dc.creatorSales, Jose Luis
dc.creatorUñac, Rodolfo Omar
dc.creatorGargiulo Almeida, María Verónica
dc.creatorZgrablich, G.
dc.date.accessioned2019-03-15T17:26:37Z
dc.date.accessioned2022-10-15T05:49:48Z
dc.date.available2019-03-15T17:26:37Z
dc.date.available2022-10-15T05:49:48Z
dc.date.created2019-03-15T17:26:37Z
dc.date.issued2000-04
dc.identifierSales, Jose Luis; Uñac, Rodolfo Omar; Gargiulo Almeida, María Verónica; Zgrablich, G.; Dynamic Effects of Promoters on Associative Desorption; American Chemical Society; Langmuir; 16; 7; 4-2000; 3462-3466
dc.identifier0743-7463
dc.identifierhttp://hdl.handle.net/11336/71763
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4351742
dc.description.abstractThe kinetics of the associative desorption of A2 in the presence of coadsorbed species B is studied under conditions of nonequilibrium using the analysis of thermal desorption spectra obtained via Monte Carlo simulation. The surface reaction is expected to be strongly influenced by the mobility of the adsorbed species B. Thus, the reaction A(s)+A(s)+B(s)→A2(g)+2s+B(s) is proposed where x indicates the adsorbed phase, and a surface site, and g denotes the gas phase. A rich variety of behaviors is found that depended on the interplay between the concentration of promoter species, the mobility of species A and B, and interparticle interactions.
dc.languageeng
dc.publisherAmerican Chemical Society
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/la991099u
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/abs/10.1021/la991099u
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectPromotors
dc.subjectAsociative desorption
dc.subjectsimulation
dc.titleDynamic Effects of Promoters on Associative Desorption
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


Este ítem pertenece a la siguiente institución