Silice mésoporeuse | EPFL Graph Search

Mesoporous silica is a form of silica that is characterised by its mesoporous structure, that is, having pores that range from 2 nm to 50 nm in diameter. According to IUPAC's terminology, mesoporosity sits between microporous (50 nm). Mesoporous silica is a relatively recent development in nanotechnology. The most common types of mesoporous nanoparticles are MCM-41 and SBA-15. Research continues on the particles, which have applications in catalysis, drug delivery and imaging. Mesoporous ordered silica films have been also obtained with different pore topologies. A compound producing mesoporous silica was patented around 1970. It went almost unnoticed and was reproduced in 1997. Mesoporous silica nanoparticles (MSNs) were independently synthesized in 1990 by researchers in Japan. They were later produced also at Mobil Corporation laboratories and named Mobil Composition of Matter (or Mobil Crystalline Materials, MCM). Six years later, silica nanoparticles with much larger (4.6 to 30 nanometer) pores were produced at the University of California, Santa Barbara. The material was named Santa Barbara Amorphous type material, or SBA-15. These particles also have a hexagonal array of pores. The researchers who invented these types of particles planned to use them as molecular sieves. Today, mesoporous silica nanoparticles have many applications in medicine, biosensors, thermal energy storage, water/gas filtration and imaging. Mesoporous silica nanoparticles are synthesized by reacting tetraethyl orthosilicate with a template made of micellar rods. The result is a collection of nano-sized spheres or rods that are filled with a regular arrangement of pores. The template can then be removed by washing with a solvent adjusted to the proper pH. Mesoporous particles can also be synthesized using a simple sol-gel method such as the Stöber process, or a spray drying method. Tetraethyl orthosilicate is also used with an additional polymer monomer (as a template).

Polyphenols as Morphogenetic Agents for the Controlled Synthesis of Mesoporous Silica Nanoparticles

Fabien Sorin, Jialuo Luo, René M. Rossi, Alina Osypova

Non-surfactant-induced synthesis of mesoporous silica nanoparticles (MSNPs) is gaining increasing interest because of their low toxicity and simple purification compared to conventional surfactant-based methods. Tannic acid (TA), considered as a glucose-derived polyphenol, was first employed a few years ago and has attracted great research interest. Despite recent progress, the mechanisms resulting in the porous structure remain to be elucidated. In this work, we have employed TA and four structurally related polyphenols (gallic acid, ethyl gallate, eudesmic acid, and quercetin) to elucidate the effect of the chemical structure and properties of polyphenols on their templating ability. Our results unravel the mechanism of MSNP formation templated by TA, which form a supramolecular framework as the skeleton for the silica species to attach. The structure of the supramolecular network results in irregular pores. Additionally, the pK(a) value of the templates may be accounted for the particle size. Small-angle X-ray scattering was used to provide precise information on the morphology, especially the porosity of the resulting MSNPs in addition to electron microscopy, dynamic light scattering, nitrogen adsorption and desorption Brunauer-Emmett-Teller method, and thermogravimetric analysis.

AMER CHEMICAL SOC2019

Preparation and Characterization of High-Surface-Area Bi(1-x)/3V1-xMoxO4 Catalysts

Lioubov Kiwi, Alexandre Nell

We report the successful application of a templating approach employing ordered mesoporous carbon to the synthesis of BiVO4, Bi2Mo3O12, and Bi0.85V0.55Mo0.45O4 and the performance of these materials as catalysts for the oxidation of propene to acrolein. Ordered mesoporous carbon templates were used to control the nucleation and growth of the mixed metal oxide crystals, allowing higher final surface areas to be obtained. The resulting materials were characterized by X-ray diffraction, Raman spectroscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and BET surface area analysis. The surface area of the mixed metal oxide catalysts was found to depend on the type of mesoporous silica used to prepare the carbon template and on the conditions under which the carbon template was formed. Through an appropriate choice of template, the surface areas of the mixed metal oxides exceeded 15 m(2)/g. Catalytic testing revealed that materials produced via templating in ordered mesoporous carbon had per-gram activities that were up to 85 times higher than those produced by a conventional hydrothermal synthesis and exhibited stable catalytic activities over 24 h.

American Chemical Society2014

Catalytic ozonation of oxalic acid using carbon nanofibres on macrostructured supports

Lioubov Kiwi, Tatiana Iouranova

Carbon nanofibres (CNFs) were grown on different macrostructured supports such as cordierite monoliths, carbon felts and sintered metal fibres. The resulting composites exhibited excellent resistance to attrition/corrosion and its porosity is mainly due to mesoporous structures. The CNF/ structured materials were tested in the ozonation of oxalic acid in a conventional semi-batch reactor after being crushed to powder form, and in a newly designed reactor that may operate in semi-batch or continuous operation. The CNFs supported on the different structured materials exhibited high catalytic activity in the mineralization of oxalic acid.

2012