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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 26 (1993), S. 1751-1757 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Fluorine Chemistry 58 (1992), S. 210 
    ISSN: 0022-1139
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 10 (1971), S. 402-407 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zusammenfassung Die vonMenefee undPeticolas entwickelte Theorie zur Abschätzung der Molekulargewichtsverteilung von Polymerschmelzen durch Messung der Relaxationsspannung bei stationärem Fließen wird auf theoretische Beispiele von polydispersen Polymeren und auf experimentelle Resultate von PMMA-Schmelzen angewendet. Es wird gezeigt, daß die erste Näherungsgleichung $$Z_c (M) = 1 - \frac{{\pi ^2 }}{6}\sum\limits_{n \geqslant 1} {\frac{{\mu (n)}}{{n^2 }}\Phi (n^2 t)} $$ kumulativeZ-Verteilungskurve,μ (n) Moebius-Funktion,Θ(t) normalisierter Spannungsrest zur Zeitt) immer breitere Molekulargewichtsverteilungen als die erwarteten ergibt. Bessere Ergebnisse erhält man mit Näherungsgleichungen höherer Ordnung.
    Notes: Summary The theoretical treatment developed byMenefee andPeticolas for evaluating the molecular weight distribution of polymer melts from measurements of stress relaxation after steady-state flow has been applied both to artificial examples of polydisperse polymers and to experimental data on poly(methylmethacrylate) melts. It has been shown that the first approximation equation $$Z_c (M) = 1 - \frac{{\pi ^2 }}{6}\sum\limits_{n \geqslant 1} {\frac{{\mu (n)}}{{n^2 }}\Phi (n^2 t)} $$ (whereZ c (M) is the cumulativeZ-distribution curve,μ(n) theMoebius function and Θ(t) the normalized stress remaining at timet which has been found satisfactory byPeticolas for a poly(ethylene)melt (J. Chem. Phys.39, 3392, 1963) gives molecular weight distributions always broader than those expected. Better results are obtained by higher approximation equation.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 10 (1971), S. 418-421 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Description / Table of Contents: Zusammenfassung Die Beziehung zwischen der Schmelzviskosität, dem mittleren Molekulargewicht und dem Verzweigungsindex wurde für polydisperse Polymere mit der wahrscheinlichsten Verteilung von primären Ketten, die ihrerseits statistisch verteilte tri- oder tetrafunktionale Verzweigungspunkte besitzen, abgeleitet. Die Ergebnisse wurden aus einer Erweiterung der vonKilb für die Berechnung der Grenzviskosität angewandten Methode erhalten. Für ausgewählte Verzweigungsindizes werden numerische Werte der Viskositätsfunktionen angegeben.
    Notes: Summary The relation of melt viscosity to weight-average molecular weight and branching index has been derived for polydisperse polymers, with the most probable distribution of primary chains, having randomly distributed tri- or tetrafunctional branch points. The results are obtained by an extension of theKilb treatment for the intrinsic viscosity calculations. Numerical values of the viscosity functions are given for selected branching indices.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 14 (1975), S. 192-199 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Rheologica acta 8 (1969), S. 304-311 
    ISSN: 1435-1528
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Conclusions From an overall analysis of the above results it appears that the rheological properties of plasticized PVC are governed, below about 200 °C, not only by the usual parameters (composition, temperature, molecular weight) but also by the crystallinity of the polymer. Recent estimations of the crystallinity degree in commercial PVC samples vary from 3% (45) to about 10% (46), the actual value depending on the thermal history of the sample. Apparently even small values of the crystallinity degree can affect rather strongly the rheological behaviour of plasticized PVC in the rubbery and flow regions. For the fractions here investigated, the fractional precipitation procedure used to carry out the separation (1) leads probably to a fractionation based not only on molecular weight but also on stereoregularity (47), the result being that the fractions precipitated firstly are more polydisperse and more crystallizable. In dilute solution, they give easily aggregates (1), stable up to relatively high temperatures (2). The dynamic-mechanical data discussed above (fig. 1) as well as the anomalies presented by the rheological results (fig. 7 to 12) can be therefore explained on the basis of a model in which supermolecular structures linked together by crystalline bonds are present in the samples. The marked dependence of PVC mechanical properties on the annealing temperature described recently byAndrews andKazama (48) seems to give considerable support to such a model.
    Type of Medium: Electronic Resource
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  • 8
    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 dynamic-mechanical properties as a function of temperature and the low- and high-speed tensile properties at 23°C have been determined on specimens of conventional suspension-polymerized PVC and of low-temperature-polymerized PVC roll milled and then compression molded at different temperatures. It has been found that the main transition α and the shear modulus above Tα depend on the thermal history and are strongly affected by crystallinity, whereas the dynamic-mechanical spectrum below Tα is not influenced by these parameters. Room-temperature tensile modulus and yield properties are very little affected by processing history and crystallinity. The elongation at break and the fracture energy, on the contrary, increase, at any fixed strain rate, for conventional PVC with milling temperature. The same trend has been found for low-temperature PVC, but the elongation at break-versus-temperature curve is shifted, as a whole, toward higher temperatures by approximately 50°C. Such results are discussed in terms of homogeneity of the specimens, which is controlled by the melting process of the crystallites. Stereoscanning electron micrographs of fracture surfaces appear to substantiate these conclusions.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 17 (1973), S. 3187-3197 
    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 thermal behavior of terpolymers of caprolactam (CL) and of hexamethylenediammonium isophthalate (IH) and terephthalate (TH) has been studied in a wide range of compositions by differential thermal analysis. It has been found that either amorphous or crystalline polymers having different crystallization rates can be obtained by changing the composition. The dependence of melting points and glass transition temperatures on the composition has been investigated. The dependence of Tg on the composition for the copolymers CL-IH, IH-TH, and CL-TH has been described by means of the Gordon-Taylor equation. It has been found that this equation fits the experimental data for the IH-TH system only if a parameter which takes into account interactions between the monomeric units is introduced. A ternary iso-Tg map has been obtained through statistical analysis. The influence of the chain stiffness and bulkiness of the monomers on the glass transition temperature is discussed.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 18 (1978), S. 742-749 
    ISSN: 0032-3888
    Keywords: Chemistry ; Chemical Engineering
    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 parison extrusion and the effects of post-extrusion swelling and sagging in the blow molding process have been studied by several authors and some qualitative relationships with rheological parameters have been attempted. The aim of this work is to show that, under some simplifying assumptions, the relevant rheological parameters - the swelling of the parison and its tensile compliance - can be directly determined from the viscoelastic analysis of the process. The reliability of the model has been tested by experiments carried out by the pinch-off mold technique which provides the parison weight profile as a function of both previous extrusion history and mold closing delay. First of all it has been shown that the proposed model is suitable to represent the data. The swelling behavior shows the expected dependence on time and shear rate and the long-time swelling data compare well with those determined by capillary extrusion experiments. It has also been found that the measured tensile compliance is of the same order of magnitude as that determined by conversion of tensile relaxation experiments; however, in the blow molding experiments the compliance of the parison decreases with increasing extrusion shear rate, i.e., by increasing the induced anisotropy of the polymer. As rheological examples, the performance displayed on both industrial and laboratory machines is discussed for three high density polyethylenes.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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