Precipitate definition

An important example has been studied by Roozboom it is furnished by the aqueous solutions of ferric chloride and of ammonium chloride. Although these two salts cannot be considered amorphous, their solutions, as had been previously shown by Lehmann, may furnish mixed crystals they may also give as precipitates definite compounds, namely, the hydrate Fe2ClQ 12H20 and the double salt (NHJj-FeClj-HjO. 

The precipitate obtained is in fact colloidal and has no definite composition. Careful drying of the precipitate gives the anhydrous oxide, SnO, which may also be prepared by heating tin(II) ethane-dioate (oxalate) ... 

The controlled thermal decomposition of dry aromatic diazonium fluoborates to yield an aromatic fluoride, boron trifluoride and nitrogen is known as the Schiemann reaction. Most diazonium fluoborates have definite decomposition temperatures and the rates of decomposition, with few exceptions, are easily controlled. Another procedure for preparing the diazonium fluoborate is to diazotise in the presence of the fluoborate ion. Fluoboric acid may be the only acid present, thus acting as acid and source of fluoborate ion. The insoluble fluoborate separates as it is formed side reactions, such as phenol formation and coupling, are held at a minimum temperature control is not usually critical and the temperature may rise to about 20° without ill effect efficient stirring is, however, necessary since a continuously thickening precipitate is formed as the reaction proceeds. The modified procedure is illustrated by the preparation of -fluoroanisole ... 

Bismuth trioxide may be prepared by the following methods (/) the oxidation of bismuth metal by oxygen at temperatures between 750 and 800°C (2) the thermal decomposition of compounds such as the basic carbonate, the carbonate, or the nitrate (700—800°C) (J) precipitation of hydrated bismuth trioxide upon addition of an alkah metal hydroxide to a solution of a bismuth salt and removal of the water by ignition. The gelatinous precipitate initially formed becomes crystalline on standing it has been represented by the formula Bi(OH)2 and called bismuth hydroxide [10361 -43-0]. However, no definite compound has been isolated. 

Theodore et al. employed Monte Carlo metliods in conjunction with the binomial and Weibull distributions to estimate out-of-compliance probabilities for electrostatic precipitators on tlie basis of observed bus section failures. The following definitions apply (see Fig. 21.6.1). 

For iridium the position is reversed. This time it is the black dioxide, Ir02, with the rutile structure (p. 961), which is the only definitely established oxide. It is obtained by heating the metal in oxygen or by dehydrating the precipitate produced when alkali is added to an aqueous solution of [IrCl6] . Contamination either by unreacted metal or by alkali is, however, difficult to avoid. The other oxide, Ir203, is said to be... 

By this means an appreciable amount of precipitate can be obtained, and definitely identified. 

The direct synthetic process is described in U.S. Patent 2,772,280. A solution of 73.3 g (0.332 mol) of (3-aminoxyalanine ethyl ester dihydrochloride in 100 ml of water was stirred in a 500 ml 3-necked round-bottomed flask cooled in an ice-bath. To the above solution was added over a 30-minute period 65.6 g (1.17 mols) of potassium hydroxide dissolved in 100 ml of water. While the pH of the reaction mixture was 7 to 10.5, a red color appeared which disappeared when the pH reached 11 to 11.5. The light yellow solution was allowed to stand at room temperature for 14 hour and then added to 1,800 ml of 1 1 ethanol-isopropanol. The reaction flask was washed twice with 10 ml portions of water and the washings added to the alcohol solution. The precipitated salts were filtered out of the alcohol solution and the filtrate cooled to 5°C in a 5 liter 3-necked round-bottomed flask. To the cold, well-stirred solution was added dropwise over a 35-minute period sufficient glacial acetic acid to bring the pH of the alcohol solution to 6.0. When the pH of the solution had reached 7 to 7.5, the solution was seeded and no further acetic acid added until Crystallization of the oil already precipitated had definitely begun. The crystalline precipitate was collected on a filter, washed twice with 1 1 ethanol-isopropanol and twice with ether. The yield of 4-amino-3-isoxazolidone was 22.7 g. 

The last definition has widespread use in the volumetric analysis of solutions. If a fixed amount of reagent is present in a solution, it can be diluted to any desired normality by application of the general dilution formula V,N, = V N. Here, subscripts 1 and 2 refer to the initial solution and the final (diluted) solution, respectively V denotes the solution volume (in milliliters) and N the solution normality. The product VjN, expresses the amount of the reagent in gram-milliequivalents present in a volume V, ml of a solution of normality N,. Numerically, it represents the volume of a one normal (IN) solution chemically equivalent to the original solution of volume V, and of normality N,. The same equation V N, = V N is also applicable in a different context, in problems involving acid-base neutralization, oxidation-reduction, precipitation, or other types of titration reactions. The justification for this formula relies on the fact that substances always react in titrations, in chemically equivalent amounts. 

After a precipitate has been filtered and washed, it must be brought to a constant composition before it can be weighed. The further treatment will depend both upon the nature of the precipitate and upon that of the filtering medium this treatment consists in drying or igniting the precipitate. Which of the latter two terms is employed depends upon the temperature at which the precipitate is heated. There is, however, no definite temperature below or above which the... 

The precipitate must be convertible into a pure substance of definite chemical composition this may be effected either by ignition or by a simple chemical operation, such as evaporation, with a suitable liquid. 

Alternatively, add pure aqueous ammonia solution (1 1) by means of a dropper pipette until a definite precipitate of iron(III) hydroxide just begins to form. Now add concentrated hydrochloric acid dropwise, stirring and allowing to stand for a minute or two after each 2-3 drops, until a clear solution is obtained then add 1.5 mL of concentrated hydrochloric acid and mix well. 

Discussion. The turbidity of a dilute barium sulphate suspension is difficult to reproduce it is therefore essential to adhere rigidly to the experimental procedure detailed below. The velocity of the precipitation, as well as the concentration of the reactants, must be controlled by adding (after all the other components are present) pure solid barium chloride of definite grain size. The rate of solution of the barium chloride controls the velocity of the reaction. Sodium chloride and hydrochloric acid are added before the precipitation in order to inhibit the growth of microcrystals of barium sulphate the optimum pH is maintained and minimises the effect of variable amounts of other electrolytes present in the sample upon the size of the suspended barium sulphate particles. A glycerol-ethanol solution helps to stabilise the turbidity. The reaction vessel is shaken gently in order to obtain a uniform particle size each vessel should be shaken at the same rate and the same number of times. The unknown must be treated exactly like the standard solution. The interval between the time of precipitation and measurement must be kept constant. 

The Bronsted definition also includes the possibility that an ion is an acid (an option not allowed by the Arrhenius definition). For instance, a hydrogen carbonate ion, HC03, one of the species present in natural waters, can act as an acid and lose a proton, and the resulting carbonate ion is removed by precipitation if suitable cations are present (Fig. 10.2) ... 

What do we mean by the rate of a chemical reaction Informally, we consider a reaction to be fast if the products are formed rapidly, as occurs in a precipitation reaction or an explosion (Fig. 13.1). A reaction is slow if the products are formed over a long period of time, as happens in corrosion or the decay of organic material (Fig. 13.2). Our first task is to set up a precise, quantitative definition of the rate of a chemical reaction. 

Extensive monitoring of the chemistry of precipitation is now available fi-om networks in both North America and Europe. Representative values of the major soluble species that account for most of the measured conductance of the samples at three United States sites are shown in (Table I) (77). It will be noted that the acidity, which is measured directly as pH, is due primarily to the presence of nitrate and sulphate ions that are not balanced by associated cations. While direct pH measurements are a valid measure of precipitation acidity, Reuss (18) has proposed that a balance of the principle ionic species, as in Equation 1 would provide a more appropriate definition of the acidity in relation to possible ecosystem responses. 

Where e is the excess acid in mol/L and ionic concentrations are expressed as mol/L. While this more precise definition may apply in some strictly chemical responses such as soil erosion, Biydges and Summers 19) have considered the more complete reactions including biological ionic utilizations and have defined an "acidifying potential" of precipitation as ... 

Acidity, definition in relation to possible ecosystem responses, 38,41 Acid precipitation, role of HO, 75 Acid rain... 

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