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Platinum-indium anodes

The electrochemical procedure for the synthesis of the complex was similar to those described by Tuck [559]. The cell was a 100-cm3 tail-form beaker fitted with a rubber bung through which the electrochemical leads enter the cell. The indium anode was suspended from a platinum wire and the cathode was a platinum wire. [(pySe)2] (0.31 g) was dissolved in acetonitrile and a small amount of tetraethylammonium perchlorate was added to the solution as a current carrier. An applied voltage of 10 V produced a current of 15 mA. During the electrolysis nitrogen gas was bubbled through the solution to provide an inert atmosphere and also to stir the solution phase. After 1 hr of reaction 70 mg of metal had been dissolved from the anode (Ey = 1.1). [Pg.270]

Ralstonia eutropha Electrochemical reaction CO2 + IT + e HCOO Microbial reaction (nonstoichiometric) HCOO —> C5H12O + C4H10O Platinum mesh anode separated by ceramic membrane from the indium foil cathode. 1.2 mM isobutanol and 0.6 mM 3-methyl-l-butanol after 1(X) h m... [Pg.1274]

The electrolytic cells shown ia Figures 2—7 represent both monopolar and bipolar types. The Chemetics chlorate cell (Fig. 2) contains bipolar anode/cathode assembhes. The cathodes are Stahrmet, a registered trademark of Chemetics International Co., and the anodes are titanium [7440-32-6] Ti, coated either with mthenium dioxide [12036-10-17, RUO2, or platinum [7440-06-4] Pt—indium [7439-88-5] Ir (see Metal anodes). Anodes and cathodes are joined to carrier plates of explosion-bonded titanium and Stahrmet, respectively. Several individual cells electrically connected in series are associated with one reaction vessel. [Pg.73]

In fact, in 1972, Fujishima and Honda (10) demonstrated that O2 evolution on n-type Ti02 occurs as a photocurrent, proportional to the light intensity (Figure 1) of wavelengths less than 415 nm, i.e. for photon energies equal to or greater than the band gap of Ti02 3.0 eV. In this work and that of Ohnishi et al. (11) a platinum black metal cathode was connected in an external circuit to an indium contact on the back side of the photo-anode (see... [Pg.222]

The reactions are carried out in a 200-mL tail-form beaker, with a tightly fitting rubber stopper through which the platinum electrode leads are inserted gas inlet and outlet tubes can be inserted as required. The cathode is a platinum wire carrying a 2 X 2 cm platinum sheet. The anode is a platinum wire onto which a shot of indium is beaten to form a 1 X 1 cm plate. The electrodes are placed 1-2 cm apart in the liquid phase, which is a mixture of organic solvents. [Pg.257]

For electropolymerization an anode made of glassy carbon (CWE), gold (Au), platinum disk or plate (Pt), or tin-doped indium-oxide-coated glass (ITO) are commonly used as working electrodes. A platinum wire or mesh is used as the counterelectrode. The potential is measured vs silver/silver chloride (Ag/AgCl) or saturated calomel (SCE) electrodes. Alternatively, a silver wire can be used as a pseudoreference with calibration to the half-wave potential of the ferrocene/ferrocenium (Fc/Fc ) redox couple. [Pg.423]


See other pages where Platinum-indium anodes is mentioned: [Pg.122]    [Pg.74]    [Pg.144]    [Pg.144]    [Pg.459]    [Pg.438]    [Pg.239]    [Pg.247]    [Pg.148]    [Pg.5422]    [Pg.182]    [Pg.254]    [Pg.5421]    [Pg.298]    [Pg.858]    [Pg.415]    [Pg.304]    [Pg.21]    [Pg.765]    [Pg.775]    [Pg.121]    [Pg.270]    [Pg.325]    [Pg.43]    [Pg.73]   
See also in sourсe #XX -- [ Pg.982 ]




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