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  • 1
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    Berkeley, Calif. : Periodicals Archive Online (PAO)
    California Management Review. 35:3 (1993:Spring) 68 
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  • 2
    ISSN: 0887-624X
    Keywords: antenna effect ; photocatalytic activity ; solubilization ; distribution coefficient ; poly(sodium styrene sulfonate-co-N-vinylcarbazole) ; poly[sodium styrene sulfonate-co-N-(acryloyloxyhexyl)carbazole] ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two new antenna polyelectrolytes, poly(sodium styrenesulfonate-co-N-vinylcarbazole) (PSSS-VCz) and poly[sodium styrenesulfonate-co-N-(acryloyloxyhexyl)carbazole](PSSS-AHCz) have been synthesized. Both polymers were found to solubilize large hydrophobic compounds such as perylene in aqueous solution, but PSSS-AHCz was much more efficient than PSSS-VCz. The distribution coefficients of perylene between the polymer pseudophase and water was determined to be (2.9 ± 0.1) × 106 and (4.0 ± 0.2) × 104 in PSSS-AHCz and PSSS-VCz, respectively. The greater solubilizing ability of PSSS-AHCz is attributed to the higher content of hydrophobic monomer units in the polymer. Both copolymers displayed photocatalytic activity, absorbing light in the UV-visible spectral region. Energy can then be transferred to a solubilized molecule or dissolved oxygen and induce photochemical reactions. The model reaction used in this study was the photosensitized oxidation of perylene solubilized in aqueous polymer solutions. PSSS-AHCz was found to be a much more efficient photocatalyst than PSSS-VCz. The enhanced photocatalytic activity of PSSS-AHCz is attributed to the greater concentration of carbazole chromophores, the higher local concentration of probe in the polymeric pseudophase and possibly to the elimination of the low-energy excimer.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 36 (1990), S. 685-700 
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The kinetics of lumped nth-order reactions are examined both asymptotically and numerically. The lumped kinetics in most cases are Mth order at large times. There exist two critical values for n, denoted by n* and n*, which are expressed explicitly as functions of the feed properties. It is shown that (1) M = n when n 〉 n*, (2) M is linear in n when n* 〈 n 〈 n*, and (3) M does not exist when n = n* or n ≤ n*. Whenever the feed contains some unconvertibles, M is independent of n for -∞ 〈 n 〈 n*. The overall effective rate constant is not continuous at n = n* nor at n = n*. Unexpectedly, when n 〉 n* the lump's long-time behavior is governed by all species, not just by the most refractory species. Although the asymptotic kinetics are developed for long times, they are useful for fitting the whole-time behavior of the lump by an mth-order model. This is true even when M does not exist in the asymptotic regime. Numerical experiments show that M and m behave similarly in many respects. For example, as n increases, they both become closer to n and less dependent on the feed properties. Some published data are rationalized in light of the present results.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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