Author
Listed:
- Roman Dychkovskyi
(AGH University of Krakow, 30 Mickiewicza Ave., 30-059 Krakow, Poland
Department of Mining Engineering and Education, Dnipro University of Technology, 19 Yavornytskoho Ave., 49005 Dnipro, Ukraine)
- Dariusz Sala
(AGH University of Krakow, 30 Mickiewicza Ave., 30-059 Krakow, Poland)
- Michał Pyzalski
(AGH University of Krakow, 30 Mickiewicza Ave., 30-059 Krakow, Poland)
- Ivan Miroshnykov
(Department of Mining Engineering and Education, Dnipro University of Technology, 19 Yavornytskoho Ave., 49005 Dnipro, Ukraine)
- Agnieszka Sujak
(Department of Biosystems Engineering, Faculty of Environmental and Mechanical Engineering, Poznan University of Life Sciences, Wojska Polskiego 50, 60-627 Poznan, Poland)
- Karol Durczak
(Department of Biosystems Engineering, Faculty of Environmental and Mechanical Engineering, Poznan University of Life Sciences, Wojska Polskiego 50, 60-627 Poznan, Poland)
- Igor Kotsan
(AGH University of Krakow, 30 Mickiewicza Ave., 30-059 Krakow, Poland)
- Andrii Pererva
(PJSC “Lviv Coal Company”, Lviv Region, 80086 Silets, Ukraine)
Abstract
The growing accumulation of coal beneficiation waste represents a significant environmental and technological challenge while simultaneously creating opportunities for the resource recovery within circular economy frameworks. This study presents the development and process-oriented evaluation of an environmentally safe technology for converting coal beneficiation waste into potassium humate, with the simultaneous recovery of molybdenum compounds via alkaline extraction. The proposed solution is designed to improve resource efficiency, reduce the volume of waste directed to landfilling, and generate a high value-added product for agricultural and technological applications. The process flow includes preliminary characterization and preparation of the waste, determination of moisture, ash, and organic matter content, and the separation of metal-bearing fractions. Alkaline extraction was carried out using potassium hydroxide under controlled temperature and reaction time conditions, followed by purification and concentration of the humate solution. The process management strategy focuses on optimizing key technological parameters, including alkali concentration, solid-to-liquid ratio, temperature, and reaction time, to maximize humate yield while preserving functional groups responsible for biological activity. Comprehensive physicochemical, thermal, and mineralogical analyses confirmed the stability of the aluminosilicate matrix and the suitability of the material for alkaline processing without adverse structural degradation. Biological tests using oat ( Avena sativa ) demonstrated that potassium humate derived from coal beneficiation waste exhibits higher growth-stimulating effectiveness than a conventional commercial humate. Economic analysis revealed a strong correlation between humic acid content and added value, confirming the feasibility of transforming coal beneficiation waste from an environmental burden into a valuable secondary resource.
Suggested Citation
Roman Dychkovskyi & Dariusz Sala & Michał Pyzalski & Ivan Miroshnykov & Agnieszka Sujak & Karol Durczak & Igor Kotsan & Andrii Pererva, 2026.
"Management of Chemical Synthesis Processes of Potassium Humate During Coal Beneficiation Waste Processing,"
Sustainability, MDPI, vol. 18(5), pages 1-19, February.
Handle:
RePEc:gam:jsusta:v:18:y:2026:i:5:p:2196-:d:1870968
Download full text from publisher
Corrections
All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jsusta:v:18:y:2026:i:5:p:2196-:d:1870968. See general information about how to correct material in RePEc.
If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.
We have no bibliographic references for this item. You can help adding them by using this form .
If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.
For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .
Please note that corrections may take a couple of weeks to filter through
the various RePEc services.