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  • Polymer and Materials Science  (248)
  • Life and Medical Sciences  (83)
  • Wiley-Blackwell  (331)
  • 1980-1984  (331)
  • 1983  (331)
  • 1
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 184 (1983), S. 585-596 
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Light scattering, viscosity and GPC measurements were performed on a homologous series of linear polyethylenes with viscosity average molar masses in decahydronaphthalene at 135°C between 1,0 · 105 and 2,7 · 106 g · mol-1 and relatively broad molar mass distributions. 1,2,4-Trichlorobenzene, α-chloronaphthalene, decahydronaphthalene (decalin) and decane were used as solvents. In the case of linear polyethylene in decahydronaphthalene and decane relationships between intrinsic viscosity and weight average molar mass were established. The values of the weight average molar masses obtained by light scattering are considerably higher than those obtained by viscosity and GPC measurements. These discrepancies are explained by molecular aggregation of the polyethylene macromolecules.
    Additional Material: 11 Ill.
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  • 2
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Scattering functions for linear polyethylenes were calculated, using different assumptions, and compared with experimentally determined scattering functions of the system polyethylene/decane. It is pointed out, that the polyethylene macromolecules in a good solvent can be treated as statistical coils with a non-uniform expansion and a constant average expansion exponent ε and not as statistical coils with uniform expansion. Comparison of the experimentally determined and the calculated scattering functions yields a molar mass distribution of polyethylene which is in agreement with the results from GPC-measurements within the limits of experimental error.
    Additional Material: 5 Ill.
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  • 3
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The effects of relative humidity on hemolymph osmolarity and on kidney ultrastructure are explored in Helix aspersa. The snails are active at 95% relative humidity and less active at 50% relative humidity. The hemolymph osmotic pressure increases with the decrease of relative humidity. Pericardial fluid and hemolymph collected from the heart contain similar amounts of total proteins, and both fluids display hemocyanin molecules in negatively stained preparations. When the snails are kept in an atmosphere of 95% relative humidity, numerous wide intercellular spaces are observed in the single-layered-kidney epithelium. The spaces are almost absent when the snails are kept at 50% relative humidity. It is suggested that prourine is formed through a paracellular junctional pathway across the single-layered kidney epithelium, and that the pericardial cavity is not the site of prourine formation. The septate junctions joining the kidney epithelial cells form a continuous belt of intimate contact in the paracellular pathway of prourine. Long septate junctions with many septa are present in the kidneys of snails from the atmosphere of 50% relative humidity, whereas short septate junctions with fewer septa are found in the kidneys of snails from the atmosphere of 95% relative humidity. It is possible that the longer septate junctions with many septa reduce prourine formation across the kidney sac epithelium.
    Additional Material: 9 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 22 (1983), S. 151-160 
    ISSN: 0730-2312
    Keywords: dog pancreatic microsomes ; signal sequences ; rotavirus glycoproteins ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Rotaviruses are nonenveloped viruses that code for two glycoproteins: a structural glycoprotein (VP7) and a nonstructural glycoprotein (NS29). The precursor to VP7 (37K) was shown to contain a 1.5K cleavable signal sequence. The 37K precursor was authentically processed (signal sequence cleaved and the polypeptide “core” glycosylated) when synthesized in a cell-free system supplemented with dog pancreatic microsomes. Similar experiments were performed with the nonstructural glycoprotein precursor (20K); however, the 20K precursor contained an integral (noncleavable) signal sequence. Both precursors were inserted into membranes cotranslationally and both glycosylated products underwent post-translational oligosaccharide processing. The results suggest a morphogenetic scheme for the simian rotavirus SA11.
    Additional Material: 4 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, N.Y. : Wiley-Blackwell
    Journal of Cellular Biochemistry 22 (1983), S. 235-244 
    ISSN: 0730-2312
    Keywords: fertilization ; egg envelopes ; glycoproteins ; molecular topography ; Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: To investigate the molecular basis of the observed morphological and biological characteristics of coelomic egg envelopes (CE), vitelline envelopes (VE), and fertilization envelopes (FE) of Xenopus laevis eggs, envelopes were radioiodinated under a variety of conditions: in situ, isolated and intact, or solubilized. The distribution of 125I in envelope components was analyzed by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. Each envelope type displayed unique profiles when iodinated in the intact state. A major constituent of VE, the 41,500 molecular weight component, was not labeled in the intact state, although the corresponding component of CE was heavily labeled. After dissociation of the envelope by guanidine-HCl or sodium dodecyl sulfate, all of the components could be radioiodinated. However, when the envelopes (VE and FE) were dissolved by heating and subsequently radioiodinated by lactoperoxidase, the resulting radioactivity profile was similar to that of the intact envelopes, suggesting that in the heat-dissolved envelope, the individual components retain similar structural relations as in the intact envelope. Quantitative but not qualitative differences were found between the inner and outer aspects of VE and FE. The significance of these findings is discussed in relation to what is known about the morphological, biological, and molecular properties of the envelopes.
    Additional Material: 4 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 255-260 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Using direct difference ir and laser Raman spectroscopy, the sequential hydration of hen egg-white lysozyme was monitored. The ir data allowed us to identify some specific molecular hydration events that occur as water is added, whereas the Raman is interpreted in terms of conformational changes. The largest of these solvent-induced changes occurs below the hydration level at which activity commences.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 2513-2516 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 2639-2665 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The problem of viscous damping of vibrating DNA polymer in solution is solved in the low-amplitude limit for all acoustic branches of the spectrum. The acoustic spectrum covers the microwave region of frequencies. Analytic solutions are obtained for a model describing the DNA polymer as a smooth circular cylinder. Numerical solutions are presented for a model describing the DNA polymer as a twisted cylinder of elliptical cross section. The amount of mass loading is determined for both models and the damped spectrum for the mass-loaded oscillator is calculated. The viscous damping is found to be a strong function of frequency, singular at very low frequencies for all modes except the torsional mode of the circular cylinder. All acoustic modes are overdamped, implying that the observation of well-defined resonances in DNA requires either highly structured water on the molecular level or very dry material.
    Additional Material: 14 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Makromolekulare Chemie 111 (1983), S. 203-212 
    ISSN: 0003-3146
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zwei Dreikomponenten-Cokondensate wurden durch Reaktion folgender Monomergruppen mit Formaldehyd hergestellt: (I) p-Chlorphenol, p-Kresol and p-Aminophenol; (II) p-Toluidin, p-Bromanilin und p-Aminobenzoesäure. Durch Zusammensetzung und Kondensationsgrad der beiden Cokondensate wurden diese charakterisiert. Die beiden Cokondensate wurden in verschiedenen stöchiometrischen Verhältnissen gemischt und die Menge an sauren und basischen Gruppen in einer bestimmten Probenmenge berechnet. Mit Hilfe der elektrometrischen Titration in nichtwäßrigen Lösungen wurden die Mengen an sauren und basischen funktionellen Gruppen in den Cokondensat-Mischungen bestimmt. Es wurde eine ausgezeichnete übereinstimmung zwischen den berechneten und den gemessenen Werten gefunden. Die Art der Titrationskurven wurde im Sinne von intramolekularer Wasserstoffbrückenbindung, Homokonjugation und Ionenassoziation in einem Medium niedriger Dielektrizitätskonstante interpretiert.
    Notes: Two three component condensation polymers have been prepared by reaction with formaldehyde from the following groups of monomeric units: (I) p-chlorophenol, p-cresol and p-aminophenol; (II) p-toluidine, p-bromoaniline and p-aminobenzoic acid. The relevant available data regarding the composition and degree of polymerization (DP) of the two copolymers have been used to characterize the samples. The two copolymers have been mixed in various stoichiometric proportions, and the amounts of acidic/basic functional groups expected to be present in a given weight of the mixture, have been calculated. Electrometric titration techniques in non-aqueous solvents have been used to determine the amount of acidic/basic functional groups present in the copolymer mixtures. An excellent correlation could be obtained between the observed and calculated values. The nature of the titration curves have been interpreted in terms of intramolecular hydrogen bonding, homoconjugation and ion-association in a medium of low dielectric constant.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 2659-2671 
    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: Carborane-substituted polyphosphazenes were prepared by the thermal polymerization of phenyl-carboranyl pentachlorocyclotriphosphazene. Successive isothermal vacuum pyrolyses were conducted on the polymer and examined for structural changes by infrared spectroscopy. The degradation products were ascertained by gas chromatography-mass spectrometric analysis. It was found that the presence of the carborane group improves the thermal stability of the polymer by retarding the ring-chain equilibrium processes of decomposition.
    Additional Material: 12 Ill.
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