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  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 381 (1911), S. 337-346 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 12
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 107 (1924), S. 383-390 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 13
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 97 (1966), S. 63-74 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: An apparatus for volumetric measurement of gas uptake with an accuracy greater than ± 0,2 μl. is described. A maximum deviation from zero of 0,2 μl./h. is observed under blank conditions when measurements are made relative to a reference chamber to assure constant pressure. The instrument has an maximum effective capacity of 30 ml. substrate. The principal part of the apparatus is a capilliary manometer for pressure equilibration coupled to a micrometer piston which functions as a gas buret.
    Notes: Es wird eine Apparatur mit folgenden Eigenschaften beschrieben: Der Gasumsatz wird nach einem Kompensationsverfahren volumetrisch bei konstantem Druck gemessen. Die Genauigkeit der Volumenmessung ist besser als ± 0,2 μl Gas. Die Nullage zeigt einen maximalen Gang von 0,2 μl/h. Substratmengen bis 30 ml können eingesetzt werden. Die wesentlichen Teile der Apparatur sind ein Kapillarmanometer als „Nullinstrument“ für die Druckmessung und eine Mikrometerschraube, mit deren Hilfe  -  ähnlich wie bei einer Kolbenbürette  -  der Gasumsatz gemessen wird.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 14
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 97 (1966), S. 75-96 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The spontaneous autoxidation of n-butyl methacrylate, i.e., the reaction of the monomer free of peroxides with oxygen in the dark without additional initiators, is a radical chain reaction. The reaction is started by radicals which are generated by an absolutely thermal primary reaction of n-butyl methacrylate and oxygen. At 50.0°C. The rate of this primary radical formation was found to be (1.0 ± 0.2)·10-8 mol·1-1·h-1.The spontaneous overall rate of autoxidation amounts to (3.0 ± 0.3)·10-5 mol·1-1·h-1 at the same temperature. In the course of the autoxidation reaction a polymeric n-butyl methacrylate peroxide is formed which further acts as an initiator for the autoxidation and causes a slightly autocatalytic course of the overall reaction. The decomposition constant of the polymeric peroxide amounts to (3.5 ± 0.2)·10-5 h-1 at 50.0°C.For determining those values it was necessary to measure the autoxidation of n-butylmethacrylate initiated by bis-azoisobutyronitrile. These results are also reported.A theoretical appendix deals with the autoxidation rate in relation with time. Besides of the values of the different reaction constants the particular form of this relation is considerably influenced by the concentration of an added initiator.
    Notes: Die spontane Autoxydation von n-Butylmethacrylat, d.h. die Reaktion des peroxidfreien Monomeren im Dunkeln ohne zugesetzte Initiatoren, ist eine Radikalkettenreaktion. Sic wird durch Radikale gestartet, die in einer rein thermischen Primärreaktion zwischen n-Butylmethacrylat und molekularem Sauerstoff entstehen. Bei 50,0°C wurde die Geschwindigkeit dieser primären Radikalbildung zu (1,0 ± 0,2)·10-8 mol·l-1·h-1. gefunden.Die spontane Bruttoautoxydationsgeschwindigkeit hat bei derselben Temperatur den Wert (3,0 ± 0,3)·10-5 mol·l-1·h-1. Im Verlauf der Autoxydationsreaktion entsteht ein polymeres n-Butylmethacrylatperoxid, das seinerseits als Autoxydationsinitiator wirkt und so einen schwach autokatalytischen Verlauf der Bruttoreaktion bedingt. Die Zerfallskonstante des polymeren Peroxides bei 50,0°C hat den Wert (3,5 ± 0,2)·10-5 h-1.Zur Ermittlung dieser Zahlenwerte waren Messungen der durch Azoisobuttersäuredinitril initiierten Autoxydation des n-Butylmethacrylates nötig, die ebenfalls mitgeteilt werden.In einem theoretischen Anhang wird die Abhängigkeit der Autoxydationsgeschwindigkeit von der Zeit behandelt. Die spezielle Form dieser Beziehung wird, außer von der Größe der verschiedenen Reaktionskonstanten, stark von der Konzentration eines zugesetzten Initiators beeinflußt.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 15
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 135 (1970), S. 131-135 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Di-2-cyanoisopropylperoxide is formed when azobisisobutyronitrile is decomposed under oxygen in isobutyronitrile as a solvent. The yield amounts to ca. 5%. Thermal decomposition of the peroxide occurs with measurable rate only above 120°C by a first order reaction. The energy of activation in cumene as a solvent was found to be 37.9 kcal · mole-1. The rate constant of the decomposition reaction at 140°C amounts to 0.057 h-1 in cumene, to 0.073 h-1 in tert-butylbenzene, to 0.18 h-1 in chlorobenzene, and to 0.23 h-1 in o-dichlorobenzene.
    Notes: Das Di-2-cyanoisopropylperoxid entsteht in etwa 5-proz. Ausbeute bei der Zersetzung von Azoisobuttersäredinitril unter Sauerstoff in Isobutyronitril als Lösungsmittel. Thermisch zerfällt das Peroxid est oberhalb von 120°C mit meßbarer Geschwindigkeit in einer Reaktion erster Ordnung. Die Aktivierungsenergie, in Cumol als Lösungsmittel, wurde zu 37,9 kcal · mol-1 bestimmt. Werte für die Zerfallskonstante bei 140°C sind in Cumol 0,057 h-1, in tert-Butylbenzol 0,073 h-1, in Chlorbenzol 0,18 h-1 und in o-Dichlorbenzol 0,23 h-1.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 16
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 5 (1978), S. 302-311 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The mass spectra of 20 differently substituted dimethylthiophosphinic esters of aromatic hydroxy compounds are presented. Fragmentation routes were investigated using high resolution mass measurements, decoupled metastable determinations and deuterium labelling. All compounds exhibited abundant molecular ions and typical phosphorus-containing ions. Characteristic elimination processes strongly dependent upon the respective type of substitution were observed. Due to their high stability, their great ease of formation and their good gas chromatographic properties these new types of derivatives are of special interest for establishing gas chromatography mass spectrometry profiles of acidic catecholamine metabolites.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 84 (1972), S. 363-363 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 18
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 44 (1911), S. 756-761 
    ISSN: 0365-9496
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 19
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 40 (1907), S. 3691-3695 
    ISSN: 0365-9496
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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