Photocatalytic hydrogen production from biomass-derived compounds: a case study of citric acid.

Highly crystalline anatase TiO2 nanoparticles with high BET surface area have been synthesized by thermal hydrolysis of titanium(IV) bis(ammoniumlactato) dihydroxide aqueous solutions. The photocatalytic H2 production from aqueous citric acid (CA) solutions over Pt-loaded TiO2 has been investigated under different experimental conditions, that is, different CA concentration, temperature, light intensity, and pH of Pt/TiO2 suspension. For comparison, the photocatalytic dehydrogenation of triethanolamine (TEA) has also been investigated. The highest H2 production rates were obtained at pH 3 and 9 for CA and TEA, respectively. This behavior is readily explained by the adsorption characteristic of the employed reagent on the surface of the charged TiO2. The effect of the photocatalyst loading and the light intensity on the H2 production rate showed the same behavior in the case of CA and TEA evincing that these parameters are catalyst dependent. The apparent activation energies have been determined to be 13.5 ± 1.8 and 14.7 ± 1.6 kJ mol(-1) for CA and TEA, respectively, indicating the existence of an activation energy barrier in a photocatalytic process which can be attributed to the desorption of adsorbed products.