Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Advertisement

Scientific Reports
  • View all journals
  • Search
  • My Account Login
  • Content Explore content
  • About the journal
  • Publish with us
  • Sign up for alerts
  • RSS feed
  1. nature
  2. scientific reports
  3. articles
  4. article
Alkaline selective separation of silicon/vanadium from vanadium-bearing shale and recovery of silica
Download PDF
Download PDF
  • Article
  • Open access
  • Published: 11 May 2026

Alkaline selective separation of silicon/vanadium from vanadium-bearing shale and recovery of silica

  • Guoliang Wei1,
  • Chaoyi Chen1,2,
  • Junqi Li1,2,
  • Xin Lin1,
  • Ruoxin Li1,
  • Jiaxing Xie1 &
  • …
  • Gangan Wang1 

Scientific Reports (2026) Cite this article

  • 569 Accesses

  • Metrics details

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

  • Chemistry
  • Environmental sciences
  • Materials science

Abstract

To overcome the lack of effective separation driving force in traditional physical pre-concentration methods for vanadium hosted in mica-type minerals, an alkaline selective pre-desilication route for silicon/vanadium separation was proposed based on the differences in reactivity and structural stability of various mineral phases in alkaline systems. By controlling the reaction conditions, preferential dissolution of SiO2 and relative retention of vanadium in the solid phase were achieved. To quantitatively evaluate the separation behavior, the selectivity coefficient α(Si/V) was introduced to characterize the relative dissolution differences between SiO2 and V2O5, and the effective selective separation window was subsequently determined. The results showed that under the conditions of NaOH concentration of 160 g/L, liquid-to-solid ratio of 4 mL/g, temperature of 190 °C, and reaction time of 20 min, the leaching rate of SiO2 reached 62.29%, while that of V2O5 was only 10.56%, corresponding to an α(Si/V) value of 5.9. The V2O5 grade in the solid phase was enriched from 1.09% to 1.87% after desilication. Under the studied conditions, the apparent leaching processes of both SiO2 and V2O5 could be described by the unreacted shrinking core model. The dissolved silicon in the desilication liquor was recovered as precipitated silica via carbonation reaction, achieving an SiO2 recovery rate exceeding 97% and a product purity higher than 99%. The carbonate system after carbonation could be further regenerated into NaOH through causticizing treatment.

Similar content being viewed by others

Hydrometallurgical process development to recycle valuable metals from spent SCR deNOX catalyst

Article Open access 11 November 2021

Learning a reactive potential for silica-water through uncertainty attribution

Article Open access 17 July 2024

Green recovery of vanadium from spent vanadium catalyst from sulfuric acid production

Article Open access 20 April 2026

Acknowledgements

This work was supported by the National Natural Science Foundation of China (No. U23A20610, 52574399, 52274260), Guizhou Province Qiankehe Platform Talent GCC [2023]017, Science and Technology Innovation Team of Guizhou University [2023]04. "Hundred Universities and Thousand Enterprises" Technological Tackling and Bid-winning & Leader-appointing Program, Department of Education of Guizhou Province (Qianjiaoji) [2025]006, China Postdoctoral ScienceFoundation under Grant Number (2025MD774069), State-funded Postdoctoral Researchers Program (GZC20252395).Guizhou Provincial Science and Technology Foundation ZD[2026]070.

Funding

National Natural Science Foundation of China (No. U23A20610, 52574399, 52274260), Guizhou Province Qiankehe Platform Talent GCC [2023]017, Science and Technology Innovation Team of Guizhou University [2023]04. "Hundred Universities and Thousand Enterprises" Technological Tackling and Bid-winning & Leader-appointing Program, Department of Education of Guizhou Province (Qianjiaoji) [2025]006, China Postdoctoral ScienceFoundation under Grant Number (2025MD774069), State-funded Postdoctoral Researchers Program (GZC20252395).Guizhou Provincial Science and Technology Foundation ZD[2026]070.

Author information

Authors and Affiliations

  1. School of Materials and Metallurgy, Guizhou University, Guiyang, 550025, China

    Guoliang Wei, Chaoyi Chen, Junqi Li, Xin Lin, Ruoxin Li, Jiaxing Xie & Gangan Wang

  2. Guizhou Province Dual Carbon and New Energy Technology Innovation and Development, Research Institute, Guiyang, 550025, China

    Chaoyi Chen & Junqi Li

Authors
  1. Guoliang Wei
    View author publications

    Search author on:PubMed Google Scholar

  2. Chaoyi Chen
    View author publications

    Search author on:PubMed Google Scholar

  3. Junqi Li
    View author publications

    Search author on:PubMed Google Scholar

  4. Xin Lin
    View author publications

    Search author on:PubMed Google Scholar

  5. Ruoxin Li
    View author publications

    Search author on:PubMed Google Scholar

  6. Jiaxing Xie
    View author publications

    Search author on:PubMed Google Scholar

  7. Gangan Wang
    View author publications

    Search author on:PubMed Google Scholar

Corresponding author

Correspondence to Chaoyi Chen.

Ethics declarations

Competing Interests

The authors declare no competing interests.

Additional information

Publisher’s note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary Information

Supplementary Information. (download DOCX )

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License, which permits any non-commercial use, sharing, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if you modified the licensed material. You do not have permission under this licence to share adapted material derived from this article or parts of it. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc-nd/4.0/.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Wei, G., Chen, C., Li, J. et al. Alkaline selective separation of silicon/vanadium from vanadium-bearing shale and recovery of silica. Sci Rep (2026). https://doi.org/10.1038/s41598-026-51423-z

Download citation

  • Received: 12 March 2026

  • Accepted: 28 April 2026

  • Published: 11 May 2026

  • DOI: https://doi.org/10.1038/s41598-026-51423-z

Share this article

Anyone you share the following link with will be able to read this content:

Sorry, a shareable link is not currently available for this article.

Provided by the Springer Nature SharedIt content-sharing initiative

Keywords

  • Vanadium-bearing shale
  • Silicon/vanadium separation
  • Alkaline selective desilication
  • Recovery of dissolved silicon
  • Alkaline solution regeneration
Download PDF

Advertisement

Explore content

  • Research articles
  • News & Comment
  • Collections
  • Subjects
  • Follow us on Facebook
  • Follow us on X
  • Sign up for alerts
  • RSS feed

About the journal

  • About Scientific Reports
  • Contact
  • Journal policies
  • Guide to referees
  • Calls for Papers
  • Editor's Choice
  • Journal highlights
  • Open Access Fees and Funding

Publish with us

  • For authors
  • Language editing services
  • Open access funding
  • Submit manuscript

Search

Advanced search

Quick links

  • Explore articles by subject
  • Find a job
  • Guide to authors
  • Editorial policies

Scientific Reports (Sci Rep)

ISSN 2045-2322 (online)

nature.com footer links

About Nature Portfolio

  • About us
  • Press releases
  • Press office
  • Contact us

Discover content

  • Journals A-Z
  • Articles by subject
  • protocols.io
  • Nature Index

Publishing policies

  • Nature portfolio policies
  • Open access

Author & Researcher services

  • Reprints & permissions
  • Research data
  • Language editing
  • Scientific editing
  • Nature Masterclasses
  • Research Solutions

Libraries & institutions

  • Librarian service & tools
  • Librarian portal
  • Open research
  • Recommend to library

Advertising & partnerships

  • Advertising
  • Partnerships & Services
  • Media kits
  • Branded content

Professional development

  • Nature Awards
  • Nature Careers
  • Nature Conferences

Regional websites

  • Nature Africa
  • Nature China
  • Nature India
  • Nature Japan
  • Nature Middle East
  • Privacy Policy
  • Use of cookies
  • Legal notice
  • Accessibility statement
  • Terms & Conditions
  • Your US state privacy rights
Springer Nature

© 2026 Springer Nature Limited

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing