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  • 1985-1989  (2)
  • 1980-1984
  • 1987  (2)
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  • 1985-1989  (2)
  • 1980-1984
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 30 (1987), S. 289-296 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: A two-column pilot scale downflow percolating fixed film (DPFF) anaerobic reactor treating deproteinized cheese whey (DPW) was used in this study. The system was operated at one-third of the maximum working volume in an attempt to avoid mass transfer limitations of the gas products (since two-thirds of the immobilized microbial culture was unsubmerged), as well as to minimize the effects of localized high volatile fatty acids (VFA) levels and low pH on its methanogenic activity. A new method to shorten the start-up period was used by growing methanogenic and acetogenic (H2-producers) bacteria on a synthetic medium until reaching a stable methane production rate and then switching the reactor over to DPW and allowing acidogenic growth. The start-up period was reduced to 35 days as a result of this operational mode. The reactor was able to handle 8 kg COD/ m3·d after 35 days of operation.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Biotechnology techniques 1 (1987), S. 115-116 
    ISSN: 1573-6784
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary The ability of a recently developed affinity membrane to adsorb commercially prepared trypsin was investigated. Several buffered solutions of trypsin which varied in their initial concentrations from 62.5 mg/l to 1,000 mg/l, were passed through a stacked bed of seven membranes; dry wt 350 mgs. The adsorbed protein was eluted using acetic acid; 2.2 mgs to 5.3 mgs of trypsin was desorbed. The adsorption capacity tended to a maximum of 16 mg /g dry wt when the initial feed concentration of trypsin was 1 g/l. There was no loss in enzyme activity after desorption; 11,500 IU ± 500 IU.
    Type of Medium: Electronic Resource
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