Adsorption-journal of The International Adsorption Society 

About: Adsorption-journal of The International Adsorption Society is an academic journal published by Springer Science+Business Media. The journal publishes majorly in the area(s): Adsorption & Activated carbon. It has an ISSN identifier of 0929-5607. Over the lifetime, 1888 publications have been published receiving 44336 citations.

Enzyme immobilization by adsorption: a review

Abstract: Endowed with unparalleled high catalytic activity and selectivity, enzymes offer enormous potential as catalysts in practical applications. These applications, however, are seriously hampered by enzymes’ low thermal and chemical stabilities. One way to improve these stabilities is the enzyme immobilization. Among various tested methods of this process that make use of different enzyme-carrier interactions, immobilization by adsorption on solid carriers has appeared most common. According to these findings, in this review we present a comparative analysis of the literature reports on the recent trends in the immobilization of the enzymes by adsorption. This thorough study was prepared in order to provide a deeper understanding of the process. Both carriers, carrier modifiers and procedures developed for effective adsorption of the enzymes are discussed. The review may thus be helpful in choosing the right adsorption scheme for a given enzyme to achieve the improvement of its stability and activity for a specific application.

Physical adsorption characterization of nanoporous materials: progress and challenges

Abstract: Within the last two decades major progress has been achieved in understanding the adsorption and phase behavior of fluids in ordered nanoporous materials and in the development of advanced approaches based on statistical mechanics such as molecular simulation and density functional theory (DFT) of inhomogeneous fluids. This progress, coupled with the availability of high resolution experimental procedures for the adsorption of various subcritical fluids, has led to advances in the structural characterization by physical adsorption. It was demonstrated that the application of DFT based methods on high resolution experimental adsorption isotherms provides a much more accurate and comprehensive pore size analysis compared to classical, macroscopic methods. This article discusses important aspects of major underlying mechanisms associated with adsorption, pore condensation and hysteresis behavior in nanoporous solids. We discuss selected examples of state-of-the-art pore size characterization and also reflect briefly on the existing challenges in physical adsorption characterization.

Amine functionalised metal organic frameworks (MOFs) as adsorbents for carbon dioxide

Abstract: Three different porous metal organic framework (MOF) materials have been prepared with and without uncoordinated amine functionalities inside the pores. The materials have been characterized and tested as adsorbents for carbon dioxide. At 298 K the materials adsorb significant amount of carbon dioxide, the amine functionalised adsorbents having the highest CO2 adsorption capacities, the best adsorbing around 14 wt% CO2 at 1.0 atm CO2 pressure. At 25 atm CO2 pressure, up to 60 wt% CO2 can be adsorbed. At high pressures the CO2 uptake is mostly dependent on the available surface area and pore volume of the material in question. For one of the iso-structural MOF pairs the introduction of amine functionality increases the differential adsorption enthalpy (from isosteric method) from 30 to around 50 kJ/mole at low CO2 pressures, while the adsorption enthalpies reach the same level at increase pressures. The high pressure experimental results indicate that MOF based solid adsorbents can have a potential for use in pressure swing adsorption of carbon dioxide at elevated pressures.

Sorption Studies of Acid Dye by Mixed Sorbents

Abstract: The sorption of Acid Blue 9 onto the mixture of activated clay and activated carbon has been studied in terms of pseudo-first order and pseudo-second order chemical sorption processes. The batch sorption model, based on the assumption of a pseudo-second order mechanism, has been developed to predict the rate constant of sorption and the equilibrium capacity with the effect of initial dye concentration, mass of mixed sorbent, temperature and initial solution pH. The rates of sorption were found to conform to pseudo-second order kinetics with good correlation. Batch isotherm studies showed that the sorption of Acid Blue 9 by the mixed sorbent from aqueous solution was described by the Langmuir isotherm equation. A comparison of the evaluated equilibrium capacity of sorption has been made by the pseudo-second order rate equation as well as by the Langmuir isotherm and operating line method. In addition, an activation energy of sorption has also been determined based on the pseudo-second order rate constants.

Why does the linear driving force model for adsorption kinetics work

Abstract: The Linear Driving Force (LDF) model for gas adsorption kinetics is frequently and successfully used for analysis of adsorption column dynamic data and for adsorptive process designs because it is simple, analytic, and physically consistent. Yet, there is a substantial difference in the characteristics of isothermal batch uptake curves on adsorbent particles by the LDF and the more rigorous Fickian Diffusion (FD) model. It is demonstrated by using simple model systems that the characteristics of the adsorption kinetics at the single pore or the adsorbent particle level are lost in (a) evaluating overall uptake on a heterogeneous porous solid, (b) calculating breakthrough curves from a packed adsorbent column, and (c) establishing the efficiency of separation by an adsorptive process due to repeated averaging of the base kinetic property. That is why the LDF model works in practice.