Integration of nickel doping with loading on graphene for enhanced adsorptive and catalytic properties of CdS nanoparticles towards visible light degradation of some antibiotics.

Water dispersible, highly efficient nickel doped CdS nanoparticles anchored on graphene nanosheets as a photocatalyst for cephalexin and sulfamethoxazole photodegradation have been prepared in a facile microwave-furnace assisted method. Each one of the two modifications has played a critical role in nanocomposite functioning. Defects originated by dopant boosted the lifetime of carriers and thereupon graphene matrix transferred them to contribute effectively the photocatalytic process. Characterization results revealed the formation of monocrystalline hexagonal phase of all products and that both doping and loading on graphene have red-shifted the absorption edge of CdS towards the visible light region. Furthermore, FTIR confirmed the successful reduction of graphene oxide by the subsequent preparation steps. Adsorption isotherms revealed the role of graphene in enhancing substrate adsorption. Nevertheless, dissimilar pathways of catalytic degradation were observed on the doped composite as cephalexin oxidation was principally mediated by the hole-hydroxyl radical mechanism, sulfamethoxazole oxidation favored the superoxide radical mechanism. This composite has shown, however, a high photostability and minimized ions release of the composite.

Kinetic and mechanistic aspects of sensitized photodegradation of ß-lactam antibiotics: microbiological implications.

Amoxicillin (Amx) and cephalexin (Cfx) are ß-lactam antibiotics widely used in human and veterinary medicine. Two points of interest surrounding these molecules are the photodegradation of the molecules and their microbiological implications, as well as the persistence and bioaccumulation in the environment which may cause resistance to bacterial strains. The kinetic and mechanistic aspects of the photosensitized degradation of Amx and Cfx have been studied in water at pH 7.4 and 10 by stationary and time-resolved methods. Kinetic evidence indicates that the Rose Bengal-sensitized photooxidation of Amx at pH 7.4 proceeds via O(2)((1)Δ(g)) and O(2•-) mechanisms while at pH 10 the degradation path occurs, principally, via O(2)((1)Δ(g)). For Cfx, this process is attributed to O(2)((1)Δ(g)) and O(2•-). Photoproducts, which arise from the addition of oxygen atoms and subsequent oxidation of the groups -CH(3) to -COOH, were detected. For both antibiotics the bacteriostatic activity decreases in parallel to their photodegradation. The results of this study could potentially help scientists to better understand and predict the photodegradability of these antibiotics on living organisms and in different environmental compartments.