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Updated: Mar 31, 2026

Electrochemically and Bioelectrochemically Induced Ammonium Recovery
Published on: January 22, 2015
From technical HCH residues to industrial relevant vicinal dichlorinated compounds: Electrochemical chlorine transfer
Simon Horsinka1, Dominik Weis1, Philipp Beeskow2
1ESy-Labs GmbH, Mainzer Str. 41, Gernsheim 64579, Germany; Department of Chemistry, Johannes Gutenberg University, Duesbergweg 10-14, Mainz 55128, Germany.
Abstract:
For over 70 years, the remains of Lindane production have contributed to tremendous global environmental problems. The manufacturing process of 1,2,3,4,5,6-hexachlorocyclohexane (HCH) yields approximately 15% of the insecticidal γ-isomer, which is called Lindane. This has led to the accumulation of estimated 7.4 million tons of waste worldwide that have in most cases not been properly disposed. In addition, the HCH has carcinogenic, genotoxic, mutagenic, and teratogenic effects. The large quantities of this persistent residue, which continue to spread into the environment, highlight the urgent need for remediation. Although numerous processes for water treatment have been extensively described, all the established methods currently rely on incineration. In this context, electrosynthesis represents a promising and sustainable approach to transform HCH into benzene, while simultaneously enabling the released chlorine to upcycle terminal alkenes into vicinal dichloro products. Since this process must be economically competitive with conventional incineration, the present study investigates the key characteristics of the proposed e-shuttle reaction. Several industrially relevant chloro compounds are optimized in terms of their molar yields related to HCH input. Additionally, the kinetics of the reaction are studied using a representative substrate, and the potential for chlorine upcycling is assessed. Finally, an economic feasibility analysis is conducted for a plant designed to upcycle annually 5 000 metric tons of HCH.
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