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  • 1
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 35 (1989), S. 507-510 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 6 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 338 (1996), S. 627-633 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On Surface Compounds of Transition Metals. XL. Characterization of Chromium Doped Silica Catalyst Systems of the Phillips Type by Scanning Electron Microscopy with Energy Dispersive Analysing System (SEM/EDS)The surface of typical supports for the Phillips catalyst was studied by SEM. The seemingly smooth surfaces are composed by closely packed, ball-shaped substructures; macro- and micro-pores can be seen. Adherent particles on the surface (φ ≪ 1 μm) show the same substructures as the usual surface. After impregnation and activation/reduction of the catalysts crystallites are seen at the surface, which are characterized as Cr2O3 by their crystal shape and EDS analysis.Polymerization of ethylene occurs at the usually doped surface, while the Cr2O3 particles do not exhibit a special activity. Mechanically inforced breaks of the catalyst grains show the formation of threadlike polyethylene with diameters of 200 to 300 nm.
    Additional Material: 10 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 38 (1987), S. 498-506 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Sulfidierung von Fe-Mn-Legierungen und Mn bei hohen TemperaturenDie Sulfidierung von Fe-Mn-Legierungen mit 20-50% Mn und von reinem Mn wurde bei 973 K, 1073 K und 1173 K in H2-H2S Atmosphären bei konstantem pS2 oder konstantem pH2S/pH2 untersucht, unter Bedingungen, bei denen nur MnS gebildet wird. Die Sulfidierungskinetik ist vorwiegend parabolisch, aber bedingt durch zwei verschiedene Diffusionsvorgänge. Bei der Sulfidierung der Fe-Mn-Legierungen bei 973 K und 1073 K ist die Diffusion der Mn-Atome in der Legierung der geschwindigkeitsbestimmende Vorgang, und es wird eine verzahnte Grenzfläche Sulfidschicht/Legierung beobachtet. Bei 1173 K erfolgt ein Übergang zur Kontrolle der Sulfidierungsgeschwindigkeit durch Diffusion des Mn in der Sulfidschicht und ein Übergang von der verzahnten Grenzfläche zur ebenen Grenzfläche.
    Notes: The sulfidation behaviour of a range of Fe-Mn alloys and pure Mn were studied at 973 K, 1073 K, and 1173 K in H2-H2S atmospheres at constant pS2 or constant pH2S/pH2. The sulfidation kinetics were parabolic in most cases, but two different diffusion processes affect the kinetics. In the sulfidation of the Fe-Mn alloys at 973 K and 1073 K, the diffusion of manganese atoms in the alloy is the rate-determining step and an interlocked scale/alloy interface is observed. At 1173 K there is a transition to rate-control by the diffusion of manganese in the sulfide scale connected with transition from rugged to a planar scale/alloy interface.
    Additional Material: 13 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 40 (1989), S. 642-650 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Influence of HCl and N2 on high temperature corrosion in atmospheres with low oxygen pressuresThe effects of HCl and N2 on the high temperature corrosion in atmospheres with low oxygen pressures were investigated.Investigations of the alloy Fe-20Cr in He-H2-H2-O-HCl atmospheres at 1173 K under conditions, where no condensed chlorides could be formed, show the simultaneous growth of Cr2O3 and evaporation of CrCl2. The kinetics of the reactions can be described by growth of Cr2O3 according to the parabolic rate law and transport of CrCl2 in the gas flow following a linear rate law.During heating of the samples in He-H2-H2O-HCl condensed chlorides are formed which decrease the adherence of the oxide layers and cause oxide spallation during cooling. This can be avoided either by preoxidation in H2-H2O or heating in dry hydrogen. The porosity of Cr2O3 layers is not enhanced when HCl is added to the gas atmosphere.The oxidation and evaporation is enhanced in N2-H2-H2O-HCl atmospheres compared to He-H2-H2O-HCl atmospheres. The Cr2O3 scales are coarse grained and poros. The enhanced porosity is caused by the nucleation and growth of chromium nitrides in the transient state of oxidation.
    Notes: Der Einfluß von gasförmigem HCl und Stickstoff auf die Hochtemperatur-Korrosion in Atmosphären mit niedrigem Sauerstoffpartialdruck wurde untersucht.Untersuchungen mit der Legierung Fe-20Cr in He-H2-H2O-HCl-Atmosphären bei 1173 K unter Bedingungen, bei denen keine kondensierten Chloride gebildet werden, zeigten, daß gleichzeitig Wachstum von Cr2O3 und Abdampfen von CrCl2 erfolgt. Die Kinetik der Gesamtreaktion läßt sich durch Überlagerung eines parabolischen Zeitgesetzes für das Oxidwachstum mit einem linearen Zeitgesetz für die Abdiffusion des Chlorides in den Gasstrom beschreiben.Beim Aufheizen der Proben in He-H2-H2O-HCl bilden sich kondensierte Chloride, die die Haftung der Oxidschichten beeinträchtigen und Abplatzen beim Abkühlen verursachen. Voroxidation in H2-H2O oder Aufheizen in getrocknetem Wasserstoff verhindern dies. Die Porosität von Cr2O3-Schichten wird durch den Zusatz von HCl zur Gasatmosphäre nicht erhöht.In N2-H2-H2O-HCl-Atmosphären ist die Oxidation und das Abdampfen beschleunigt gegenüber He-H2-H2O-HCl-Atmosphären. Die gebildeten Cr2O3-Schichten sind grobkörnig und porös. Ursache der erhöhten Porosität ist die Keimbildung und das Wachstum von Chromnitriden im Anfangsstadium der Oxidation.
    Additional Material: 16 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 41 (1990), S. 303-307 
    ISSN: 0947-5117
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Description / Table of Contents: Influence of HCl and Cl2 on high temperature corrosion of 2 1/4Cr 1 Mo Steel in atmospheres with high oxygen pressuresThe oxidation of the 2 1/4 Cr 1 Mo steel was investigated at 773 K in oxidizing He-O2-HCl atmospheres. The addition of HCl to He-O2 atmospheres leads to accelerated oxidation rates. Below porous and cracked oxide scales condensed chlorides are formed. At low HCl pressures 0-1000 vppm the “active oxidation” is determining the corrosion process; i.e. oxidation of evaporating chlorides within the oxide scale. For higher HCl contents 1000-3000 vppm the corrosion behaviour changes to paralinear; i.e. simultaneous parabolic oxide growth and linear mass loss by chloride evaporation.
    Notes: Die Oxidation des 2 1/4Cr1Mo-Stahls in oxidierenden He-O2-HCl-Atmosphären bei 773 K wurde untersucht. Der Zusatz von HCl zu He-O2-Atmosphären führt zu stark beschleunigter Oxidation. Unter porösen und rissigen Oxidschichten bilden sich feste Chloride. Bei niedrigen HCl-Drücken 0-1000 vppm bestimmt „aktive Oxidation“ den Korrosionsprozeß; d.h. Oxidation flüchtiger Chloride innerhalb der Oxidschicht. Bei höheren HCl-Drücken 1000-3000 vppm erfolgt ein Übergang zum paralinearen Korrosionsverhalten, d.h. gleichzeitiges parabolisches Oxidwachstum und lineare Massenabnahme durch das Abdampfen von Chloriden.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1982), S. 390-394 
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Geographic variations in the carbon isotope composition of the human diet and human hair were investigated. The carbon isotopic composition of common foodstufls purchased in Chicago, USA, Tokyo, Japan and Munich, FRG, were determined by combustion and differential isotope ratio mass spectrometry. The dietary protein carbon for the United States (-18.1‰) was calculated to be enriched in 13C relative to the Japanese (-21.2‰) and the German (-23.6‰) diets. To a large degree, the differences reflected the consumption of corn-fed animal products in the United States and Japan, as well as seafood in Japan. The carbon isotopic composition of hair (-16.4, -18.0 and -20.4%) for the three respective populations correlated with the calculated values of the dietary protein, but were 2-3% enriched in 13C. Changes in the isotopic composition of beard hair were shown to record the changes in dietary composition in travelers visiting the respective regions.
    Additional Material: 1 Ill.
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  • 7
    ISSN: 0323-7648
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The r-values of the monomer pair acrylonitrile/allylbenzene in the radical bulk and solution polymerization, using hexamethylphosphoric acid triamide, dimethylsulfoxide, γ-butyrolactone, ethylene carbonate and nitromethane as solvents, have been determind. A copolymerization equation is derived, considering the degradative chain transfer, associate formation and solvent effect, by which the deviations from the Mayo-Lewis concept and the solvent effects can be explained.
    Notes: Die r-Werte des Monomerpaares Acrylnitril/Allylbenzol wurden bei der radikalischen Copolymerisation in Substanz bzw. in den Lösungsmitteln Hexamethylphosphorsäuretriamid, Dimethylsulfoxid, γ-Butyrolacton, Ethylencarbonat und Nitromethan bestimmt. Unter Berücksichtigung der degradativen Kettenübertragung, der Assoziatbildung und des Lösungsmitteleinflusses wurde eine Copolymerisationsgleichung abgeleitet, mit deren Hilfe die Abweichung vom Mayo-Lewis-Modell und Lösungsmitteleffekte interpretierbar sind.
    Additional Material: 1 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 203 (1880), S. 118-137 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 207 (1881), S. 320-347 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 207 (1881), S. 348-360 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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