96 research outputs found

    A novel and disposable amperometric hydrazine sensor based on polydimethyldiallylamine stabilized copper(II)hexacyanoferrate nanocubes modified screen-printed carbon electrode

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    © 2017 The Authors. A cubic shaped copper(II)hexacyanoferrate was prepared by wet chemical method by mixing an equimolar concentration of CuCl 2 with K 3 [Fe(CN) 6 ] 2 in the presence of poly(diallyldimethylammonium chloride) (PDDA). The X-ray diffraction, field emission scanning electron microscopy, elementa l analysis, Fourier transform infrared spectroscopy and thermal gravimetric analysis were used to confirm the formation of PDDA stabilized copper(II)hexacyanoferrate nanocubes (PDDA@copper(II)hexacyanoferrate nanocubes). The electrocatalytic behavior of the PDDA@copper(II)hexacyanoferrate nanocubes modified screenprinted carbon electrode (SPCE) towards electrochemical oxidation of hydrazine was studied by cyclic voltammetry (CV). The CV results revealed that PDDA@copper(II)hexacyanoferrate nanocubes modified SPCE exhibits an enhanced electrocatalytic activity and lower oxidation potential towards hydrazine than bare SPCE. Under optimized conditions, amperometric i-t method was used for the determination hydrazine, and PDDA@copper(II)hexacyanoferrate nanocubes modified SPCE can able to detect hydrazine in the linear concentration ranges from 0.03 to 533.6 μM with a detection limit of 10 nM. The PDDA@copper(II)hexacyanoferrate nanocubes modified SPCE is highly selective in the presence of potentially active interfering compounds including high concentration of ascorbic acid. In addition, the developed hydrazine sensor shows acceptable practicality with excellent long-term stability towards the detection of hydrazine

    A robust nitrobenzene electrochemical sensor based on chitin hydrogel entrapped graphite composite

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    © 2017 An amperometric nitrobenzene (NB) sensor has been developed based on a glassy carbon electrode (GCE) modified with the composite of chitin hydrogel stabilized graphite (GR-CHI) composite. The physicochemical characterization confirmed the formation of GR-CHI composite and was formed by the strong interaction between GR and CHI. Furthermore, GR-CHI composite modified GCE was used to study the electrochemical reduction behavior of NB by cyclic voltammetry (CV) and compared with GR and CHI modified GCEs. The CV results confirmed that GR-CHI composite modified electrode has high catalytic ability and lower reduction potential toward NB than other modified electrodes due to the combined unique properties of exfoliated GR and CHI. The GR-CHI composite modified electrode can be able to detect the NB in the linear response range from 0.1 to 594.6 µM with the lower detection limit of 37 nM by amperometric i–t method. The selectivity of the sensor is evaluated in the presence of nitroaromatic, biologically active and dihydroxybenzene compounds. The sensor shows appropriate practicality and good repeatability toward detection of NB in lab water samples

    Transcriptional recapitulation and subversion of embryonic colon development by mouse colon tumor models and human colon cancer

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    Colon tumors from four independent mouse models and 100 human colorectal cancers all exhibited striking recapitulation of embryonic colon gene expression from embryonic days 13.5-18.5

    Influence of aluminium sources on the synthesis and catalytic activity of mesoporous AlMCM-41 molecular sieves

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    Mesoporous AIMCM-41 molecular sieves were synthesized using various aluminium sources, viz., sodium aluminate, aluminium sulphate, aluminium isopropoxide and pseudoboehmite. The influence of different aluminium sources on the framework substitution of aluminium as well as on the catalytic properties of t-butylation of phenol was studied. Among the aluminium sources, the use of sodium aluminate for the AIMCM-41 synthesis showed maximum incorporation of aluminium in the framework. Further, the catalyst also showed good catalytic activity for the chosen reaction. (C) 2000 Elsevier Science B.V. All rights reserved

    Acid sites distribution and their influence on the catalytic properties of mesoporous H-AlMCM-41 and H-FeMCM-41

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    The acid properties of mesoporous H-AlMCM-41 and H-FeMCM-41 catalysts were studied by temperature programmed desorption of ammonia. The results suggest the existence of four different types of acid sites. They are assigned to: (i) weak acid sites due to surface/terminal hydroxyl groups; (ii) moderate structural (Bronsted) acid sites associated with symmetrical tetrahedral AI(III) or Fe(III); (iii) strong structural (Bronsted) acid sites fi om a highly distorted tetrahedral AI(III) or Fe(III) and (iv) Lewis acid sites arising from tricoordinated Al(III) or Fe(III) in the framework. The t-butylation reaction of phenol over H-AlMCM-41 and H-FeMCM-41 showed high substrate conversion in the case of the former than the fatter. This could be attributed to presence of large excess of type (ii) and type (iii) acid sites in H-AlMCM-41

    Tertiary butylation of phenol over mesoporous H-FeMCM-41

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    Trivalent-iron-substituted mesoporous molecular sieve catalysts (FeMCM-41) were synthesized hydrothermally and characterized systematically by various analytical and spectroscopic techniques. Temperature-programmed desorption studies of ammonia of the protonated catalyst (H-FeMCM-41) indicate a broad distribution of the acid sites. Vapour-phase alkylation of phenol with t-butyl alcohol (2-methyl-2-propanol) was carried out over this solid acid catalyst and p-t-butyl phenol was obtained as the major product with high selectivity
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