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Dripping electrolyte

We can measure arc resistance on dry surfaces or when they are wetted by an electrolyte dripping on the surface between pairs of sharp electrodes, We report arc resistance as the time it takes to form a conductive track into which the arc disappears. [Pg.184]

Metal-Complex (Formazan) Dyes. The hydrazone from 2-carboxyphenylhydra-zine-4-sulfonic acid and benzaldehyde is suspended in water and then dissolved by adding aqueous sodium hydroxide to obtain pH 6.5 -7.0. This solution is added to the aqueous diazonium salt solution obtained from a typical aqueous diazotiza-tion of 4-(2-sulfooxyethylsulfonyl)-2-aminophenyl-6-sulfonic acid. The mixture is then dripped into an aqueous solution of copper sulfate, while the pH is maintained with soda at 5.5 - 6.5. After complete coupling the pH is adjusted to 1 with concentrated hydrochloric acid. The strongly acidic solution is then neutralized with alkali to pH 5.5. The copper - formazan complex is salted out along with sodium chloride, filtered, washed with dilute aqueous sodium chloride solution, and dried. A dark powder results which gives a dark blue solution in water. It consists of an electrolyte-containing powdered sodium salt of the acid 25 ... [Pg.123]

A new type of background electrolyte feeding has now been proposed (P5). A horizontal channel, which has a series of small holes, provides a drip of electrolyte which falls onto the folded edge of the curtain. The folded edge lies on a drain board, and while the paper is able to suck the amount of water it needs, the excess flows from the drain board into... [Pg.107]

Soluble insulin, preferably from the same species the patient has been using (never a sustained-release form), should be given by continuous i.v. infusion of a 1 unit/ml solution of insulin in isotonic sodium chloride. It is best to use a pump, which allows independent control of insulin and electrolyte administration more readily than an i.v. drip. If a pump is not available, the insulin should be added in a concentration of 1 unit/ml to 50-100 ml of sodium chloride in a burette. The infusion rate is determined by a sliding scale, as illustrated in Table 35.2. The rate is adjusted hourly using the same scale. If an i.v. drip is used instead of a pump the concentration should be lower (40 units/I). Stringent precautions against septicaemia are necessary in these patients. Continuous infusion i.m. (not s.c.) can also be equally effective, provided the patient is not in shock and provided there is not an important degree of peripheral vascular disease. [Pg.693]

A slow flow of anhydrous hydrogen chloride gas is now introduced through the capillary tube E. This hydrogen chloride addition should continue throughout the electrolysis to maintain a saturated solution. A trickle of water is allowed to drip into the porous cup. The rate of water addition determines the voltage requirement of the electrolytic cell. Thus, changes in the rate may be required during the electrolysis, but a convenient initial rate of addition is about 4 1./24 hr. [Pg.141]

With a dripping mercury electrode the surface is ideal and the double layer is modeled as a pure, frequency independent capacitor, somewhat voltage-dependent. The capacitance values are very high because of the small double-layer thickness, Cdi is about 20 pF/cm. With solid electrode materials, the surface is of a more fractal nature, with a distribution of capacitive and resistive properties. The actual values are dependent on the type of metal, the surface conditions, the type of electrolyte, and the applied voltage. The capacitance increases with higher electrolyte concentration. The double-layer capacitor is inevitable it is there as long as the metal is wetted. Cdi may dominate the circuit if there are no sorption or electrode reaction processes, or if the frequency is high. [Pg.216]

Plutonium metal is often purified by electrolytic refining the plutonium sample is immersed in a molten chloride salt under an inert atmosphere, comprising the anode in an electrolytic cell. Liquid Pu metal is collected on the surface of a tungsten cathode and drips off into a collector. Transition-metal contaminants remain in the residue of the anode, and rare earths and other actinides concentrate in the molten salt. The yield of purified Pu metal can be as high as 97%. Zone melting is also used to purify metallic plutonium the plutonium is fabricated into a bar along which a high-temperature zone is passed. As the melt zone is moved... [Pg.2883]

From this I conclude that if a rapidly dripping and otherwise insulated mass of mercury is in contact with an electrolyte through the dripping tip, then the mercury and the electrolyte cannot have different potentials. Had they different potentials - for example, if the mercury were to be positive - then each falling drop would form a double layer on its surface, which would take away +E from the mercury and render its positive potential smaller and smaller until it was the same as that of the liquid. [Pg.130]

Amalgam electrodes are of value because they allow active metals, e.g. Na and K, to be used as electrodes. Reproducible, reversible potentials can be obtained at very low concentrations of the metal it is best to use dropping electrodes, in which the amalgam drips slowly into the electrolyte, so that the surface is always fresh. The potential of the amalgam is compared with that of the pure metal by using both in a cell in which the electrolyte is dissolved in a solvent which does not attack the pure metal (e.g. ethylamine). Thus, to determine E (K, K), the sum of the standard e.m.f. values of the two cells ... [Pg.11]


See other pages where Dripping electrolyte is mentioned: [Pg.215]    [Pg.215]    [Pg.131]    [Pg.1029]    [Pg.338]    [Pg.326]    [Pg.124]    [Pg.428]    [Pg.498]    [Pg.364]    [Pg.378]    [Pg.207]    [Pg.15]    [Pg.313]    [Pg.1058]    [Pg.403]    [Pg.192]    [Pg.299]    [Pg.366]    [Pg.276]    [Pg.363]    [Pg.364]   
See also in sourсe #XX -- [ Pg.215 ]




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