|
| << vorige | volgende >> |
Tijdschrift beschrijving
Alle jaargangen van het bijbehorende tijdschrift
Alle afleveringen van het bijbehorende jaargang
Alle artikelen van de bijbehorende aflevering
Details van artikel 5 van 43 gevonden artikelen
| Titel: |
Application of the density functional method to study phase transitions in an associating Lennard-Jones fluid adsorbed in energetically heterogeneous slit-Like pores |
| Auteur: |
HUERTA, ADRIAN PIZIO, OREST BRYK, PAWEŁ SOKOŁOWSKI, STEFAN |
| Verschenen in: |
Molecular physics |
| Paginering: | Jaargang 98 (2002) nr. 22 pagina's 1859-1869 |
| Jaar: |
2002-11-20 |
| Inhoud: |
A density functional approach is used to study the adsorption of the four-bonding-site model associating Lennard-Jones fluid in slit-Like pores with energetically heterogeneous walls. The fluid-wall potential is qualitatively similar to that invoked by Rocken, P., Somoza, A., Tarazona, P., and Findenegg, G. H., 1999, J. chem. Phys., 108, 8089, i.e. it consists of a homogeneous part that varies in the direction perpendicular to the wall and a periodic part, varying also in one direction parallel to the wall. Both parts are modelled by Lennard-Jones 9,3-type functions. The structure of the adsorbed film is characterized by the local densities of all particles and the densities of the monomers. The phase diagrams are evaluated for several systems characterized by different corrugation of the adsorbing potential. The adsorbing field is strong enough to allow for the layering transition. As well as the formation of the so-called bridge phase that fills the pore space over the most energetic parts of the wall and of capillary condensation, the layering transition is observed within the first layer adjacent to the pore walls. If the adsorbing potential due to each pore wall is shifted in phase by π/2, the bridge phase is not formed. |
| Uitgever: |
Taylor & Francis |
| Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
Details van artikel 5 van 43 gevonden artikelen
| << vorige | volgende >> |