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81.
Ali MOGHIMI Mohammad SABER‐TEHRANI Syed WAQIF‐HUSAIN Majid MOHAMMADHOSSEINI 《中国化学》2007,25(12):1859-1865
A novel and selective method for the fast determination of trace amounts of chromium species in water samples has been developed. The procedure is based on the selective formation of chromium diethyldithiocarbamate complexes at different pH in the presence of Mn(II) as an enhancement agent of chromium signals followed by elution with organic eluents and determination by atomic flame absorption spectrometry. The maximum capacity of the employed disks was found to be (396±3) µg and (376±2) µg for Cr(III) and Cr(VI), respectively. The detection limit of the proposed method is 49 and 43 ng·L?1 for Cr(III) and Cr(VI), respectively. The proposed method was successfully applied for determination of chromium species Cr(III) and Cr(VI) in different water samples. 相似文献
82.
Ensafi AA Keyvanfard M 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2002,58(8):1567-1572
A new kinetic-spectrophotometric method is described for the determination of ultra trace amounts of Pd(II). The methods based on catalytic action of Pd(II) on the oxidation of pyrogallol red (PGR) with hydrogen peroxide at pH 9.7. The reaction was monitored spectrophotometrically by measuring the decrease in absorbance of the PGR at 540 nm, for the first 4.5 min from initiation of the reaction. Calibration curve was linear in the range of 0.02-1.00 microg ml(-1) Pd(II). The limit of detection is 0.017 microg ml(-1) Pd(II). The relative standard deviation (R.S.D.) for ten replicate analyses of 0.03 and 0.60 microg ml(-1) Pd(II) was 1.5 and 0.9%, respectively. The influence of more than 40 potential interfering ions was studied for the selectivity. The proposed method was used for the determination of palladium in catalytic material. 相似文献
83.
Ali G. Ozkabak Surya N. Thakur Lionel Goodman 《International journal of quantum chemistry》1991,39(3):411-422
C6H6 Raman scattering activities calculated from harmonic model ab initio Hartree–Fock 6–311 ++ G(d, p) polarizability derivatives (and harmonic force fields calculated at the same level) accurately simulate experiment (to within 1% for the a1g modes). Accurate predictions are also made for the e2g modes (to within 5% for ν7 and ν9, and more poorly for ν6 and ν8 [in Fermi resonance with ν6 + ν1]) and for the e1g out-of-plane mode, ν10. Only the ν6 in-plane CCC bending mode scattering activity is found to be anomalous. Systematic variation of the basis set indicates that the benzene scattering activities and depolarization ratios are strongly dependent on inclusion of both carbon and hydrogen atom diffuse functions in the basis set. Predictions are also made for 12C6D6 and for unmeasured intensities in 13C6H6. Measurements of a1g mode scattering activities in the latter molecule are predicted to be useful in testing the harmonic Hartree–Fock Raman intensity model. 相似文献
84.
Ali Taha Viktor Gutmann Wolfgang Linert 《Monatshefte für Chemie / Chemical Monthly》1991,122(5):327-339
Summary The solvatochromic and thermochromic behaviour of a series of mixed Ni(II) complexes with unsubstituted and substituted -diketones and diamines in the solvents 1,2-dichloroethane (DCE), acetonitrile (An), acetone (AC),n-butanol (n-BuOH), formamide (FA), N,N-dimethylformamide (DMF), dimethylsulfoxide (DMSO) and pyridine (PY) has been studied and characterized on the basis of electronic spectra. Spectrophotometric methods have been used to evaluate equilibrium constants and their enthalpic and entropic terms for the formation of Ni(-dik)(diam)L
+ and Ni(-dik)(diam)L
2
+
. Increasing donor strength of the donor-solvents (L) and (or) increasing electronwithdrawing parameters of the substituents at the -diketone and the diamine ligands lead to increasing formation constants, paralleled by relative increase in the stability of the five-coordinated species Ni(-dik)(diam)L
+. The results are discussed in terms of the extended donor-acceptor concept.On leave of absence from the Faculty of Education, Ain Schams University, Roxy, Cairo, Egypt 相似文献
85.
An analytical method using alumina modified with water-soluble polyacrylic acid polymer for the simultaneous separation and
preconcentration of trace Cu and Cd in a column system, and their determination by flame atomic absorption spectrometry was
developed. The conditions for coating Al2O3 with polyacrylic acid were optimized, then the column was packed with 50 mg of this sorbent. Cd and Cu solution was passed
through a glass column at pH 4.5, and elution was carried out with 5 mL of 0.05 M HCl at a flow rate of 1 mL min−1. A sorption capacity of 10 mg Cu and 12 mg Cd was obtained for 1 g sorbent. The detection limit was calculated as 4.5 μg L−1 for Cu and 1.54 μg L−1 for Cd in the final solution. Enrichment factors of 300 for Cd and 400 for Cu were obtained. 相似文献
86.
Sigman MB Ghezelbash A Hanrath T Saunders AE Lee F Korgel BA 《Journal of the American Chemical Society》2003,125(51):16050-16057
Cu(2)S nanocrystals with disklike morphologies were synthesized by the solventless thermolysis of a copper alkylthiolate molecular precursor. The nanodisks ranged from circular to hexagonal prisms from 3 to 150 nm in diameter and 3 to 12 nm in thickness depending on the growth conditions. High resolution transmission electron microscopy (HRTEM) revealed the high chalcocite (hexagonal) crystal structure oriented with the c-axis ([001] direction) orthogonal to the favored growth direction. This disk morphology is thermodynamically favored as it allows the extension of the higher energy [100] and [110] surfaces with respect to the [001] planes. The hexagonal prism morphology also appears to relate to increased C-S bond cleavage of adsorbed dodecanethiol along the more energetic [100] facets relative to [001] facets. Monodisperse Cu(2)S nanodisks self-assemble into ribbons of stacked platelets. This solventless approach provides a new technique to synthesize anisotropic metal chalcogenide nanostructures with shapes that depend on both the face-sensitive thermodynamic surface energy and the surface reactivity. 相似文献
87.
Ali M. Emran Th E. Boothe R. D. Finn M. M. Vora P. J. Kothari 《Journal of Radioanalytical and Nuclear Chemistry》1985,91(2):277-284
An analytical technique using reversed-phase liquid chromatography has been developed for the determination of urea at quantities as low as 1 ng to quantitate the amount of non-labelled urea produced during the synthesis of no-carrier-added {11C}urea starting from11CN–. As a result, the specific activity of the {11C} urea thus prepared was calculated to be as high as 3.5±0.8 Ci/mol.Research supported in part by PHS Grant NINCDS 1 PO1 NS 15639. 相似文献
88.
Summary Resolution of enantiomeric mixtures of DL-amino acids (Nine) using silica gel layers impregnated with (-)-bruncine is reported.
The solvent system used was Butanol: Acetic acid: Chloroform (3∶1∶4). The diastereomers were formed and hydrolysed, by dilute
HCl spray, on the chromatogram only and the amino acids thus resolved were located by ninhydrin spray. The cross resolution
possibilities of enantiomers were also calculated. 相似文献
89.
Acidity constants of six substituted 1-benzyl-1-methoxy-2-nitroethylenes (2-Z with Z = m-NO(2), m-CF(3), m-Cl, H, p-Me, p-MeO) and their respective nitronic acids were determined in 50% DMSO-50% water (v/v) at 20 degrees C. Kinetic data were obtained on the reversible deprotonation of all six 2-Z by OH(-) and piperidine and on the reversible deprotonation of 2-NO(2)() by piperazine, 1-(2-hydroxyethyl)piperazine, and morpholine in the same solvent. These data allowed a determination of the Br?nsted coefficients alpha (dependence on acidity of 2-Z) and beta (dependence on amine basicity). The fact that alpha > beta indicates the presence of a transition state imbalance which, however, is much smaller than that for the deprotonation of arylnitromethanes. The reasons for this reduction in the imbalance and their relevance to a recent study of the deprotonation of Fischer carbene complexes are discussed. 相似文献
90.
The effect of anion concentration and the dependence of uranyl ascorbate on the nature of anion present is systematically studied for nine different anions over the concentration range (0.2–2.0) × 10−2 M. These anions, commonly encountered in pharmaceutical preparations with ascorbic acid (vitamin C) are nitrate, sulfate, chloride, bromide, fluoride, phosphate, citrate, oxalate, and tartrate. Based on the absorbance data, and on the value of the replacement constant K calculated, the studied anions may be arranged according to their complexing power on uranium as follows: citrate > tartrate > phosphate > oxalate > fluoride > sulfate > nitrate > chloride > bromide.This order is substantiated by the calculated values of the side reaction coefficients αM of the uranyl ligand complex or the conditional stability constant of uranyl-ascorbate calculated at different ligand concentrations. 相似文献