A SiO2/pHEMA-Based Polymer-Infiltrated Ceramic Network Composite for Dental Restorative Materials

SiO2-poly(2-hydroxyethyl methacrylate) (pHEMA)-based composites have been widely used as biomaterials owing to their biocompatibility. However, they have not yet been applied as tooth restorative materials because of their poor mechanical properties. In the present paper, we develop a novel SiO2/pHEMA-based composite with a polymer-infiltrated network (PICN) structure for use in dental restorative materials. A mixture of SiO2 nanoparticles and a poly(vinyl alcohol) binder was sintered at 950 °C to fabricate a porous SiO2 block. A monomer mixture containing 70 wt%-HEMA/30 wt%-ethylene glycol dimethacrylate and a benzoyl peroxide initiator was infiltrated into the porous SiO2 block and heat-polymerized to fabricate the SiO2/pHEMA-based composite with a PICN structure. The composite was characterized according to its mechanical properties, surface free energy, and bonding properties with a dental adhesive. The flexural strength was 112.5 ± 18.7 MPa, the flexural modulus was 13.6 ± 3.4 GPa, and the Vickers hardness was 168.2 ± 16.1, which are similar values to human teeth. The surface free energy of the polar component of the composite was 19.6 ± 2.5 mN/m, suggesting that this composite has an active surface for bonding with the adhesive. The composite bonded well to the adhesive, in the presence of a silane coupling agent. The SiO2/pHEMA-based composite was demonstrated to be a potential candidate for dental restorative materials.

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.

A Study on the Heat Effect and Kinetics During Magnesiothermic Reduction of Porous SiO2

Magnesiothermic reduction reaction (MRR) is an effective method to synthesis Si nanoparticles. In this paper, the heat effect and MRR kinetics were investigated by real-time temperature monitoring and analyzing the DSC curve of the MRR. It was found that the MRR onset temperature is about 465 °C, and the system temperature rose sharply at 535 °C. After the disappearance of the magnesium phase, the system temperature remained consistent with the set value. The exothermic peak lags and the spike decreases when adding NaCl into the system. The MRR was chemical reaction control, corresponding with the apparent activation energy was 193.456 kJ·mol-1 (without NaCl) and 191.434 kJ·mol-1 (with NaCl) in the temperature interval 465 °C −700 °C, respectively. NaCl affects the reaction mechanism by lowering the temperature of the system. Our work successfully prepared the spherical Si nanoparticles, which average grain size increased from 25 nm to 40 nm with the extended reaction duration. The conversion rate of porous SiO2 precursor was as high as 92%.