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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Langmuir 9 (1993), S. 2496-2498 
    ISSN: 1520-5827
    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
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 930-933 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 98 (1994), S. 5622-5626 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 57 (1999), S. 61-64 
    ISSN: 1572-879X
    Keywords: heteropoly acids ; hydrates ; tungstosilicic acid ; hydrogen bond
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The dehydration of H4SiW12 O40·15.6 H2O was studied in situ in the IR chamber. On evacuation at room temperature the departure of most loosely bonded water characterized by bands at 3550 and 1616 cm−1 was observed. In the remaining hexahydrate the band at 3445 cm−1 was ascribed to the hydrogen bond between the Od oxygen atom of the Keggin unit and dioxonium H5O 2 + ion, the presence of which is manifested by the 1710 and 1100 cm−1 vibrations. All these bands vanish in the case of anhydrous H4SiW12O40, in which the band at 3106 cm−1 ascribed to the hydrogen bond between neighbouring HPA anions Od−H+−Oc is still present. The dehydration of hexahydrate is accompanied by splitting of the W=Od band into 987 and 1010 cm−1 reflecting the change of the kind of hydrogen bond in which the Od oxygen atom is involved. Based on the above results it was concluded that protons forming oxonium ions in hydrated solid heteropoly acid are more strongly bonded than those in anhydrous one which are forming hydrogen bonds between neighbouring Keggin units.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1572-9028
    Keywords: CuZSM-5 ; NO activation ; IR frequencies ; DFT calculations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract In this paper we study the properties of Cu ions and their interactions with diatomic molecules in Cu-exchanged ZSM-5. We present DFT quantum chemical calculations for models composed of the Cu site and a diatomic molecule accompanied by IR investigations for various forms of CuZSM-5. Two series of calculations with density functional theory have been undertaken in order to investigate the influence of zeolitic framework on properties of exchanged cations: (i) for small models built of free mono- and divalent copper cation interacting with CO, N2 and NO and (ii) 5- or 6-member ring models of ZSM-5 hosting the cation and a diatomic molecule. Comparison of calculated and experimental IR X–Y frequencies supports our model and brings some insight into the activation mechanism.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of thermal analysis and calorimetry 53 (1998), S. 217-225 
    ISSN: 1572-8943
    Keywords: desorption energy distribution functions ; heterogeneity of Si-OH-Al groups in HNa-mordenites ; infrared spectroscopic studies of ammonia desorption ; temperature-programmed desorption (TPD) of ammonia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract We have investigated the temperature-programmed desorption (TPD) of ammonia during the activation of NH4Na-mordenites of different exchange degrees. Using a regularization method, desorption energy distribution functions have been calculated. The obtained results indicate the heterogeneity of the bridging Si-OH-Al groups in HNa-mordenites. This was concluded from the width of the distribution functions and from the presence of submaxima. For HNa-mordenites of exchange degrees below 50%, containing only hydroxyls in the broad channels, two distinct submaxima are present, thus suggesting the presence of at least two kinds of bridging hydroxyls of various acid strengths. In HNa-mordenites of exchange degrees above 50%, the hydroxyls appear in narrow channels and the distribution of ammonia desorption energy broadens on the side of higher energies. This may be related to a strong stabilization of ammonium ions inside narrow channels. The maximum concentrations of hydroxyls of desorption energies between 95 and 135 kJ mol-1 and between 135 and 165 kJ mol-1 calculated from TPD data were 3.9 and 3.3 OH per unit cell (u.c.). These values agree well with our previous IR results of concentrations of hydroxyls in broad and in narrow channels (3.7 and 2.8 OH per u.c.). The TPD data obtained for the heterogeneity of OH groups in HNa-mordenites are in accordance with the IR data concerning ammonia desorption. The IR band of OH groups restoring upon saturation of all the hydroxyls with ammonia and subsequent step-by-step desorption at increasing temperatures shifts to lower frequencies indicating that there are hydroxyls of various acid strengths and the less acidic hydroxyls restore first at lower desorption temperatures.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Reaction kinetics and catalysis letters 51 (1993), S. 161-166 
    ISSN: 1588-2837
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The 3609 cm−1 OH-groups in NaHZSM-5 zeolites are heterogeneous, 5 kinds of OH-groups being found. Benzene is more strongly bonded to more acidic hydroxyls and n-hexane to less acidic hydroxyls.
    Type of Medium: Electronic Resource
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