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The article presents a study of mesoporous silicates through the controllable soft-templating method. The synthesis of mesoporous silicate from the surfactant templating approach is demonstrated with the aim of controllable synthesis on the micro-, meso-, and macroscale. The use of EISA method combined with other synthetic techniques for the preparation of mesoporous silica thin films is explored.

Highly ordered mesoporous carbons and silicas with ultralarge accessible pores have been successfully synthesized by using laboratory-made poly(ethylene oxide)-b-polystyrene (PEO-b-PS) diblock copolymers as templates via the evaporation-induced self-assembly (EISA) approach. Resols and tetraethyl orthosilicate (TEOS) serve as carbon and silica precursors, respectively. Small-angle X-ray scattering (SAXS) and transmission electron microscopy (TEM) measurements show that the mesoporous carbons (denoted as C-FDU-18) possess face centered cubic closed-packing (fcc) mesostructure (Fm3m) with large-domain ordering. N2 sorption isotherms reveal a large mesopore at the mean value of 22.6 nm with a narrow pore-size distribution. Mesoporous silicas (Si-FDU-18) also display a highly ordered fcc closed-packing mesostructure with an ultralarge unit cell (a = 54.6 nm). A hydrothermal recrystallization was introduced for the first time to produce micropores in thick silica walls (∼7.7 nm) and thus to generate ultralarge accessible mesopores (30.8 nm). Notably, the amphiphilic diblock copolymer with high molecular weight (PEO125-PS230, 29700 g mol-1) in this report was prepared via a simple method of atom transfer radical polymerization (ATRP). It can be easily available for chemists even without any experience in polymer synthesis. [ABSTRACT FROM AUTHOR]

Highly ordered mesoporous polymer-silica and carbon-silica nanocomposites with interpenetrating networks have been successfully synthesized by the evaporation-induced triconstituent co-assembly method, wherein soluble resol polymer is used as an organic precursor, prehydrolyzed TEOS is used as an inorganic precursor, and triblock copolymer F127 is used as a template. It is proposed for the first time that ordered mesoporous nanocomposites have ‘reinforced concrete’-structured frameworks. By adjusting the initial mass ratios of TEOS to resol, we determined the obtained nanocomposites possess continuous composition with the ratios ranging from zero to infinity for the two constituents that are ‘homogeneously’ dispersed inside the pore walls. The presence of silicates in nanocomposites dramatically inhibits framework shrinkage during the calcination, resulting in highly ordered large-pore mesoporous carbon-silica nanocomposites. Combustion in air or etching in HF solution can remove carbon or silica from the carbon-silica nanocomposites and yield ordered mesoporous pure silica or carbon frameworks. The process generates plenty of small pores in carbon or/and silica pore walls. Ordered mesoporous carbons can then be obtained with large pore sizes of ∼6.7 nm, pore volumes of ∼2.0 cm3/g, and high surface areas of ∼2470 m2/g. The pore structures and textures can be controlled by varying the sizes and polymerization degrees of two constituent precursors. Accordingly, by simply tuning the aging time of TEOS, ordered mesoporous carbons with evident bimodal pores at 2.6 and 5.8 nm can be synthesized. [ABSTRACT FROM AUTHOR]

A coordination-assisted synthetic approach is reported here for the synthesis of highly active and stable gold nanoparticle catalysts in ordered mesoporous carbon materials using triblock copolymer F127 as a structure-directing agent, thiol-containing silane as a coordination agent, HAuCl4 as a gold source, and phenolic resin as a carbon source. Upon carbonization, the gold precursor becomes reduced to form monodispersed Au nanoparticles of ca. 9.0 nm, which are entrapped or confined by the "rigid" mesoporous carbonaceous framework. Nanoparticle aggregation is inhibited even at a high temperature of 600 °C. After removal of the silica component, the materials possess the ordered mesostructure, high surface area (~1800 m2/g), large pore volume (~1.19 cm3/g), and uniform bimodal mesopore size (<2.0 and 4.0 nm). The monodispersed gold nanoparticles are highly exposed because of the interpenetrated bimodal pores in the carbon framework, which exhibit excellent catalytic performance. A completely selective conversion of benzyl alcohol in water to benzoic acid can be achieved at 90 °C and 1 MPa oxygen. Benzyl alcohol can also be quantitatively converted to benzoic acid at 60 °C even under an atmospheric pressure, showing great advantages in green chemistry. The catalysts are stable, poison resistant, and reusable with little activity loss due to metal leaching. The silane coupling agent played several functions in this approach: (1) coordinating with gold species by the thiol group to benefit formation of monodispersed Au nanoparticles; (2) reacting with phenolic resins by silanol groups to form relatively "rigid" composite framework; (3) pore-forming agent to generate secondary pores in carbon pore walls, which lead to higher surface area, larger pore volumes, and higher accessibility to to the gold nanoparticles. Complete removal of the silica component proves to have little effect on the catalytic performance of entrapped Au nanoparticles. [ABSTRACT FROM AUTHOR]

Here, we report a facile method for the preparation of monodisperse lanthanide-doped titania-coated silica nanoparticles. By hydrolysis of titanium alkoxide precursors in the presence of lanthanide ions, titania coatings have been deposited on the surface of the silica nanoparticles dispersed in the pure ethanol. Lanthanide ions were directly incorporated into the coating during the coating process. For a given ratio of titanium alkoxide to water, the density of the doped ions is determined by the concentration of the lanthanide ions in the reactant mixture. The final particles were nanosized, discrete, and exhibiting luminescence when excited. [ABSTRACT FROM AUTHOR]

Pd/mesoporous silica-carbon nanocomposites with 3.2 nm Pd particles, prepared by a simple wetness impregnation method, have demonstrated high activity at 258 K for the hydrodechlorination of chlorophenols with a high selectivity. [ABSTRACT FROM AUTHOR]