Carbon Dioxide Capture in a Fixed Bed of Coconut Shell Activated Carbon Impregnated With Sodium Hydroxide: Effects of Carbon Pore Texture and Alkali Loading

  • Suravit Naksusuk Suranaree University of Technology
  • Chaiyot Tangsathitkulchai Suranaree University of Technology

Abstract

Performance of CO2 adsorption was investigated in a fixed bed of coconut shell activated carbon impregnated with sodium hydroxide with emphasis on the effect of alkali loading and carbon pore texture. CO2 adsorption capacity increased with the increase of NaOH loading and passed through a maximum value at the optimum loading of 180 g NaOH/g carbon. This optimum loading appeared to be the same, independent of the surface area of activated carbon in the range of 766-1052 m2/g. A pore blocking phenomenon was proposed to account for the effect of alkali loading on the CO2 adsorption behavior. Empirical equations were also developed to correlate the breakthrough time, the adsorption capacity at breakthrough time and the equilibrium adsorption capacity with alkali loading and surface area of activated carbon. The breakthrough equation based on the LDF model was found to describe the experimental breakthrough data reasonably well. The transport of CO2 molecules in the pore structure of activated carbon to the adsorption sites is governed by the mechanism of surface diffusion and the surface diffusivity is about two orders of magnitude larger than the pore diffusivity.

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Author Biographies

Suravit Naksusuk

School of Chemical Engineering, Institute of Engineering, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand

Chaiyot Tangsathitkulchai

School of Chemical Engineering, Institute of Engineering, Suranaree University of Technology, Nakhon Ratchasima 30000, Thailand

Published In
Vol 23 No 4, Aug 8, 2019
How to Cite
[1]
S. Naksusuk and C. Tangsathitkulchai, “Carbon Dioxide Capture in a Fixed Bed of Coconut Shell Activated Carbon Impregnated With Sodium Hydroxide: Effects of Carbon Pore Texture and Alkali Loading”, Eng. J., vol. 23, no. 4, pp. 29-48, Aug. 2019.