ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • Chemistry  (8)
  • charge reduction  (2)
  • Bronsted acid catalysts  (1)
  • Family behavior  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 18 (1993), S. 235-241 
    ISSN: 1572-879X
    Keywords: Montmorillonite ; clay ; charge reduction ; cation migration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 9 (1991), S. 115-119 
    ISSN: 1572-879X
    Keywords: Clays ; montmorillonites ; charge reduction ; charge regeneration ; lithiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 5 (1990), S. 203-210 
    ISSN: 1572-879X
    Keywords: Montmorillonite ; swectite ; Bronsted acid catalysts ; intercalation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In this short review the special attributes that make modified layered clays such versatile and effective catalysts for the conversions of organic molecules are discussed and exemplified.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 3 (1980), S. 195-195 
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Columns, packed ; High resolution ; Packing apparatus ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 7 (1984), S. 375-381 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Reverse phase columns ; Window diagrams ; Aromatic carboxylic acids ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 6 (1983), S. 569-570 
    ISSN: 0935-6304
    Keywords: Serially coupled capillary columns ; Window diagram ; Optimization ; Compressibility ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 4 (1981), S. 344-345 
    ISSN: 0935-6304
    Keywords: 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
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Homologized series ; Retention volumes ; Family behavior ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 5 (1973), S. 1007-1021 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 4 (1972), S. 657-666 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...