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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 28 (1994), S. 283-289 
    ISSN: 1572-879X
    Keywords: alumina pillars ; montmorillonite ; catalytic activity ; pillar density
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Controlled calcination of Texas montmorillonite provides a family of materials differing only in cation exchange capacity (cec). Introduction of alumina pillar precursor ions, followed by calcination at 500°C, then provides a family of pillar densities ranging from near zero to the maximum attainable (ca. 0.16 pillars per unit cell) all, however, having cec below 10 mequiv./100 g dry clay and catalytically inactive. Cec and activity are regenerated by exposure to cyclohexylamine. All members of the regenerated family have cec of 36 ± 1 but the proton concentrations vary widely, with a maximum of about 45 mequiv./100 g. The reactivity with respect to pentan-1-ol dehydration to alkene or ether varies with pillar density in similar manner to the proton count and these parameters are essentially linearly related so that there is no correlation between reactivity and pillar density per se. The reactivity of the pillared variety is a maximum with that pre-calcined at ca. 200°C but is only about two-thirds that of the unpillared analogue. The pillared variety is highly selective towards alkene formation, whereas the unpillared analogue strongly favours ether formation. It is suggested that future emphasis be given to improving regeneration techniques, and that since unpillared montmorillonite predominantly catalyses addition of water to alkene to yield ethers, the pillared analogue may be more useful in alkanol production.
    Type of Medium: Electronic Resource
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  • 2
    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
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  • 3
    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
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 10 (1991), S. 63-69 
    ISSN: 1572-879X
    Keywords: Montmorillonite ; Bentonite, clay ; charge reduction/regeneration ; cation migration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Controlled calcination of ion-exchanged Wyoming Bentonite in the presence and absence of ammonia leads to layer charge reductions. Detailed chemical analyses of both unexchangeable and exchangeable species lead to the conclusion that in no case is there migration of the original interlamellar cations into the octahedral region of the layers although, in terms of ionic radius alone, Mg2+, Ni2+ and, possibly Co2+, might be expected to do so. The production of unexchangeable Mg, Ni or Co, is identified as resulting from high temperature hydrolysis leading to hydroxide or oxide formation.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-879X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    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
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 14 (1992), S. 11-13 
    ISSN: 1572-879X
    Keywords: Pillared layered materials ; synthesis ; characterisation ; pillar density
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A practical approach to the synthesis from a given layered host of pillared derivatives of varied, and controlled, pillar density is described. An analytical technique allowing measurement of the pillar density is outlined and it is shown that, if the stoichiometric composition of the host is known, the measurements permit elucidation of the charge on the ionic pillar precursor. Once established for fixed conditions of synthesis this would allow calculation of pillar density from a knowledge of the cation exchange capacity of the original host.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-879X
    Keywords: Montmorillonites ; layered materials ; pillared layered materials ; synthesis ; pillar precursor charge ; pillar density
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Controlled calcination of Texas montmorillonite has allowed production of a range of materials of cation exchange capacity from ≈ 70 mequiv./100 g dry clay to virtually zero. Pillaring of these with Chlorhydrol precursor solution has then provided a family of materials of pillar density ranging from about one per six unit cells to zero. The analytical technique based on isomorphous metal dilution (IMD) that follows pillaring is validated. The results provide a consistent value for the precursor (Keggin) ion charge, in the conditions normally used, of 3.15±0.10 rather than the “formal” value of 7. An approach to the attainment of pillar densities consistent with the introduction of shape/size selectivity on pillared layered materials is outlined.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Journal of radioanalytical and nuclear chemistry 242 (1999), S. 663-669 
    ISSN: 1588-2780
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Notes: Abstract The gas chromatographic technique of elution by characteristic point (ECP) has been used to determine partition data for HN3 at finite concentrations with tributyl phosphate (TBP) in hydrocarbon (hexadecane) solution in the presence of nitric acid and uranyl nitrate. The data are used to derive predictive equations for calculating gas-liquid and liquid-liquid partition coefficients for varying temperature and varying concentrations of TBP, HNO3, UO2(NO3)2, and HN3 in hydrocarbon solvents simulating nuclear fuel reprocessing flow sheets. The chromatographically derived partition data presented, being based on more precise measurements than were previously possible using conventional methods, allowed demonstration and quantification of the logarithmic temperature effect expected, but previously unobservable.
    Type of Medium: Electronic Resource
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  • 10
    Publication Date: 1999-12-01
    Print ISSN: 0236-5731
    Electronic ISSN: 1588-2780
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering
    Published by Springer
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