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Single horizontal electrode

Single horizontal electrode When a grounding electrode with length x and radius r is buried horizontally in soil at depth h, Sunde s formula for resistance R and capacitance C... [Pg.484]

The electron gun consists of a spiral-shaped tungsten cathode and a Wehnelt cylinder. These two components not only constitute the electrodes of the acceleration gap, but also form the optical assembly to control and shape the electron beam. Current signals are linear and have repetition frequency about 800 Hz. They are used to deflect the electron beam horizontally and vertically over the exit window plane. The scanner can be equipped by two cathodes for maximum output. Then, the width of the exit window is more than double that of a standard unit with a single cathode. The exit window containing the 12-15 prn-thick titanium foil is relatively large to assure an effective cooling of the foil. [Pg.53]

Fig. 16.3. Cyclic voltammogram of 13.6 U PP2A from Upstate (blank) and 0.3 mM catechol monophosphate+13.6 U PP2A from Upstate (CMP+PP) at lOOrnVs-1 using a single-drop configuration on a horizontally supported screen-printed two-electrode system, with graphite as working and Ag/AgCl as reference/auxiliary electrode. Reprinted from Campas et al. [86], with permission from Elsevier. Fig. 16.3. Cyclic voltammogram of 13.6 U PP2A from Upstate (blank) and 0.3 mM catechol monophosphate+13.6 U PP2A from Upstate (CMP+PP) at lOOrnVs-1 using a single-drop configuration on a horizontally supported screen-printed two-electrode system, with graphite as working and Ag/AgCl as reference/auxiliary electrode. Reprinted from Campas et al. [86], with permission from Elsevier.
UMEs used in our laboratory were constructed by sealing of carbon fibre into low viscosity epoxy resin (see Fig. 32.4) [118]. This method is simple, rapid and no specialised instrumentation is required. Firstly, the fibres are cleaned with this aim. They are immersed in dilute nitric acid (10%), rinsed with distilled water, soaked in acetone, rinsed again with distilled water and dried in an oven at 70°C. A single fibre is then inserted into a 100- iL standard micropipette tip to a distance of 2 cm. A small drop of low-viscosity epoxy resin (A. R. Spurr, California) is carefully applied to the tip of the micropipette. Capillary action pulls the epoxy resin, producing an adequate sealing. The assembly is placed horizontally in a rack and cured at 70°C for 8h to ensure complete polymerization of the resin. After that, the electric contact between the carbon fibre and a metallic wire or rod is made by back-filling the pipette with mercury or conductive epoxy resin. Finally, the micropipette tip is totally filled with epoxy resin to avoid the mobility of the external connection. Then, the carbon fibre UME is ready. An optional protective sheath can be incorporated to prevent electrode damage. [Pg.781]

Most separations are done with an agarose gel in a horizontal position, called a submarine gel because it is underneath the buffer in the chamber. However, when DNA sequencing is done (see Section 13.8), a polyacrylamide gel is run in a vertical position. Many different samples can be separated on a single gel. Each sample is loaded at a given place (a distinct well) at the negative-electrode end of the gel, and an electric current flows until the separation is complete (Figure 13.2). [Pg.364]


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