Fabrication of Silica-Titanium Composite Film on Wood Surface and Optimization of Its Structure and Properties

In this thesis, wood loaded with a silica-titanium (Si-Ti) composite film was prepared using the sol-gel method in order to achieve improved wood with high hydrophobicity and photocatalytic activity under visible light. The factors affecting the structure and properties of the composite film, as well as the optimization process, were discussed. Infrared analysis revealed that the vibrational intensity of Si-O-Si, Ti-O-Ti, and Ti-O-Si telescopic vibration peaks increased with an increase in vinyltriethoxysilane (VETS). Additionally, the number of Ti-O-Ti telescopic vibration peaks also increased with an increase in VETS. Furthermore, the intensity of -NO3, Si-O-Si, and Ti-O-Ti telescopic vibrational peaks was enhanced with a higher dosage of nitric acid. Conversely, the intensity of -OH telescopic vibrational peaks decreased with an increase in drying temperature. XRD analysis showed that nitric acid could promote the transformation of TiO2 from amorphous to anatase, while SiO2 would reduce the grain size of anatase TiO2 and promote the growth of rutile TiO2. Additionally, wood surfaces loaded with Si-Ti composite film changed from hydrophilic to hydrophobic, with significant differences observed between different levels of each factor. The photocatalytic activity of surface-loaded Si-Ti composite films on wood was most affected by the amount of nitric acid, which influenced crystallinity of TiO2 and thus impacted the photocatalytic activity. Furthermore, changes in VTES dosage not only affected the crystalline phase of TiO2 and the grain size of Si-Ti composite film but also influenced the crystallinity of TiO2 through generating SiO2. Finally, based on optimal preparation process (titanium-alcohol ratio of 1:5, titanium-silicon ratio of 1:0.2, titanium-acid ratio of 1:0.5, and drying temperature of 100 degrees C), wood surfaces loaded with Si-Ti composite film achieved a contact angle up to 125.9 degrees and exhibited a decolorization rate for rhodamine B under UV light reaching 94% within 180 min.