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Membranes silica

The synthesis of silica membranes has only recently been described. Silica forms sols and gels very easily both by the colloidal suspension and by the polymeric gel route. Its chemical resistance and its thermal stability in the presence of water vapor or metal impurities are not very good however. Larbot et al. (1989) have described the synthesis of silica membranes starting with a commercially available silica sol (Cecasol Sobret) in an aqueous solution at pH 8. [Pg.37]


Silica membranes Silica-PDMS Silica-phenolic resin... [Pg.886]

Methods for DNA extraction Silica-membrane column-t)rpe kit Qiagen DNeasy Plant Mini kit Anion-exchange column-type kit Qiagen Genomic-tip kit CTAB method... [Pg.157]

Fig. 10.14 Schematic representation of the membrane = 47 mm), mesostructured silica-synthetic route to dynamic functionalized me- surfactant before (B) and after (C) calcination, sostructured silica membranes in the AAMs ODS-hydrophobized silica before (D) and after... Fig. 10.14 Schematic representation of the membrane = 47 mm), mesostructured silica-synthetic route to dynamic functionalized me- surfactant before (B) and after (C) calcination, sostructured silica membranes in the AAMs ODS-hydrophobized silica before (D) and after...
Hwang, G.-J. et al., Separation of hydrogen from a H2-H20-HI gaseous mixture using a silica membrane, AIChE., 46, 92,2000. [Pg.158]

Pex, P.P.A.C. and Y.C. van Delft, Silica membranes for hydrogen fuel production by membrane water gas shift reaction and development of a mathematical model for a membrane reactor, in Carbon Dioxide Capture for Storage in Deep Geologic Formations—Results from the C02 Capture Project Capture and Separation of Carbon Dioxide from Combustion Sources, eds., D. Thomas, and B. Sally, Vol. 1, Chapter 17, 2005. [Pg.322]

The only ceramic membranes of which results are published, are tubular microporous silica membranes provided by ECN (Petten, The Netherlands).[10] The membrane consists of several support layers of a- and y-alumina, and the selective top layer at the outer wall of the tube is made of amorphous silica (Figure 4.10).[24] The pore size lies between 0.5 and 0.8 nm. The membranes were used in homogeneous catalysis in supercritical carbon dioxide (see paragraph 4.6.1). No details about solvent and temperature influences are given but it is expected that these are less important than in the case of polymeric membranes. [Pg.80]

Membranes with extremely small pores ( < 2.5 nm diameter) can be made by pyrolysis of polymeric precursors or by modification methods listed above. Molecular sieve carbon or silica membranes with pore diameters of 1 nm have been made by controlled pyrolysis of certain thermoset polymers (e.g. Koresh, Jacob and Soffer 1983) or silicone rubbers (Lee and Khang 1986), respectively. There is, however, very little information in the published literature. Molecular sieve dimensions can also be obtained by modifying the pore system of an already formed membrane structure. It has been claimed that zeolitic membranes can be prepared by reaction of alumina membranes with silica and alkali followed by hydrothermal treatment (Suzuki 1987). Very small pores are also obtained by hydrolysis of organometallic silicium compounds in alumina membranes followed by heat treatment (Uhlhom, Keizer and Burggraaf 1989). Finally, oxides or metals can be precipitated or adsorbed from solutions or by gas phase deposition within the pores of an already formed membrane to modify the chemical nature of the membrane or to decrease the effective pore size. In the last case a high concentration of the precipitated material in the pore system is necessary. The above-mentioned methods have been reported very recently (1987-1989) and the results are not yet substantiated very well. [Pg.18]

Kaiser, A. and H. Schmidt. 1984. Generation of silica-membranes from alkoxisilanes on porous supports. J, Non-Cryst. Solids 63 261-71. [Pg.60]

A similar scheme can be used to concentrate proteins R. S. Foot, J. Khandurina, S. C. Jacobson, and J. M. Ramsey, Preconcentration of Proteins on Microfluidic Devices Using Porous Silica Membranes, Anal. Chem 2005,77, 57. [Pg.683]

N. Benes, Mass Transport in Thin Supported Silica Membranes" PhD Thesis, Univ. of Twente, Enschede, The Netherlands, 2000... [Pg.350]

Subramanian and coworkers developed polymeric sorbents using different support materials (such as Merrifield chloromethylated resin, Amberlite XAD 16) and complexing ligands (amides, phosphonic acids, TTA), and evaluated their binding affinity for U(VI) over other diverse ions, even under high acidities. The practical utility of these sorbents was demonstrated using simulated waste solutions (220-222). Shamsipur et al. reported the solid-phase extraction of ultra trace U(VI) in natural waters using octadecyl silica membrane disks modified by TOPO (223). The method was found satisfactory for the extraction and determination of uranium from different water samples. [Pg.97]

Shamsipur, M. Ghiasvand, A.R. Yamini, Y. Solid-phase extraction of ultratrace uranium(VI) in natural waters using octadecyl silica membrane disks modified by tri-N-octylphosphine oxide and its spectrophotometric determination with dibenzoylmethane, Anal. Chem. 65 (1999)4892 1895. [Pg.114]

Kurungot, S., Yamaguchi, T., Nakao, S.-L, Rh/y-AljOj catalytic layer integrated with sol-gel synthesized microporous silica membrane for combact membrane reactor applications, Catal. Lett. 2003, 86, 273-278. [Pg.402]

A. Nijmeijer, Flydrogen-selective silica membranes for use in membrane steam reforming, PhD dissertation, University of Twente, the Netherlands, 1999. [Pg.135]

In addition to the Pd-based membranes, microporous silica membranes for hydrogen permeation [8] can be produced by a special type of chemical vapor deposition [140] named chemical vapor infiltration (CVI) [141], A large amount of studies have been carried out on silica membranes made by CVI for hydrogen separation purposes [8,121], CVI [141] is another form of chemical vapor deposition (CVD) [140] (see Section 3.7.3). CVD involves deposition onto a surface, while CVI implies deposition within a porous material [141], Both methods use almost similar equipment [140] and precursors (see Figure 3.19) however, each one functions using different operation parameters, that is, flow rates, pressures, furnace temperatures, and other parameters. [Pg.485]


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