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  • Chemistry  (891)
  • Physics  (141)
  • MATERIALS, METALLIC  (81)
  • 1970-1974  (584)
  • 1965-1969  (506)
  • 1940-1944  (23)
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  • 1
    Publication Date: 2011-08-16
    Description: The effect of vacuum on the cyclic strength of metals is examined. Experimental data are presented of studies to clarify the mechanism of vacuum influence on fatigue failure. The dependence of copper and armco-iron fatigue life on vacuum level is studied. It is found that the presence of saturation on the curve of fatigue life versus vacuum level is common for the materials studied. The effect of vacuum on fatigue fracture of copper is studied over a wide range of deformations. It is shown that fatigue life increase under vacuum conditions and the observed characteristics of the fatigue fracture itself in vacuum are associated with homogenization of the plastic deformation under these conditions.
    Keywords: MATERIALS, METALLIC
    Type: Space Studies in the Ukraine, No. 1 (NASA-TT-F-15535); p 45-64
    Format: text
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  • 2
    Publication Date: 2019-06-27
    Description: Phase diagram of titanium-rich aluminum alloys, using thermal, microstructural, dilatometric, and X-ray analyses
    Keywords: MATERIALS, METALLIC
    Type: NASA-TT-F-11011
    Format: text
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  • 3
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: The methyl methacrylate polymerization initiated by anion-radicals of aromatic hydrocarbons biphenyl, naphthalene, 2-phenyl naphthalene, phenanthrene, anthracene, and acenaphthylene have been studied by IR spectroscopy. From the IR spectra of the reaction mixtures as well as from the UV spectra of the polymers obtained conclusions on the initiation mechanism were drawn.
    Notes: Die von Anionen-Radikalen der aromatischen Kohlenwasserstoffe Biphenyl, Naphthalin, 2-Phenylnaphthalin, Phenanthren, Anthracen und Acenaphthalin initierte Methylmethacrylat-Polymerisation wurde mit Hilfe der IR-Spektroskopie untersucht. Aus den IR-Spektren der Reaktionsgemische sowie aus den UV-Spektren der Polymeren wurden Schlußfolgerungen über den Initiierungsmechanismus gezogen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 80 (1968), S. 620-620 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 11 (1973), S. 2135-2142 
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An attempt was made to evaluate stresses on chemical bonds in axially stressed polymers from the shift of skeletal vibration frequencies in chain molecules. The maximum stress on chemical bonds was found to be at least ten times the average stress on the specimen.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 5 (1973), S. 263-264 
    ISSN: 0030-4921
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The correlation between the puckering angle of the four-membered cycle and 4J has been obtained from analysis of the PMR spectra of some 2-substituted azetidines and oxetanes. The absolute values of 4Jcis and 4Jtrans were found to decrease with decreasing of the puckering angle.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 9 (1971), S. 71-77 
    ISSN: 0449-2986
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 380 (1971), S. 202-211 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: By means of spectrophotometric methods the interaction of CeIV in sulphate and nitrate containing solutions with diethylenetriaminepentaacetic acid (DTPE, H5L), ethylenetriaminetetraacetic acid (ÄDTE, H4A), nitrilotriacetic acid (NTE, H3X), iminodiacetic acid (IMDE, H2Z), acids, and glycine (HGL) has been investigated. In weakly acidic acid redox-stable CeIV complexomates are formed with DTPE, ÄDTE and NTE; CeIV reduction proceeds the more slowly, the more stable the complexonate is. The reverse holds for strongly acidic solutions. Inorganic anions in the solutions display a strong influence on composition and redoxactivity of the CeIV complexonates. The stability of CeIV in its complexonates depends on the type of metal-ligand bonding.
    Notes: Mittels spektrophotometrischer Methoden wird die Reaktion von Cer(IV) in sulfat- und nitrathaltigen Lösungen mit Diäthylentriaminpentaessigsäure (DTPE, H5L), Äthylentriamintetraessigsäure (ÄDTE, H4A), Nitrilotriessigsäure (NTE, H3X), Iminodiessigsäure (IMDE, H2Z), Säuren und Glycin (HGl) untersucht. In schwach sauren Lösungen bilden sich mittlere Komplexonate des Cer(IV) mit DTPE, ÄDTE und NTE, was zur Redoxstabilität der Systeme führt. Eine Reduktion von Cer(IV) durch Komplexon verläuft um so langsamer, je stabiler das Komplexonat ist. In stark sauren Medien beobachtet man eine umgekehrte Gesetzmäßigkeit. Großen Einfluß auf Zusammensetzung und Redoxaktivität von Cer(IV)-Komplexonaten haben in der Lösung befindliche anorganische Anionen. Die Stabilität von Cer(IV) in thermodynamisch stabilen Komplexonaten erklärt sich durch eine andere Bindung zwischen Cer(IV) und Komplexon.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 358 (1968), S. 90-96 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The ternary compounds with the structure of the NaZn13 type were found in the course of the X-ray investigation of the systems lanthanum-nickel-silicon (∼ LaNi10.5Si2.5, a = 11.27-11.35 Å) and lanthanum-iron-silicon (∼ LeFe11.5Si1.5, a = 10.51-10.52 Å); one can regard these compounds as the members of two isoelectronic series, one beginning with LaZn13 and other with LaCo13. The ternary phases of the NaZn13 type in the systems lanthanum-cobalt-silicon and lanthanum-cobalt-aluminium are solid solutions based on LaCo13. Compounds of the NaZn13 type are formed also in the systems cerium-cobaltsilicon (Ce(Co, Si)13, a = 11.36 Å), praseodymium-cobalt-silicon (∼ PrCo10.5Si2.5, a = 11.28 Å) and neodymium-cobalt-silicon (∼ NdCo10.5Si2.5, a = 11.24 Å).
    Notes: Die ternären Verbindungen vom NaZn13-Typ wurden bei der röntgenographischen Strukturuntersuchung der Systeme Lanthan-Nickel-Silicium (∼ LaNi10,5Si2,5, a = 11,27 bis 11,35 Å) und Lanthan-Eisen-Silicium (∼ LaFe11,5Si1,5, a = 10,51-10,52 Å) gefunden; diese Verbindungen kann man als Glieder der isoelektronischen Reihen, die mit LaZn13 bzw. LaCo13 beginnen, ansehen. Die ternären Phasen von demselben Typ in den Systemen Lanthan-Kobalt-Silicium und Lanthan-Kobalt-Aluminium sind LaCo13-Mischkristalle. Die Verbindungen vom NaZn13-Typ bilden sich auch in den Systemen Cer-Kobalt-Silicium (Ce(Co, Si)13, a = 11,36 Å), Praseodym-Kobalt-Silicium (∼ PrCo10,5Si2,5, a = 11,28 Å) und Neodym-Kobalt-Silicium (∼ NdCo10,5Si2,5, a = 11,24 Å).
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 344 (1966), S. 95-101 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The existence of the ternary compounds R3Ni6Si2 (R = Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tu, Yb, Lu) with the superstructure of the Ca3Ag8 type has been established by means of X-ray diffraction analysis. The lattice constants are given. The atoms in the Ce3Ni6Si2 structure have the following positions (space group Im3m—Oh9): 12 (e) x 0 0 with x = 0.280, 24 Ni in 24 (h) 0 x x with x = 0.670, 8 Si in 8 (c) 1/4 1/4 1/4.
    Notes: Die Existenz der ternären Verbindungen R3Ni6Si2 (R = Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tu, Yb, Lu) mit der Überstruktur des Ca3Ag8-Typs wurde röntgenographisch festgestellt. Die Gitterkonstanten sind in Tab. 2 zusammengefaßt. Die Atome in der Ce3Ni5Si2-Struktur besetzen folgende Lagen (Raumgruppe Im3m—Oh9): 12 Ce in 12 (e) x 0 0 mit x = 0,280, 24 Ni in 24 (h) 0 x x mit x = 0,670, 8 Si in 8 (c) 1/4 1/4 1/4.
    Additional Material: 3 Ill.
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