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Sodium consumption concentration

In addition to scaling, system performance also deteriorated. Only 86% SO removal efficiency was obtained at 150,000 ppm chloride, significantly lower than the 93% at base case conditions. Filter cake insoluble solids also decreased to 39% compared with 53% for the base case. Decreases of T0S and total alkalinity concentrations were observed and reflected the increased liquor loss and sodium consumption. [Pg.195]

When the chloride ion concentration is above 100,000 ppm, system performance deteriorated with the increase of chloride ion concentration. In addition to the decreasing scrubbing solution pH and SO removal efficiency, the filter cake insoluble solids also decreased and resulted in increased liquor losses and sodium consumptions. [Pg.198]

Potassium Carbonate. Except for small amounts produced by obsolete processes, eg, the leaching of wood ashes and the Engel-Precht process, potassium carbonate is produced by the carbonation, ie, via reaction with carbon dioxide, of potassium hydroxide. Potassium carbonate is available commercially as a concentrated solution containing ca 47 wt % K CO or in granular crystalline form containing 99.5 wt % K CO. Impurities are small amounts of sodium and chloride plus trace amounts (<2 ppm) of heavy metals such as lead. Heavy metals are a concern because potassium carbonate is used in the production of chocolate intended for human consumption. [Pg.532]

In soils too saline for traditional crops, there is the possibility of developing halophytes for crop or forage production. An important consideration is that the produce (e.g. leaves or grain) should contain only low concentrations of sodium or chloride, or it will be unsuitable for human or animal consumption. [Pg.246]

In the decomposer, deionized water reacts with the amalgam, which becomes the anode to a short-circuited cathode. The caustic soda produced is stored or evaporated, if higher concentration is required. The hydrogen gas is cooled by refrigeration to remove water vapor and traces of mercury. Some of these techniques are employed in different facilities to maximize the production of chlorine, minimize the consumption of NaCl, and also to prevent the buildup of impurities such as sulfate in the brine.26 The production of pure chlorine gas and pure 50% sodium hydroxide with no need for further concentration of the dilute solution is the advantage that the mercury cell possesses over other cells. However, the cell consumes more energy and requires a very pure brine solution with least metal contaminants and above all requires more concern about mercury releases into the environment.4... [Pg.924]

Sears 189) and Heston et al. 190) used the adsorption of sodium hydroxide for the determination of the surface area of colloidal silica. An empirical factor was used for the conversion of alkali consumption into surface area. This is permissible provided the packing density of surface silanols is constant. The determination was performed in concentrated sodium chloride solution in order to keep down the dissolution of silica. Using the same technique, it was found in my laboratory that all surface silanol groups as determined by other methods are neutralized at pH 9.0. At higher pH, siloxane bonds in the surface were opened. A maximum in the sorption of Na+ ions occurred usually at pH 10.5-10.6 which corresponded to a packing density of ca. 5 OH/100 A. On further addition of alkali, silicate ions H3Si04 went into solution. [Pg.229]

This must obviously be the opposite of passive transport. Active transport does require energy, usually in the form of the consumption of ATP or GTP, because the molecules are moving against the concentration gradient from an area of lower concentration to an area of higher concentration. The most well known active transport system is the Sodium-Potassium-ATPase Pump (Na" "- K+ZATPase) which maintains an imbalance of sodium and potassium ions inside and outside the membrane, respectively. See Figure 3. [Pg.20]

This method can be used for the determination of the ozone concentration in the gas and/or liquid phase. The measurement takes place in the liquid phase, though, so that to measure a process gas containing ozone, the gas must first be bubbled through a flask containing potassium iodide KI. For the measurement of the liquid ozone concentration, a water sample is mixed with a KI solution. The iodide F is oxidized by ozone. The reaction product iodine 12 is titrated immediately with sodium thiosulfate Na2S203 to a pale yellow color. With a starch indicator the endpoint of titration can be intensified (deep blue). The ozone concentration can be calculated by the consumption of Na2S203. [Pg.68]

Fio. 8.—Relation between Consumption of Sodium Hydroxide and Concentration of Carbohydrate m Aqueous Solution.1 (Concentration of polysaccharides is expressed in mole of n-glucose residue per liter of solution. Initial concentration of sodium hydroxide is 0.25 M. mole of sodium hydroxide consumed per mole of carbohydrate. Carbohydrates D-glucose O, D-fructose , sucrose X, lactose , maltose , starch , and dextrin A.)... [Pg.240]


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See also in sourсe #XX -- [ Pg.193 , Pg.194 ]




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Sodium concentration

Sodium consumption

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