of direct methanol fuel cells.
dc.languageeng
dc.publisherSPRINGER
dc.relationJournal of Solid State Electrochemistry
dc.rightsCopyright SPRINGER
dc.rightsrestrictedAccess
dc.subjecttungsten carbide
dc.subjectDEMS
dc.subjectmethanol
dc.titleOn-line mass spectrometry of the electro-oxidation of methanol in acidic media on tungsten carbide
dc.typeArtículos de revistas


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