Surface polyacrylonitriles

Nacimiento, R, Gonzalez, J. R, Alcantara, R, Ortiz, G. R, and Tirado, J. L. (2013]. Improving the electrochemical properties of self-organized titanium dioxide nanotubes in lithium batteries by surface polyacrylonitrile electropolymerization, J. Electrochem. Soc., 160, PP.A3026-A3035. 

The way in which these factors operate to produce Type III isotherms is best appreciated by reference to actual examples. Perhaps the most straightforward case is given by organic high polymers (e.g. polytetra-fluoroethylene, polyethylene, polymethylmethacrylate or polyacrylonitrile) which give rise to well defined Type III isotherms with water or with alkanes, in consequence of the weak dispersion interactions (Fig. S.2). In some cases the isotherms have been measured at several temperatures so that (f could be calculated in Fig. 5.2(c) the value is initially somewhat below the molar enthalpy of condensation and rises to qi as adsorption proceeds. In Fig. 5.2(d) the higher initial values of q" are ascribed to surface heterogeneity. 

The white cell adsorption filter layer is typically of a nonwoven fiber design. The biomaterials of the fiber media are surface modified to obtain an optimal avidity and selectivity for the different blood cells. Materials used include polyesters, eg, poly(ethylene terephthalate) and poly(butylene terephthalate), cellulose acetate, methacrylate, polyamides, and polyacrylonitrile. Filter materials are not cell specific and do not provide for specific filtration of lymphocytes out of the blood product rather than all leukocytes. 

More than 95% of current carbon fiber production for advanced composite appHcations is based on the thermal conversion of polyacrylonitrile (PAN) or pitch precursors to carbon or graphite fibers. Generally, the conversion of PAN or pitch precursor to carbon fiber involves similar process steps fiber formation, ie, spinning, stabilization to thermoset the fiber, carbonization—graphitization, surface treatment, and sizing. Schematic process flow diagrams are shown in Eigure 4. However, specific process details differ. 

Select mobile phases for HPSEC based on their ability to dissolve the sample and their compatibility with the column. Zorbax PSM columns are compatible with a wide variety of organic and aqueous mobile phases (Table 3.4), but analysts should avoid aqueous mobile phases with a pH greater than 8.5. As mentioned earlier, select mobile phases that minimize adsorption between samples and silica-based packings. Sample elution from the column after the permeation volume indicates that adsorption has occurred. If adsorption is observed or suspected, select a mobile phase that will be more strongly adsorbed onto the silica surface than the sample. For example, N,N-dimethyl-formamide (DMF) is often used for polyurethanes and polyacrylonitrile because it eliminates adsorption and dissolves the polymers. When aqueous mobile phases are required, highly polar macromolecules such as Carbowax can be used to coat the silica surface and eliminate adsorption. Table 3.5 provides a list of recommended mobile-phase conditions for some common polymers. 

The chitosan-heparin polyelectrolyte complex was covalently immobilized onto the surface of polyacrylonitrile membrane. The immobilization caused the water contact angle to decrease, thereby indicating an increase in hy-... 

Membranes UF membranes consist primarily of polymeric structures (polyethersulfone, regenerated cellulose, polysulfone, polyamide, polyacrylonitrile, or various fluoropolymers) formed by immersion casting on a web or as a composite on a MF membrane. Hydrophobic polymers are surface-modified to render them hydrophilic and thereby reduce fouling, reduce product losses, and increase flux [Cabasso in Vltrafiltration Membranes and Applications, Cooper (ed.). Plenum Press, New York, 1980]. Some inorganic UF membranes (alumina, glass, zirconia) are available but only find use in corrosive applications due to their high cost. 

SPAN module. It was mentioned at the beginning that the special polyacrylonitrile fibers of SPAN have a wall thickness of 30 gm, which is considerably thicker than the 8 gm wall thickness of the SMC modules [19]. As a consequence, the presence of stronger capillary effects from the special porous fiber material of the SPAN module would be a reasonable conclusion. Furthermore, the texture of the special polyacrylonitrile fibers is expected to have better surface properties, supporting the permeation of molecules as compared with synthetically modified cellulose. In conclusion, both convection and diffusion effectively contribute to the filtration efficiency in a SPAN module, whereas for the SMC membrane, diffusion is the driving force for molecular exchange, the efficiency of which is also considerable and benefits from the large surface-to-volume ratio. 

Moafi et al. [143] studied the ability of titania versus zirconia to photocatalyze methylene blue and eosin yellow on polyacrylonitrile fibers. Ti02 particles ranging from 10-20 nm in size and Zr02 particles ranging from 20-40 nm in size were dispersed on the fiber surface. Photocatalytic activity of Ti02 was greater. 

Fischer-Colbrie, G., Matama, T., Heumann, S. et al. (2007) Surface hydrolysis of polyacrylonitrile with nitrile hydrolysing enzymes from Micrococcus luteus BST20. Journal of Biotechnology, 129, 62-68. 

Polyacrylonitrile (PAN) cloth with surface density of 1.0 kg/m2 and thickness of 10 mm was utilized as the raw material for making ion-exchange sorbents. 

In practical application, it was reported that the platinum particles dispersed in highly porous carbonized polyacrylonitrile (PAN) microcellular foam used as fuel-cell electrocatalyst160 have the partially active property. The fractal dimension of the platinum particles was determined to be smaller than 2.0 by using the potentiostatic current transient technique in oxygen-saturated solutions, and it was considered to be a reaction dimension, indicating that not all of the platinum particle surface sites are accessible to the incoming oxygen molecules. 

The surface properties of carbon fibers are intimately related to the internal structure of the fiber itself, which needs to be understood if the surface properties are to be modified for specific end applications. Carbon fibers have been made from a number of different precursors, including polyacrylonitrile (PAN), rayon (cellulose) and mesophase pitch. The majority of commercial carbon fibers currently produced are based on PAN, while those based on rayon and pitch are produced in very limited quantities for special applications. Therefore, the discussion of fiber surface treatments in this section is mostly related to PAN-based carbon fibers, unless otherwise specified. 

Fig. 2.24 The production process for C fibers. Starting with pitch or polyacrylonitrile the fluids are spun into oriented fibers, thermoset, carbonized, and graphi-tized to carbon fibers. Surface treatment improves bonding to resin matrix.

Wang HY, Kobayashi T, Fujii N. Surface molecular imprinting on photosensitive dithiocar-bamoyl polyacrylonitrile membranes using photograft polymerization. J Chem Technol Biotechnol 1997 70 355-362. 

Keywords Cutinase Polyacrylonitrile Polyamide Polyethyleneterphthalate Surface hydrolysis... 

Fischer-Colbrie G, Matama T, Heumann S et al (2007) Surface hydrolysis of polyacrylonitrile with a nitrilase of a new strain of Micrococcus luteus. J Biotechnol 128 849-857... 

Fischer-Colbrie G, Herrmann M, Heumann S et al (2006) Surface modification of polyacrylonitrile with nitrile hydratase and amidase from Agrobacterium tumefaciens. Biocatal Biotrans 24 419-425... 

Chapter 5 shows that the application of hydrolytic enzymes is a powerful yet mild strategy to directly improve polymer surface properties (i.e. hydrophilicity) or activate materials for further processing. The surface hydrolysis of polyamides (PA), polyethyleneterphthalates (PET) and polyacrylonitriles (PAN) is discussed, as well as the mechanistic details on the enzymatic surface hydrolysis. The mechanistic data, combined with advances in structural and molecular biology, help to explain different activities of closely related enzymes on polymer surfaces. 

Two different polyacrylonitrile precursor carbon fibers, an A fiber of low tensile modulus and an HM fiber of intermediate tensile modulus were characterized both as to their surface chemical and morphological composition as well as to their behavior in an epoxy matrix under interfacial shear loading conditions. The fiber surfaces were in two conditions. Untreated fibers were used as they were obtained from the reactors and surface treated fibers had a surface oxidative treatment applied to them. Quantitative differences in surface chemistry as well as interfacial shear strength were measur-ed. 

To understand the mechanism of polyblending, experiments have been carried out with polymeric solution. W. Borchard and G. Rehage mixed two partially miscible polymer solutions, measured the temperature dependence of the viscosity, and determined the critical point of precipitation. When two incompatible polymers, dissolved in a common solvent, are intimately mixed, a polymeric oil-in-oil emulsion is formed. Droplet size of the dispersed phase and its surface chemistry, along with viscosity of the continuous phase, determine the stability of the emulsion. Droplet deformation arising from agitation has been measured on a dispersion of a polyurethane solution with a polyacrylonitrile solution by H. L. Doppert and W. S. Overdiep, who calculated the relationship between viscosity and composition. 

The surface of polymeric materials such as polypropylene (PP), PS, polyacrylonitrile (PAN), and nylon was oxidized by immersing them in aqueous solution of oxidizing agents such as potassium peroxy disulfate under nitrogen purging at high temperatures [14]. Graft polymerization of water-soluble monomers such as AAm, methacrylic acid, and 3-aminopropyl methacrylate has been frequently performed in aqueous solution with the use of ceric ion, for instance, at... 

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