Ammonium chloride solubility

Aqueous ammonia can also behave as a weak base giving hydroxide ions in solution. However, addition of aqueous ammonia to a solution of a cation which normally forms an insoluble hydroxide may not always precipitate the latter, because (a) the ammonia may form a complex ammine with the cation and (b) because the concentration of hydroxide ions available in aqueous ammonia may be insufficient to exceed the solubility product of the cation hydroxide. Effects (a) and (b) may operate simultaneously. The hydroxyl ion concentration of aqueous ammonia can be further reduced by the addition of ammonium chloride hence this mixture can be used to precipitate the hydroxides of, for example, aluminium and chrom-ium(III) but not nickel(II) or cobalt(II). 

Caution.—If the ethanol used to extract the methylamine hydrochloride is not absolute, i.e., if it contains traces of water, considerably less than the above suggested quantity will be required for the extraction, because the solubility of the hydrochloride will be markedly increased by the water present. The recrystallised material will now, however, contain traces of ammonium chloride. 

Dilute hydrochloric or sulphuric acid finds application in the extraction of basic substances from mixtures or in the removal of basic impurities. The dilute acid converts the base e.g., ammonia, amines, etc.) into a water-soluble salt e.g., ammonium chloride, amine hydrochloride). Thus traces of aniline may be separated from impure acetanilide by shaking with dilute hydrochloric acid the aniline is converted into the soluble salt (aniline hydrochloride) whilst the acetanilide remains unaffected. 

The absence of ammonium chloride and methylamine hydrochloride may be shown by the complete solubility of the product in chloroform. 

Footnote 4 - The solubility of Ammonium Chloride in absolute Ethanol is 0.6g/100g at 15C. The solubility in n-Butyl Alcohol is neglible, even at its boiling point. If you use n-Butyl Alcohol, you will only need to perform 3 reflux/filter operations to obtain sufficiently pure Methylamine Hydrochloride. 

Dilead hexacyanokisferrate [14402-61 -0] Pb2[Fe(CN)g], is a white precipitate that forms when lead acetate is added to Ca2[Fe(CN)g]. It is insoluble in water or dilute acids but is soluble in hot ammonium chloride or ammonium succinate solutions. It has been used as a quaUtative analytical reagent in tests for cadmium and chromate. 

Several commercial grades are available fine crystals of 99 to 100% purity, large crystals, pressed lumps, rods, and granular material. Double-Decomposition Methods. Double-decomposition processes all iavolve the reaction of sodium chloride, the cheapest chlorine source, with an ammonium salt. The latter may be suppHed directiy, or generated in situ by the reaction of ammonia and a supplementary iagredient. Ammonium chloride and a sodium salt are formed. The sodium salt is typically less soluble and is separated at higher temperatures ammonium chloride is recovered from the filtrate by cooling. 

Some polymers from styrene derivatives seem to meet specific market demands and to have the potential to become commercially significant materials. For example, monomeric chlorostyrene is useful in glass-reinforced polyester recipes because it polymerizes several times as fast as styrene (61). Poly(sodium styrenesulfonate) [9003-59-2] a versatile water-soluble polymer, is used in water-poUution control and as a general flocculant (see Water, INDUSTRIAL WATER TREATMENT FLOCCULATING AGENTs) (63,64). Poly(vinylhenzyl ammonium chloride) [70304-37-9] h.a.s been useful as an electroconductive resin (see Electrically conductive polya rs) (65). 

Precipitated or synthetic barium carbonate is the most commercially important of all the barium chemicals except for barite. Barium carbonate is an unusually dense material, that is almost kisoluble ki water and only slightly soluble ki carbonated water. It does dissolve ki dilute hydrochloric, nitric, and acetic acids and is also soluble ki ammonium nitrate and ammonium chloride solutions. 

CeOCl. The anhydrous cerous chloride [7790-86-5] can be made from the hydrated salt by suppressing oxyhahde formation during thermal dehydration by the presence of hydrogen chloride or ammonium chloride. The anhydrous salt is soluble in a variety of organic solvents, eg, alcohols and ethers, has mp 817°C, and can be volatilized at high temperatures in vacuum. 

Liquid-phase chlorination of butadiene in hydroxyhc or other polar solvents can be quite compHcated in kinetics and lead to extensive formation of by-products that involve the solvent. In nonpolar solvents the reaction can be either free radical or polar in nature (20). The free-radical process results in excessive losses to tetrachlorobutanes if near-stoichiometric ratios of reactants ate used or polymer if excess of butadiene is used. The "ionic" reaction, if a small amount of air is used to inhibit free radicals, can be quite slow in a highly purified system but is accelerated by small traces of practically any polar impurity. Pyridine, dipolar aptotic solvents, and oil-soluble ammonium chlorides have been used to improve the reaction (21). As a commercial process, the use of a solvent requites that the products must be separated from solvent as well as from each other and the excess butadiene which is used, but high yields of the desired products can be obtained without formation of polymer at higher butadiene to chlorine ratio. 

Ammonium cyanide may be prepared in solution by passing hydrogen cyanide into aqueous ammonia at low temperatures. It may also be prepared from barium cyanide and ammonium sulfate, or calcium cyanide with ammonium carbonate. It may be prepared in the dry state by gentiy heating a mixture of potassium cyanide or ferrocyanide and ammonium chloride, and condensing the vapor in a cooled receiver. Ammonium cyanide is soluble in water or alcohol. The vapor above soHd NH CN contains free NH and HCN, a very toxic mixture. 

Solid particulates are captured as readily as hquids in fiber beds but can rapidly plug the bed if they are insoluble. Fiber beds have frequently been used for mixtures of liqmds and soluble sohds and with soluble solids in condensing situations. Sufficient solvent (usually water) is atomized into the gas stream entering the collector to irrigate the fiber elements and dissolve the collected particulate. Such nber beds have been used to collect fine fumes such as ammonium nitrate and ammonium chloride smokes, and oil mists from compressed air. 

The entire amount of the ammonium chloride-mandelic acid mixture may be boiled with the benzene but this gives a supersaturated solution of the acid in the benzene and much difficulty is met in the filtration. The solubility of mandelic acid in hot benzene is approximately i g. in 50 cc. 

O-Acetyl-p-methylcholine chloride [Methacholine chloride, Amechol, Provocholine, 2-acetoxypropyl-ammonium chloride] [62-51-1] M 195.7, m 170-173", 172-173". It forms white hygroscopic needles from Et20 and is soluble in H2O, EtOH and CHCI3. It decomposes readily in alkaline solns and slowly in H2O. It should be handled and stored in a dry atmosphere. The bromide is less... 

Ammonium chloride solutions are slightly acidic, so they are better solvents than water for insoluble hydroxides such as Mg(OH)2. Find the solubility of Mg(OH)2 in moles per liter in 0.2 M NH4CI and compare with the solubility in water. Hint Find K for the reaction... 

Rh(N02)6 is of some importance in the traditional extraction of rhodium. Impure RI1CI3 is neutralized and treated with NaN02 Na3Rh(N02)6 is soluble under these conditions (though base metals precipitate), but when ammonium chloride is added, (NH4)3Rh(N02)6 precipitates. The potassium salt is similarly relatively insoluble. All these salts are believed... 

Ammonium chloride passes into solution with increase of total volume, and hence its solubility should be diminished by increase of pressure. Sodium chloride, on the contrary, dissolves with contraction, and its solubility should be increased by rise of pressure. Above 1,530 atm., however, the latter salt dissolves with expansion, and its solubility then decreases with pressure. These deductions from the equation have been confirmed. 

The efficient hydrogenation of various benzene compounds in biphasic systems has also been described by similar surfactant-protected irid-ium(O) nanoparticles [47]. The solubility of the nanoparticles was assured by 10 equivalents of water-soluble N,N-dimethyl-N-cetyl-Ar-(2-hydroxyethyl)-ammonium chloride salt. TEM observations show that the particles are monodispersed in size with an average diameter of 1.9 0.7 nm (Fig. 7). 

These compounds should be dissolvable in a clean-up solution containing a quaternary organic ammonium salt, or simply ammonium chloride [1749]. The solubilities of some selected particulate bridging agents are shown in Table 9-1. A chelating agent such as citric acid or its salts is also included in the clean-up solution. 

A terpolymer can be obtained from a water-soluble nonionic monomer, such as acrylamide a cationic monomer, such as 3-acrylamidopropyltrimethyl ammonium chloride and a hydrophobic monomer, such as an alkyl-acrylamide... 

Ammonium chloride is soluble in water (see the solubility rules on page 116). Therefore, the concentration NH4+ and that of Cl are both 0.20 M. 

The temperature dependences of solubilities of the trichlorides of lanthanum, praseodymium, and neodymium in aqueous ammonium chloride solutions (212) are so irregular that no estimate of solution enthalpies can be made from them by the van t Hoff method. 

Addition of ammonium chloride increases the solubility of SmCl3, ErCl3, and TmCl3 in HMPA (159). 

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