Although researchers recognized comparable photodegradation mechanisms with both ZnO and TiO2, they proved that ZnO was the superior photocatalyst in degrading pesticide carbetamide, herbicide triclopyr, pulp mill bleaching wastewater, 2-phenylphenol, phenol, blue 19, and acid red 14. This superiority of ZnO photocatalytic activity is because it has more active sites, higher reaction rates, and is more effective in generating hydrogen peroxide [18]. Due to its direct, wide bandgap of 3.37 eV, ZnO has a wide range of applications in optoelectronic devices [19] such as light-emitting diodes, photodetectors, and p-n homojunctions. The large exciton binding

energy of 60 meV [19], compared to that of GaN (approximately 25 meV) [20], enhances the MDV3100 concentration luminescence efficiency of the emitted light even at room temperature and higher. The visible

photoluminescence (PL) emission at approximately 2.5 eV (approximately 495 nm), originated from intrinsic defects [21], makes ZnO suitable for applications in field emission and vacuum fluorescent displays. Many techniques including chemical vapor deposition [22], pulsed laser deposition [23], molecular beam epitaxy [24], sputtering [25], hydrothermal synthesis [26], and oxidation of metallic zinc powder [27, 28] have been used to prepare ZnO in different forms and structures for various applications. Nanoparticulate form enhances the catalytic activity due to its large surface area and the presence of vacancies and uncoordinated Silibinin atoms at corners this website and edges. The photocatalytic activity is also improved by bandgap engineering, as a result of the quantum MK 8931 concentration confinement effect

[29–31]. A well-controlled synthesis process at room temperature is needed for the economical use of ZnO in catalytic applications such as water treatment and other environmental applications. Herein, we are reporting, for the first time to the best of our knowledge, a direct, simple, room-temperature synthesis method for ZnO nanoparticles using cyclohexylamine (CHA), as a precipitating agent, and zinc nitrate hexahydrate, as a source of zinc, in both aqueous and ethanolic media. The synthesized ZnO nanoparticles were examined as a photocatalyst for the degradation of the highly toxic cyanide anion [CN- (aq)] in the aqueous medium at room temperature. The kinetics for cyanide photodegradation were investigated with respect to ZnO concentration of weight percentage. Method Materials Zinc nitrate hexahydrate (pure, POCH), cyclohexylamine (GC >99%, Merck, Whitehouse Station, NJ, USA), absolute ethanol (EtOH, 99.9%, Scharlau, Sentmenat, Barcelona, Spain), potassium cyanide (≥97%, Sigma-Aldrich, St. Louis, MO, USA), potassium iodide (≥99.5%, Sigma-Aldrich), and ammonia solution (28-30% NH3 basis, Sigma-Aldrich) were commercially available and were used as received. Deionized water (18.2 MΩ.