Abstract

To solve the problem of water pollution, using environment friendly and cost effective method in short time is the need of hour. In this work, chromium (Cr) and nitrogen (N) co-doped TiO2 nanoparticles were synthesized and were used for the photocatalytic degradation of dyes under visible light. The synergistic effect of metal and non-metal co-dopants added would result in appropriate reduction of band gap {from 3.2 eVof TiO2 to 2.67eV}, decrease in recombination rate of charge carriers by trapping electrons and holes, and in better light harvesting capacity. Nanoparticles were synthesized by sol-gel method and characterized using ultraviolet-visible (UV-VIS) spectroscopy, fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), zeta potential, X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET)analysis, field emission scanning electron microscopy (FE-SEM), and RAMAN spectroscopy. Eosin yellow (EY) and rose bengal (RB) were subjected to photocatalytic degradation under solar light to check the photocatalytic activity of the synthesized nanoparticles. Effects of dye concentration, the concentration of nanoparticles, time, and pH were investigated to optimize the parameters. The results obtained were remarkable for 20ppm EY solution took 10min using 1 gL-1 NPs at pH 3 and 10ppm RB solution took 5min using 0.75 gL-1 NPs at pH 5.78 (original pH) for complete degradation. Kinetics studies were also performed and both dyes followed pseudo-second-order kinetics with R2 values 0.99312 and 0.99712 for EY and RB, respectively. The study of degraded products was conducted using high-performance liquid chromatography (HPLC) hyphenated with electron spray ionization mass spectroscopy (ESI-MS) (LC-MS) and possible degradation pathways were made for both dyes. A reusability test was also performed showing the efficiency of the particles was up to 88% after 3 cycles of use. These notable results can be attributed to the efficient removal of organic pollutants using the proposed dopants in this study.

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