A continuous electroreduction cell composed of palladium nanocatalyst immobilized on discarded cigarette filters as an active bed for Cr(VI) removal from groundwater. (15th June 2020)

• Record Type: Journal Article
• Authors: Dorosti, Mostafa; Baghdadi, Majid; Nasimi, Sorour
• Is Part Of: Journal of environmental management. Volume 264(2020)
• Publication Date: 2020-06-15
• Subjects: Chromium hexavalent -- Palladium -- Hydrogenation -- Electroreduction -- Groundwater; Environmental policy -- Periodicals; Environmental management -- Periodicals; Environment -- Periodicals; Ecology -- Periodicals; 363.705
• DOI: 10.1016/j.jenvman.2020.110409
• Languages: English
• ISSNs: 0301-4797

Abstract

Abstract: In this research, a unique continuous electrochemical cell was designed and applied for the disinfection of groundwater and simultaneous Cr(VI) reduction and Cr(III) precipitation. Discarded cigarette filters (DCFs) were utilized as an efficient bed for palladium nanoparticles (PdNPs) immobilization located between porous anode and cathode made of graphite felt. The characterization of the bed was performed using FE-SEM, EDS, BET, and FT-IR analysis. The results confirmed the distribution of palladium nanoparticles on the surface of DCFs. The proposed design for electrochemical cell obviated the need to divide the anolyte and catholyte because the anode was located at the outlet of the cell, thereby avoiding the reaction between hydrogen radicals produced on the surface of PdNPs and oxygen and chlorine produced in the anode. The hydrogen gas produced in the cathode was converted to hydrogen radicals, acting as the most prominent species for the reduction. Hydroxide ions produced in the cathode increased the pH of the solution between electrodes, resulting in the precipitation of Cr (III) with an efficiency of 96%. Furthermore, free chlorine at the concentration of 1 mg L −1 was generated through chloride ion oxidation in the anode, which can be effective for disinfection. The effect of initial Cr (VI) concentration (C0 ), flow rate (Q), and current (I) was investigated, and the maximum removal efficiency (99.7%) was observed at the flow rate of 5 mL min −1 and current of 0.05 A, respectively. No interference ensued from the various coexisting ions in groundwater. The findings of this study suggested that the proposed electrochemical cell is capable of in-situ total chromium removal and free chlorine production in groundwater simultaneously. Graphical abstract: Image 1 Highlights: Continuous electrochemical cell with an active bed was designed for Cr(VI) removal. This design obviated the need to divide the anolyte and catholyte. Palladium nanoparticles were immobilized on discarded cigarette filters. Simultaneous in-situ Cr(VI) reduction and Cr(III) precipitation were achieved. Oxygen gas and free chlorine had no contact with hydrogen radicals in the cell.