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Main Authors: Sergienko, Natalia, Lumbaque, Elisabeth Cuervo, Radjenovic, Jelena
Format: Preprint
Published: 2024
Subjects:
Online Access:https://arxiv.org/abs/2411.15162
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author Sergienko, Natalia
Lumbaque, Elisabeth Cuervo
Radjenovic, Jelena
author_facet Sergienko, Natalia
Lumbaque, Elisabeth Cuervo
Radjenovic, Jelena
contents MnxOy coated over TiO2 nanotube array substrate was doped with Mo and polyaniline (PANI) and applied for electrochemical desulfurization of concentrated sulfide (HS) solutions at basic pH, typical of biogas scrubbing solutions and industrial wastewater. Mo and PANI co-dopants significantly enhanced the anode activity towards sulfide oxidation and ensured its complete stability even in highly corrosive sulfide solutions (e.g., 200 mM HS). This was due to the increased electrochemically active surface area, improved coating conductivity and reduced charge transfer resistance. The (electro)catalytic oxidation of HS- demonstrated robust performance with very limited impact of different operational parameters (e.g., dissolved oxygen, anode potential, HS concentration). Due to the formation of elemental sulfur (S0) layer at the anode surface at basic pH, longer term anode usage requires its periodic removal. Chemical dissolution of S0 with toluene allows its rapid removal without affecting the anode activity, and easy recrystallization and recovery of pure sulfur.
format Preprint
id arxiv_https___arxiv_org_abs_2411_15162
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle (Electro)catalytic oxidation of sulfide and recovery of elemental sulfur from sulfide-laden streams
Sergienko, Natalia
Lumbaque, Elisabeth Cuervo
Radjenovic, Jelena
Chemical Physics
Materials Science
MnxOy coated over TiO2 nanotube array substrate was doped with Mo and polyaniline (PANI) and applied for electrochemical desulfurization of concentrated sulfide (HS) solutions at basic pH, typical of biogas scrubbing solutions and industrial wastewater. Mo and PANI co-dopants significantly enhanced the anode activity towards sulfide oxidation and ensured its complete stability even in highly corrosive sulfide solutions (e.g., 200 mM HS). This was due to the increased electrochemically active surface area, improved coating conductivity and reduced charge transfer resistance. The (electro)catalytic oxidation of HS- demonstrated robust performance with very limited impact of different operational parameters (e.g., dissolved oxygen, anode potential, HS concentration). Due to the formation of elemental sulfur (S0) layer at the anode surface at basic pH, longer term anode usage requires its periodic removal. Chemical dissolution of S0 with toluene allows its rapid removal without affecting the anode activity, and easy recrystallization and recovery of pure sulfur.
title (Electro)catalytic oxidation of sulfide and recovery of elemental sulfur from sulfide-laden streams
topic Chemical Physics
Materials Science
url https://arxiv.org/abs/2411.15162