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UV-activated assisted electrochemical process for mine water deep mineralization and resource recovery
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  • Published: 03 March 2026

UV-activated assisted electrochemical process for mine water deep mineralization and resource recovery

  • Xiangyun Liu1,
  • Youzheng Chai1,
  • Yuwei Gu1,
  • Yongqi Li1,
  • Xiao Wang2,
  • Qiancheng Wang3,
  • Gong Zhang  ORCID: orcid.org/0009-0003-6996-28811,4,
  • Huijuan Liu  ORCID: orcid.org/0009-0002-9358-78851,4 &
  • …
  • Jiuhui Qu  ORCID: orcid.org/0000-0001-9177-093X1 

Nature Communications , Article number:  (2026) Cite this article

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We are providing an unedited version of this manuscript to give early access to its findings. Before final publication, the manuscript will undergo further editing. Please note there may be errors present which affect the content, and all legal disclaimers apply.

Subjects

  • Pollution remediation
  • Sustainability

Abstract

High-salinity mine water generated during membrane concentration of mine water contains structurally stable complex organic matter that resists removal and mineralization by conventional advanced oxidation processes, ultimately producing low-value by-product salts that hinder the resource utilization pathway. Leveraging the ultraviolet sensitivity of inherent chromophore groups and conjugated structures, this study developed an ultraviolet-activated assisted electrochemical process. By harnessing ultraviolet/oxidant synergies, this approach achieves ~89.9% total organic carbon removal, with minimal performance decay over 1000 hours. Combined with ultraviolet-visible spectroscopy, fluorescence excitation-emission-matrix spectroscopy, fourier transform ion cyclotron resonance mass spectrometer, and model contaminant experiments, this study elucidates an ultraviolet activation and radical attack synergistic mechanism driving organic mineralization. The direct integration of purified brine with bipolar membrane electrodialysis successfully produces acid, high-purity alkali (>99%), and reusable water, thereby closing the loop of impurities removal and resource recovery. This integrated system offers a strong strategy for high-value resource recovery and sustainable mine water management.

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Data availability

All the data supporting the findings of this study are available within the Article and its Supplementary Information files. Source experimental data are available via figshare (https://doi.org/10.6084/m9.figshare.31220905)59. All the raw data relevant to the study are available from the corresponding author upon request. Source data are provided with this paper.

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Acknowledgments

We gratefully acknowledge the financial support from the Major Program of the Ministry of Science and Technology (MOST) of China (no. 2023YFC 3210300).

Author information

Authors and Affiliations

  1. Center for Water and Ecology, State Key Laboratory of Regional Environment and Sustainability, School of Environment, Tsinghua University, Beijing, China

    Xiangyun Liu, Youzheng Chai, Yuwei Gu, Yongqi Li, Gong Zhang, Huijuan Liu & Jiuhui Qu

  2. State Key Laboratory of Water Resource Protection and Utilization in Coal Mining, National Institute of Clean and Low Carbon Energy, China Energy Investment Group, Beijing, China

    Xiao Wang

  3. Department of Chemistry, Tsinghua University, Beijing, China

    Qiancheng Wang

  4. Beijing Laboratory of Environmental Frontier Technologies (BLEFT), School of Environment, Tsinghua University, Beijing, China

    Gong Zhang & Huijuan Liu

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Contributions

X.L. and G.Z. conceived the idea. X.L. performed the experimental studies. X.W. provided the actual high-salinity mine water samples. X.L., Y.C., Y.G., Y.L., Q.W., G.Z., H.L., and J.Q. carried out the analysis. X.L. and G.Z. wrote the manuscript. All authors contributed to its preparation and approved the final version.

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Correspondence to Gong Zhang.

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Liu, X., Chai, Y., Gu, Y. et al. UV-activated assisted electrochemical process for mine water deep mineralization and resource recovery. Nat Commun (2026). https://doi.org/10.1038/s41467-026-70043-9

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  • Received: 24 July 2025

  • Accepted: 12 February 2026

  • Published: 03 March 2026

  • DOI: https://doi.org/10.1038/s41467-026-70043-9

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