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Updated: Jan 26, 2026

Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
Dual-stage electrochemical system enabling reagent-free nickel-ammonia decomplexation and resource recovery
Chi Zhang1, Pengfei Chen1, Jiazhou He2
1Guangdong Basic Research Center of Excellence for Ecological Security and Green Development, Key Laboratory for City Cluster Environmental Safety and Green Development of the Ministry of Education, School of Ecology, Environment and Resources, Guangdong University of Technology, Guangzhou 510006, China.
Abstract:
Nickel-ammonia chelated wastewater generated by electroplating and battery manufacturing is difficult to treat using conventional precipitation-based methods that require high chemical input and offer limited resource recovery. Here, we report a reagent-free dual-stage electrochemical membrane reactor that resolves the intrinsic pH-speciation mismatch between nickel removal and ammonia stripping. In the cathodic chambers, in situ generation of hydroxide ions dissociates nickel-ammonia complexes, enabling nickel recovery through electrodeposition and hydroxide precipitation, while anodically generated protons drive ammonia capture across a gas-permeable membrane. The dual-stage configuration independently optimized the pH conditions required for nickel and ammonia removal, reducing effluent Ni and NH4+-N concentrations to below 0.1 and 25 mg L-1, respectively, while producing reusable metallic Ni, β-Ni(OH)2, and ammonia solution. Life cycle assessment shows that although the dual-stage electrochemical process requires higher primary energy input than chemical precipitation, selective recovery of nickel and ammonia substantially lowers overall environmental damage. This work demonstrates a compact and sustainable electrochemical pathway for nickel-ammonia decomplexation and resource recovery, providing a circular-economy solution for metal-finishing and battery wastewater treatment.
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