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1.
Ghodratollah Absalan Mohammad Soleimani Mozaffar Asadi Mohammad Bagher Ahmadi 《Analytical sciences》2004,20(10):1433-1436
A new ammonia optical sensor was designed using bis(acetylacetoneethylendiamine)tributylphosphin cobalt(III) tetraphenylborate complex, coated on transparent triacetylcellulose film as membrane. The change in the absorbance of the optode at the maximum wavelength of 408 nm was related to ammonia concentration in aqueous samples. A buffer solution with a pH of 9 (sodium borate-HCl) was used. The optode was fully regenerated in pH 2. The linear dynamic range for determination of ammonia was 3.3 x 10(-4) to 6.9 x 10(-3) mol l(-1) with a detection limit of 5.0 x 10(-5) mol l(-1) and a response time range of 4 - 6 min. This membrane was successfully applied for determination of ammonia in drinking water. 相似文献
2.
One of the open questions in the geometry of line arrangements is to what extent does the incidence lattice of an arrangement determine its fundamental group. Line arrangements of up to 6 lines were recently classified by K.M. Fan (Michigan Math. J. 44(2) (1997) 283), and it turns out that the incidence lattice of such arrangements determines the projective fundamental group. We use actions on the set of wiring diagrams, introduced in (Garber et al. (J. Knot Theory Ramf.), to classify real arrangements of up to 8 lines. In particular, we show that the incidence lattice of such arrangements determines both the affine and the projective fundamental groups. 相似文献
3.
An approximate method is developed to solve the full nonlinear equations governing two-dimensional irrotational flow in a free waterfall, falling under the influence of gravity, at high Froude number based on conditions far upstream. Schwarz—Christoffel transformation is used to map the region, in the complex potential-plane, onto the upper half-plane. The Hilbert transformation as well as the perturbation technique, for large Froude number, are used as a basis for the approximate solution of the problem. A complete solution, up to second-order approximation, for the downstream free-surfaces profiles, for different Froude number, is discussed and illustrated. The obtained approximate solutions are compared with those of other authors. Favourable agreement with other results suggests that this method is effective in dealing with flow problems strongly influenced by gravity and high Froude number. The results obtained by this method are sufficiently accurate for practical purposes. 相似文献
4.
Youssef Z. Boutros Mina B. Abd-el-Malek Nagwa A. Badran Hossam S. Hassan 《Applied Mathematical Modelling》2007
The non-linear equations of motion describing the laminar, isothermal and incompressible flow in a rectangular domain bounded by two weakly permeable, moving porous walls, which enable the fluid to enter or exit during successive expansions or contractions, are considered. We apply Lie-group method for determining symmetry reductions of partial differential equations. Lie-group method starts out with a general infinitesimal group of transformations under which given partial differential equations are invariant, then, the determining equations are derived. The determining equations are a set of linear differential equations, the solution of which gives the infinitesimals of the dependent and independent variables. After the group has been determined, a solution to the given partial differential equation may be found from the invariant surface condition such that its solution leads to similarity variables that reduce the number of independent variables in the system. Effect of the permeation Reynolds number Re and the dimensionless wall dilation rate α on self-axial velocity have been studied both analytically and numerically and the results are plotted. 相似文献
5.
N. Jiten Singh Adriana C. Olleta Anupriya Kumar Mina Park Hai-Bo Yi Indrajit Bandyopadhyay Han Myoung Lee P. Tarakeshwar Kwang S. Kim 《Theoretical chemistry accounts》2006,115(2-3):127-135
In earlier studies, the interactions of isolated ionic species with various solvents were investigated using ab initio calculations.
The ionic species investigated included cations (proton, hydronium, ammonium, and metal cations) and anions (single electron,
hydroxide, and halide anions). However in the present study, we investigate the interactions of these ionic species with the
solvent in the presence of other competing ionic species. We also elaborate on how the information obtained from these extensive
studies have been employed in designing and synthesizing various kinds of novel ionophores and receptors. 相似文献
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The equilibrium constants and the thermodynamic parameters were spectrophotometrically measured for the 1:1 adduct formation of [Co(Salen)(PPh3)]ClO4.H2O, and [Co(7,7′-Me2Salen)(PPh3)]ClO4.H2O as acceptors, with P(OR)3 (R = methyl, ethyl, and i-propyl) as donors, in acetonitrile (CH3CN) and dimethylformamide (DMF) as solvents at constant ionic strength (I = 0.1 M NaClO4), and various temperatures (t = 10–50 °C). Our results revealed the following trends: stability of the cobalt(III) Schiff base complexes toward a given phosphite donor, [Co(7,7′-Me2Salen)(PPh3)]+ < [Co(Salen)(PPh3)]+; binding of the donors (phosphites) toward a given cobalt(III) Schiff base complex, P(OEt)3 > P(OMe)3 > P(O-iPr)3; influence of solvent on the stability of a given cobalt(III) Schiff base complex toward a given phosphite donor, CH3CN < DMF. 相似文献
9.
A chemically modified carbon paste electrode with 3,4-tetra pyridinoporphirazinatocobalt(II) (Co(3,4 tppa) was applied to the determination of free cyanide ion. The electrode has a linear range between 1.5 × 10−5 M and 1.0 × 10−2 M with a Nernstian slope of 60 ± 1.5 mV/decade and its detection limit is 9 × 10−6 M. The response time of electrode is 5 min. The proposed electrode was applied successfully for the determination of cyanide in commercially available spring water. Some anions, such as SCN−, I−, Cl−, Br− and oxalate that are usually serious interfering species for most of cyanide selective electrodes, did not have any interfering effect for this proposed electrode. 相似文献
10.
The vibrational spectrum of the vinyl bromide cation in the first excited electronic state A 2A' was obtained by one-photon mass-analyzed threshold ionization (MATI) spectroscopy. The use of an improved vacuum-ultraviolet radiation source based on four-wave sum frequency mixing in Hg resulted in excellent sensitivity for MATI signals. From the MATI spectrum, the ionization energy to the A 2A' state of the cation was determined to be 10.9150+/-0.0006 eV. Nearly complete vibrational assignments for the MATI peaks were possible by utilizing the vibrational frequencies and Franck-Condon factors calculated at the density-functional theory (DFT) and time-dependent DFT/B3LYP levels with the 6-311+G(df,p) basis set. 相似文献