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Poly transfer film

Photomechanical stencils are of two types direct coatings and transfer films. Direct coatings are either bichromated gelatin or bichromated poly(vinyl alcohol) (PVA). The coated screens are exposed through a positive, washed, and inspected. These screens are used for printing electronic components. They are not practical for commercial work because of the difficulty of reclaiming the screen after use. [Pg.50]

Gorton and coworkers have been particularly active in this field and produced an excellent review of the methods and approaches used for the successful chemical modification of electrodes for NADH oxidation [33]. They concentrated mainly on the adsorption onto electrode surfaces of mediators which are known to oxidise NADH in solution. The resulting systems were based on phenazines [34], phenoxazines [35, 36] and pheno-thiazines [32]. To date, this approach has produced some of the most successful electrodes for NADH oxidation. However, attempts to use similar mediators attached to poly(siloxane) films at electrode surfaces have proved less successful. Kinetic analysis of the results indicates that this is because of the slow charge transfer between the redox centres within the film so that the catalytic oxidation of NADH is restricted to a thin layer nearest the electrode surface [37, 38]. This illustrates the importance of a charge transfer between mediator groups in polymer modified electrodes. [Pg.45]

Redox cycling of poly(thionine) films in aqueous acetic acid solution involves not only electron transfer (coupled with proton transfer to maintain electroneutrality), but also film solvation and acetic acid coordination... [Pg.518]

Redox cycling of poly(vinylferrocene) films involves not only coupled electron/anion transfer, but also solvation and polymer configuration changes. The situation is further complicated by both reversible and irreversible elements of solvation and configuration changes, commonly referred to as break-in", immediately following deposition. Here, a dou-... [Pg.519]

Homogeneous charge transfer can take place between chemically similar redox species of one redox couple, e.g., Fe3+ and Fe2+ ions in solution or ferrice-nium and ferrocene moieties in poly(vinylferrocene) films, the electron transfer (- electron hopping or electron exchange reaction) can be described in terms of second-order kinetics and according to the - Dahms-Ruff theory [viii-x] it may be coupled to the isothermal diffusion ... [Pg.86]

The poly-Si films obtained by ALILE process always show p-type behavior. On high temperature resistant foreign substrates, the p-type poly-Si can be transferred to n-type poly-Si by overdoping, e.g., by phosphorous diffusion at 950°C [68], This allows for other solar cell configurations (e.g., substrate/ n+-type ALILE seed layer/n-type absorber/p+-type emitter). [Pg.213]

Low-damage SIMS has distinguished thin transfer films of the homologous series of poly(methyl, ethyl, isobutyl, n-butyl and lauryl) methacrylates. Figure 10 is a SIMS spectrum from a poly-lauryl methacrylate films on a silver substrate (8). [Pg.297]

Dupoet P. D., Miyamoto S., Murakami T., Kimura J., and Karube I., Direct electron transfer with glucose oxidase immobilized in an electropolymerized poly(Nmethylpyrrole) film on a gold electrode. Anal. Chem., 235, 255-263, 1990. [Pg.70]

M. Tsionsky, AJ. Bard, D. Dini, and F. Decker, Polymer films on electrodes. 28. Scanning electrochemical microscopy study of electron transfer at poly(alkylterthiophene) films. Chem. Mater., 10, 2120 (1998). [Pg.159]

Many redox enzymes can be denatured if the pH of the solution is taken too far from neutral or if nonaqueous solvents are used. It is therefore desirable, although not always essential, to use neutral aqueous solutions in the electropolymerization process, thus restricting the choice of monomers that can be used. One way to overcome this problem is to incorporate, or immobilize, the enzyme after deposition of the polymer film. This allows a much wider choice of deposition conditions. In addition to adsorbing the enzyme onto preformed poly(pyrrole) films, " GOx has also been covalently immobilized onto a wide range of preformed 3- and N-derivatized pyrrole carboxylates or onto N-amino-substituted pyrroles. This technique may increase current densities at a given glucose concentration by as much as twentyfold when compared to the best results obtained elsewhere. The authors make no claims for direct electron transfer between enzyme... [Pg.250]

GOx-poly(aniline) films have been grown from aqueous solutions, although acidic solutions (around pH 1) are necessary for electropolymerization, which can also adversely affect the enzyme. Although direct electron transfer between GOx and poly(aniline) has been postulated, " evidence to support this is not unequivocal. Based on experiments using poly(aniline) poly(aniline)/glucose oxidase bilayers, Hoa et al. have concluded that there is negligible direct electron transfer.This difference may reflect different deposition conditions used in the two sets of experiments. [Pg.254]

Audebert, P, G. Bidan, and M. Lapkowski. 1986. Reduction by two successive one-electron transfers of anthraquinone units bonded to electrodeposited poly(pyrrole) films. J Chem Soc Chem Commun 887-889. [Pg.897]

The ruthenium oligothienylacetylide complexes 93 (Chart 5.30) [106] and the oligothienylferrocene complexes 94a and b were electrochemically polymerized [107]. The voltammetry of poly-94a and poly-94b films contains redox waves due to both the ferrocene and backbone redox couples. Low-energy absorption bands appear upon oxidation of both the Fe centers and the conjugated backbone in the UV-Vis-near-IR spectrum of the films, and these have been attributed to charge-transfer processes. The poor solubility of 94b prevents electropolymerization at room temperature however, polymer films can be prepared at elevated temperatures. Electropolymerization of 95, in which hexyl chains have been added to increase the monomer solubility, has also been reported [108]. [Pg.313]

This cube was based ou a previous scheme of squares visual approach. Here, the axes x, y and z, respectively, represent coupled electron/proton transfer, solvent transfer and acetic acid coordination. Four equilibrium constants describe the coordination reactions for the four pairs of species on the left and right faces of the cube. The authors interpreted their data on partial redox switching of poly(vinylferrocene) films imder permselective conditions in aqueous perchlorate bathing electrolytes which produce films that reach... [Pg.175]


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