Sulphates, organic

Note. (1) TBSH should be stored in a dark bottle preferably at 4°C. Under these conditions decomposition occurs to only a small extent (5% in 9 months). The purity of TBSH may be assessed by t.l.c. analysis (CHCl3-MeOH, 9 1 v/v). Impure TBSH may be purified as follows TBSH (60 g) is dissolved in ether (600ml) and the solution washed first with aqueous sodium hydroxide solution (3 x 50 ml, 0.75 m), and then with water (25 ml). Light petroleum (1 litre, b.p. 30-40 °C) is added to the dried (magnesium sulphate) organic layer. The precipitated TBSH (50 g) is collected by filtration and dried in vacuo over phosphorus pentoxide for 24 hours at room temperature. 

Calcium Calcite, sulphates, organic association, silicates, phosphates... 

Several methods of wine sample concentration by precipitation of proteins, including use of ammonium sulphate, organic solvents (such... 

Minerals and acid mine drainage Chloride, sulphate, organic compounds, etc. 

However, AP is capable of forming complex compoxmds. It interacts with fluoride, sulphate, organic acids and even in pure water is capable of forming compounds Al(OH) +, Al (OH) and AJ (OH). That is why gibbsite dissolution reaction at high pH values even in the absence of foreign components acquires the following format... 

Ammonia may be estimated by dissolving the gas in a known volume of standard acid and then back-titrating the excess acid. In a method widely used for the determination of basic nitrogen in organic substances (the Kjeldahl method), the nitrogenous material is converted into ammonium sulphate by heating with concentrated sulphuric acid. The ammonia is then driven off by the action of alkali and absorbed in standard acid. 

Phenylhydrazine on exposure to light slowly darkens and eventually becomes deep red in colour salts of the base share this property but to a lesser degree, the sulphate and acetate (of the common salts) being most stable to light. Phenylhydrazine is largely used in organic chemistry to characterise aldehydes and ketones as their phenyl-hydrazones (pp. 342, 345), and carbohydrates as their osazones (pp. 136-140). It is readily reduced thus in the process of osazone formation some of the phenylhydrazine is reduced to aniline and ammonia. On the... 

Principle. A known weight of the substance is heated with fuming nftric acid in a sealed tube, the organic material being oxidised to carbon dioxide and water, and the sulphur to sulphuric acid. The latter is subsequently washed out of the tube, precipitated as barium sulphate, and estimated as such... 

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. 

Metallic sodium. This metal is employed for the drying of ethers and of saturated and aromatic hydrocarbons. The bulk of the water should first be removed from the liquid or solution by a preliminary drying with anhydrous calcium chloride or magnesium sulphate. Sodium is most effective in the form of fine wire, which is forced directly into the liquid by means of a sodium press (see under Ether, Section II,47,i) a large surface is thus presented to the liquid. It cannot be used for any compound with which it reacts or which is affected by alkalis or is easily subject to reduction (due to the hydrogen evolved during the dehydration), viz., alcohols, acids, esters, organic halides, ketones, aldehydes, and some amines. 

Organic acids Anhydrous sodium, magnesium or calcium sulphate. 

In the isolation of organic compounds from aqueous solutions, use is frequently made of the fact that the solubility of many organic substances in water is considerably decreased by the presence of dissolved inorganic salts (sodium chloride, calcium chloride, ammonium sulphate, etc.). This is the so-called salting-out effect. A further advantage is that the solubility of partially miscible organic solvents, such as ether, is considerably less in the salt solution, thus reducing the loss of solvent in extractions. 

To prepare the solid phenyldlazonlum chloride or sulphate, the reaction is conducted in the absence of water as far as possible. Thus the source of nitrous acid is one of its organic esters (e.g., amyl nitrite) and a solution of hydrogen chloride gas in absolute alcohol upon the addition of ether only the diazonium salt is precipitated as a crystalline solid, for example ... 

The palladium may be recovered by heating the spent catalyst to redness in order to remove organic impurities this treatment may reduce some of the barium sulphate to barium sulphide, which acts as a catalytic poison. The palladium is then dissolved out with aqua regia and the solution evaporated the residue is dissolved in hot water and hydrochloric acid to form palladium chloride. 

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