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1.
Brett Ammundsen Gary R. Burns Ali Amran Stig E. Friberg 《Journal of Sol-Gel Science and Technology》1995,4(1):23-29
The effects of thermal treatment on composite materials prepared by the gelation of sols comprising large concentrations of metal oxide precursor salts have been investigated, in order to determine the compositional and thermal requirements for forming spinel magnesium manganates in such systems. The preparative technique has been found to give rise to derived gel materials in which the metal oxide phase, in the form of regular spherical particles, is dispersed throughout a continuous silica matrix. Silica-supported mixed magnesium and manganese spinel oxide phases were obtained for systems comprising at least 30 wt% metal nitrate after heating to temperatures between 700 and 850°C, but not without concomitant formation of Mn2O3 and modification of the silica network by magnesium. 相似文献
2.
Stig Veibel 《Fresenius' Journal of Analytical Chemistry》1964,205(1):94-109
Zusammenfassung Der grundsätzliche Unterschied zwischen anorganischer und organischer Analyse wird diskutiert, wobei dargelegt wird, daß die Gruppenreaktionen der funktioneilen Gruppen in der organischen Analyse die Funktionen der Ionenreaktionen der anorganischen Analyse übernommen haben.Als Beispiele werden sowohl chemische Reaktionen als auch instrumentelle Methoden zur Identifikation von Hydroxylverbindungen, Carboxylsäuren, Carbonylverbindungen, Aminen, einschließlich Aminosäuren, N-Oxiden, schwefelhaltige Verbindungen, Alkoxyverbindungen und Kohlenwasserstoffen erwähnt.Es wird betont, daß sich die endgültige Identifikation einer organischen Verbindung nur durch Konbination qualitativer und quantitativer Methoden durchführen läßt.
Summary The fundamental difference between inorganic and organic analysis is discussed, and it is shown how group reactions in organic analysis have assumed the function of ionic reactions in inorganic analysis.Chemical reactions and instrumental methods for the identification of the following compounds are mentioned hydroxy compounds, carboxylic acids, carbonyl compounds, amines, including amino-acids, N-oxides, sulphur containing compounds, alkoxy compounds and hydrocarbons. It is emphasized that a combination of qualitative and quantitative methods is necessary for obtaining a final identification.相似文献
3.
Water samples from the Arctic Sea were analyzed by the potentiometric stripping technique. Lead(II) and cadmium(II) were determined after pre-electrolysis for 32 min at—1.1 V vs. Ag/AgCl, the detection limits being 0.06 and 0.04 nM, respectively. Zinc(II) was determined after the addition of gallium(III) by pre-electrolysis for 16 min at —1.4 V vs. Ag/AgCl, the detection limit being 0.25 nM. Problems in the determination of copper(II) at the very low concentrations found in oceanic waters are outlined. The average zinc(II), cadmium(II) and lead(II) concentrations in eight different samples were 2.5, 0.16 and 0.10 nM as determined by potentiometric stripping analysis and 1.9, 0.16 and 0.09 nM as determined by solvent extraction/atomic absorption spectrometry. The advantages of this computerized technique for the analysis of sea water are discussed. 相似文献
4.
Liquid-phase microextraction of protein-bound drugs under non-equilibrium conditions 总被引:1,自引:0,他引:1
Recently, we introduced an inexpensive and disposable hollow fiber-based device for liquid-phase microextraction (LPME) where ionic analytes typically were extracted and preconcentrated from 1-4 mL aqueous samples (such as plasma and urine) through an organic solvent immobilized in the pores of a polypropylene hollow fiber and into a 10-25 microL volume of acceptor phase present inside the lumen of the hollow fiber. Subsequently, the acceptor phase was directly subjected to the final analysis by a chromatographic or electrophoretic method. In the present work, attention was focused on LPME of the basic drugs amphetamine, pethidine, promethazine, methadone and haloperidol characterized by substantial differences in the degree of protein binding. Drug-protein interactions in plasma resulted in reduced recoveries and substantially increased extraction times compared with extraction of the drugs from a pure water matrix. However, by addition of 5-50% methanol to the plasma samples, recoveries were comparable with LPME from water samples and ranged between 75 and 100%. The addition of methanol was found not to speed up the LPME process and extractions from plasma were performed in 45 min to reach equilibrium. Because approximately 55-70% of the final analyte concentrations were achieved within the initial 10 min of the LPME process, validation was accomplished after 10 and 45 min of LPME. In general, the results with 10 and 45 min were almost comparable, with precision data in the range 1.2-11.1% (RSD) and with linearity in the concentration range 20-1000 ng mL(-1) (r = 0.999). In conclusion, excellent LPME results may be achieved in a short time under non-equilibrium conditions with a minor loss of sensitivity. In cases of drug-protein interactions, methanol may be added to ensure a high extraction recovery. 相似文献
5.
A high-performance liquid chromatographic procedure is described for the quantitative determination of epinephrine, norepinephrine, and dopamine in human plasma. The method, which is based on adsorption of the catecholamines to alumina and, after liberation, separation on a microparticulate bonded strong cation-exchange resin and amperometric detection, has been optimized to give complete baseline separation of the substances of interest. Dihydroxybenzylamine, a nonendogenous catecholamine, is used as the internal standard. The detection limit is about 0.1 pmol for dopamine. Analysis of data obtained for norepinephrine and epinephrine from a total of 59 plasma samples showed a good correlation to the corresponding values obtained with a radioenzymatic method. Some results from normal and pathological conditions are compared. 相似文献
6.
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8.
Johan Sjöblom Hege Ebeltoft Alf Bjørseth Stig E. Friberg Chris Brancewicz 《Journal of Dispersion Science and Technology》2013,34(1):21-34
Hydrolysis and condensation of monomolecular alkyloxysilane films by the Langmuir technique is presented. Octadecyltrimethoxysilane formed monolayers on aqueous subphases with different properties depending on the bulk pH. At pH 1 a solid condensed film was directly formed with a molecular area of 23 Å2 and a surface pressure/surface area variation similar to that on non-ionized stearic acid. At pH 5.6 and 11 several phase transitions were observed during the compression of the monolayer with a final collapse at a molecular area of 20 Å2. Relaxation measurements confirmed the stability of the films for longer than 12 hours at different surface pressures below a critical value. 相似文献
9.
Stig E. Friberg Ibrahim Kayali Tatang Suhery Linda D. Rhein F. Anthony Simion 《Journal of Dispersion Science and Technology》2013,34(3):337-347
Water uptake in natural and reaggregated stratum corneum was determined by weight difference after storage in an atmosphere of controlled relative humidity. Interlayer spacing in separated lipids as a function of their water content was determined by low-angle X-ray diffractometry. These values were used as a calibration curve to determine the water content of the lipid bilayers in reaggregated stratum corneum. The results revealed different behavior of the lipid models compared to natural lipids of the stratum corneum. The additional water taken up after reaggregation of equilibrated lipids and proteins, was equally partitioned between the protein and the natural lipid fraction, while the models gave a proportionally higher water uptake into the lipids at high relative humidity. It is obvious that the models, so far, do not mimic all the properties of the natural stratum corneum lipids. 相似文献
10.
Stig R. Erlander 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(6):1181-1193
Abstract Previous developed theories were applied in explaining the mechanism for the salting-in and -out of various amino acids. Glycine is salted-in according to the cationic sequences Li+ > Na+ > K+ > Rb+ and Ca2+ > Ba2+ > Sr2+. The ability of a cation to increase the solubility of an amino acid therefore corresponds to the destruction of the ion-ion bond between the - CO-2and the -NH+ 2group of the amino acid by forming an insoluble ion-ion bond between the added cation and the - CO?2 group. This insolubilizing effect produces a positive charge on the amino acid. If, however, the anion of the added salt forms a relatively insoluble ion-ion bond with the -NH+2 group of the amino acid, then the effect is minimized because now both charges on the amino acid are reduced. Consequently, the more insoluble the cation amino acid salt and the more soluble the anion amino acid salt (or vice versa), the greater will be the salting-in effect. Titration of either charged group on the amino acid zwitterion has the same effect, since now the ion-ion bond of the amino acid is again destroyed. Aliphatic and carboxylic acid groups also effect the salting-in sequence, since these groups are salted-out by addition of salt when D± < DH2o. These mechanisms explain how leucine is first salted-out, then salted-in (at 4 M) and finally salted-out again (at 9 M) in LiCl solutions. Urea salts-in hydrophobic amino acids by increasing the dielectric constant and salts-out polar amino acids by increasing the interaction between the two charge groups on the amino acid. Glycine reverses the salting-in effect of NaCl on asparagine by competing for the Na+ ion. 相似文献