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Salts reducing concentration

Leading Examples Electrodialysis has its greatest use in removing salts from brackish water, where feed salinity is around 0.05-0.5 percent. For producing high-purity water, ED can economically reduce solute levels to extremely low levels as a hybrid process in combination with an ion-exchange bed. ED is not economical for the produc tion of potable water from seawater. Paradoxically, it is also used for the concentration of seawater from 3.5 to 20 percent salt. The concentration of monovalent ions and selective removal of divalent ions from seawater uses special membranes. This process is unique to Japan, where by law it is used to produce essentially all of its domestic table salt. ED is very widely used for deashing whey, where the desalted product is a useful food additive, especially for baby food. [Pg.2029]

Addition of hexafluorophosphate salts reduces the dediazoniation rate of 4-me-thylbenzenediazonium tetrafluoroborate in TFE/H20 (1 1) (Maskill and McCrud-den, 1992). However, as the concentration of these salts (0.12 — 0.23 M) does not affect the rate, it is evident that these salts are intercepting one of the intermediates, i.e., either the ion-molecule pair or the aryl cation. [Pg.174]

Element Insoluble Salt Expected Concentration in Seawater, log(mole/l) Observed Concentration in Seawater, log(mole/l) Observed Concentration in Reducing Muds, log(mole/l)... [Pg.604]

Since the crown ethers are very effective complexing agents, the amount of free M+ in solution, as in (33)—(36), is expected to be small the crown ether competes very well with Rh and X for M +. Indeed, it is found that the addition of excess salt causes a much lower degree of rate inhibition in [18]-crown-6 as compared to some other solvents. For example, Fig. 10 illustrates the differences between [18]-crown-6 and tetraglyme as the level of salt promoter is increased. The capability of using an excess of salt reduces the criticality of precisely controlling the salt concentration and is beneficial for the stability of the catalyst (92). [Pg.364]

Hydrogen trisulphide is much more easily combustible than the crude parent hydrogen polysulphide. Exposure to light tends to accelerate its decomposition. It slowly reduces concentrated sulphuric acid to sulphur dioxide, whilst on contact with dry silver oxide, cupric oxide, lead dioxide or mercuric oxide, it bursts into explosive combustion,2 a residue of the metallic sulphide being obtained. Many other metallic oxides and most salts bring about a less vigorous decomposition metals in the massive condition only react with it slowly. With potassium permanganate or dichromate the reaction is violent. [Pg.71]

The effective solute (ts) transport number, ranged from 93% to 98%, even if reduced to 88% for sodium lactate. The water transport number (tw) increased from 9.3 to 15.6 and correspondently the maximum salt weight concentration in the concentrated stream (CBc,max) ranged from 286 to 350 kg/m3. Finally, while the surface resistance (rc) of the cation-exchange membranes was found to be about constant (5 2fl cm2), ra tended to increase with A/b. However, the specific electric energy consumption (e) slightly increased from 0.19 to 0.22 kWh/kg of salt recovered. [Pg.345]

Fig. 11 Interaction of polyelectrolyte rods in salt-free solution SAXS-intensities measured for different polyelectrolyte concentrations at smallest scattering angles [71]. The respective concentrations are filled trangles 3 g/L hollow triangles lOg/L crosses 15 g/ L circles 20 g/L. The inset displays the maximum of the scattering intensity as function of the reduced concentration c/c where c=L 3... Fig. 11 Interaction of polyelectrolyte rods in salt-free solution SAXS-intensities measured for different polyelectrolyte concentrations at smallest scattering angles [71]. The respective concentrations are filled trangles 3 g/L hollow triangles lOg/L crosses 15 g/ L circles 20 g/L. The inset displays the maximum of the scattering intensity as function of the reduced concentration c/c where c=L 3...
The observations discussed above may have implications for any system where water, dissolved salts and hydrophobic entities are present and there must be many. Currently the separation of hydrophobic proteins can be achieved using a hydrophobic chromatography column, by elution with salt solutions. There is no adequate theory for this process and present understanding is purely empirical. Suppose then, that while all salts reduce electrostatic forces, only those salts that reduce bubble coalescence also reduce the hydrophobic attraction. Further, these salts have a significant effect on the hydrophobic attraction only above their transition concentration. With this notion in mind the experimental results are explained. This then enables separations to be simplified, as the salt type and concentration gradient required are easily determined. [Pg.135]

Hyponitrous acid, HgNgOg, has been made from its salts. A solution of sodium hyponitrite is produced by reducing concentrated aqueous NaNOg with sodium amalgam. The insoluble silver salt, precipitated from neutral solution, when treated with anhydrous HCl in dry ether gives the acid ... [Pg.333]

Electrolytic solutions used for extra-renal infusion and dialysis contain metal chlorides of Na, K, Ca and Mg salts at concentrations that are critical for effective treatment. These solutions also contain dextrose, citrate and lactate additives as part of this special formulation. The analysis for these metals must be precise and accurate and this can be achieved with ICP-OES using yttrium or scandium as internal standard to correct for matrix affects. The method of standard addition may also be used with similar success but is a more tedious method. The ability to dilute the sample several fold due to the high concentrations of metals reduces/eliminates the effect of EIE (easily ionised elements) caused by other elements in the same solution. The dilution and the ease of detection and corrections with an internal standard using the multi-element capability make this an excellent method. [Pg.235]

Special considerations zinc oxide decreases thermal stability combination of zinc oxide with carbon black reduces UV stability high concentrations of TiO2 or carbon black are needed to improve UV stability, at lower concentrations these fillers will reduce UV stability copper-containing compounds, iron salts, cadmium, cobalt, manganese, lead salts reduce thermal stabihty of PVC (also fillers containing these metals) sand was found to protect PVC from UV degradation calcium carbonate interferes with radiation crosslinking of... [Pg.682]


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See also in sourсe #XX -- [ Pg.1327 ]




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