Adsorption and photocatalytic degradation of cysteine in presence of TiO2

Abstract

Abstract Amino-acids are elemental constituents of microorganisms, e.g. bacteria, fungi, virus, mold, among others and are at the origin of the formation of odorous compounds after chlorination treatment due to the filtration of these microorganisms. Our study aims at studying the photocatalytic degradation of cysteine chosen as model of amino acid for understanding better the photocatalytic chemical pathway of microorganisms. The kinetics of adsorption in the dark and under UV light, the kinetics of photocatalytic oxidation, the effect of pH and the main initial pathways of cysteine degradation have been investigated in aerated TiO 2 Degussa P-25 aqueous suspensions illuminated at λ > 340 nm. Langmuir and Langmuir–Hinshelwood kinetics were observed respectively in the dark and under UV light. The coverage of TiO 2 surface under UV revealed a coverage of TiO 2 equivalent to that in the dark, indicating no modification of adsorption sites under irradiation. This behaviour is in agreement with a geometrical adsorption of cysteine as proved by using the molecular surface of cysteine and by taking into account the accessibility of water molecules. The effect of pH on adsorption and photocatalytic degradation showed a good correlation between dark adsorption and photocatalytic degradation. The mineralisation of organic carbon and nitrogen shows the presence of traces of organics hardly mineralisable but also the formation of similar amount of NH 4 + and NO 3 − ions from the beginning of the reaction contrarily to what was observed for other amino-acids. This behaviour is explained by the different ionisation states of cysteine. Taking into account the evolution of Total Organic Carbon, sulphate, nitrate and ammonium, an initial reaction pathway has been proposed.