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Water ammonia determination

Analytical Procedures. Standard methods for analysis of food-grade adipic acid are described ia the Food Chemicals Codex (see Refs, ia Table 8). Classical methods are used for assay (titration), trace metals (As, heavy metals as Pb), and total ash. Water is determined by Kad-Fisher titration of a methanol solution of the acid. Determination of color ia methanol solution (APHA, Hazen equivalent, max. 10), as well as iron and other metals, are also described elsewhere (175). Other analyses frequendy are required for resia-grade acid. For example, hydrolyzable nitrogen (NH, amides, nitriles, etc) is determined by distillation of ammonia from an alkaline solution. Reducible nitrogen (nitrates and nitroorganics) may then be determined by adding DeVarda s alloy and continuing the distillation. Hydrocarbon oil contaminants may be determined by ir analysis of halocarbon extracts of alkaline solutions of the acid. [Pg.246]

Methods of EGA using selective sorption, condensation of effluent gases, infrared absorption and thermoparticulate analysis have been reviewed by Lodding [144]. The use of simple gas burette systems should not be forgotten and an Orsat gas analysis apparatus can provide useful measurements in studies of the decomposition of formates [169]. Problems have been encountered in the determination of water released Kiss et al. [170—172] have measured the formation of this compound from infrared analyses of the acetylene evolved following reaction of water with calcium carbide. Kinetic data may be obtained by wet methods ammonia, determined by titration after absorption in an aqueous solution, has been used to measure a—time values for the decomposition of ammonium salts in a fluidized bed [173],... [Pg.23]

Mertens etal. [11] and Stevens [12] designed semiautomated versions of the micro Kjeldahl which avoided the distillation step altogether. In their versions, after the digestion step the digestion solution was diluted and the ammonia determined with an ammonia probe. The limitation on the sensitivity, then, is the sensitivity of the ammonia probe. This limits the method to the more productive oceanic waters. [Pg.482]

In solution, the drug may hydrolyze to yield diethylaminoethanol and 4-aminobenzoic acid. For the analysis, the sample solution is treated with 0.2 M (NH4>2Zn(SCN)4, heated to the onset of boiling, and cooled with slow rotational mixing for 4 minutes. This process yields clear solution and an oily precipitate, which is filtered through cotton wool. The filter is washed with 10% NH4SCN solution, and cooled to IT C. The precipitate is dissolved in acetone or dimethylformamide. Water, ammonia buffer solution (pH unspecified), and acid chrome black special indicator are added, and the mixture titrated with 10 mM EDTA to determine Zn(II), and hence procaine. [Pg.427]

As can be seen from Figure 2.1.2, the water and ammonia concentrations have a significant influence on the reaction rate, and the corresponding reaction orders with respect to the water and ammonia concentrations can also be determined. The following overall equation can then relate the different reaction parameters to the growth rate of the particles. The equation is given for the TEOS, water, ammonia, ethanol system in the temperature range between 20 and 60°C. [Pg.129]

The experimental data of Espiard et al. (21,22), based on the AOT/ toluene/water/ammonia system, showed an increase in particle size with increase in R. This observation led the authors to conclude that the droplet size of the microemulsion water pool was a key determinant of particle size. The effect of R on particle size was also investigated for silica nanoparticles synthesized in AOT/ decane/water/ammonia microemulsions (31). No particles were observed below about R = 4. However, as R increased from 5 to 9.5, the particle size also increased, in agreement with the observations of Espiard et al. (21,22). As noted previously (see Figure 2.2.3), in this microemulsion system, free water pools do not become... [Pg.168]

Acid-Base. The pH of natural waters is determined primarily by the carbonate equilibria. However, organisms may produce amounts of organic matter or ammonia sufficient to influence the pH and buffer capacity of the waters. It would be of interest to determine titration curves of high organic, high color, low alkalinity waters leached from some marshes. It is possible that these waters contain sufficient amounts of organic acids to be significant. [Pg.339]

Look at the following computer-generated ball-and-stick models of water, ammonia, and methane. Each of these molecules—and every other molecule as well— has a specific three-dimensional shape. Often, particularly for biologically important molecules, three-dimensional shape plays a crucial part in determining the molecule s chemistry. [Pg.263]

The organic substance and the ammonia were oxidized and the drop method (Shatenshtein et al., 1957b) was used to determine the concentration of deuterium in the resulting purified water (Shatenshtein and Antonchik, 1959 Shatenshtein and Yakovleva, 1958). The activity of tritium in the combustion water was determined as described by Yakushin and Shatenshtein (1960). [Pg.160]

If, however, the precipitate of diphenylurea is too small to weigh accurately, it is converted to ammonia and determined colorimetrically by the Nessler method. In this procedure, the filter paper is removed from the funnel and placed in a small beaker 4 ml. pure sulphuric acid (66° Be) are added, allowing this to flow slowly over the platinum spiral and through the funnel so as to wash off all traces of adherent precipitate. To the mixture obtained in this way 10 mgm. mercuric sulphate are added and the whole is then kept near boiling temperature for 2 hours. After allowing to cool, 20 ml. distilled water are added and the mixture is transferred to a 200-ml. flask containing 0-25 gm. sodium thiosulphate dissolved in 100 ml. water to remove the mercury. The beaker is washed with water which is added to the contents of the flask until the total volume is about 150 ml. and the ammonia determined in this. [Pg.83]

I) Ammonolysis of Esters. (1) To 5 ml of saturated solution of ammonia in methanol add 2 ml of ethyl acetate. Cork, and allow to stand until the next laboratory period. Place the contents of the tube in an evaporating dish and evaporate the alcohol over a water bath. Determine the weight of the amide. [Pg.210]

The smoke consists mainly of water, ammonia, ammonium chloride and iiiiro-gen. However, its composition has still not been exactly determined, and it is possible that highly toxic compounds may be present in small amounts. [Pg.51]

NH4+ + NH2 ). If instead of water, ammonia is used as a solvent (a) What is the formula of the cation that would indicate that a compound is an acid (b) What is the formula of the anion produced if a compound is a base (c) Look at the way that NaCl is formed from an acid-base reaction on earth and determine if NaCl can be a salt on Baseacidopolous. [Pg.398]

The amount of an evolved gas can be determined by a continuous titration method. A carrier gas removes the evolved gas from the furnace chamber and transports it to an aqueous-absorbing solution where it is continuously titrated. The titrant used will depend on the type of evolved gas to be determined. For example, ammonia is titrated with dilute hydrochloric acid, whereas water is determined by the Karl Fischer method. Compounds that can be determined include water, hydrogen chloride, ammonia, sulfur dioxide, carbon dioxide, and chlorine (80). [Pg.518]

The temperature of the system is 288 K and the total pressure is 1 atm. The diffusivity of ammonia in air under these conditions is 0.215 cm2/s and in liquid water is 1.77 x 10 5 cm2/s. Neglecting water evaporation, determine the rate of diffusion of ammonia, in kg/m2-h. Assume that the gas and liquid are in equilibrium at the interface. [Pg.84]

Figure 6.21 summarises the results described above. The deomposition products shown in this figure for a CPC, system B sample, were also measured for the CPC, system A samples, only differences in the measured intensities of released water (quantitatively determined with the aid of a MS calibration curve) and ammonia (quantitatively determined with the aid of a FTIR calibration curve) were found ... [Pg.214]


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See also in sourсe #XX -- [ Pg.184 , Pg.205 , Pg.242 , Pg.266 , Pg.267 ]




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