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  • Chemical Engineering  (1)
  • bioconversion  (1)
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 45 (1995), S. 27-32 
    ISSN: 0006-3592
    Keywords: esterification ; lipase ; glycerides ; organic solvent ; surfactant ; bioconversion ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Several surfactant-coated enzymes have been prepared by coating lipases of various origins with a nonionic surfactant, glutamic acid dioleylester ribitol (2C18Δ9GE). Enzymatic interesterification of tripalmitin with oleic acid using the surfactant-coated lipase was carried out in organic media. The surfactant-coated lipases could effectively catalyze the interesterification of glycerides better than did the powder lipases. A suitable organic solvent was an aliphatic hydrocarbon such as isooctane. The enzymatic activity for the interesterification strongly depended on the origin of the lipase. The surfactant-coated lipase prepared by Mucor javanicus showed the highest enzymatic activity for the interesterification of glycerides, although its powder lipase did not show enzymatic activity. Selective interesterification of glycerides could be performed by adjusting the concentration ratio of oleic acid to tripalmitin in isooctane. Di-substituted glyceride could be selectively produced when the concentration ratio of carboxylic acid to glycerides was 7. © 1995 John Wiley & Sons, Inc.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Hoboken, NJ : Wiley-Blackwell
    AIChE Journal 27 (1981), S. 277-284 
    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 calculational method is proposed for the simulation of steady-state, multisolute, countercurrent extraction with axial dispersion. The method provides for complex chemical-equilibrium and phase-equilibrium relationships, and accounts for the individual resistances of the liquid phases in the calculation of mass-transfer rates. The solution procedure follows that developed by Newman (1967, 1968) for systems of simultaneous, second-order difference equations.Three example problems are solved to demonstrate the efficiency and flexibility of the method. These include (1) an example from McSwain and Durbin (1966), (2) calculation of axial-dispersion and mass-transfer parameters from experimental data for the extraction of acetic acid from water by a tertiary amine in an RDC extractor, and (3) simultaneous extraction of solutes that interact in an acid-base complexing reaction at the liquid-liquid interface. The examples all assume that extraction is governed by interphase mass-transfer rates and cell-wise backmixing; however, the method is also applicable to equilibrium-stage separators, separators described by the diffusional model of axial dispersion, and other countercurrent separation processes.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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