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  • Electronic Resource  (4)
  • Polymer and Materials Science  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 36 (1998), S. 1547-1556 
    ISSN: 0887-6266
    Keywords: gas permeation ; plasticization ; semiinterpenetrating polymer network ; polyimide ; Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: CO2-induced plasticization may significantly spoil the membrane performance in high-pressure CO2/CH4 separations. The polymer matrix swells upon sorption of CO2, which accelerates the permeation of CH4. The polymer membrane looses its selectivity. To make membranes attractive for, for example, natural gas upgrading, plasticization should be minimized. In this article we study a polymer membrane stabilization by a semiinterpenetrating polymer network (s-ipn) formation. For this purpose, the polyimide Matrimid 5218 is blended with the oligomer Thermid FA-700 and subsequently heat treated at 265°C. Homogeneous films are prepared with different Matrimid/Thermid ratios and different curing times. The stability of the modified membrane is tested with permeation experiments with pure CO2 as well as CO2/CH4 gas mixtures. The original membrane shows a minimum in its permeability vs. pressure curves, but the modified membranes do not indicating suppressed plasticization. Membrane performances for CO2/CH4 gas mixtures showed that the plasticizing effect indeed accelerates the permeation of methane. The modified membrane clearly shows suppression of the undesired methane acceleration. It was also found that just blending Matrimid and Thermid was not sufficient to suppress plasticization. The subsequent heat treatment that results in the s-ipn was necessary to obtain a stabilized permeability. © 1998 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 36: 1547-1556, 1998
    Additional Material: 10 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 16 (1972), S. 2567-2576 
    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: Comparison of the reflectance spectrum of cellulose with that of myoinositol, cycloheptaamylose, and other model compounds indicates that the acetal linkage does not contribute significantly to the absorption peak at 260 nm. The spectra of photolyzed and photo-oxidized cellulose suggest that ketonic carbonyl groups are a more likely cause of this peak. Photolysis of cellulose and amylose under vacuum with 253.7 nm light increases the concentration of ketonic carbonyls and thus promotes yellowing. Photo-oxidation with 253.7-nm light bleaches both carbohydrates owing to the formation of carboxyl groups. Other investigators had previously reported that this last reaction yellows cellulose, but it appears that this was an effect caused by the 184.9-nm component in the light of the lamp used. Comparison of the spectra of thermally and photolytically yellowed cellulose indicates that the end products of the two degradations are quite different.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 833-852 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The initial stages of the photolysis of cellulose under vacuum can be followed by the gas production. A photolysis cell is described which allows a rigorous temperature control and gives a reproducible photolysis surface of the solid carbohydrate sample. A mass spectrometer was used to analyze the gases. To measure accurately the small amounts produced in a small volume requires careful calibration of this instrument, together with a fixed routine for the experimental procedure. Using this apparatus, we have photolyzed hydrocellulose under vacuum with 253.7 nm light. Only H2, CO, and CO2 were evolved, the rate of H2 production increasing to a constant value, that of CO increasing more slowly without becoming constant, and that of CO2 decreasing rapidly to a constant value. No induction periods were observed. The gas evolution was not caused by residual O2 or CO2 adsorbed on the polymer, but the rates were altered by leaving the photolyzed sample under vacuum overnight or heating the unphotolyzed sample under vacuum at 100°C. The rates of gas production increased markedly when the light filter was changed to allow a combined photolysis by 253.7 and 184.9 nm light. The results illustrate that stringent precautions must be taken to filter off the latter line in polymer photolyses with Hg arc light if the results are to be meaningfully interpreted in terms of 253.7 nm light photolysis. On photolyzing hydrocellulose previously boiled in NaOH solution, a larger H2 production rate and a smaller CO2 rate (compared with untreated hydrocellulose) were observed. It is suggested that this standard alkali treatment is the reason for the differences between our results and the results of the photolysis of cellulose reported in the literature.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 12 (1974), S. 2283-2293 
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cellobiose and myoinositol, both as received and in physically modified form, were photolyzed at 60.0°C under vacuum with 253.7 nm light. The rates of hydrogen production were compared with the H2 rate obtained from analogous photolyses of hydrocellulose. The similar physical state and optical properties of cellobiose and hydrocellulose allowed a direct comparison of H2 production rates, from which it is clear that neither the glycosidic linkage, nor the number of primary or secondary hydroxyl groups, is the basis for observed differences in rates. The relative rates of H2 production from myoinositol and levoglucosan indicate that strain in the pyranose ring has only a slight effect on the photolysis rate, and further, since published carbohydrate structures show that the local skeletal environment about each hydroxyl in a “defectless” unstrained carbohydrate structure is very similar in all the relevant compounds thus far determined, differences in H2 rates must therefore arise as a result of possible differences in the hydrogen-bonding environment of the hydroxyl. From an extrapolation of optical properties of simple alcohols in hydrogen-bond-free environments, together with a consideration of possible cage effects during photolysis, it is concluded that the precursors of the H2 are hydrogen-bond-free hydroxyl groups of the carbohydrates. Confirmation of this hypothesis has been obtained from the H2 rates observed on photolyzing cellobiose and myoinositol after these compounds had been freeze-dried or recrystallized, which treatment results in a concentration of “defective” hydroxyls differing from the original solid, but is without effect on the overall numbers of “ordinary” hydroxyls.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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