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  • 2000-2004
  • 1990-1994  (3)
  • 1990  (3)
  • Chemistry  (3)
  • 25.70
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  • 2000-2004
  • 1990-1994  (3)
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  • 1
    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.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Polymers for Advanced Technologies 1 (1990), S. 143-150 
    ISSN: 1042-7147
    Keywords: Reinforcement ; Amorphous ; Matrix ; LC-polyester ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: The preparation and the mechanical properties of binary blends of amorphous thermoplastics and a para-linked liquid crystalline polyester, which is expected to act as a reinforcement, are reported. The LC-polyester has the advantage that it is soluble in common organic solvents, that it has a low transition temperature, and that it does not crystallize readily. Polycarbonate, polystyrene, poly(methyl methacrylate), and poly(ether sulfone) were selected as matrix materials. Most of the films cast from the blends turned out to be turbid and thus phase separated, the sizes of the dispersed phases ranging between 0.2 μm (in polycarbonate) and 1 μm (in polystyrene).The LC-polyester causes a substantial increase of the stiffness in blends with polycarbonate, poly(methyl methacrylate), and poly(ether sulfone) and almost no increase in the case of polystyrene. These differences are attributed to the particular magnitudes of the strength of the phase coupling between the matrix and the dispersed phase, which is controlled by their compatibility.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Characterization of Selenium Compounds with the 2,4,6-tris(trifluoromethyl)phenyl SubstituentReaction of 2,4,6-tris(trifluoromethyl)phenyl lithium and red selenium results in a product which by acidic hydrolysis yields bis[2,4,6-tris(trifluoromethyl)phenyl] diselenide 1. With diazomethane this compound reacts to form bis[2,4,6-tris(trifluoromethyl)phenylselenenyl] methane 2, with bis(triphenylphosphine)ethene platinum(0) the corresponding bis(triphenylphosphine)bis-[2,4,6-tris(trifluoromethyl)phenylselenenyl] platinum(II) 3 is formed. Chlorine and bromine cleave the selenium-selenium bond in 1 and 2,4,6-tris(trifluoromethyl)phenylselenenyl chloride 4 and -bromide 5 are formed. The selenenyl halides are starting materials for the preparation of N,N′-bis-[2,4,6-tris(trifluoromethyl)phenylselenenyl] sulfur(IV) diimide 6 and sulfinylimino-2,4,6-tris(trifluoromethyl)phenyl selenide 7. The X-ray structures of 1 and 7 are discussed.
    Notes: Durch Reaktion von 2,4,6-Tris(trifluormethyl)phenyllithium mit rotem Selen und anschließender saurer Hydrolyse des Reaktionsprodukts bildet sich Bis[2,4,6-tris(trifluormethyl)phenyl]diselenid 1. Mit Diazomethan reagiert diese Verbindung zu Bis[2,4,6-tris(trifluormethyl)phenylselenenyl]methan 2, mit Ethen-bis(triphenylphosphan)-platin(0) entsteht Bis[2,4,6-tris(trifluormethyl)phenylselenenyl]bis(triphenylphosphan) platin(II) 3. Chlor und Brom spalten die Selen-Selen Bindung in 1 unter Bildung von 2,4,6-Tris(trifluormethyl)phenylselenenylchlorid 4 und -bromid 5. Die Selenenylhalogenide sind Ausgangsstoffe für N,N′-Bis[2,4,6-tris(trifluormethyl)phenyl-selenenyl]schwefel(IV)-diimid 6 und Sulfinylimino-2,4,6-tris(trifluormethyl)phenyl-selenid 7. Die Einkristall-Röntgenstrukturen von 1 und 7 werden diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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