Faculty Publications
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Item Solar light induced photocatalytic degradation of Reactive Blue 220 (RB-220) dye with highly efficient Ag@TiO2 core-shell nanoparticles: A comparison with UV photocatalysis(2014) Khanna, A.; Shetty K, K.Ag core-TiO2 shell (Ag@TiO2) structured nanoparticles with Ag to TiO2 molar ratio of 1:1.7 were synthesized using one pot synthesis method and post calcination was carried out at 450°C for 3h to convert it from amorphous to crystalline form. The Ag core and TiO2 shell formation was confirmed by TEM and AFM. The particle size analysis revealed the average size of Ag@TiO2 as approximately around 30nm. EDS spectra showed the presence of O, Ag, and Ti elements. The improvement in optical properties was proved by DRS which showed significant red shift by Ag core in visible region. Ag@TiO2 exhibited better photocatalytic activity as compared to Degussa P25-TiO2, synthesized TiO2, and the Ag doped TiO2 photocatalysts under UV and solar light irradiation for degradation of Reactive Blue 220 (RB-220) dye. Higher rate of photocatalysis of RB-220 with Ag@TiO2 was obtained under solar light irradiation as compared to UV light irradiation, confirming the capability of the catalyst to absorb both UV and visible light. The kinetics of degradation of dye was found to follow modified Langmuir Hinshelwood (L-H) kinetic model. Ag@TiO2 can be recycled without much decline in the efficacy. Ag@TiO2 has been found to be the effective photocatalyst for degradation of water contaminated with azo dyes under both UV and solar light irradiations. © 2013 Elsevier Ltd.Item Ag-TiO2 nanoparticles for photocatalytic degradation of lomefloxacin(Taylor and Francis Inc. 325 Chestnut St, Suite 800 Philadelphia PA 19106, 2016) Kulkarni, R.M.; Malladi, R.S.; Hanagadakar, M.S.; Doddamani, M.R.; Bhat, K.U.The photocatalytic activity of silver-doped TiO2 (Ag-TiO2) nanoparticles was studied by photocatalytic degradation of lomefloxacin (LMF) using a photoreactor with a mercury lamp (PHILIPS, TUV 8 W T5, Emax = 254 nm). The 1 and 2% silver-doped TiO2 nanoparticles were synthesized by liquid impregnation (LI) method. The resulting nanoparticles were characterized by surface analytical methods such as X-ray diffraction (XRD), scanning electron microscope (SEM), energy dispersive X-ray analysis and transmission electron microscope (TEM). The study shows 2% Ag-TiO2 nanoparticles exhibited better results (95% degradation) in 1 h for the degradation of lomeofloxacin compared to 1% Ag-TiO2 and pure TiO2. XRD analysis indicated that the crystallite size of TiO2 was 17.00 nm, while the crystallite size of 1% Ag-TiO2 and 2% Ag-TiO2 was 13.07 to 14.17 nm. TEM images show the particle size of Ag-TiO2 nanoparticles were in the range 40–45 nm in length and 10–15 nm in breadth. Pseudo-first-order rate constants were found to decrease with increase in pH. The effect of UV intensity, catalyst dosage and initial concentration of LMF on the degradation rate were also studied and elaborately discussed. © 2015 Balaban Desalination Publications. All rights reserved.Item Photocatalytic degradation of phenol using Ag core-TiO2 shell (Ag@TiO2) nanoparticles under UV light irradiation(Springer Verlag service@springer.de, 2016) Shet, A.; Shetty K, K.V.Ag@TiO2 nanoparticles were synthesized by one pot synthesis method with postcalcination. These nanoparticles were tested for their photocatalytic efficacies in degradation of phenol both in free and immobilized forms under UV light irradiation through batch experiments. Ag@TiO2 nanoparticles were found to be the effective photocatalysts for degradation of phenol. The effects of factors such as pH, initial phenol concentration, and catalyst loading on phenol degradation were evaluated, and these factors were found to influence the process efficiency. The optimum values of these factors were determined to maximize the phenol degradation. The efficacy of the nanoparticles immobilized on cellulose acetate film was inferior to that of free nanoparticles in UV photocatalysis due to light penetration problem and diffusional limitations. The performance of fluidized bed photocatalytic reactor operated under batch with recycle mode was evaluated for UV photocatalysis with immobilized Ag@TiO2 nanoparticles. In the fluidized bed reactor, the percentage degradation of phenol was found to increase with the increase in catalyst loading. © 2015, Springer-Verlag Berlin Heidelberg.Item Photocatalytic degradation of Irgalite violet dye using nickel ferrite nanoparticles(IWA Publishing 12 Caxton Street London SW1H 0QS, 2019) Vijay, S.; Mohan Balakrishnan, R.M.; Rene, E.R.; Uddandarao, P.Nanotechnologies have prominent applications in the field of science and technology owing to their size-tunable properties providing a promising approach for degradation of various pollutants. In this scenario, the present work aims to study the effect of nickel ferrite nanoparticles on the degradation of Irgalite violet dye by Fenton’s reaction using oxalic acid as an oxidizing agent in the presence of sunlight. The effect of pH and adsorbent dosage on the rate of dye degradation was monitored. Based on these studies it was observed that 99% dye degradation was achieved for catalyst dosage of 0.2 g, 400 ppm dye concentration and 2.0 mM oxalic acid at pH 3.0 within 60 min. The studies reveal that the degradation follows pseudo-first-order kinetics and the catalyst reusability remained constant almost for five cycles. Further, nickel ferrite nanoparticles are proven to be an efficient alternative for the removal of dyes from coloured solutions. © IWA Publishing 2019Item Reusable floating polymer nanocomposite photocatalyst for the efficient treatment of dye wastewaters under scaled-up conditions in batch and recirculation modes(John Wiley and Sons Ltd vgorayska@wiley.com Southern Gate Chichester, West Sussex PO19 8SQ, 2019) Das, S.; Mahalingam, H.BACKGROUND: In the last decade, research on floating photocatalysts has increased rapidly with polymer substrates being a popular choice. However, most of the published work is on very small volumes and there is very little work on scale-up of such systems. RESULTS: Polystyrene–titanium dioxide nanocomposite floating films were prepared using a facile solvent casting method and tested for the photocatalytic degradation of four different dyes under UV irradiation. The prepared film was characterised by Fourier-transform infrared (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), inductively coupled plasma optical emission spectrometry (ICP-OES) and profilometry. Scale-up studies were done in batch mode under optimised conditions, and for the larger reactor volume, the effect of recirculation was studied. Complete decolourisation of the model dye (Remazol Turquoise Blue) was observed within 80 min in the scaled-up batch process. In the recirculation mode, for a much larger volume of the dye solution, around 75% decolourisation in 6 h was observed. The reusability of the photocatalytic film was tested, and the results promise a minimum decolourisation efficiency of around 70%. Finally, total organic carbon (TOC) and liquid chromatography mass spectrometry (LC-MS) analysis were used to assess the degradation of the dye. The maximum TOC reduction observed was around 25% possibly due to the complex nature of the dye used in this study. The intermediate products of degradation were identified, and a tentative mechanism is suggested. CONCLUSION: This work demonstrates the recirculation aspects of the photocatalytic reactor under the scaled-up conditions for a complex dye. The prepared film showed excellent stability with satisfactory wastewater decontamination under UV irradiation even after repeated use. © 2019 Society of Chemical Industry. © 2019 Society of Chemical IndustryItem Solar assisted photocatalytic degradation of organic pollutants in the presence of biogenic fluorescent ZnS nanocolloids(Elsevier Ltd, 2019) Uddandarao, P.; Hingnekar, T.A.; Mohan Balakrishnan, R.M.; Rene, E.R.The main aim of this study was to ascertain the photocatalytic degradation of organic pollutants present in aqueous phase using fluorescent biogenic ZnS nanocolloids produced from an endophytic fungus Aspergillus flavus. The degradation studies were carried out using different organic pollutants such as methyl violet (MV), 2,4-dichlorophenoxyacetic acid (2,4-D) and paracetamol (PARA) for 120 min, 270 min and 240 min, respectively, at pH varying from 3.0 to 11.0. The results from this study indicate that the degradation efficiency of ZnS nanocolloids for MV, 2,4-D and PARA were 87%, 33% and 51%, respectively, at the optimum concentration of 100 mg/L of the tested organic pollutants. At different time intervals, the samples were analyzed for their chemical oxygen demand (COD) and total organic carbon (TOC) contents. The reduction of COD and TOC were 78% and 74% for MV at 120 min; 55.5% and 57.2% for 2,4-D at 270 min and 47.6% and 44.5% for PARA at 240 min, respectively. The degradation pathway was determined based on the mass spectrum and the intermediates formed; in addition, the interaction between organic pollutants and nanocolloids was also elucidated based on atomic force microscopy (AFM) and fluorescence spectrum. © 2019 Elsevier LtdItem An efficient system for electro-Fenton oxidation of pesticide by a reduced graphene oxide-aminopyrazine@3DNi foam gas diffusion electrode(Elsevier B.V., 2020) Senthilnathan, J.; Younis, S.A.; Kwon, E.E.; Surenjan, A.; Kim, K.-H.; Yoshimura, M.A stable rGO-AmPyraz@3DNiF gas diffusion electrode was prepared via modification of 3D nickel foam (3D-NiF) with aminopyrazine functionalized reduced graphene oxide (rGO-AmPyraz) for the electro Fenton (EF) process. The generation capacity of H2O2 and OH radicals by this electrode was assessed relative to 3DNiF and rGO-AmPyraz@indium tin oxide (ITO) electrodes and with/without a coated Fe3O4 plate. The rGO-AmPyraz@3DNiF electrode showed the maximum production of these radicals at 2.2 mmol h?1 and 410 ?mol h?1, respectively (pH 3) with the least leaching of Ni2+ such as < 0.5 mg L?1 even after 5 cycles (e.g., relative to 3DNiF (24 mg L?1). Such control on Ni ion leaching was effective all across the tested pH from 3 to 8.5. Its H2O2 generation capacity was far higher than that of the nanocarbon supported on commercially available ITO conductive glass. The mineralization of dichlorvos (at initial concentration: 50 mg L?1) was confirmed with its complete degradation as the concentrations of the end products (e.g., free Cl?1 (5.36 mg L?1) and phosphate (12.89 mg L?1)) were in good agreement with their stoichiometric concentration in dichlorvos. As such, the proposed system can be recommended as an effective electrode to replace nanocarbon-based product commonly employed for EF processes. © 2020 Elsevier B.V.Item Photocatalytic degradation of p-nitrophenol using biologically synthesized ZnO nanoparticles(Springer Science and Business Media Deutschland GmbH, 2021) Kadam, V.V.; Shanmugam, S.D.; JagadeeshBabu, J.; Mohan Balakrishnan, R.M.The present work deals with the photocatalytic degradation of p-nitrophenol as it is a United States Environmental Protection Agency-listed priority pollutant and has adverse environmental and health effects. To eradicate the detrimental environmental impact of p-nitrophenol, the biologically synthesized ZnO nanoparticles were used as a photocatalyst. The degradation of p-nitrophenol was confirmed by decreasing the absorbance value at a characteristic wavelength of 317 nm using the UV-vis spectrophotometer. Reaction parameters such as ZnO photocatalyst concentration of 0.1 g/L at pH 11 in the presence of H2O2 (5 mM) were found to be optimum conditions for p-nitrophenol degradation. The photocatalytic degradation was slowly enhanced in the presence of H2O2 as an electron acceptor. The kinetics of nitrophenol degradation was studied, which follows the pseudo-first-order reaction. The photocatalytic degradation of p-nitrophenol was characterized by using total organic carbon, chemical oxygen demand, and high-performance liquid chromatography analyses. This method is found to be effective as it is environmentally friendly, free of toxic chemicals. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.Item Auto-combustion synthesis of narrow band-gap bismuth ferrite nanoparticles for solar photocatalysis to remediate azo dye containing water(Springer Science and Business Media Deutschland GmbH, 2021) Kalikeri, S.; Shetty K, V.Narrow band gap of ferrites makes it a good photocatalyst, and it plays very prominent role in the level of degradation of organic dyes by photocatalysis. In the current study, bismuth ferrite (BFO) nanoparticles were synthesized by auto-combustion technique. The synthesized BFO particles have the average crystallite size of 33 nm and band gap energy of 1.9 eV. As revealed by microscopic images, uniform, distinct, and hexahedral shaped BFO nanoparticles of 42.7 nm are formed. The BFO nanoparticles exhibited visible and solar light-mediated photocatalytic activity in degrading Acid Yellow-17. The optimum pH and catalyst loading were found to be pH 5 and 0.2 g/L respectively. Around complete degradation under solar and 95% degradation under visible light could be achieved within 135 min of irradiation. Around 85% and 83% chemical oxygen demand (COD) removal could also be achieved under solar and visible light respectively. The degradation followed first-order kinetics in terms of COD removal. The BFO nanoparticles are promising as solar light active catalysts for wastewater treatment. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.Item Suspended and polycaprolactone immobilized Ag @TiO2/polyaniline nanocomposites for water disinfection and endotoxin degradation by visible and solar light-mediated photocatalysis(Springer Science and Business Media Deutschland GmbH, 2021) Gadgil, D.J.; Shetty K, V.In the present study, water contaminated with Escherichia coli (E. coli) cells was photocataytically disinfected using Ag core-TiO2 shell/Polyaniline nanocomposite (Ag@TiO2/PANI) under visible light irradiation. Ag@TiO2/PANI containing 13 weight % of Ag@TiO2 was found to offer maximum disinfection activity. Band gap energy of Ag@TiO2/PANI was found to be 2.58 eV. Ag@TiO2/PANI nanocomposites were efficient in water disinfection in their suspended and immobilized form. Rate of disinfection with Ag@TiO2/PANI was faster than that with Ag@TiO2 nanoparticles. Water containing 50 × 108 CFU/mL cells was completely disinfected within 120 min with 1 g/L Ag@TiO2/PANI nanocomposite. Simultaneous disinfection and endotoxins degradation were achieved. The photocatalytic disinfection of water and endotoxin degradation using Ag@TiO2/PANI nanocomposite under visible light irradiation followed second order kinetics. The nanocomposite also exhibited a good solar photocatalytic activity. © 2020, Springer-Verlag GmbH Germany, part of Springer Nature.