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Membrane polymer potential

Since most other modeling techniques for polymers are extremely demanding, the limited capabilities of COSMO-RS for efficient prediction of solubilities in polymers can be of great help in practical applications when suitable polymers with certain solubility requirements are desired. One application may be the selection of appropriate membrane polymers for certain separation processes. Predictions of drug solubility in polymers are sometimes of interest for pharmaceutical applications. Furthermore, it is most likely that COSMO-RS can also be used to investigate the mutual compatibility of polymers for blends. This aspect, and many other aspects of the potential of COSMO-RS for polymer modeling, still awaits systematic investigation. [Pg.160]

Figure 6.13. Impedance plots for single cells at 80°C with the reactant gases humidified at 95°C for hydrogen and 85°C for oxygen, a Nafion 117 membrane. Cell potential and ohmic drop corrected cell potential (in parentheses) ( ) 0.70 V (0.75 V), ( ) 0.60 V (0.74 V), ( ) 0.50 V (0.73 V), (T) 0.40 V (0.72 V). b Nafion l 12 membrane. Cell potential and ohmic drop corrected cell potential (in parentheses) ( ) 0.60 V (0.67 V), ( ) 0.50 V (0.63 V), (A) 0.40 V (0.57 V), (T) 0.30 V (0.50 V). Plots were corrected for the high-frequency resistances [9], (Reprinted from Journal of Electroanalytical Chemistry, 503, Freire TJP, Gonzalez ER. Effect of membrane characteristics and humidification conditions on the impedance response of polymer electrolyte fuel cells, 57-68, 2001, with permission from Elsevier and the authors.)... Figure 6.13. Impedance plots for single cells at 80°C with the reactant gases humidified at 95°C for hydrogen and 85°C for oxygen, a Nafion 117 membrane. Cell potential and ohmic drop corrected cell potential (in parentheses) ( ) 0.70 V (0.75 V), ( ) 0.60 V (0.74 V), ( ) 0.50 V (0.73 V), (T) 0.40 V (0.72 V). b Nafion l 12 membrane. Cell potential and ohmic drop corrected cell potential (in parentheses) ( ) 0.60 V (0.67 V), ( ) 0.50 V (0.63 V), (A) 0.40 V (0.57 V), (T) 0.30 V (0.50 V). Plots were corrected for the high-frequency resistances [9], (Reprinted from Journal of Electroanalytical Chemistry, 503, Freire TJP, Gonzalez ER. Effect of membrane characteristics and humidification conditions on the impedance response of polymer electrolyte fuel cells, 57-68, 2001, with permission from Elsevier and the authors.)...
Baradie, B., Dodelet, J.R, and Guay, D., Hybrid Nafion -inorganic membrane with potential applications for polymer electrolyte fuel cells, J. Electroanal. Chem., 489, 101, 2000. [Pg.305]

Production of New Pol3miers. The polybenzimidazole developed as a raw material for specially thermal-stable textile fibers by the Celanese Research Company proved to be a potential membrane polymer due to the exceptionally high water absorption (17). [Pg.212]

There are several potential routes to the preparation of composite reverse osmosis membranes, whereby the ultrathin semipermeable film is formed or deposited on the microporous sublayer.1 2 The film can be formed elsewhere, then laminated to the microporous support, as was done in the earliest work on this membrane approach. Or it can be formed in place by plasma polymerization techniques. Alternatively, membrane polymer solution or polymer-forming reactants can be applied in a dipcoating process, then dried or cured in place. The most attractive approach from a commercial standpoint, however, has been the formation of the semipermeable membrane layer in situ by a classic "non-stirred" interfacial reaction method. Several examples of membranes made by this last approach have reached commercial status. [Pg.309]

Under ideal conditions, a thermodynamic equilibrium will be reached when the chemical potential of the solute i is equal at the membrane surface and the feed phase adjacent to it. The sorption of these solutes at the membrane surface creates a solute concentration gradient across the membrane, resulting in a diffusive net flux of solute across the membrane polymer (Fig. 3.6-lOB). In vapor permea-tion/pervaporation, any solute that has diffused toward the membrane downstream surface is ideally instantaneously desorbed and subsequently removed from the downstream side of the membrane (Fig. 3.6-lOC). This can be achieved either by applying a vacuum (vacuum vapor permeation/pervaporation), or by passing an inert gas over the membrane downstream surface (sweeping-gas vapor permea-... [Pg.272]

In the synthesis of polymers with functional groups suitable for drug attachments, hydrophilic hydroxyl-containing polymers and copolymers of divinyl ether and maleic anhydride are commonly used as precursor backbones for further modification. Polyfvinyl alcohol) has also been used in this way, both as the starting point for enzyme immobilization work, sometimes via azido group reactions, and also as a precursor for new membranes of potential interest in the haemodialysis field. ... [Pg.358]

The conductive polymer layer contains doping ions, which activity determines the drop in the potential at the membrane/polymer interface. If, during measurement, there is no change in the oxidation state of the polymer and in the concentration of the ion doping the polymer, the drops in the potential at the membrane/polymer and polymer/metal interfaces will also be constant. Any changes in the potential of such sensor will be determined by changes in the activity of ions in the analyzed solution, which also determine the potential at the solution/membrane interface (similar to conventional sensors) [53]. [Pg.209]

In addition, more synthesis on PBl polymers has been made by using a variety of diacids with active groups such as pendant amino [100, 101], carboxyl [102-104], sulfonic acid [105-107], hydroxyl [83, 108, 109], tert-butyl [5] or nitrile [110]. These functional groups are expected to be reactive with e.g., cross-linking agents containing epoxy or alkyl halide moieties, which provide polymers potential to be further modified for superior properties of PBl membranes. A comprehensive summary of different PBl main-chain stracture derivatives considered for fuel cell applications is given in Table 7.1. [Pg.159]

PIMs have the potential to overcome many of these limitations mentioned above. The encapsulation of the extractant within the membrane polymer matrix significantly lessens reagent losses to the aqueous solutions in contact with the membrane. Although PIMs suffer from relatively slow mass transport through the membrane, due to their mechanical stability the membranes can be made into very thin films which can somewhat mitigate the diffusive resistance effects (Nghiem et al, 2006). [Pg.239]

Thus began the search for an alternative low-cost polymer material. The current challenge is to improve the membrane properties in terms of thermal stability and proton conductivity while reducing methanol crossover. This may be achieved by the creation of new low-cost membranes. It has been mentioned by Smitha et al. [1] in their study that Gilpa and Hogarth identified 60 alternatives to the PFI membranes. Among these, 15 membranes showed potential for replacing Nafion membranes. To develop new polymer membrane with similar and improved properties by a less expensive route, the properties of Nafion polymers need to be understood consequently, research on Nafion membranes was carried out. [Pg.11]

The potential applications of such a polymerization technique for preparing novel polymeric materials include microfiltration, separation membranes, polymer blends with a unique microstructural morphology, and porous microcarriers for cultures of living cells and enzymes [7]. Some other interesting ideas about the preparation of novel materials include the conductive composite film [95] and microporous silica gel [96]. [Pg.170]

Zhang, C. Hu, J. Nagatsu, M. Meng, Y. Shen, W. Toyoda, H. Shu, X. (2011). High-Performance Plasma-Polymerized Alkaline Anion-Exchange Membranes for Potential Application in Direct Alcohol Fuel Cells. Plasma Process. Polym., Vol. 8, pp. 1024-1032... [Pg.138]

Wang, G., Weng, Y., Zhao, J., Chen, R., Xie, D. (2009) Preparation of a fimctional poly (ether imide) membrane for potential alkaline fuel cell applications chloromethylation. Journal of Applied Polymer Science, 112, 721-727. [Pg.356]

Zhao, C.J., Lin, H.D., Li, X.F., Na, H., Morphological investigations of block sulfonated poly(arylene ether ketone) copolymers as potential proton exchange membranes, Polym. Adv. TechnoL, 2011, 22, 2173-2181. [Pg.242]

Many complex systems have been spread on liquid interfaces for a variety of reasons. We begin this chapter with a discussion of the behavior of synthetic polymers at the liquid-air interface. Most of these systems are linear macromolecules however, rigid-rod polymers and more complex structures are of interest for potential optoelectronic applications. Biological macromolecules are spread at the liquid-vapor interface to fabricate sensors and other biomedical devices. In addition, the study of proteins at the air-water interface yields important information on enzymatic recognition, and membrane protein behavior. We touch on other biological systems, namely, phospholipids and cholesterol monolayers. These systems are so widely and routinely studied these days that they were also mentioned in some detail in Chapter IV. The closely related matter of bilayers and vesicles is also briefly addressed. [Pg.537]


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