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  • Polymer and Materials Science  (58)
  • Wiley-Blackwell  (58)
  • 1980-1984  (58)
  • 1925-1929
  • 1
    Electronic Resource
    Electronic Resource
    Crystal and molecular structure of isoleucinomycin, cyclo[-(D-Ile-Lac-Ile-D-Hyi)3-](C60H102N6O18) (1980)
    New York : Wiley-Blackwell
    Biopolymers 19 (1980), S. 1517-1534 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The crystal structure of a synthetic analog of valinomycin, cyclo[-(D-Ile-Lac-Ile-D-Hyi)3-] (C60H102N6O18), has been determined by x-ray diffraction procedures. The crystals are orthorhombic, space group P212121, with cell parameters a = 11.516, b = 15.705, c = 39.310 Å, and Z = 4. The atomic coordinates for the C, N, O atoms were refined in the anisotropic thermal motion approximation and for the H atoms in the isotropic approximation. Values of standard (R) and weighted (Rw) reliability factors after refinement are 0.073 and 0.056, respectively. The structure is completely asymmetric. The cyclic molecular backbone is stabilized by six intramolecular hydrogen bonds N—H…O=C, five bonds being of the 4→1 type and one being of the 5→1 type. The side chains are located on the molecular periphery. The conformational state of isoleucinomycin in the crystal is intermediate between the corresponding crystalline states of valinomycin and meso-valinomycin. The observed conformation suggests that complexation could proceed via entry of the ion at the face possessing the L-Lac residues, the less crowded face.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.1980.360190808
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  • 2
    Electronic Resource
    Electronic Resource
    Genetic and biochemical analysis of in vivo protein folding and subunit assembly (1983)
    New York : Wiley-Blackwell
    Biopolymers 22 (1983), S. 125-129 
    Details
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The in vivo pathway of folding and subunit assembly of a trimeric bacteriophage protein has been studied by characterizing precursors to the native protein and by analyzing temperature-sensitive mutations that kinetically block the pathway. The native trimer is formed via an intermediate composed of three partially folded chains, the protrimer. At 39°C, temperature-sensitive mutations prevent the formation of both the native trimer and the protrimer, possibly by destabilizing earlier intermediates. However, the mutations do not affect the stability of the native protein, formed at 30°C. Thus, these mutations identify amino acid residues involved in interactions that determine the folding pathway.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/bip.360220120
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  • 3
    Electronic Resource
    Electronic Resource
    Studies in ring opening polymerisation, 6Part 5: cf.1.. Tertiary base initiated polymerisation of 5-phenyl-1,3-dioxolan-2,4-dione (1981)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 313-324 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: 5-Phenyl-1,3-dioxolan-2,4-dione (the anhydrocarboxylate derivative of mandelic acid) has been shown to undergo polymerisation in the presence of tertiary organic bases such as pyridine in a reaction that has somewhat unusual characteristics. Thus, although the reaction in nitrobenzene shows first-order kinetic dependence on both monomer and pyridine over a reasonable concentration range, the pyridine is not consumed and does not appear to control the molecular weight of the resultant polymer. The most important factor in controlling molecular weight is the presence of adventitious moisture which enters into the polymerisation process producing poly-α-esters that are hydroxyl/carboxyl terminated. The rate of polymerisation increases progressively as pyridine is replaced by 2-methylpyridine and 2,6-dimethylpyridine but decreases dramatically when 2-methoxypyridine is used, indicating the importance of the basicity of the attacking species. The results are interpreted in terms of the interaction of the basic nitrogen and the C-4 ring carbonyl leading to the formation of a transient charge transfer complex which subsequently decomposes to form pyridine, carbon dioxide and the α-lactone. The chain growth process involves the interaction of the α-lactone with any nucleophiles present which control the molecular weight and nature of the end groups.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1981.021820204
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  • 4
    Electronic Resource
    Electronic Resource
    Chemistry of naked persulfate, 3Part 2: cf.2.. Phase transfer free radical reactions: polymerization of acrylic monomers in organic solution using potassium peroxydisulfate in the presence of quaternary ammonium salts (1981)
    New York : Wiley-Blackwell
    Die Makromolekulare Chemie 182 (1981), S. 701-703 
    Details
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/macp.1981.021820243
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  • 5
    Electronic Resource
    Electronic Resource
    Metal acetylacetonates as latent accelerators for anhydridehyphen;cured epoxy resins (1981)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 979-986 
    Details
    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: Twenty-two metal acetylacetonate compounds have been evaluated as possible latent accelerators for epoxy-anhydride solventless resins. Experimental data have revealed that titanium (IV) oxyacetylacetonate, chromium (III), zirconium (IV), cobalt (III), and cobalt (II) acetylacetonates are particularly effective with anhydride cured epoxy resins. When added to the resin at a level of 0.05-0.10% (w/w), they provide very fast gel times at 150-175°C combined with very good storage stabilities (〉 six months) at room temperature. The power factor values of cured resin samples, containing these preferred metal acetylacetonates, have been found to be between 2.0 and 2.5% at 150°C and 60 Hz. Correlation between the catalytic effectiveness of these metal acetylacetonates, as latent accelerators for epoxy-anhydride resins, and their thermal stabilities suggest that decomposition products may be the active species responsible for initiating polymerization in epoxyanhydride resin systems.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1981.070260320
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  • 6
    Electronic Resource
    Electronic Resource
    Equilibrium acid concentrations in hydrolyzed polyesters and polyester-polyurethane elastomersPresented in part at the 184th meeting of the American Chemical Society, Kansas City, MO, September 12-17, 1982, Ref. 1. (1983)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 3779-3792 
    Details
    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: Equilibrium acid concentrations, [Ae], were determined in butylene adipate and caprolactone polyesters, of low molecular weight, and in thermoplastic polyurethane elastomers based on these polyesters. Values of [Ae] of the polyesters at 85°C were 0.7, 1.3, and 3-4 × 10-3 mol/g at relative humidities (RH) of 25%, 50%, and 93%, respectively. [Ae] of the thermoplastic elastomers at 85°C were about 3 and 7 × 10-4 mol/g at 10% and 25% RH, respectively. Values of [Ae] were not very dependent on temperature at constant RH. Equilibrated thermoplastic elastomers had low molecular weights and poor physical properties. Consequently, equilibration does not set a practical limit on hydrolytic degradation, even at low RH. Equations were developed that described the variation in acid content with time. Rate constants for hydrolysis and esterification increased as RH decreased. Reesterification in the elastomers in the absence of water is too slow to be a useful method of decreasing hydrolytic damage.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1983.070281218
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  • 7
    Electronic Resource
    Electronic Resource
    Compatibility of poly(∊-caprolactone) (PCL) and poly(styrene-co-acrylonitrile) (SAN) blends. I. Blends containing SAN with 24 wt% acrylonitrile (1984)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 1781-1795 
    Details
    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: Polymer blends of poly(∊-caprolactone) (PCL) and poly(styrene-co-acrylonitrile) (SAN), containing 24 wt % acrylonitrile (AN), were prepared, and their transition behavior was examined by thermal analysis and dynamic mechanical testing. The blends were judged to be compatible on the basis of the presence of a single, compositionally dependent glass transition. The results of thermal treatment upon blends glass transition behavior and the dependence of thermal history upon the crystallization of semicrystalline PCL were also studied. The crystallization of PCL from SAN/PCL blends was found to be retarded by the presence of SAN, and crystalline PCL was found to exist only in blends containing a high PCL concentration. Blends which do not contain crystalline PCL were transparent, and their glass transition behavior can be correlated by the Gordon-Taylor equation. Phase separation, which was characterized by lower critical solution temperature (LCST) behavior, was found to occur when blends were heated to elevated temperatures.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1984.070290531
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  • 8
    Electronic Resource
    Electronic Resource
    The oxidation of 18/8 type stainless steel in high pressure CO2/2% CO (1981)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 32 (1981), S. 1-7 
    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: Die Oxidation von 18/8 Stählen in Kohlendioxid + 2% Kohlenmonoxid bei hohem DruckDie Oxidation verschiedener 18/8 Stähle in Gemischen aus Kohlendioxid und 2% Kohlenmonoxid wurde im Temperaturbereich 550 bis 650°C durch intermittierende Messung der Gewichtszunahme, metallographische Untersuchung, Fraktographie und Rasterelektronenmikroskopie verfolgt. Schon in einem frühen Oxidationsstadium entsteht eine Duplex-Zunderschicht. Die Gewichtszunahme/Zeit-Kurven zeigen zwei Prozeßstufen, und zwar ein Anfangsstadium, das sich exponentiell dem zweiten langsameren Stadium annähert. Die Geschwindigkeit der Duplex-Zunderbildung zeigte nicht die übliche Temperaturabhängigkeit; indessen wurde bei etwa 600°C ein Maximum der Geschwindigkeit festgestellt. Die sekundären Verzunderungsgeschwindigkeiten waren bei 650 und 550°C deutlich zu erkennen und lagen bei der niedrigeren Temperatur höher. Im Zunder traten verschiedene Spinelle auf. Die erhaltenen Ergebnisse werden mit der Annahme gedeutet, daß Kationendiffusion durch verschiedene innere Spinelle der geschwindigkeitsbestimmende Schritt ist.
    Notes: The oxidation of a variety of 18/8 stainless steels in high pressure CO2/2% CO has been followed in the temperature range 550-650°C using intermittent weight gain measurement metallography, fractography and scanning electron microscopy. Duplex scales formed at an early stage of oxidation. The weight gain curves were analysed in terms of a two stage process, the initial stage exponentially approaching a slower secondary stage. The primary rate of duplex scale formation did not show the usual temperature dependence. Rather a maximum in the rate was observed at ∼600°C. Secondary rates were well established at 650°C and 550°C the secondary rate at 550°C, however, being higher than that at 650°C. Various spinels occurred and the results are explained in terms of the rate controlling process being cation diffusion through different inner spinels.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19810320102
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  • 9
    Electronic Resource
    Electronic Resource
    The detailed examination of two stainless steel specimens oxidised for 20,000 hours in high pressure CO2/2% CO (1982)
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 33 (1982), S. 77-82 
    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: Detaillierte Untersuchung von zwei nichtrostenden Stählen nach 20 000 Stunden Oxidation in CO2/2% CO bei hohem DruckMit Hilfe von Rasterelektronenmikroskopie, Mikrosonde und Kernmikrosonde wurden zwei Proben von 18/8-Stählen eingehend untersucht; die Proben waren repräsentativ für die beiden Extreme des nach einem parabolischen Zeitgesetz bei 600°C gewachsenen Zunders. Auf dem im Vakuum angelassenen Stahl 316 erfolgte die Zunderbildung mit hoher Geschwindigkeit, wobei innen eine vorwiegend einheitliche Spinellschicht vorlag, jedoch mit einem chromreichen und nickelarmen Spinell (geheiltes Oxid) an der Grenzfläche Metall/Zunder. Das darunter befindliche Metall war stark aufgekohlt, wobei die Kohlenstoffkonzentration in der Nähe der Metalloberfläche etwa 1 Gew.-% betrug. Bei dem Material mit geringerer Verzunderungsgeschwindigkeit war die innere Zunderschicht komplexer aufgebaut und das Metall weniger stark aufgekohlt. Die Ergebnisse werden unter Berücksichtigung der Zusammensetzung der inneren Oxidschicht und der unter Ausheilung erfolgenden Schichtbildung erläutert, wobei dem dort vorliegenden Sauerstoffpotential der geschwindigkeitsbestimmende Einfluß zugeschrieben wird.
    Notes: Detailed examination has been carried out on two specimens of 18/8 steels representing the extremes of the rates of parabolic duplex scale growth at 600°C using metallography, scanning electron microscopy, microprobe and nuclear microprobe analysis.The high growth rate material, vacuum annealed 316, had an inner layer of mainly a uniform spinel but with a chromium rich low nickel spinel (healed oxide) at the metal interface. The underlying alloy was extensively carburised with a carbon concentration near the metal surface of ∼1 wt%. The low growth rate material had a more complex inner layer and a much lower degree of carburisation. The results are explained in terms of the composition of the inner oxide and the rate of healing layer formation being controlled by the prevailing oxygen potential there.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/maco.19820330202
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  • 10
    Electronic Resource
    Electronic Resource
    Determination of pendant allyl and monomer content in polydiallylphthalate (1984)
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 29 (1984), S. 407-411 
    Details
    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: Methods are described for the determination of diallylphthalate monomer and pendant allyl contents in homopolymers of diallylphthalate. The monomer content was determined by gel permeation chromatography. The total allyl content was determined by FTIR and computer subtraction of solvent spectrum. The pendent allyl content can be calculated from the difference between total allyl and allyl caused by monomer. Determination of both monomer and pendant allyl content in the prepolymer is essential for accurate prediction of the physical properties of the cured polymer.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/app.1984.070290138
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