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Tetraethylorthosilicate TEOS

Another important recent advance is the development of the CVD of Si02 from tetraethylorthosilicate (TEOS) and ozone (see Ch. 11). This deposition reaction is becoming prominent for the many production advantages it provides. ]... [Pg.373]

Two kinds of solution were prepared in advance. Solution A was a water solution containing an Si source, which was obtained by hydrolyzing metal alkoxide (tetraethylorthosilicate, TEOS) with a dilute tetrapropylammoniumhydroxide (TPA-OH)/water solution at room temperature. The molar ratio of Si to the template was 3. In peparation of ZSM-S zeolite nanoerystals, aluminium isopropoxide as an A1 source and sodium chloride were added into solution A. Solution B was an oi mic solution containing surfectant Nonionie surfactants, poljraxyethylene (15) cxslylether (C-15), polyoxyethylene (15) nonylphenylether (NP-15), and polyoxyethylene (15) oleylether (O-15), and ionic surfoctnnts, sodium bis(2-ethylhexyl) sulfosucdnate (AOT) and... [Pg.185]

American scientists prepared the organo-silica sol-gel membranes60 and demonstrated in a single layer format for pH measurement and multiple-layer format for both C02 and NH3. The sensors used a hydroxypyrenetrisulfonic acid (HPTS) as the indicator immobilizes in a base-catalyzed sol-gel containing poly(dimethyl)siloxane, aminopropyl-triethoxysilane (APTES) and tetraethylorthosilicate (TEOS). This indicator gel was over coated with a hydrophobic sol-gel to reduce cross reactivity to pH when either carbon dioxide or ammonia were examined. [Pg.367]

It is possible to modify the matrix hydrophilicity-lipophilicity balance (HLB) by using different alkyl-modified trialkoxysilanes as co-reagents with tetraethylorthosilicate (TEOS), to greatly alter (reduce) the release rate of heparin, as then water access to the entrapped drug is considerably reduced (Figure 2.10).4... [Pg.213]

Figure 4.23 Synthesis space diagram for a ternary system composed of tetraethylorthosilicate (TEOS), cetyltrimethylammonium bromide (CTAB), and sodium hydroxide (H, hexagonal phase [MCM-41] C, cubic phase [MCM-48] L, lamellar phase [MCM-50] H20/Si02 = 100, reaction temperature 100°C, reaction time 10 days). (Reprinted from Science, Vol. 267, A. Firouzi, D. Kumar, L.M. Bull, T. Besier, R Sieger, Q. Huo, S.A. Walker, J.A. Zasadzinski, C. Glinka, J. Nicol, D.l. Margolese, G.D. Stucky, B.F. Chmelka, Cooperative Organization of Inorganic-Surfactant and Biomimetic Assemblies, pp. 1138-1143. Copyright 1995. With permission of AAAS.)... Figure 4.23 Synthesis space diagram for a ternary system composed of tetraethylorthosilicate (TEOS), cetyltrimethylammonium bromide (CTAB), and sodium hydroxide (H, hexagonal phase [MCM-41] C, cubic phase [MCM-48] L, lamellar phase [MCM-50] H20/Si02 = 100, reaction temperature 100°C, reaction time 10 days). (Reprinted from Science, Vol. 267, A. Firouzi, D. Kumar, L.M. Bull, T. Besier, R Sieger, Q. Huo, S.A. Walker, J.A. Zasadzinski, C. Glinka, J. Nicol, D.l. Margolese, G.D. Stucky, B.F. Chmelka, Cooperative Organization of Inorganic-Surfactant and Biomimetic Assemblies, pp. 1138-1143. Copyright 1995. With permission of AAAS.)...
Hybrid membranes composed of poly(vinyl alcohol) (PVA) and tetraethylorthosilicate (TEOS), synthetised via hydrolysis and a co-condensation reaction for the pervaporation separation of water-isopropanol mixtures has also been reported [32], These hybrid membranes show a significant improvement in the membrane performance for water-isopropanol mixture separation. The separation factor increased drastically upon increasing the crosslinking (TEOS) density due to a reduction of free volume and increased chain stiffness. However, the separation factor decreased drastically when PVA was crosslinked with the highest amount of TEOS (mass ratio of TEOS to PVA is 2 1). The highest separation selectivity is found to be 900 for PVA TEOS (1.5 1 w/w) at 30°C. For all membranes, the selectivity decreased drastically up to 20 mass % of water in the feed and then remained almost constant beyond 20 mass %, signifying that the separation selectivity is much influenced at lower composition of water in the feed. [Pg.127]

A recent paper [69] presents a new type of PVA hybrid membrane prepared by hydrolysis followed by condensation of a PVA and a tetraethylorthosilicate (TEOS) mixture, which shows a significant performace in water-acetic acid mixture separation. The highest separation selectivity (1116) with a flux of 3.33xft)"2 kg m"2 h"1 at 30 °C for 10% mass of water in the feed has ben obtained by using the membrane containing 1 2 mass ratio of PVA and TEOS. The performance of these membranes was explained on the basis of a reduction of free volume and a decrease of the hydrophylic character owning to the formation of... [Pg.132]

The variety of finely divided silica known as hexagonal mesoporous silica (HMS) [6,34] is generally prepared by the copolymerization of a silica precursor such as tetraethylorthosilicate (TEOS), in presence of a suitable template. This acid or base catalyzed reaction follows the sol-gel route and it has been found [28] that during silica preparation by this technique, it is also possible to add an organotriethoxysilane [RSi(OEt)3] that would... [Pg.116]

Nakamura and Matsui [71] prepared silica nanotubes as a spin-off product of sol-gel synthesis wherein tetraethylorthosilicate (TEOS) was hydrolyzed in the presence of ammonia and D, L-tartaric acid. Ono et al. [72] showed that certain cholesterol derivatives can gelate tetraethyl orthosilicate (TEOS) to obtain tubular silica structures. Using cholesterol based gelators nanotubes of transition metal (Ti, V and Ta) oxides can also be prepared. The organogelators used in these processes are chiral diamino... [Pg.261]

In the case of fluorescence spectra, it is the emission of the radiation from the excited state that is measured, rather than its absorption. This also provides valuable information. As an example, tetraethylorthosilicate (TEOS)-based gels were doped with two optically active organic indicators, thionin and nile blue A. Before trapping in a solgel host, thionin and nile blue A were both evaluated for solvent and protonation effects on their spectral properties. Only extreme pH values provided by HCl, NaOH, and NH4OH produced new absorption and/or fluorescence bands. The absorption and fluorescence spectra revealed a decrease in a pH 11 solution of NH4OH compared to neutral conditions (Krihak et al., 1997). [Pg.84]

Aerosol (97% Si02), tetraethylorthosilicate (TEOS), Na2Si03 and superfine Si02 as Si source have been studied, respectively. Using... [Pg.198]

PCH materials offer new opportunities for the rational design of heterogeneous catalyst systems, because the pore size distributions are in the supermicropore to small mesopore range (14-25A) and chemical functionality (e.g., acidity) can be introduced by adjusting the composition of the layered silicate host. The approach to designing PCH materials is based on the use of intercalated quaternary ammonium cations and neutral amines as co-surfactants to direct the interlamellar hydrolysis and condensation polymerization of neutral inorganic precursor (for example, tetraethylorthosilicate, TEOS) within the galleries of an ionic lamellar solid. [Pg.401]

Synthesis of Acid-Prepared Mesoporous Spheres (APMS).3 Tetraethylorthosilicate (TEOS, 5.65 g, 27.1 mmol) was added to a solution of cetyltrimethylammonium bromide (CTAB, 1.20 g, 3.30 mmol) in aqueous acid (4.40 g cone. HC1, 55.5 g H20). This mixture was stirred for 1 hour and then transferred to a teflon-lined Parr autoclave and heated at 150 °C for 40 minutes. The mixture was cooled and filtered to recover a white powder. APMS could also be prepared at temperatures between 80 and 230 °C by adjusting the heating time (lower temperatures, longer times). [Pg.748]

A purely siliceous MCM-41 and Ti-containing MCM-41 were synthesized according to the following procedure. Ethanol and methanol were used as solvents respectively. The calculated amount of titanium isopropoxide (TIP Fluka) and tetraethylorthosilicate (TEOS Aldrich, 50 g) were put into the ethanol(33 g) solution and stirred vigorously for 30 min. This mixture was added to a pure water (35 g) and heated to reflux(60 C). 1.25 g HC1 was... [Pg.782]


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See also in sourсe #XX -- [ Pg.127 ]




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