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Peer-reviewedCC BY-NCRSC advances

Sulfate-driven enhancement of TiO₂ anatase photocatalysis for cationic dye degradation: mechanistic insights and degradation optimization.

  1. 1Department of Pure and Industrial Chemistry, Faculty of Physical Sciences, Bayero University Kano P.M.B. 3011 Kano State Nigeria [email protected].
  2. 2Department of Chemical Engineering, Faculty of Engineering, University of Malaya 50603 Kuala Lumpur Malaysia.

Abstract

The influence of inorganic ions in wastewater matrices on the activity and reuse of TiO₂ photocatalysts is an important consideration in photocatalytic water treatment. This study investigates the effect of sulfate ions (SO₄ ²⁻) on the photocatalytic degradation of the cationic dye methylene blue (MB) using anatase TiO₂ under different irradiation and pH conditions. Photocatalytic performance across repeated treatment cycles was evaluated using cumulative percent degradation (CPD), a parameter introduced in this study, and related to changes in the percent atomic concentration (PAC) of elements detected on the recovered TiO₂ surface by X-ray photoelectron spectroscopy (XPS). Under UV irradiation, SO₄ ²⁻-containing systems exhibited the highest CPD values, reaching 248.10% at pH 4 (TMB4) and 294.23% at pH 10 (TMB8), indicating enhanced cumulative MB degradation in the presence of sulfate under these conditions. Surface characterization revealed changes in the carbon-, nitrogen-, oxygen-, and sulfur-containing species associated with the TiO₂ surface following photocatalytic treatment. Carbon-containing surface species increased in the recovered samples and were associated with changes in photocatalytic performance. XPS analysis indicated that sulfur detected on irradiated sulfate-containing samples was attributable to surface-bound sulfate-derived species, with no evidence supporting the formation of discrete molecular sulfur species. Overall, the results demonstrate that SO₄ ²⁻, particularly in combination with UV irradiation, can enhance the cumulative photocatalytic degradation of MB while influencing the surface chemistry of anatase TiO₂. The findings provide further insight into the relationship between wastewater ionic composition, photocatalytic performance, and surface transformations associated with the repeated application of TiO₂ photocatalysts.

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BibTeX
@article{farouk2026sulfatedriven,
  title = {{Sulfate-driven enhancement of TiO₂ anatase photocatalysis for cationic dye degradation: mechanistic insights and degradation optimization.}},
  author = {Hamisu Umar Farouk and Abdul Aziz Abdul Raman and Wan Mohd Ashri Wan Daud},
  journal = {RSC advances},
  year = {2026},
  month = oct,
  doi = {10.1039/d6ra02604d},
  url = {https://europepmc.org/article/MED/42852249},
  note = {CC BY-NC},
}
RIS
TY  - JOUR
TI  - Sulfate-driven enhancement of TiO₂ anatase photocatalysis for cationic dye degradation: mechanistic insights and degradation optimization.
AU  - Hamisu Umar Farouk
AU  - Abdul Aziz Abdul Raman
AU  - Wan Mohd Ashri Wan Daud
PY  - 2026
DA  - 2026/10/08
JO  - RSC advances
DO  - 10.1039/d6ra02604d
UR  - https://europepmc.org/article/MED/42852249
AB  - The influence of inorganic ions in wastewater matrices on the activity and reuse of TiO₂ photocatalysts is an important consideration in photocatalytic water treatment. This study investigates the effect of sulfate ions (SO₄ ²⁻) on the photocatalytic degradation of the cationic dye methylene blue (MB) using anatase TiO₂ under different irradiation and pH conditions. Photocatalytic performance across repeated treatment cycles was evaluated using cumulative percent degradation (CPD), a parameter introduced in this study, and related to changes in the percent atomic concentration (PAC) of elements detected on the recovered TiO₂ surface by X-ray photoelectron spectroscopy (XPS). Under UV irradiation, SO₄ ²⁻-containing systems exhibited the highest CPD values, reaching 248.10% at pH 4 (TMB4) and 294.23% at pH 10 (TMB8), indicating enhanced cumulative MB degradation in the presence of sulfate under these conditions. Surface characterization revealed changes in the carbon-, nitrogen-, oxygen-, and sulfur-containing species associated with the TiO₂ surface following photocatalytic treatment. Carbon-containing surface species increased in the recovered samples and were associated with changes in photocatalytic performance. XPS analysis indicated that sulfur detected on irradiated sulfate-containing samples was attributable to surface-bound sulfate-derived species, with no evidence supporting the formation of discrete molecular sulfur species. Overall, the results demonstrate that SO₄ ²⁻, particularly in combination with UV irradiation, can enhance the cumulative photocatalytic degradation of MB while influencing the surface chemistry of anatase TiO₂. The findings provide further insight into the relationship between wastewater ionic composition, photocatalytic performance, and surface transformations associated with the repeated application of TiO₂ photocatalysts.
SN  - 2046-2069
ER  -