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  • Polymer and Materials Science  (1,882)
  • Analytical Chemistry and Spectroscopy  (859)
  • AERODYNAMICS  (526)
  • SPACECRAFT DESIGN, TESTING AND PERFORMANCE
  • 2020-2024
  • 1980-1984  (2,008)
  • 1975-1979  (1,517)
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Keywords
Publisher
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Raman spectra and normal vibrations of dipeptides. II. Glycyl-L-proline (1983)
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 1285-1300 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Raman and ir spectra of the glycyl-L-proline (GP) dipeptide were recorded. A normal-coordinate treatment was performed on the basis of the experimental spectra, using a modified Urey-Bradley force field (MUBFF). Cyclic redundancies were eliminated, and those due to the ring methylene groups, particularly distorted in regard to the tetrahedral conformation, were treated. An assignment of the experimental frequencies is proposed on the basis of the normal treatment.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360220504
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  • 2
    Electronic Resource
    Electronic Resource
    Phase separation by synthesis of semi-interpenetrating network on the basis of polystyrene and poly(butyl methacrylate) from homogeneous solution (1984)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 185 (1984), S. 347-351 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Phase separation by semi-interpenetrating polymeric network formation based on the copolymer styrene-divinylbenzene (PS-DVB) and poly(butyl methacrylate) (PBMA) was investigated by light scattering. The time for phase separation was measured as a function of the rate of the copolymerization reaction and of the composition of the initial blend. The time until the outset of phase separation decreases with increasing content of PBMA in the blend. The change in concentration of DVB does not influence the process of phase separation.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1984.021850211
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  • 3
    Electronic Resource
    Electronic Resource
    Corrosion fatigue behaviour of nitrogen-implanted steel in water (1980)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 31 (1980), S. 783-789 
    Details
    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: Schwingungskorrosionsverhalten von nitriertem Stahl in WasserDas Schwingungskorrosionsverhalten von nitriertem Stahl in neutralen Lösungen wurde unter Verwendung von schwingenden, einseitig eingespannten Proben (cantilever beam method) elektrochemisch (Ekorr/Zeit, Rp-Messung) und mittels Rasterelektronenmikroskopie untersucht.Die Korrosionsgeschwindigkeit in stagnierenden Flüssigkeiten ist bei dem nitrierten Stahl, unabhängig von der Stickstoffkonzentration, niedriger als bei unbehandeltem Stahl; die an der Oberfläche entstehenden Oxidschichten besitzen deutlich bessere Schutzwirkung.Bei einer zyklischen Belastung (25,4 kg/mm-2, 16,6 Hz) ist die Rißauslösung verzögert. Die Zeit bis zum Bruch ist beträchtlich kürzer als bei nicht nitrierten Proben (zumindest unter den verwendeten Versuchsbedingungen). Die Erhöhung der Rißausbreitungsgeschwindigkeit läßt sich erklären durch die Gefügeschädigungen, die durch das Nitrieren hervorgerufen werden. Die Bruchmorphologie wird ebenfalls erörtert.
    Notes: The corrosion fatigue behaviour of nitrogen implanted iron in neutral solutions has been investigated utilizing the oscillating cantilever beam method, by means of electrochemical (Ecorr vs. time plots, Rp measurements) and S. E. M. techniques.The calculated corrosion rate under stagnant conditions is lowered for the implanted iron at all nitrogen doses with respect to untreated iron. The surface oxide layers achieve enhanced protecting capacity.Consequently under a cyclic load of 25.4 kg mm-2, at a frequency of 16.6 Hz, cracks nucleation is delayed. The time to breaking of implanted specimens is considerably lower in our experimental conditions compared to untreated iron. The increase in the crack growth rate is consistent with the detrimental action of structural damage following implantation. The fracture morphology is also discussed.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19800311006
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  • 4
    Electronic Resource
    Electronic Resource
    Condensation of Co++ ions on chondroitin sulfate from transport coefficients and proton NMR measurements in aqueous solutions (1979)
    New York : Wiley-Blackwell
    Biopolymers 18 (1979), S. 1849-1857 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The “condensed” counterions which characterize high-charge-density polyelectrolyte solutions can be analyzed into two subpopulations: (1) site-bound counterions and (2) atmospherically entrapped counterions. The distinction is achieved experimentally by combining the data from self-diffusion coefficient or electrical mobility measurements, which give the amount of “condensed” ions, and those from nmr, chemical shift measurements, which indicate the amount of site-bound ions. In the case of a solution of chondroitin sulfate with excess Co++ counterions, it can be estimated that 20% of the structural charge of the polyion is neutralized by site-bound, dehydrated, condensed counterions, while a further 30% is neutralized by atmospherically entrapped, hydrated counterions.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1979.360180803
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  • 5
    Electronic Resource
    Electronic Resource
    Separation of dextrans by gel permeation chromatography (1978)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Physics Edition 16 (1978), S. 2147-2155 
    Details
    ISSN: 0098-1273
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The role of the intrinsic viscosity [η] as separation parameter in gel permeation chromatography (GPC) was studied for dextrans (from Leuconostoc mesenteroids B512) dissolved in water with deactivated silicagel (Porasil) as the column-filling material. For that purpose specific viscosities of dextran fractions eluted by GPC were measured as a function of the elution volume v. Provided that the elution volumes are corrected for zonal spreading, they are related to the intrinsic viscosities in an unambiguous way, probably reflecting a unique relationship between degree of branching and molecular weights. This was further investigated by developing an iteration method to prepare two calibration curves γ(v) and g(v), respectively, relating ln[\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}] and InM (M is the molecular weight) to v. It required that the weight-average molecular weight Mw, the number-average molecular weight Mn, and the average intrinsic viscosity [\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}] for a number of dextran samples (broad distributions) be previously known. The calibration curves found lead to consistent values of the above-mentioned averages. Moreover, they allow-establishment of the [\documentclass{article}\pagestyle{empty}\begin{document}$\left[ {\bar \eta } \right]$\end {document}]-M relationship over the range 5000 〈 M 〈 500,000.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1978.180161205
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  • 6
    Electronic Resource
    Electronic Resource
    Methods for the determination of the number of polytetrahydrofuran branches in neoprene-g-polytetrahydrofuran (1980)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 2021-2031 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methods for the determination of the number of the number of polytetrahydrofuran branches in neoprene-g-polytetrahydrofuran were examined. Only two suitable methods were found; namely, termination of oxonium ions by triphenylphosphine followed by 31P-NMR and termination with NH4OH—NH4Cl buffer and reaction with fluorescamine followed by fluorescence spectroscopy. Both methods led to the conclusion that Neoprene W has 9 ± 1 active halogens per mole that can be used to initiate tetrahydrofuran polymerization when silver salts are added. Among the methods examined in this study the fluorescence method was the most reliable, most reproducible, fastest, and simplest.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1980.170180637
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  • 7
    Electronic Resource
    Electronic Resource
    Quantitative analysis of 5-fluorouracil and 5,6-dihydrofluorouracil in plasma by gas chromatography mass spectrometry (1982)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 9 (1982), S. 336-339 
    Details
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 5-Fluorouracil and 5,6-dihydro-5-fluorouracil were analysed in the plasma of patients by combined gas chromatography mass spectrometry. 5-Bromouracil was the internal standard. After extraction from plasma with an isopropanol-diethyl ether mixture (20/80) the components were pentylated and the derivatives produced extracted into diethyl ether. Electron impact mass spectrometry was used for the simultaneous quantitative determinations of 5-fluorouracil and 5,6-dihydro-5-fluorouracil (detection limit 10 ng mI-1 5-fluorouracil, 80 ng mI-1 5,6-dihydro-5-fluorouracil). Chemical ionization was utilized to measure 5,6-dihydro-5-fluorouracil concentrations 〈80 ng mI-1 (sensitivity 10 ng mI-1). The biological applicability of these two techniques was demonstrated by analysing plasma samples from patients after administration of 5-fluorouracil or 5′-deoxyfluorouridine by intravenous injections and infusions.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200090806
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  • 8
    Electronic Resource
    Electronic Resource
    Synthesis of secondary hydroxyl-terminated telechelic polybutadiene prepolymers using a new azobisnitrile initiator (1983)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 21 (1983), S. 3591-3595 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1983.170211219
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  • 9
    Electronic Resource
    Electronic Resource
    Letters to the editor (1982)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 17 (1982), S. 643-645 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210171211
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  • 10
    Electronic Resource
    Electronic Resource
    Californium-252 plasma desorption time of flight mass spectroscopy of proteins (1984)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 11 (1984), S. 242-257 
    Details
    ISSN: 0306-042X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Fast heavy ions, i.e. fission fragments from a 252Cf-source, have been used to desorb and ionize peptides and proteins from a sample surface. Masses of the desorbed ions have been determined by the time-of-flight technique. The mass interval of the molecules studied is 1000-14 000 u. Quasi-molecular ions of higher masses than earlier reported have been observed. The results include the detection of quasi-molecular ions of proinsulins, cytochrome-C, ribonuclease and two phospholipases. The general features of mass spectra of proteins using this ionization method are described. Emphasis is put on the discussion of metastable ion decay, neutral components, multiply charged ions, isotopic broadening, and cluster ion formation. Also the precision which can be obtained with a straight time-of-flight mass spectrometer will be discussed. Future applications of the technique are outlined.
    Additional Material: 22 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bms.1200110509
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