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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 97 (1993), S. 12819-12827 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 19 (1980), S. 537-541 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial & engineering chemistry research 26 (1987), S. 32-39 
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 4
    ISSN: 1520-5045
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 21 (1982), S. 42-48 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Industrial and engineering chemistry 23 (1984), S. 465-470 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Catalysis letters 22 (1993), S. 1-32 
    ISSN: 1572-879X
    Keywords: Hydrodesulfurization ; hydrodenitrogenation ; hydrodemetallation ; hydrogenation ; hydrocracking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The petroleum industry gets confronted with more stringent requirements with respect to transportation fuels: diminution by a factor of 10, or more, of the sulphur content, and a drastic diminution of the aromatic content. Besides, the quality of the crude oil supply keeps diminishing on an average. For this, the hydrotreating processes (HDS, HDN, HDM, hydrogenation, hydrocracking) will occupy a still increasing place in the refining processes. In a first part, we shall select some of the most important results published recently: use of new modifiers and supports (TiO2, ZrO2, mixed oxides), of metals not yet used in hydrotreating (Ru, Rh, Pd, Pt, possibly Nb, associations RuU, PdU, VU etc.), confirmation of the existence of distinct catalytic sites (hydrogenation and hydrogenolysis of the heteroatom-carbon bonds). Other new results should contribute to clarify the controversies and uncertainties concerning the origin of synergy between different elements and the changes of selectivity as a function of the experimental conditions. For this last topic, reference shall be made to the CoMoS model and the remote control theory. In a second part, we shall summarise the new constraints that the hydrotreating processes will face. It will be necessary to save still more energy. It will also be necessary to achieve a better balance of the various reactions taking place in a given process. The overall selectivity of catalysts and processes will have to be improved. In the third part, we shall try to emphasize directions of research which could help reach the objectives. We shall shortly outline the future contributions of chemical engineering. We shall examine with more details the problems concerning the genesis of adequate catalytic sites (underlining the enormous influence of the activation steps) and the modification of activity by means of the composition of the reacting medium. As the problem of synergy remains crucial for the future developments, we shall also present results with new synergetic systems (WS2 + supported Rh or Pd; MoS2 + supported Pt). The new results give hope that the mechanisms of synergy could get clarified in the near future.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1572-9028
    Keywords: iron–molybdenum–antimony catalysts ; solid-state reactions in catalysts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Catalysts were prepared by impregnation of Fe2(MoO4)3 with different quantities of antimony butoxide. BET surface area measurement, XRD, Mössbauer spectroscopy, CTEM-AEM, XPS and ISS were used to characterize phase and surface architectures and their changes after calcination and catalytic reaction. Before calcination, antimony was present as pure oxide or hydroxide, partly as particles and partly as an incomplete monolayer on the surface of Fe2(MoO4)3. After calcination at 400°C, antimony got detached from the Fe2(MoO4)3 surface and aggregated very intensively, partly as Sb2O4 and partly, through reaction with the iron molybdate, as a mixture of distorted FeSbO4 and MoO3. After reaction or calcination at 500°C, more distorted FeSbO4 and MoO3 are formed, separated from Fe2(MoO4)3. Selective oxidation of isobutene to methacrolein was carried out on the calcined material. Impregnated catalysts show considerably improved catalytic performances compared to the pure Fe2(MoO4)3 phase or mechanical mixtures of it with α-Sb2O4. The catalytic performances are explained by several catalytic cooperations via spillover oxygen. These cooperative effects involve all the oxide phases present in the material having worked as catalyst: Fe2(MoO4)3 (pure or possibly contaminated by small amounts of antimony oxide), FeSbO4, MoO3 and SbyOx.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 41 (1995), S. 1543-1549 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Special kinetic behaviors in isothermal reactions on heterogeneous catalysts composed of two components with different roles are studied with the focus on hi stabilities that could occur in stirred-tank flow reactors when control of catalytic sites on one component by mobile (spillover) species produced by the other operates. The comprehensive kinetic model involves: (1) generation of spillover species on the second phase, their transfer to the potentially catalytic phase, and their reaction with this acceptor to generate selective sites; (2) the kinetics of the catalytic reaction. We developed a model for selective catalytic oxidation, where catalyst sites change from nonselective to selective under the influence of the control by spillover oxygen. The model is based on the system of differential equations. By integration and iteration to the steady state for each value of the external control parameter under investigation, the oxygen and hydrocarbon reactant consumption, as well as the state of the catalyst, is calculated. These calculations predict bistable selectivity for certain ranges of concentration in the feed. Data on the boundaries of the hysteresis loops as a function of catalyst composition and oxygen partial pressure are discussed, as well as the variation of these hysteresis boundaries as a function of the internal parameters.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester [u.a.] : Wiley-Blackwell
    Surface and Interface Analysis 9 (1986), S. 195-206 
    ISSN: 0142-2421
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Physics
    Notes: This paper is written for specialists of surface techniques not perfectly familiar with catalysis, as well as for scientists working in the area of heterogeneous catalysis. It is aimed at suggesting the problems of characterization that surface analysis is faced with, because of the complexity of real catalysts. We first present the various typical ‘architectures’ to which catalysts may correspond. We shall then illustrate typical problems, and their solutions, by selecting examples in the field of hydrodesulfurization (HDS) catalysts. We shall show how 10 out of the 12 theories proposed for explaining catalytic activity were eliminated thanks to surface techniques. HDS catalysts are remarkable in several respects, especially because they undergo many ‘metamorphoses’ (activation, modifications during catalytic work, ageing, regeneration) from the time of their preparation to that of their death by irreversible deactivation. They therefore provide a large body of illustrative examples concerning the characterization of several ‘architectures’. In spite of the achievements of surface techniques in clarifying many features of HDS catalysts during their life, investigators are still faced with unsolved problems; many such problems are related to the very fine scale (of the order of 1 nm or less) of the details of importance for catalysis. This might suggest directions for new improvements or the development of new surface techniques. As a conclusion, we shall recall that, because complete characterization needs the joint use of several techniques, a methodology of study had to be developed, now exists, and still continues to improve. The main lines of this general methodology are not restricted to catalysts, but can be used for the study of all complex highly dispersed solids.
    Additional Material: 13 Ill.
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