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1.
Priya Jaiswal Vijaykumar Ijeri Ashwini Srivastava 《Journal of inclusion phenomena and macrocyclic chemistry》2004,49(3-4):219-224
This paper is a report on the complexation studies of silverions with certain water soluble crown ethers viz., 15-crown-5,18-crown-6, cyclam, diaza 15-crown-5 and certain water insolublecrown ethers viz., benzo 15-crown-5, dibenzodiaza 15-crown-4,dibenzyldiaza 18-crown-6 in some nonionic surfactants viz.,polyoxyethylated alkyl phenol (TX 100), polyoxyethylene (20)sorbiton monolaurate (Tween 20), polyoxyethylene (20) sorbitonmonoleate (Tween 80) and polyoxyethylated glyco monolaurylether (Brij 35) by potentiometry. In addition, conductometry wasalso used to study the complexation of oxa crown ethers to comparethe results obtained by potentiometry, which were found to be ingood agreement with each other. The complexation studies indicate1:1 complex formation between the silver ion and macrocycle, thelogML n+ values being in the range 1 to 9. 相似文献
2.
B Ramachandra Reddy P Radhika J Rajesh Kumar D Neela Priya K Rajgopal 《Analytical sciences》2004,20(2):345-349
Cyanex 923 has been proposed as a sensitive analytical reagent for the direct extractive spectrophotometric determination of cobalt(II). Cobalt(II) forms a blue-colored complex with Cyanex 923 in the organic phase. The maximum absorbance of the complex is measured at 635 nm. Beer's law was obeyed in the range 58.9 - 589.0 microg of cobalt. The molar absorptivitiy and Sandell's sensitivity of the complex was calculated to be 6.79 x 10920 l mol(-1) cm(-1) and 0.088 microg cm(-2), respectively. The nature of the extracted species was found to be Co(SCN)2 x 2S. An excellent linearity with a correlation coefficient value of 0.999 was obtained for the Co(II)-Cyanex 923 complex. Stability and regeneration of the reagent (Cyanex 923) for reuse is the main advantage of the present method. The method was successfully applied to the determination of cobalt in synthetic mixtures and pharmaceutical samples was found to give values close to the actual ones. Standard alloy samples, such as high-speed tool BCS 484 and 485, have been tested for the determination of cobalt for the purpose of validating the present method. The results of the proposed method are comparable with atomic absorption spectrometry and were found to be in good agreement. 相似文献
3.
4.
Rajeev K. Thakur C. Villette J.M. Aubry G. Delaplace 《Colloids and surfaces. A, Physicochemical and engineering aspects》2007,310(1-3):55-61
Formulation–composition map is an interesting tool to predict the nature of an emulsion, stability, viscosity and nevertheless to decide the mixing protocol of its ingredients. Information based on optimum formulation (environmental conditions at which the affinity of an emulsifier for oil and for aqueous phase is same), which is depicted through hydrophilic–lipophilic deviation (HLD) concept, is necessary to make a formulation–composition map of an emulsion. In order to apply this concept in food emulsions, it is necessary to determine characteristic constants of each component of the system, i.e. the aqueous phase, the oil phase and the emulsifier at equilibrium. In this work formulation–composition map of a sunflower oil–water–lecithin system, based on the knowledge of phase behavior of lecithin at equilibrium and emulsification, was made. The shape of inversion line on formulation–composition map was not the classical stair type rather an almost vertical inversion line at water-fraction (fw) near 0.20 was observed. It was supposed to be linked to the viscosity of oil phase which was 50 times the viscosity of aqueous phase. Additionally, emulsions were of oil-in-water (O/W) type for fw higher than 0.20, but their viscosity and the drop size behavior with respect to salt concentration as formulation variable did not show the existence of transitional inversion line on formulation–composition map. Such map in advance can certainly facilitate the guidelines for dynamic emulsification. 相似文献
5.
A. N. Thakur 《Journal of Radioanalytical and Nuclear Chemistry》1997,215(2):161-167
Neutron induced -ray spectra from various geological samples were analyzed to evaluate the usefulness of continuum spectra in deriving the chemical composition information. A fast Fourier transform technique has been used to estimate the signal content of selected energy bands of the continuum spectra. Monte Carlo calculations have been performed using the major -ray energy sources (due to Fe, Ca, Si and Al) to generate the corresponding detected -ray spectra. The experimental spectra are compared to the simulated spectra to check the consistency of the signal distribution between the peak and the continuum. The continuum above and below a chosen -ray line is calculated to find what fraction of the lower energy continuum is due to that line. The accuracy of the relative elemental concentrations determined by this method is confirmed through comparison with laboratory elemental analysis of the samples. It is found that using the continuum could greatly increase the sensitivity and precision of the measurement of elemental concentrations determined from -ray spectra of thick target sources, for spectra having peaks of poor statistical significance. However, for thin target sources or spectra with very good statistics in their peaks, this method may not be very advantageous. 相似文献
6.
The extraction behaviour of thorium(IV) from aqueous nitric acid employing 3-phenyl-4-benzoyl-5-isoxazolone (HPBI) in the presence of tri-n-octyl phosphine oxide (TOPO) as well as tri-n-butyl phosphate (TBP) in xylene medium was investigated. The extraction constant (log k(ex)) for the binary organic phase species Th(PBI)(4) was determined to be 8.26 which is by far the largest amongst the corresponding values known for other beta-diketones. The overall extraction constant (log K) for the ternary species Th(PBI)(4) TBP and Th(PBI)(4).2TOPO were estimated to be 14.96 and 20.96 respectively. An inverse correlation of the adduct formation constant (log K(s)) with the pK(a) of the beta-diketones, 2-thenoyltrifluoroacetone, 1-phenyl-3-methyl-4-benzoyl-5-pyrazolone and HPBI, was observed. The steric as well as the electronic effects of adduct formation have been discussed. Analytical application of HPBI for the separation of (234)Th radiotracer from natural uranium (99.3% (238)U) has been suggested. 相似文献
7.
Das DD Mahapatra R Pradhan J Das SN Thakur RS 《Journal of colloid and interface science》2000,232(2):235-240
Removal of hexavalent chromium from aqueous medium by using activated cow dung carbon was studied. Cow dung was carbonized and activated by treating with concentrated H(2)SO(4) followed by heating for 24 h at 120 degrees C. The extent of adsorption was studied as a function of pH, contact time, amount of adsorbent, concentration of adsorbate, and temperature. At lower pH (<3.5), the prepared sorbent was capable of removing approximately 90% Cr(VI) at 5 ppm concentration from aqueous synthetic solution. The dynamics of migration of the sorbate ions from the bulk onto the sorbent surface was studied and the results obtained under various experimental conditions were found to follow standard adsorption isotherms. The reaction kinetics was found to be of first order. Copyright 2000 Academic Press. 相似文献
8.
C.S. Hoad R.W. Matthews M.M. Thakur D.G. Gillies 《Journal of organometallic chemistry》1977,124(3):c31-c36
Thallium-205, carbon-13 and proton NMR spectra have been determined for some monomethylthallium(III) derivatives CH3TlX2 (X anion) permitting comparison of NMR parameters in the series CH3TlX2, (CH3)2TlX, (CH3)3Tl. 相似文献
9.
Colorimetric method for the determination of captafol (difolatan) in commercial formulations and residues on grains and apples. 总被引:1,自引:0,他引:1
A simple and rapid colorimetric method for the microdetermination of captafol (difolatan), based on its reaction with a dithiocarbamate, has been developed. The bright yellow colour which develops instantaneously on mixing the fungicide with the reagent is stable for at least 12 h. The method has been successfully adapted to the determination of captafol in its formulated products and residues on grains and apples. 相似文献
10.
Semi-interpenetrating polymer networks (IPNs) of poly(ethylene glycol), poly(vinyl alcohol) and polyacrylamide were prepared as a support for enzyme immobilization and kinetic studies were performed for the immobilization of -amylase. The effect of IPN composition on the extent of immobilization was investigated and the percentage of relative activity of the immobilized enzyme was evaluated as a function of the chemical architecture of the IPNs, pH and temperature, taking starch as a substrate. The kinetic constants and the maximum reaction velocity were also evaluated. The IPNs were characterized by IR spectral analysis. 相似文献