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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Analytical chemistry 47 (1975), S. 940-942 
    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
    Industrial and engineering chemistry 18 (1979), S. 148-150 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Biochemistry 18 (1986), S. 465-471 
    ISSN: 0020-711X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
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  • 4
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    International Journal of Biochemistry 18 (1986), S. 725-729 
    ISSN: 0020-711X
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Transition metal chemistry 4 (1979), S. 109-111 
    ISSN: 1572-901X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary The thermodynamic ionisation and formation constant at different ionic strengths of some divalent metal ions ofN-m-tolyl-p-methoxybenzohydroxamic acid at 25 and 35° were determined in several dioxan∶water media. The solid complexes of CuII, NiII and MnII withN-m-tolylbenzo-,N-m-tolyl-p-methylbenzo- andN-m-tolyl-p-methoxybenzohydroxamic acids were prepared and their magnetic susceptibilities measured at room temperature.
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  • 6
    ISSN: 1436-5073
    Keywords: molybdenum ; AAS ; solvent extraction of Mo
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A selective and sensitive method for the extraction and microgram determination of molybdenum (VI) with hydroxamic acid as yellow molybdenum-hydroxamate complex from acidic medium is described. The molybdenum-PCPPSAHA complex has λmax 388 nm, molar absorptivity 5.0 × 103l mol−1 cm−1. The system obeys Beer's law in the range of 1–28 μg/ml of molybdenum(VI). Sandell's sensitivity is 0.0192 μg cm2 and stoichiometry of the complex is 1∶2, molybdenum: PCPPSAHA while mixed complex molybdenum-PCPPSAHA-morin has λmax 400 nm and molar absorptivity 5.9 × 103lmo1−1 cm−1 and stoichiometry of the complex is 1∶2∶1. The molybdenum is determined by graphite furnace atomic absorption spectrophotometry after directly pipetted the extract into the furnace which increases the sensitivity 20 fold.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Microchimica acta 66 (1976), S. 595-601 
    ISSN: 1436-5073
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Eine Methode zur schnellen Extraktion und spektrophotometrischen Bestimmung von Cer(IV) wurde beschrieben. Der Cer-Komplex mit N-p-Tolylbenzohydroxamsäure wird bei pH 8,4–9,8 mit Chloroform extrahiert. Das Absorptionsmaximum liegt zwischen 460 und 470 nm. Bei 465 nm sind die Ablesungen reproduzierbar und wird das Beersche Gesetz zwischen 0,03 und 40μg Cer/ml erfüllt. Die molare Extinktion des genannten Komplexes beträgt bei 465 nm 4,6 · 103 l · mol−1 · cm−2. Es wurde versucht, den Cergehalt von Meerwasser zu bestimmen.
    Notes: Summary A method for rapid extraction and spectrophotometric determination of cerium (IV) is described. The cerium-N-p-tolylbenzo-hydroxamic acid complex is extracted into chloroform at the pH 8.4 to 9.8. Maximum absorbance occurs between 460 and 470 nm. The values are reproducible at 465 nm and Beer's law is obeyed at this wavelength over the range of 0.03–40,μ per ml of the cerium(VI). The molar absorptivity of the cerium-p-TBHA complex is 4.6×103 l · mole−1 · cm−2 at 465. An attempt has been made to determine the cerium in sea water.
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  • 8
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The data presented here were acquired during 1985-1987 as part of the WAVES (Water-Air Vertical Exchange Study) programme in Lake Ontario. Observations were collected from a research tower standing in 12m of water, 1.1 km east of the western shore of the lake. The tower was designed to minimize ...
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 7 (1975), S. 635-641 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Résumé On a étudié l'oxyde d'antimoine trivalent (Sb2O3) par TG, ATD et diffraction des rayons X, dans l'air, l'azote et l'argon. Dans l'air, l'oxydation de Sb2O3 en Sb2O4 se produit au-dessus de 510°. La réaction d'oxydation se déroule en deux étapes, comme le montrent les courbes TG et ATD. Le comportement de Sb2O3 est similaire dans l'azote et l'argon. Sb2O3 reste stable jusqu'à 430°; au-dessus de cette température, il se produit cependant une perte de poids lente et continue, jusqu'à 550°. Au-delà, Sb2O3 se volatilise, ce qui entraîne une perte de poids considérable. L'étude par rayons X indique que la partie sublimée consiste en la forme cubique de Sb2O3 (Sénarmontite) et que le résidu possède une structure orthorhombique (Valentinite). On a estimé à 610° environ la température de la transition cubique-orthorhombique, d'après les courbes ATD obtenues dans l'air, l'azote et l'argon.
    Abstract: Zusammenfassung Untersuchungen zur Thermogravimetrie (TG), Differential-Thermoanalyse (DTA), sowie Röntgendiffraktion von Antimon(III)-oxid (Sb2O3) wurden in Luft, Stickstoff- und Argon-Atmosphäre durchgeführt. In Gegenwart von Luft wird Sb2O3 oberhalb 510° zu Sb2O4 oxidiert. Die Oxidationsreaktion vollzieht sich in zwei Stufen, wie aus den TG- und DTA-Kurven hervorgeht. Das Verhalten von Sb2O3 ist ähnlich in N2 und Ar. Bis zu 430° bleibt es unverändert, bei höheren Temperaturen macht sich bis 550° ein langsamer, kontinuierlicher Gewichtsverlust bemerkbar. Über 550° verflüchtigt sich Sb2O3 was in einem überaus großen Gewichtsverlust deutlich wird. Die Röntgenuntersuchungen des Sublimats und des Rückstandes zeigen, daß Ersteres der kubischen Form von Sb2O3 (Senarmontit) und Letzterer der rhombischen Form (Valentinit) entspricht. Aus den in Luft, N2 und Ar erhaltenen DTA-Kurven wurde die Übergangstemperatur von der kubischen in die orthorhombische Modifikation bei etwa 610° geschätzt.
    Notes: Abstract Thermogravimetry (TG), differential thermal analysis (DTA) and X-ray diffraction studies of antimony(III) oxide, (Sb2O3), in air, nitrogen and argon atmospheres have been made. In air Sb2O3 becomes oxidized to Sb2O4 above 510°. The oxidation reaction proceeds in two stages as revealed by the TG and DTA curves. The behaviour of Sb2O3 is similar in both N2 and Ar. Sb2O3 remains unaffected up to 430°, above which there is a slow, and continuous mass loss up to 550°. Above 550° Sb2O3 volatilizes resulting in an enormous weight loss. X-ray studies of the sublimate and the residue indicate the former to be the cubic form of Sb2O3 (Senarmontite) while the residue is the orthorhombic (Valentinite) structure. From the DTA curves in air, N2 and Ar, the transition temperature for the cubic to the orthorhombic modification has been estimated to be around 610°.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 14 (1978), S. 335-336 
    ISSN: 1572-8943
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The thermal dissociation of N-phenylbenzohydroxamic acid was studied by differential thermal analysis (DTA) and thermogravimetry (TG). The DTA curve showed two exothermic peaks caused by melting and/or decomposition of the compound.
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