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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Macromolecules 26 (1993), S. 1751-1757 
    ISSN: 1520-5835
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    Amsterdam : Elsevier
    Journal of Fluorine Chemistry 58 (1992), S. 210 
    ISSN: 0022-1139
    Quelle: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 10 (1971), S. 418-421 
    ISSN: 1435-1528
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: 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.
    Notizen: 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.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 10 (1971), S. 402-407 
    ISSN: 1435-1528
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Beschreibung / Inhaltsverzeichnis: 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.
    Notizen: 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.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 5
    ISSN: 1435-1528
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 6
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 14 (1975), S. 192-199 
    ISSN: 1435-1528
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 7
    Digitale Medien
    Digitale Medien
    Springer
    Rheologica acta 8 (1969), S. 304-311 
    ISSN: 1435-1528
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Chemie und Pharmazie , Physik
    Notizen: 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.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 8
    Digitale Medien
    Digitale Medien
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 829-834 
    ISSN: 0032-3888
    Schlagwort(e): Chemistry ; Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Three copolymeric perfluoroethers with the structure CF3[(OCF2CF2)p(OCF2)q] OCF3, having different p/q ratios, have been fractionated. The fractions obtained have been characterized by Gel Permeation Chromatography and 19F-NMR. The viscosity η the specific volume v and the glass transition temperature, Tg have been measured by standard techniques for all the above samples as well as for some other perfluorinated polyethers.The temperature dependence of viscosity of the unfractionated samples is described by the W.L.F. equation. The values of fg (fractional free-volume at Tg) and of af (free-volume expansion coefficient) are independent of composition, for p/q ratios from 0.53 to 1.15. The critical molecular weight, Mc, is of the order of 8-9,000. From the molecular weight dependence of specific volume, the contribution to the molar volume of the in-chain CF2 group and the excess molar free volume of the chain ends have been determined. The limiting value of Tg for an infinite molecular weight polymer was found to depend linearly on the compositional ratio O/C and the extrapolated values for polytetrafluoroethylene and for the homopolymer (CF2O)n were found to be respectively 200 K and 120 K.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 9
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 14 (1970), S. 79-88 
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: Measurements of melt viscosity on samples of polytetrafluoroethylene of different molecular weight were carried out at 360°C by means of tensile creep tests in the linear viscoelasticity range. The apparent activation energy for viscous flow in the range between 330° and 380°C was estimated to be 20 kcal/mole. A value of about 7,500 was also determined for the average molecular weight between entanglement points (Me), from the equilibrium compliance (De). Melt viscosity data were compared with zero strength time (ZST) values and a linear correlation was found on a bilogarithmic scale. The dependence of ZST on the applied stress and temperature was also studied and the results are discussed on the basis of Bueche's theory on the creep at rupture above the glass transition temperature.
    Zusätzliches Material: 8 Ill.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 10
    ISSN: 0021-8995
    Schlagwort(e): Chemistry ; Polymer and Materials Science
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie , Maschinenbau , Physik
    Notizen: A method for the evaluation of the amount of defects in the comonomer alternation included in the crystalline phase of alternating ethylene-tetrafluoroethylene (ETFE) and ethylene-chlorotrifluoroethylene (ECTFE) copolymers, is proposed. The method is based on a comparison between X-ray fiber diffraction profiles and calculated Fourier transforms for isolated chain models. The proposed method is not affected by the regioirregularities and stereoirregularities possible for ECTFE. For the considered ECTFE sample, the chains in the crystalline phase present an amount of defects in the comonomer alternation much lower than those evaluated for all the considered ETFE samples. Substantial differences in the melting temperatures between ETFE samples are accounted for by the different amounts of defects in the comonomer alternation included in the crystalline phase. © 1995 John Wiley & Sons, Inc.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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