Abstract

Polypropylene (PP) surfaces with reversible switching between superhydrophobicity and superhydrophilicity were fabricated by a simple dip-coating method. The reversibility was obtained using a combination of UV and thermal treatment cycles. Superhydrophobic polymeric surfaces were prepared by dipping PP substrates in a hot suspension of xylene containing TiO2 nanoparticles (NPs) functionalized with trimethoxypropyl silane (TMPSi). This resulted in superhydrophobic PP surfaces with water contact angles (WCA) of 158° that were converted to superhydrophilic (WCA ~0°) by UV irradiation. However, the superhydrophobic state can be easily recovered using a soft thermal treatment (100 °C for 2 h). A continuous switch in the extreme wettability properties of the surfaces was achieved using cycles of UV irradiation and thermal treatments. Additionally, the hydrophilicity obtained by UV illumination improved the weak adhesion that existed between the nanocoating and the PP surface before the UV treatment by about 90 %. Detailed high-resolution X-ray photoelectron spectroscopy data showed that the relative concentration of the hydrophilic component, Ti–OH, in the O 1s signal increased from 32 % to more than 50 % when the surface was irradiated. Simultaneously, the Ti 2p signal showed a reduction of Ti(IV) to Ti(III) after the photochemical treatment leading to a surface hydroxylation and the superhydrophilicity found after UV irradiation. This paper reports the preparation of PP surfaces with excellent controllable wettability with important applications where improvement in the coating adhesion is necessary.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.