Abstract

Biodegradability of polyesteramides prepared by anionic ring-opening copolymerization of ε-caprolactone and ε-caprolactam and of aromatic-aliphatic co-polyesters (PETP/LA) synthesized by solvolysis of poly(ethyleneterephthalate) with water solutions of lactic acid by microorganisms producing extracellular esterase and lipase was investigated. The bacterium Pseudomonas aeruginosa, yeast Candida guilliermondii and micromycete Aspergillus fumigatus exhibiting strong esterase and lipase activities on agar plates with artificial nitrophenyl substrates were selected to be used in six-week degradation experiments at 28°C. PETP/LA samples exhibited mass reductions of up to 5-10% in both the presence of the three microorganisms and in abiotic controls where the polymers were exposed only to Nutrient Broth or malt extract-glucose medium. Scanning electron microscopy revealed breaks in PETP/LA fibres when polymers were exposed to A. fumigatus and C. guilliermondii, attributable to microbial action. Polyesteramides were resistant to biodegradation. Degradation of both polymer types resulted in a 5-10-fold increase of toxicity of culture supernatans measured with Vibrio fischeri bioluminescence test and Sinapis alba germination plant test, as compared to the biotic and abiotic controls. No genetic toxicity was detected with Salmonella typhimurium His- test. The study suggests that ecotoxicity of compounds produced by biodegradation of polymers should be monitored.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.