4.7 Article

Comparative biodeterioration at air interfaces of adipate-based polyester polyurethane coatings by fungal microcolonies of Aureobasidium sp. W12

Journal

POLYMER DEGRADATION AND STABILITY
Volume 214, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.polymdegradstab.2023.110386

Keywords

Coating; Aliphatic polyester; Polyurethane; Fungal; Aureobasidium; Unsaturated environments

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Understanding the conditions that promote microbial deterioration of polymer materials is crucial for predicting and controlling their environmental fate. In this study, fungal degradation of commercial polyester polyurethanes was investigated under nutrient limitation and high humidity conditions at air/polymer interfaces. Results showed rapid deterioration of the polymer materials, with the rate of degradation depending on the properties of the materials.
Understanding conditions that enable environmentally common microbes to aggressively deteriorate polymer materials are important for predicting and controlling the environmental fates of these materials. For protective paints and coatings in terrestrial environments, processes at air interfaces are among important factors to understand. Here, we track fungal biodeterioration at air/solid polymer interfaces under nutrient limitation and high humidity, using polymer compositions common in commercial polyester polyurethanes. A fungal isolate, Aureobasidium sp. W12, was collected from an aircraft and identified as a polyester degrader through screening assays. Two polyadipate-based materials were then used for W12 coating deterioration analysis: a commercial polyester polyurethane, Irogran (R) PS455-203, and a model polyester urethane, PEA-HM. Single and micro-aggregated cell clusters distributed within similar to 1.5 mm diameter regions were prepared on the polymer surfaces and incubated with no supplemental nutrients at >95% relative humidity for up to 13 days. Coating deterioration was semi-quantitatively monitored through ester carbonyl loss by transmission FTIR spectroscopy and both materials were rapidly deteriorated, although at different rates. With similar to 0.5 monolayer cell surface coverage, PEA-HM showed about 6 x greater molar ester deterioration versus Irogran (R) over the first 24 h. By 13 days, the polyester fractions of Irogran coatings were deteriorated to an average depth of about 0.1 mu m, while PEA-HM coatings about 1 mu m thick were completely deteriorated in 5 days within and beyond cell covered regions. Localized analysis of non-uniform PEA-HM deterioration showed that quantities on the order of 10 individual Aureobasidium yeast cells could locally deteriorate through 1-2 mu m of PEA-HM coating within 12 days (with deterioration rates up to about 2 x 10 6 mu mol ester / (cell x day)). These results correlate conditions and polymer properties that promote high deterioration potentials of Aureobasidium W12 microcolonies at air / coating interfaces.

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