Faculty Publications

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    Self-assembly synthesis of Co3O4/multiwalled carbon nanotube composites: An efficient enzyme-free glucose sensor
    (Royal Society of Chemistry, 2015) Prasad, R.; Badekai Ramachandra, B.R.
    Self-assembled cobalt oxide-multiwalled carbon nanotube composites were synthesized by simple and effective wet chemical routes. Using these materials, a modified glassy carbon electrode was fabricated and investigated for enzyme-free glucose sensor applications. The fabricated sensor exhibited a high sensitivity of 5089.1 ?A mM-1 cm-2 with a detection limit of 10.42 ?M over a glucose concentration ranging from 0.05 to 12 mM. The sensor also shows promising sensor features like stability, selectivity and fast detection. Moreover, the detection of glucose in human blood serum samples with the as-developed sensor agreed well with the results obtained from commercial glucose meters. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
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    A new colorimetric chemosensors for Cu2+ and Cd2+ ions detection: Application in environmental water samples and analytical method validation
    (Elsevier B.V., 2017) Tekuri, V.; Trivedi, D.R.
    A new heterocyclic thiophene-2-caboxylic acid hydrazide based chemosensor R1 to R4 were designed, synthesized and characterized by various spectroscopic techniques like FT-IR, UV-Vis, 1H NMR, 13C NMR, Mass and SC-XRD. The chemosensor R3 showed a significant color change from colorless to yellow in the presence of Cu2+ ions and chemosensor R4 showed a significant color change from colorless to yellow in the presence of Cd2+ ions over the other tested cations such as Cr3+, Mn2+, Fe2+, Fe3+, Co2+, Ni2+, Zn2+, Ag2+, Al3+, Pb2+, Hg2+, K+, Ca2+ and Mg2+. The high selective and sensitivity of R3 towards Cu2+ and R4 towards Cd2+ ions was confirmed by UV-Vis spectroscopic study. The R3 showed a red shift in the presence of Cu2+ ions by ??max 67 nm and R4 showed a red shift in the presence of Cd2+ ions by ??max 105 nm in the absorption spectrum. The binding stoichiometric ratio of the complex between R3 - Cu2+ and R4 - Cd2+ ions have been found to be 1:1 using the B-H plot. Under optimized experimental conditions, the R3 and R4 exhibits a dynamic linear absorption response range, from 0 to 50 ?M for Cu2+ ions and 0 to 30 ?M for Cd2+ ions, with the detection limit of 2.8 × 10?6 M for Cu2+ and 2.0 × 10?7 M for Cd2+ ions. The proposed analytical method for the quantitative determination of Cu2+ and Cd2+ ions was validated and successfully applied for the environmental samples with good precision and accuracy. © 2017 Elsevier B.V.
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    Colorimetric and fluorometric turn-on sensor for selective detection of fluoride ions: Sol-gel transition studies and theoretical insights
    (Royal Society of Chemistry, 2018) Pangannaya, S.; Mohan, M.; Trivedi, D.R.
    A new organic receptor R1 based on a naphthyl unit covalently linked to a long alkyl chain has been designed, synthesized and characterized by standard spectroscopic techniques. The colorimetric response of receptor R1 from colorless to a pale yellow color and blue fluorescence emission in the presence of F- ions revealed its selective sensing ability in the solution phase. UV-Vis titration, fluorescence titration and 1H NMR titration studies confirmed the formation of the R1-F- complex. Receptor R1 formed a stable gel in DMSO and was confirmed through the standard heating-and-cooling method. Addition of F- ions resulted in disruption of the gel forming a solution that exhibited blue fluorescence emission. The binding constant of the R1-F- complex was found to be of the order of 5.9 × 105 M-1. DFT studies revealed the formation of the receptor-anion complex agreeing well with the experimental results. The detection limit was calculated and found to be 0.8 ppm, implying the potential for application of receptor R1 in environmental applications. © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.
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    Colorimetric anion sensors based on positional effect of nitro group for recognition of biologically relevant anions in organic and aqueous medium, insight real-life application and DFT studies
    (Elsevier B.V., 2018) Singh, A.; Sahoo, S.K.; Trivedi, D.R.
    A new six colorimetric receptors A1-A6 were designed and synthesized, characterized by typical common spectroscopic techniques like FT-IR, UV–Visible, 1H NMR, 13C NMR and ESI-MS. The receptor A1 and A2 exhibit a significant naked-eye response towards F? and AcO? ions in DMSO. Due to presences of the NO2 group at para and ortho position with extended ?-conjugation of naphthyl group carrying –OH as a binding site. Compared to receptor A2, A1 is extremely capable of detecting F? and AcO? ions present in the form of sodium salts in an aqueous medium. This is owed to the occurrence of –NO2 group at para position induced in increasing the acidity of –OH proton. Consequently, it easily gets deprotonated in aqueous media. The detection limit of receptor A1 was turned out to be 0.40 and 0.35 ppm for F? and AcO? ions which is beneath WHO permission level (1.0 ppm). Receptor A1 shows a solitary property of solvatochromism in different aprotic solvents in presence of AcO? ion. Receptor A1 depicts high selectivity towards AcO? ion in DMSO: HEPES buffer (9:1, v/v). Receptor A1 proved itself for real life application by detecting anion in solution and solid state. The binding mechanism of receptor A1 with AcO? and F? ions was monitored from 1HNMR titration and DFT study. © 2017 Elsevier B.V.
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    Acetaminophen micropollutant: Historical and current occurrences, toxicity, removal strategies and transformation pathways in different environments
    (Elsevier Ltd, 2019) Vo, H.N.; Le, G.K.; Nguyen, T.M.; Bui, X.-T.; Nguyen, K.H.; Rene, E.R.; Vo, T.D.H.; Cao Ngoc, N.-D.; Mohan, R.
    Acetaminophen (ACT) is commonly used as a counter painkiller and nowadays, it is increasingly present in the natural water environment. Although its concentrations are usually at the ppt to ppm levels, ACT can transform into various intermediates depending on the environmental conditions. Due to the complexity of the ACT degradation products and the intermediates, it poses a major challenge for monitoring, detection and to propose adequate treatment technologies. The main objectives of this review study were to assess (i) the occurrences and toxicities, (2) the removal technologies and (3) the transformation pathways and intermediates of ACT in four environmental compartments namely wastewater, surface water, ground water, and soil/sediments. Based on the review, it was observed that the ACT concentrations in wastewater can reach up to several hundreds of ppb. Amongst the different countries, China and the USA showed the highest ACT concentration in wastewater (?300 ?g/L), with a very high detection frequency (81–100%). Concerning surface water, the ACT concentrations were found to be at the ppt level. Some regions in France, Spain, Germany, Korea, USA, and UK comply with the recommended ACT concentration for drinking water (71 ng/L). Notably, ACT can transform and degrade into various metabolites such as aromatic derivatives or organic acids. Some of them (e.g., hydroquinone and benzoquinone) are toxic to human and other life forms. Thus, in water and wastewater treatment plants, tertiary treatment systems such as advanced oxidation, membrane separation, and hybrid processes should be used to remove the toxic metabolites of ACT. © 2019 Elsevier Ltd
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    Design and synthesis new colorimetric receptors for naked-eye detection of biologically important fluoride and acetate anions in organic and arsenite in aqueous medium based on ICT mechanism: DFT study and test strip application
    (Elsevier B.V., 2020) Singh, A.; Mohan, M.; Trivedi, D.R.
    Novel three colorimetric anion receptors R1, R2 and R3 have been designed and synthesized via condensation reaction and characterized using IR, MS, and NMR spectroscopic techniques. Anion sensing properties were studied using colorimetric, UV–vis titration, 1H NMR titration, and Cyclic Voltammetric Studies. Comparing the UV–visible titration data of the receptors R1 and R2, R2 showed high redshift (??max) in the mixed competitive solution (DMSO: H2O, 9: 1; v/v) of about 155 nm, 157 nm, 169 nm for Na+F?, Na+AcO?, and Na+AsO2 ? ions with LOD of 0.23 ppm, 0.18 ppm, and 0.30 ppm, respectively. The observed spectral change of receptor R2 is due to the anion-induced deprotonation of the OH proton, which is confirmed by UV–vis titration, 1HNMR titration, and cyclic voltammetric studies. Theoretical studies via DFT calculation were carried for R1 and R2 to optimize the structure and to explain the anion-binding mechanism. The application of designed receptor R2 was successfully demonstrated for the detection of F? and AsO2 ? ions using a test strip. The receptors R1 and R2 proved itself to be potentially useful for real-life application by sensing F? and AcO? ions in real samples like toothpaste, mouthwash, vinegar and seawater in a complete aqueous medium. © 2019 Elsevier B.V.
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    Design and synthesis of malonohydrazide based colorimetric receptors for discrimination of maleate over fumarate and detection of F?, AcO? and AsO2 ? ions
    (Elsevier B.V., 2020) Singh, A.; Mohan, M.; Trivedi, D.R.
    In this study, we have designed and synthesized two new organic receptors R1 and R2 based on malonohydrazide for the recognition of biologically important anions. The receptor R1 capable of colorimetric discrimination of maleate over fumarate ion, exhibit significant color change from pale yellow to wine red due to intermolecular hydrogen bond between the R1 and maleate ion, supported by 1HNMR titration, where the peak at ?12.0 ppm attributed to the NH proton experiences a downfield shift upon binding with maleate ion. Receptor R1, equipped with two electron-withdrawing [sbnd]NO2 moieties as the chromogenic signaling unit enhance the hydrogen bonding tendency and acidity, and thus when comparing with receptor R2, R1 displayed substantial higher redshift (??max) of 148 nm, 143 nm, and 140 nm towards F?, AcO?, and maleate anion in the DMSO. In addition, the synthesized receptors R1 and R2 are able to detect F?, AcO?, and AsO2 ? ions as their sodium salts in an aqueous solution with visual color change. Receptor R1 exhibit electrochemical response towards F? and AcO? ions. The receptors R1 and R2 are successfully applied for quantitative detection of F? ion in the toothpaste solution in an aqueous medium. Additionally, R1 and R2 exhibit fluorescence enhancement towards F? and AcO? ions in the DMSO. As well, R1 and R2 demonstrate to be potentially useful colorimetric chemosensor for sensing maleate ion using the test strip. The theoretical calculation based on TD-DFT corroborates well with the experimental results of the receptors R1 and R2 with fluoride, acetate and maleate. © 2019 Elsevier B.V.
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    Real-time interrogation of fiber optic biosensor using TiO2coated etched long-period grating
    (American Institute of Physics Inc., 2020) Singh, M.; Raghuwanshi, S.K.
    In this work, a TiO2 coated etched long-period grating (e-LPG) fiber optic biosensor is developed for the detection of Escherichia coli (E. coli) bacteria in food items. Label-free Escherichia coli bacteria monitoring is done over the detection range of 0 cfu/ml-50 cfu/ml using an advanced spectral interrogation mechanism. The thin film deposition of 40 nm TiO2 over the e-LPG is confirmed by the microscopy method, such as scanning electron microscopy. In our proposed biosensor design, T4-bacteriophage is covalently immobilized over the TiO2 coated fiber surface. This biosensor system has reached sensitivity at 2.55 nm/RIU. Our experiments confirm the resolution and the limit of detection (3?/S) of 0.0039 RIU and 10.05 ppm, respectively. The proposed biosensor with enhanced sensitivity is suitable for monitoring harmful pathogens/infectious agents in various food products. © 2020 Author(s).
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    Colorimetric chemosensors for the selective detection of arsenite over arsenate anions in aqueous medium: Application in environmental water samples and DFT studies
    (Elsevier B.V., 2023) K, K.; Nityananda Shetty, A.N.; Trivedi, D.R.
    Novel organic receptors N3R1- N3R3 were developed for the selective colorimetric recognition of arsenite ions in the organo-aqueous media. In the 50% aq. acetonitrile media and 70% aq. DMSO media, receptors N3R2 and N3R3 showed specific sensitivity and selectivity towards arsenite anions over arsenate anions. Receptor N3R1 showed discriminating recognition of arsenite in the 40% aq. DMSO medium. All three receptors formed a 1:1 complex with arsenite and stable for a pH range of 6–12. The receptors N3R2 and N3R3 achieved a detection limit of 0.008 ppm (8 ppb) and 0.0246 ppm, respectively, for arsenite. Initial hydrogen bonding on binding with the arsenite followed by the deprotonation mechanism was well supported by the UV–Vis titration, 1H- NMR titration, electrochemical studies, and the DFT studies. Colorimetric test strips were fabricated using N3R1- N3R3 for the on-site detection of arsenite anion. The receptors are also employed for sensing arsenite ions in various environmental water samples with high accuracy. © 2023 Elsevier B.V.
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    Colorimetric differentiation of arsenite and arsenate anions using a bithiophene sensor with two binding sites: DFT studies and application in food and water samples
    (Royal Society of Chemistry, 2024) K, K.; Nityananda Shetty, A.N.; Trivedi, D.R.
    Chemosensor N7R1 with two acidic binding sites was synthesized, and the ability of the sensor to differentiate arsenite and arsenate in the organo-aqueous medium was evaluated using colorimetric sensing methods. N7R1 distinguished arsenite with a peacock blue color and arsenate with a pale green color in a DMSO/H2O (9 : 1, v/v) solvent mixture. The specific selectivity for arsenite was achieved in DMSO/H2O (7 : 3, v/v). The sensor demonstrated stability over a pH range of 5 to 12. The computed high binding constant of 9.3176 × 1011 M−2 and a lower detection limit of 11.48 ppb for arsenite exposed the chemosensor's higher potential for arsenite detection. The binding mechanism with a 1 : 2 binding process is confirmed using UV-Vis and 1H NMR titrations, electrochemical studies, mass spectral analysis and DFT calculations. Practical applications were demonstrated by utilizing test strips and molecular logic gates. Chemosensor N7R1 successfully detected arsenite in real water samples, as well as honey and milk samples. © 2024 The Royal Society of Chemistry.