scholarly journals Electroadsorptive Removal of Gaseous Pollutants

2019 ◽  
Vol 9 (6) ◽  
pp. 1162 ◽  
Author(s):  
Mattia Pierpaoli ◽  
Gabriele Fava ◽  
Maria Ruello

Adsorption is a consequence of surface energy distribution, and the existence of electrostatic bonding suggests that the presence of an external electric field may affect adsorbate/adsorbent interactions. Nevertheless, this aspect has been poorly studied in the literature, except under non-thermal plasma or corona discharge conditions. After having demonstrated in our previous work that the adsorption kinetics of gaseous organic compounds can be enhanced by the presence of an external applied electric field, in this study, we focus on the influence of the electric field on adsorbent and adsorptive interactions. By using a commercially available activated carbon cloth, in addition to increasing the adsorbent mass transfer coefficient by virtue of the increasing intensity of the applied electric field, the results suggest that adsorbent morphology is only influenced by the formation of new surface functional groups. Moreover, enhanced adsorption kinetics and capacity may result from the electrohydrodynamic force induced by the movement of charged and neutral particles towards the adsorbent, as confirmed by the reversibility of the process. Such enhancement results in a negligible increase, of about 3%, in adsorption capacity (i.e., from 91 mmol m−2 Pa−1 for only adsorption to 94 mmol m−2 Pa−1 in the presence of the applied electric field), but also in a dramatic doubling of adsorption kinetics (i.e., from 0.09 min−1 for only adsorption to 0.19 min−1 in the presence of the applied electric field). In reality, the application of an electric field to an activated carbon cloth leads to faster adsorption kinetics, without substantially altering its adsorption capacity.

Carbon ◽  
2012 ◽  
Vol 50 (6) ◽  
pp. 2226-2234 ◽  
Author(s):  
Alain Perrard ◽  
Laurence Retailleau ◽  
René Berjoan ◽  
Jean-Pierre Joly

Water ◽  
2021 ◽  
Vol 13 (5) ◽  
pp. 598
Author(s):  
David Ribes ◽  
Emilia Morallón ◽  
Diego Cazorla-Amorós ◽  
Francisco Osorio ◽  
María J. García-Ruiz

The adsorption and electroadsorption of bromide from natural water has been studied in a filter-press electrochemical cell using a commercial granular activated carbon as the adsorbent. During electroadsorption experiments, different voltages were applied (2 V, 3 V and 4 V) under anodic conditions. The presence of the electric field improves the adsorption capacity of the activated carbon. The decrease in bromide concentration observed at high potentials (3 V or 4 V) may be due to the electrochemical transformation of bromide to Br2. The anodic treatment produces a higher decrease in the concentration of bromide in the case of cathodic electroadsorption. Moreover, in this anodic electroadsorption, if the system is again put under open circuit conditions, no desorption of the bromide is produced. In the case of anodic treatment in the following adsorption process after 24 h of treatment at 3 V, a new decrease in the bromide concentration is observed as a consequence of the decrease in bromide concentration after the electrochemical stage. It can be concluded that the electroadsorption process is effective against the elimination of bromide and total bromine in water, with a content of 345 and 470 µg L−1, respectively, reaching elimination values of 46% in a single-stage electroadsorption process in bromide and total bromine. The application of the electric field to the activated carbon with a positive polarization (anodic electroadsorption) increases the adsorption capacity of the activated carbon significantly, achieving a reduction of up to 220 µg L−1 after 1 h of contact with water. The two stage process in which a previous electrochemical oxidation is incorporated before the electroadsorption stage significantly increased the efficiency from 46% in a single electroadsorption step at 3 V, to 59% in two stages.


2000 ◽  
Vol 126 (6) ◽  
pp. 562-568 ◽  
Author(s):  
Albert Subrenat ◽  
Jean-Noël Baléo ◽  
Pierre Le Cloirec

Chemosphere ◽  
2016 ◽  
Vol 144 ◽  
pp. 982-988 ◽  
Author(s):  
S. López-Bernabeu ◽  
R. Ruiz-Rosas ◽  
C. Quijada ◽  
F. Montilla ◽  
E. Morallón

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