Voici les éléments 1 - 4 sur 4
Pas de vignette d'image disponible
Publication
Accès libre

On the determination of surface areas in activated carbons

2005, Stoeckli, Fritz, Centeno, Teresa A.

The paper examines the validity of two approaches frequently used to determine surface areas in activated carbons, namely the BET method and the use of immersion calorimetry. The study is based on 21 well characterized carbons, whose external and microporous surface areas, Se and Smi, have been determined by a variety of independent techniques. It appears clearly that SBET and the real surface area Smi + Se are in agreement only for carbons with average pore widths Lo around 0.8–1.1 nm. Beyond, SBET increases rapidly and SBET− Se is practically the monolayer equivalent of the micropore volume Wo. This confirms that a characterization of surface properties based on SBET is, a priori, not reliable. The study of the enthalpy of immersion of the carbons into benzene at 293 K, based on Dubinin’s theory, shows that ΔiH consists of three contributions, namely from the interactions with the micropore walls (−0.136 J m−2), the external surface (−0.114 J m−2), and from the volume W*o of liquid found between the surface layers in the micropores (−141 J cm−3). It appears that for carbons where Lo> 1 nm, the real surface area cannot be determined in a reliable way from the enthalpy of immersion and a specific heat of wetting alone.

Pas de vignette d'image disponible
Publication
Accès libre

The physical and chemical characterization of a sulphur-impregnated active carbon, by combined adsorption and immersion techniques

1991, Rebstein, Patrick, Stoeckli, Fritz

A commercially available active carbon, impregnated with sulphur, has been characterized and compared to the original carbon by using adsorption and immersion techniques. The specific reaction of liquid CS2 with sulphur, following the preadsorption of various amounts of n-nonane, shows that the accessibility of sulphur decreases rapidly. It is also found that the impregnated carbon becomes hydrophilic but, in the case of SO2 adsorption, no change in adsorption capacity is detected.

Pas de vignette d'image disponible
Publication
Accès libre

On the mechanisms of phenol adsorption by carbons

2001, Stoeckli, Fritz, Hugi-Cleary, D.

The removal of phenol and related compounds from dilute aqueous solutions by activated carbons corresponds to the coating of the micropore walls and of the external surface by a monolayer. This process is described by an analog of the Dubinin—Radushkevich—Kaganer equation. On the other hand, as suggested by immersion calorimetry at 293 K, in the case of concentrated solutions, the mechanism corresponds to the volume filling of the micropores, as observed for the adsorption of phenol from the vapor phase. The equilibrium is described by the Dubinin—Astakhov equation. It follows that the removal of phenol from mixtures with water depends on the relative concentrations, and the limiting factor for adsorption is either the effective surface area of the carbon, or the micropore volume.

Pas de vignette d'image disponible
Publication
Accès libre

Evolution of microporosity during activation of carbon

1991, Stoeckli, Fritz, Ballerini, Luca

Various adsorption and immersion techniques and a recent model for micropore distributions have been used to assess quantitatively the evolution of the main properties of active carbon. The precursors used in this study were of vegetable and polymeric origin. One activation series based on natural coal was also included.