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Metal-impregnated carbon applied as adsorbent for removal of sulphur compounds using fixed-bed column technology.

Authors :
Martins AV
Ramos JE
Coelho JA
Vidal CB
Cavalcante CL Jr
Azevedo DC
Source :
Environmental technology [Environ Technol] 2014 May-Jun; Vol. 35 (9-12), pp. 1367-77.
Publication Year :
2014

Abstract

Metal-impregnated carbons (Cu--AC; Ag--AC and Pd--AC) were studied as adsorbents for the desulphurization of liquid fuels. A real gasoline was examined for sulphur compounds. Textural characteristics of adsorbents were determined by nitrogen adsorption/desorption isotherms at 77 K. The adsorption isotherms were obtained by frontal analysis in a single fixed bed at 30 degrees C and 45 degrees C. Breakthrough curves were simulated according to a mathematical model that assumed axially dispersed flow and mass transfer described by a linear driving force approximation and nonlinear adsorption equilibrium reached instantaneously on the external surface of the adsorbents particles. The model was solved numerically by orthogonal collocation in finite elements, using the commercial solver gPROMS. The proposed model matched experimental data reasonably well. Resistance to mass transfer was significant and thought to be due to intraparticle diffusion kinetics. The results confirmed the efficiency of the use of activated carbon (AC) in the adsorption of sulphur compounds, especially when its surface is modified with metals. Comparing adsorption capacities of sulphur compounds from real gasoline, AC-Pd material appeared more selective than other materials, even presenting a behaviour of rapid saturation explained by the presence of other components competing for adsorption sites, reducing their effectiveness in removing sulphur compounds. Both pristine AC and Pd--AC showed good regenerability. The regenerated Pd--AC sorbent can recover about 85% of the desulphurization capacity.

Details

Language :
English
ISSN :
0959-3330
Volume :
35
Issue :
9-12
Database :
MEDLINE
Journal :
Environmental technology
Publication Type :
Academic Journal
Accession number :
24701935
Full Text :
https://doi.org/10.1080/09593330.2013.868530