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251.
2,3-Dihydroxypyridine loaded (via –N=N–linker) Amberlite XAD-2 (AXAD-2-DHP) was prepared and characterized by elemental analyses, TGA and FT-IR spectra. It (1g packed in a column of 1cm diameter; surface area 135.5m2g–1) was found to be an effective solid phase sorbent for enriching Zn2+, Mn2+, Ni2+, Pb2+, Cd2+, Cu2+, Fe3+ and Co2+ at pH 3.5 to 7.0 using flow rates between 1.0–5.0mLmin–1. For desorption (recovery 97.0–99.8%) of the metal ions, 8 to 10mL of 2.0molL–1 HCl or 1.5molL–1 HNO3 at a flow rate of between 2.0 and 4.0mLmin–1 were found most suitable. The t1/2 (time for 50% sorption) is between 2 and 10min when a 50mL solution (containing a total amount of metal of 2mg) was equilibrated with 0.5g of resin. Sorption of all metal ions except Pb2+ follows the Langmuir model, whereas for Pb the data fits with the Freundlich model. The sorption capacity is between 60.7 (for Cd) and 406.7 (for Cu) µmolg–1. The resin can withstand an acid concentration of 6molL–1 and can be reused for thirty cycles of sorption–desorption. The preconcentration factor varies between 100 and 300. For Cd, Ni and Cu the sorption capacity of 2,3-dihydroxypyridine loaded cellulose is lower than that of the present resin. The tolerance limits of electrolytes, humic acid, complexing agents, Ca2+ and Mg2+ in the enrichment of all metal ions are reported. The limits of detection are 3.88, 5.37, 8.72, 13.88, 4.71, 1.24, 0.59 and 0.30µgL–1 for Zn2+, Mn2+, Ni2+, Pb2+, Cd2+, Cu2+, Fe3+ and Co2+, respectively. The calibration curves for flame AAS determination were linear in the ranges 0.018–1.0, 0.067–5.0, 0.2–5.0, 0.9–20, 0.028–2.0, 0.077–5.0, 0.19–10 and 0.1–3.5µgmL–1, respectively. All the eight metal ions in river and synthetic water samples, Co in vitamin tablets and Zn in milk samples have been quantitatively enriched with Amberlite XAD-2-DHP and determined by flame atomic absorption spectrometry. 相似文献
252.
D. Rekha K. Suvardhan K. S. Kumar G. R. K. Naidu P. Chiranjeevi 《Journal of Analytical Chemistry》2006,61(12):1177-1182
A simple, sensitive, and rapid flow-injection spectrophotometric method was developed for the determination of trace amounts
of selenium(IV). The method is based on the oxidation reaction of 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH)
by selenium(IV) followed by the coupling reaction with chromotropic acid (4.5-dihydroxy naphthalene-2.7-disulphonic acid)
in a basic medium (phosphate buffer, pH 10.5) to give a pink derivative with λmax 530 nm that is stable for more than 7 days at 35°C. The reaction and flow conditions of the full experimental design were
optimized. A detection limit (2s) of 0.25 μg/L Se(IV) was obtained at a sampling rate of 10 samples per hour. Beer’s law is
obeyed for a Se(IV) concentration range of 0.05–0.5 μg/mL at the wavelength of maximum absorption. The detailed study of various
interference ions indicates that the method is highly selective. The method was successfully applied to the determination
of traces of selenium(IV) in various water samples. The results obtained were in good agreement with those obtained by the
reported methods at the 95% confidence level.
The text was submitted by the authors in English. 相似文献
253.
Lu Z Prouty MD Guo Z Golub VO Kumar CS Lvov YM 《Langmuir : the ACS journal of surfaces and colloids》2005,21(5):2042-2050
We explored using a magnetic field to modulate the permeability of polyelectrolyte microcapsules prepared by layer-by-layer self-assembly. Ferromagnetic gold-coated cobalt (Co@Au) nanoparticles (3 nm diameter) were embedded inside the capsule walls. The final 5 mum diameter microcapsules had wall structures consisting of 4 bilayers of poly(sodium styrene sulfonate)/poly(allylamine hydrochloride) (PSS/PAH), 1 layer of Co@Au, and 5 bilayers of PSS/PAH. External alternating magnetic fields of 100-300 Hz and 1200 Oe were applied to rotate the embedded Co@Au nanoparticles, which subsequently disturbed and distorted the capsule wall and drastically increased its permeability to macromolecules like FITC-labeled dextran. The capsule permeability change was estimated by taking the capsule interior and exterior fluorescent intensity ratio using confocal laser scanning microscopy. Capsules with 1 layer of Co@Au nanoparticles and 10 polyelectrolyte bilayers are optimal for magnetically controlling permeability. A theoretical explanation was proposed for the permeability control mechanisms. "Switching on" of these microcapsules using a magnetic field makes this method a good candidate for controlled drug delivery in biomedical applications. 相似文献
254.
The kinetics of substitution of aqua ligands fromcis-diaqua-bis(biguanide)cobalt(III) and chromium(III) ions by aspartic acid in EtOH–H2O media have been studied spectrophotometrically in the 30 to 45°C range. We propose the following rate law for the anation
相似文献
255.
Indoles undergo smooth coupling with phenylacetylene in the presence of 10 mol % of gallium(III) chloride or gallium(III) bromide under mild conditions to afford the corresponding 1,1-bis(1H-3-indolyl)-1-phenylethanes in high yields and with high selectivity. 相似文献
256.
Titanium oxide on silica-alumina support is described to be an efficient regenerable catalyst for alkylation of aromatic compounds with alkyl halides, alcohols and olefins, and the reaction is proposed to be initiated by the protonated metal active species present in the catalyst. 相似文献
257.
Raj Kumar 《Colloid and polymer science》1979,257(1):95-97
Summary Estimation of zeta potential from experimental data on electroosmotic and electrophoretic effects for Zeokarb 225 (Na+ form)/methanol-water system has been made and discussed. Results indicate that zeta potentials estimated from electroosmotic flux and electrophoretic mobility are not in agreement and vary with applied potential difference in a linear manner. Reasons for the variation of zeta potential with electrical field have been discussed. It has been argued that zeta potentials estimated from electroosmotic data are more reliable in comparison to the values obtained from electrophoretic data.With 2 figures and 2 tables 相似文献
258.
Acid catalysed dehydration of the diols 5 , derived from the cyclohexenone 3 affords mixtures of 8 and 11 . The product ratio 8/11 , although strongly dependent on both the reaction conditions and the substituent R, is independent of the diol configuration; this indicates a cationic intermediate 6 . Conditions were found, which allow the sequence A → B → C → D (Scheme 2) to be applied to the syntheses of the enones 8, 21 and 25 in fair to good yields from the corresponding cyclohexenones 3, 18 and 22 . 相似文献
259.
Sachindra Kumar Datta 《Fresenius' Journal of Analytical Chemistry》1959,168(6):418-424
Summary Eighteen anilic acids have been prepared from maleic anhydride and various aromatic amines and their properties and analytical reactions with various metal ions have been studied. The acid prepared from benzidine was insoluble in all common solvents and, hence, its application could not be studied. Most of these reagents, except those obtained from aniline, o- and p-chloroanilines, nitranilines, p-amino-acetanilide and o-phenylenediamine, produced more or less quantitative precipitations with both thorium and zirconium. Their actions towards thorium and zirconium were very much alike. They also gave precipitations with mercury(I), lead and cerium(IV), but such precipitations were not complete. Ferrous iron showed greyish turbidity with most of the reagents, but ferric iron produced colourations varying from brown to violet, such colours were, however, found to be unstable either on standing for a while or on heating. Gold and platinum underwent reduction in presence of these reagents.Part VIII: See Z. analyt. Chem. 163, 403 (1958).The work has been carried out in the chemical laboratories of Darjeeling Government College, Darjeeling. The author is grateful to the authorities of the College for the laboratory facilities. 相似文献
260.
Kotha A Raman RC Ponrathnam S Kumar KK Shewale JG 《Applied biochemistry and biotechnology》1998,74(3):191-203
Various glycidyl methacrylate (GMA) copolymers were synthesized by suspension polymerization, using pentaerythritol triacrylate (PETA), trimethylolpropane triacrylate (TMPTA), and trimethylolpropane trimethacrylate (TRIM) as crosslinking comonomers. These copolymers were evaluated for the immobilization of penicillin G acylase. Broad pore-size distribution that was observed was in the range 5-300 nm. Both surface area and pore volume increased with increase in the mole fraction of crosslinking comonomer (increasing crosslink density). The pore volume of the copolymers was more than doubled by including lauryl alcohol as porogen. Binding of penicillin G acylase (PGA) was quantitative on highly crosslinked copolymers. The expression of bound PGA was better on the relatively more hydrophilic GMA-TMPTA and GMA-PETA copolymer supports compared to the GMA-TRIM copolymers. Among the different copolymers studied, GMA-TMPTA copolymer 7411 exhibited highest activity of immobilized penicillin G acylase (167.4 IU/g) with 35.1% expression. 相似文献
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