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Hybrids organosilicas

In this work, lacnnarity analysis of TEM images of a previously synthesized hybrid organosilica material incorporating a biphenyl moiety was carried out. The results obtained snch as degree of connectedness of holes in sample material were correlated to the visnally observed degree of roughness of the materiaTs surface. [Pg.398]

In this research study an ordered, mesoporous hybrid organosilica material incorporating a biphei rl moiety was fabricated. The polymerization process was surfactant-mediated to ensure uniform pore pattern and narrow pore size distribution. The synthesis of the organosilica precursor was done and investigated by the research group of the Inorganic Synthesis and Computational Research Laboratory of Institute of Chemistry, Diliman, Quezon City. [Pg.398]

The possible compositions for the walls of the ordered mesoporous materials go beyond the field of inorganic chemistry, and materials with hybrid organosilica walls have been prepared [81-84], Some mesoporous benzene-silica hybrids are stable at a temperature higher than 500 °C [84], Mesoporous materials prepared from polysilazanes and nonionic surfactants can be activated to form silicon carbonilride ceramics, which retain an ordered mesoporosity up to 1500 °C [85],... [Pg.6]

Lacunarity Analysis of TEM Images of Heat-Treated Hybrid Organosilica Materials... [Pg.397]

Abstract The lacunarity of TEM images of heat-treated hybrid organosilica materials incorporating a biphenyl moiety was determined. The measured lacunarity of the samples correlated with the degree of observed clumping. Heat treatment was found to be desirable in decreasing the lacunarity of the samples, leading to an increase in the available surface area of the material. [Pg.397]

Thus, the H, C, and Si NMR spectroscopy was frequently used to study silica thin films, hybrid organosilica, and other films. However, these applications deal with chemical structure of the films. These are no publication with NMR cryoporometry applied to thin silica films. [Pg.338]

Fischer, C.E., Raith, A., Mink, J., Raudaschl-Sieber, G., Cokoja, M., and Kiihn, F.E. 2011. Organic-inorganic nanotube hybrids Organosilica-nanotubes containing ethane, ethylene and acetylene groups. J. Organometal. Chem. 696 2910-2917. [Pg.963]

Mesoporous materials present exceptionally high surface area, and thermal and mechanical stability thus, mesoporous hybrid organosilica represents a suitable solid support for the design of organocatalysts (Nandi et al., 2011 Jain et al., 2011). [Pg.32]

The evolution in the nature of aerogel materials also followed the progress in sol—gel chemistry, with the synthesis of hybrid organosilica aerogels [17] and some nmi-oxide aerogels (e.g., sulfides) [18] (Chap. 17). [Pg.6]

Fousseret, B., Mougenot, M., Rossignol, F., Baumard, J.F., Soulestin, B., Boissiere, C., Ribot, F., Jalabert, D., Carrion, C., Sanchez, C., and Lejeune, M. (2010) Inkjet-printing-engineered functional microdot arrays made of mesoporous hybrid organosilicas. Chem. Mater., 22 (13), 3875-3883. [Pg.314]

Kapoor et al [131] demonstrated that the synthesis of hybrid organosilicas with mesoscopically ordered pores and molecularly ordered pore walls was not confined to symmetrically linear bridged organosilane precursors, but a similar arrangement could also be obtained with nonlinear symmetric bridged organosilane precursors, such as 1,3-BTEB. [Pg.590]

Castricum, H.L., Paradis, G. G., Mittelmeijer-Hazeleger, M.C., Bras, W., Eeckhaut, G., Vente, J.F., Rothenberg, G., and ten Elshof, f.E. (2014) Tuning the nanopore structure and separation behavior of hybrid organosilica membranes. Microporous Mesoporous Mater., 185, 224-234. [Pg.707]

Preparation and textural characterization trans-(IR, 2R)-diaminocyclohexane The synthesis of hybrid organosilica containing trans-(l/ ,2i )-diaminocyclohexane was achieved by sol-gel under different synthesis conditions. It was conducted either in water or in propanol as solvent in the presence of an acid catalyst ... [Pg.488]

These and several other researchers extended the methodology with the aim to widen functionality, using dopant molecules and silicon precursors derivatized with organic moities giving place to a vast class of hybrid organic-inorganic organosilica nanocomposites capable to meet numerous, advanced requirements in fields as diverse as catalysis,... [Pg.13]

Figure 3.7 Schematic of the incorporation of organic groups in the pore walls of mesoporous silica using bridged organosilane precursors (top). Schematic of the structure of a phenylene-bridged hybrid mesoporous organosilica with both atomic and mesoporous periodicity (bottom) [36],... Figure 3.7 Schematic of the incorporation of organic groups in the pore walls of mesoporous silica using bridged organosilane precursors (top). Schematic of the structure of a phenylene-bridged hybrid mesoporous organosilica with both atomic and mesoporous periodicity (bottom) [36],...
Since the discovery of this first benzene-bridged mesoporous hybrid material with crystal-like pore walls, the series of organosilica precursors that give PMOs exhibiting molecular-scale periodicity was considerably extended. Kapoor et al. demonstrated with the formation of PMO products from the precursor 1,3 -bis(triethox-ysilyl)benzene (10) that a crystal-like organization of the organic bridges within the pore walls is not restricted to linear-substituted precursors.264... [Pg.77]

Figure 3.23 Photographs of powders of mesoporous hybrid materials with various conjugated ir-electron systems (from left to right) ethene-, benzene-, 1,4-divinylbenzene-, 4,4 -divinylstilbene-, and 4,4 -divinylazobenzene-bridged organosilicas. (See color insert.)... Figure 3.23 Photographs of powders of mesoporous hybrid materials with various conjugated ir-electron systems (from left to right) ethene-, benzene-, 1,4-divinylbenzene-, 4,4 -divinylstilbene-, and 4,4 -divinylazobenzene-bridged organosilicas. (See color insert.)...

See other pages where Hybrids organosilicas is mentioned: [Pg.398]    [Pg.48]    [Pg.398]    [Pg.402]    [Pg.127]    [Pg.583]    [Pg.584]    [Pg.398]    [Pg.48]    [Pg.398]    [Pg.402]    [Pg.127]    [Pg.583]    [Pg.584]    [Pg.240]    [Pg.260]    [Pg.261]    [Pg.262]    [Pg.213]    [Pg.233]    [Pg.233]    [Pg.30]    [Pg.672]    [Pg.399]    [Pg.118]    [Pg.603]    [Pg.261]    [Pg.267]    [Pg.53]    [Pg.53]    [Pg.41]    [Pg.46]    [Pg.52]    [Pg.57]    [Pg.66]    [Pg.71]   
See also in sourсe #XX -- [ Pg.127 ]




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