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  • Chemistry  (8)
  • charge reduction  (2)
  • Family behavior  (1)
  • 1
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 18 (1993), S. 235-241 
    ISSN: 1572-879X
    Schlagwort(e): Montmorillonite ; clay ; charge reduction ; cation migration
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Controlled calcination of ion-exchanged Texas montmorillonite leads to layer charge reduction. Detailed chemical analyses of both exchangeable and unexchangeable metal species lead to the conclusion that, in complete contrast to the situation with Wyoming bentonite, Ni2+, Co2+ and Zn2+ are all capable of migrating from the interlamellar space into the octahedral region of the sheets where they are (i) isomorphously exchanged for Mg2+, and to a proportionately smaller extent, for Fe2+, (ii) trapped in the octahedral vacancies. In addition, they are converted to unexchangeable species on the interlamellar sheet surfaces by high temperature hydrolysis leading to hydroxide or oxide formation. It is suggested that protons within the octahedral region are bound as -OH+ 2rather than simply physically trapped.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 9 (1991), S. 115-119 
    ISSN: 1572-879X
    Schlagwort(e): Clays ; montmorillonites ; charge reduction ; charge regeneration ; lithiation
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Thermally induced migration of Li+-cations from the interlamellar region into the sheet structure of montmorillonite clays has long been known to lead to charge reduction which, depending on conditions, may be partial or virtually complete. Charge regeneration by treatment with strong base involves H+-extraction from the sheets and detailed structural and interlamellar analysis establishes a 1∶1 balance between Li+ and H+ arising from the structural exchange -OH + Li+→-OLi + H+. Such lithiated clays are substantially more thermally and solvent stable than their precursors.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 7 (1984), S. 375-381 
    ISSN: 0935-6304
    Schlagwort(e): Liquid chromatography, HPLC ; Reverse phase columns ; Window diagrams ; Aromatic carboxylic acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The optimization of the separation of eight aromatic carboxylic acids, using Hypersil SAS and MOS reverse phase columns, with respect to eluent (methanol : water) composition, pH, and temperature, is described. Window diagram techniques are used and the pH of the aqueous buffer and elution temperature are shown to be more critical than eluent composition.
    Zusätzliches Material: 11 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 6 (1983), S. 569-570 
    ISSN: 0935-6304
    Schlagwort(e): Serially coupled capillary columns ; Window diagram ; Optimization ; Compressibility ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 195-195 
    ISSN: 0935-6304
    Schlagwort(e): Gas chromatography ; Columns, packed ; High resolution ; Packing apparatus ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 4 (1981), S. 344-345 
    ISSN: 0935-6304
    Schlagwort(e): Gas chromatography ; Capillary, glass/fused silica ; Gas phase deactivation reaction ; Readily adjustable thickness of silicon layers for deactivation ; Wettability for any known stationary phase ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 11 (1988), S. 649-660 
    ISSN: 0935-6304
    Schlagwort(e): Gas chromatography ; Homologized series ; Retention volumes ; Family behavior ; Chemistry ; Analytical Chemistry and Spectroscopy
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 657-666 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Study of n-butane pyrolysis at high temperature in a flow system allows measurement of the sum of the rate constants of the initiation reactions \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {(1)} & {{\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm 2C}_{\rm 2} {\rm H}_{\rm 5} ^{\rm .} } \\ \end{array} \\ \begin{array}{*{20}c} {(2)} & {{\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm CH}_{\rm 3} ^{\rm .} } \\ \end{array} + {\rm C}_{\rm 3} {\rm H}_{\rm 7} ^{\rm .} \\ \end{array}$$\end{document} and of the Arrhenius parameters of the reactions \documentclass{article}\pagestyle{empty}\begin{document}$$\begin{array}{l} \begin{array}{*{20}c} {(3)} & {{\rm CH}_{\rm 3} ^{\rm .} + {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm CH}_{\rm 4} + {\rm C}_{\rm 4} {\rm H}_{\rm 9} ^{\rm .} } \\ \end{array} \\ \begin{array}{*{20}c} {(4)} & {{\rm C}_{\rm 2} {\rm H}_{\rm 5} ^{\rm .} + {\rm C}_{\rm 4} {\rm H}_{{\rm 10}} \to {\rm C}_{\rm 2} {\rm H}_{\rm 6} } \\ \end{array} + {\rm C}_{\rm 4} {\rm H}_{\rm 9} ^{\rm .} \\ \end{array}$$\end{document} Established data for k1/k2 allow estimation of k1 for 951°K and this, with recent thermochemical data, yields the result log k-1 (l.mole s-1) = 8.5, in remarkable agreement with a recent measurement [20] but over si×ty times smaller than conventional assumption. The product k3k4 (l.2mole-2s-2) is found to be associated with the Arrhenius parameters log (A3A4) = 21.90 ± 0.6 and (E3 + E4) = 38.3 ± 2.7 kcal/mole. These values are much higher than would be e×pected on the basis of low temperature estimates. Independent evaluation gives log A4 = 10.5 ± 0.4 (l.mole-1s-1) and E4 = 20.1 ± 1.7 kcal/mole, hence log A3 = 11.4 ± 0.8 (l.mole-1s-1) and E3 = 18.2 ± 3.2 kcal/mole. These values are shown to be entirely consistent with a wide range of results from pyrolytic studies, and it is argued that they further confirm the view that Arrhenius plots for alkyl radical-alkane metathetical reactions are strongly curved, in part due to tunneling and, appreciably, to other as yet unidentified effects. Since there is published evidence that metathetical reactions involving hydrogen atoms show even greater curvature, it is suggested that this may be a characteristic of many metathetical reactions.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 2 (1970), S. 69-70 
    ISSN: 0538-8068
    Schlagwort(e): Chemistry ; Physics Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Erwartet Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 1007-1021 
    ISSN: 0538-8066
    Schlagwort(e): Chemistry ; Physical Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The pyrolysis of isobutane was investigated in the ranges of 770° to 855°K and 20 to 150 Torr at up to 4% decomposition. The reaction is homogeneous and strongly self-inhibited. A simple Rice-Herzfeld chain terminated by the recombination of methyl radicals is proposed for the initial, uninhibited reaction. Self-inhibition is due to abstraction of hydrogen atoms from product isobutene giving resonance-stabilized 2-methylallyl radicals which participate in termination reactions. The reaction chains are shown to be long. It is suggested that a previously published rate constant for the initiation reaction (1)\documentclass{article}\pagestyle{empty}\begin{document}$$ i - C_4 H_{10} \to CH_3 + i - C_3 H_7 $$\end{document} is incorrect and the value k1 = 1016.8 exp (-81700 cal mol-1/RT)s-1 is recommended. The values of the rate constants for the reactions (4i) \documentclass{article}\pagestyle{empty}\begin{document}$$ CH_3 + i - C_4 H_{10} \to CH_3 + i - C_4 H_9 $$\end{document} (4t) \documentclass{article}\pagestyle{empty}\begin{document}$$ CH_3 + i - C_4 H_{10} \to CH_4 + t - C_4 H_9 $$\end{document} (8) \documentclass{article}\pagestyle{empty}\begin{document}$$ CH_3 + i - C_4 H_8 \to CH_4 + 2 - methylallyl $$\end{document} are estimated to be \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{4i} = 10^{13.16} \exp (- 16300calmol^{ - 1} /RT)cm^3 mol^{ - 1} s^{ - 1} $$\end{document} \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{4t} = 10^{12.51} \exp (- 12900calmol^{ - 1} /RT)cm^3 mol^{ - 1} s^{ - 1} $$\end{document} and \documentclass{article}\pagestyle{empty}\begin{document}$$ k_{8} = 10^{14.05} \exp (- 17600calmol^{ - 1} /RT)cm^3 mol^{ - 1} s^{ - 1} $$\end{document} From a recalculation of previously published data on the pyrolysis of isobutane at lower temperatures and higher pressures, the value k11c, = 109.6 cm3 mol-1 s-1 is obtained for the rate constant of recombination of t-butyl. A calculation which is independent of any assumed rate constants or thermochemistry shows that the predominant chain termination reaction is the recombination of two methyl radicals in the conditions of the present work and the recombination of two t-butyl radicals in those of our previous study at lower temperatures and higher pressures.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
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