Major considerations for using surface energy models as a tool for surface modification and adhesion improvement purposes

Direct measurement of Surface Free Energy (SFE) for solid surfaces is not feasible; thus, the Young-Dupre<acute accent> equation, in conjunction with appropriate SFE models, is employed for its estimation. This study explores the impact of surface treatment of polyethylene (PE) on its SFE and adhesion properties and addresses two main challenges: identifying the ideal contact angle (CA) and selecting a reliable SFE model. Five distinct surface treatments were applied to PE and as-placed, advancing, and receding CAs were measured with five probe liquids. Comparative analysis with Attenuated Total Reflectance - Fourier Transform Infrared Spectroscopy (ATR-FTIR) and X-ray Photoelectron Spectroscopy (XPS) revealed inconsistencies with as-placed and advancing CAs, while receding CAs provided better correlation with surface modifications. SFE and work of adhesion (Wad) calculations were performed using multiple SFE models, including the two-component OWRK, the threecomponent VOGC, and a novel four-component Partial Solvation Parameters (PSPs) model. Using as-placed CAs led to unreliable adhesion predictions, while employing receding CAs aligned more closely with adhesion measurements. All models underestimated the contribution of non-dispersive interactions to the total SFE and Wad, particularly when using as-placed CA. A new two-step method utilizing both advancing and receding CAs is proposed, demonstrating improved correlation with FTIR, XPS, and adhesion data, and attributing most adhesion improvements to non-dispersive interactions. This work highlights the need for refined SFE models and CA measurement techniques for accurately assessing modified surfaces in adhesion studies.