Super water repellent fabrics produced by silica nanoparticle-containing coating

In this paper, we report on superhydrophobic fabrics (polyester, wool and cotton) produced by a wet-chemical coating technique. The coating solutions were synthesized by the co-hydrolysis of two silane precursors, tetraethyl orthosilicate (TEOS) and an alkylsilane, in an alkaline condition. Without any purification, the as-hydrolyzed solutions were directly used to treat fabrics, and the treated fabrics had water contact angles (CA) as high as 170º and sliding angles (SA) as low as 5º. Three alkylsilanes have been used for the synthesis of the coating solutions, and all contain three hydrolysable alkoxyl groups and one non-hydrolysable alkyl, but with different chain lengths (C1, C8 and C16). It was found that the CA value increased with an increase in the alkyl chain length, while the SA showed a reverse trend. When the functional group had a C16 alkyl, the treated fabric surfaces were highly superhydrophobic, with the CA not being affected much by the fabric type, while the SA values were slightly affected by the original wettability of the fabric substrates. The superhydrophobic feature was attributed to a highly rough surface formed by the particulate coating. Aside from the superhydrophobicity, the influence of the coating on the fabric softness was also examined.

Photochromic textiles from hybrid silica coating with improved photostability

Photochromic surface coating on textiles may create new fashion opportunities. It also enhances the ultraviolet (UV) protection ability of the coated products. In this study, a spirooxazine dye and a silane that bears a long alkyl chain have been used to produce hybrid photochromic silica coatings on wool fabrics. Four stabilisers are added separately to the photochromic silica coatings to examine their influence on photostability and photochromic behaviour. It is found that the addition of UV stabilisers slightly reduces the photochromic response speed and photochromic absorption. However, the addition of UV stabilisers to the photochromic coating considerably improves the photochromic lifetime. Among the four UV stabilisers studied, the quencher results in the best improvement to photostability with the lowest reduction in photochromic absorption.

Superhydrophobic fabrics from hybrid silica sol-gel coatings: Structural effect of precursors on wettability and washing durability

Particle-containing silica sol was synthesized by co-hydrolysis and co-condensation of two silane precursors, tetraethylorthosilicate (TEOS) and an organic silane composed of a non-hydrolyzable functional group (e.g., alkyl, flourinated alkyl, and phenyl), and used to produce superhydrophobic coatings on fabrics. it has been revealed that the non-hydrolyzable functional groups in the organic silanes have a considerable influence on the fabric surface wettability. When the functional group was long chain alkyl (C16), phenyl, or flourinated alkyl (C8), the treated surfaces were highly superhydrophobic with a water contact angle (CA) greater than 170°, and the CA value was little affected by the fabric type. The washing durability of the superhydrophobic coating was improved by introducing the third silane containg epoxide group, 3-glycidoxypropyltrimethoxsilane (GPTMS), for synthesis. Although the presence of epoxide groups in the coating slightly reduced the fabrics' superhydrophobicity, the washing durability was considerably improved when polyester and cotton fabrics were used as substrates.

Photochromic fabrics from hybrid silica surface coatings

In this study, hybrid silica prepared by a sol-gel technique and doped with a photochromic dye was used to produce photochromic coatings on fabric surfaces. The coated fabrics showed a strong photochromic effect with very fast optical response speed. Good coating adhesion was obtained on wool fabrics. The photostability of the photochromic fabrics was improved by three different processes: adding a photo stabilizer, adjusting the surface wettability and sealing off the dye-containing pores with additional silica coating. Four UV stabilizers were added separately to the photochromic silica coatings to investigate their influence on the photostability and photochromic behaviour. The addition of UV stabilizers retarded the photochromic response and reduced photochromic absorption, but increased photochromic lifetime. Among the four UV stabilizers studied, the quencher resulted in the best improvement to the photostability with minimal reduction in the photochromic absorption. Increasing the hydrophobicity of the coating, and sealing-off the dye-containing pores were also found to improve photostability.

Synthesis of silica-coated ZnO nanocomposite : the resonance structure of polyvinyl pyrrolidone (PVP) as a coupling agent

Abstract The preparation of silica-coated ZnO nanocomposite using polyvinyl pyrrolidone (PVP) as a coupling agent was investigated. Transmission electron microscopy analysis revealed that silica has been deposited on the surface of PVP-capped ZnO nanoparticles as a continuous thin layer. Two-dimensional correlation analysis based on the time-dependent UV–vis spectra was introduced to study the interaction governing the deposition of silica on to PVP-capped ZnO. Strong hydrogen bonds formed between the amphiphilic PVP molecules and silica in the silicacoated PVP-capped ZnO composites. The reduced photocatalytic activity of silica-coated ZnO nanoparticles will enhance their performance as durable, safe, and nonreactive UV blockers in plastics, paints, and coating for outdoor textile and timber products.

Diatoms : self assembled silica nanostructures, and templates for bio/chemical sensors and biomimetic membranes

In this review we highlight recent advances in the understanding of biosilica production, biomodification of diatom frustules and their subsequent applications in bio/chemical sensors, and as a model membrane for filtration and separation.

Double-layer and hydration forces measured between silica sheets subjected to various surface treatments

Force measurements between silica surfaces in aqueous solutions of NaCl are reported. Silica is prepared with one of three surface treatments: (i) flaming, (ii) exposure to steam for 150 h, and (iii) brief exposure to ammonia vapor. Analysis of electrical double-layer interactions indicates that the surface density of silanol groups increases with steam treatment, and that exposure to ammonia etches the surface slightly and renders it porous. The force at short range is dominated by a strong repulsion which is attributed to hydration of the surface. The hydration component of the force is not significantly affected by the surface treatments, nor by electrolyte concentration over the range investigated (up to 0.1 M).

Measuring surface forces to explore surface chemistry : mica, sapphire and silica

In this paper measurements of the forces acting between two solid surfaces separated by a thin liquid film are discussed. By investigating these forces in a range of different liquids and solutions, it is possible to acquire an understanding of the surface properties of the solid material. The surface of mica has been studied extensively in this way, and the results obtained are reviewed to illustrate how the surface force measurements can give surface chemical information. Recent measurements on two other materials, sapphire and silica, which are of greater practical interest are also discussed.

Photoreactive azido-containing silica nanoparticle/polycation multilayers : durable superhydrophobic coating on cotton fabrics

In this study, we report the functionalization of silica nanoparticles with highly photoreactive phenyl azido groups and their utility as a negatively charged building block for layer-by-layer (LbL) electrostatic assembly to produce a stable silica nanoparticle coating. Azido-terminated silica nanoparticles were prepared by the functionalization of bare silica nanoparticles with 3-aminopropyltrimethoxysilane followed by the reaction with 4-azidobenzoic acid. The azido functionalization was confirmed by FTIR and XPS. Poly(allylamine hydrochloride) was also grafted with phenyl azido groups and used as photoreactive polycations for LbL assembly. For the photoreactive silica nanoparticle/polycation multilayers, UV irradiation can induce the covalent cross-linking within the multilayers as well as the anchoring of the multilayer film onto the organic substrate, through azido photochemical reactions including C–H insertion/abstraction reactions with surrounding molecules and dimerization of azido groups. Our results show that the stability of the silica nanoparticle/polycation multilayer film was greatly improved after UV irradiation. Combined with a fluoroalkylsilane post-treatment, the photoreactive LbL multilayers were used as a coating for superhydrophobic modification of cotton fabrics. Herein the LbL assembly method enables us to tailor the number of the coated silica nanoparticles through the assembly cycles. The superhydrophobicity of cotton fabrics was durable against acids, bases, and organic solvents, as well as repeated machine wash. Because of the unique azido photochemistry, the approach used here to anchor silica nanoparticles is applicable to almost any organic substrate.