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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Ground water monitoring & remediation 16 (1996), S. 0 
    ISSN: 1745-6592
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Notes: Aerobic biodegradation of vapor-phase petroleum hydrocarbons was evaluated in an intact soil core from the site of an aviation gasoline release. An unsaturated zone soil core was subjected to a flow of nitrogen gas, oxygen, water vapor, and vapor-phase hydrocarbons in a configuration analogous to a biofilter or an in situ bioventing or sparging situation. The vertical profiles of vapor-phase hydrocarbon concentration in the soil core were determined by gas chromatography of vapor samples. Biodegradation reduced low influent hydrocarbon concentrations by 45 to 92 percent over a 0.6-m interval of an intact soil core. The estimated total hydrocarbon concentration was reduced by 75 percent from 26 to 7 parts per million. Steady-state concentrations were input to a simple analytical model balancing advection and first-order biodegradation of hydrocarbons. First-order rate constants for the major hydrocarbon compounds were used to calibrate the model to the concentration profiles. Rate constants for the seven individual hydrocarbon compounds varied by a factor of 4. Compounds with lower molecular weights, fewer methyl groups, and no quaternary carbons tended to have higher rate constants. The first-order rate constants were consistent with kinetic parameters determined from both microcosm and tubing cluster studies at the field site.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of polymers and the environment 7 (1999), S. 117-125 
    ISSN: 1572-8900
    Keywords: Depolymerase ; enzymatic degradation ; hydrolase ; PHB hydrolysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Energy, Environment Protection, Nuclear Power Engineering , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract A strain of Aspergillus fumigatus, which was observed to rapidly degrade poly-3-hydroxybutyrate (PHB) in a leaf compost, was found to secrete an extracellular hydrolase when grown on PHB as the sole carbon source. Isolation and characterization of the PHB hydrolase (depolymerase) from this fungus revealed that the enzyme had a molecular weight of 57 kDa, an isoelectric point of 7.2, and a PHB hydrolysis activity maxima which occurred at 70°C and pH 8.0. Affinity labeling experiments suggested that this fungal hydrolase is a type of serine esterase. The cyclic trimers of 3-hydroxybutyrate were found to reversibly inhibit the enzymes.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2381-2387 
    ISSN: 0887-624X
    Keywords: bacterial polyesters ; epoxidation of polyesters ; polyhydroxyalkanoates ; crosslinking polyesters ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Poly(3-hydroxyoctanoate-co-3-hydroxy-10-undecenoate)s (PHOUs) with controlled amounts of unsaturated repeating units were epoxidized to various extents with m-chloroperbenzoic acid (MCPBA) in homogeneous solution. The epoxidation reaction was second order, with an initial rate constant of 1.1 × 10-3Lmol-1.s-1 at 20°C, regardless of the unsaturated unit content in PHOU. No substantial change in either molecular weight or molecular weight distribution occurred as a result of epoxidation, but the melt transition temperature and enthalpy of melting both decreased as the unsaturated groups were increasingly converted into epoxide groups. In contrast, the glass transition temperature (Tg) increased by approximately 0.25°C for each 1 mol % of epoxidation, irrespective of the composition of the PHOU. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2381-2387, 1998
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 36 (1998), S. 2389-2396 
    ISSN: 0887-624X
    Keywords: bacterial polyesters ; epoxidation of polyesters ; polyhydroxyalkanoates ; crosslinking polyesters ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The vinyl groups in the pendant substituents of a series of poly(3-hydroxyoctanoate-co-3-hydroxy-10-undecenoate)s, PHOUs, were completely converted into epoxide groups with m-chloroperbenzoic acid to produce a series of copolymers, poly(3-hydroxyoctanoate-co-3-hydroxy-10,11-epoxyundecenoate)s, PHOEs containing 5, 9, 14, and 22 mol % of epoxide repeating units. The epoxidized polymers were crosslinked by reactions with succinic anhydride, using 2-ethyl-4-methylimidazole as an initiator, at 90°C during a period of 0.5-4 h. Mild conditions were used for the crosslinking reactions to prevent degradation or rearrangement reactions, and the extent of crosslinking was evaluated from the sol-gel content. Both Tg and gel content increased after crosslinking, depending upon the amount of epoxide group in the initial PHOE sample. Kinetic parameters for the crosslinking reaction were determined by use of the Kissinger and the Ozawa methods. The activation energy (15.6-16.0 kcal/mol) for the crosslinking reaction was the same for each sample, and the frequency factors were of the same order of magnitude, regardless of epoxide group content in the PHOE. The values obtained from the Ozawa method were slightly higher than those obtained from the Kissinger method. © 1998 John Wiley & Sons, Inc. J. Polym. Sci. A Polym. Chem. 36: 2389-2396, 1998
    Additional Material: 8 Ill.
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  • 5
    Publication Date: 1996-02-01
    Print ISSN: 1069-3629
    Electronic ISSN: 1745-6592
    Topics: Energy, Environment Protection, Nuclear Power Engineering , Geosciences
    Published by Wiley
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  • 6
    Publication Date: 1998-02-13
    Print ISSN: 0024-9297
    Electronic ISSN: 1520-5835
    Topics: Chemistry and Pharmacology , Physics
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