Design of Co3O4@SiO2 Nanorattles for Catalytic Toluene Combustion Based on Bottom-Up Strategy Involving Spherical Poly(styrene-co-acrylic Acid) Template

Bearing in mind the need to develop optimal transition metal oxide-based catalysts for the combustion of volatile organic compounds (VOCs), yolk-shell materials were proposed. The constructed composites contained catalytically active Co3O4 nanoparticles, protected against aggregation and highly dispersed in a shell made of porous SiO2, forming a specific type of nanoreactor. The bottom-up synthesis started with obtaining spherical poly(styrene-co-acrylic acid) copolymer (PS30) cores, which were then covered with the SiO2 layer. The Co3O4 active phase was deposited by impregnation using the PS30@SiO2 composite as well as hollow SiO2 spheres with the removed copolymer core. Structure (XRD), morphology (SEM), chemical composition (XRF), state of the active phase (UV-Vis-DR and XPS) and reducibility (H2-TPR) of the obtained catalysts were studied. It was proven that the introduction of Co3O4 nanoparticles into the empty SiO2 spheres resulted in their loose distribution, which facilitated the access of reagents to active sites and, on the other hand, promoted the involvement of lattice oxygen in the catalytic process. As a result, the catalysts obtained in this way showed a very high activity in the combustion of toluene, which significantly exceeded that achieved over a standard silica gel supported Co3O4 catalyst.

Theoretical and Experimental Study on the Functionalization Effect on the SERS Enhancement Factor of SiO2-Ag Composite Films

Herein we addressed a study to determine the enhancement factor (EF) of the Raman signal reached by composite films with two main components, Ag nanoparticles and SiO2 spheres. The study involves the synthesis, structural composition and optical response by using experimental techniques and theoretical-numerical modeling. A colloid with single NPs and agglomerates of them, with a tannic acid layer on its surface, was produced. Separately, porous SiO2 spheres were obtained. A mixture of both, Ag NPs and SiO2 particles was used to produce the films by solvent evaporation method. It is shown that single or agglomerated Ag NPs are preferentially located at the interstices of the SiO2 spheres. Using discrete dipole approximation, the SERS EF has been estimated considering the agglomeration and tannic acid layer. Both, the dielectric spheres and tannic acid layer diminish the electric field intensity and therefore the SERS EF. When a Ag NP with/without a dielectric shell is touching a SiO2 sphere, the EF is as high as 1 × 103, the zones where this value is reached are smaller when the dielectric layer is present. With a cluster of 3 nude Ag NPs surrounded by SiO2 spheres an EF of 2.4 × 103 is obtained.

Surface Modification Design for Improving the Strength and Water Vapor Permeability of Waterborne Polymer/SiO2 Composites: Molecular Simulation and Experimental Analyses

Polymer-based nanocomposites properties are greatly affected by interfacial interaction. Polyacrylate nanocomposites have been widely studied, but few studies have been conducted on their interface mechanism. Therefore, there was an urgent demand for providing a thorough understanding of the polymethyl acrylate/SiO2 (PMA/SiO2) nanocomposites to obtain the desired macro-performance. In this paper, a methodology, which combined molecular dynamics simulation with experimental researches, was established to expound the effect of the surface structure of SiO2 particles which were treated with KH550, KH560 or KH570 (KH550-SiO2, KH560-SiO2 and KH570-SiO2) on the mechanical characteristic and water vapor permeability of polymethyl acrylate/SiO2 nanocomposites. The polymethyl acrylate/SiO2 nanocomposites were analyzed in binding energy and mean square displacement. The results indicate that PMA/KH570-SiO2 had the highest tensile strength, while PMA/KH550-SiO2 had the highest elongation at break at the same filler content; KH550-SiO2 spheres can significantly improve water vapor permeability of polyacrylate film.