Preparation, nano-mechanics and particle deposition behavior of thin, antifouling hydrogel coatings

Abstract

Hydrogels based on hydrophilic, crosslinked polymer networks can reduce surface contamination in aqueous environments and continue attracting research interest due to their low adhesion, biocompatibility and tunable properties. In particular, sub-micron hydrogel films can potentially screen a surface from interaction with foulant colloids and microorganisms without compromising original functions, such as water permeation in membranes. This study focuses on the preparation of thin hydrogel films with the goal of understanding their adhesive and micromechanical properties, as well as factors affecting the dynamics of microparticle deposition on such films, mimicking the initial stages of surface fouling with colloids, microparticles and microorganisms. For this purpose, a simple procedure was developed to simultaneously crosslink and covalently anchor multi-arm-PEG precursors to a surface to form a submicron coating as a representative model. The effects of synthetic parameters and external conditions on adhesion and viscoelasticity were studied by force spectroscopy using polystyrene colloidal probes. The same particles were also employed in macroscopic deposition experiments in a parallel plate flow cell under identical solution conditions. Microscopic adhesion and elasticity were unaffected by the hydrogel crosslinking density and by salinity, but strongly affected by solution pH and dwell time, whereas macroscopic deposition was strongly affected both by salinity and by pH. These differences were ascribed to the effect of long-range double-layer forces, involved in deposition but absent in measurements of adhesion and elasticity. The results highlight the differences and similarities between the two types of measurements and underlying phenomena, as a step towards the understanding and rational design of soft antifouling coatings.