Subir material

Suba sus trabajos a SEDICI, para mejorar notoriamente su visibilidad e impacto

 

Mostrar el registro sencillo del ítem

dc.date.accessioned 2023-04-12T14:08:08Z
dc.date.available 2023-04-12T14:08:08Z
dc.date.issued 2016-08
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/151335
dc.description.abstract We report on experimental (thermodynamics and kinetics) and computer simulation results for Xe sorption in ZIF-8. At temperatures below ∼145 K, there are two substeps present in adsorption isotherms (before saturation is reached). The substep that occurs at higher loadings was identified as corresponding to ZIF-8’s gate-opening transition. Above 145 K, this higher-loading substep is no longer resolvable. We determined the isosteric heat of adsorption for this system and obtained a value of 244 meV for sorption on the more strongly binding sites in the ZIF-8. We found that there is a peak in the isosteric heat of adsorption, as a function of sorbent loading, associated with the gate-opening transition. We estimated the heat of transition for gate-opening to have an upper bound of ∼30 meV. Our results for the isotherms and the isosteric heats are compared with those from our Monte Carlo computer simulations, obtained using both the structure of ZIF-8 before and after the gate-opening transition and a new set of mixed Lennard-Jones parameters. We conducted measurements for the sorption kinetics for this system. We found that, while the sorption occurs faster as the loading increases before the gate-opening transition, the equilibration times increase with loading in the gate-opening region, resulting in an unusual nonmonotonic behavior for the variation of this quantity as a function of sorbent loading. en
dc.format.extent 16649-16657 es
dc.language en es
dc.subject Adsorption es
dc.subject Chemical structure es
dc.subject Isotherms es
dc.subject Metal organic frameworks es
dc.subject Sorption es
dc.title Evidence of Gate-Opening on Xenon Adsorption on ZIF-8: An Adsorption and Computer Simulation Study en
dc.type Articulo es
sedici.identifier.other https://doi.org/10.1021/acs.jpcc.6b03481 es
sedici.identifier.issn 1932-7447 es
sedici.identifier.issn 1932-7455 es
sedici.creator.person Gallaba, Dinuka H. es
sedici.creator.person Albesa, Alberto Gustavo es
sedici.creator.person Migone, Aldo D. es
sedici.subject.materias Física es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution 4.0 International (CC BY 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle The Journal of Physical Chemistry C es
sedici.relation.journalVolumeAndIssue vol. 120, no. 30 es


Descargar archivos

Este ítem aparece en la(s) siguiente(s) colección(ones)

Creative Commons Attribution 4.0 International (CC BY 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution 4.0 International (CC BY 4.0)