Photocatalytic-photothermal evaporators are emerging as promising water purification technologies capable of removing both inorganic and organic pollutants while offering low-cost and low-energy desalination. Despite their potential, the interplay between photocatalysis and photothermal evaporation remains poorly understood. Here, we investigate the sequential application of the two processes and demonstrate, for the first time, the existence of synergistic effects that are independent of the specific materials used. We show that pollutant rejection by evaporation is very effective on the aromatic intermediates formed via hydroxyl-radical attack – an insight of general relevance to advanced oxidation processes. However, we also identify p-benzoquinone as a critical volatile intermediate whose concentration remains significant in the distillate after conventional liquid-phase photocatalysis combined with evaporation. By examining the role of the water matrix, including common inorganic electrolytes and non-volatile organic compounds, we further reveal conditions under which the combined process becomes practically ineffective – an issue not previously recognized for photocatalytic–photothermal systems. Building on these findings, we propose an improved treatment sequence in which the evaporation step is brought forward, mitigating the inhibitory effects of non-volatile species and enabling robust synergistic coupling. This work highlights the overlooked importance of gas-phase photocatalysis and provides a rational framework for the future design and optimization of photocatalytic-photothermal evaporators.

Combined photocatalysis and solar distillation: Promoting synergistic effects for a more efficient VOC/SVOC rejection / H. Hamza, M. Schiavoni, B. Aksu, A.B. Shah Syed, V. Lughi, M.V. Diamanti, D. Meroni. - In: CHEMICAL ENGINEERING JOURNAL. - ISSN 1385-8947. - 531:(2026 Mar 01), pp. 174182.1-174182.9. [10.1016/j.cej.2026.174182]

Combined photocatalysis and solar distillation: Promoting synergistic effects for a more efficient VOC/SVOC rejection

H. Hamza
Primo
;
M. Schiavoni
Secondo
;
D. Meroni
Ultimo
2026

Abstract

Photocatalytic-photothermal evaporators are emerging as promising water purification technologies capable of removing both inorganic and organic pollutants while offering low-cost and low-energy desalination. Despite their potential, the interplay between photocatalysis and photothermal evaporation remains poorly understood. Here, we investigate the sequential application of the two processes and demonstrate, for the first time, the existence of synergistic effects that are independent of the specific materials used. We show that pollutant rejection by evaporation is very effective on the aromatic intermediates formed via hydroxyl-radical attack – an insight of general relevance to advanced oxidation processes. However, we also identify p-benzoquinone as a critical volatile intermediate whose concentration remains significant in the distillate after conventional liquid-phase photocatalysis combined with evaporation. By examining the role of the water matrix, including common inorganic electrolytes and non-volatile organic compounds, we further reveal conditions under which the combined process becomes practically ineffective – an issue not previously recognized for photocatalytic–photothermal systems. Building on these findings, we propose an improved treatment sequence in which the evaporation step is brought forward, mitigating the inhibitory effects of non-volatile species and enabling robust synergistic coupling. This work highlights the overlooked importance of gas-phase photocatalysis and provides a rational framework for the future design and optimization of photocatalytic-photothermal evaporators.
Interfacial distillation; Photocatalysis; Photothermal evaporator; Pollutant rejection; Volatile organic compounds; Wastewater treatment;
Settore CHEM-02/A - Chimica fisica
   COmposite nanomaterials coupling Photothermal Evaporation and photocatalysis for durable water purification systems (COPE)
   COPE
   MINISTERO DELL'UNIVERSITA' E DELLA RICERCA
   P2022TLMK7_001
1-mar-2026
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1235177
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