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131.
The preconcentration of cadmium from aqueous colloid solution containing 8-hydroxyquinoline as extractant, laurylsulphate natrium as surfactant,n-butanol as co-surfactant was performed using micellar ultrafiltration technique. Filters with different pore size and materials were used to achieve a separation from liquid solutions. The cadmium recoveries depending on different conditions (pH, concentration of surfactant) were determined and the results are explained in the terms of colloidal parameters in the compare with the classical solvent extraction.  相似文献   
132.
Summary There were studied the process of styrene polymerization in PVC swollen surface layer initiated by free radicals generated under the action of chemical potential gradient as an external force. It was found that conversion of styrene into the block copolymer is an diffusion controlled process.
Zusammenfassung Die Initiation des Prozesses der Polymerization von Styrol in den Oberflächenquellungsschichten von PVC wurde untersucht.Dabei wurde festgestellt, daß die freien Radikale, welche bei Zerreißung von spannungsbeanspruchten Bindungen, wie sie durch Einfluß von äußeren Kräften auf den Gradienten des chemischen Potentials des Quellungsmittels an Oberflächenquell bildungsmittel Polymer entstehen können, Polymerizationsprozesse des olefinischen Quellungsmittels initiieren können.


Dedicated to ProfessorV. Kellö in celebration of his 60th birthday.  相似文献   
133.
Ascorbate oxidase fromCucurbita sp. was isolated by ammonium sulfate precipitation and DEAE-dextran-silochrome column chromatography. The thermal and pH stabilities of the purified enzyme were investigated. TheK M forl-ascorbic acid (1.5 mM) and chlorohydroquinone (0.37 mM) was determined. Substrate specificity of ascorbate oxidase was investigated and compared with those of laccases fromCoriolus hirsutus andCerrena maxima. Ascorbate oxidase was covalently bound to a polymeric membrane and used in an enzyme electrode for ascorbic acid.  相似文献   
134.
The estimation scheme of uncertainty of determination of 1-hydroxypyrene (1-OHP) in urine was developed analysing the main stages of the analytical procedure: (1) preparation of 1-OHP standards, (2) creation of the calibration curve for the high performance liquid chromatography (HPLC) analysis method with the evaluation of recovery, (3) measuring procedure of aliquot of urine, (4) adjusting the pH of aliquot and hydrolysis with enzyme, (5) solid phase extraction, (6) concentration of the extract, (7) injection of the extract to chromatograph and analysing by the HPLC method, (8) calculation of 1-OHP mass from the calibration curve, (9) calculation of 1-OHP concentration in urine. The evaluation of the uncertainty is based on quantification of individual components. Combined uncertainty was calculated using the law of propagation of uncertainties according to the EURACHEM/CITAC guidelines. Level dependence of the uncertainty arises from the calibration curve. The limits of detection and quantification were found to be equal to 0.03 and 0.1 ng/mL, respectively. The calculated expanded level-dependent uncertainty covers 47–27–25% within the concentration range 0.03–0.1–0.4 ng/mL with the materials and equipment used. These parameters could easily be recalculated according to the proposed scheme if there are some changes in the analysis procedure.  相似文献   
135.
Titanium - catalyzed dimerization of cycloheptatriene affords pentacyclo[7.5.0.02,8.05,14.07,11]tetradeca-3,12-diene, 3, and pentacyclo[8.4.0.03,7.04,14.06,11]tetradeca-8,12-diene, 4. By heating, 3 is converted quantitatively into 4.  相似文献   
136.
The a complexes of furan, thiophene, pyrrole, pyridine, and benzene with the hydride ion were calculated by the MINDO/3 method. The affinities of the indicated aromatic rings and a number of substituted furans for the H ion were estimated. It is shown that the relative magnitude of the affinity correlates qualitatively with the experimental data on the relative rates of the reaction of the examined compounds with nucleophilic reagents. The following order of increasing reactivities of unsubstituted aromatic rings was obtained: pyrrole相似文献   
137.
This paper presents qualitative and quantitative comparative results on the simultaneous TG-DTG DTA of five commercial and low-grade bauxites. The methodology of qualitative determination of the basic mineral forms contained in bauxites is currently being established. The weight losses relating to the steps in the TG curve allow determination of the contents of the basic minerals in bauxite. These are recalculated as percentages of Al2O3, SiO2, CaO moisture and total volatiles. The final results are in accordance with the results of classical chemical analyses, and this jusitifies the use of this technique as a quick method for qualitative and quantitative determinations of both commercial and low-grade bauxites.
Zusammenfassung Qualitative und quantitative Ergebnisse vergleichender simultaner TG-DTG-DTA-Untersuchungen an 5 kommerziellen und geringwertigen Bauxiten werden vorgestellt. Die Methodologie der qualitativen Bestimmung der wichtigsten im Bauxit enthaltenen Minerale wird ausgearbeitet. Die Gewichtsverluste bei den entsprechenden TG-Stufen erlauben die Berechnung der Gehalte an den wichtigsten Mineralen. Diese werden umgerechnet in die Anteile an Al2O3, SiO02, CaO, Feuchtigkeit und Glühverlust. Letztere Resultate stimmen mit denen klassisch-chemischer Analyse überein. Das erlaubt die Anwendung thermoanalytischer Methoden als Schnellverfahren für qualitative und quantitative Bestimmungen in kommerziellen und geringwertigen Bauxiten.

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138.
Radionuclide X-ray fluorescence method with a Si/Li semiconductor detector and238Pn exciting source was used in the study of Mn, Fe, Cu, Zn, and Pb content of solid emissions, raw and final materials of a brick factory. From the point of view of metal content, the working environment of the brick factory is safe for workers.  相似文献   
139.
The kinetics of the reaction of manganese(III) with oxalic acid (OA) has been studied in H2SO4 solutions. Under the experimental conditions of 6 × 10–3 <>0 < 0.4=" mol=">–3 and [H2SO4]0 0.2 mol dm–3 the observed pseudo-first order rate constant k obs follows the expression
  相似文献   
140.
The effect of sample volume, tube length, tube diameter, peak height and sampling rate on the determination of phosphorus in acidic plant digests was investigated, and optimal conditions for the flow injection method are described. Sampling rates of 420 samples per hour were achieved without incurring problems from carryover of samples, and evidence was obtained that rates as high as 700 samples per hour are possible. The flow injection method was proved to be suitable for routine analyses and has obvious advantages over other automated or manual methods in sampling rate, simplicity of design and cost.  相似文献   
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