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Liquid Crystals as Multifunctional Interfaces for Trapping and Characterizing Microplastics
Summary
This study explored the use of liquid crystal (LC) films as multifunctional interfaces for trapping and classifying common microplastics including polyethylene (PE) and polystyrene (PS). PE and PS microparticles exhibited distinct two-dimensional aggregation patterns at the LC interface, with differences amplified by adding low concentrations of surfactant. Machine learning models applied to fractal geometry analysis of the aggregation patterns classified PE versus PS with over 99% accuracy, suggesting a novel approach for microplastic identification.
Identifying and removing microplastics (MPs) from the environment is a global challenge. This study explores how the colloidal fraction of common MPs behave at aqueous interfaces of liquid crystal (LC) films. We observed polyethylene (PE) and polystyrene (PS) microparticles to be captured at the LC interface and exhibit distinct two-dimensional aggregation patterns. The addition of low concentrations of surfactant (sodium dodecylsulfate (SDS)) was found to further amplify the differences in PS/PE aggregation patterns, with PS changing from a linear chain-like morphology to a singly dispersed state with increasing SDS concentration and PE forming dense clusters at all SDS concentrations. Statistical characterization of assembly patterns using fractal geometric theory-based machine learning and a deep learning image recognition model yielded highly accurate classification of PE vs PS (>99%). Additionally, by performing feature importance analysis on our deep learning model, dense, multi-branched assemblies were confirmed to be unique features of PE relative to PS. To obtain additional insight into the origin of these key features, we performed microscopic characterization of LC ordering at the microparticle surfaces. These observations led us to predict that both microparticle types should generate LC-mediated interactions (due to elastic strain) with a dipolar symmetry, a prediction consistent with the observed interfacial organization of PS but not PE. We conclude that the non-equilibrium organization of the PE microparticles arises from their polycrystalline nature, which leads to rough particle surfaces and weakened LC elastic interactions and enhanced capillary forces. Overall, our results highlight the potential utility of LC interfaces for surface-sensitive characterization of colloidal MPs.