Faculty Publications
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Item An analytical model for spiral wound Reverse Osmosis membrane modules: Part I - Model development and parameter estimation(2011) Sundaramoorthy, S.; Srinivasan, G.; Murthy, D.V.R.A mathematical model for spiral wound Reverse Osmosis membrane module is presented in this work. The model incorporates spatial variations of pressure, flow and solute concentration in the feed channel and uniform conditions of pressure in the permeate channel. Assuming solution-diffusion model to be valid, explicit analytical equations were derived for spatial variations of pressure, flow, solvent flux and solute concentration on the feed channel side of the module. Analytical procedures for estimation of model parameters were presented. Graphical linear fit methods were developed for estimation of parameters Aw (solvent transport coefficient), Bs (solute transport coefficient) and b (feed channel friction parameter). The mass transfer coefficient k was assumed to vary along the length of the feed channel with varying conditions of flow, solute concentration and pressure. Explicit analytical equations for estimation of mass transfer coefficient were presented. In this paper (Part I), theoretical studies on development of mathematical model and methods for estimation of model parameters are presented. In Part II of this paper series [1], Studies on validation of this model with experimental data are presented. The studies cover experimental work on a spiral wound RO module with an organic compound namely chlorophenol as a solute. © 2011 Elsevier B.V.Item Enhancement of propyl gallate yield in nonaqueous medium using novel cell-associated tannase of bacillus massiliensis(2013) Aithal, M.; Belur, P.D.Enzymatic synthesis of propyl gallate in organic solvent was studied using cell-associated tannase (EC 3.1.1.20) of Bacillus massiliensis. Lyophilized biomass showing tannase activity was used as the biocatalyst. The effects of solvent, surfactant treatment, and bioimprinting on the propyl gallate synthesis were studied and subsequently optimized. Among various solvents, benzene followed by hexane was found to be the most favorable. Treatment of the biocatalyst with Triton X-100 at a lower concentration (0.2% w/v), before lyophilization, increased the propyl gallate yield by 24.5% compared to the untreated biocatalyst. The biocatalyst was imprinted with various concentrations of gallic acid and tannic acid. Biocatalyst imprinted with tannic acid showed 50% enhancement in the propyl gallate yield compared to the non-imprinted biocatalyst. © 2013 Taylor & Francis Group, LLC.Item Dual colorimetric receptor with logic gate operations: Anion induced solvatochromism(Royal Society of Chemistry, 2014) Kigga, M.; Swathi, N.; Manjunatha, J.R.; Das, U.K.; Nityananda Shetty, A.N.; Trivedi, D.R.A receptor R1 was designed and synthesised for colorimetric detection of F- ions as well as Cu2+ ions via intramolecular charge transfer mechanism. Upon addition of F- ions in dry DMSO, the color of the receptor R1 changed from pale yellow to blue. The receptor showed a unique property of solvatochromism by displaying different coloration with different solvents only in the presence of F- ions, which were applied to determine the percentage composition of binary solvent mixtures. The receptor R1 was able to detect Cu2+ ions colorimetrically where it exhibited a color change from pale yellow to orange-red. In addition, the receptor was subjected to molecular logic gate applications, wherein it showed 'ON-OFF' switching operations. © 2014 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.Item New luminescent 2-methoxy-6-(4-methoxy-phenyl)-4-p-tolyl-nicotinonitrile: Synthesis, crystal structure, DFT and photophysical studies(2014) Ahipa, T.N.; Kamath, P.R.; Kumar, V.; Vasudeva Adhikari, A.V.In the current communication, we report the synthesis, spectroscopic, crystal structure, DFT and photophysical studies of a new nicotinonitrile derivative, viz. 2-methoxy-6-(4-methoxy-phenyl)-4-p-tolyl-nicotinonitrile (2) as a potential blue light emitting material. The compound 2 was synthesized in good yield via a simple route. The acquired spectral and elemental analysis data were in consistent with the chemical structure of 2. The single crystal study further confirms its three dimensional structure, molecular shape, and nature of short contacts. Its DFT calculations reveal that compound 2 possesses a non-planar structure and its theoretical IR spectral data are found to be in accordance with experimental values. In addition, its UV-visible and fluorescence spectral measurements prove that the compound exhibits good absorption and fluorescence properties. Also, it shows positive solvatochromic effect when the solvent polarity was varied from non-polar to polar. © 2014 Elsevier B.V. All rights reserved.Item Preparation and characterization of novel PSf/PVP/PANI-nanofiber nanocomposite hollow fiber ultrafiltration membranes and their possible applications for hazardous dye rejection(Elsevier, 2015) Kajekar, A.J.; Dodamani, B.M.; Isloor, A.M.; Zulhairun, A.K.; Cheer, N.B.; A.F., A.F.; Shilton, S.J.In the present study, PANI (polyaniline)-nanofibers were synthesized by interfacial polymerization technique, dispersed in n-Methyl-2-Pyrrolidone (NMP) solvent and blended with PVP (Polyvinylpyrrolidone)/PSf (Polysulfone) for preparing the novel hollow fiber membrane by dry-wet spinning technique. The newly prepared nanocomposite ultrafiltration hollow fiber membrane is characterized by Scanning Electron Microscope (SEM), Contact Angle, Zeta Potential and Differential Scanning Calorimeter (DSC). Filtration studies are conducted to measure the membrane pure water flux (PWF), rejection of hazardous dye (Reactive Red 120) and fouling resistance. The maximum rejections are obtained for M 0.5 membrane with 99.25% rejection of RR120 hazardous dye at 2. bar pressure. The pure water flux, percentage rejection, antifouling property and thermal resistance increased with an increase in PANI-nanofiber concentration. The contact angle of the membrane decreased with increasing PANI-nanofiber concentration, which indicated increased hydrophilicity of the new membranes. © 2015 Elsevier B.V.Item Extraction, characterization and biological studies of phytochemicals from Mammea suriga(Xi'an Jiaotong University, 2015) Poojary, M.M.; Vishnumurthy, K.A.; Vasudeva Adhikari, A.V.Abstract The present work involves extraction of phytochemicals from the root bark of a well-known Indian traditional medicinal plant, viz. Mammea suriga, with various solvents and evaluation of their in vitro antimicrobial and antioxidant activities using standard methods. The phytochemical analysis indicates the presence of some interesting secondary metabolites like flavonoids, cardiac glycosides, alkaloids, saponins and tannins in the extracts. Also, the solvent extracts displayed promising antimicrobial activity against Staphylococcus aureus, Bacillus subtilis and Cryptococcus neoformans with inhibition zone in a range of 20-33 mm. Further, results of their antioxidant screening revealed that aqueous extract (with IC50 values of 111.51±1.03 and 31.05±0.92 ?g/mL in total reducing power assay and DPHH radical scavenging assay, respectively) and ethanolic extract (with IC50 values of 128.00±1.01 and 33.25±0.89 ?g/mL in total reducing power assay and DPHH radical scavenging assay, respectively) were better antioxidants than standard ascorbic acid. Interestingly, FT-IR analysis of each extract established the presence of various biologically active functional groups in it. © 2015 Xi'an Jiaotong University.Item An Efficient Three-component, One-pot Synthesis of Quinazolines under Solvent-free and Catalyst-free Condition(HeteroCorporation support@jhetchem.com, 2015) Bhat, S.I.; Das, U.K.; Trivedi, D.R.An efficient green protocol for the synthesis of quinazolines in the absence of solvent and catalyst has been developed. 2,4-Disubstituted quinazolines have been synthesized from three-component one-pot reactions of 2-aminoaryl ketones, orthoesters, and ammonium acetate. The present method has advantages of operational simplicity, substrate generality, clean reaction, high yields (76-94%), and moderate reaction time. The plausible mechanism of the reaction has been proposed based on the spectral characterization and single crystal X-ray analysis of isolated intermediate. © 2014 HeteroCorporation.Item Dissolution of kraft lignin using Protic Ionic Liquids and characterization(Elsevier B.V., 2016) Rashid, T.; Chong, C.F.; Iyyaswami, I.; Murugesan, T.In the present research three Protic Ionic Liquids (pyridinium formate, pyridinium acetate and pyridinium propionate) were synthesized and tested for the dissolution and subsequent regeneration of kraft lignin. Among the investigated solvents, pyridinium formate showed a higher dissolution capacity (70% w/w) i.e. (710 g/L) at 75 °C within 1 h. The results indicated that the introduced solvent is thermally stable, noncorrosive, possesses low viscosity and is easy to recycle. The dissolution process is purely physical and the physicochemical analysis of the regenerated lignin showed high thermal stability, with reduction in polydispersity and the average molecular weight was reduced from 4119 g/mol to 1249 g/mol. FTIR spectroscopy and 1H NMR results proved that the regenerated lignin is less degraded. Moreover the OH vibrations of regenerated lignin showed a weak inter and intramolecular interaction in regenerated lignin, which could positively help in reducing its chemical resistance towards processing for further commercial applications. Due to the higher solubility of lignin and its stability towards recyclability, the pyridinium formate proved that present selective dissolution and regeneration of lignin could significantly enhance the pretreatment techniques for lignocellulosic biomass. © 2016 Elsevier B.V.Item Optimised microwave-assisted biosynthesis of silver nanoparticles from Nothapodytes foetida leaf extracts and its anti-microbial activities(Taylor and Francis Ltd. michael.wagreich@univie.ac.at, 2016) Roopesh, R.; Geedhika, G.; D'Souza, J.; Anandhan, S.; Bhat, K.U.; Jaya M, J.; Fathima B, S.; Mohan Balakrishnan, R.M.The present investigation reports the biogenesis of silver nanoparticles (Ag NPs) using extracts of a medicinal plant Nothapodytes foetida. Total phenolic content (TPC) and ferric reducing antioxidant power (FRAP) assay were carried out for the microwave-assisted extract (MAE) of N. foetida using methanol as solvent and the conditions for extraction were optimised by response surface methodology (RSM). The effects of operating variables such as extraction time, temperature and ratio of sample to solvent were studied using central composite design (CCD). A mathematical model with a high determination coefficient (R2) for TPC (0.991) and FRAP (0.995) was obtained. The optimal conditions of extraction for TPC were 48.6 ºC, 23.15 min and 2.04:30 (g/mL) and for FRAP 52.31ºC, 12.32 min and 1.67: 30 (g/mL). Under these conditions, the experimental yields of TPC and FRAP were 2.426 mg gallic acid equivalents (GAE)/g dry powder and 14.985mg of FeSO4·7H2O/g of dry powder, respectively. Ag NPs were characterised using UV–Vis spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD) and Fourier transform infrared (FTIR) spectroscopy. The synthesised Ag NPs have also shown potent activity against the human pathogenic Staphylococcus aureus. © 2016 Informa UK Limited, trading as Taylor & Francis Group.Item A new strategy to refine crude Indian sardine oil(Japan Oil Chemists Society yukagaku@jocs-office.or.jp, 2017) Charanyaa, S.; Belur, B.D.; Iyyaswami, R.Current work aims to develop a refining process for removing phospholipids, free fatty acids (FFA), and metal ions without affecting n-3 polyunsaturated fatty acid (n-3 PUFA) esters present in the crude Indian sardine oil. Sardine oil was subjected to degumming with various acids (orthophosphoric acid, acetic acid, and lactic acid), conventional and membrane assisted deacidification using various solvents (methanol, ethanol, propanol and butanol) and bleaching with bleaching agents (GAC, activated earth and bentonite) and all the process parameters were further optimized. Degumming with 5%(w/w) ortho phosphoric acid, two stage solvent extraction with methanol at 1:1 (w/w) in each stage and bleaching with 3% (w/w) activated charcoal loading, at 80ºC for 10 minutes resulted in the reduction of phospholipid content to 5.66 ppm from 612.66 ppm, FFA to 0.56% from 5.64% with the complete removal of iron and mercury. Under these conditions, the obtained bleached oil showed an enhancement of n-3 PUFA from 16.39% (11.19 Eicosapentaenoic acid (EPA) + 5.20 Docosahexaenoic acid (DHA)) to 17.91% (11.81 EPA + 6.1 DHA). Replacing conventional solvent extraction with membrane deacidification using microporous, hydrophobic polytetrafluoroethylene membrane (PTFE), resulted in a lesser solvent residue (0.25% (w/w)) in the deacidified oil. In view of lack of reports on refining of n-3 PUFA rich marine oils without concomitant loss of n-3 PUFA, this report is significant. © 2017 by Japan Oil Chemists’ Society.