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901.
In this study, a syringe was filled with silica gel loaded with 3-aminopropyltriethoxysilane, for the separation and preconcentration of copper, cadmium and chromium prior to their determination by graphite furnace atomic absorption spectrometry (GFAAS) in seawater. For this purpose, a syringe was filled with 0.5 g of modified silica gel and the sample solution was drawn into the syringe and ejected back again. The analyte elements were quantitatively retained at pH 5. Then, the elements sorbed by the silica gel were eluted with 2.0 M of HCl and determined by GFAAS. At optimum conditions, the recovery of Cu, Cd and Cr were 96-98%. Detection limits (3delta) were 6.6, 7.5 and 6.0 micro g L(-1) for Cu, Cd and Cr, respectively. The elements could be concentrated by drawing and discharging several portions of sample successively but eluting only once. Cu, Cd and Cr added to a seawater sample were quantitatively recovered (>95%) in the range of the 95% confidence level. The method proposed in this paper was compared with a column technique. Optimum experimental conditions, reproducibility, precision and recoveries of both techniques are the same, but the syringe technique is much faster, easier and more practical than the column technique. It is a portable system and allows one to make the sorption process in the source of sample. In addition, the risk of contamination is less than in the column technique. 相似文献
902.
Kinetic study on the cleavage of N‐phenylphthalimide (NPhPT) in the presence of 0.05 M NH2NH2 and mixed H2O‐CH3CN solvents reveals the occurrence of reaction scheme where A, B, C, C1, An, E, and F represent NPhPT, o‐CO?2C6H4CONHC6H5, o‐CONHNH2C6H4‐ CONHC6H5, N‐aminophthalimide, aniline, o‐CO?2C6H4CONHNH2, and o‐CONHNH2C6H4‐CONHNH2, respectively. But, in the presence of either nonbuffered ?0.20 M NH2NH2 hydrazine buffer of pH ~7.30–8.26 with total buffer concentration ([Buf]T) of >0.02 M, further conversion of F to 2,3‐dihydrophthalazine‐1,4‐dione (DHPD) has been detected depending upon the length of the reaction time (t), the values of [Buf]T, and pH. It has been shown that the rate of conversion of C1 to F is much faster than that of C to C1 which is much faster than that of F to DHPD. The reaction step A → C involves general base (GB) catalysis, while step C → C1 seems to involve specific base–general acid (GA) and GB‐GB catalysis. © 2005 Wiley Periodicals, Inc. Int J Chem Kinet 37: 147–161, 2005 相似文献
903.
The adsorption/desorption process of borate was studied at Pt(111) in acidic solution by cyclic voltammetry. A so-called butterfly
wave in the cyclic voltammogram of Pt(111) in HClO4 shifted to negative direction upon the addition of boric acid with the disappearance of its sharp spikes. The shift in potential
was found to be −57 mV with a tenfold increase of boric acid concentration. This illustrates that this anomalous wave is due
to borate adsorption/desorption by a one-electron transfer process. The borate adsorption/desorption wave was observed to
shift by −63 mV/pH. At pH>3, the anomalous wave splits forming two separate waves, depending on the pH and the scan rate.
The appearance of two waves is assigned to the change in the adsorption mode of borate or the participation of OH in the adsorption
process. 相似文献
904.
Vijayasarathi Nagarajan Barbara Müller Oksana Storcheva Klaus Köhler Andreas Pöppl 《Research on Chemical Intermediates》2007,33(8):705-724
Interactions and binding sites of the solvent molecules chloroform and ethanol to bis(acetylacetonate)oxovanadium(IV) (VO(acac)2) complexes in (frozen) solutions have been investigated by pulsed electron nuclear double resonance, sum peak electron spin
echo envelope modulation and hyperfine sublevel correlation spectroscopy. The experimental proton hyperfine coupling data
of coordinating solvent molecules have been interpreted using quantum chemical calculations (density functional theory). Experimental
and computed hyperfine couplings indicate that ethanol coordinates to vanadium in the equatorial plane of VO(acac)2 and chloroform interacts via hydrogen bonding to oxygens of the acac ligands. 相似文献
905.
Elena Blanco J. M. Ruso J. Sabín G. Prieto F. Sarmiento 《Journal of Thermal Analysis and Calorimetry》2007,87(1):211-215
The interactions of lysozyme and myoglobin with anionic surfactants
(hydrogenated and fluorinated), at surfactant concentrations below the critical
micelle concentration, in aqueous solution were studied using spectroscopic
techniques. The temperature conformational transition of globular proteins
by anionic surfactants was analysed as a function of denaturant concentration
through absorbance measurements at 280 nm. Changes in absorbance of protein-surfactant
system with temperature were used to determine the unfolding thermodynamics
parameters, melting temperature, T
m,
enthalpy, ΔH
m,
entropy, ΔS
m
and the heat capacity change, ΔC
p,
between the native and denatured states. 相似文献
906.
Let G be a finite group, H be a proper subgroup of G, and S be a unitary subring of C. The kernel of the restriction map S[Irr(G)] → S[Irr(H)] as a ring homomorphism is studied. As a corollary, the main result in [Isaacs, I. M. and Navarro, G., Injective restriction of characters, Arch. Math., 108, 2017, 437–439] is reproved. 相似文献
907.
908.
Koichi Kikuta Koji Noda Shin Okumura Toshiaki Yamaguchi Shin-ichi Hirano 《Journal of Sol-Gel Science and Technology》2007,42(3):381-387
Orientation control of perovskite compounds was investigated by the application of a seed layer prepared from oxide nanosheets.
An aqueous suspension of oxide nanosheets was prepared by the exfoliation of a layered compound of KCa2Nb3O10 oxide grains. A seed layer composed of (TBA)Ca2Nb3O10 nanosheets (TBA = tetrabutylammonium) was formed on a glass substrate by simply dip coating it in the suspension. Two kinds
of perovskite compounds, LaNiO3 (LNO) and Pb(Zr,Ti)O3 (PZT) with a preferred orientation of (00l) were successfully grown on this seeded glass substrate. In this study, the relation between lattice mismatch and electrical
properties is investigated. A large, oriented PZT film with a size of 5 ×4 cm shows an improved P-E hysteresis behavior by
use of this orientation control. 相似文献
909.
John M. Charnes Howard Marmorstein Walter Zinn 《The Journal of the Operational Research Society》1995,46(8):1006-1013
We consider a periodic-review inventory replenishment model with an order-up-to-R operating doctrine for the case of deterministic lead times and a covariance-stationary stochastic demand process. A method is derived for setting the inventory safety stock to achieve an exact desired stockout probability when the autocovariance function for Gaussian demand is known. Because the method does not require that parametric time-series models be fit to the data, it is easily implemented in practice. Moreover, the method is shown to be asymptotically valid when the autocovariance function of demand is estimated from historical data. The effects on the stockout rate of various levels of autocorrelated demand are demonstrated for situations in which autocorrelation in demand goes undetected or is ignored by the inventory manager. Similarly, the changes to the required level of safety stock are demonstrated for varying levels of autocorrelation. 相似文献
910.
This paper studies the optimal operation of an M/E k /1 queueing system with a removable service station under steady-state conditions. Analytic closed-form solutions of the controllable M/E k /1 queueing system are derived. This is a generalization of the controllable M/M/1, the ordinary M/E k /1, and the ordinary M/M/1 queueing systems in the literature. We prove that the probability that the service station is busy in the steady-state is equal to the traffic intensity. Following the construction of the expected cost function per unit time, we determine the optimal operating policy at minimum cost. 相似文献