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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Zeolite-based composite materials prepared by the embedding of the beta zeolite nanophase from aqueous colloidal solution into matrices of preformed Si(Al)MCM-41 mesoporous molecular sieves have been characterized by different methods (XRD, SEM, FTIR, N2 adsorption, and TPD of NH3). Their potential as catalysts for toluene disproportionation has been compared to mechanical mixtures of freeze-dried nanobeta crystallites with Si(Al)MCM-41 mesoporous materials. It is found that the zeolite catalyst efficiency is not substantially changed by the presence of mesopores belonging to the matrix. It is suggested that formation of intergrown aggregates from the colloidal nanobeta particles provides own highly developed textural mesoporosity that makes the contribution of the diffusional alleviation of the support negligible.
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PMID:Beta zeolite colloidal nanocrystals supported on mesoporous MCM-41. 1584 27

Nanosize mesoporous material MCM-48 was synthesized under the hydro-thermal system. The results of TEM and SEM show that the obtained MCM-48 is well organized on a 100 A length scale. Both the Nanosize and the superior organization provide this material with good thermal stability.
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PMID:Synthesis of nanosize mesoporous MCM-48 material. 1624 42

The present study reports a green synthesis method for preparing pure (free of fly ash) and ordered MCM-41 materials from coal fly ash at room temperature (25 degrees C) during 24 h of reaction. It was shown that the impurities in the coal fly ash were not detrimental to the formation of MCM-41 at the tested conditions. The influence of initial synthesis pH on material properties of calcined MCM-41 samples was investigated by various techniques such as XRF, XPS, XRD, FTIR, DR-UV-vis, solid state NMR, N2 physisorption, TG-DTA, SEM and TEM. The experimental results showed that the amount of trace elements such as Al, Na, Ti and Fe incorporated into the sample increased with synthesis pH value. More aluminum species were incorporated with tetrahedral coordination in the framework under a high pH value. The particle size of the sample decreased with the synthesis pH value. Samples synthesized at high pH values had a larger pore size and were more hydrothermally stable than those at low pH values. From thermal analysis, it was observed that the synthesized MCM-41 samples showed a high thermal stability. These properties made the synthesized MCM-41 suitable for further processing into more useful materials in a wide range of applications.
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PMID:Synthesis of MCM-41 from coal fly ash by a green approach: influence of synthesis pH. 1664 13

MWNTs (multi-walled carbon nanotubes) were made by catalytic CVD process using iron-containing mesoporous silica, Fe-MCM-41, with 4 mol% Fe loading prepared by direct synthesis route. Uniform 5 nm size Fe2O3 nano-particles impregnated onto a mesoporous silica support, SBA-15 were also prepared for CNTs synthesis. The catalysts were characterized using XRD, SEM/TEM, N2 physisorption, UV-vis diffuse reflectance and FT-IR spectroscopies. Acetylene gas was introduced as a carbon source, and the gas mixture of Ar:H2:C2H2 = 14:5:1 pyrolyzed at 750 degrees C for 60 min was found to be the optimum synthesis condition. Fe-MCM-41 due to higher dispersion of nano-sized Fe-species was efficient as catalyst for MWNTs with more uniform size distribution. Cobalt-impregnated Fe-MCM-41 (Co/Fe = 1) produced a small fraction of SWNTs of ca. 2 nm diameter mixed with MWNTs.
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PMID:Synthesis of carbon nanotubes using mesoporous Fe-MCM-41 catalysts. 1725 85

Ce-containing MCM-41 materials were prepared via a direct, nonhydrothermal method at room temperature from tetra-ethoxysilane, n-hexadecyl trimethyl ammonium bromide, ammonia solution, and cerium(IV) ammonium nitrate precursors. Composite materials containing the nominated ratios of 5 and 10% (w/w) CeO2/MCM-41 were targeted. The obtained materials were investigated by TGA, DSC, FTIR, diffuse reflectance UV-vis, XRD, N2 adsorption/desorption isotherms, and SEM. Results indicated the insertion of cerium ions in tetrahedral environment in the framework of MCM-41. BET surface area amounting to 824 and 726 m2/g; total pore volume amounting to 0.427 and 0.515 cm3/g; and narrow pore size distribution maximizing at 22.5 and 23.7 A, respectively were obtained for the 5 and 10% CeO2/MCM-41 calcined composites. SEM showed a spherical type morphology for the composites which is rather similar to their blank MCM-41, and no clear ceria aggregates were observed on the external surfaces of composites spherical particles. Thus, the adopted method allows the persistence of MCM-41 texture with cerium inserts in the framework of MCM-41 and/or forms finely divided ceria nanoparticles on the wall of MCM-41 materials. Moreover, stabilization of any formed ceria nanoparticles was attributed to the short nonintersecting porous nature of MCM-41 matrix, which hinders their aggregation upon calcinations.
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PMID:Cerium modified MCM-41 nanocomposite materials via a nonhydrothermal direct method at room temperature. 1771 29

Al-MCM-41 mesoporous sieves were synthesized at the ambient temperature by using TEOS as silica source, Al(NO)3 x 9H2O as Al source, and cetyl trimethylammonium bromide as templating agent. The framework and surface structures of the synthesized samples were characterized by XRD, N2-adsorption/desorption isotherms, FTIR and SEM etc. The results showed that the samples were the typical Al-MCM-41 mesoporous sieves with the higher ordered-degree and specific surface area (up to 816 m2 x g(-1)) and the narrower pore diameter distribution. Controlling the highest value of Al/Si with the range of 0.06-0.13, and taking temperature programmed calcination would be beneficial to the formation of the highly ordered Al-MCM-41 mesoporous sieves. The evaluating results showed that the synthesized Al-MCM-41 molecular sieves have a higher catalytic activity for isomerization of endo-tetrahydrodicyclo-pentadiene (endo-TCD) into exo-tetrahydrodicyclo-pentadiene (exo-TCD) and adamantane.
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PMID:[Synthesis and catalytic-isomerization performance of Al-MCM-41 mesoporous sieves]. 1794 16

Sulfated zirconia and SZ/MCM-41 were used as catalysts for the synthesis of beta-aminoalcohols via epoxide aminolysis. Sulfated zirconia was prepared by sol-gel and SZ/MCM-41 was obtained by impregnation. Solid catalysts were characterized by XRD, SEM-EDS, UV-Vis, FT-IR pyridine desorption and Nitrogen physisorption. Both acid materials were useful as catalysts, even when they were recycled several times. The beta-aminoalcohols were characterized by FT-IR, (1)H- and (13)C-NMR and GC-MS.
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PMID:Comparative study of regioselective synthesis of beta-aminoalcohols under solventless conditions catalyzed by sulfated zirconia and SZ/MCM-41. 1806 55

The present investigation covers immobilization of TiO2 using a simple solid state dispersion technique over mesoporous Al-MCM-41 support for the treatment of isoproturon herbicide. Catalysts are characterized by XRD, X-ray photo electron spectroscopy (XPS), surface area, UV-Vis diffused reflectance spectra (DRS), SEM and TEM. A detailed photocatalytic degradation study of isoproturon under solar light in aqueous suspensions is reported. The 10 wt% TiO2/Al-MCM-41 composite system found to be optimum with high degradation activity. The reaction follows pseudo-first order kinetics. The parameters like TiO2 loading over Al-MCM-41, amount of catalyst, concentration of substrate, pH effect, durability of the catalyst, activity comparison of TiO2 and Al-MCM-41 supported system are studied. The mineralization of isoproturon is monitored by TOC. Based on the degradation products detected through LC-MS, a plausible degradation mechanism is proposed. The data indicates that TiO2/Al-MCM-41 composite system is an effective photocatalyst for treatment of isoproturon in contaminated water.
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PMID:Photocatalytic degradation of isoproturon herbicide over TiO2/Al-MCM-41 composite systems using solar light. 1839 14

Postalkoxysilylation with diethoxydimethylsilane has been carried out on the zeolitic lamellar precursors of various topologies such as MWW, FER, CDO and MCM-47 aiming to construct new crystalline structures with expanded pore apertures between the layers. The silylation process and the crystalline and pore structures of the resulting materials have been investigated with the techniques of XRD, IR, (13)C and (29)Si MAS NMR, ICP, SEM, HRTEM, elemental analyses, and N 2 adsorption. In contrast to forming known three-dimensional zeolite structures after direct calcination of the lamellar precursors, the silylation led to new crystalline structures with opener pores, as evidenced by the shift of layer-related diffractions to the lower-angle region in XRD patterns and the enlarged interlayer pores found by HRTEM images. After optimizing the treatment conditions, particularly the amount of silane agent, a maximum and homogeneous silylation was realized, which guaranteed the phase purity in interlayer expanded zeolites. The expanded structures were well preserved after calcination at 823 K or reflux in water for 1 to 2 weeks, indicating a high thermal stability and also a hydrothermal stability. The interlayer expanded zeolites prepared from the metallosilicate precursors of MWW topology exhibited higher catalytic activities in the redox and solid acid-catalyzed reactions of bulky molecules than that of their counterparts with conventional MWW topology.
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PMID:Methodology for synthesizing crystalline metallosilicates with expanded pore windows through molecular alkoxysilylation of zeolitic lamellar precursors. 1852 90

We report here a detailed study on the surface topology of well-known ordered mesoporous silica (SBA-15, MCM-41, and KIT-6) and a series of nanocast Co 3O 4, Co 3O 4/CoFe 2O 4 composites by high resolution scanning electron microscopy (HR-SEM). Images of the MCM-41 structure were obtained at a resolution of the pore size, as well as a real space image of the gyroid silica surface of KIT-6 for two different aging temperatures, clearly revealing the differences of the aging procedures. By using the low voltage HR-SEM technique with extremely high resolution, we could very clearly show the influence of the template properties on the structure of the nanocast metal oxides.
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PMID:Direct imaging of surface topology and pore system of ordered mesoporous silica (MCM-41, SBA-15, and KIT-6) and nanocast metal oxides by high resolution scanning electron microscopy. 1867 51


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