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Photocatalytic reduction and recovery of copper by polyoxomelalates

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dc.contributor.author Troupis, A en
dc.contributor.author Hiskia, A en
dc.contributor.author Papaconstantinou, E en
dc.date.accessioned 2014-03-01T01:18:12Z
dc.date.available 2014-03-01T01:18:12Z
dc.date.issued 2002 en
dc.identifier.issn 0013-936X en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/14863
dc.subject.classification Engineering, Environmental en
dc.subject.classification Environmental Sciences en
dc.subject.other Catalysts en
dc.subject.other Copper en
dc.subject.other Light absorption en
dc.subject.other Oxidation en
dc.subject.other Precipitation (chemical) en
dc.subject.other Reducing agent en
dc.subject.other Photocatalysis en
dc.subject.other chloride ion en
dc.subject.other copper en
dc.subject.other metal derivative en
dc.subject.other acetic acid derivative en
dc.subject.other chlorate en
dc.subject.other chloride en
dc.subject.other nitrate en
dc.subject.other polymer en
dc.subject.other silicon derivative en
dc.subject.other tungsten derivative en
dc.subject.other photochemistry en
dc.subject.other article en
dc.subject.other catalysis en
dc.subject.other concentration (parameters) en
dc.subject.other light absorption en
dc.subject.other molecular stability en
dc.subject.other oxidation en
dc.subject.other particulate matter en
dc.subject.other pH en
dc.subject.other pollution en
dc.subject.other reaction analysis en
dc.subject.other reduction en
dc.subject.other algorithm en
dc.subject.other chemical model en
dc.subject.other chemistry en
dc.subject.other light en
dc.subject.other oxidation reduction reaction en
dc.subject.other radiation exposure en
dc.subject.other Acetates en
dc.subject.other Algorithms en
dc.subject.other Chlorates en
dc.subject.other Chlorides en
dc.subject.other Copper en
dc.subject.other Hydrogen-Ion Concentration en
dc.subject.other Light en
dc.subject.other Models, Chemical en
dc.subject.other Nitrates en
dc.subject.other Oxidation-Reduction en
dc.subject.other Polymers en
dc.subject.other Silicon Compounds en
dc.subject.other Tungsten Compounds en
dc.title Photocatalytic reduction and recovery of copper by polyoxomelalates en
heal.type journalArticle en
heal.identifier.primary 10.1021/es020933q en
heal.identifier.secondary http://dx.doi.org/10.1021/es020933q en
heal.language English en
heal.publicationDate 2002 en
heal.abstract A series of polyoxometalates PW12O403-, SiW12O404-, and P2Mo18O626- have been used as photocatalysts for recovery, of copper and production of fine metal particles. The process involves absorption of light by polyoxometalates, oxidation of an organic substrate, for instance, propan-2-ol as sacrificial reducing reagent, and reoxidation of the reduced polyoxometalates by Cu2+ ions, closing the photocatalytic cycle. Copper(II) ions are reduced to copper-(I) and finally to zero-state particles in a 2-electron process, as also suggested by the half-order dependence. Increase of catalyst or propan-2-ol concentration, or both, accelerates the photodeposition of copper until a saturation value is reached. The method is operational at a wide range of copper concentrations varying from 3 to 1300 ppm, leading to very low final concentrations (<0.2 ppm). The presence of dioxygen suppresses the initiation of copper recovery, though the process is equally effective after dioxygen is consumed. The process is independent of pH within the range 0.3-5.0. Addition of ClO4-, NO3-, or CH3COO- has no effect on the removal of copper ions. Chloride ions retard the enhancement of copper precipitation through stabilization of copper(I). This homogeneous, polyoxometalate-based process exhibits some benefits in comparison with the semiconductor-based (heterogeneous) recovery of metals: The final zero-state metal particles are obtained in pure form. No separation from the catalyst is needed, and moreover, the process is catalytic as the photodeposited metal particulates do not hinder the photocatalytic action of polyoxometalate anions. en
heal.publisher AMER CHEMICAL SOC en
heal.journalName Environmental Science and Technology en
dc.identifier.doi 10.1021/es020933q en
dc.identifier.isi ISI:000179833400011 en
dc.identifier.volume 36 en
dc.identifier.issue 24 en
dc.identifier.spage 5355 en
dc.identifier.epage 5362 en


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