Meso-porous

In these systems, the interface between two phases is located at the high-throughput membrane porous matrix level. Physicochemical, structural and geometrical properties of porous meso- and microporous membranes are exploited to facilitate mass transfer between two contacting immiscible phases, e.g., gas-liquid, vapor-liquid, liquid-liquid, liquid-supercritical fluid, etc., without dispersing one phase in the other (except for membrane emulsification, where two phases are contacted and then dispersed drop by drop one into another under precise controlled conditions). Separation depends primarily on phase equilibrium. Membrane-based absorbers and strippers, extractors and back extractors, supported gas membrane-based processes and osmotic distillation are examples of such processes that have already been in some cases commercialized. Membrane distillation, membrane... 

The rather low value obtained with the copper phthalocyanine, a low-energy solid (line (v)), is probably explicable by some reversible capillary condensation in the crevices of the aggregate, the effect of which would be to increase the uptake at a given relative pressure the plausibility of this explanation is supported by the fact that very low values of s, 1-47-1-77, were obtained with certain other phthalocyanines known to be meso-porous (cf. Chapter 3). 

In the field of materials synthesis, T8[CH = CH2]8 has been used to prepare three-dimensional (meso)porous polymers with high surface area via reactions with TgHg or T8[OSiMe2H]8 in the presence of a Pt catalyst as described in Section Xu et al. prepared a POSS-based monomer by reaction... 

As surface area and pore structure are properties of key importance for any catalyst or support material, we will first describe how these properties can be measured. First, it is useful to draw a clear borderline between roughness and porosity. If most features on a surface are deeper than they are wide, then we call the surface porous (Fig. 5.16). Although it is convenient to think about pores in terms of hollow cylinders, one should realize that pores may have all kinds of shapes. The pore system of zeolites consists of microporous channels and cages, whereas the pores of a silica gel support are formed by the interstices between spheres. Alumina and carbon black, on the other hand, have platelet structures, resulting in slit-shaped pores. All support materials may contain micro, meso and macropores (see text box for definitions). 

Summarizing, the in situ UV-Vis, XANES, and EXAFS studies of Bonino et al. [49] and of Prestipino et al. [50] on hydrated and anhydrous peroxo/hy-droperoxo complexes on crystalhne microporous and amorphous meso-porous titanosilicates have shown, for the first time, the equilibriiun between r] side-on and end-on complexes. The amount of water is the key factor in the equilibrium displacement. In this regard please note that, owing to the hydrophobic character of TS-1, substrates such as olefins are the dominant species in the channels. This fact assures a relatively local low concentration of water, which in turn guarantees a sufficient presence of the active end-on... 

Marra GL, Artioli G, Fitch AN, MUanesio M, Lamberti C (2000) Microporous Meso-porous Mater 40 85... 

Wang X-X, Veyre L, Lefebvre P, Patarin J, Basset J-M (2003) Microporous and Meso-porous Materials 66 169... 

Thomas and his colleagues in Cambridge have pioneered the development of nanoparticles prepared from cluster compounds and supported in meso-porous silica.31 Highly active and effective catalysts have been developed for a number of hydrogenation reactions. The significant factors controlling... 

D.W. Aksnes, K. Forland, L. Kimtys 2001, (Pore size distribution in meso-porous materials as studied by H NMR), Phys. Chem. Chem. Phys. 3, 3203. 

Various other classes of catalysts have been investigated for NH3-SCR, in particular, metal-containing clays and layered materials [43 15] supported on active carbon [46] and micro- and meso-porous materials [31b,47,48], the latter also especially investigated for HC-SCR [25,3lb,48-53], However, while for NH3-SCR, either for stationary or mobile applications, the performances under practical conditions of alternative catalysts to V-W-oxides supported on titania do not justify their commercial use if not for special cases, the identification of a suitable catalyst, or combination of catalysts, for HC-SCR is still a matter of question. In general terms, supported noble metals are preferable for their low-temperature activity, centred typically 200°C. As commented before, low-temperature activity is a critical issue. However, supported noble metals have a quite limited temperature window of operation. 

At higher reaction temperatures (>300°C), micro- or meso-porous materials and/or oxides containing transition metals are preferable. The performances are considerably dependent on the type of reductant, besides the characteristics of the catalyst and the type of transition metal. Although all possible combinations have been explored, including the usage of high-throughput methods, identification of a suitable catalyst formulation active in HC-SCR under practical conditions, especially to decrease by more than... 

Physisorption measurements showed that carbon nanomaterials exhibit rather meso- and macroporous structures (maximum micropore fraction, 15% see Table 2.1). The lowest specific surface area was measured with the platelet fiber catalyst exhibiting slightly more than 100 m2/g. The Co/HB material offers 120 m2/g of surface area, and the highest BET value was determined with the Co/ MW catalyst featuring nearly 290 m2/g. Carbon nanomaterials, though, are not really porous, as the space between the graphene layers is too small for nitrogen molecules to enter. The only location of adsorption is the external surface of the nanomaterials and the inner surface of the nanotubes. 

Khenkin, A.M. and Neumann, R. (2000). Aerobic photochemical oxidation in meso-porous Ti-MCM-41 epoxidation of alkenes and oxidation of sulfides. Catal. Lett. 68(1-2), 109-111... 

A. Clearfield, Organically pillared micro- and meso-porous materials , Chem Mater. 1998,10,2801-2810. 

The supported Co2+-substituted Wells-Dawson POM, Cs6H2[P2W17061Co(OH2)], on silica was stable up to 773 K and catalyzed the heterogeneous oxidation of various aldehydes to the corresponding carboxylic acids with 02 as a sole oxidant [116], The H5PV2Mo10O40 POM, impregnated onto meso-porous MCM-41, catalyzed the aerobic oxidation of alkanes and alkenes using isobutyraldehyde as a... 

Fig. 9 Schematic representation of three approaches to generate nanoporous and meso-porous materials with block copolymers, a Block copolymer micelle templating for mesoporous inorganic materials. Block copolymer micelles form a hexagonal array. Silicate species then occupy the spaces between the cylinders. The final removal of micelle template leaves hollow cylinders, b Block copolymer matrix for nanoporous materials. Block copolymers form hexagonal cylinder phase in bulk or thin film state. Subsequent crosslinking fixes the matrix hollow channels are generated by removing the minor phase, c Rod-coil block copolymer for microporous materials. Solution-cast micellar films consisted of multilayers of hexagonally ordered arrays of spherical holes. (Adapted from [33])...

Another group working on silica monoliths is the one of A. and M. Kuehn [41]. Their Continuous-Bed-Silica (CB-Silica) is a highly porous monolith having meso- and micropores. The structure of the CB-Silica is very porous and con-... 

The thermal conductivity of bulk silicon (148 W K m ) is dominated by phonons electronic contributions are negligible. Due to restrictions of the mean free path of phonons in the porous network the thermal conductivity of micro PS is reduced by two or three orders of magnitude at RT, compared to the bulk value. Because of the larger dimensions of its network, meso PS shows a thermal conductivity several times larger than that of micro PS, for the same value of porosity. Thermal oxidation at low temperatures (300°C) is found to decrease the thermal conductivity of meso PS by a factor of about 0.5 [Pe9]. In contrast to bulk Si the thermal conductivity of PS is found to decrease with decreasing temperature [Be21, La4, Ge9, Lyl]. 

A certain anisotropy of the refractive index along specific crystallographic axes indicates that the microstructures in the porous network are not spherical but somewhat elongated along the PS growth direction [Mi4], This birefringence is below 1% for micro PS, while it may reach values in the order of 10% for meso PS films formed on (110) oriented silicon wafers [Ko22]. 

Fig. 7.6 Spectral dependence of the absorption coefficient for free-standing micro PS (72% porosity), meso PS (45% porosity), bulk Si and amorphous Si H at RT. While the meso porous film can be roughly fitted to a Bruggeman effective medium calculation for...

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