Ammonia density

Colorless volatile liqnid with an odor of ammonia density 0.694 at 15°C (59°F) boils at 33-34°C (91-93°F) freezes at -lOLC ( 149°F) soluble in water, alcohol, and ether strongly alkaline. 

Colorless liquid with a strong odor of ammonia density 0.832 at 20°C (68°F) bp 56°C (132°F) solidifies at -74°C (-101°F) infinitely soluble in water, soluble in most organic solvents aqueous solution strongly alkaline. 

Test Yourself Find the true mass of 28.0 wt% ammonia (density = 0.90 g/mL) when the apparent mass is 20.000 g. (Answer 20.024 g)... 

Procedure. One drop of ammonia (density 0.91) and 1 drop of the reagent solution are added to 1-2 drops of the test solution on a spot plate. The mixture is stirred with a glass rod previously wetted with ether. Red-violet spots on the porcelain indicate the presence of calcium. 

The extent of dissociation at a given temperature can be determined by measuring the density of the vapour. Since anhydrous sulphuric acid is less volatile than hydrogen chloride, ammonium sulphate does not readily sublime on heating some ammonia is evolved to leave the hydrogensulphate ... 

Ammoniameter. This hydrometer, employed in finding the density of aqueous ammonia solutions, has a scale graduated in equal divisions from 0° to 40°. To convert the reading to specific gravity multiply by 3 and subtract the resulting number from 1000. 

The density of concentrated ammonia, which is 28.0% w/w NH3, is 0.899 g/mL. What volume of this reagent should be diluted... 

TiF is a colorless, very hygroscopic soHd and is classified as a soft fluorinating reagent (4), fluorinating chlorosilanes to fluorosilanes at 100°C. It also forms adducts, some of them quite stable, with ammonia, pyridine, and ethanol. TiF sublimes at 285.5°C, and melts at temperatures >400° C. It is soluble in water, alcohol, and pyridine, hydroly2ing in the former, and has a density of 2.79 g/mL. 

Ammonia—water systems operate under moderate pressures and care must be taken to avoid leaks of the irritating and toxic ammonia (qv). Sometimes a third material with a widely different density, eg, hydrogen, is added to the cycle in order to eliminate the need for mechanical pumping. 

Like the other alkah metals (45), lithium has appreciable solubiUty in Hquid ammonia. A saturated solution at —33.2° C contains 15.7 mol lithium in 1000 g of ammonia, and at 19°C has a density of 0.477, lower than that of any other known Hquid. Lithium reacts readily in Hquid ammonia to form... 

Nickel Carbonate. Nickel carbonate [3333-67-3], NiCO, is a light-green, rhombic crystalline salt, density 2.6 g/cm, that is very slightly soluble in water. The addition of sodium carbonate to a solution of a nickel salt precipitates an impure basic nickel carbonate. The commercial material is the basic salt 2NiCo2 3Ni(OH)2 4H20 [29863-10-3]. Nickel carbonate is prepared best by the oxidation of nickel powder in ammonia and CO2. Boiling away the ammonia causes precipitation of pure nickel carbonate (32). 

AH ammonium haUdes exhibit high vapor pressures at elevated temperatures, and thus, sublime readily. The vapor formed on sublimation consists not of discrete ammonium haUde molecules, but is composed primarily of equal volumes of ammonia and hydrogen haUde. The vapor densities are essentiaHy half that expected for the vaporous ammonium haUdes. Vapor pressures at various temperatures are given in Table 2 (11). Latent heats of sublimation, assuming complete dissociation of vapors and including heats of dissociation are 165.7, 184.1, and 176.6 kJ /mol (39.6, 44.0, and 42.2... 

Iron, cobalt, and nickel catalyze this reaction. The rate depends on temperature and sodium concentration. At —33.5°C, 0.251 kg sodium is soluble in 1 kg ammonia. Concentrated solutions of sodium in ammonia separate into two Hquid phases when cooled below the consolute temperature of —41.6°C. The compositions of the phases depend on the temperature. At the peak of the conjugate solutions curve, the composition is 4.15 atom % sodium. The density decreases with increasing concentration of sodium. Thus, in the two-phase region the dilute bottom phase, low in sodium concentration, has a deep-blue color the light top phase, high in sodium concentration, has a metallic bronze appearance (9—13). 

Supercritical Fluid Chromatography. Supercritical fluid chromatography (sfc) combines the advantages of gc and hplc in that it allows the use of gc-type detectors when supercritical fluids are used instead of the solvents normally used in hplc. Carbon dioxide, -petane, and ammonia are common supercritical fluids (qv). For example, carbon dioxide (qv) employed at 7.38 MPa (72.9 atm) and 31.3°C has a density of 448 g/mL. 

Coppet(II) oxide [1317-38-0] CuO, is found in nature as the black triclinic tenorite [1317-92-6] or the cubic or tetrahedral paramelaconite [71276-37 ]. Commercially available copper(II) oxide is generally black and dense although a brown material of low bulk density can be prepared by decomposition of the carbonate or hydroxide at around 300°C, or by the hydrolysis of hot copper salt solutions with sodium hydroxide. The black product of commerce is most often prepared by evaporation of Cu(NH2)4C02 solutions (35) or by precipitation of copper(II) oxide from hot ammonia solutions by addition of sodium hydroxide. An extremely fine (10—20 nm) copper(II) oxide has been prepared for use as a precursor in superconductors (36). 

These effects can be attributed mainly to the inductive nature of the chlorine atoms, which reduces the electron density at position 4 and increases polarization of the 3,4-double bond. The dual reactivity of the chloropteridines has been further confirmed by the preparation of new adducts and substitution products. The addition reaction competes successfully, in a preparative sense, with the substitution reaction, if the latter is slowed down by a low temperature and a non-polar solvent. Compounds (12) and (13) react with dry ammonia in benzene at 5 °C to yield the 3,4-adducts (IS), which were shown by IR spectroscopy to contain little or none of the corresponding substitution product. The adducts decompose slowly in air and almost instantaneously in water or ethanol to give the original chloropteridine and ammonia. Certain other amines behave similarly, forming adducts which can be stored for a few days at -20 °C. Treatment of (12) and (13) in acetone with hydrogen sulfide or toluene-a-thiol gives adducts of the same type. 

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