Sulfur electrode

Sulfur poisons catalytic sites in the fuel cell also. The effect is aggravated when there are nickel or iron-containing components including catalysts that are sensitive to sulfur and noble metal catalysts, such as found in low temperature cell electrodes. Sulfur tolerances are described in the specific fuel cell sections of this handbook." In summary, the sulfur tolerances of the cells of interest, by percent volume in the cleaned and altered fuel reformate gas to the fuel cells from published data, are ... 

Sulfur analytical scheme. The polarographlc analysis of many of the major sulfur species which are found in porewaters has been described in detail by Luther et al(22). Tables I and II show the relevant reactions of sulfur species at the mercury electrode. Sulfur species are quantified by the method of standard additions. Briefly, the samples are split in the following manner. 

In spite of their low solubility ( 5 x 10 M litre), HFeOJ ions diffuse to the positive electrode and are oxidized to solid FeOOH causing further dissolution of iron and its continous transfer to the positive electrode. The process is irreversible, the potential of the nickel electrode being too positive, even during discharge, for the reduction of trivalent iron. Further decrease of capacity is caused by the lowering of oxygen overpotential on the nickel oxide in the presence of FeOOH. The self-discharge and iron transfer processes are somewhat inhibited by additives to the electrode (sulfur) or electrolyte (e.g., lithium and sulfide ions, or hydrazine sulfate). 

Later there was a suggestion to employ sulfur and fhen chalcogenides, primarily sulfides, as active materials for the positive electrode. Sulfur is liquid at the working temperature of the battery. The sulfur elecfrode was manufactured from a mixture of sulfur and carbon or in fhe form of a niobium box wifh niobium filler packed wifh sulfur. The high volafilify of sulfur (af 507°C fhe pressure of sulfur vapor is... 

At the negative electrode, sulfur in solution is transformed between poly sulfide and sulfide ... 

AlCla-NaCl (63-37 to 50-50 mole %) 140-165 Linear sweep voltammetry (Pt and W electrodes) Sulfur heterocycles 157b So a... 

The coking process produces electrode quality coke from vacuum residues of good quality (low metal and sulfur contents) or coke for fuel in the case of heavy crude or vacuum residue conversion having high impurity levels. 

Toney M F, Howard J N, Richer J, Borges G L, Gordon J G, Melroy O R, Yee D and Sorenson L B 1995 Electrochemical deposition of copper on a gold electrode in sulfuric acid Resolution of the interfacial structure Phys. Rev. Lett. 75 4472-5... 

Platinum is a beautiful silvery-white metal, when pure, and is malleable and ductile. It has a coefficient of expansion almost equal to that of soda-lime-silica glass, and is therefore used to make sealed electrodes in glass systems. The metal does not oxidize in air at any temperature, but is corroded by halogens, cyanides, sulfur, and caustic alkalis. 

V. a term used to describe a voltage difference between one electrode and another VCDT. Vienna canyon diabolo troilite (actually silver sulfide used as a replacement standard for CDT [sulfur isotopes])... 

Polyaniline (PANI) can be formed by electrochemical oxidation of aniline in aqueous acid, or by polymerization of aniline using an aqueous solution of ammonium thiosulfate and hydrochloric acid. This polymer is finding increasing use as a "transparent electrode" in semiconducting devices. To improve processibiHty, a large number of substituted polyanilines have been prepared. The sulfonated form of PANI is water soluble, and can be prepared by treatment of PANI with fuming sulfuric acid (31). A variety of other soluble substituted AJ-alkylsulfonic acid self-doped derivatives have been synthesized that possess moderate conductivity and allow facile preparation of spincoated thin films (32). 

The most popular device for fluoride analysis is the ion-selective electrode (see Electro analytical techniques). Analysis usiag the electrode is rapid and this is especially useful for dilute solutions and water analysis. Because the electrode responds only to free fluoride ion, care must be taken to convert complexed fluoride ions to free fluoride to obtain the total fluoride value (8). The fluoride electrode also can be used as an end poiat detector ia titration of fluoride usiag lanthanum nitrate [10099-59-9]. Often volumetric analysis by titration with thorium nitrate [13823-29-5] or lanthanum nitrate is the method of choice. The fluoride is preferably steam distilled from perchloric or sulfuric acid to prevent iaterference (9,10). Fusion with a sodium carbonate—sodium hydroxide mixture or sodium maybe required if the samples are covalent or iasoluble. 

The electrolytic processes for commercial production of hydrogen peroxide are based on (/) the oxidation of sulfuric acid or sulfates to peroxydisulfuric acid [13445-49-3] (peroxydisulfates) with the formation of hydrogen and (2) the double hydrolysis of the peroxydisulfuric acid (peroxydisulfates) to Caro s acid and then hydrogen peroxide. To avoid electrolysis of water, smooth platinum electrodes are used because of the high oxygen overvoltage. The overall reaction is... 

The zinc electrolyte contains ca 60 kg/m zinc as sulfate and ca 100 kg/m free sulfuric acid. It is electrolyzed between electrodes suspended vertically in lead or plastic-lined, eg, poly(vinyl chloride), concrete tanks. The insoluble anodes are made of lead with small amounts of silver. The anodic... 

A number of simple, standard methods have been developed for the analysis of ammonium compounds, several of which have been adapted to automated or instmmental methods. Ammonium content is most easily deterrnined by adding excess sodium hydroxide to a solution of the salt. Liberated ammonia is then distilled into standard sulfuric acid and the excess acid titrated. Other methods include colorimetry (2) and the use of a specific ion electrode (3). 

Dilution with water reverses the reaction, and heating the solution Hberates sulfur dioxide. Upon being added to a solution of teUurides, teUurium forms colored polyteUurides. Unlike selenium, teUurium is not soluble in aqueous sodium sulfite. This difference offers a method of separating the two elements. Like selenium, teUurium is soluble in hot alkaline solutions except for ammonium hydroxide solutions. Cooling reverses the reaction. Because teUurium forms solutions of anions, Te , and cations, Te" ", teUurium films can be deposited on inert electrodes of either sign. 

Fluoride. A fluoride concentration of ca 1 mg/L is helpful in preventing dental caries. Eluoride is deterrnined potentiometrically with an ion-selective electrode. A buffer solution of high total ionic strength is added to the solution to eliminate variations in sample ionic strength and to maintain the sample at pH 5—8, the optimum range for measurement. (Cyclohexylenedinitrilo)tetraacetic acid (CDTA) is usually added to the buffer solution to complex aluminum and thereby prevent its interference. If fluoroborate ion is present, the sample should be distilled from a concentrated sulfuric acid solution to hydrolyze the fluoroborate to free fluoride prior to the electrode measurement (26,27). 

This reaction is accelerated by iacreased temperature, iacreased electrolyte concentration, and by the use of sodium hydroxide rather than potassium hydroxide ia the electrolyte. It is beheved that the presence of lithium and sulfur ia the electrode suppress this problem. Generally, if the cell temperature is held below 50°C, the oxidation and/or solubiUty of iron is not a problem under normal cell operating conditions. 

At the cathode, or positive electrode, lead dioxide [1309-60-0] Pb02, reacts with sulfuric acid to form lead sulfate [7446-14-2] PbSO, and water in the discharging reaction... 

To calculate the open circuit voltage of the lead—acid battery, an accurate value for the standard cell potential, which is consistent with the activity coefficients of sulfuric acid, must also be known. The standard cell potential for the double sulfate reaction is 2.048 V at 25 °C. This value is calculated from the standard electrode potentials for the (Pt)H2 H2S04(yw) PbS04 Pb02(Pt) electrode 1.690 V (14), for the Pb(Hg) PbS04 H2S04(yw) H2(Pt) electrode 0.3526 V (19), and for the Pb Pb2+ Pb(Hg) 0.0057 V (21). 

Paste Mixing. The active materials for both positive and negative plates are made from the identical base materials. Lead oxide, fibers, water, and a dilute solution of sulfuric acid are combined in an agitated batch mixer or reactor to form a pastelike mixture of lead sulfates, the normal, tribasic, and tetrabasic sulfates, plus PbO, water, and free lead. The positive and negative pastes differ only in additives to the base mixture. Organic expanders, barium sulfate [7727-43-7] BaSO carbon, and occasionally mineral oil are added to the negative paste. Red lead [1314-41 -6] or minium, Pb O, is sometimes added to the positive mix. The paste for both electrodes is characterized by cube weight or density, penetration, and raw plate density. 

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