Faculty Publications
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Item Effect of pH on the geotechnical properties of laterite(2006) Sunil, B.M.; Nayak, S.; Shrihari, S.Environmental Geotechnology has emerged as an interdisciplinary science, aiming and forecasting, analyzing and solving the geotechnical problems involving the influence of environmental factors. Lateritic soil of west coast region of India was studied to investigate the effect of soaking on the engineering properties and chemical characteristics of soil, soaked in different pH solutions (pH = 5.0, pH = 7.0, pH = 8.0). 12 N hydrochloric acid and 15 M ammonia solution were used to monitor the pH of the solution for about ninety days. Results showed that the pH of the solution has strong influence on the chemical characteristics of lateritic soil. The engineering properties of soil are altered when compared with the initial characteristics of the soil. The reason for this observed behavior of the soil is addressed in this paper. © 2006 Elsevier B.V. All rights reserved.Item A rapid extractive spectrophotometric determination of copper(II) in environmental samples, alloys, complexes and pharmaceutical samples using 4-N,N(dimethyl)amino]benzaldehyde thiosemicarbazone(2011) Karthikeyan, J.; Naik, P.P.; Nityananda Shetty, A.N.4-[N,N-(Dimethyl)amino]benzaldehyde thiosemicarbazone (DMABT) is proposed as an analytical reagent for the extractive spectrophotometric determination of copper(II). DMABT forms yellow colored complex with copper(II) in the pH range 4.4-5.4. Beer's law is obeyed in the concentration range up to 4.7 ?g mL -1. The optimum concentration range for minimum photometric error as determined by Ringbom plot method is 1.2-3.8 ?g mL-1. The yellowish Cu(II)-DMABT complex shows a maximum absorbance at 420 nm, with molar absorptivity of 1.72 × 104dm3 mol-1 cm-1 and Sandell's sensitivity of the complex obtained from Beer's data is 0.0036 ?g cm-2. The composition of the Cu(II)-DMABT complex is found to be 1:2 (M/L). The interference of various cations and anions in the method were studied. Thus the method can be employed for the determination of trace amount of copper(II) in water, alloys and other natural samples of significant importance. © 2010 Springer Science+Business Media B.V.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 Inhibitory and stimulating effect of single and multi-metal ions on hexavalent chromium reduction by Acinetobacter sp. Cr-B2(Kluwer Academic Publishers, 2014) Hora, A.; Shetty K, V.Potential application of chromium reducing bacteria for industrial scale wastewater treatment demands that effect of presence of other metal ions on rate of Cr(VI) reduction be investigated, as industrial wastewaters contain many toxic metal ions. In the current study, the effect of different heavy metal ions (nickel, zinc, cadmium, copper, lead, iron) on chromium reduction by a novel strain of Acinetobacter sp. Cr-B2 that shows high tolerance up to 1,100 mg/L and high Cr(VI) reducing capacity was investigated. The alteration in Cr(VI) reduction capacity of Cr-B2 was studied both in presence of individual metal ions and in the presence of multi-metal ions at different concentrations. The study showed that the Cr(VI) reduction rates decreased in presence of Ni2+, Zn2+ and Cd2+ when present individually. Pb2+ at lower concentration did not show significant effect while Cu2+ and Fe3+ stimulated the rate of Cr(VI) reduction. In the studies on multi-metal ions, it was observed that in presence of Cu2+ and Fe3+, the inhibiting effect of Ni2+, Zn2+, Cd2+ and Pb2+ on Cr(VI) reduction was reduced. Each of these metals affect the overall rate of Cr(VI) reduction by Cr-B2. This work highlights the need to consider the presence of other heavy metal ions in wastewater when assessing the bioreduction of Cr(VI) and while designing the bioreactors for the purpose, as rate of reduction is altered by their presence. © 2014, Springer Science+Business Media Dordrecht.Item Evaluation of pyrolyzed areca husk as a potential adsorbent for the removal of Fe2+ ions from aqueous solutions(Academic Press, 2019) Sheeka Subramani, B.; Shrihari, S.; Manu, B.; BabuNarayan, K.S.[No abstract available]Item Solvent selection for highly reproducible carbon-based mixed-cation hybrid lead halide perovskite solar cells via adduct approach(Elsevier Ltd, 2020) Keremane, K.S.; Prathapani, S.; Haur, L.J.; Damodaran, D.; Vasudeva Adhikari, A.V.; Priyadarshi, A.; Mhaisalkar, S.G.The major problem identified in carbon-based mixed cation perovskite solar cells (PSCs) is the selection of a suitable solvent for single-step solution-processed perovskite deposition in order to promote their scalable production. Herein we report a detailed study on the selection of appropriate solvent for the one-step deposition of cesium-formamidinium lead iodide (Cs0.1FA0.9PbI3) perovskite via Lewis acid-base adduct approach for fully printable mesoporous PSCs with mesoporous TiO2/ZrO2/C architecture. Highly reproducible Cs0.1FA0.9PbI3 solar cells were fabricated via adducts of PbI2 with eco-friendly dimethyl sulfoxide (DMSO). The best cells fabricated with the above approach yielded a photoconversion efficiency (PCE) of 12.33% for a small area device (active area: 0.09 cm2) and 10.1% for a large area device (active area 0.7cm2). The average power conversion efficiency for 62 PSCs was found to be 10.5% under an AM 1.5G illumination. Finally, the mixed cation perovskite in carbon architecture using the Lewis acid-base adduct approach is remarkably stable, with less than 1% change from the initial PCE after 1800h of storage under dark ambient conditions (25 °C, 60–70% RH). © 2020 International Solar Energy SocietyItem Enhanced Recovery of Iron Values from Low-Grade Ores and Tailings through Reverse Cationic Flotation(World Researchers Associations, 2025) Varma, R.M.; Harsha, V.; Reddy, B.R.R.; Shanmugam, S.B.; Harish, H.India is well-known for its rich deposits of high-quality hematite ores, making it a vital player in the global market. As the availability of high-grade iron ores diminishes, the need to process low-grade ores, fines and slimes through beneficiation is becoming increasingly important to meet market requirements. The creation of fines and slimes leads to a mineral loss of about 20 to 25% of the overall mineral value during processing. This research investigates the beneficiation of iron ore tailings using reverse cationic flotation, with Sokem reagent acting as a collector and starch serving as a depressant. A series of comparative assessments involving magnetic separation and gravity separation were performed. An initial mineralogical examination showed that hematite and goethite were the main iron-bearing minerals, accompanied by quartz and kaolinite as significant gangue materials. The selective flocculation technique proved effective, enhancing the iron grade from 41.05% to 57.03% Fe, with a recovery rate of 47.35%. After desliming, the outcomes improved further, yielding 58.25% Fe and a recovery of 29.00%. These results underline the potential for successful beneficiation of iron ore tailings, offering valuable insights for enhancing the recovery of high-grade iron from low-grade ores and reducing mineral losses during processing. © 2025, World Researchers Associations. All rights reserved.Item Coconut shell biochar–Bacillus cereus DKBovi-5 based biocomposite as a sustainable additive for cement mortar: Effect of pyrolysis temperature on characterization, strength, hydration, and healing(Elsevier B.V., 2025) Anoop, P.P.; Palanisamy, T.Although biochar–bacteria composites have been explored for self-healing in cementitious materials, the influence of pyrolysis temperature on microbial compatibility and healing performance has been insufficiently investigated. This study addresses this gap by examining how pyrolysis temperature affects the physicochemical properties of coconut shell biochar and its effectiveness as a microbial carrier in mortar. Biochar produced at 300 °C, 400 °C, and 500 °C was characterized, and Bacillus cereus DKBovi-5 was immobilized onto it to form biocomposites. The biocomposites were incorporated into mortar to evaluate mechanical, microstructural, and crack healing performances. Characterization of biochar showed enhanced crystallinity at 500 °C as indicated by XRD, development of primary and secondary pores confirmed by FESEM, and increased micronutrient concentrations due to thermal enrichment observed through ICP-MS. Compressive strength restoration increased from 80.21 % to 91.23 % between 300 °C and 500 °C temperatures. TGA analysis, interpreted using Bhatty's method, indicated an increase in the degree of hydration from 61.65 % to 65.33 %. Rietveld refinement of XRD data revealed a rise in calcite content from 24 % to 51 %. FESEM imaging confirmed the deposition of hydration products within the biochar pores. Healing evaluation showed closure of cracks up to 0.762 mm and 0.920 mm in mortars with 300 °C and 500 °C biocomposites, respectively, corresponding to healed areas of 92.49 % and 100 %. The healed products in all biocomposites were confirmed as calcite through FESEM-EDS and XRD analyses. Optimized pyrolysis at 500 °C yielded a biocomposite with superior microbial healing performance, establishing its suitability as a self-healing admixture in bio-mortar applications. © 2025 Elsevier B.V.Item Rotational Flexibility in Dication Drives Ambient Temperature Ferroelectricity in an Organic–Inorganic Hybrid Halide(John Wiley and Sons Inc, 2025) Hassan, N.; Panday, R.; Chandru, P.G.; Ananthram, K.S.; Jose, T.M.; Bhoi, U.; Sieradzki, A.; Zar?ba, J.K.; Boomishankar, R.; Tarafder, K.; Ballav, N.Organic–inorganic hybrid halides (OIHHs) have gained attention as potential ferroelectric materials due to structure-property synergy of the organic and inorganic constituents. This study introduces an unusual Ag(I)-based ternary OIHH, (4,4?-bpy)Ag2Br4, featuring rotational flexibility in the organic dication to induce asymmetry into the structure. The compound crystallizes in a monoclinic crystal system with a non-centrosymmetric polar P21 space group at room-temperature and undergoes a structural phase transition to a centrosymmetric phase (P21/c) at Curie temperature (Tc) of 330 K which was further supported by differential scanning calorimetry (DSC), second harmonic generation (SHG) signals, dielectric anomaly, current-voltage (I–V) profiles, and X-ray photoelectron spectroscopy (XPS) data. Ferroelectricity is confirmed through polarization–electric field (P–E) hysteresis loops and piezoresponse force microscopy (PFM), exhibiting switchable polar domains. Density functional theory (DFT) calculations revealed electronic structures of the ferroelectric and paraelectric phases, identified the (?-AgBr2)nn? inorganic anionic chain contributing to the net polarization, and in general, complemented the experimental results. Comparative studies with structurally analogous Ag(I)-based OIHHs lacking dication rotational freedom endorse the critical role of organic flexibility in driving ferroelectricity. This study provides insights into the role of organic dications in controlling ferroelectric behavior and offers a promising pathway for developing coinage metal-based OIHH ferroelectric materials. © 2025 Wiley-VCH GmbH.