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991.
Determination of sulfametoxazole, sulfadiazine and associated compounds in pharmaceutical preparations by capillary zone electrophoresis 总被引:3,自引:0,他引:3
Berzas Nevado JJ Castañeda Peñalvo G Guzmán Bernardo FJ 《Journal of chromatography. A》2001,918(1):205-210
A capillary zone electrophoresis method is presented to separate sulfadiazine, sulfamethoxazole, trimethoprim, bromhexine and guaiacol by using a fused-silica capillary (60.2 cm x 75 microm I.D.). The separation was carried out at 30 kV and 25 degrees C in a 15 mM phosphate buffer adjusted to pH 6.2 as electrolyte. Under these conditions, the run time was 6 min and the limits of quantification were about 1 mg/l for every component. The method was applied to pharmaceutical preparations and the results provided recoveries close to 100%. 相似文献
992.
Pospísil M Kalendová A Capková P Simoník J Valásková M 《Journal of colloid and interface science》2004,277(1):154-161
Na(+)-montmorillonite type Wyoming, cloisite Na(+) from Southern Clay Products, Inc., was intercalated (i) with octadecylammonium cations and subsequently intercalated with octadecylamine molecules, (ii) with dodecylamine molecules, and (iii) with octylamine molecules to determine the applicability of these intercalates for nanocomposite materials on the base of polymer/clay. The structures were determined on the basis of a combination of results from X-ray diffraction and molecular simulations. The calculated values of basal spacings are in good agreement with experimental basal spacings when experimental samples were prepared. The interlayer space of intercalated montmorillonite shows a monolayer or bilayer arrangement of alkyl chains in dependence on the concentration of the intercalation solution. The values of the total sublimation energy, interaction energy, and exfoliation energy were calculated for all investigated samples. Low values of exfoliation energies lead to better exfoliation of intercalated silicate layers and this material appears suitable for use as a precursor for polymer/clay nanocomposites. The values of exfoliation energy for the investigated samples show that montmorillonite intercalated with dodecylamine or octadecylamine molecules is suitable for exfoliation of silicate layers. 相似文献
993.
J. J. Ramírez-García M. Jiménez-Reyes M. Solache-Ríos E. Fernández-Ramírez H. López-González A. Rojas-Hernández 《Journal of Radioanalytical and Nuclear Chemistry》2003,255(2):299-303
The solubility of europium at 0.02M, 0.1M and 0.7M NaClO4 ionic strength solutions was determined by a radiometric method and pEus-pCH diagrams were obtained. Hydrolysis constants were also determined at the same ionic strengths by pH titration and the values found were log *1 = -7.68±0.11, -8.07±0.10 and -8.20±0.11. The log K
sp values were -23.5±0.2, -22.7±0.2 and -21.9±0.2 for 0.02M, 0.1M and 0.7M NaClO4 ionic strengths, respectively, at 303 K under CO2-free conditions and the extrapolated value at zero ionic strength was log K
sp
0 = -24.15. The working pCH ranges for the calculation of the hydrolysis constants were selected from the pEus-pCH diagrams in the region where precipitation of europium oxide or hydroxide was less than 20%. Europium removal from aqueous solutions with zeolites was explored. 相似文献
994.
Anna Painelli Francesca Terenziani Zoltán G. Soos 《Theoretical chemistry accounts》2007,117(5-6):915-931
We discuss electron-transfer processes that govern the physics of several materials or systems of interest for advanced applications.
The discussion touches upon several topics, ranging from solvatochromism to solvent-induced symmetry breaking, from excitonic
to cooperative effects in molecular crystals, from phase transitions to vibrational contributions to the dielectric constant
in organic materials, from spectroscopy to molecular transport. In all these diverse systems electron transfer (ET) plays
a major role and is discussed with reference to simple models for delocalized charges. 相似文献
995.
Aranka Pilbáth Ilona Felhősi Gyula Tolnai Erika Kálmán 《Journal of Solid State Electrochemistry》2006,10(9):721-729
Due to the toxic and carcinogenic properties of hexavalent chromium ion, the corrosion protection with chromating technique needs replacement. Several environmentally friendly alternative metal pretreatments have already been proposed. One of these methods is the application of self-assembling molecules to form mono- or multilayers on the metal surfaces. These layers can prevent metal dissolution due to their dense and stable structure. The objective of our studies was to protect zinc surface against corrosion, with a thin phosphonate layer. Aqueous solutions of diphosphonic acid with different alkyl chain lengths were applied with different treatment times. The layer formation, stability, and corrosion protection of these films were monitored by electrochemical impedance spectroscopy and the effect of 1,5-diphosphono-pentane (DPP) on zinc was studied by polarization curves. The wetting properties were determined by static contact angle measurement. 1,5-Diphosphono-pentane forms a thin layer, with a pronounced protective ability in neutral aqueous solutions. The application of self-assembling molecules can be a promising method to replace the chromating technique on zinc surface. 相似文献
996.
Ascorbic acid (AA) is determined by amperometric detection based on the photochemical reduction of Methylene Blue (MB(+)) in 0.1 M phthalate buffer at pH 3.8. In this medium, MB(+) using flow-injection analysis. The carrier stream is 1 mM MB(+) is reduced quasi-reversibly at a glassy carbon electrode at -0.34 V vs. Ag/AgCl, while AA is oxidized irreversibly at about 0.3 V. The reactor is irradiated with a 500 W halogen lamp to facilitate the development of the photochemical reaction. A laboratory-built wall-jet electrode system was used. The Leucomethylene Blue formed in the reaction is detected at +0.050 V. At 2.2 ml min(-1) and using a sample loop of 43 mul, the method allows the determination of AA in the range 5.0-90.0 mug ml(-1), with a relative standard deviation of 1.3-4.8%, a detection limit of 1.9 mug ml(-1) and a sampling frequency of 45-50 h(-1). 相似文献
997.
P. Baláž K. Tkáčová E. G. Avvakumov 《Journal of Thermal Analysis and Calorimetry》1989,35(5):1325-1330
Experimental results on the influence of preliminary mechanical activation on the thermal decomposition of chalcopyrite are presented and discussed. The following experimental facts were found:
The intensive grinding of chalcopyrite leads to a shift in temperature of the endothermic DTA peak and brings about a decrease in the activation energy of the thermal decomposition of CuFeS2. These results can be attributed to the mechanically produced alterations in structure and surface properties of the mineral. 相似文献
1. | a decrease in the temperature of the endothermic DTA peak of-CuFeS2 from 821 K for a non-activated sample to 763 K for an optimally activated one; |
2. | a decrease in the apparent activation energy of the thermal decomposition of CuFeS2 from 238 kJ mol–1 for a non-activated sample to 72 kJ mol–1 for an optimally activated sample. |
998.
Résumé Dans la première partie de ce travail, les auteurs mettent en évidence que la vitesse d'une réaction en régime non isotherme dépend d'un facteur supplémentaire: le régime de montée en température. Cette assertion est basée sur le fait que le taux de réactionx est une fonction de trois variables: températureT, tempst, et vitesse de chauffeT, variable qui n'avait pas été prise en considération jusqu'ici par les autres auteurs travaillant sur ce problème.Puis, se basant sur les deux hypothèses suivantes: a) l'équation de vitesse en régime isotherme est la forme limite de l'équation de vitesse en régime dynamique, b) la variation de température en régime dynamique affecte la fréquence d'apparition des germes de la nouvelle phase, une formulation théorique des loisg(x) est proposée pour le régime non-isotherme. Cette formulation est explicitée en fonction de l'écart, à une température donnée, entre les valeurs de Lnk
i (isotherme) et Lnk
d (dynamique) dans le diagramme Lnk = f(1/T).L'étude, par thermogravimétrie, de la décomposition du gypse, du sulfate de calcium semihydraté, et de l'oxalate de calcium monohydraté, réalisée en montée linéaire de température, permet de vérifier expérimentalement la formulation théorique proposée.Pour obtenir une bonne interprétation cinétique d'une réaction chimique en régime dynamique, la vitesse de chauffe ne doit pas excéder 20°/heure.
In the first part of this paper, the authors point out that the rate of reaction with non-isothermal kinetics depends on a supplementary factor: the heating rate. This assertion is based on the fact that the degreex of reaction is a function of three variables:T (temperature),t (time) andT (heating rate); this was not taken into account by other authors concerned with the subject.Then from the two following hypotheses: a) the rate equation for isothermal conditions is the limit form of the rate equation for non-isothermal conditions, b) the temperature change under dynamic conditions affects the frequency of nucleus formation of the new phase, a theoretical formulation of non-isothermalg(x) laws is proposed. This formulation involves the value of the difference, at constant temperature, between Ink i (isothermal) and In kd (dynamic) in the Ink=f(1/T) diagram.The thermogravimetric study of the dehydration of gypsum, of calcium sulfate hemihydrate, and of calcium oxalate monohydrate, under non-isothermal conditions, allows experimental verification of the theoretical formulation proposed.For a good kinetic approach of a chemical reaction under dynamic conditions, the heating rate must not exceed 20°/hour.
Zusammenfassung Im ersten Teil dieser Arbeit wird von den Autoren bewiesen, daß die Geschwindigkeit einer Reaktion unter nicht-isothermen Bedingungen von einem zusätzlichen Faktor, den Bedingungen des Temperaturenstiegs, abhängt. Diese Behauptung beruht auf der Tatsache, daß der Reaktionsverlauf eine Funktion dreier Variablen ist: der TemperaturT, der Zeitt und der AufheizungsgeschwindigkeitT, wobei letztere Variable bisher von den auf diesem Gebiet arbeitenden Autoren außer Acht gelassen worden ist.Nachfolgend wird an Hand der zwei Voraussetzungen, daß a) die Geschwindigkeitsgleichung unter isothermen Bedingungen die Grenzform der Geschwindigkeitsgleichung unter dynamischen Bedingungen ist und b) die Temperaturänderung unter dynamischen Bedingungen sich auf die Erscheinungsfrequenz der Keime der neuen Phase auswirkt, eine theoretische Formulierung der Gesetzeg(x) für nicht-isotherme Bedingungen vorgeschlagen. Diese Formulierung wird als Funktion der Abweichung ausgedrückt, welche bei einer gegebenen Temperatur zwischen den Werten von Lnk i (isotherm) und Lnk d (dynamisch) im Diagramm Lnk=f(1/T) besteht.Die bei linearem Temperaturanstieg thermogravimetrisch durchgeführte Untersuchung der Zersetzung von Gips, von Calciumsulfat Semihydrat und von Calciumoxalat Monohydrat ermöglicht die vorgeschlagene theoretische Formulierung experimentell zu bestätigen.Um unter dynamischen Bedingungen eine gute kinetische Interpretation einer chemischen Reaktion zu erhalten, darf die Aufheizungsgeschwindigkeit den Wert von 20° pro Stunde nicht überschreiten.
, : . , : (),t () ' ( ), , . : ) ) t(x) . Lnk j () Lnk d ( ) Lnk=f(1/T) . , , . , 20° .相似文献
999.
The new alkaloid oxytriphine, the parent of natural 2-oxazoline derivatives, has been isolated from the epigeal part ofOxytropis trichophysa; and its structure has been established as (5S)-(+)-2,5-diphenyl-2-oxazoline. (-)-N-Benzoyl-2-phenyl-2-hydroxyethylamine and benzoic acid have been detected in this plant for the first time. A hypothesis of the possible biogenetic interrelationship of the compounds isolated is put forward.Institute of the Chemistry of Plant Substances. Uzbekistan Academy of Sciences, Tashkent. Translated from Khimiya Prirodnykh Soedinenii. No. 6, pp. 873–876, November–December, 1993. 相似文献
1000.
The possibilities of amperometric enzyme electrodes in reversed micellar systems for the determination of phenol, 4-chloro-3-methylphenol and 2,4-dimethylphenol are illustrated. The used enzymatic reaction consisted of the oxidation of the phenolic compounds by oxygen, catalysed by tyrosinase. The reduction of the liberated quinones was amperometrically detected. The concentration of the components of the reversed micelles, as well as the potential applied to the tyrosinase electrode have been optimized. The stability of the enzyme electrode with time was also evaluated. The effect of the analyte solubility in water upon the analytical performance of the electrode was explored. Advantages of amperometric biosensors in reversed micelles are shown with respect to aqueous media and organic phase enzyme electrodes. 相似文献