Search results for "silica"
showing 10 items of 1092 documents
Prehnite: Structural similarity of the monoclinic and orthorhombic polymorphs and their Si/Al ordering
1990
Abstract Two modifications of the naturally occurring mineral prehnite, Ca 2 Al(Si 3 AlO 10 )(OH) 2 , are characterized by precise single crystal diffraction methods. The two forms are topologically identical. They differ only in the siting of one Al and one Si atom per unit cell: these switch their places in two of the tetrahedrally coordinated sites. This appears to be the only known case where a silicate occurs with two differently ordered tetrahedral distributions of Al and Si atoms. The two forms are not polytypes according to the current definition of polytypes. The two modifications are so similar to each other that they differ only in the eighth coordination sphere.
Synthesis of a Hydrothermally Stable, Periodic Mesoporous Material Containing Magnetite Nanoparticles, and the Preparation of Oriented Films
2006
Magnetite nanoparticles modified covalently with triethoxysilane having a quaternary dicetyl ammonium ion are used together with tetraethylorthosilicate as building blocks to prepare a mesoporous material. Cetyltrimethylammonium bromide is used as a structure-directing agent under conditions typically used for mesoporous MCM-41 silicas. The resulting mesoporous material (MAG-MCM-41), containing up to 15 wt % of magnetite is characterized by transmission electron microscopy (TEM), isothermal gas adsorption, and X-ray diffraction. In contrast to siliceous MCM-41, mesoporous MAG-MCM-41 exhibits a remarkable hydrothermal stability. The magnetic properties of MAG-MCM-41 are characterized by DC a…
Enhanced surface area in thermally stable pure mesoporous TiO2
2000
Abstract We describe here for the first time the surfactant-assisted synthesis of thermally stable mesoporous pure TiO 2 having a high surface area. Our synthetic approach to the chemistry of this system is based on the equilibrium between the hydrolysis and condensation reactions of the inorganic species and the organic–inorganic self-assembling processes. The use of titanatrane complexes helps to retard the hydrolysis and condensation reactions, thus allowing us to overcome the difficulties in preparing titanium dioxide mesoporous materials starting from highly reactive Ti-alkoxides. The mesoporous material has been characterized by TEM, XRD and N 2 adsorption–desorption isotherms and dis…
Large monolithic silica-based macrocellular foams with trimodal pore system.
2003
Silica-based materials with hierarchical pore systems at three different length scales (small mesopores–large mesopores–macropores) have been prepared through a nanotectonic approach by using mesoporous nanoparticles as building blocks; the resulting materials present a highly accessible foam-like architecture and can be prepared as large monoliths. Huerta Morillo, Lenin Jose, Lenin.Huerta@uv.es ; Latorre Saborit, Julio, Julio.Latorre@uv.es ; Beltran Porter, Aurelio, Aurelio.Beltran@uv.es ; Beltran Porter, Daniel, Daniel.Beltran@uv.es ; Amoros del Toro, Pedro Jose, Pedro.Amoros@uv.es
Stable anchoring of dispersed gold nanoparticles on hierarchic porous silica-based materials
2010
The nanometric organization of MOx (M = Co, Zn, Ni) domains partially embedded inside the mesoporous silica walls but accessible to the pore voids, which is achieved through a simple one-pot surfactant-assisted procedure, define optimal anchors for the nucleation and growth of gold nanoparticles, which in turn favours an exceptional thermal stability for the final Au-supported materials. As silica support we have selected a UVM-7 silica having a highly accessible architecture defined by two hierarchic pore systems. The combination of nanometric pore length, tortuous mesopores and MOx inorganic anchors favours the stability of the final Au/CoOx-UVM-7 nanocomposites.
Incorporation of Mn12single molecule magnets into mesoporous silica
2003
The incorporation of four Mn12 derivatives, namely [Mn12O12(O2CR)16(H2O)4] (R = CH3 (1), CH3CH2 (2), C6H5 (3), C6F5 (4)), into the hexagonal channels of the MCM-41 mesoporous silica has been studied. Only the smallest clusters 1 and 2, i.e. those with compatible size with the pores of MCM-41, could enter into the mesoporous silica. Powder X-ray diffraction analysis, HRTEM images and N2 adsorption–desorption isotherm experiments show that the well-ordered hexagonal structure of MCM-41 is preserved and that the Mn12 clusters are inside the pores. The magnetic properties of the MCM-41/2b nanocomposite material obtained in CH2Cl2 indicate that the structure of the cluster is maintained after in…
CsPbX3/SiOx (X = Cl, Br, I) monoliths prepared via a novel sol-gel route starting from Cs4PbX6 nanocrystals
2019
We developed a facile synthesis of nanocomposite powders of CsPbX3 nanocrystals (NCs) embedded in silica. The synthesis starts from colloidal Cs4PbX6 NCs that are mixed with tetraethyl orthosilicate in the presence of nitric acid, which triggers the sol-gel reaction yielding the formation of SiOx and the conversion of starting NCs into CsPbX3 ones. The overall reaction delivers CsPbX3 NCs encased in a silica matrix. The resulting CsPbX3/SiOx nano-composite powders exhibited enhanced moisture and thermal stability in air. Also, when mixing different CsPbX3/SiOx samples having diverse anion compositions, no interparticle anion exchange processes were observed, which is a further indication th…
Synthesis and Properties of Amine-Cured Epoxy/Organophilic Layered Silicate Nanocomposites
2009
Epoxy-layered silicate composites have been prepared by dispersing an organically modified montmorillonite (Nanofil 919) in an epoxy resin and curing in the presence of an aromatic hardener. Dispersion of the layered silicate within the epoxy matrix was verified using X-ray diffraction and transmission electron microscopy revealing that interaction improves upon organic silicate modification. Flexural properties and toughness increase with the organic silicate loading whereas glass transition temperature decreases and thermal stability remains practically unmodified.
Dispersions of nanosilica in biocompatible copolymers
2010
Dispersions of nanosilica in matrices of biocompatible copolymers were prepared by melt blending. Copolymers with variable molecular size at fixed hydrophilic/hydrophobic ratio and nanosilicas with different interfacial areas were studied. For comparison, a nanoclay was also investigated. The interfacial area played a relevant role in conferring peculiar properties on the nanohybrids. Amazingly, the macromolecule adsorbed on the nanosilica surface maintains some crystallinity which was quantitatively evaluated. In contrast, all the macromolecule anchored to the nanoclay surface is amorphous. The change of the crystalline state was reflected in the dielectric and the electrical conductivity …
Graphene oxide-silica nanohybrids as fillers for PA6 based nanocomposites
2014
Graphene oxide (GO) was prepared by oxidation of graphite flakes by a mixture of H2SO4/H3PO4 and KMnO4 based on Marcano's method. Two different masterbatches containing GO (33.3%) and polyamide-6 (PA6) (66.7%) were prepared both via solvent casting in formic acid and by melt mixing in a mini-extruder (Haake). The two masterbatches were then used to prepare PA6-based nanocomposites with a content of 2% in GO. For comparison, a nanocomposite by direct mixing of PA6 and GO (2%) and PA6/graphite nanocomposites were prepared, too. The oxidation of graphite into GO was assessed by X-ray diffraction (XRD), Micro-Raman spectroscopy, scanning electron microscopy (SEM), X-ray photoelectron spectrosco…