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Homogeneous Hydrophobicity

PGC sorbents have even more highly homogeneous hydrophobic surfaces than GCB sorbents. PGCs are macroporous materials composed of flat, two-dimensional layers of carbon atoms arranged in graphitic structure. The flat, homogeneous surface of PGC arranged in layers of carbons with delocalized n electrons makes it uniquely capable of selective fractionation between planar and nonplanar analytes such as the polychlorinated biphenyls [92,94,95],... [Pg.89]

Solid surface properties homogeneous, hydrophobic surface, not promoting any specific biochemical interaction. [Pg.818]

Figure 12.4 Schema of DCMD mechanism of transport through porous membranes (a) homogenous hydrophobic and (b) composite bydropbobic/hydiophilic. Tbe concentration profiles correspond to nonvolatile solutes. (Adapted liom Khayet et al., 2005b.)... Figure 12.4 Schema of DCMD mechanism of transport through porous membranes (a) homogenous hydrophobic and (b) composite bydropbobic/hydiophilic. Tbe concentration profiles correspond to nonvolatile solutes. (Adapted liom Khayet et al., 2005b.)...
The Smith-Ewart expression (eq. 1) accurately predicts the particle number for hydrophobic monomers like styrene and butadiene (21), but fails to predict the particle number (22) for more hydrophilic monomers like methyl methacrylate and vinyl acetate. A new theory based on homogeneous particle... [Pg.23]

These are the components of the formulation that do all or most of the actual foam control work. Traditionally, defoamers were single component Hquids or homogeneous solutions of vegetable or mineral oils, but more recendy a number of active hydrophobic soHds have been utilized so effectively that in a dispersion of hydrophobic soHds in a traditional oil such as castor oil [8001-79-4] the oil could be classed as a carrier oil rather than an active ingredient. [Pg.463]

Thiourea will react with neutralised formalin at 20-30°C to form methylol derivatives which are slowly deposited from solution. Heating of methylol thiourea aqueous solutions at about 60°C will cause the formation of resins, the reaction being accelerated by acidic conditions. As the resin average molecular weight increases with further reaction the resin becomes hydrophobic and separates from the aqueous phase on cooling. Further reaction leads to separation at reaction temperatures, in contrast to urea-formaldehyde resins, which can form homogeneous transparent gels in aqueous dispersion. [Pg.692]

Soluble tetrameric form (G4) Composed of four identical monomers and stabilized by hydrophobic interactions of hydrophobic amino acids at the C terminus of monomers. Abundant for brain AChE and BChE in mammalian body fluids and in the soluble fraction of tissue homogenates. [Pg.359]

Another SBU with open metal sites is the tri-p-oxo carboxylate cluster (see Section 4.2.2 and Figure 4.2). The tri-p-oxo Fe " clusters in MIL-100 are able to catalyze Friedel-Crafts benzylation reactions [44]. The tri-p-oxo Cr " clusters of MIL-101 are active for the cyanosilylation of benzaldehyde. This reaction is a popular test reaction in the MOF Hterature as a probe for catalytic activity an example has already been given above for [Cu3(BTC)2] [15]. In fact, the very first demonstration of the catalytic potential of MOFs had aheady been given in 1994 for a two-dimensional Cd bipyridine lattice that catalyzes the cyanosilylation of aldehydes [56]. A continuation of this work in 2004 for reactions with imines showed that the hydrophobic surroundings of the framework enhance the reaction in comparison with homogeneous Cd(pyridine) complexes [57]. The activity of MIL-lOl(Cr) is much higher than that of the Cd lattices, but in subsequent reaction rans the activity decreases [58]. A MOF with two different types of open Mn sites with pores of 7 and 10 A catalyzes the cyanosilylation of aromatic aldehydes and ketones with a remarkable reactant shape selectivity. This MOF also catalyzes the more demanding Mukaiyama-aldol reaction [59]. [Pg.81]

The recombination between Ru(bipy)j and viologen radicals nearby the inner surface of the vesicle is found to be strongly inhibited as compared to homogeneous solution, presumably due to a fast extraction of hydrophobic viologen radicals into the depth of the membrane. [Pg.40]

Oily crops such as soybeans and canola (oilseed rape) cannot be extracted with aqueous buffers, because the extraction solvent cannot permeate the hydrophobic plant tissue matrix. In these cases, homogenization in acetonitrile-hexane is recommended. This solvent mixture is able to extract sulfonylureas from these samples with a minimum of co-extracted oil. After extraction, the sulfonylureas partition into the acetonitrile phase while most of the oil stays in the hexane phase. Further cleanup is accomplished using a silica SPE cartridge and normal-phase conditions. [Pg.406]

The reaction mechanism for the heterogeneous and homogeneous acid-catalysed esterification were reported to be similar (17). However, there is a major difference concerning the snrface hydrophobicity. Reaction pockets are created inside a hydrophobic environment, where the fatty acid molecules can be absorbed and react further. Water molecules are unlikely to be absorbed on sites enclosed in hydrophobic areas. [Pg.295]

Affinity chromatography involves precisely the same kind of electrostatic, hydrophobic, dipolar, and hydrogen-bonding interactions described above, but the specificity of binding is extraordinarily high. Demands on the homogeneity of the stationary phase and on the rigidity of the support are often... [Pg.11]

Liposomes are formed due to the amphiphilic character of lipids which assemble into bilayers by the force of hydrophobic interaction. Similar assemblies of lipids form microspheres when neutral lipids, such as triglycerides, are dispersed with phospholipids. Liposomes are conventionally classified into three groups by their morphology, i.e., multilamellar vesicle (MLV), small unilamellar vesicle (SUV), and large unilamellar vesicle (LUV). This classification of liposomes is useful when liposomes are used as models for biomembranes. However, when liposomes are used as capsules for drugs, size and homogeneity of the liposomes are more important than the number of lamellars in a liposome. Therefore, "sized" liposomes are preferred. These are prepared by extrusion through a polycarbonate... [Pg.30]


See other pages where Homogeneous Hydrophobicity is mentioned: [Pg.1246]    [Pg.809]    [Pg.1893]    [Pg.1897]    [Pg.137]    [Pg.1174]    [Pg.825]    [Pg.1026]    [Pg.1246]    [Pg.809]    [Pg.1893]    [Pg.1897]    [Pg.137]    [Pg.1174]    [Pg.825]    [Pg.1026]    [Pg.478]    [Pg.495]    [Pg.233]    [Pg.237]    [Pg.381]    [Pg.188]    [Pg.14]    [Pg.61]    [Pg.873]    [Pg.894]    [Pg.3]    [Pg.142]    [Pg.149]    [Pg.368]    [Pg.241]    [Pg.317]    [Pg.144]    [Pg.75]    [Pg.218]    [Pg.405]    [Pg.9]    [Pg.231]    [Pg.232]    [Pg.270]    [Pg.228]    [Pg.332]    [Pg.260]    [Pg.257]   
See also in sourсe #XX -- [ Pg.210 ]




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