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Chakravarti, S. K.
- Multiple Equilibrium in Humic Acid-Metal System: Determination of Successive Stability Constants of Cu(II) and Ca-Complexes with the Aid of Ion Selective Electrodes
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1 Department of Chemistry, University of North Bengal, Derjeeling, IN
1 Department of Chemistry, University of North Bengal, Derjeeling, IN
Source
Journal of Surface Science and Technology, Vol 1, No 1 (1985), Pagination: 63-68Abstract
Multiple equilibria in humic acid-Cu(II) and humic acid-Ca systems in 0.1 N KNO3, have been studied at different pH's using ion selective electrodes. At pH 4.8, Ca has been found to form only MA+, where as Cu(II) forms both MA+ and MA2, complexes. Significant negative co-operative effect has been observed in all the systems studied, which is more prominent in Ca-humic acid complex at low pH. Logarithms of intrinsic stability constant, K0, ranged from 7.5 to 8.5 for Cu(II) and 5.8 to 6.0 for Ca-complexes. Results are compared with those for the two synthetic model humic acid-metal systems.- Determination of Limit of Solubilization of a Series of Thiazine Dyes in Different Surfactants
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Authors
Affiliations
1 Department of Chemistry, North Bengal University, Darjeeling-734430, IN
1 Department of Chemistry, North Bengal University, Darjeeling-734430, IN
Source
Journal of Surface Science and Technology, Vol 3, No 1 (1987), Pagination: 67-70Abstract
Tha solubilizations of a series of thiazine dyes have been studied with three anionic surfactants having different hydrocarbon chain. The quality of the solubilized dye is found to decrease with the increase of chain length of the surfactants and their order in respect of solubilization is sodium dodecyl sulfate (NaDS) > sodium heptadecyl sulfate (NaHS) > Dodecyl benzene sodium sulfonate (DBSS). In aqueous medium the nature of the dyes, their structure and size are important parameters to influence the behaviour of the solubilizers.Keywords
Limit of Solubilization, Thiazine Dyes, Micelles.- Interaction of some New Thiazine Dyes with Polyacrylic Acid in Presence of Alkali Halides And Surfactants
Abstract Views :244 |
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Authors
Affiliations
1 Department of Chemistry, North Bengal University, Darjeeling-734430, IN
1 Department of Chemistry, North Bengal University, Darjeeling-734430, IN
Source
Journal of Surface Science and Technology, Vol 3, No 1 (1987), Pagination: 75-77Abstract
The effect of alkali metal chlorides on the metachromatic behaviour of Trimethyl propyl thionine (TMPT) and Diethyl methyl propyl thionine (DEMPT) as induced by polyacrylic acid (PAA) was investigated spectrophotometrically. The size of hydrated ion and hydrophobicity of substituents were not found to be significant factors to influence the above behaviour. The alkali metal cation affinity sequence was observed as Li+ > K+ > Cs+ for polyacrylic acid exchangers. A large amount of destruction of metachromasy was observed in PAA-TMPT and PAA-DEMPT on addition of small amounts of cetyl trimethyl ammonium chloride (CTACI) and Decyl trimethyl ammonium chloride (DTACI) and their order CTACI > DTACI.Keywords
Polyacrylic Acid Metachromasy, Micelles, Thiazine Dyes, TMPT & DEMPT, Hydrophobicity.- Exchange Behaviour of Coen33+ on Soil and Pest Fulvic Acid
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Authors
Affiliations
1 Department of Chemistry, University of North Bengal, Dist. Darjeeling, West Bengal, 734 430, IN
1 Department of Chemistry, University of North Bengal, Dist. Darjeeling, West Bengal, 734 430, IN
Source
Journal of Surface Science and Technology, Vol 3, No 2 (1987), Pagination: 143-149Abstract
The study of the exchange pattern on soil and peat fulvic acids (SFA and PFA) reveals that the uptake of Coen33+ increases with increase in pH but, after reaching a maximum at pH 6.5 it starts decreasing, and finally attains a steady value. The release isotherms indicate the following order of reactivity: Li ≈ Na < K < Rb < Cs < H for monovalent cations, (the reversal of exchangeability for Li and Na taking place at lower concentration) and Mg < Ca < Sr < Ba for the divalent cations. However, for organic cations the order of exchangeability is (C2H5)4N > (CH3)4N at lower concentration but the reverse is observed at higher concentration. The release isotherms with monovalent cations distinctly display that the exchange processes occur in three stages. Kielland's equation has been harnessed to find out the thermodynamic equilibrium constants and Gibbs free energy change for exchange reactions involving bivalent cations. It is found that Log of corrected selectivity coefficients or thermodynamic equilibrium constants, when plotted separately against hydrated ionic radii and the reciprocal of Debye-Huckel parameter a0, the relative affinities of the counter ions for the exchange substrates are much better correlated with a0 rather than with hydrated ionic radii.Keywords
Fulvic Acid, Coen3, Uptake, Exchangeability, Selectivity Coefficients, Thermodynamic Equilibrium Constant.- 2020 Conference Announcement:Nanotech Forum 2020
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Authors
Affiliations
1 SK Chakravarti, Professor, Physics, National Institute of Technology
1 SK Chakravarti, Professor, Physics, National Institute of Technology