Photocatalytic Degradation of Allura Red by Mn-Ni co-doped Nanotitania under Visible Light Irradiation

Abstract

Photocatalyst has been extensive interest because of it’s new innovation to the reduce the contamination in the environment. A straight forward and economical procedure has been employed by sol-gel technique for the co-doping of Mn2+ and Ni2+ into TiO2 . The co-doped and undoped photocatalysts were described by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive X-ray Spectroscopy (EDX), Fourier transform infrared spectroscopy (FT-IR), UV-Visible Diffused Reflectance Spectroscopy (UV Vis-DRS), Transmission electron Microscopy (TEM) and Brunauer-Emmett-Teller (BET). The portrayal results shows that anatase and rutile mixed phase was observed for some co-doped nanocatalysts and the remaining catalysts exhibits anatase phase only. It was observed by FT-IR that the shifting of frequency of Ti-O-Ti in the catalysts was seen due to substitutional doping of Mn and Ni by replace Ti and O, further the photocatalysts shows rough morphology, irregular shape of particle with size (6.5nm) and having high surface area (135.70 m2/g), less band energy (2.7 eV). The photocatalytic action of these materials was assessed by the degradation of Allura red (AR) as a contaminant. The results shows that AR has degraded within 60 minutes at doping concentrations 0.25 Wt% of Mn2+ion and 1.0 Wt% of Ni2+ ion in TiO2 (NMT2) at an optimum reaction parameters pH-4, catalyst dose 0.070g/L and at AR initial dye concentration 0.010g/L.

Synthesis and antibacterial activity of transition metal (Ni/Mn) co-doped TiO2 nanophotocatalyst on different pathogens under visible light irradiation

“…An appended benefit of transition metal doping like Mn, Cr, Ni, Cu is to improve the trapping of electron to inhibit the e + /h − recombination during irradiation of light [6,7]. "Transition metal doped TiO 2 nanoparticles demonstrated that Ni or Mn doped TiO 2 possess better absorption ability of visible light and Ni/Mn either substitutes Ti 4+ site or embeds in the vacancy of TiO 2 lattice" [8].…”