Synthesis of Ag/ZnO-AC composite photocatalyst: spectroscopic investigation, parameter optimization, synergistic effect and performance enhancement for cost-effective photocatalytic degradation of phenols and dyes.

A ternary photocatalyst composite-Silver decorated on ZnO supported with activated carbon (Ag/ZnO-AC) was investigated for the synthesis, characterization and UV assisted photocatalytic degradation of phenols and dyes present in wastewater. XPS and TEM revealed the elemental composition and formation of ternary Ag/ZnO-AC composite. Different operational parameters including the effect of calcination temperature, catalyst dose, initial concentration of pollutant and the effect of H2O2 and ethanol were studied. The photocatalytic activity was assessed for the degradation of p-Nitrophenol (PNP), o-Nitrophenol (ONP), and dye methyl orange (MO) under UV irradiation by ZnO, Ag/ZnO and Ag/ZnO-AC catalyst. The degradation for PNP, ONP and MO in presence of UV light were found to be in the order Ag/ZnO-AC>Ag/ZnO>ZnO. Improved degradation by Ag/ZnO-AC is attributed to high charge separation and greater adsorption of pollutant because of the combination of Ag and AC leading to a synergistic effect in the catalyst. Along with the high reusability, the composite catalyst Ag/ZnO-AC was found to be non-selective and cost-effective for the degradation of phenols as well as dyes. The as synthesized ternary composite Ag/ZnO-AC can be efficiently used as a photocatalyst for the degradation of recalcitrant and other deleterious contaminants present in wastewater.

Photo-catalyzed degradation of p-nitrophenol employing TiO2 and UV radiations.

Heterogeneous photocatalysis on metal oxide semiconductor particles is an advanced oxidation technology (AOT), which has been effective means of removing organic pollutants from water streams as it utilizes ultraviolet light with semiconductors acting as photocatalyst and leads to complete mineralization of pollutants to environmentally harmless compounds. In the present investigation, the photo-catalyzed degradation studies of p-Nitrophenol (PNP) were carried out in laboratory scale immersion well UV photo-reactor using semiconductor photo-catalyst TiO2 in suspension. For this purpose, low pressure 12 W mercury lamp was used and the effect of (i) time of irradiation, (ii) dose of TiO2, (iii) initial concentration of PNP and (iv) the addition of H2O2 to the system was studied to arrive at optimum process parameters for the complete degradation and decolorization of PNP. Simple UV irradiation could not achieve significant degradation of PNP. But UV+aeration+TiO2+ H2O2 combination achieved almost complete degradation of PNP. The spectrophotometric analysis showed that the rate of degradation of PNP was very fast in initial two hours and the maximum degradation was achieved in 5 hours. The degradation was found to increase in the order UV < UV + aeration < UV + aeration + TiO2 < UV + aeration + TiO2+ H2O2, and the degradation was found to be almost 100% for UV + aeration + TiO2 + H2O2, 91% for UV + aeration + TiO2, 43% for UV + aeration and only 26% for UV irradiation.