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  • Chemistry  (10)
  • erosion  (3)
  • Wiley-Blackwell  (10)
  • Springer  (3)
  • Blackwell Publishing Ltd
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 34 (1990), S. 47-70 
    ISSN: 1573-4889
    Keywords: erosion ; oxidation ; angle of incidence ; nickel ; cobalt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The combined erosion-oxidation of cobalt and nickel at 600 and 780°C over a range of particle-impact angles has been studied by using weight change vs. time measurements and extensive morphological and microstructural characterization of exposed specimens. The oxidation process has been found to affect the angular dependence of the degradation rates. The effect is especially significant at low-impact angles where ripples and flakes are developed upon the surfaces of specimens.
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 34 (1990), S. 23-45 
    ISSN: 1573-4889
    Keywords: erosion ; oxidation ; high-temperature corrosion ; interactions ; nickel ; cobalt
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The combined erosion-oxidation of nickel, cobalt, and the oxides of these metals have been studied at 780°C in air to examine two regimes of interactionnamely, a regime of erosion-enhanced oxidation during which an oxide scale of constant thickness covers metal specimens, and a regime of oxidation-affected erosion that is characterized by a composite surface layer of metal, oxide, and erodent. In the case of cobalt, these two regimes have been documented and the transition from one regime to another described. For the range of conditions examined, only the oxidation-affected erosion regime was observed for nickel due to its lower oxidation rate compared to cobalt.
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Oxidation of metals 34 (1990), S. 71-100 
    ISSN: 1573-4889
    Keywords: erosion ; oxidation ; alloys interaction
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The modes of interaction of erosion and high-temperature oxidation, occurring simultaneously on an alloy surface, have been studied using Ni-30Cr, MA754, Ni-20Al, and Co-22Cr-11Al-0.2Y alloys to examine the influence of chromia and alumina scale formation on the erosion of nickel and cobalt base alloys. The results have shown that, in the presence of a rapidly flowing oxidizing gas stream, the evaporation of volatile metal oxides becomes important at lower temperatures where normally it can be ignored. Otherwise, the erosion and oxidation of alloys parallels the behavior of pure metals but also introduces additional factors derived from lengthening of the period of transient oxidation and modification of concentration profiles in the alloy adjacent to the alloy/scale interface. Higher erosion intensities extend the transient oxidation behavior which adversely affects the formation of protective scales. As with pure metals, the presence of erosion and oxidation together always produced increased rates of degradation.
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  • 4
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The high-resolution nmr spectrum of baker's yeast tRNACUALeu, a recently sequenced non-denaturable tRNA, has been compared with the spectra of the native and denatured conformers of the closely related species tRNAUUGLeu. Because of the presence of many common base pairs in the different tRNA's, it is possible to assign most of the low-field resonances to specific secondary-structure base pairs. A comparison of the observed positions of the various resonances with those predicted by a semiempirical ring-current shift theory shows a root-mean-square deviation of 0.14, 0.11, and 0.12 ppm for tRNAUUGLeu (native), and tRNAUUGLeu (denatured), respectively. These results support the ring-current shift theory currently used to interpret the low-field nmr spectra of the tRNA molecules. Differences between the predicted and observed positions of some resonances provide new evidence for higher order effects such as shifts from second nearest neighbors, anomalous shifts exerted by G·U base pairs, and tertiary-structure effects. A model that was previously proposed for the denatured conformer of tRNAUUGLeu is also supported.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 16 (1977), S. 1557-1566 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Yeast tRNA3Leu is one of several tRNA molecules which can adopt a stable, biologically inactive, denatured conformation. The circular dichroism of the native and denatured conformers differs, providing the basis for the present study of the mechanism for the renaturation process. Conversion of the denatured structure to the native takes place in two steps: a rapid change occurring immediately on addition of Mg++, followed by a slower, strongly temperature-dependent step which returns the molecule to its biologically active state. Optimal kinetic data for the second step could be obtained at 285 nm. Analysis of the time dependence of Δε285 by the Guggenheim method demonstrated that this step follows first-order kinetics. The temperature dependence of the rate constants over the range 32-41°C yielded the following parameters for the rate-limiting step: Ea = 69 kcal/mole, ΔH
    Additional Material: 6 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 25 (1987), S. 3127-3141 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Isobutylene has been polymerized in a continuous stirred tank reactor using a catalyst system comprised of 1-bromoadamantane and diethylaluminum chloride. The polymerization was carried out in hexane solvent at -15 to -27°C and gave 100% conversion to polyisobutylene (PIB) of 1000-3000 Mw. The results of pyrolysis-gas chromatography-mass spectrometry analyses are consistent with a mechanism involving the formation of the adamantyl cabocation and its addition to an isobutylene molecule to initiate polymerization. 13C-NMR analyses show that the PIB products contain R2C—CR2 and R2C—CHR olefin types. Information on the nature of these olefins and the route to their formation has been developed.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 1405-1406 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 40 (1990), S. 1053-1057 
    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
    Additional Material: 2 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 43 (1991), S. 1293-1299 
    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: The individual, competitive, and displacement adsorption of polyvinyl alcohol (PVOH), hydroxyethyl cellulose (HEC), and hydroxypropylmethyl cellulose (HPMC) in aqueous solution onto an attapulgite clay has been systematically studied. For the individual adsorption experiments, the amount of polymer adsorbed at equilibrium decreased in the order PVOH, HEC, HPMC. In the competitive adsorption experiments, the adsorption level of each polymer is diminished by the presence of a competing polymeric species. Binary mixtures of a cellulosic polymer (HEC or HPMC) with PVOH result in a substantial reduction in the amount of cellulosic polymer adsorbed. In the displacement adsorption studies, the sequential addition of HEC or HPMC is not able to displace previously adsorbed PVOH molecules to any appreciable extent. However, the addition of PVOH to previously equilibrated HEC/clay or HPMC/clay suspensions results in a large amount of the adsorbed cellulosic polymer being displaced by PVOH, especially under conditions of high surface coverage. These results indicate that PVOH is preferentially adsorbed on the clay surface and the strength of attachment to the surface is greater for PVOH than for either cellulosic polymer.
    Additional Material: 7 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 23 (1988), S. 129-134 
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fragment-molecule (F+M) adduct ions of a variety of heterocyclic systems have been observed in positive methane chemical ionization spectra at relatively low sample concentrations, i.e. in the microgram range. The relative abundance of these adduct ions increases with sample concentration. Possible mechanisms of formation of F+M are discussed. Formation of such ions should be recognized as an artifact, otherwise such F+M adduct ions in chemical and electron ionization may be mistaken for impurities present in a sample.
    Additional Material: 1 Ill.
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