Enhanced photoelectrocatalytic oxidation of hypophosphite and simultaneous recovery of metallic nickel via carbon aerogel cathode

Carbon aerogel (CA) cathode was adopted to an undivided-chamber photoelectrocatalytic system with TiO2 nanotube arrays (TNA) photoanode to enhance the oxidation of hypophosphite (H2PO2−) and simultaneous recovery of metallic nickel (Ni). Both the efficiencies of H2PO2− oxidation and Ni recovery were...

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Veröffentlicht in:Journal of hazardous materials 2023-04, Vol.448, p.130601-130601, Article 130601
Hauptverfasser: Zhang, Juanjuan, Li, Yibing, Xie, Tengfei, Cui, Yuexin, Mao, Ran, Zhao, Xu
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container_end_page 130601
container_issue
container_start_page 130601
container_title Journal of hazardous materials
container_volume 448
creator Zhang, Juanjuan
Li, Yibing
Xie, Tengfei
Cui, Yuexin
Mao, Ran
Zhao, Xu
description Carbon aerogel (CA) cathode was adopted to an undivided-chamber photoelectrocatalytic system with TiO2 nanotube arrays (TNA) photoanode to enhance the oxidation of hypophosphite (H2PO2−) and simultaneous recovery of metallic nickel (Ni). Both the efficiencies of H2PO2− oxidation and Ni recovery were significantly enhanced after replacing Ti or carbon fiber paper cathode with CA cathode. With 1.0 mM H2PO2− and 1.0 mM Ni2+, the ratio of PO43− production increased from ∼41% or ∼54% to ∼100%, and the ratio of Ni recovery increased from ∼20% or ∼ 37% to ∼93% within 180 min at 3.0 V. H2PO2− was finally oxidized to PO43− by •OH radicals, which was speculated to be generated from UV/H2O2 and bound on TNA photoanode. Meanwhile, Ni2+ was eventually electro-reduced to metallic Ni by a two-electron reduction reaction. The efficiencies of H2PO2− oxidation and Ni recovery were favored at higher cell voltage, faintly acid conditions and larger H2PO2− concentration. The stability of this system exhibited that the ratio of PO43− production increased significantly in each cycle, which was attributed to the increase of H2O2 in-situ-generation via CA cathode caused by deposition of metallic Ni. Finally, the treatment of actual electroless nickel plating effluents was demonstrated. [Display omitted] •H2PO2− oxidation and Ni recovery were largely enhanced via carbon aerogel cathode.•The pathways of H2PO2− oxidation by •OH radicals and Ni2+ deposition were proposed.•Oxidation of H2PO2− and cathodic deposition of metallic Ni were mutually promoted.•The treatment of actual electroless nickel plating effluents was demonstrated.
doi_str_mv 10.1016/j.jhazmat.2022.130601
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Both the efficiencies of H2PO2− oxidation and Ni recovery were significantly enhanced after replacing Ti or carbon fiber paper cathode with CA cathode. With 1.0 mM H2PO2− and 1.0 mM Ni2+, the ratio of PO43− production increased from ∼41% or ∼54% to ∼100%, and the ratio of Ni recovery increased from ∼20% or ∼ 37% to ∼93% within 180 min at 3.0 V. H2PO2− was finally oxidized to PO43− by •OH radicals, which was speculated to be generated from UV/H2O2 and bound on TNA photoanode. Meanwhile, Ni2+ was eventually electro-reduced to metallic Ni by a two-electron reduction reaction. The efficiencies of H2PO2− oxidation and Ni recovery were favored at higher cell voltage, faintly acid conditions and larger H2PO2− concentration. The stability of this system exhibited that the ratio of PO43− production increased significantly in each cycle, which was attributed to the increase of H2O2 in-situ-generation via CA cathode caused by deposition of metallic Ni. Finally, the treatment of actual electroless nickel plating effluents was demonstrated. [Display omitted] •H2PO2− oxidation and Ni recovery were largely enhanced via carbon aerogel cathode.•The pathways of H2PO2− oxidation by •OH radicals and Ni2+ deposition were proposed.•Oxidation of H2PO2− and cathodic deposition of metallic Ni were mutually promoted.•The treatment of actual electroless nickel plating effluents was demonstrated.</description><identifier>ISSN: 0304-3894</identifier><identifier>EISSN: 1873-3336</identifier><identifier>DOI: 10.1016/j.jhazmat.2022.130601</identifier><identifier>PMID: 36746082</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Carbon aerogel cathode ; Hypophosphite oxidation ; Nickel recovery ; OH radicals ; Photoelectrocatalytic</subject><ispartof>Journal of hazardous materials, 2023-04, Vol.448, p.130601-130601, Article 130601</ispartof><rights>2023</rights><rights>Copyright © 2023. 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Both the efficiencies of H2PO2− oxidation and Ni recovery were significantly enhanced after replacing Ti or carbon fiber paper cathode with CA cathode. With 1.0 mM H2PO2− and 1.0 mM Ni2+, the ratio of PO43− production increased from ∼41% or ∼54% to ∼100%, and the ratio of Ni recovery increased from ∼20% or ∼ 37% to ∼93% within 180 min at 3.0 V. H2PO2− was finally oxidized to PO43− by •OH radicals, which was speculated to be generated from UV/H2O2 and bound on TNA photoanode. Meanwhile, Ni2+ was eventually electro-reduced to metallic Ni by a two-electron reduction reaction. The efficiencies of H2PO2− oxidation and Ni recovery were favored at higher cell voltage, faintly acid conditions and larger H2PO2− concentration. The stability of this system exhibited that the ratio of PO43− production increased significantly in each cycle, which was attributed to the increase of H2O2 in-situ-generation via CA cathode caused by deposition of metallic Ni. 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Both the efficiencies of H2PO2− oxidation and Ni recovery were significantly enhanced after replacing Ti or carbon fiber paper cathode with CA cathode. With 1.0 mM H2PO2− and 1.0 mM Ni2+, the ratio of PO43− production increased from ∼41% or ∼54% to ∼100%, and the ratio of Ni recovery increased from ∼20% or ∼ 37% to ∼93% within 180 min at 3.0 V. H2PO2− was finally oxidized to PO43− by •OH radicals, which was speculated to be generated from UV/H2O2 and bound on TNA photoanode. Meanwhile, Ni2+ was eventually electro-reduced to metallic Ni by a two-electron reduction reaction. The efficiencies of H2PO2− oxidation and Ni recovery were favored at higher cell voltage, faintly acid conditions and larger H2PO2− concentration. The stability of this system exhibited that the ratio of PO43− production increased significantly in each cycle, which was attributed to the increase of H2O2 in-situ-generation via CA cathode caused by deposition of metallic Ni. Finally, the treatment of actual electroless nickel plating effluents was demonstrated. [Display omitted] •H2PO2− oxidation and Ni recovery were largely enhanced via carbon aerogel cathode.•The pathways of H2PO2− oxidation by •OH radicals and Ni2+ deposition were proposed.•Oxidation of H2PO2− and cathodic deposition of metallic Ni were mutually promoted.•The treatment of actual electroless nickel plating effluents was demonstrated.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>36746082</pmid><doi>10.1016/j.jhazmat.2022.130601</doi><tpages>1</tpages></addata></record>
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subjects Carbon aerogel cathode
Hypophosphite oxidation
Nickel recovery
OH radicals
Photoelectrocatalytic
title Enhanced photoelectrocatalytic oxidation of hypophosphite and simultaneous recovery of metallic nickel via carbon aerogel cathode
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