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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 35 (1988), S. 1065-1084 
    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: Quantitative size exclusion chromatography (SEC) was considered a system with the following components: sample preparation, fractionation, detection, calibration, and resolution correction. Four systems were evaluated: I was 3 columns with “conventional single detector interpretation”; II was 4 columns with concentration correction and detector assessment; III was concentration correction applied to the data of I; IV was two development “mixed bed” columns. Analysis of polystyrene standards included calculation of their molecular weight averages and use of the Glöckner “T” measure of resolution as well as “specific resolution index.” Systems I and III provided the best high molecular weight results. System IV allowed 12-20 min analysis times and provided a highly linear calibration curve with very good reproducibility; however, it showed significantly worse resolution at high molecular weights. Plots of molecular weight averages determined from SEC versus their known true values were particularly useful. Concentration correction using the Rudin model moved different concentration data toward a common universal calibration curve and generally lowered molecular weight averages. Narrow polystyrene standards required relatively high concentrations for precise molecular weight averages and therefore, their averages were not good indicators of the need for concentration correction. Analysis of polypropylene samples corroborated the lower high molecular weight resolution of System III. Concentration correction did significantly change the polypropylene molecular weight distribution but did not affect the result of the kinetic model fitting.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1685-1700 
    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: Five different types of calibration curve currently used in size exclusion chromatography-differential viscometer (SEC-DV) systems were identified and their use summarized. A simple method of deriving weighting factors for fitting local intrinsic viscosity calibration curves was shown to greatly improve the precision of calculated molecular weight distributions. The problem of reliably extrapolating the fitted curves to allow for differences in sensitivity among detectors has yet to be examined. With regard to Mark - Houwink constants, a method of fitting data from the SEC-DV system to obtain more statistically sound values was derived. For the data used here, the new method involves fitting a plot of logarithm of the local intrinsic viscosity of the sample vs. logarithm of the universal calibration curve parameter, Ji. Results for the data obtained appeared only slightly more precise than those for the traditional method. However, the new method promises improved reliability. © 1993 John Wiley & Sons, Inc.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 30 (1990), S. 1063-1072 
    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 objective of this work was to investigate the compatibilization of a blend of linear low density polyethylene with polypropylene by Injection of a free radical initiator during extrusion. The reactive extrusion process utilized a single screw extruder equipped with two static mixers. The initiator was injected into the extruder feedport and temperature programming used to cause most reaction to occur within the static mixers. Although elongation at yield was increased by 37 percent, impact strength and yield strength decreased by 17 and 54 percent, respectively. Scanning electron microscopy showed that the maximum size of the dispersed phase decreased from a maximum size of four microns to less than two microns upon addition of initiator. Size exclusion chromatography (SEC), temperature rising elution chromatography (TREF), and differential scanning calorimetry showed that the polypropylene in the blend was degrading while the polyethylene was increasing in molecular size. The combination of SEC and TREF was particularly useful in elucidating this result. No copolymer was discerned by any of the methods used.
    Additional Material: 14 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1701-1706 
    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 closely related topics of resolution correction and the determination of interdetector volume were examined. In determining the interdetector volume (δ) by searching to superimpose two types of intrinsic viscosity calibration curve (one from narrow standards and one from a broad standard), the underlying equation based upon symmetrical axial dispersion theory was derived. This equation combined with experimental results showed that the local intrinsic viscosity value is very similarly affected by interdetector volume and by band spreading. The result supported the idea of using an effective δ to effect an axial dispersion correction to local intrinsic viscosity data. However, it also increased the difficulty of finding both δ and standard deviation (δ) simultaneously by numerical search. Furthermore, attempts to apply the method to the chromatograms of narrow standards showed inadequate superposition. Following calculation of skewing factors, the superposition problems were attributed to skewing of the chromatograms of the monodisperse polymer standards used. © 1993 John Wiley & Sons, Inc.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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