Evaluation of kinetics and mechanism properties of CO adsorption onto the palm kernel shell activated carbon.

Abstract

The volumetric adsorption kinetics of carbon dioxide (CO) onto the synthesized palm kernel shell activated carbon via single-stage CO activation and commercial Norit® activated carbon were carried out at an initial pressure of approximately 1 bar at three different temperatures of 25, 50, and 100 °C. The experimental kinetics data were modelled by using the Lagergren's pseudo-first-order model and pseudo-second-order model. Comparing these two, the non-linear pseudo-second-order kinetics model presented a better fit towards CO adsorption for both adsorbents, owing to its closer coefficient of determination (R) to unity, irrespective of the adsorption temperature. In addition, kinetics analysis showed that the corresponding kinetics coefficient (rate of adsorption) of both activated carbons increased with respect to adsorption temperature, and thereby, it indicated higher mobility of CO adsorbates at an elevated temperature. Nevertheless, CO adsorption capacity of both activated carbons reduced at elevated temperatures, which signified exothermic and physical adsorption (physisorption) behaviour. Besides, process exothermicity of both carbonaceous adsorbents can be corroborated through activation energy (E) value, which was deduced from the Arrhenius plot. E values that were in range of 32-38 kJ/mol validated exothermic adsorption at low pressure and temperature range of 25-100 °C. To gain an insight into the CO adsorption process, experimental data were fitted to intra-particle diffusion model and Boyd's diffusion model, and findings revealed an involvement of both film diffusion and intra-particle diffusion during CO adsorption process onto the synthesized activated carbon and commercial activated carbon.