Thermodegradation of medium-chain-length poly(3-hydroxyalkanoates) produced by Pseudomonas putida from oleic acid
Medium-chain-length poly(3-hydoxyalkanoates) (mcl-PHA), comprising six to fourteen carbon-chain-length monomers, are natural thermoplastic polyesters synthesized by fluorescent pseudomonades. In this study, mcl-PHA was produced by Pseudomonas putida from oleic acid in aerobic shake flask fermentatio...
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Veröffentlicht in: | Polymer degradation and stability 2010-12, Vol.95 (12), p.2334-2342 |
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Sprache: | eng |
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Zusammenfassung: | Medium-chain-length poly(3-hydoxyalkanoates) (mcl-PHA), comprising six to fourteen carbon-chain-length monomers, are natural thermoplastic polyesters synthesized by fluorescent pseudomonades. In this study, mcl-PHA was produced by
Pseudomonas putida from oleic acid in aerobic shake flask fermentation. Thermal degradation of mcl-PHA was performed at temperatures in the range of 160–180 °C. Thermodynamic parameters of mcl-PHA thermal degradation were determined where degradation activation energy,
E
d
and pre-exponential factor,
A equal to 85.3 kJ mol
−1 and 6.07 × 10
5 s
−1, respectively; and exhibited a negative activation entropy (∆
S) of −139.4 J K
−1 mol
−1. Titration was carried out to determine the carboxylic terminal concentration and used to correlate number-average molecular weight (
M
n
) of the polymers. Thermally-degraded PHA contained higher amount of carboxylic terminals and lower
M
n
compared to the initial PHA and these results coincide with the decreased
M
n
in GPC analysis. Thermal properties of initial and degraded mcl-PHA were characterized by thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The thermal decomposition mechanism was investigated following the analyses of the degradation products using 400-MHz
1H NMR, FTIR spectroscopy and GC analysis. The overall decomposition reaction is the hydrolysis of ester linkages to produce hydroxyl and carboxylic terminals. A small proportion of unsaturated side chain fragments would undergo oxidative cleavage at C
C linkages, producing minor amount of low-molecular weight esters and acids. At higher temperatures, the hydroxyl terminal can undergo dehydration to form an alkenyl terminal. |
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ISSN: | 0141-3910 1873-2321 |
DOI: | 10.1016/j.polymdegradstab.2010.08.027 |