Capacitive deionization of chloride ions by activated carbon using a three-dimensional electrode reactor

• Published in: Separation and purification technology Vol. 191; pp. 424 - 432
• Main Authors: Sun, Zhumei, Chai, Liyuan, Liu, Mingshi, Shu, Yude, Li, Qingzhu, Wang, Yunyan, Wang, Qingwei, Qiu, Dingfan
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 2018
• Subjects: Activation energy; Capacitive deionization; Electrosorption; External diffusion; Intraparticle diffusion; Three-dimensional electrode; Three-dimensional electrode; Capacitive deionization; Intraparticle diffusion; Electrosorption; External diffusion; Activation energy
• ISSN: 1383-5866; 1873-3794
• DOI: 10.1016/j.seppur.2017.09.015

[Display omitted] •A three-dimensional electrode reactor for CDI was constructed.•Parameter studies were performed figured out the optimized operating condition.•Application of anode potentials effectively reduce activation energy and improve the adsorption rate.•Intraparticle mass transfer diffusion and surface adsorption process were the rate-limiting mechanism. A three-dimensional electrode reactor was introduced into capacitive deionization (CDI). Electrosorption kinetic and the thermodynamic parameters on removal of chloride ions from aqueous solutions at various temperatures (298–323K), anode potentials (0.3–1.2V), circulation velocities (75–168mLmin−1), pH (1–10), ionic strengths (0.028–3.028M) and thickness of packed-bed (3.5 & 5cm), on granular activated carbon (GAC) were studied in the three-dimensional electrode reactor. Electrosorption of chloride ions was found to be pH dependent. The result showed that the electrosorption capacity of the chloride ions increased with increasing anode potential, but decreased with increasing temperature, ionic strength and thickness of packed-bed. Batch kinetic data from experimental investigations have been described by pseudo-first-order, pseudo-second-order, external mass transfer and intraparticle diffusion models. It was found that the electrosorption of chloride ions onto GAC electrodes followed pseudo-first-order kinetics model, and intraparticle diffusion and adsorption had rate limiting effects on the electrosorption process. The value of activation energy and rate constants of electrosorption were found to reduce and increase compared to adsorption. This may be the main reasons that anode potential enhanced significantly adsorption capacity. The thermodynamics analyses indicated that the electrosorption is spontaneous and exothermic in nature.