Ammonia Potassium, Sodium

Alkali Ammonia Biocides Sodium hydroxide (caustic soda) Potassium hydroxide (caustic potash) Calcium oxide (lime) Calcium hydroxide Sodium, potassium and calcium carbonates Ammonia (q.v.)... 

The ethereal solution of crude quinidine and cinchonidine, obtained as described under cinchonine, is shaken with dilute hydrochloric acid, the excess acid neutralised with ammonia and sodium potassium tartrate added. The base is recovered from the precipitated tartrate by dissolving the latter in dilute acid and pouring the filtered solution in a thin stream, slowly and with constant stirring, into excess of ammonia solution. The crude alkaloid is converted into the neutral sulphate, and this recrystallised... 

Acetylene and Potassium in Liquid Ammonia Potassium (40 g) is dissolved in 1 liter of dry liquid ammonia. Dry acetylene is then bubbled into the solution until the blue color is discharged. A solution of 15 g of estrone in 300 ml of dioxane is prepared and diluted with 300 ml of ether, cooled, and added to the potassium acetylide solution over a period of 10 min. The liquid ammonia is allowed to evaporate, an additional 500 ml of ether is added, and the mixture is allowed to stand overnight. About 3 liters of 5 % sulfuric acid is added and the organic layer separated. The water layer is re-extracted with fresh ether, and the combined ether extracts are washed twice with 5 % sodium carbonate solution, th6n several times with water, and finally evaporated under reduced pressure. The residue is dissolved in 150 ml of methanol, then an equal quantity of hot water is added and the mixture cooled. The precipitated solid is collected, washed with cold 60 % methanol and crystallized once from methanol-water to give 14.8 g (85%) of 17a-ethynylestradiol mp 143-144°. 

Potassium chloride is crystallized from sea bitterns containing chlorides of potassium, sodium and calcium by ammoniation (Jagadesh etai, 1992). This process is less energy intensive and more efficient than by fractional crystallization by evaporation, as the ammonia used is recovered by distillation. Crystallization produces a better quality product in terms of both size and purity than by other methods. 

Chlorites Chloroform Ammonia, organic matter, metals Aluminum, magnesium, potassium, sodium, aluminum chloride, ethylene, powerful oxidants... 

The method described is essentially that of Pollard and Par-cell.4 N-Ethylallenimine has been prepared by treating N-(2-bromoallyl)ethylamine in liquid ammonia with sodium amide,4-6 lithium amide,6 or potassium amide.6... 

Nitric acid, Sulfuric acid, Resorcinol diacetate, Urea Nitrourea, Formaldehyde, Sodium hydroxide, Ammonia Nitroglycerin, Sodium nitrate, Nitrocellulose, Woodmeal, Potassium nitrate... 

Several tetrammino-derivatives of gold salts have been prepared. When dilute ehloraurie acid saturated with ammonium nitrate is added to a cold saturated solution of ammonium nitrate and the mixture treated with ammonia gas at ordinary temperature, a precipitate of fetrammino-auric nitrate, [Au(NH3)4](N03)3, is obtained. Tctrammino-aurie nitrate is soluble in water and may be crystallised from warm water. It may be precipitated from solution by the addition of any soluble nitrate, but with potassium, sodium, or ammonium nitrate it forms double salts. Thus, potassium nitrate if added to a concentrated solution of tetrammino-auric nitrate forms the compound [Au (NH 3).,] (NO 3)j.KNO. j, which crystallises from solution in needles. 

The bromide, [Co(NH3)5OH]Br,.H20, is prepared from the corresponding aquo-salt in the same manner as the chloride, and separates from alcohol and water as a violet powder. The iodide, [Co(NHs)5OH]I2, is obtained from the chloride by dissolving it in aqueous ammonia and adding solid potassium iodide. The dithionate, [Co(NH3)5OH]S206. H,0, obtained from the chloride by treating it with ammonia and sodium dithionate, crystallises in short red prisms or leaflets. 

H. Riesenfeld found the solubility of ammonia in soln. of sodium sulphide to be a linear function of the Na2S-conc. and they measured the ammonia press, of A-soln. of ammonia in sodium sulphide. With soln. containing 0 5, 1, and 1 5 mol. of sodium monosulphide, the respective press, of the ammonia were 15 18, 16 94, and 18 55 mm., when the press, of the ammonia in 2V-aq. soln. was 13 45 mm. According to W. P. Bloxam, potassium sulphide is stable at a low red heat and does not decompose when it is melted. P. Berthier stated that it is volatilized at high temp. When it is roasted in the air, potassium sulphide... 

According to E. Laurent,58 a soln. of sodium nitrate is decomposed in sunlight with the evolution of oxygen, while in darkness it is stable. Zinc dust reduces a soln. of potassium nitrate to the nitrite and hydroxide with the evolution of some oxygen above 60°, only a little nitrite but much nitrogen and ammonia are given off.59 The copper-zinc couple also reduces soln. of the nitrate, first to nitrite, and then to ammonia. Potassium amalgam, stannous chloride, etc., also reduce the nitrates in a similar way. 

Of the homoleptic carbonylmetallates(l -) we have attempted to reduce, [Co(CO)4] appears to be the most difficult. Although the sodium salts of [M(CO)6] (M = V, Nb, and Ta) were quickly reduced in liquid ammonia by sodium metal to provide the corresponding trianions, [M(CO)5]3 (vide supra), it seems unlikely that we have ever effected complete reduction of Na[Co(CO)4] to Na3[Co(CO)3]. Even after 2 days of refluxing (at — 33°C) anhydrous ammonia solutions of Na[Co(CO)4] with excess Na, considerable amounts of the tetracarbonylcobaltate(l —) remained. Low yields of a heterogeneous-appearing brown to olive-brown insoluble solid were isolated this solid has been shown to contain Na3[Co(CO)3] (vide infra). As in the case of [Re(CO)s], we found that solutions of potassium in liquid ammonia were far more effective at reducing [Co(CO)4]-. However, unlike [Re(CO)s], [Rh(CO)4], or [Ir(CO)4] (vide infra), there was no evidence that [Co(CO)4] was reduced by sodium or potassium metal in hexa-methylphosphoric triamide. We observed that excess sodium naphthalenide slowly (over a period of 40-50 hr at room temperature) converted Na[Co(CO)4] in THF to an impure and insoluble brown powder that contained Na3[Co(CO)3], but this synthesis appeared to be of little or no utility. 

H. M. Dawson and J. McCrae, D. P. Konowaloff, and W. Gaus also used soln. of various salts of the alkali metals, and of potassium, sodium, cupric, or barium hydroxide in place of water and also copper sulphate, copper chloride, zinc sulphate, and cadmium iodide while M. 8. Sherrill and D. E. Russ examined the effect of ammonium chromate. W. Herz and A. Kurzer examined the distribution of ammonia between water and a mixture of amyl alcohol and chloroform. Observations on the distribution of ammonia between water and chloroform were made by T. S. Moore and T. F. Winmill, G. A. Abbott and W. C. Bray, and J. M. Bell. J. H. Hildebrand gave for the molar fraction N X104 of ammonia at 1 atm. press., and 25°, dissolved by ethyl alcohol, 2300 methyl alcohol, 2730 and water, 3300. 

H. Stamm also measured the solubilities of the salts of the alkalies in liquid ammonia —potassium hydroxide, nitrate, sulphate, chromate, oxalate, perchlorate, persulphate, chloride, bromide, iodide, carbonate, and chlorate rubidium chloride, bromide, and sulphate esesium chloride, iodide, carbonate, and sulphate lithium chloride and sulphate sodium phosphate, phosphite, hypophosphite, fluoride, chloride, iodide, bromate, perchlorate, periodate, hyponitrire, nitrite, nitrate, azide, dithionate, chromate, carbonate, oxalate, benzoate, phtnalate, isophthalate ammonium, chloride, chlorate, bromide, iodide, perchlorate, sulphate, sulphite, chromate, molybdate, nitrate, dithionate, thiosulphate, persulphate, thiocyanate, phosphate, phosphite, hypophosphite, arsenate, arsenite, amidosulphonate, ferrocyanide, carbonate, benzoate, methionate, phenylacetate, picrate, salicylate, phenylpropionate, benzoldisulphonate, benzolsulphonate, phthalate, trimesmate, mellitate, aliphatic dicarboxylates, tartrate, fumarate, and maleinate and phenol. 

The ammonium theory.—In the ammonium theory of H. Davy, A. M. Ampere, and J. J. Berzelius, it was assumed. that the ammonium compounds contain a metallic radicle, NH4 (4.31,38), which may replace potassium, sodium, etc., in different salts. When ammonia unites with hydrogen chloride, the NH4-radicle is formed which unites with chlorine to form ammonium chloride in the same way that potassium united with chlorine forms potassium chloride. The ammonium theory thus corresponds with the ethyl theory of J. J. Berzelius, and J. von Liebig. The nitrogen is assumed to be quinquevalent, and this is in harmony with the work of V. Meyer and M. T. Lecco, A. Ladenburg, and W. Lossen on the quaternary ammonium baseb, and with the isomorphism of the ammonium and the potassium salts. 

Attempts by A. W. Titherley to make sodium imide, Na2NH, by the action of ammonia on sodium oxide gave sodamide, NaNH2t and water Na20+2NH3 ->2NaNH2+H20. The water at once decomposes the sodamide, forming sodium hydroxide and ammonia, but if the action be suddenly stopped some of the primary product—sodamide—can be obtained sodium oxide and sodamide do not react to any appreciable extent. Bee potassium and sodium amides for the properties. 

N. Blondlot said that red phosphorus is formed by the action of soln. of potassium, sodium, or ammonium hydroxide on ordinary phosphorus A. Commaille said that with aq. ammonia, some phosphorus hydride is formed—vide infra—and A. Stock and co-workers found that red phosphorus is produced by the aq. ammonia treatment. E. J. Houston considered the phosphorus produced by a protracted heating under potash-lye to be a special modification. B. Lepsius found that red phosphorus is formed when phosphine is decomposed by an electric arc and A. Stock and co-workers, when the solid hydride is heated in vacuo for 24 hrs. at 340°-360°. 

Copper (I) iodide is a dense, pure white solid, crystallizing with a zinc-blende structure below 300°. It is less sensitive to light than either the chloride or bromide, although passage of air over the solid at room temperature in daylight for 3 hours results in the liberation of a small amount of iodine. It melts at 588°, boils at 1,293°, and unlike the other copper halides, is not associated in the vapor state. Being extremely insoluble (0.00042 g./l. at 25°), it is not perceptibly decomposed by water. It is insoluble in dilute acids, but dissolves in aqueous solutions of ammonia, potassium iodide, potassium cyanide, and sodium thiosulfate. It is decomposed by concentrated sulfuric and nitric acids. 

Industrial poisoning. The production of silicone products uses substances harmful for human health. These are inorganic substances (ammonia, chlorine, sodium and potassium hydroxides, sulfuric and hydrochloric acids, hydrogen chloride) and organic compounds of various types, such as hydrocarbons (methane, benzene and its homologues), chlorine derivatives (methyl- and ethylchloride, chlorobenzene), alcohols (methyl, ethyl, n-butyl, hydrosite), acetone, pyridine, etc. The information about their toxicity, explosion hazard, effect on human body, as well as maximum allowable concentrations of gases and vapours in the air at workplace can be found in special references.(Ryabov 1970). A comprehensive description of silicone substances is given in Table 29. 

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