Chemistry

Mineralization of phenazopyridine, 1, in water, under solar-simulator radiation was efficiently achieved using nanoparticle CdS-sensitized rutile TiO2, TiO2/CdS, 2, as photo-catalysts. Despite that, 2 showed two main drawbacks. Firstly, the system was difficult to recover by simple filtration, and demanded centrifugation. Secondly, the sensitizer CdS showed relatively high tendency to leach out hazardous Cd2+ ions under photo-degradation reaction conditions. In an attempt to solve out such difficulties, 2 was supported onto sand surface. The sand/TiO2/CdS system, 3, was easier to recover but showed slightly lower catalytic activity compared to 2. On the other hand, the support failed to prevent leaching of Cd2+. This indicates limited future applicability of CdS-sensitized TiO2 photo-catalyst systems, in solar-based water purification strategies, unless leaching out tendency is completely prevented.

Thin films of CdS, deposited by chemical bath deposition (CBD) onto films of fluorine-doped tin oxide/glass (glass/FTO) substrates were prepared and investigated for photoelectrochemical conversion (PEC) of light into electricity. Knowing the hazardous nature of CdS, the focal theme of this work was to modify the electrodes by simple economic ways to maximize their conversion efficiency and minimize their degradation under PEC conditions. This was to avoid leaching out of hazardous Cd2+ ions. Different parameters have been investigated for this purpose. Multi-deposition preparation, redox couple, and electrode etching affected electrode PEC characteristics. Consistent with earlier literature, annealing the electrode enhanced its conversion efficiency and stability. On the other hand, effect of cooling rate of pre-annealed CdS electrodes, prepared by CBD, on their PEC characteristics has been investigated here for the first time. Controlling the cooling rate was one major factor that affected CdS surface morphology, conversion efficiency and stability under PEC conditions. The major recommendation coming out here is that PEC characteristics of CdS thin film electrodes can be significantly enhanced by pre-annealing the electrode at ∼250 °C followed by its slow cooling.

Natural molecular dye, anthocyanin, is described here as safe sensitizer for TiO2 particles in photo-degradation of organic contaminants in water. The dye is a promising replacement for the more costly and hazardous heavy metal based systems, such as CdS particles and Ru-compounds. TiO2/anthocyanin effectively catalyzed the photo-degradation of methyl orange contaminant under solar simulator radiation. The new TiO2/anthocyanin catalyst showed comparable efficiency to earlier systems, while avoiding their hazardous nature. When supported onto activated carbon (AC) particles, the resulting AC/TiO2/anthocyanin system showed enhanced efficiency and ease of recovery from the catalytic reaction mixture. The natural dye molecules showed the tendency to degrade under photo-degradation conditions, just like earlier hazardous sensitizers. However, complete mineralization of anthocyanin occurred leaving no traces of organic species in solution. Sensitizer degradation caused deactivation of the supported catalyst on recovery. Such a shortcoming was overcome by re-treatment of the recovered catalysts with fresh dye.Effects of different reaction parameters on the catalyst efficiency were studied. A mechanism, similar to earlier CdS-sensitized catalyst systems, is proposed for the TiO2/anthocyanin catalyst.

In search for safe techniques to manage waste pharmaceutical compounds drained in water, solar-driven degradation of phenazopyridine (a model drug) was investigated in aqueous media using different ZnO-based catalyst systems. Naked ZnO, CdS-sensitized ZnO (ZnO/CdS) and activated carbon-supported ZnO (AC/ZnO) have been studied. Both naked ZnO and AC/ZnO were highly efficient in mineralizing phenazopyridine, reaching complete removal in ∼50 min, with AC/ZnO having the higher edge. The ZnO/CdS system showed lower efficiency, due to screening of light by CdS. Moreover, the tendency of CdS to leach out Cd2+ ions discouraged the use of CdS as sensitizer in this work. In both ZnO and AC/ZnO systems, the photo-degradation reaction was induced by the UV tail of the solar light. The visible region, with wavelength longer than 400 nm, failed to induce photo-degradation. The reaction was faster with higher catalyst loading, until a maximum efficiency was reached at a certain concentration. The rate of reaction increased with higher drug concentrations up to a certain limit. The effect of pH value was studied, and the catalysts showed highest efficiencies at pH close to 7. Stability of ZnO to degradation was studied. Both catalyst systems showed lowered efficiencies on recovery and reuse. The results suggest that complete mineralization of waste drugs, commonly dumped in sewage water, with direct solar light is a potentially feasible strategy using the AC/ZnO catalyst.Naked ZnO and activated carbon-supported ZnO particle catalysts for complete mineralization of phenazopyridine by direct solar light. Future strategy for safe management of waste drugs.

Mineralization of phenazopyridine, 1, in water, under solar-simulator radiation was efficiently achieved using nanoparticle CdS-sensitized rutile TiO2, TiO2/CdS, 2, as photo-catalysts. Despite that, 2 showed two main drawbacks. Firstly, the system was difficult to recover by simple filtration, and demanded centrifugation. Secondly, the sensitizer CdS showed relatively high tendency to leach out hazardous Cd2+ ions under photo-degradation reaction conditions.

In search for safe techniques to manage waste pharmaceutical compounds drained in water, solar-driven degradation of phenazopyridine (a model drug) was investigated in aqueous media using different ZnO-based catalyst systems. Naked ZnO, CdS-sensitized ZnO (ZnO/CdS) and activated carbon-supported ZnO (AC/ZnO) have been studied. Both naked ZnO and AC/ZnO were highly efficient in mineralizing phenazopyridine, reaching complete removal in∼ 50 min, with AC/ZnO having the higher edge.

Thin films of CdS, deposited by chemical bath deposition (CBD) onto films of fluorine-doped tin oxide/glass (glass/FTO) substrates were prepared and investigated for photoelectrochemical conversion (PEC) of light into electricity. Knowing the hazardous nature of CdS, the focal theme of this work was to modify the electrodes by simple economic ways to maximize their conversion efficiency and minimize their degradation under PEC conditions. This was to avoid leaching out of hazardous Cd2+ ions.