AI Article Synopsis

  • Microplastics are a significant environmental issue, necessitating a reduction in both petrochemical and bio-based plastics, as they accumulate in food chains and pose risks to animals and humans.
  • The study explored various advanced oxidation processes (AOPs) like ultrasounds and ultraviolet irradiation to enhance the biodegradability of polylactic acid (PLA) films, treating them for durations of 1 to 6 hours.
  • Results showed that PLA films achieved up to 90% weight loss using a commercial enzyme cocktail during composting, and notably, PLA was transformed into bacterial nanocellulose post-enzymatic hydrolysis.

Article Abstract

It is well acknowledged that microplastics are a major environmental problem and that the use of plastics, both petro- and bio- based, should be reduced. Nevertheless, it is also a necessity to reduce the amount of the already spread plastics. These cannot be easily degraded in the nature and accumulate in the food supply chain with major danger for animals and human life. It has been shown in the literature that advanced oxidation processes (AOPs) modify the surface of polylactic acid (PLA) materials in a way that bacteria more efficiently dock on their surface and eventually degrade them. In the present work we investigated the influence of different AOPs (ultrasounds, ultraviolet irradiation, and their combination) on the biodegradability of PLA films treated for different times between 1 and 6 h. The pre-treated samples have been degraded using a home model compost as well as a cocktail of commercial enzymes at mesophilic temperatures (37 °C and 42 °C, respectively). Degradation degree has been measured and degradation products have been identified. Excellent degradation of PLA films has been achieved with enzyme cocktail containing commercial alkaline proteases and lipases of up to 90% weight loss. For the first time, we also report valorization of PLA into bacterial nanocellulose after enzymatic hydrolysis of the samples.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10110681PMC
http://dx.doi.org/10.1007/s11274-023-03605-4DOI Listing

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