Search results for "Mesoporous material"

Synthesis and characterization of mesoporous Mn-MCM-41 materials

2011

Si { 1 H} CP-MAS NMR X-ray photo-emission spectroscopy a b s t r a c t MCM-41 has been synthesized at two different pH using cetyl-trimethylammonium bromide (CTAB) surfactant as template and adding the silica precursor to aqueous solutions containing CTAB. The obtained solids were calcined at 600 ◦ C for 4 h. Mn-MCM-41 powders with different Mn/Si molar ratios were prepared using the incipient wetness method, followed by calcination at 550 ◦C for 5 h. At the end of the impregnation process the powders colour changed from white to brown whose intensity depends on manganese quantity. The materials characterization was performed by X-ray diffraction, N2 adsorption, 29 Si Cross Polarization–Mag…

Nano-sized mesoporous carbon particles with bimodal pore system and semi-crystalline porous walls

2008

Acetylene CVD carbon replication of a hierarchical pore silica-based material, Fe-UVM-7, is reported. The original template organization, which is based on the aggregation of mesoporous nanoparticles, is accurately replicated in the final carbon material: a bimodal porous carbon combining mesoporous nanoparticles and inter-particle textural-like pores which provide high surface area, a highly accessible pore system and semi-crystalline pore walls in the form of graphitic-like nanodomains is presented.

Surfactant-Assisted Synthesis of Mesoporous Alumina Showing Continuously Adjustable Pore Sizes

1999

Porous materials displaying tailor-made pore sizes and shapes are particularly interesting in a great variety of real and potential applications where molecular recognition is needed, such as shape-selective catalysis, molecular sieving, and selective adsorption. Classically, apart from silica, materials most commonly used for catalysis and catalyst supports have been those based on high surface aluminas, owing to their thermal, chemical, and mechanical stability and their low cost. Earlier aluminas with high surface areas (~500 m/g) had been prepared using structure-directing agents. However, they were X-ray amorphous materials and their porosity was purely textural, characterized by wide …

A Novel Pathway for Synthesis of Submicrometer-Size Solid Core/Mesoporous Shell Silica Spheres

1998

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…

MCM-41, MCM-48 and related mesoporous adsorbents: their synthesis and characterisation

2001

MCM-41, MCM-48, MCM-41 analogue materials and disordered silica xerogels were compared with respect to their long range and short range order, their specific surface area, pore structure and pore structural parameters, pore wall thickness and their surface hydroxyl group concentration. Based on X-ray diffraction data it could be seen that the degree of long range order decreased in the order MCM-41>MCM-48>MCM-41 analogues >amorphous silica xerogels. The particle porosity and pore wall thickness increased in the same sequence such that MCM-41 analogues and amorphous silica xerogels were more stable towards water and water vapour. The concentration of the surface hydroxyl groups increased whe…

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

Selective hydrogenation of nitroderivatives over Au/TiO2/UVM-7 composite catalyst

2020

Abstract Hydrogenation of nitroderivatives (4-nitrostyrene or 7-nitro-1-tetralone) was performed using as support a silica mesoporous material with high specific surface area (1091 m2/g) and a bimodal pore size distribution (UVM-7). Gold and/or TiO2 were deposited inside the pores of this support with the aim to achieve high activity and selectivity for this reaction. The morphology and structure of the powders have been characterized by adsorption-desorption isotherms, XRD, TEM, STEM-HAADF, XPS and ATR-FTIR. Structural characterizations shown differences between the catalysts with and without titania. The presence of TiO2 provides a better size distribution of the spherical gold nanopartic…

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.