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  • 1
    Electronic Resource
    Electronic Resource
    Comparison of linear distributed-parameter filters to lumped approximants (1986)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 186-194 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Optimal distributed-parameter filters are commonly implemented using approximating lumped Kalman filtering theory. The effect of such an approximation is investigated. A theoretical development shows that there is a loss in the spatial noise correlation for the lumped approximants. Two numerical examples of engineering significance illustrate that one result of this loss is slower filter convergence for the lumped approximants relative to the full distributed-parameter filters.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690320203
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Optimal, real-time monitoring of particle size distribution in a fluidized bed (1986)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 32 (1986), S. 389-396 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A novel method for tracking particle size distribution dynamics in a fluidized bed yields on-line, real-time measurements of particle size distribution that are representative of actual conditions. These measurements are somewhat corrupted with noise (random error), however, and are available to the computer only at discrete time intervals. An optimal filtering algorithm combines the measurements with predictions from an idealized dynamic model to yield particle size distribution estimates that are not only on-line and real-time, but also virtually continuous and well-behaved.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690320305
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    Paper (German National Licenses)
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  • 3
    Electronic Resource
    Electronic Resource
    Real-time estimation of dynamic particle-size distributions in a fluidized bed: Theoretical foundation (1985)
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 31 (1985), S. 1202-1212 
    Details
    ISSN: 0001-1541
    Keywords: Chemistry ; Chemical Engineering
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Significant noise (random error) is common in an on-line signal when measuring the particle size distribution in a fluidized bed. The application of optimal estimation theory to obtain a filtering algorithm that can rectify such measurements is detailed. Off-line simulation studies demonstrate that the filtering algorithm yields a measure of particle size distribution that is well-behaved, accurate, and able to track in real time as conditions change in the bed.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/aic.690310718
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    Paper (German National Licenses)
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  • 4
    Electronic Resource
    Electronic Resource
    Poly α-ester degradation studies. V. Thermal degradation of polyglycollide (1973)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 11 (1973), S. 2045-2056 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal degradation of polyglycollide [poly(methylene carboxylate)] has been studied over the temperature range 250-400°C by using the combined kinetic and analytical technique previously described. The results obtained from thermogravimetry and product analysis were in many ways similar to those from previous work involving higher poly-α-esters. Thus the reaction was predominantly first-order and the major degradation product was glycollide monomer. This confirms the observations of Carothers and is best interpreted in terms of an intramolecular ester interchange process. Kinetic studies have shown that the first-order rate constant k is related to temperature T by the expression: \documentclass{article}\pagestyle{empty}\begin{document}$$ k = 2.1 \times 10^8 e^{ - 32,{{600} \mathord{\left/ {\vphantom {{600} {RT}}} \right. \kern-\nulldelimiterspace} {RT}}{\rm sec}^{ - {\rm 1}} } $$\end{document} The results from gas evolution analysis showed consistent and marked deviation from first-order behavior. This is interpreted in terms of the greater sensitivity of this technique to traces of acidic degradation products. Solution viscometry was used to demonstrate the effect of degradation conditions on molecular weight change in both thermogravimetric and gas evolution techniques.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1973.170110823
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  • 5
    Electronic Resource
    Electronic Resource
    Poly-α-ester degradation studies. VI. Thermal degradation of poly(3-pentylidene carboxylate) (1980)
    New York : Wiley-Blackwell
    Journal of Polymer Science: Polymer Chemistry Edition 18 (1980), S. 123-146 
    Details
    ISSN: 0360-6376
    Keywords: Physics ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The thermal degradation of poly(3-pentylidene carboxylate) has been studied kinetically over the temperature range 200-300°C using thermogravimetry, gas evolution analysis, and rheogoniometry together with isolation and analysis of the reaction products. The observed behavior is completely different from that previously reported for poly(isopropylidene carboxylate) and poly(methylene carboxylate). Whereas in the latter cases the decomposition occurs by a first-order intramolecular ester interchange process characterized by an activation energy in the region of 27 kcal mole-1, poly(3-pentylidene carboxylate) decomposition occurs by random chain scission superimposed on a first-order hydrogen abstraction process. The activation energy associated with this decomposition reaction is in the region of 47 kcal mole-1, and the major degradation products are cis- and trans-2-ethyl crotonic acid.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/pol.1980.170180113
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    Paper (German National Licenses)
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