Silica thin films with a two-dimensional (2D) hexagonal structure were produced from TEOS and the F127 triblock copolymer PEO106PPO70PEO106. The structure of the films was deduced from transmission electron microscopy (TEM) performed on microtomed sections and from a 2D X-ray scattering technique adapted for film characterization. Both methods are complementary and allow for a detailed characterization of the film structure. The pore channels within the coatings are organized in domains, which spin and curve inside the film, but align with the surface plan at the air/film and film/substrate interfaces. The formation of the film was monitored by in situ time-resolved SAXS experiments to follow the structural evolution during the first minutes after deposition. Cylindrical micelles, which gives rise to a wormlike structure, form first at the air/film interface and extend toward the film/substrate interface via solvent evaporation. When most of the liquid phase is evaporated, the well-aligned domains located at both interfaces are obtained by a self-arrangement of the micelles parallel to the interfaces. This rearrangement occurs when the film is considered to be dry. The atom content profiles in the as-prepared films were obtained by Rutherford backscattering (RBS) and show homogeneous distribution of atoms throughout the film thickness. To stiffen the network and remove the surfactant, various postsynthesis treatments were applied to the coatings, that is, thermal treatment, base-catalyzed condensation, and solvent extraction. Each method induces shrinkage, leading to 2D-centered rectangular films through a contraction of the initial 2D hexagonal structure. As-prepared and treated films exhibit excellent optical transparency and high degree of organization. Ellipsometry measurements and N2 adsorption/desorption isotherms were thus used to estimate the refractive index and the porosity of the films. Refractive index down to 1.2 was obtained in the film that was pretreated under a NH3 atmosphere before solvent extraction of the surfactant. This shows the efficiency of this treatment to minimize the network shrinkage. N2 adsorption-desorption measurement performed on films calcined at 350 °C gives a surface area of 800 m2 g-1 and a porosity of 63%.@en

A novel catalyst preparation procedure is proposed in order to enhance the noble metal distribution at low loadings, while controlling the hierarchical porosity of the support material. Thus, a silica-supported platinum catalyst with hierarchical porosity was prepared using a combination of three processes performed in aqueous medium: emulsion polymerisation, sonochemistry and sol-gel synthesis. First, a polystyrene latex template of ca. 130 nm was synthesised by emulsion polymerisation and subsequently decorated with Pt nanoparticles of ca. 2.1 nm by sonochemical reduction of sodium tetrachloroplatinate. Then, the mesoporous silica support was prepared by a two-step acid-base catalysed sol-gel synthesis around the Pt-loaded latex spheres. Materials with specific surface areas and total pore volumes as high as 615 m2 g−1 and 0.74 cm3 g−1, respectively, were obtained.@en

As a follow-up of the paper “Engineering of silica-supported platinum catalysts with hierarchical porosity combining latex synthesis, sonochemistry and sol-gel process – I. Material preparation” (A.F. Sierra-Salazar, et at., Microporous Mesoporous Mater. 234 (2016) 207–214. http://dx.doi.org/10.1016/j.micromeso.2016.07.009), we propose waterborne Pt-based catalysts with hierarchical porosity and controlled Pt nanoparticles (NPs) distribution within the support. The materials exhibit specific surface areas and total pore volumes as high as 490 m2 g−1 and 0.77 cm3 g−1, with ∼5 nm Pt NPs mainly located in the macropores. The Pt NPs were characterised using X-ray photoemission spectroscopy (XPS) and high resolution transmission electron microscopy (HR-TEM). Considering the selectivity challenge of the catalytic hydrogenation of halonitrobenzenes to produce haloanilines, which are important raw materials for several industrial products, we evaluated these hierarchically porous catalysts for the hydrogenation of p-chloronitrobenzene (p-CNB) in batch mode to produce p-chloroaniline (p-CAN). It was possible to obtain up to 100% selectivity at 80% conversion and initial reaction rates up to 34 molCNB min−1 molPt −1. Such selectivity was higher than that exhibited by a commercial Pt/SiO2 catalyst (up to 92%).@en