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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 52 (1980), S. 1292-1296 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 59 (1987), S. 2551-2555 
    ISSN: 1520-6882
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Microchimica acta 108 (1992), S. 221-226 
    ISSN: 1436-5073
    Keywords: platinum ; ion chromatography ; UV-detection ; biotic materials
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A method for the determination of platinum is presented. The procedure consists of a high-pressure digestion of the sample followed by an ion Chromatographic separation. Then the platinum chloro complex is detected by UV-absorption.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Microchimica acta 101 (1990), S. 173-188 
    ISSN: 1436-5073
    Keywords: ceramics ; atomic spectrometry ; inorganic analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The analytical characterization required in the development and in the quality control of new ceramics is discussed. For the basic substances, the problems encountered in the development of routine techniques for a direct and reliable analysis of Al2O3, AlN, Si3N4, SiC, and ZrO2 powders are reported. Among the atomic spectrometric methods, especially slurry atomization ICP-spectrometry is described. Also the problems encountered in the development of combined procedures as required for the characterization of reference samples are presented. Methods for the direct bulk analysis of ceramics and microdistributional analysis, as they are now under development with laser-based techniques and various probe techniques, are described as well.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1436-5073
    Keywords: platinum ; biotic and environmental material ; high pressure ashing ; separation ; graphite furnace AAS
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A simple and reliable procedure for the determination of platinum including high pressure ashing, separation and detection by graphite furnace AAS has been developed. It was put to practical use in the analysis of biotic and environmental materials polluted with platinum in the concentration rangeμg/kg to g/kg.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1436-5073
    Keywords: electrochemical preconcentration of Mn ; flow-through cell ; GF AAS ; water analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A flow system incorporating a 2-electrode electrochemical microcell with a working electrode made from crushed reticulated vitreous carbon and a graphite furnace AAS instrument was used for the preconcentration and determination of trace amounts of Mn. The sample, rinsing and elution solutions were pneumatically transported through the system. Mn2+ ions can be quantitatively deposited both anodically and cathodically at a voltage of +1.5 to + 3 V and −2.5 to −4V, respectively applied to the cell. Samples of 0.1 to 1 ml volume were analyzed within 5–10 min. The limits of detection and determination were 8.7 and 29 pg, respectively. The reproducibility was 1.5 to 5%. The electrochemical behaviour of Mn in the flow system was studied by using a 3-electrode flow-through cell coupled on-line to a flame AAS instrument.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1436-5073
    Keywords: decomposition ; mass spectrometry ; ceramics ; fluorine ; isotope ratio
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The features of a combustion with elementary fluorine for the case of compact SiC ceramics and model substances for boron containing ceramics (H3BO3 and Na2B4O7) were investigated with the aim of their decomposition and analysis. On-line detection of the gaseous decomposition products by quadrupole mass spectrometry using electron impact ionisation was studied. Limitations by blanks and transport interferences were investigated. Standard addition as well as the isotope dilution technique were used for calibration in the case of B, C and W at the trace and major component level.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 203 (1964), S. 20-33 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary A simple titrimetric ultramicro method allows the determination of carbon in not easily volatile organic compounds using sample weights of 10–30 μg. Comparable quantities of S, P, N, Cl, Br, I do not interfere. The standard deviation of the method is ± 0,08 μg C. Sulphur-free substances are burnt at 1000°C in pure oxygen, sulphur containing substances at 550°C in presence of an Ag-Mn-PbCrO4 catalyst. The combustion is carried out with an electrically heated Pt-spiral in a slow stream of oxygen. The carbon dioxide is absorbed in 0.01 M Ba(OH)2 solution. Complete absorbance is attained by using a special stirrer. The excess of Ba2+ ions is photometrically back-titrated with a 0.01 M EDTA solution and phthalein purple as indicator.
    Notes: Zusammenfassung Eine einfache titrimetrische Ultramikromethode gestattet die Bestimmung des Kohlenstoffs schwerflüchtiger organischer Substanzen (10–30 μg) nach Lösungsteilung. Schwefel, Phosphor, Stickstoff, Chlor, Brom und Jod stören nicht, wenn sie in der gleichen Größenordnung wie der Kohlenstoff vorliegen. Die Standardabweichung der Methode beträgt ±0,08 μg Kohlenstoff. Schwefelhaltige Substanzen werden bei 550°C mit einem Ag-Mn-Bleichromatkatalysator, alle anderen Verbindungsklassen in einem reinen Sauerstoffstrom bei über 1000°C verbrannt. Gezündet wird mit einer elektrisch heizbaren Platinspirale. Zur Bestimmung wird das Kohlendioxid in 0,01 m Bariumhydroxidlösung unter Zuhilfenahme eines hochtourigen Glockenrührers absorbiert und der Überschuß der Bariumionen in 60% dioxanhaltiger Lösung gegen Phthaleinpurpur komplexometrisch zurücktitriert. Die Endpunktsanzeige wurde photometrisch vorgenommen.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 205 (1964), S. 29-40 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary For the determination of chlorine in ultramicro amounts of nonvolatile organic compounds 1–10μg of the substance are measured by taking an aliquot of a solution of known strength. This aliquot is filled into a small quartz tube, the solvent is evaporated by blowing with a stream of filtered air, and the remaining substance is burnt in a stream of oxygen at 1000–1100° C. The HCl formed is absorbed in glacial acetic acid and titrated by help of differential electrolytic potentiometry. The relative standard deviation is ±1,5%. Quantities of N, P, S and F comparable to the amount of chlorine do not interfere. For the determination of chlorine in substances containing bromine and iodine silver electrodes are to be used.
    Notes: Zusammenfassung Zur Ultramikrobestimmung schwerfüchtiger organischer Stoffe werden 1–10 μg Substanz durch Lösungsteilung abgemessen und nach Entfernung des Lösungsmittels im Sauerstoffstrom bei 1000–1100°C verbrannt. Der gebildete Chlorwasserstoff wird in einer Vorlage in Eisessig absorbiert und argentometrisch titriert. Die Endpunktsanzeige erfolgt durch differentielle elektrolytische Potentiometrie mit AgCl-Elektroden. Die relative Standardabweichung beträgt 1,5%. Stickstoff-, P-, S- und F-Mengen in der Größenordnung des Chlorgehaltes verursachen keine Störungen. Bei brom- bzw. jodhaltigen Verbindungen müssen reine Silberelektroden verwendet werden.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Fresenius' Zeitschrift für analytische Chemie 205 (1964), S. 40-50 
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Summary For the determination of nitrogen in ultramicro amounts of nonvolatile organic compounds 5–20 μg of the substance are measured by taking an aliquot of a solution of known strength. This aliquot is filled into a small quartz tube, the solvent is evaporated by blowing with filtered air, and the remaining substance is pyrolyzed in streaming hydrogen at 〉1000°C. Thereafter the nitrogen is converted to ammonia by an iron catalyst at 400°C, and the ammonia is titrated iodometrically with biamperometrical indication. The standard deviation of the method is ±0,016 μg N. Quantities of S, F, Cl, Br and J comparable to the amount of nitrogen do not interfere.
    Notes: Zusammenfassung Zur Ultramikrobestimmung von Stickstoff in schwerflüchtigen organischen Verbindungen werden 5–20 μg Substanz durch Lösungsteilung abgemessen und nach der Entfernung des Lösungsmittels bei 〉1000°C im Wasserstoffstrom pyrolysiert. Der Stickstoff wird anschließend durch einen Eisenkontakt bei 400°C quantitativ in Ammoniak überführt, das jodometrisch mit biamperometrischer Endpunktsanzeige titriert wird. Die Standardabweichung des Verfahrens beträgt ±0,016 μg N. Die Bestimmung wird durch Schwefel und Halogene nicht gestört.
    Type of Medium: Electronic Resource
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