Adsorbents derived from nitric acid-oxidised coal and activated with potassium hydroxide

Authors

  • Volodymyr Kucherenko L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine
  • Yuliia Tamarkina L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine
  • Anastasiia Redko L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine
  • Iryna Frolova L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine

DOI:

https://doi.org/10.30857/2786-5371.2025.3.2

Keywords:

oxicarbon, alkaline thermochemolysis, porous carbon material, pore structure, ecotoxicant adsorption

Abstract

Alkaline activation is the most effective method for producing carbon-based adsorbents with a highly developed surface area (≥1,000 m2/g). However, its major drawback – the requirement for large quantities of alkali – necessitates research aimed at improving the process. This study aimed to quantitatively assess the effect of nitric acid oxidation of long-flame coal on the porous structure and adsorption properties of adsorbents produced by alkaline activation at a low KOH-to-coal ratio (≤1 g/g). Experimental, analytical and comparative scientific methods were employed. The properties of the adsorbents were characterised using infrared spectroscopy, porometry, and the kinetics and isotherms of 4-chlorophenol, methylene blue dye, and lead cation adsorption from aqueous solutions (at 25°C). It was found that pre-oxidation of the coal with nitric acid introduces ether, ester, phenolic, carboxylic, and nitro groups into the carbon matrix, resulting in a mass increase of up to 16% and significantly influencing the formation of the adsorbents. Increasing the HNO3-to-carbon ratio from 0 to 1.0 mol/mol reduces the adsorbent yield (from 50.2% to 33.85%), increases the specific surface area (from 1,685 m2/g to 2,216 m2/g), and improves adsorption properties by 25%-51%. The dominant portion (~80%) of the effect occurs within the range of ≤0.4 mol/mol. A comparison of the porous structure characteristics of the adsorbents revealed that oxidation primarily promotes the formation of subnanopores and mesopores with diameters of 2-5 nm. A comparison of adsorption properties showed that adsorbents derived from oxidised coal adsorb greater quantities of adsorbates (by a factor of 1.20-1.43) and with a higher initial rate (by a factor of 1.2-4.0). This property is particularly important for the rapid removal of highly toxic compounds from water. The adsorbent produced from oxidised coal possesses a more developed surface and a subnanoporous structure, and it exhibits greater adsorption activity than the material derived from non-oxidised coal. Pre-oxidation significantly enhances the adsorption capacity of activated carbon in capturing ecotoxicants from aqueous environments

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Author Biographies

Volodymyr Kucherenko, L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine

Doctor of Chemical Sciences, Senior Researcher

https://orcid.org/0000-0001-7234-947X

Yuliia Tamarkina, L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine

PhD in Chemical Sciences, Senior Researcher

https://orcid.org/0000-0002-8747-4481

Anastasiia Redko, L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine

Iryna Frolova, L.M. Litvinenko Institute of Physical-Organic and Coal Chemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine

PhD in Chemical Sciences, Researcher

https://orcid.org/0000-0001-9660-5474

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Published

2025-09-25

How to Cite

Kucherenko, V., Tamarkina, Y., Redko, A., & Frolova, I. (2025). Adsorbents derived from nitric acid-oxidised coal and activated with potassium hydroxide. Technologies and Engineering, 26(3), 24–37. https://doi.org/10.30857/2786-5371.2025.3.2

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