Publications Scientifiques

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    Understanding the rate-limiting step adsorption kinetics onto biomaterials for mechanism adsorption control
    (SAGE Publications Ltd, 2024) Sahmoune, Mohamed Nasser; Abbas, Moussa; Trari, Mohamed
    Biomaterials are a class of porous materials that have been widely exploited over the past two decades. However, the implications of controlling adsorption by rate-limiting steps are still not adequately established. Identifying the rate-limiting step is a promising approach for the design of adsorption systems. In this review, we study in detail the rate-limiting step of the adsorption of dyes in aqueous media on biomaterials to rationalize the factors governing the rate-limiting step involved in the adsorption process using empirical kinetics and mass transfer models. This knowledge is then applied to identify the best fit of these models to study the rate-controlling step involved in the adsorption process, which is crucial for the design of the adsorption system. This review first studies the limiting step of adsorption of dyes in an aqueous medium on biomaterials. Kinetic modeling is used to better understand the rate control step involved in biosorption. Generally, the equations used are empirical models of kinetics and mass transfer and the biomaterials come from the following categories: agricultural and industrial waste, algae, fungi, bacteria, and plants. In most adsorption studies reported in this review, the pseudo second-order model was found to be best suited for fitting the kinetic data of dyes on biomaterials, indicating that chemisorption is the rate-limiting step that controls adsorption. Concerning the diffusion effects of mass transfer, intraparticle diffusion is among the most often used models to examine the rate-limiting step which is controlled by both film diffusion and intraparticle diffusion. The first takes place when the external transfer is greater than the internal transfer while the opposite occurs in the case of porous diffusion. However, the majority of works do not study the real step of controlling the overall adsorption kinetics, namely, film diffusion or intraparticle diffusion.
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    Adsorption of auramine-O using activated globe artichoke leaves : kinetic and isotherm studies
    (Chemic Publishing Company, 2017) Laribi, Kahina; Sahmoune, Mohamed Nasser
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    Adsorption of auramine-O using activated globe artichoke leaves : kinetic and isotherm studies
    (Chemic Publishing Company, 2017) Laribi, Kahina; Sahmoune, Mohamed Nasser
    The aim of this work was to study the removal of auramine-O (Au-O) from aqueous solution using powder prepared from globe artichoke leaves chemically activated with NaOH solution. The physico-chemical characteristics of the samples were performed and the characterization by FT-IR analysis has been carried out to examine the structure of globe artichoke leaves before and after activation. Scanning electron microscope was used to analyze the surface change of the globe artichoke leaves before and after adsorption of dye solution. A comparison of two models on the overall adsorption rate showed that the kinetic of adsorption was better described by the pseudo-second order model. The equilibrium data fitted very well to Langmuir model with maximum monolayer adsorption capacity of 344.8 mg g-1 at 298 K. This study shows that the globe artichoke leaves can be used as low cost alternative adsorbent for removal of auramine-O
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    Adsorptive removal of diazinon : kinetic and equilibrium study
    (Taylor and Francis, 2014) Ouznadji, Z.B.; Sahmoune, Mohamed Nasser; Mezenner, N.Y.
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    Effect of calcium competition on chromium adsorption by fungi biomass
    (2006) Louhab, K.; Sahmoune, Mohamed Nasser; Addad, J.; Bar, S.
    The kinetics and thermodynamic of adsorption of a mono-solute of chromium ions and of a bi-solute of chromium and calcium ions by fungi biomass (Streptomycine rimosus) was investigated in a batch system. The experimental data were analyzed based by Langmuir isotherm and a Pseudo second order mechanism, in the both the mono-and bi-solute adsorption systems, in order to predict the rate constant of adsorption, the equilibrium capacity. The results indicate that the adsorption mechanism is described by Langmuir isotherm and a Pseudo-second-order. The equilibrium adsorption capacity and the equilibrium rate constant increased with an increase in the initial chromium concentration in both mono-and bi-solute adsorption systems. The adsorption capacity of chromium decreased with an increase in calcium concentration