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  • Artikel: DFG Deutsche Nationallizenzen  (10)
Datenquelle
  • Artikel: DFG Deutsche Nationallizenzen  (10)
Materialart
Erscheinungszeitraum
  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 70 (1966), S. 3738-3740 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 16 (1976), S. 507-509 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: In a previous paper, results of morphological studies using electron microscopy and X-ray diffraction were reported concerning random and non-random olefin copolymers of ethylene. As comonomers, relatively low concentrations of n-alpha alkenes and 5-methyl norbornene-2 were used. It was tentatively concluded that one possibility for morphological changes observed in the n-alpha alkene copolymers was a change in direction of chain folding. These studies have been continued with copolymers of ethylene and acenaphthylene. The intent was to pursue effects of vicinal substitution; however, the result was to produce ethylene copolymers of quite high comonomer content which were crystalline and showed no evidence of an independent beta mechanical transition. Further, definite evidence was found to indicate a change in the direction of chain folding in the polymer crystals.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 16 (1976), S. 510-511 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Polyolefins are generally known either as partially crystalline thermoplastics or as elastomers. With the finding in the ethylene-acenaphthylene copolymer system of the unusual properties of high crystallinity, high modulus, and no independent beta thermomechanical transition at high comonomer contents, it appeared that it might be possible to prepare a block polymer system which would retain the desirable low temperature transition near -110°C and “hard” acenaphthylene copolymer segments as well. Attempts were made, and the resulting terpolymer is described. An intermediate crystallinity polymer of apparently broad composition distribution was obtained with the modulus of high density polyethylene but the elongational characteristics of low density polyethylene.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 16 (1976), S. 734-734 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 15 (1975), S. 842-847 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Studies have been published relating the mechanical properties of ethylene copolymers with short chain branching structures. Other work has emphasized that crystallites in these copolymer systems participate in superstructures and that stress distribution during mechanical testing depends on the arrangement of these structures, the morphology. While developing structure-property correlations, morphologies of some random and non-random olefin copolymers have been examined. Surprising morphological differences were found depending on the length, concentration and degree of randomness of the n-alkyl branch and on vicinal substitution with norbornene derivatives as comonomers. X-ray diffraction yielded unexpected results which can be explained by a change in the direction of chain folding. Linear side chains randomly introduced into an otherwise high density polyethylene result in a two to three fold increase in the 110:200 x-ray intensity ratios, a slight reduction in the 110:020 intensity and a 5 to 10 fold decrease in the 200:02 intensities. These results cannot be explained by orientations introduced in sample preparation. There are associated morphological changes. Vincinal substitution with norbornene comonomers has little effect on crystal habit but does change the morphology, tending to shift superstructures from lamellar to fibrillar in nature.
    Zusätzliches Material: 13 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 37 (1959), S. 555-558 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 38 (1959), S. 141-155 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: A surface-etching technique has been devised which reveals the spherulites in molded Polyethylene for study with the electron microscope. By means of this technique it is possible to observe the effect of various heating cycles and polymer structures on the size and perfection of the spherulites. The etching technique shows that two different types of large spherulites may be formed in polyethylene. One, which may be formed on molding, contains a relatively low amount of internal order. The other, which forms on long heat aging or annealing, contains a high degree of internal order. Heat aging at temperatures well below the melting point will induce the poorly ordered type of spherulite to break up and regrow in the highly ordered form. Spherulite structure was observed to depend not only on heat treatment, but also on chain branching and molecular weight. Increased linearity induces the formation of a more regular, sheetlike or laminated structure within the spherulites, while lower molecular weight causes the lamellae and spherulites as well to be larger in size. Extremely high molecular weight linear resins showed no spherulitic structure as such, but were fibrillar in appearance. Annealing or long heat aging of these resins induced the formation of a row type aggregate structure rather than the typical spherulites observed in normal molecular weight resins. Electron microscope studies of stress-cracked surfaces indicate that a high degree of internal spherulitic order such as is formed on long heat aging may well be the primary cause of stress-cracking in polyethylene. This is further indicated by resins such as the ethylene/propylene copolymers, in which highly ordered spherulites do not form with heat aging. These resins are very resistant to stress cracking. Structural studies show that the ethylene/propylene copolymers are very nonrandom, and it is believed that this interferes with the formation of perfect, and consequently crack-prone, spherulites.
    Zusätzliches Material: 14 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 561-562 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 1 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 21 (1956), S. 557-559 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    Hoboken, NJ : Wiley-Blackwell
    Journal of Polymer Science 56 (1962), S. 225-231 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Both the glass transition temperature and the melting point of poly(vinyl chloride have been found to increase as the temperature at which the ample is polymerized is decreased). The glass transition temperature changes from about 70°C. for polymer prepared at 125°C. to about 100°C. for polymer prepared at -80°C. It is believed the increase in percentage of syndiotactic structure which results from decreasing the polymerization temperature is responsible for the change in glass transition temperature. The effect of polymerization temperature on melting point is even more striking. The melting point changes from approximately 160 to above 300°C. on lowering the polymerization temperature from 125 to -80°C. X-ray diffraction studies show that polymers prepared at low temperature form crystals which have a substantial increase in perfection along the chain axis. It seems probable that this increase in crystalline perfection along the chain axis is responsible for the very marked increase in melting point.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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