Photocatalytic hydrogen production from alkanol-amines as sacrificial agents by using Cu-modified TiO-P25 prepared via in situ photodeposition of cupric ions under UV-A light irradiation was investigated. A direct comparison among different sacrificial agents (monoethanolamine, diethanolamine, and triethanolamine) was preliminarily performed. Diethanolamine was selected for further investigation, due to its higher hydrogen production rate with respect to other alkanol-amines. Effect of pH, starting concentration of sacrificial agent, and catalyst/co-catalyst loads were studied. Solution pH exerts major impact on the photoefficiency for hydrogen generation: reaction mechanisms at different pH values were extensively examined. For the first time, a validated kinetic model estimated the unknown rate constants of (i) reaction between diethanolamine and photogenerated holes, (ii) proton reduction, and (iii) diethanolamine adsorption on the photocatalyst surface.
Hydrogen production upon UV-light irradiation of Cu/TiO2 photocatalyst in the presence of alkanol-amines
Di Somma I
2020
Abstract
Photocatalytic hydrogen production from alkanol-amines as sacrificial agents by using Cu-modified TiO-P25 prepared via in situ photodeposition of cupric ions under UV-A light irradiation was investigated. A direct comparison among different sacrificial agents (monoethanolamine, diethanolamine, and triethanolamine) was preliminarily performed. Diethanolamine was selected for further investigation, due to its higher hydrogen production rate with respect to other alkanol-amines. Effect of pH, starting concentration of sacrificial agent, and catalyst/co-catalyst loads were studied. Solution pH exerts major impact on the photoefficiency for hydrogen generation: reaction mechanisms at different pH values were extensively examined. For the first time, a validated kinetic model estimated the unknown rate constants of (i) reaction between diethanolamine and photogenerated holes, (ii) proton reduction, and (iii) diethanolamine adsorption on the photocatalyst surface.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
