Precipitation electrical conductivity

The potassium combines with the sulfur to form potassium sulfate, which condenses as a soHd primarily in the electrostatic precipitator (ESP) or baghouse. The recovered potassium sulfate is then deUvered to a seed regeneration unit where the ash and sulfur are removed, and the potassium, in a sulfur-free form such as formate or carbonate, is recycled to the MHD combustor. It is necessary also to remove anions such as Cf and E which reduce the electrical conductivity of the generator gas flow. These are present in the coal ash in very small and therefore relatively harmless concentrations. As the seed is recycled, however, the concentrations, particularly of CF, tend to build up and to become a serious contaminant unless removed. 

Commercial precipitation hardening copper alloys are based on beryUium, chromium, and nickel, this last in combination with siUcon or tin. The principal attributes of these alloys are high strength in association with adequate formabiUty. Electrical conductivity varies according to alloy and ranges from around 20 to 80% lACS. 

As a solution of barium hydroxide is mixed with a solution of sulfuric acid, a white precipitate forms and the electrical conductivity decreases markedly. Write equations for the reactions that occur and account for the conductivity change. 

Sonication of 0.05 M Hg2(N03)2 solution for 10,20 and 30 min and the simultaneous measurements of conductivity, temperature change and turbidity (Table 9.2) indicated a rise in the turbidity due to the formation of an insoluble precipitate. This could probably be due to the formation of Hg2(OH)2, as a consequence of hydrolysis, along with Hg free radical and Hg° particles which could be responsible for increase in the turbidity after sonication. The turbidity increased further with time. Mobility of NO3 ions was more or less restricted due to resonance in this ion, which helped, in the smooth and uniform distribution of charge density over NO3 ion surface. Hence the contribution of NOJ ion towards the electrical conductance was perhaps much too less than the conduction of cationic species with which it was associated in the molecular (compound) form. Since in case of Hg2(N03)2, Hg2(OH)2 species were being formed which also destroyed the cationic nature of Hg22+, therefore a decrease in the electrical conductance of solution could be predicted. The simultaneous passivity of its anionic part did not increase the conductivity due to rise in temperature as anticipated and could be seen through the Table 9.2. These observations could now be summarized in reaction steps as under ... 

A prerequisite for a precise and accurate titration is the reproducible identification of an end point which either coincides with the stoichiometric point of the reaction or bears a fixed and measurable relation to it. An end point may be located either by monitoring a property of the titrand which is removed when the stoichiometric point is passed, or a property which can be readily observed when a small excess of the titrant has been added. The most common processes observed in end-point detection are change of colour change of electrical cell potential change of electrical conductivity precipitation or flocculation. (Electrochemical methods are discussed in Chapter 6 precipitation indicators find only limited use.)... 

The electrical conductance of a solution is a measure of its current-carrying capacity and is therefore determined by the total ionic strength. It is a nonspecific property and for this reason direct conductance measurements are of little use unless the solution contains only the electrolyte to be determined or the concentrations of other ionic species in the solution are known. Conductometric titrations, in which the species of interest are converted to non-ionic forms by neutralization, precipitation, etc. are of more value. The equivalence point may be located graphically by plotting the change in conductance as a function of the volume of titrant added. 

In the case of Lysimeter Teuftal, most dissolved heavy metal and metalloid concentrations are directly correlated to electrical conductivity. The plot in Fig. 7 shows the relative dilution of different components during a rain event in comparison to that of electrical conductivity. The trend is independent of the speciation of these components. It should be noted that there are three notable exceptions, namely Ni(H), Co(II), and Cu(II). The common property of these cationic species is that they are extremely insoluble under the highly basic conditions encountered in the leachates of cement-stabilized residues (pH 12.8). It is possible that precipitation is the cause of such behaviour. 

Electrically conducting polymer particles such as polypyrrole and polyaniline could also be prepared by dispersion polymerization in aqueous ethanol (31). The oxidation polymerization of pyrrole and aniline has been carried out at the electrode surfaces so far and formed a thin film of conducting polymer. On the other hand, polypyrrole precipitates as particles when an oxidizing reagent is added to a pyrrole dissolved ethanol solution, which contains a water-soluble stabilizer. In this way electrically conducting polymer particles are obtained and, in order to add more function to them, incorporation of functional groups, such as aldehyde to the surface, and silicone treatment were invented (32). 

Influence of catalase activity and electrical conductivity. Parallel to the determination of the oxygen activity. Beck and co-workers 38> investigated the activity for the decomposition of hydrogen peroxide by various chelates. In each case, 1 mg of freshly precipitated pigment was added to 1% hydrogen peroxide solution and the velocity of oxygen evolution was determined volumetri-cally. The results summarized in Table 5 show no correlation between electro-catalytic activity and catalase activity. 

---