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    A simple, rapid, selective and sensitive spectrophotometric method for the determination of platinum has been proposed based on the colour reaction between platinum(IV) and piperonal thiosemicarbazone (PATS) in 0.008 - 0. 032 M sulphuric acid medium. The greenish yellow complex has an absorption maximum at 360 nm. Beer's law is obeyed upto 6.5 ppm of Pt and the optimum concentration range is 1 - 5.1 ppm of Pt. The molar absorptivity and Sandell's sensitivity are 3. 239 x 104 1 mol-1 cm-1 and 0.006 ?g cm-2, respectively. The optimum conditions for complete colour development have been investigated by studying parameters like effect of medium, acidity, reagent concentration, time period and effect of diverse ions. The method is used for the determination of platinum in hydrogenation catalysts and platinum complexes.
    (Rapid spectrophotometric determination of platinum (IV) using piperonal thiosemicarbazone) Shetty, P.; Nityananda Shetty, A.N.; Gadag, R.V.
    2002
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    Spectrophotometric determination of platinum(IV) in alloys, complexes, environmental, and pharmaceutical samples using 4-[N,N-(diethyl)amino] benzaldehyde thiosemicarbazone
    (2010) Naik, P.P.; Karthikeyan, J.; Nityananda Shetty, A.N.
    4-[N,N-(Diethyl)amino] benzaldehyde thiosemicarbazone (DEABT) is proposed as an analytical reagent for the spectrophotometric determination of platinum(IV). The DEABT forms 1:2 yellow complex with Pt(IV), which is sparingly soluble in water and completely soluble in water-ethanol-DMF medium. The Pt(IV)-DEABT complex shows maximum absorbance at 405 nm. Beer's law is valid up to 7.80 ?g cm-3, and optimum concentration range for the determination of platinum(IV) is 0.48-7.02 ?g cm-3. The molar absorptivity and Sandell's sensitivity of the method are found to be 1.755 × 104 dm3 mol-1 cm-1 and 0.0012 ?g cm-2, respectively. The relative error and coefficient of variation (n=6) for the method does not exceed ±0.43% and 0.35%, respectively. Since the method tolerates a number of metal ions commonly associated with platinum, it can be employed for the determination of platinum in environmental samples, pharmaceutical samples, alloys, catalysts, and complexes. The method is rapid as the Pt(IV)-DEABT complex is soluble in water-ethanol-DMF medium and not requiring any time consuming extraction method for the complex. © 2010 Springer Science+Business Media B.V.
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    Synthesis and biological evaluation of aminoketones
    (2010) Sankappa Rai, U.; Isloor, A.M.; Shetty, P.; Isloor, N.; Malladi, S.; Fun, H.-K.
    A three-component Mannich reaction of different ketones with aromatic aldehydes and different amines in microwave irradiation under solvent free condition afforded corresponding ?-amino carbonyl compounds in excellent yields. This method proved as a novel and improved modification of the reported three-component Mannich reaction in terms of milder reaction conditions, reaction times, clean reaction profiles, very small quantity of catalyst and simple workup procedure. Newly synthesized ?-aminoketones were characterized by spectral studies. Structure of compound 4a was also confirmed by single-crystal X-ray analysis. All the compounds were screened for their antimicrobial activity by MIC method. Few of the molecules were found to be biologically potent. © 2010 Elsevier Masson SAS. All rights reserved.
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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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    Synthesis of worm-shaped carbon nanofibers over a sodium chloride support
    (2012) Ravindra, R.; Badekai Ramachandra, B.R.
    Worm-shaped carbon nanofibers (WCNFs) were synthesized in bulk by chemical vapour deposition at 680 °C using iron carboxylate as catalyst precursors and sodium chloride as catalyst support. The products were characterized by scanning electron microscopy, transmission electron microscopy, Raman spectroscopy and X-ray diffraction method. The purity of the purified products was determined by thermal analysis. TheWCNFyield was 6700% relative to catalyst. The simplicity, environmental friendliness and use of easily available low-cost precursors are the advantage of this synthesis technique. © Springer Science+Business Media B.V. 2012.
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    A catalyst- and solvent-free three-component reaction for the regioselective one-pot access to polyfunctionalized pyrroles
    (2013) Bhat, S.I.; Trivedi, D.R.
    A facile method for the regioselective synthesis of tetrasubstituted pyrroles, from readily accessible 1,3-dicarbonyls, benzoin derivatives and ammonium acetate, has been developed. The one-pot three-component reactions were performed to afford tetrasubstituted pyrroles under solvent- and catalyst-free conditions. © 2013 Elsevier Ltd. All rights reserved.
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    Palladium complex in a room temperature ionic liquid: A convenient recyclable reagent for catalytic oxidation
    (Taylor and Francis Ltd., 2014) Dileep, R.; Badekai Ramachandra, B.; Suresha Kumara, T.H.S.
    Palladium (Pd)-catalyzed carbonylation of alcohols proceeds in ionic liquid (IL) media (1-ethyl-3-methylimidazolium hexafluorophosphate). Carbonylation of primary/secondary alcohols to aldehydes/ketones was greatly accelerated by the use of a Pd-based catalyst in the presence of NaOCl as an oxidant. The catalyst was more easier to recycle in the IL [Emim]PF6 with an equal-proportioned CH2Cl2 than in the single CH2Cl2 or IL. © 2014 The Author(s). Published by Taylor & Francis.
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    Conversion of waste polypropylene to liquid fuel using acid-activated kaolin
    (SAGE Publications Ltd, 2014) Panda, A.K.; Singh, R.K.
    Waste polypropylene was subjected to thermal degradation in the presence of kaolin and acid-treated kaolin, with different catalyst-to-plastics ratios, in a semi-batch reactor at a temperature range of 400-550°C to obtain optimized process conditions for the production of liquid fuels. The effects of process temperature, catalyst and feed composition on yield and quality of the oil were determined. For a thermal decomposition reaction at up to 450°C, the major product is volatile oil; and the major products at a higher temperature (475-550°C) are either viscous liquid or wax. The highest yield of condensed fraction in the thermal reaction is 82.85% by weight at 500°C. Use of kaolin and acid-treated kaolin as a catalyst decreased the reaction time and increased the yield of liquid fraction. The major product of catalysed degradation at all temperatures is highly volatile liquid oil. The maximum oil yield using kaolin and acidtreated kaolin is 87.5% and 92%, respectively, at 500°C. The oil obtained was characterized using GC-MS for its composition and different fuel properties by IS methods. © The Author(s) 2014.
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    Novel one-pot green synthesis of graphene in aqueous medium under microwave irradiation using a regenerative catalyst and the study of its electrochemical properties
    (Royal Society of Chemistry, 2015) Subramanya, B.; Bhat, D.
    In this work we report an economic, eco-friendly, high yielding and facile one-pot method for the large scale synthesis of few layer graphene (FLG) nanosheets directly from graphite in aqueous medium using a regenerative catalyst, sodium tungstate. This method is fast and makes use of environmental friendly chemicals and microwave radiation. The as-synthesized FLG nanosheets are characterized by field emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. Raman analysis indicates that the as-synthesized graphene is bilayered with a smaller domain size of 3.9 nm which is responsible for a higher specific surface area of FLG nanosheets (1103.62 m2 g-1). Moreover, XPS analysis of FLG nanosheets shows a high C:O ratio (?9.6) which is the best among the graphene prepared from green chemicals. The electrochemical performance of as-synthesized FLG nanosheets is analysed by cyclic voltammetry (CV), chronopotentiometry and electrochemical impedance spectroscopy (EIS) in neat 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIMBF4) electrolyte. The superior capacitive performance with large capacitance (219 F g-1), high energy density (83.56 W h kg-1) and excellent cyclability (3000 cycles) exhibited by these graphene nanosheets make them an excellent candidate for supercapacitor material. © The Royal Society of Chemistry and the Centre National de la Recherche Scientifique 2015.
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    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.