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    SHAO Xining, FU Guotao, SANG Jiarong. Experimental and theoretical study on the temperature dependence of water contact angle on Polydimethylsiloxane filmJ. Journal of Chemical Engineering of Chinese Universities, 2026, 40(3): 396-402. DOI: 10.3969/j.issn.1003-9015.2026.00.001
    Citation: SHAO Xining, FU Guotao, SANG Jiarong. Experimental and theoretical study on the temperature dependence of water contact angle on Polydimethylsiloxane filmJ. Journal of Chemical Engineering of Chinese Universities, 2026, 40(3): 396-402. DOI: 10.3969/j.issn.1003-9015.2026.00.001

    Experimental and theoretical study on the temperature dependence of water contact angle on Polydimethylsiloxane film

    • To investigate the effect of temperature on the contact angle of water droplets on polydimethylsiloxane (PDMS) films, a self-built high-temperature and high-pressure sessile-drop visualization system was adopted in this study. Combined with the low-bond axisymmetric drop shape analysis, the morphologies of water droplets on the PDMS surface were systematically captured, and their corresponding contact angles were accurately measured at a constant pressure of 5 MPa over a temperature range of 30–210 °C. The experimental data revealed that the contact angle remains essentially constant at ~96° throughout the entire temperature range, exhibiting negligible temperature sensitivity. On the theoretical side, the water-PDMS interaction was represented by a Steel 10-4-3 potential, with the water-PDMS attraction energy treated as an adjustable parameter. After calibrating this parameter to the experimental contact angle at a single arbitrary temperature, classical density functional theory combined with Young’s equation was used to predict the contact angle evolution. The calculations indicated a slight increase in the contact angle with temperature at low temperatures, followed by a pronounced decrease at higher temperatures, a trend that deviates from the experimentally observed plateau. This discrepancy suggests that the interaction potential requires further refinement. The present work not only enlarges the high-temperature, high-pressure contact angle database for water-solid systems but also provides a valuable guidance for future theoretical development.
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