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  • 1
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Surface Science 18 (1969), S. 245-267 
    ISSN: 0039-6028
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Topics in catalysis 3 (1996), S. 337-354 
    ISSN: 1572-9028
    Schlagwort(e): amorphous silica ; titanium ; FT-IR studies ; ammoximation ; cyclohexanone oxime
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The catalytic behavior and the role of the acidic sites and of the activated forms of molecular oxygen in the ammoximation reaction of cyclohexanone to cyclohexanone oxime were investigated on pure and titanium doped amorphous silicas. The samples were prepared by the sol-gel method under acidic and basic conditions. The introduction of low amounts of titanium on silicas, prepared under basic conditions, strongly increased the oxime yield and conversion. The sample containing 0.25% titanium resulted in a very active and selective catalyst. A further increase of the titanium content decreased the catalytic activity and also the catalyst deactivation, because of a decrease of the tars formation rate. The comparison of the catalytic data and the results of FT-IR and EPR analysis confirmed the bifunctional nature of the amorphous silica catalyst. On the first step of the reaction pathway, the imine formation, the paramount parameter is an intrinsic property of pure silica, related to its textural and structural features. The adsorption experiments showed that the silica prepared under basic conditions, the only active in ammoximation, was able to form surface imine on acidic sites. The nature and the role of the oxidizing sites seem more complex. EPR results showed the presence of radical species on titanium modified silica and also, in small amount, on silica itself; however, the oxime formation did not seem to be a property related only to the presence of activated oxygen species anchored to titanium sites. It has been proposed that the formation of oxime is due to a combined effect of the presence of tars and of the activated oxygen species due to the titanium, which are able to oxidize the imine to oxime.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Catalysis letters 1 (1988), S. 223-228 
    ISSN: 1572-879X
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Temperature programmed description of small amounts of preadsorbed and converted methanol (TPD-C) was studied on acidic forms of modified Y zeolites. The modification consisted of generation of various types and amounts of non-skeletal Al species which yield Al Lewis acid sites, and, consequently, of changes of the number and strength of the Brönsted acid sites. All the non-skeletal Al species enhanced the methanol conversion to products whose composition was dependent on their properties as well as on the remaining skeletal hydroxyls.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    ISSN: 1572-879X
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The simulation of 4 K 1H broad-line NMR spectra of CD3OH interacting with the acidic OH groups of H-mordenite zeolite shows no CD3OH2 + ions but hydrogen-bonded complexes. For high CD3OH concentrations, clusters of hydrogen-bonded methanol molecules are formed, also hydrogen-bonded to Brønsted acid sites of the zeolite. The 300 K 1H MAS spectra prove that the desorbed H-mordenite sample contains also silanol groups in electrostatic interaction with the framework; these silanols do not interact with methanol under our experimental conditions.
    Materialart: Digitale Medien
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  • 5
    ISSN: 1572-879X
    Schlagwort(e): anionic Pt-carbonyl complexes ; CO chemisorption on Pt ; IR spectroscopy ; UV/VIS diffuse reflectance spectroscopy ; faujasites
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract The temporal generation of anionic platinum-carbonyl complexes in platinum ionexchanged zeolites X and Y by reductive carbonylation at 105 Pa and 363 K is monitored by in situ UV/VIS and FTIR spectroscopy. A monomer [Pt3(CO)6]2−, exhibiting bands at 318 and 456 nm in the UV/VIS spectra and at 1790 and 2025 cm−1 in the FTIR spectra, is the only platinum/species formed in NaX. The monomer as well as oligomers are generated in NaY, where the formation of the latter species is due to the stronger acidity in the NaY as compared to NaX. The decomposition of the complexes results in the generation of Pt clusters of the size ≤1 nm.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    ISSN: 1572-879X
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Notizen: Abstract Adsorption of various octenes and octanes was studied with a 10-membered ring molecular sieve, H-[B]ZSM-5. Adsorption of octane was very fast, the double-branched octane diffused slowly, and the triple-branched molecules could not enter the channels of the sample. Since the 10-membered ring molecular sieves are the best catalysts for skeletal isomerisation of n-butene, trimethylpentenes or other larger oligomers cannot be intermediates in this reaction. By contrast, skeletal isomerisation of n-butane which is known to require 12-membered ring channels, can involve a trimethylpentane-like molecule as an intermediate.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Czechoslovak journal of physics 19 (1969), S. 1421-1424 
    ISSN: 1572-9486
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Physik
    Notizen: Abstract The construction of an infrared cell for spectrometric measurements of surface complexes on solids at temperatures up to 450 °C is described. A Pt resistance element measures the temperature of the sample caused by radiation from the source of infrared spectrometer.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Springer
    Reaction kinetics and catalysis letters 4 (1976), S. 151-157 
    ISSN: 1588-2837
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Abstract Обмен C3D6 с гидроксилированным и частично дегидроксилированным HY цеолитом был исследован в газовой (МС) и твердой (ИК) фазах при 300°C и при температуре инфракрасного луча.
    Notizen: Abstract The exchange of C3D6 with hydroxylated and partially dehydroxylated HY zeolites was studied by the analysis of the gas (MS) and the solid (IR) phase at 300°C and at the temperature of the IR beam.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Springer
    Reaction kinetics and catalysis letters 5 (1976), S. 479-487 
    ISSN: 1588-2837
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Abstract Было исследовано взаимодействие пропилена с CoNaX и NaX цеолитами и обмеи водородов пропилена CoNaX цеолитом при температурах инфракрасного луча и 300°C с помощью ИК и МС анализа. Также были измерены теплоты адсорбции. Было овнаружено, что присутствие Co2+ ионов оказывает влияние на структуру адсорбированного комплекса пропилена. Сопоставлены кислотные свойства OH групп цеолитов НУ, НХ и CoNaX и обсужден механизм овмена.
    Notizen: Abstract Interaction of propene with CoNaX and NaX zeolites and exchange of propene hydrogens with CoNaX zeolite was studied at the temperature of the IR beam and at 300°C by means of IR and MS analysis. In addition, the heats of adsorption were measured. The structure of adsorbed propene complexes was found to be influenced by the presence of Co2+ ions. The mechanism of the exchange is discussed and the properties of the OH groups of HY, HX and CoNaX zeolites are compared.
    Materialart: Digitale Medien
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  • 10
    Digitale Medien
    Digitale Medien
    Springer
    Reaction kinetics and catalysis letters 2 (1975), S. 297-303 
    ISSN: 1588-2837
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Abstract Изотопный обмен D2 с OH группами HY цеолитов был исследован в твердой и газовой фазах с помощю ИК и масс-снектроскопии Скорость обменов O2−OH и O2−H2 порышается с дегидроксилированием образцов. Активные центры возникают, вероятно, за счет отрыва решеточного кислорода, и катализируют диссоциацию O2. Дегидроксилирование сопровоздается возникновением групп OH, поглощающих при 3740 см−1, обмен которюх медленнее, чем для остальных OH и оказывает влияние на кинетику обмена в газовой фазе.
    Notizen: Abstract The exchange reaction of D2 with OH groups of HY zeolites was followed both in the solid and gas phase by IR and MS. The rates of D2−OH and D2−H2 exchange increase considerably with dehydroxylation of the sample. The active centers are probably vacancies formed by removal of oxygen from the lattice, they catalyze the dissociation of D2. Dehydroxylation of the sample is accompanied by the formation of 3 740 cm−1 hydroxyls, whose exchange with D2 is slower than that with other OH groups and which affect the kinetics in the gas phase.
    Materialart: Digitale Medien
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