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  • 1960-1964  (9)
  • Polymer and Materials Science  (9)
  • Gastric cancer
Materialart
Erscheinungszeitraum
Jahr
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 3 (1960), S. 122-124 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 4 (1960), S. 38-44 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: It is known that polyethylene extruding from a capillary viscometer does not attain a steady-state output rate immediately following a pressure imposition. The time dependence of output rate was studied quantitatively, and under some extrusion conditions was found to be of surprisingly large magnitude. The most notable effect is an overall rise in the output rate; its magnitude and duration depends on the extrusion pressure and temperature and on the entry geometry of the die employed. The magnitude of the effect is also characteristic of particular polyethylene samples and seems associated with smooth filament extrusion of the polymer. The steady-state output rate can exceed the initial rate by as much as 40%. The rising output rate characteristic has been associated with a decreasing melt viscosity. This is taken to be the result of configurational changes occurring in the extruding melt. The data are shown to be qualitatively consistent with this postulate.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. S45 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 6 (1962), S. S49 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 5
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 4 (1960), S. 362-363 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Zusätzliches Material: 1 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 44 (1960), S. 261-264 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Zusätzliches Material: 3 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 58 (1962), S. 29-48 
    ISSN: 0022-3832
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: The relationship at 190°C. between Newtonian melt viscosity η0 and the weight-average molecular weight, M̄w for polyethylenes has been developed by use of melt viscosities obtained from capillary viscometry and molecular weights from intrinsic viscosity and bulk flow measurements in addition to the usual light-scattering determinations. The same η0 vs. M̄w relationship is obeyed by whole and fractionated linear polyethylenes and also by ethylene-butene and ethylene-propylene copolymers. The Newtonian viscosity therefore seems virtually independent of molecular weight distribution and the influence of short (ethyl, methyl) chain branches. Low density polyethylenes have consistently lower Newtonian melt viscosities at given M̄w than their linear counterparts. At constant M̄w and temperature, therefore, η0 depends primarily on long-chain branching. A viscosity index of long-chain branching (v.b.i.) is defined by the ratio of Newtonian viscosities of a linear and a branched polyethylene of the same M̄w. The v.b.i. correlates well with an intrinsic viscosity branching index provided long branch incidence is high. The correlation breaks down otherwise, because the intrinsic viscosity is also sensitive to molecular weight distribution and the presence of short-chain branches. The v.b.i. is therefore more useful as a long branching index. It is a comparative index, however, and not an absolute evaluation of the number of long branches per molecule. The η0 vs. M̄w relationship of linear polyethylenes does not obey the often reported 3.5 power law for linear polymers, but is well fitted by a 4.2 power factor. The present work indicates the necessity of using polyethylenes which have been stabilized against the effects of thermally induced changes if meaningful values of Newtonian viscosity are to be obtained.
    Zusätzliches Material: 6 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Letters 1 (1963), S. 365-368 
    ISSN: 0449-2986
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York : Wiley-Blackwell
    Journal of Polymer Science Part A: General Papers 2 (1964), S. 1655-1668 
    ISSN: 0449-2951
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: Light-scattering evaluations of molecular weight and gyration radii have been carried out over a range of temperatures for linear and branched polyethylenes in α-chloronaphthalene solutions. In a number of cases the molecular size parameters have been found to depend on the solution temperature. When observed, the temperature dependence can change molecular weight values by as much as 50%. The temperature dependence tends to be more pronounced at higher molecular weights, in linear than in branched polyethylenes, and is particularly noticeable at solution temperatures below that of the normal crystalline melting temperature of the polymer. It is suggested that the temperature dependence of molecular weight parameters may be due to a gradual dissociation in solution of polymer aggregates arising from persisting interchain entanglements. A relationship was established between intrinsic viscosity and molecular weight for selected fractionated polyethylenes by using molecular weight data obtained under conditions unfavorable to the persistence of polymer aggregates. A number of published viscosity-molecular weight functions for polyethylenes was compared with the calibrated relationship. Some of the published equations gave results in good agreement with the present function, but a number of others resulted in gross overestimates of molecular weight. Polymer aggregation problems may have been encountered in the derivation of some of these viscosity-molecular weight functions. The comparison indicates the danger of indiscriminate choice of viscosity-molecular weight functions for use in rapid estimates of polymer molecular weight.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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