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Free membranes

Once the membrane was successfully produced, it was analysed for characterisation and scanning. The sol-gel technique was successfully used to obtain a crack-free unsupported membrane, which was expected to have pore size of 1-2 nm. The development of the crack-free membrane may not have the same strength without strong, solid support. The next stage of this work was to characterise the fabricated membrane. Hie objectives of this study were to develop a zirconia-coated 7-alumina membrane with inorganic porous support by the sol-gel method and to characterise the surface morphology of the membrane and ceramic support. [Pg.384]

The following are some of the reasons that microreactors can be be used (i) reduced mass and heat transfer limitations, (ii) high area to volume ratio, (iii) safer operation, and (iv) ease of seating up by numbering out. The advantages of scaling down zeolite membranes are that it could be easier to create defect-free membranes and... [Pg.224]

State-of-the-art thin film Li" cells comprise carbon-based anodes (non-graphitic or graphite), solid polymer electrolytes (such as those formed by solvent-free membranes, for example, polyethylene oxide, PEO, and a lithium salt like LiPFe or LiCFsSOs), and metal oxide based cathodes, in particular mixed or doped oxides... [Pg.325]

Many different glycosyltransferase activities involved in higher plant wall biosynthesis have been identified in cell free membrane fractions, but in only a few cases has glycosyltransferase activity been retained in detergent-solubilized preparations, and in even fewer cases have any purified polypeptides been identified as plant cell wall glycosyltransferases (29,33). [Pg.111]

This chapter is devoted to the behavior of double layers and inclusion-free membranes. Section II treats two simple models, the elastic dimer and the elastic capacitor. They help to demonstrate the origin of electroelastic instabilities. Section III considers electrochemical interfaces. We discuss theoretical predictions of negative capacitance and how they may be related to reality. For this purpose we introduce three sorts of electrical control and show that this anomaly is most likely to arise in models which assume that the charge density on the electrode is uniform and can be controlled. This real applications only the total charge or the applied voltage can be fixed. We then show that predictions of C < 0 under a-control may indicate that in reality the symmetry breaks. Such interfaces undergo a transition to a nonuniform state the initial uniformity assumption is erroneous. Most... [Pg.66]

Use of ionophore-incorporated membranes leads thus to the same conclusions as described above for the ionophore-free membranes. Here too, the SHG measurements suggest that a permanent, primary ion-dependent charge separation at the liquid-liquid interface, and therefore a potentiometric response, is only possible when the membrane contains ionic sites. [Pg.468]

OP Hamill, A Marty, E Neher, B Sakman, FJ Sigworth. (1981). Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches. Pfluegers Arch 391 85-100. [Pg.380]

While ionophore-free membranes based on classical ion exchangers are still in use for the determination of lipophilic ions, such sensors often suffer from insufficient selectivity, as it is governed solely by the lipophilicity pattern of ions, also known for anions as the Hofmeister sequence. This pattern for cations is Cs+ > Ag+ >K+ > NH > Na+ > Li+ > Ca2+ > Mg2+ and for anions CIOT > SCN- > I > Sal- > N03- > Br > N02- > Cl- > OAc- HC03- > SO - > HPO4. While the ion exchanger fixes the concentration of hydrophilic analyte ions in the membrane on the basis of the electroneutrality condition within the membrane, the second key membrane component is the ionophore that selectively binds to the analyte ions. The selectivity of... [Pg.102]

The main classes of plasticizers for polymeric ISEs are defined by now and comprise lipophilic esters and ethers [90], The regular plasticizer content in polymeric membranes is up to 66% and its influence on the membrane properties cannot be neglected. Compatibility with the membrane polymer is an obvious prerequisite, but other plasticizer parameters must be taken into account, with polarity and lipophilicity as the most important ones. The nature of the plasticizer influences sensor selectivity and detection limits, but often the reasons are not straightforward. The specific solvation of ions by the plasticizer may influence the apparent ion-ionophore complex formation constants, as these may vary in different matrices. Ion-pair formation constants also depend on the solvent polarity, but in polymeric membranes such correlations are rather qualitative. Insufficient plasticizer lipophilicity may cause its leaching, which is especially undesired for in-vivo measurements, for microelectrodes and sensors working under flow conditions. Extension of plasticizer alkyl chains in order to enhance lipophilicity is only a partial problem solution, as it may lead to membrane component incompatibility. The concept of plasticizer-free membranes with active compounds, covalently attached to the polymer, has been intensively studied in recent years [91]. [Pg.124]

Size-related problems may become important for all microsensors. Leakage of sensing materials from a small membrane may lead to rapid deterioration of sensor properties [104], While the lipophilicity of membrane components cannot be increased infinitely, immobilization of ionophore and ion exchanger in the polymer by covalent attachment or molecular imprinting along with utilization of plasticizer-free membranes could help solve the leakage problem. [Pg.128]

Tsutsumi K, Obata Y, Takayama K, Isowa K, Nagai T (1999) Permeation of several drugs through keratinized epithelial-free membrane of hamster cheek pouch. IntJ Pharm 177 7-14... [Pg.110]

Doyle, D. A., Lee, A., Lewis, J., Kim, E., Sheng, M., and MacKinnon, R. Crystal structures of a complexed and peptide-free membrane protein-binding domain Molecular basis of peptide recognition by PDZ. Cell 1996, 85, 1067-1076. [Pg.282]

There exist a maximum allowable thickness of the supported gel layers above which it is not possible to obtain crack-free membranes after calcination. For Y-alumina membranes this thickness depends on a number of (partly unknown) parameters and has a value between 5 and 10 /im. One of the important parameters is certainly the roughness and porosity of the support system, because unsupported membranes (cast on teflon) are obtained crack-free up to 100 )xm. The xerogel obtained after drying was calcined over a wide range of temperatures. At 390°C the transition of boehmite to y-AljOj takes place in accordance with the overall reaction... [Pg.30]

One difficulty in framing this discussion is a lack of commonality in units for the expression systems. For example, the same substrate may not have been examined in all systems or activity may be expressed per mg total cell lysate protein, per mg cytosol-free cell membrane protein, per mg microsomal protein or per million cells. In this section, activity levels will be compared in the units originally reported. The following values, as determined in the human lymphoblast system, may be used to compare among the alternative methods of enzyme preparation cytosol-free membranes provide about a 2-fold enrichment in activity, microsomes provide 5-fold enrichment in activity and there are about 7 million cells per mg total protein. These ratios may differ somewhat for other mammalian cell systems but they are unlikely to be off by more than 2-fold. [Pg.205]

The shift to longer wavelengths of the ORD Cotton effects upon aggregation of lipid-free membrane protein must arise from a unique kind of association or an association which, if not qualitatively unique, is more dominant in membrane protein than in other proteins. Since the... [Pg.280]

With some experience, no staining of the membrane is necessary. When the PVDF membrane is illuminated with white light immediately after transfer, protein bands appear as white, opaque areas surrounded by translucent protein-free membrane. Taking care not to dry the membrane, a protein band to be eluted can be marked with a pencil. [Pg.84]

DEVELOPMENTS IN DISPERSION-FREE MEMBRANE-BASED EXTRACTION-SEPARATION PROCESSES Anil Kumar Pabby and Ana-Maria Sastre... [Pg.670]


See other pages where Free membranes is mentioned: [Pg.322]    [Pg.383]    [Pg.229]    [Pg.234]    [Pg.116]    [Pg.116]    [Pg.120]    [Pg.67]    [Pg.84]    [Pg.84]    [Pg.123]    [Pg.124]    [Pg.62]    [Pg.149]    [Pg.19]    [Pg.22]    [Pg.25]    [Pg.36]    [Pg.56]    [Pg.311]    [Pg.209]    [Pg.266]    [Pg.288]    [Pg.301]    [Pg.305]    [Pg.306]    [Pg.75]    [Pg.78]   
See also in sourсe #XX -- [ Pg.333 , Pg.334 , Pg.335 , Pg.336 , Pg.340 ]




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Defect-free membranes

Dense crack-free membranes

Emulsion-free liquid membranes

Free energy of membranes

Free fatty acids membrane separation

Free radical formation membrane lipid peroxidation

Importance of Free-standing Smectic Membranes

Membrane disruption, free radical

Membrane free energy

Membrane matrix fraction free volume

Membrane transport free energy

Pinhole-free membrane, palladium

Synthesis thin defect-free membranes

Thin defect-free membranes

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