SO <sub>2</sub> hydro-desulfurization to H <sub>2</sub> S production on metal doped nanotubes and nanocages (Mn-Si <sub>60</sub> , Mn-C <sub>60</sub> , Mn-B <sub>30</sub> P <sub>30</sub> , Mn-SiNT(7, 0), Mn-CNT(7, 0) and Mn-BPNT(7, 0))
Abstract The trying to propose the novel catalysts to increase the Claus reactions in order to remove the SO 2 and H 2 S with high performances is very important. Here, the capacities of metal doped nanostructures as catalysts for SO 2 hydro-desulfurization to produce the H 2 S are examined. The possible mechanisms and reactions pathways for SO 2 hydro-desulfurization to H 2 S production on Mn doped nanostructures are investigated. The important species for SO 2 hydro-desulfurization are adsorbed on Mn atoms of nanostructures. The H 2 S molecule is generated on Mn doped nanostructures through following reaction steps: SO 2 * → SO* → S* → SH* → H 2 S. The H 2 S is desorbed from surfaces of metal doped nanostructures, easily. The final performances of used catalysts for SO 2 hydro-desulfurization to H 2 S production are changed in this order: Mn-SiNT(7, 0) > Mn-BPNT(7, 0) > Mn-CNT(7, 0) > Mn-Si 60 > Mn-B 30 P 30 > Mn-C 60 . Finally, the Mn-SiNT(7, 0), Mn-CNT(7, 0) and Mn-BPNT(7, 0) as catalysts have effective ability for SO 2 hydro-desulfurization to H 2 S production from thermodynamic view point.
Authors
- Mariem Alwan
- Hiba Mushtaq
- Tiang Hengo
- Farag M. A. Altalbawy
- Ahmed Salih Sahib
- Nawfal Yousif Jamil
- Mahmood Jawad
- Aseel Smerat
- Zahraa Saad Abdulali
- Fadhil F. Sead
Institutions
- Al-Ahliyya Amman University (JO)
- University of Baghdad (IQ)
- Shaoxing University (CN)
- Ahl Al Bayt University (IQ)
- National University of Science and Technology (ZW)
- Iraqi University (IQ)
- Al-Nisour University College (IQ)
- University of Kerbala (IQ)
- University of Tabuk (SA)
Publication Details
- Journal
- Chemical Product and Process Modeling
- Published
- 2026-02-12
- DOI
- https://doi.org/10.1515/cppm-2025-0141
- Primary Topic
- Industrial Gas Emission Control
- Type
- article
- Field-Weighted Citation Impact
- 0.00