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Measurement of Rate and Equilibrium Parameters for Physicochemical Processes Pertaining to the Atmosphere by Gas Chromatography

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dc.contributor.author Roubani-Kalantzopoulou, F en
dc.contributor.author Sotiropoulou, V en
dc.contributor.author Metaxa, H en
dc.contributor.author Katsanos, NA en
dc.date.accessioned 2014-03-01T01:13:54Z
dc.date.available 2014-03-01T01:13:54Z
dc.date.issued 1998 en
dc.identifier.issn 1040-7685 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/12770
dc.subject Atmospheric equilibrium parameters en
dc.subject Atmospheric rate parameters en
dc.subject Reversed-flow gas chromatography en
dc.subject.classification Chemistry, Analytical en
dc.subject.other WALL REACTION PROBABILITIES en
dc.subject.other DENUDER TUBES en
dc.subject.other DEPOSITION VELOCITIES en
dc.subject.other DIFFUSION en
dc.title Measurement of Rate and Equilibrium Parameters for Physicochemical Processes Pertaining to the Atmosphere by Gas Chromatography en
heal.type journalArticle en
heal.identifier.primary 10.1002/(SICI)1520-667X(1998)10:1<141::AID-MCS18>3.0.CO;2-6 en
heal.identifier.secondary http://dx.doi.org/10.1002/(SICI)1520-667X(1998)10:1<141::AID-MCS18>3.0.CO;2-6 en
heal.language English en
heal.publicationDate 1998 en
heal.abstract Laboratory kinetic experiments can be performed under conditions of concentration, temperature, pressure, humidity, and so on very close to those prevailing in the atmosphere and in the presence of heterogeneous sinks by the reversed-flow gas chromatography (RF-GC) technique. It is an absolute rate constant technique, but the system is neither a static nor a flow one. It is a diffusion controlled system by means of which rate constants and reaction orders with respect to time n(t) of unimolecular and bimolecular chemical reactions of atmospheric species with other substances can be measured. In the presence of heterogeneous sinks, the following physicochemical parameters are determined under unsteady-state conditions: the local adsorption parameter k(1) of the analyte A under study and the experimental isotherm, the desorption rate constant of A from the solid surface k(-1), the rate constant k(2) of a possible first-order or pseudo-first-order surface reaction of the adsorbed analyte, and the deposition velocity V-d and the reaction probability gamma of A on the heterogeneous sink. (C) 1998 John Wiley & Sons, Inc. en
heal.publisher JOHN WILEY & SONS INC en
heal.journalName Journal of Microcolumn Separations en
dc.identifier.doi 10.1002/(SICI)1520-667X(1998)10:1<141::AID-MCS18>3.0.CO;2-6 en
dc.identifier.isi ISI:000071418800018 en
dc.identifier.volume 10 en
dc.identifier.issue 1 en
dc.identifier.spage 141 en
dc.identifier.epage 146 en


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