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  • Polymer and Materials Science  (171)
  • SPACE RADIATION  (37)
  • 1980-1984  (140)
  • 1960-1964  (68)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 3 (1960), S. 213-223 
    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 interaction between a carbon black filler and styrene-butadiene rubber is increased if the material is heated after milling. This effect has been attributed to the polymeric free radicals which are presented after milling but which require a high temperature to increase their mobility to the point where they can react. The extent of interaction increases with time of heating and with the amount of milling before heating. The postulated mechanism is supported by the experimental activation energies and by the predictable influence of free radical scavengers on the system.
    Additional Material: 12 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 26 (1981), S. 223-230 
    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: Poly(ethylene terephthalate) filament yarn has been annealed in nitrogen atmosphere, in silicone oil, or in nonreacting organic solvents. Morphological changes resulting from the annealing processes have been followed by Raman spectroscopy. Crystallinity, as evidenced by the width of the 1730 cm-1 carbonyl stretching vibration, is shown to affect the macroscopic properties of these filaments. Furthermore, these spectroscopic results, together with shrinkage measured, suggest that the shrinkage and the crystallization processes in the polymer fiber proceed at different rates in different fluid media.
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Biopolymers 21 (1982), S. 1435-1450 
    ISSN: 0006-3525
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The dissociation of beef liver and bacterial (Micrococcus lysodeikticus) catalases by the action of sodium n-dodecyl sulfate (SDS) has been investigated as a function of SDS concetration and time by ultracentrifugation. The rate of dissociation of beef liver catalase is found to be much faster than that for bacterial catalase in 25 mM SDS at pH 7.0. Beef liver catalase is dissociated into its four subunits after 24 h, whereas bacterial catalase is not completely dissociated after 36 days of incubation. The binding of SDS to beef liver catalase obeys a Hill equation with a cooperativity exponent of 2.0 and a binding constant of 440. The initial interaction of SDS with beef liver catalase can be detected by microcalorimetry, whereas the mixing of SDS with bacterial catalase is athermal. Bacterial catalase retains enzymic activity in the presence of SDS, whereas beef liver catalase is completely deactivated at SDS concentrations above 5 mM. Beef liver catalase is more sensitive to acid denaturation than bacterial catalase, and the rate of dissociation for both catalases is sixth-order in proton concentration. Comparison of the amino acid analysis of the two catalases shows that bacterial catalase has a smaller number of lysyl residues and a larger number of glutamyl residues than beef liver catalase. Taken together these structural differences could lead to a reduced affinity of bacterial catalase for the binding of SDS as observed.
    Additional Material: 10 Ill.
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  • 4
    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: An improved cell which permits the measurement of permeabilities of membranes to gases over a wide range of temperatures and gas pressures is described. The measurements are made by the variable volume method, under constant pressure differential across the membrane. The cell lends itself particularly well to routine tests, because it does not require calibration or the use of vacuum techniques. The performance of the cell is discussed, and typical experimental results are presented. A modified permeability cell of the same type for high-pressure studies is also described. Measurements with this apparatus show that the rate of gas permeation obeys, in some cases, a single from of Fick's law, even under pressure differentials across the membrane as high as 800 psi (54 atm.). The paper also compares permeability data obtained by the variable volume and the variable pressure methods. The permeability of 0.002 in.-thick Alathon 15 polyethylene to oxygen and nitrogen was determined between 0 and 50°C. by the two methods, using the same sample of membrane in situ, and the measurements were found to agree within experimental error. Permeabilites of 0.010 in.-thick samples of Alathon 15 polyethylene to nitrogen, oxygen, helium, and carbon dioxide obtained in the same temperature range by the variable volume method were 15-30% higher than the corresponding data determined by the variable pressure method. This discrepancy could be due to the fact that the variable pressure measurements with the thicker membrances may not have been made under true steady-state conditions, although permeabilities were determined from apparently linear sections of permeated gas pressure vs. time curves. A critical re-examination of the methods used to determine permeability constants is suggested.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 28 (1983), S. 283-294 
    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 room-temperature aging of two nitrile rubber-epoxy adhesives has been examined. Both are 121°C curing systems, based on DGEBA-type epoxy resins, one of which has been available for about 15 years while the other is a more recent development. It has been found that hydrolysis of the epoxide and polymerization both occur slowly, reducing the epoxide content and solubility. A major reduction in honeycomb peel strength of joints made with aged material was evident in the older system and to a lesser extent in the newer adhesive. This is a result of diminished adhesive flow. Tensile strength was less affected by aging.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim [u.a.] : Wiley-Blackwell
    Materials and Corrosion/Werkstoffe und Korrosion 34 (1983), S. 500-504 
    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: Einfluß der Kaltverformung auf die Oxidation einiger nichtrostender StahleOxidationsversuche in Verbindung mit optischer Interferenzmikroskopie liefern Aussagen über die Anfangsstadien der Oxidation im Mikrobereich. Die auf dem Substrat entstehende dünne Oxidschicht führt zum Auftreten einer Interferenzfarbe, die direkt mit der Dicke dieser Schicht korrelierbar ist. Es wird gezeigt, daß das Verhalten der nichtrostenden Stähle auch bei gleicher Vorbehandlung verschieden ist. So ist das Oxidationsverhalten von gezogenem Stahl AlSI 304 und 321 vollkommen anders als das von Incoloy 800 H, während unverformte und rekristallisierte Proben sich gleich verhalten. Dieses Verhalten der Stähle 304 und 321 ist wahrscheinlich der Bildung von α- Martensit in der verformten austenitischen Matrix zuzuschreiben.
    Notes: Oxidation experiments, performed by means of light interference microscopy, give information of the initial oxidation on a microscopic scale. A thin oxide layer on the substrate gives rise to an interference colour, which is directly correlated to the thickness of this layer. It is shown that not all stainless steels react in the same way to the same pretreatments. The oxidation behaviour of drawn AlSI 304 and AlSI 321 is completely different from that of Incoloy 800 H, while the undeformed and recrystallized samples all show the same oxidation behaviour. It is suggested that this behaviour of AlSI 304 and AlSI 321, is caused by the formation of α martensite in the deformed austenitic matrix.
    Additional Material: 9 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 4 (1960), S. 86-91 
    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: Previous time-consuming, destructive methods for examination of infrared spectra of cured, black-loaded rubbers have been replaced almost entirely by a rapid new technique which examines the rubber in its original form. By use of ultrathin microtomed sections (ca. 2 μ thick) of the rubber and electrical amplification of the absorptions on a recorder quite good infrared spectra of the rubber may be obtained. Characterization and structure determination of the rubber can then be carried out. Many different polymers, copolymers, and mixtures of polymers which have been loaded with up to 60 parts phr of carbon black and cured have been characterized in this way. Typical applications to determinations of polymers in tires, etc. are described. The effect of variation in particle size of carbon black is considered.
    Additional Material: 4 Ill.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 53-57 
    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: Many cured, black-loaded rubbers contain varying amounts of inorganic fillers: to characterize the rubber, absorptions due to fillers must be recognized and identified. Reference spectra of all the common inorganic fillers used in the rubber industry have been recorded and their recognition in infrared spectra of ultra-thin microtomed sections of known and unknown samples is described. Both rubbers and inorganic fillers can usually be identified in cured samples.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 171-174 
    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: Infrared absorption spectroscopy has been used to demonstrate dose rate dependence of trans-vinylene unsaturation in irradiated Marlex 50 polyethylene. When the irradiated polymer is stored in vacuum a decrease is observed in trans-vinylene absorbance over a period of several weeks. After high dose rate irradiation the decay is preceded by an initial increase. These phenomena are ascribed to the reaction of “trapped” radicals.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. 20-31 
    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 properties of chlorinated and chlorosulfonated ethylene polymers and copolymers have been examined. The effect of such variables as polymer chain structure, molecular weight, degree of chlorination, and chlorination conditions was studied. A variation in physical properties of different polyolefins chlorinated to the same degree is attributed to differences in residual crystallinity in the chlorinated product. Chlorinated linear polyethylenes are more crystalline than chlorinated branched polyethylene and are semicrystalline, flexible plastics in the 15-35 wt. % range. The chlorinated branched polyethylenes of this chlorine content are soft and rubbery. Chlorination conditions can influence the degree of residual crystallinity in the chlorinated product, and hence have a pronounced effect on the properties of the products Molecular weight of the polymer and degree of chlorination influence the properties of the chlorinated product. Chlorosulfonated linear ethylene polymers and copolymers were tested as elastomers. Stress-strain properties were better for the chlorosulfonated linear copolymers as compared to chlorosulfonated linear polyethylene or branched polyethylene. Poor residual elongation was characteristic of the chlorosulfonated linear polymers. An increase in the number of side groups in the basic polymer chain did not affect residual elongation.
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