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  • Polymer and Materials Science  (13)
  • Chemical Engineering  (10)
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 12 (1968), S. 509-525 
    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: In a systematic study of the elution column fractionation of a well characterized branched polyethylene sample it was found that one of the most important factors contributing to the efficiency was the composition selected for the p-xylene-butyl cellosolve eluting mixture. With a mixture representing the critical solvent composition at 126°C., as determined by cloud point measurements, and deposition to an amorphous phase on a fine sand support, viscosity-distribution curves were obtained which were highly reproducible and completely free of any reversal. No further improvement was gained by using an elution temperature other than 126°C. or by the substitution of tetralin or mesitylene for p-xylene. Precipitation down a temperature gradient to produce a physical separation of species provided enhanced fractionation but is of doubtful practical interest. Fractionation was readily scaled up from 2g. to 4 or 6g., merely by increasing the mixing vessel size from 500 cc. to 1000 cc. There was no loss of efficiency, and fractions with M̄w = 8 × 106, more than twentyfold higher than the sample value, were obtained despite eluted polymer concentrations exceeding 0.2%. There is evidence that many of the expected differences in the fractionation behavior of linear and branched polyethylene are erased when a solvent mixture is used which has been adjusted to the appropriate critical composition.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 2
    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: Fractions from several elution column runs on samples of up to 6 g. of a well-characterized high-pressure polyethylene were analyzed by absolute molecular weight methods and several other techniques. The Mn and Mw integral distribution curves are free from any reversal, as was the viscosity distribution curve. Fractions with Mw as high as 8 × 106 were recovered, more than 20 times higher than the original sample's Mw. The polydispersity of the fractions increases from Mw/Mn = 1.5 or less in the low molecular weight fractions to a nearly constant value of 4.5-5.0 in fractions above 60% cumulative sample weight. Nonetheless, refractionation on the elution column shows that the fractions are narrowly distributed in terms of solubility, while GPC analysis reveals that the fractions have an extremely narrow size distribution. It is concluded from the combined results that long-chain branching plays an important role in determining the equilibrium solubility and, further, that long-chain branching increases the polymer solubility. Sample calculations are provided, which illustrate the effect of fraction polydispersity on calculated original sample molecular weights and the fit of the fractionation results to several model distribution functions.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 5 (1961), S. 354-363 
    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 elution method is essentially a single-stage process, whereas the thermal gradient method is a multistage process which depends upon a thermal gradient to bring about reprecipitation of polymer in the fractions. As a test of the effectiveness of the thermal gradient, comparisons have been made of fractionation by these two column methods on high molecular weight polystyrene samples. It was found that the thermal gradient method definitely provides superior resolution and reproducibility, as expected. However, the degree of fractionation obtained by the elution method was surprising, accounting for at least 80% of the sample under the usual conditions and giving complete fractionation with certain modifications of conditions. These results indicate the difference in performance of the two methods is less than expected from an elementary consideration of the operation of the columns, and fractionation by the elution method, as conducted here, exceeds that expected for a single-stage extraction process. Although the reasons for the observed behavior are not clear, the following conclusions have been reached about certain factors which influence fractionation. Alternative methods of controlling the concentration of polymer in the fractions give almost equivalent results but enhanced resolution of the high molecular weight portion of the sample is obtained with extended solvent gradients. The inhibitor, tert-butyl catechol, which it was necessary to add to the solvents to limit degradation of the very high molecular weight sample, plays a specific role in the fractionation due to a reaction with the polystyrene which alters the fractionation behavior without affecting the molecular weight. Also, trace amounts of chemical heterogeneity in the polymers, presumably hydroxyl groups, have a marked adverse effect on fractionation by the elution method and probably account for molecular weight reversals observed in some fractionations by the thermal gradient method. It is suggested that adsorption on the surface of the beads is responsiblp for the adverse effect of chemical heterogeneity on the fractionation and that possibly an adsorption which increases with molecular weight contributes to fractionation by the elution and thermal gradient methods.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 3 (1960), S. 251-251 
    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
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 17 (1977), S. 73-80 
    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: Prior studies of two series of segmented polyurethanes based on 2, 4 toluene cliisocyanate (2, 4 TDI) or 2, 8 TDI, butanediol, and a 1000 molecular weight polytetramethyleneoxide (PTMO-1000) soft segment revealed a rapid increase in soft segment glass transition temperature (Tg) with increasing urethane content in the 2, 4 TDI series. The change in Tg couldbe correlated with estimates of hard segment-soft segment phase mixing obtained by infrared analysis of the urethane NH and carbonyl bands. In the present paper, the infrared data have been reevaluated using improved procedures for resolving the carbonyl band into H-bonded and nonbonded components, and the relation between the estimated extent of phase mixing and Tg has been reexamined. The transition behavior in an extensive series of related polymers has also been determined, including 2, 4 TDI arid 2, 6 TDI samples with PTMO2000 as well as polybutyleneadipate (PBA-1000 and PBA-2000) soft segments. The results indicate the effectiveness, of increased soft segment molecular weight in promoting phase segregation, imply that much greater phase mixing occurs in polyester than polyether samples, suggest that anchoring the ends of the soft segments has only a small effect on Tg, and provide some evidence that H-bonding not only increases Tg but can also impede soft segment crystallization.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 26 (1986), S. 1547-1551 
    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 sorption and diffusion of a series of liquids in a segmented polyurethane have been studied to determine how the behavior is affected by the choice of solvent and the heterophase nature of the polymer. The polyurethane was composed of methylene-di-para-phenylene isocyanate (MDI) butanediol, and poly(tetramethylene oxide) (1000) with a mole ratio 3:2:1. Immersion experiments in n-heptane liquid, a poor solvent, and incremental sorption experiments in n-heptane vapor showed normal Fickian havior. In the set of liquids of increasing polarity, which included 1-chloroheptane, three dichloroalkanes and orthodichlorobenzene, the swelling increased to very high levels. Effective values of the molecular weight between crosslinks computed from the Flory Rhener equation, assuming complete phase segregation, varied widely with the different liquids. Agreement could be improved by allowing 30 percent mixing of hard segments with the soft segment phase. The sorption and desorption curves for the highly swelling liquids showed various anomalies some of which might be the result of solvent induced relaxation of hard segment domains.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 47 (1993), S. 1419-1425 
    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 saturation water uptake and nonfreezing water, determined as a function of temperature in a polyurethane containing the pure polyethylene oxide soft segment (I) and in polyurethanes containing block copolymer polyethylene oxide/polypropylene oxide soft segments (II), show significantly different behavior. In sample I, the water content and nonfreezing water are only weakly dependent on temperature from 276 to 333 K. In the samples based on II, with various ratios of the hydrophilic and hydrophobic segments, there is a strong decrease in solubility with temperature and a steep drop above 303 K. The nonfreezing water exhibits a parallel trend. This behavior is interpreted in terms of the temperature-dependent phase compatibility of the polyethylene oxide and polypropylene oxide segments of II. © 1993 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 12 (1972), S. 25-29 
    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: Dynamical mechanical relaxation spectra of a number of polyurethane-polyether block copolymers have been studied as a function of composition, temperature and frequency. At low temperatures these copolymers are characterized by a high glass-like modulus which decreases to a much lower typically elastomeric value in a narrow temperature range. The latter is a function in certain cases of the composition of the polymer. The rubbery plateau is maintained up to at least 140°C. In addition, a secondary relaxation is observed around -130°C. These observations can be interpreted in terms of an overall structure consisting of a polyether matrix containing segregated polyurethane domains, the latter serving as physical crosslinks in the system at ambient temperatures and above.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Stamford, Conn. [u.a.] : Wiley-Blackwell
    Polymer Engineering and Science 19 (1979), S. 304-312 
    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 curing behavior of two commercial dicy-containing resins (I & II), both with recommended cures of 127°C/2 h, has been studied by differential scanning calorimetry (DSC), torsional braid analysis (TBA) and Fourier Transform infrared spectroscopy. Compositional analysis reveals that the two resins differ primarily in the amine/epoxy ratio and the nature of the main epoxy components. Factors contributing to the complex curing behavior observed with II are identified. Isothermal kinetic runs by DSC and TBA lead to estimates for the conversion at the gel point, and to results which suggest that the reactions of epoxy with amine and hydroxyl occur with similar activation energies and similar heats of reaction.
    Additional Material: 15 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 19 (1979), S. 313-318 
    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 curing behavior of two commercially formulated epoxy resins composed of the tetrafunctional amine dicyandiamide and with differing epoxy components, 4,4′-bisglycidylphenyl-2,2′-propane and the tetraglycidyl ether of methylene dianiline, is characterized by dynamic spring analysis. This supported viscoelastic technique is well suited to the determination of the onset of gelation under isothermal conditions but the method is not useful for monitoring later stages of reaction when the resins become more rigid. The activation energy for the curing of the two resins is about 87 kJ/mole (20.7 kcal/mole). Rate constants for the first order curing reaction are given. Additional studies of films cured below the ultimate Tg show that two relaxations can be observed upon heating. The first relaxation occurs near the original isothermal cure temperature with a low activation energy, about 250 kJ/mole, whereas the second relaxation occurs near the ultimate Tg, under the conditions used here, with an activation energy of 500-650 kJ/mole. It is believed that these activation energies provide a unique method of characterizing the molecular mobility of epoxy resins at various states of cure.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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