Faculty Publications

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    Insights on the advanced processes for treatment of inorganic water pollutants
    (Elsevier, 2020) Mohan Balakrishnan, R.M.; Uddandarao, P.; Manirethan, V.; Raval, K.
    A remarkable increase in the discharge of inorganic pollutants globally from various sources such as mines, industries, or agricultural lands is a major threat to the environment. Development of novel methodologies to mitigate the effects caused by inorganic pollutants in water is crucial in addressing environmental issues. In this regard, various biological sources as nanosorbents and biosensors are venerated as superior entities for the detection and removal of inorganic contaminants. This chapter summarizes the utility of marine bacterial melanin- and fungal-based selenium nanoparticles for the adsorption and further reports endophytic fungal–based ZnS and PbS nanoparticles for the detection of inorganic pollutants from the aqueous systems; moreover, it gives a perspective on current challenges for the removal of contaminants. © 2020 Elsevier Inc. All rights reserved.
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    Isolation of Thiobacillus sp from aerobic sludge of distillery and dairy effluent treatment plants and its sulfide oxidation activity at different concentrations
    (Triveni Enterprises, 2007) Ravichandra, P.; Mugeraya, G.; Rao, A.G.; Ramakrishna, M.; Jetty, A.
    In the present study two strains of Thiobacillus sp were isolated from aerobic sludge of distillery and dairy effluent treatment plant using standard methods of isolation and enrichment. Experiments were conducted using isolated cultures in batch bioreactor with initial sulfide concentration of 75 and 150 mg/l. The effect of initial sulfide concentration on the activity of isolated Thiobacillus sp was studied. Sulfide oxidizing capacity was also determined at different initial sulfide concentrations. The results from the study indicate the possible isolation of Thiobacillus cultures from native source and application in the full-scale reactor. © Triveni Enterprises.
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    Characterization and proinflammatory response of airborne biological particles from wastewater treatment plants
    (2011) Gangamma, S.; Patil, R.S.; Mukherji, S.
    Wastewater contains a variety of microorganisms, and unit operations in the plants could release these biological components into the air environment. These airborne biological particles could have adverse health effects on plant workers and the downwind population. This study provides a first report on the concentration and characterization of the airborne biological particles in six wastewater treatment plants in Mumbai, India. The study indicates that 49% and 27% of the samples exceed, respectively, the exposure limit for airborne endotoxin and bacteria in occupational settings. Endotoxin was identified as the single most important component of the particulate matter responsible for induction of proinflammatory indicator (tumor necrosis factor-?) in in vitro assay. Identification of several clinically important bacterial species in the samples suggests that the workers at the treatment plant are exposed to opportunistic and infectious bacteria. Principal component analysis was used to identify the groups among the bacterial species which serves as the signature for transport study. Analysis also shows that the component related to spore-forming bacteria is present in all samples. © 2011 American Chemical Society.
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    Degradation of paracetamol in aqueous solution by Fenton Oxidation and photo-Fenton Oxidation processes using iron from Laterite soil as catalyst
    (2011) Manu, B.; Mahamood
    For the treatment of paracetamol in water, the photo-Fenton Oxidation process and Classic Fenton oxidation process have been demonstrated and found effective. An iron catalyst extracted from lateritic soil is used to exhibit the degradation and mineralization of paracetamol. Paracetamol reduction and chemical oxygen demand (COD) removal are measured as the objective functions to be maximized. The experimental conditions of the degradation of paracetamol are optimized by Fenton process. the optimum conditions observed for 10 mg/L initial paracetamol concentration are influent pH 3, initial H 2O 2 dosage 30 mg/L, [paracetamol]/[H 2O 2] ratio 1:3 (w/w) and [H 2O 2] / [Laterite iron] ratio 30:0.75 (w/w). At the optimum conditions, for 10 mg/L of initial paracetamol concentration, 76% paracetamol reduction and 69% COD removal by Fenton oxidation and 79% paracetamol reduction and 77% COD removal by UV-C Fenton process are observed in 120 minutes reaction time. At the above optimum conditions, HPLC analysis has demonstrated 100% removal of paracetamol for Fenton oxidation process in 240 minutes and for UV-C photo- Fenton process in 120 minutes. The methods are effective and they may be used in the paracetamol industry. © 2011 CAFET-INNOVA TECHNICAL SOCIETY.
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    Enhanced degradation of paracetamol by UV-C supported photo-Fenton process over Fenton oxidation
    (2011) Manu, B.; Mahamood, S.
    For the treatment of paracetamol in water, the UV-C Fenton oxidation process and classic Fenton oxidation have been found to be the most effective. Paracetamol reduction and chemical oxygen demand (COD) removal are measured as the objective functions to be maximized. The experimental conditions of the degradation of paracetamol are optimized by the Fenton process. Influent pH 3, initial H 2O 2 dosage 60 mg/L, [H 2O 2]/[Fe 2+] ratio 60 : 1 are the optimum conditions observed for 20 mg/L initial paracetamol concentration. At the optimum conditions, for 20 mg/L of initial paracetamol concentration, 82% paracetamol reduction and 68% COD removal by Fenton oxidation, and 91% paracetamol reduction and 82% COD removal by UV-C Fenton process are observed in a 120 min reaction time. By HPLC analysis, 100% removal of paracetamol is observed at the above optimum conditions for the Fenton process in 240 min and for the UV-C photo-Fenton process in 120 min. The methods are effective and they may be used in the paracetamol industry. © IWA Publishing 2011.
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    Preparation and characterization of polysulfone and modified poly isobutylene-alt-maleic anhydride blend NF membrane
    (2012) Ganesh, B.M.; Isloor, A.M.; Padaki, M.
    Recently nanofiltration (NF) is gaining more importance for water treatment. It is replacing the conventional method of water treatment due to advantages of NF membranes over RO system. In this work, we are discussing the preparation of NF membrane for desalination of sea water. We herein report the synthesis of polymer, by the reaction of p-amino benzoic acid (PABA) and poly isobutylene-alt-maleic anhydride (PIAM) and its blend membrane preparation with polysulfone (PSf). The new membranes were characterized by SEM images, surface wettability to investigate the hydrophilic nature of the membrane, water swelling, pure water flux, molecular weight cut-off and salt rejection of the membranes. The membranes showed nano size (<50nm) pores in SEM image, and the contact angle data revealed that membrane surface is moderately hydrophilic. Membrane with 70:30 (PSf:modified PIAM) composition has shown good salt rejection of 96% at 200kPa for 3500ppm of NaCl solution with a pure water flux of 38.36Lm -2h -1. © 2011 Elsevier B.V.
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    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.
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    Removal of acutely hazardous pharmaceuticals from water using multi-template imprinted polymer adsorbent
    (Ecomed Publishers susanne.kuehbandner@hjr-verlag.de, 2014) Venkatesh, A.; Chopra, N.; Krupadam, R.J.
    Molecularly imprinted polymer adsorbent has been prepared to remove a group of recalcitrant and acutely hazardous (p-type) chemicals from water and wastewaters. The polymer adsorbent exhibited twofold higher adsorption capacity than the commercially used polystyrene divinylbenzene resin (XAD) and powdered activated carbon adsorbents. Higher adsorption capacity of the polymer adsorbent was explained on the basis of high specific surface area formed during molecular imprinting process. Freundlich isotherms drawn showed that the adsorption of p-type chemicals onto polymer adsorbent was kinetically faster than the other reference adsorbents. Matrix effect on adsorption of p-type chemicals was minimal, and also polymer adsorbent was amenable to regeneration by washing with water/methanol (3:1, v/v) solution. The polymer adsorbent was unaltered in its adsorption capacity up to 10 cycles of adsorption and desorption, which will be more desirable in cost reduction of treatment compared with single-time-use activated carbon. © 2014 Springer-Verlag Berlin Heidelberg.
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    Isotherm, kinetics, and process optimization for removal of Remazol Brilliant Blue dye from contaminated water using adsorption on acid-treated red mud
    (Taylor and Francis Inc. 325 Chestnut St, Suite 800 Philadelphia PA 19106, 2016) Ratnamala, G.M.; Shetty K, K.V.; Srinikethan, G.
    Red mud, which is a waste product from alumina production, has been utilized after activation with concentrated sulphuric acid treatment for removal of Remazol Brilliant Blue (RBB) dye from dye-contaminated water to investigate its potential as a low-cost adsorbent. The activation has enhanced the surface area of red mud from 20.2 to 32.28 m2/g, thus enhancing its adsorption capacity. The effect of initial dye concentration, contact time, initial pH and adsorbent dosage on percentage removal of dye using concentrated sulphuric acid-treated red mud (CATRM) was investigated. The ranges of these variables for optimization were selected based on batch studies. Acidic pH favoured adsorption and 300 min contact time was found to be suitable for attainment of equilibrium under shaking conditions of 145 rpm. Langmuir isotherm model has been found to represent the equilibrium data for RBB-CATRM adsorption system better in comparison with Freundlich model. The adsorption capacity of CATRM was found to increase with the increase in temperature, and at 40°C, it was found to be 125 mg dye/g of CATRM. The adsorption kinetics was represented by second-order kinetic model, and the kinetic constant was estimated to be 0.0063 g/mg min. Factors affecting the adsorption process were optimized by response surface methodology based on experiments designed as per central composite design. The effects of individual variables and their interaction effects on dye removal were determined. The results of the study showed that dye removal efficiency of almost 100% can be obtained with optimal conditions of initial dye concentration at 105 mg/l, red mud dosage of 2.05 g/l, initial pH of 1 and temperature of 31.65°C. pH and temperature were found to have high interaction effect on adsorption. © 2015 Balaban Desalination Publications. All rights reserved.
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    Microbial disinfection of water with endotoxin degradation by photocatalysis using Ag@TiO2 core shell nanoparticles
    (Springer Verlag service@springer.de, 2016) Sreeja, S.; Shetty K, K.V.
    The studies on photocatalytic disinfection of water contaminated with Escherichia coli using Ag core and TiO2 shell (Ag@TiO2) nanoparticles under UV irradiation showed that these nanoparticles are very efficient in water disinfection both in their free and immobilised form. Complete disinfection of 40 × 108 CFU/mL could be achieved in 60 min with 0.4 g/L catalyst loading and in 35 min with 1 g/L catalyst loading. Ag@TiO2 nanoparticles were found to be superior to TiO2 nanoparticles in photocatalytic disinfection of water. Kinetics of disinfection followed Chick’s law, and the pseudo-first-order rate constant was 0.0168 min?1 for a catalyst loading of 0.1 g/L. Disinfection of water and degradation of endotoxins (harmful disinfection residual) occurred simultaneously during photocatalysis thereby making the treated water safe for use. Endotoxin degradation showed a shifting order of kinetics. The rate of photocatalysis with nanoparticles immobilised in cellulose acetate film was marginally lower as compared to that of free nanoparticles. Negligible Ag ion leakage and re-growth of cells post-photo-catalytic treatment of water confirmed that complete disintegration of E. coli occurred during photocatalysis making the treated water safe for use. Therefore, Ag@TiO2 nanoparticles have a potential for large-scale application in drinking water treatment plants and household purification units. © 2016, Springer-Verlag Berlin Heidelberg.