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  • Articles  (1,006)
  • Chemistry  (1,006)
  • Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics  (969)
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  • Articles  (1,006)
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  • 1
    ISSN: 0948-1907
    Keywords: 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
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 61 (1996), S. 1465-1471 
    ISSN: 0021-8995
    Keywords: 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 , Physics
    Notes: New methods of preparing polymer suspensions of narrow particle size distribution with amino and carboxylic groups on the particle surface have been suggested. The effects of various factors on the diameter and size distribution of polymer particles, their stability, and concentration of functional groups on the particle surface were investigated. The application of such polymer suspensions for immunochemical studies was shown. © 1996 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
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  • 3
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    American Association for the Advancement of Science (AAAS)
    In: Science
    Publication Date: 2017-08-25
    Description: We imaged the interfacial structure and dynamics of water in a microscopically confined geometry, in three dimensions and on millisecond time scales, with a structurally illuminated wide-field second harmonic microscope. The second harmonic images reported on the orientational order of interfacial water, induced by charge-dipole interactions between water molecules and surface charges. The images were converted into surface potential maps. Spatially resolved surface acid dissociation constant (p K a,s ) values were determined for the silica deprotonation reaction by following pH-induced chemical changes on the curved and confined surfaces of a glass microcapillary immersed in aqueous solutions. These values ranged from 2.3 to 10.7 along the wall of a single capillary because of surface heterogeneities. Water molecules that rotate along an oscillating external electric field were also imaged.
    Keywords: Chemistry
    Print ISSN: 0036-8075
    Electronic ISSN: 1095-9203
    Topics: Biology , Chemistry and Pharmacology , Geosciences , Computer Science , Medicine , Natural Sciences in General , Physics
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 27 (1982), S. 1249-1258 
    ISSN: 0021-8995
    Keywords: 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 , Physics
    Notes: Polymerization of allyl methacrylate (AMA) with wool fabrics using different initiators, namely, potassium persulphate, Fe2+—H2O2, benzoyl peroxide, ceric ammonium nitrate, and vanadium pentanitrate, was investigated. The percent of polymer add-on depends upon the type and concentration of the initiator. Addition of metallic salts such as Fe3+ to the polymerization system enhances polymerization significantly when benzoyl peroxide and potassium persulphate are used independently as initiator. The opposite holds true for ceric ammonium nitrate and vanadium pentanitrate. With Fe2+—H2O2, on the other hand, the enhancement is marginal. Also studied was the incorporation of Li+, Cu++, and Fe3+ at different concentrations in AMA - wool-benzoyl peroxide polymerization systems. Determination of the polymer add-on on the basis of double bond analysis revealed that the remained double bond is governed by the magnitude of the polymer add-on as well as by the type of initiator.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Materialwissenschaft und Werkstofftechnik 27 (1996), S. 307-312 
    ISSN: 0933-5137
    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
    Notes: Es werden elektronenmikroskopische Untersuchungsergebnisse an Al2O3-Keramiken, die verschiedenen Oberflächenbearbeitungsverfahren unterworfen wurden, vorgestellt.Die Untersuchungen dienen dem Ziel der Optimierung der Oberflächenbearbeitung von keramischen Werkstoffen, wobei der Einfluß leistungsfähiger Bearbeitungsverfahren auf die Ausbildung möglichst schädigungsarmer Oberflächenschichten, die keinen negativen Einfluß auf Festigkeitskennwerte aufweisen, betrachtet wird.Die Wirkung verschiedener Schleif- und Polierprozesse auf Oberflächenveränderungen bearbeiteter Werkstücke wird dargestellt. Es wurde sowohl die Mikrostruktur der geschädigten Randzonenschicht als auch die des unbeeinflußten Grundmaterials mit elektronenmikroskopischen Methoden charakterisiert. Die verschiedenen Schädigungsstadien gestatten eine Einschätzung der Stärke des Störungseintrages in das Material durch verschiedene Schleif- und Polierprozesse.
    Additional Material: 11 Ill.
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  • 6
    ISSN: 0935-9648
    Keywords: 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 , Physics
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 23 (1972), S. 25-30 
    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: Temperaturabhängigkeit der anodischen Oxidation von Titan unterhalb des Potentials der SauerstoffentwicklungDas Wachstum von dünnen anodischen Oxidfilmen auf Ti im Temperaturbereich zwischen 20 und 70 °C läßt sich rein coulometrisch erfassen. In verdünnten, belüfteten Boratlösungen nimmt dabei das Potential mit zunehmender Zeit linear zu; die Steigung der Kurven nimmt dabei mit zunehmender Stromstärke zu; nach 10 bis 20 min zeigen alle Kurven eine Abflachung. Mit der Änderung der Temperatur ändert sich der Kurvencharakter nur unwesentlich; der Übergang zum flacheren Teil erfolgt ebenfalls nach etwa 20 min, doch bei um so niedrigeren Potenitalen, je höher die Temperatur liegt. Die Werte der aus den Ergebnissen berechneten Aktivierungsenergie zeigen, daß die Schichtbildung nicht nur durch Grenzschichtreaktionen bestimmt wird, sondern daß dabei auch rämliche Einflüsse eine Rolle spielen.
    Notes: The growth of thin anodic oxide films on Ti in the temperature range between 20 and 70° C can be expressed in purely coulometric terms. In diluted and aerated borate solutions the potential increases linearly with time; the slope of the curves increases with increasing current intensity; after 10 to 20 min all the curves show a transition to a flattened shape. Temperature changes have but an insignificant influence on the general character of the curves; the transition to the flatter portion occurs after about 20 min, too, but potentials are the lower, the higher the temperature. The values of the activation energy calculated from the results show, that the layer formation is not only controlled by the bound are face reactions, but also by certain factors coming from the bulk of the solution.
    Additional Material: 10 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Advanced Materials 3 (1991), S. 211-212 
    ISSN: 0935-9648
    Keywords: 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 , Physics
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 25 (1974), S. 749-750 
    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: Der Einfluß von Kupfersulfat und Eisen-III-sulfat auf die Korrosion und das elektrochemische Verhalten von Titan in 47 n PhosphorsäureDer Einfluß von Cu-Sulfat und Fe-III-sulfat wurde potentiodynamisch und gravimetrisch untersucht. Dabei wurden wirksame (kritische) Inhibitorkonzentrationen gefunden. Die Ergebnisse zeigen, daß beide Salze die Korrosion des Titans in Phosphorsäure bei höheren Temperaturen durch Passivierung inhibieren. Der kathodische Prozeß wird dabei erleichtert und das anodische Potential steigt auf Werte oberhalb des Passivierungspotentials. Dem entsprechend gibt es bei Anwesenheit dieser Salze keine Zone aktiver Korrosion.
    Notes: The influecne of Cu- and Fe-III sulfates has been investigated by potentiodynamic and gravimetric methods. The results show that there are effective (critical) inhibitor concentrations. According to the results obtained both salts inhibit the corrosion of titanium in phosphoric acid at elevated temperatures by passivating the metal. The cathodic process is then facilitated and the anodic potential is increased to values above the passivation potential. Correspondingly, there is no zone of active corrosion in the presence of these salts.
    Additional Material: 2 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 39 (1988), S. 338-343 
    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: Einfluß von Kohlenstoff auf die Sulfidierung von Kobalt-Tantal-LegierungenDie Sulfidierung von Kobalt-Tantal-Kohlenstofflegierungen (10 bzw. 15 Massen-% Ta, 0-1 C) wurde in einem H2/H2S-Gemisch mit 10 Vol.-% H2S durchgeführt. Die Reaktionskinetik bei 800-1000°C wurde gravimetrisch untersucht, und der Zunder wurde mittels metallographischer Methoden und Röntgenbeugung analysiert. Unter diesen Bedingungen konnte die Bildung von flüssigen kobaltreichen Sulfiden durch die genannten Tantalmengen nicht unterdrückt werden, weshalb die Sulfidierung mit hoher Geschwindigkeit erfolgte. Bei abnehmender Temperatur kam es zur Verteilung der Tantalsulfide in einer dünnen Zunderschicht, wobei der Transport von Kobalt durch die innere Schicht mit ausreichender Geschwindigkeit erfolgte und eine äußere geschmolzene Zunderschicht entstehen konnte. Der enttäuschende Einfluß des Tantals auf die Sulfidierungsbeständigkeit wird der Tatsache zugeschrieben, daß tantalreiche Sulfide nicht in der Lage sind, eine durchgehende Schicht zu bilden. Zunehmende Kohlenstoffgehalte in der Legierung führen zu einer allerdings nicht dramatischen Erhöhung der Sulfidierungsgeschwindigkeit.
    Notes: The sulphidation of cobalt-tantalum-carbon alloys containing 10 and 15 wt% Ta and carbon in the range 0-1 wt%, was carried out in H2-H2S mixture containing 10% by volume H2S. The reaction kinetics at 800-1000°C were followed thermo-gravimetrically and the scale products examined in detail using metallographic and X-ray diffraction techniques. In these sulphidation conditions (10% H2S - 90% H2) addition of 10 and 15% Ta to cobalt was unable to suppress the formation of liquid cobalt-rich sulphides; consequently, very rapid rates of alloy consumption were attained. Decreasing the temperature resulted in the distribution of the tantalum sulphides in a fine scale. Transport of cobalt through the inner layer was sufficiently rapid to form an outer, molten sulphide layer. The inability of tantalum-rich sulphides to develop into a continuous layer appears to be responsible for the disappointing effect of tantalum on the sulphidation resistance. Increasing carbon contents in the alloy increase the sulphidation rate, but the increase is not very dramatic.
    Additional Material: 7 Ill.
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