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
Hauptverfasser: Chan Sin, Mei, Gan, Seng Neon, Mohd Annuar, Mohd Suffian, Ping Tan, Irene Kit
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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.
ISSN:0141-3910
1873-2321
DOI:10.1016/j.polymdegradstab.2010.08.027