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Carbon graphite electrodes

Electrodes. Because of the numerous different processes, there are many different types of electrodes in use (9), eg, prefabricated graphite, prefabricated carbon, self-baking, and composite electrodes (see Carbon). Graphite electrodes are used primarily in smaller furnaces or in sealed furnaces. Prebaked carbon electrodes, made in diameters of <152 cm or 76 by 61 cm rectangular, are used primarily in smelting furnaces where the process requkes them. However, self-baking electrodes are preferred because of thek lower cost. [Pg.123]

Manufacturing of industrial of industrial carbons, graphite electrodes, anodes, midget electrodes, graphite blocks, graphite crucibles, gas carbons, activated carbon, synthetic diamonds, carbon black, channel black, and lamp black... [Pg.533]

Carbon—Graphite electrodes are often used, but they are less stable toward corrosion/phys-ical degradation than platinum. Graphite is available in many forms, including woven cloths, reticulated foam, and glassy (vitreous) carbon rods and plates. Organic products at different types of graphite anodes may differ considerably [60]. [Pg.1783]

DNA oxidation at carbon electrodes is associated with the irreversible oxidation of guanine and adenine [33], For example, the G oxidation signal observed at -i-1.0 V, without external labels, has been used to monitor telomerase activity by using a carbon graphite electrode (CGE) as an electrochemical transducer [5], Telomerase activity has been detected in cell extracts containing as low as 100 ng pl of protein. This label-free assay is practical in the quantitative determination of telomerase activity providing a cheap and simple detection protocol for the diagnosis of cancer that can also be extended to the analysis of food related to DNA. [Pg.298]

Graphite reacts with alkali metals, for example potassium, to form compounds which are non-stoichiometric but which all have limiting compositions (for example K C) in these, the alkaU metal atoms are intercalated between the layers of carbon atoms. In the preparation of fluorine by electrolysis of a molten fluoride with graphite electrodes the solid compound (CF) polycarbon fluoride is formed, with fluorine on each carbon atom, causing puckering of the rings. [Pg.169]

With the exception of carbon use in the manufacture of aluminum, the largest use of carbon and graphite is as electrodes in electric-arc furnaces. In general, the use of graphite electrodes is restricted to open-arc furnaces of the type used in steel production whereas, carbon electrodes are employed in submerged-arc furnaces used in phosphoms, ferroalloy, and calcium carbide. [Pg.516]

A variety of products are made in submerged-arc furnaces. Among them are various alloys and compounds. Each uses a particular type or grade of carbon electrode to hold production costs at the lowest possible level. Graphite electrodes could be and are used in some submerged-arc furnaces. Such a choice is the result of special conditions that warrant use of the more expensive graphite in Heu of carbon. [Pg.518]

Production of carbon electrodes is a capital-intensive business. Two suppHers dominate the prebaked market. Carbon paste producers are more numerous and tend to serve local markets. There is no international standard for the threaded joints on carbon electrodes. Manufacturers of straight pin carbon electrodes have followed the physical specifications adopted for graphite electrodes (37). Unified standards do not exist for pinless joints resulting in limited interchangeability among brands. Electrode diameters are offered in both English and metric sizes with no restrictions on new or unique diameters. [Pg.520]

Figure 3.6-1 The electrochemical window of 76-24 mol % [BMMIM][(CF3S02)2N]/Li [(Cp3S02)2N] binary melt at a) a platinum working electrode (solid line), and b) a glassy carbon working electrode (dashed line). Electrochemical window set at a threshold of 0.1 mA cm. The reference electrode was a silver wire immersed in 0.01 m AgBp4 in [EMIM][BF4] in a compartment separated by a Vicor frit, and the counter-electrode was a graphite rod. Figure 3.6-1 The electrochemical window of 76-24 mol % [BMMIM][(CF3S02)2N]/Li [(Cp3S02)2N] binary melt at a) a platinum working electrode (solid line), and b) a glassy carbon working electrode (dashed line). Electrochemical window set at a threshold of 0.1 mA cm. The reference electrode was a silver wire immersed in 0.01 m AgBp4 in [EMIM][BF4] in a compartment separated by a Vicor frit, and the counter-electrode was a graphite rod.
In redox flow batteries such as Zn/Cl2 and Zn/Br2, carbon plays a major role in the positive electrode where reactions involving Cl2 and Br2 occur. In these types of batteries, graphite is used as the bipolar separator, and a thin layer of high-surface-area carbon serves as an electrocatalyst. Two potential problems with carbon in redox flow batteries are (i) slow oxidation of carbon and (ii) intercalation of halogen molecules, particularly Br2 in graphite electrodes. The reversible redox potentials for the Cl2 and Br2 reactions [Eq. (8) and... [Pg.241]

Whereas the electrochemical decomposition of propylene carbonate (PC) on graphite electrodes at potentials between 1 and 0.8 V vs. Li/Li was already reported in 1970 [140], it took about four years to find out that this reaction is accompanied by a partially reversible electrochemical intercalation of solvated lithium ions, Li (solv)y, into the graphite host [64], In general, the intercalation of Li (and other alkali-metal) ions from electrolytes with organic donor solvents into fairly crystalline graphitic carbons quite often yields solvated (ternary) lithiated graphites, Li r(solv)yC 1 (Fig. 8) [7,24,26,65,66,141-146],... [Pg.394]

Lithium carbonate and hydrocarbon were identified in XPS spectra of graphite electrodes after the first cycle in LiPF6/EC-DMC electrolyte [104]. Electrochemical QCMB experiments in LiAsF6/EC-DEC solution [99] clearly indicated the formation of a surface film at about 1.5 V vs. (Li/Li+). However the values of mass accumulation per mole of electrons transferred (m.p.e), calculated for the surface species, were smaller than those of the expected surface compounds (mainly (CF OCC Li ). This was attributed to the low stability of the SEI and its partial dissolution. [Pg.441]


See other pages where Carbon graphite electrodes is mentioned: [Pg.164]    [Pg.351]    [Pg.289]    [Pg.164]    [Pg.274]    [Pg.274]    [Pg.178]    [Pg.255]    [Pg.264]    [Pg.265]    [Pg.350]    [Pg.373]    [Pg.52]    [Pg.164]    [Pg.351]    [Pg.289]    [Pg.164]    [Pg.274]    [Pg.274]    [Pg.178]    [Pg.255]    [Pg.264]    [Pg.265]    [Pg.350]    [Pg.373]    [Pg.52]    [Pg.122]    [Pg.348]    [Pg.422]    [Pg.429]    [Pg.585]    [Pg.497]    [Pg.499]    [Pg.518]    [Pg.299]    [Pg.210]    [Pg.1]    [Pg.8]    [Pg.47]    [Pg.137]    [Pg.296]    [Pg.52]    [Pg.53]    [Pg.71]    [Pg.242]    [Pg.385]    [Pg.439]    [Pg.440]    [Pg.115]    [Pg.125]   
See also in sourсe #XX -- [ Pg.120 ]




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Carbon electrode

Carbonate electrode

Graphite electrode

Graphite, graphitic carbons

Graphitic Electrodes

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