Biodegradation of PBAT ‐Silane Functionalized Nanocellulose Composite Films Under Industrial Composting Condition

Efforts to develop biodegradable plastics are ongoing in response to growing environmental concerns. However, the post‐use fate of these materials is not always well understood. This study aimed to evaluate the biodegradation behavior of poly(butylene adipate‐co‐terephthalate) (PBAT) and its composi...

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Bibliographic Details
Published inPolymer engineering and science
Main Authors Dhali, Kingshuk, Daver, Fugen, Cass, Peter, Sangwan, Parveen, Adhikari, Benu
Format Journal Article
LanguageEnglish
Published 12.08.2025
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Summary:Efforts to develop biodegradable plastics are ongoing in response to growing environmental concerns. However, the post‐use fate of these materials is not always well understood. This study aimed to evaluate the biodegradation behavior of poly(butylene adipate‐co‐terephthalate) (PBAT) and its composites. The aim of this study was to determine the biodegradation of poly(butylene adipate‐co‐terephthalate) (PBAT) and its composites. The nanocomposites were produced by melt blending PBAT with either 5 wt% unmodified cellulose nanocrystals (PBAT‐CNC) or 5 wt% phenyl silane modified cellulose nanocrystals (PBAT‐CNC PhS ). The aerobic biodegradation of the composite films was studied for their physical disintegration behavior under simulated industrial composting conditions (58°C ± 2°C) for 120 days. Additionally, respirometric biodegradation tests were separately carried out to assess CO 2 evolution and the extent of mineralization under the identical conditions. Surface morphology and thermal degradation of representative partially degraded samples were also analyzed. The effect of unmodified and silane modified cellulose nanocrystals (CNCs) on the biodegradation of the composites was evaluated. Both PBAT‐CNC and PBAT‐CNC PhS composite films exhibited faster fragmentation and mass loss compared to that of PBAT. The hydrolysis of the nanocomposite was moderately restricted by phenyl silane modified CNCs, but this effect was only observed for the first 28 days. The composites demonstrated the following order in terms of fragmentation and CO 2 evolution: PBAT‐CNC > PBAT‐CNC PhS > PBAT. The composite materials produced using silane‐modified CNCs are suitable for use as biodegradable plastics.
ISSN:0032-3888
1548-2634
DOI:10.1002/pen.70099