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Concentration ordinary

At low concentrations, ordinary temperatures, and constant valence, the extent of exchangeincreases with increasing atomic number of the exchanging ion. [Pg.272]

The Big Bang hypothesis requires an instantaneous beginning of our universe at a point to which all energy (in the Planck-Einstein matter-radiation-energy concept Ch. 12) is concentrated. Ordinary nuclear reactions cannot model this beginning and we must turn to particle physics for information (Ch. 10). [Pg.447]

Surfactants have also been of interest for their ability to support reactions in normally inhospitable environments. Reactions such as hydrolysis, aminolysis, solvolysis, and, in inorganic chemistry, of aquation of complex ions, may be retarded, accelerated, or differently sensitive to catalysts relative to the behavior in ordinary solutions (see Refs. 205 and 206 for reviews). The acid-base chemistry in micellar solutions has been investigated by Drummond and co-workers [207]. A useful model has been the pseudophase model [206-209] in which reactants are either in solution or solubilized in micelles and partition between the two as though two distinct phases were involved. In inverse micelles in nonpolar media, water is concentrated in the micellar core and reactions in the micelle may be greatly accelerated [206, 210]. The confining environment of a solubilized reactant may lead to stereochemical consequences as in photodimerization reactions in micelles [211] or vesicles [212] or in the generation of radical pairs [213]. [Pg.484]

The slightly different physical properties of deuterium allow its concentration in ordinary hydrogen (or the concentration of a deuterium-containing compound in a hydrogen compound) to be determined. Exchange of deuterium and hydrogen occurs and can be used to elucidate the mechanism of reactions (i.e. the deuterium is a non-radioactive tracer). Methanol exchanges with deuterium oxide thus ... [Pg.116]

Hence, under ordinary conditions, manganeseflV) oxide oxidises concentrated hydrochloric acid to chlorine, but the above shows that the oxidation process is essentially ... [Pg.388]

Meanwhile assemble the apparatus shown in Fig. 62, or that in Fig. 23(D), p. 45, having a distilling-flask of at least 500 ml. capacity in either case. If an ordinary condenser C (Fig. 62) is employed, fit the lower end of the condenser by means of a short piece of rubber tubing to a small inverted funnel. Arrange the latter so that its lip is just below the surface of 25 ml. of concentrated hydrochloric acid diluted with 75 ml. of water contained in a 250 ml. beaker B the hydro-. chloric acid is thereby prevented from being sucked back into the... [Pg.128]

The purification train. The oxygen is led from the cylinder through Ordinary flexible rubber condenser tubing to the constant level device A (Fig. 85). This consists of two concentric tubes (approximately 2 cm. and 0-5 cm. respectively, in diameter the inner tube being narrowed and curved at the bottom as shown) immersed in 50% aqueous potassium hydroxide contained in the outer vessel (diameter 3-5 cm.). Then by adjusting the liquid level in A the pressure of oxygen may be kept constant, and at a maximum of about... [Pg.467]

The relatively concentrated hydrochloric acid is employed so that with ordinary use of the apparatus, spent liquor does not accumulate very rapidly the concentrated acid also ensures a brisk and delicately controlled flow of gas. When the generator is replenished with acid, marble or both, the de-aeration procedure detailed above is repeated until a sufficiently air-free gas supply is obtained. [Pg.483]

Suspend the bomb by a wire or a metal rod through F. Fill with water the annular space between the pillar F and the hole in the top of H. Now heat the base of A with a pointed flame, e.., from a blowpipe pointing upwards. The time required for heating in this way is usually about i minute, but an ordinary Bunsen flame, used without concentration on the bottom of A, may require about 4 minutes. The... [Pg.506]

We may now understand the nature of the change which occurs when an anhydrous salt, say copper sulphate, is shaken with a wet organic solvent, such as benzene, at about 25°. The water will first combine to form the monohydrate in accordance with equation (i), and, provided suflScient anhydrous copper sulphate is employed, the effective concentration of water in the solvent is reduced to a value equivalent to about 1 mm. of ordinary water vapour. The complete removal of water is impossible indeed, the equilibrium vapour pressures of the least hydrated tem may be taken as a rough measure of the relative efficiencies of such drying agents. If the water present is more than sufficient to convert the anhydrous copper sulphate into the monohydrate, then reaction (i) will be followed by reaction (ii), i.e., the trihydrate will be formed the water vapour then remaining will be equivalent to about 6 mm. of ordinary water vapour. Thus the monohydrate is far less effective than the anhydrous compound for the removal of water. [Pg.41]

Sulphuric acid. Ordinary concentrated acid, sp. gr. 1-84, is a constant boiling point mixture, b.p. 338°/760 mm., and contains 98 per cent. H2SO4. The 100 per cent, acid may be prepared by the addition of the calculated quantity of oleum it is also available commercially. [Pg.188]

Hydrolysis of p-tolunitrile to p-toluic acid. Boil a mixture of 5 g. of p-tolunitrile, 80 ml. of 10 per cent, aqueous sodium hydroxide solution and 15 ml. of alcohol under a reflux condenser. (The alcohol is added to prevent the nitrile, which volatUises in the steam, from crystalhsing in the condenser it also increases the speed of hydrolysis. The alcohol may be omitted in the hydrolysis of nitriles which are hquid at the ordinary temperature, e.g., benzo-nitrUe.) The solution becomes clear after heating for about 1 hour, but continue the boiling for a total period of 1 - 5 hours to ensure complete hydrolysis. Detach the condenser and boil the solution for a few minutes in the open flask to remove dissolved ammonia and incidentally some of the alcohol CAUTION /). Cool, and add concentrated hydrochloric acid until precipitation of the p-toluic acid is complete. When cold, filter off the p-toluic acid with suction and wash with a little cold water. Recrystallise from a mixture of equal volumes of water and alcohol (methylated spirit) or from benzene. The yield of p-toluic acid, m.p. 178°, is 5-5 g. [Pg.608]

Normal Superphosphate. From its beginning as the first commercial phosphate fertilizer, normal superphosphate (NSP), also called ordinary or single superphosphate, has continued among the top fertilizers of the world (Fig. 8). Use of normal superphosphate decreased steadily on a percentage basis because of growing production of more concentrated materials, but grew on a P2 s basis to a maximum of 6.7 x 10 t... [Pg.223]

Chiral nematic Hquid crystals are sometimes referred to as spontaneously twisted nematics, and hence a special case of the nematic phase. The essential requirement for the chiral nematic stmcture is a chiral center that acts to bias the director of the Hquid crystal with a spontaneous cumulative twist. An ordinary nematic Hquid crystal can be converted into a chiral nematic by adding an optically active compound (4). In many cases the inverse of the pitch is directiy proportional to the molar concentration of the optically active compound. Racemic mixtures (1 1 mixtures of both isomers) of optically active mesogens form nematic rather than chiral nematic phases. Because of their twist encumbrance, chiral nematic Hquid crystals generally are more viscous than nematics (6). [Pg.193]

At ordinary temperatures, mercury is stable and does not react with air, ammonia (qv), carbon dioxide (qv), nitrous oxide, or oxygen (qv). It combines readily with the halogens and sulfur, but is Htde affected by hydrochloric acid, and is attacked only by concentrated sulfuric acid. Both dilute and concentrated nitric acid dissolve mercury, forming mercurous salts when the mercury is in excess or no heat is used, and mercuric salts when excess acid is present or heat is used. Mercury reacts with hydrogen sulfide in the air and thus should always be covered. [Pg.106]

Disinfection. Ozone is a more effective broad-spectmm disinfectant than chlorine-based compounds (105). Ozone is very effective against bacteria because even concentrations as low as 0.01 ppm are toxic to bacteria. Whereas disinfection of bacteria by chlorine involves the diffusion of HOGl through the ceU membrane, disinfection by ozone occurs with the lysing (ie, mpture) of the ceU wall. The disinfection rate depends on the type of organism and is affected by ozone concentration, temperature (106), pH, turbidity, clumping of organisms, oxidizable substances, and the type of contactor employed (107). The presence of oxidizable substances in ordinary water can retard disinfection until the initial ozone demand is satisfied, at which point rapid disinfection is observed. [Pg.501]

Thermodynamic Properties. Ordinary water contains three isotopes of hydrogen [1333-74-0] (qv), ie, H, H, and H, and three of oxygen [7782 4-7] (qv), ie, O, and The bulk of water is composed of and O. Tritium [15086-10-9] H, and are present only in extremely minute concentrations, but there is about 200-ppm deuterium [16873-17-9], H, and 1000-ppm in water and steam (see Deuterium and tritium). The thermodynamic properties of heavy water are subtly different from those of ordinary water. lAPWS has special formulations for heavy water. The properties given herein are for ordinary water having the usual mix of isotopes. [Pg.350]

Although the most sensitive line for cadmium in the arc or spark spectmm is at 228.8 nm, the line at 326.1 nm is more convenient to use for spectroscopic detection. The limit of detection at this wavelength amounts to 0.001% cadmium with ordinary techniques and 0.00001% using specialized methods. Determination in concentrations up to 10% is accompHshed by solubilization of the sample followed by atomic absorption measurement. The range can be extended to still higher cadmium levels provided that a relative error of 0.5% is acceptable. Another quantitative analysis method is by titration at pH 10 with a standard solution of ethylenediarninetetraacetic acid (EDTA) and Eriochrome Black T indicator. Zinc interferes and therefore must first be removed. [Pg.388]


See other pages where Concentration ordinary is mentioned: [Pg.172]    [Pg.557]    [Pg.60]    [Pg.172]    [Pg.557]    [Pg.60]    [Pg.2490]    [Pg.83]    [Pg.167]    [Pg.437]    [Pg.17]    [Pg.157]    [Pg.166]    [Pg.566]    [Pg.81]    [Pg.133]    [Pg.287]    [Pg.388]    [Pg.395]    [Pg.476]    [Pg.369]    [Pg.378]    [Pg.8]    [Pg.340]    [Pg.512]    [Pg.227]    [Pg.386]    [Pg.20]    [Pg.66]    [Pg.297]    [Pg.65]    [Pg.470]    [Pg.63]    [Pg.64]    [Pg.294]    [Pg.290]   
See also in sourсe #XX -- [ Pg.436 , Pg.437 ]




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