Options
Stoeckli, Fritz
Nom
Stoeckli, Fritz
Affiliation principale
Fonction
Professeur.e émérite
Email
fritz.stoeckli@unine.ch
Identifiants
Résultat de la recherche
Voici les éléments 1 - 6 sur 6
- PublicationAccès libreModelling of water adsorption by activated carbons: effects of microporous structure and oxygen content(2005)
;Slasli, Abdou ;Jorge, M.; Seaton, N. A.The present paper examines the adsorption of water by microporous carbons containing various amounts of surface oxygen and a smaller proportion of basic centres. The modelling of water adsorption for 293 and 310 K, using variable pore size distributions (PSD), confirms that the overall type IV isotherm is the sum of a type I isotherm associated with the specific interactions, and a type V isotherm reflecting the non-specific interactions. The principle of temperature invariance is followed by these isotherms, which indicates that modelling leads to the Dubinin–Astakhov equation.
The present approach allows the prediction of water adsorption near room temperature, on the basis of the PSD and the density of oxygen present on the surface area of the micropores. It is assumed, to a first and good approximation, that the pores are slit-shaped and the oxygen distribution is random. - PublicationMétadonnées seulementModelling of water adsorption by activated carbons: effects of microporous structure and oxygen content(2004)
;Slasli, A M ;Jorge, M; Seaton, N AThe present paper examines the adsorption of water by microporous carbons containing various amounts of surface oxygen and a smaller proportion of basic centres. The modelling of water adsorption for 293 and 310 K, using variable pore size distributions (PSD), confirms that the overall type IV isotherm is the sum of a type I isotherm associated with the specific interactions, and a type V isotherm reflecting the non-specific interactions. The principle of temperature invariance is followed by these isotherms, which indicates that modelling leads to the Dubinin-Astakhov equation. The present approach allows the prediction of water adsorption near room temperature, on the basis of the PSD and the density of oxygen present on the surface area of the micropores. It is assumed, to a first and good approximation, that the pores are slit-shaped and the oxygen distribution is random. (C) 2004 Elsevier Ltd. All rights reserved. - PublicationAccès libreWater adsorption by activated carbons in relation to their microporous structure(2003)
;Slasli, Abdou ;Jorge, M.; Seaton, N. A.The present paper examines the adsorption of water by microporous carbons in the absence of specific interactions. The modelling of water adsorption for 293 and 310 K, using variable pore size distributions (PSD), shows that the type V isotherms follow the Dubinin–Astakhov (DA) equation and fulfill the requirement for temperature invariance. Furthermore, the parameters of the DA equation can be related in a simple way to structural properties of the model carbons. For a number of well-characterized carbons, the type V isotherms generated by combining model isotherms with the corresponding PSDs are in good agreement with the limiting isotherms at 293 and 310 K derived on the basis of a recent development of Dubinin’s theory. This approach will provide the basis for further studies including specific interactions. - PublicationAccès libreThe comparison of experimental and calculated pore size distributions of activated carbons(2002)
; ;Guillot, André ;Slasli, AbdouHugi-Cleary, DeirdreActivated carbons are disorganized materials with variable pore size distributions (PSD). If one assumes that the porosity consists mainly of locally slit-shaped micropores, model isotherms can be obtained by computer simulations and used to assess the PSD on the basis of experimental isotherms. In the present study, CO2 isotherms have been measured at 273 K on seven well-characterized microporous carbons with average micropore widths between 0.65 and 1.5 nm and analysed with model isotherms obtained with standard Monte Carlo simulations. The resulting PSD are in good agreement with those obtained from a modified Dubinin equation, from liquid probes of molecular dimensions between 0.4 and 1.5 nm, from STM and from modelling based on CH4 adsorption at 308 K. The present study validates the determination of micropore distributions in active carbons based on CO2 isotherms, provided that no gate effects are present. - PublicationAccès libreMicroporosity in carbon blacks(2002)
; ;Guillot, André ;Slasli, AbdouHugi-Cleary, DeirdreMicroporous carbon blacks can be characterized by the same techniques as activated carbons, using the classical DR equation and comparison plots based on non-porous materials. The CO2 adsorption isotherm at 273 K, combined with computer modelling, also leads to an assessment of microporosity. The results agree with independent techniques such as immersion calorimetry into liquids of variable molecular dimensions and a modified Dubinin equation. The study also confirms that the comparison plots based on N2 (77 K), CO2 (273 K) and C6H6 (293 K) do not necessarily lead to overlapping results for the total micropore volume and the external surface area of the carbons. - PublicationAccès libreThe characterization of microporosity in carbons with molecular sieve effects(2002)
; ;Slasli, Abdou ;Hugi-Cleary, DeirdreGuillot, AndréThe apparent and the real micropore size distributions (PSDs) of molecular sieve carbons can be assessed by combining the adsorption of CO2 at 273 K with immersion calorimetry into liquids of increasing molecular dimensions. On the basis of model isotherms resulting from computer simulations, the adsorption of carbon dioxide, a relatively small probe, leads to the overall PSD of the carbon (essentially the internal micropore system). Immersion calorimetry, on the other hand, reveals the distribution of the pores accessible directly from the liquid phase, that is without constrictions. Liquid CS2 probes the same volume as CO2 and can be used as a reference. The paper describes the case of an industrial molecular sieve carbon obtained by blocking partly the entrance to a relatively broad micropore system, thus limiting its accessibility to molecules with diameters below 0.5–0.6 nm. It is shown how activation by steam at 900 °C removes the constrictions and leads to a gradual overlap of the two PSDs. The distribution of the pore widths on the surface, observed directly by scanning tunnelling microscopy, is also given.