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Concentration of ammonia

Adding nitric acid lowers the concentration of ammonia. Decreasing ammonia s concentration causes reaction 6.29 to move from products to reactants, decreasing the solubility of AgCl. [Pg.149]

Feedwater treatment is designed to protect the feedwater system and, to some extent, the boiler. Most systems contain carbon steel piping. Carbon steel corrosion (Fig. 23a) is considerably slower at a pH between 9.0 and 11.0. In aH-ferrous feedwater systems, the preferred pH range is therefore 9.2 to 9.6, although some systems are operated at a pH as high as 10. In systems where copper alloys are present, high concentrations of ammonia accelerate corrosion of the copper alloys. In those systems the preferred pH is 8.8—9.2. [Pg.362]

The majority of the cyanuric acid produced commercially is made via pyrolysis of urea [57-13-6] (mp 135°C) primarily employing either directiy or indirectly fired stainless steel rotary kilns. Small amounts of CA are produced by pyrolysis of urea in stirred batch or continuous reactors, over molten tin, or in sulfolane. The feed to the kilns can be either urea soHd, melt, or aqueous solution. Since conversion of urea to CA is endothermic and goes through a plastic stage, heat and mass transport are important process considerations. The kiln operates under slight vacuum. Air is drawn into the kiln to avoid explosive concentrations of ammonia (15—27 mol %). [Pg.420]

Molal concentration of ammonia in the solutions in percentages (Weight concentration of ammonia in die solution in percentages)... [Pg.129]

Wastage was caused by waters containing high concentrations of ammonia. Steam containing high levels of ammonia condensed, ran down the tube sheet, and collected at tube ends, causing pronounced localized wastage. [Pg.198]

The results indicate that 2000 people will be exposed to a concentration of ammonia greater than the emergency response planning guideline concentration (e.g., ERPG-2). [Pg.15]

The extent of coupling is also influenced by the solvent. In the hydrogenation of aniline over ruthenium oxide, coupling decreased with solvent in the order methanol > ethanol > isopropanol > t-butanol. The rate was also lower in the lower alcohols, probably owing to the inhibiting effect of greater concentrations of ammonia (44). Carboxylic acid solvents increase the amount of coupling (42). [Pg.125]

For this reason, operation around atmospheric pressures is typical. Space velocity should he high to avoid the reaction of ammonia with oxygen on the reactor walls, which produces nitrogen and water, and results in lower conversions. The concentration of ammonia must he kept helow the inflammahility limit of the feed gas mixture to avoid explosion. Optimum nitric acid production was found to he obtained at approximately 900°C and atmospheric pressure. [Pg.148]

The reagent is employed for the determination of ammonia in very dilute ammonia solutions and in water. In the presence of interfering substances, it is best to separate the ammonia first by distillation under suitable conditions. The method is also applicable to the determination of nitrates and nitrites these are reduced in alkaline solution by Devarda s alloy to ammonia, which is removed by distillation. The procedure is applicable to concentrations of ammonia as low as 0.1 mgL-1. [Pg.679]

Certain internal chemical treatments employed also need strict control to avoid risks of adverse chemical reaction and resultant corrosion. In particular, nitrogen-containing chemicals such as hydrazine and amines require effective monitoring to limit the concentration of ammonia release into steam because the presence of ammonia may, under certain conditions, cause stress corrosion cracking of copper and brasses. [Pg.170]

In a packed column, operating at approximately atmospheric pressure and 295 K, a 10% ammonia-air mixture is scrubbed with water and the concentration of ammonia is reduced to 0.1%. If the whole of the resistance to mass transfer may be regarded as lying within a thin laminar film on the gas side of the gas-liquid interface, derive from first principles an expression for the rate of absorption at any position in the column. At some intermediate point where the ammonia concentration in the gas phase has been reduced to 5%. the partial pressure of ammonia in equilibrium with the aqueous solution is 660 N/nr and the transfer rate is ]0 3 kmol/m2s. What is the thickness of the hypothetical gas film if the diffusivity of ammonia in air is 0.24 cm2/s ... [Pg.853]

In many titrations, one solution—either the analyte or the titrant—contains a weak acid or base and the other solution contains a strong base or acid. For example, if we want to know the concentration of formic acid, the weak acid found in ant venom (1), we can titrate it with sodium hydroxide, a strong base. Alternatively, to find the concentration of ammonia, a weak base, in a soil sample, titrate it with hydrochloric acid, a strong acid. Weak acids are not normally titrated with weak bases, because the stoichiometric point is too difficult to locate. [Pg.575]

Figure 2.1. Equilibrium concentration of ammonia in a mixture of initially 1 3 N2 H2 as a function of temperature for several total pressures. Note the slight deviation due to non-ideality of the gases. Figure 2.1. Equilibrium concentration of ammonia in a mixture of initially 1 3 N2 H2 as a function of temperature for several total pressures. Note the slight deviation due to non-ideality of the gases.
The gas reacts over the ammonia catalyst in an exothermic process at 450-500 °C, leading to an exit concentration of ammonia of about 15-19%. The ammonia is extracted by condensation and the unreacted gas recycled to the reactor. A fraction is purged to prevent the accumulation of inert components. The ammonia condensation is not complete, meaning that the real inlet gas of the reactor already contains several percent of ammonia. [Pg.330]

Koch and Leitner (1998) have recently conducted the oxoreaction of 1-octene with CO and H2, using a Rh-based catalyst, in SC CO2. Fischer era/. (1999) have reported enhancements in selectivity by a factor of 4 to 18 with near critical ammonia, during Co- and Ni-catalysed synthesis of 1,3-diaminopropane. This is attributed to a higher concentration of ammonia at the catalyst surface. [Pg.173]

It may be noted that enhancement of the concentration of ammonia gives rise to two opposing effects. Precipitation is encouraged on account of destruction of the liberated acid, but at the same time, precipitation is retarded on account of the reduction of the availability of reducible metal ions, Cu2+, due to the prevalent complexing action by ammonia. It is for this reason that an optimum [NH3]/[Cu2+] ratio must be maintained so that the opposing effects are at balance. [Pg.542]

The inlet concentration of ammonia will be taken as 11 per cent v/v. [Pg.152]


See other pages where Concentration of ammonia is mentioned: [Pg.50]    [Pg.157]    [Pg.317]    [Pg.368]    [Pg.45]    [Pg.42]    [Pg.43]    [Pg.189]    [Pg.224]    [Pg.2320]    [Pg.191]    [Pg.467]    [Pg.31]    [Pg.38]    [Pg.258]    [Pg.1123]    [Pg.339]    [Pg.75]    [Pg.313]    [Pg.314]    [Pg.317]    [Pg.427]    [Pg.344]    [Pg.69]    [Pg.585]    [Pg.255]    [Pg.299]    [Pg.297]    [Pg.157]    [Pg.446]   
See also in sourсe #XX -- [ Pg.21 , Pg.22 , Pg.31 , Pg.41 , Pg.59 , Pg.150 , Pg.297 , Pg.337 , Pg.440 , Pg.504 , Pg.555 , Pg.558 , Pg.559 , Pg.560 , Pg.650 , Pg.651 , Pg.652 , Pg.660 , Pg.662 , Pg.664 , Pg.665 , Pg.669 , Pg.670 , Pg.671 , Pg.676 , Pg.686 , Pg.694 , Pg.700 , Pg.738 , Pg.741 , Pg.742 , Pg.745 , Pg.746 , Pg.750 , Pg.752 , Pg.754 , Pg.756 , Pg.775 , Pg.778 , Pg.782 , Pg.834 ]




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Ammonia concentrations

Equilibrium concentration of ammonia

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