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Concentration units hydrates

The heat of hydration is approximately —70 kj /mol (—17 kcal/mol). This process usually produces no waste streams, but if the acrylonitrile feed contains other nitrile impurities, they will be converted to the corresponding amides. Another reaction that is prone to take place is the hydrolysis of acrylamide to acryhc acid and ammonia. However, this impurity can usually be kept at very low concentrations. American Cyanamid uses a similar process ia both the United States and Europe, which provides for their own needs and for sales to the merchant market. [Pg.135]

Sodium metaborate tetrahydrate can be prepared by cooling a solution containing borax and an amount of sodium hydroxide just in excess of the theoretical amount. The dihydrate is prepared by United States Borax Chemical Corp. by mixing appropriate quantities of borax penta- or decahydrate hydrate and aqueous NaOH to give a 46 to 52% solution concentration of Na20 20 (107). The mixture is then heated to about 90°C to dissolve all soHds and slowly cooled to 60—75°C. Crystals of the dihydrate ate then harvested and dried. [Pg.202]

C4 cuts, after extraction of butadiene, are preferred as feed to isobutylene extraction units because the isobutylene concentration (about 30-40%) is higher than in C4 streams from catalytic cracking. The basic reaction in isobutylene extraction is the reversible hydration of isobutylene to tertiary butyl alcohol in the presence of sulfuric acid. [Pg.105]

Pourbaix has evaluated all possible equilibria between a metal M and HjO (see Table 1.7) and has consolidated the data into a single potential-pH diagram, which provides a pictorial summary of the anions and cations (nature and activity) and solid oxides (hydroxides, hydrated oxides and oxides) that are at equilibrium at any given pH and potential a similar approach has been adopted for certain M-H2O-X systems where A" is a non-metal, e.g. Cr, CN , CO, SOj , POj", etc. at a defined concentration. These diagrams give the activities of the metal cations and anions at any specified E and pH, and in order to define corrosion in terms of an equilibrium activity, Pourbaix has selected the arbitrary value of 10 ° g ion/1, i.e. corrosion of a metal is defined in terms of the pH and potential that give an equilibrium activity of metal cations or anions > 10 g ion/1 conversely, passivity and immunity are defined in terms of an equilibrium activity of < 10 g ion/1. (Note that g ion/1 is used here because this is the unit used by Pourbaix in the S.I, the relative activity is dimensionless.)... [Pg.65]

Osmotic swelling is a second type of swelling. Where the concentration of cations between unit layers in a clay mineral is higher than the cation concentration in the surrounding water, water is osmotically drawn between the unit layers and the c-spacing is increased. Osmotic swelling results in larger overall volume increases than surface hydration. However, only certain clays, like sodium montmorillonite, swell in this manner. [Pg.60]

At this time diffraction data for ion-ion distributions in aqueous solutions of moderate concentration are beginning to become available. In aqueous NiCl2 solutions very refined neutron diffraction studies indicate that the Ni2+-Cl pair correlation function has a peak near 3.l8 under conditions in which the Cl does not penetrate the Ni(H20)g2+ unit. (J+2 ) It is reported that EXAFS studies give the same result. (1 3) While the information is most welcome it is puzzling because a geometrical calculation indicates that the closest center to center distance for the Ni2+ and a Cl that does not penetrate the hydration shell is closer to 3.98. (7)... [Pg.557]

Fig. 8-90. Normalized cathodic cur> rent of redox reactions of hydrated redox particles as a function of standard redox potential at n-type electrodes of zinc oxide / (n, cqx) = normalized cathodic reaction current n, = concentration of interfacial electrons Cqx = concentration of oxidant particles au = arbitrary unit. [From Morrison, 1969,1980.]... Fig. 8-90. Normalized cathodic cur> rent of redox reactions of hydrated redox particles as a function of standard redox potential at n-type electrodes of zinc oxide / (n, cqx) = normalized cathodic reaction current n, = concentration of interfacial electrons Cqx = concentration of oxidant particles au = arbitrary unit. [From Morrison, 1969,1980.]...
A polyelectrolyte solution contains the salt of a polyion, a polymer comprised of repeating ionized units. In dilute solutions, a substantial fraction of sodium ions are bound to polyacrylate at concentrations where sodium acetate exhibits only dissoci-atedions. Thus counterion binding plays a central role in polyelectrolyte solutions [1], Close approach of counterions to polyions results in mutual perturbation of the hydration layers and the description of the electrical potential around polyions is different to both the Debye-Huckel treatment for soluble ions and the Gouy-Chapman model for a surface charge distribution, with Manning condensation of ions around the polyelectrolyte. [Pg.57]

Isopropanol is manufactured in the United States by the indirect hydration of propylene in processes which may involve the use of concentrated or dilute sulfuric acid, whereas, in European countries and Japan, a direct hydration process is used in which propylene reacts with water in the presence of a catalyst. It is used mainly for the production of acetone, but also as a solvent and in the manufacture of other chemicals and in pharmaceutical and cosmetic formulations (lARC, 1977). [Pg.1027]

Thermal anomalies ( kinks ) in the properties of water and aqueous solutions appear to be manifestations of higher-order phase transitions in structured elements of water. Some concentration-dependent anomalies are also described and discussed in terms of (a) the occurrence of discrete structural units of water in the unaffected solvent, (b) the possible separate existence of somewhat similarly structured units in the ionic hydration atmospheres, and (c) overlapping of large (but not necessarily structured) hydration atmospheres. [Pg.76]


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See also in sourсe #XX -- [ Pg.2 ]




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