Applications sodium hydroxide

United States goes to this application. Sodium hydroxide is also an important raw material in the manufacture of soap. The method by which soap is made has not changed very much for thousands of years. A fat or oil is added to a boiling solution of sodium hydroxide in water. The fat or oil hydrolyzes into its component parts, glycerol and fatty acids. The sodium hydroxide then reacts with the fatty acids, forming sodium salts. The sodium salt of a fatty acid is a soap. Sodium hydroxide is also an important raw material in the manufacture of inorganic compounds, especially sodium and calcium hypochlorite, sodium cyanide, and a number of sulfur-containing compounds. Some other important uses of sodium hydroxide include ... 

Silver oxide-zinc cells are often specified for electronic watch applications. Sodium hydroxide electrolyte, which has a lower conductivity than potassium hydroxide, is often used because it has a lower tendency to creep at the seal. The separator in the silver oxide system must retain soluble silver species produced by chemical dissolution of the oxide, and a multiple layer separator of low-porosity film achieves this. 

In general, benzoylation of aromatic amines finds less application than acetylation in preparative work, but the process is often employed for the identification and characterisation of aromatic amines (and also of hydroxy compounds). Benzoyl chloride (Section IV, 185) is the reagent commonly used. This reagent is so slowly hydrolysed by water that benzoylation can be carried out in an aqueous medium. In the Schotten-Baumann method of benzoylation the amino compound or its salt is dissolved or suspended in a slight excess of 8-15 per cent, sodium hydroxide solution, a small excess (about 10-15 per cent, more than the theoretical quantity) of benzoyl chloride is then added and the mixture vigorously shaken in a stoppered vessel (or else the mixture is stirred mechanically). Benzoylation proceeds smoothly and the sparingly soluble benzoyl derivative usually separates as a solid. The sodium hydroxide hydrolyses the excess of benzoyl chloride, yielding sodium benzoate and sodium chloride, which remain in solution ... 

Oximes (compare Section III,74,B). The following procedure has wide application. Dissolve 0-5 g. of hydroxylamine hydrochloride in 2 ml. of water, add 2 ml. of 10 per cent, sodium hydroxide solution and 0-2 g. of the aldehyde (or ketone). If the latter is insoluble, add just sufficient alcohol to the mixture to give a clear solution. Heat the mixture under reflux for 10-15 minutes, and then cool in ice. If crystals separate, filter these off, and recrystallise from alcohol, dilute alcohol, benzene or light petroleum (b.p. 60-80°). If no solid separates on cooling, dilute with 2-3 volumes of water, filter the precipitated sohd, and recrystallise. 

Compound 1, 2,2-diniethyl-4-pentenal, has been prepared by the Claisen rearrangement route described above and by reaction of isobutyraldehyde with allyl chloride in the presence of aqueous sodium hydroxide and a phase-transfer catalyst. Both routes are applicable to the synthesis of a variety of substituted 4-pentenals. 

Sodium hydroxide. Properties and applications are similar to those for potassium... 

Other industrial applications of electrolysis include extraction/purification of metals from ores, electroplating, and the manufacture of certain chemicals such as sodium hydroxide. In the latter, sodium chloride solution when electrolysed is converted to sodium hydroxide to produce chlorine at the anode and hydrogen at the cathode. Both of these gaseous by-products are collected for industrial use chlorine is used in the production of bleach and PVC hydrogen is used as a fuel, to saturate fats, and to make ammonia. 

Resoles are usually those phenolics made under alkaline conditions with an excess of aldehyde. The name denotes a phenol alcohol, which is the dominant species in most resoles. The most common catalyst is sodium hydroxide, though lithium, potassium, magnesium, calcium, strontium, and barium hydroxides or oxides are also frequently used. Amine catalysis is also common. Occasionally, a Lewis acid salt, such as zinc acetate or tin chloride will be used to achieve some special property. Due to inclusion of excess aldehyde, resoles are capable of curing without addition of methylene donors. Although cure accelerators are available, it is common to cure resoles by application of heat alone. 

The development of electrical power made possible the electrochemical industry. Electrolysis of sodium chloride produces chlorine and either sodium hydroxide (from NaCl in solution) or metallic sodium (from NaCl fused). Sodium hydroxide has applications similar to sodium carbonate. The ad vantage of the electrolytic process is the production of chlorine which has many uses such as production of polyvinyl chloride. PVC, for plumbing, is produced in the largest quantity of any plastic. 

This formula was confirmed hy Haworth and Perkin s synthesis of a-flZZocryptopine from herherine, the first application of a process, of which examples have heen given already in the syntheses of cryptopine (p. 298) and protopine (p. 301) hy the same authors. Anhydrotetrahydromethyl-herherine (I cf. hase (a), p. 346) in dry chloroform was added to a solution of perhenzoic acid in ether cooled helow 5°. The amine oxide, C21H23O5N (II), separated as an oil, which after shaking with sodium hydroxide solution, solidified and was crystallised from water in slender prisms, m.p. 135°. It was dissolved in acetic acid, hydrochloric acid added, the mixture heated in boiling water for an hour and the hase precipitated hy addition of potassium hydroxide. The precipitate was dissolved in methyl alcohol, ether added, the alcohol washed out with water and the ethereal... 

Deuterioboration of 5a-cholest-2-ene (171), followed by oxidation of the alkylborane intermediate with hydrogen peroxide in the presence of sodium hydroxide, illustrates the application of this method for the preparation of c/5-deuterium labeled alcohols.(For the preparation of tra 5 -deuterium labeled alcohols see section VII-A.) The predominant reaction product is 2a-di-5a-cholestan-3a-ol (172, 1.03 D/mole) which is accompanied by 3a-di-5a-cholestan-2a-ol (173) and other minor products." ... 

Isotope labeling by derivative formation with deuterated reagents is useful for the preparation of analogs such as dg-acetonides, da-acetates, da-methyl ethers, dg-methyl esters, etc. The required reagents are either commercially available or can be easily prepared. (The preparation of da-methyl iodide is described in section IX-F. Various procedures are reported in the literature for the preparation of dg-acetone, da-diazometh-ane57.i63.i73 and da-acetyl chloride. ) These reactions can be carried out under the usual conditions and they need no further discussion. A convenient procedure has been reported for the da-methylation of sterically hindered or hydrogen bonded phenolic hydroxyl functions by using da-methyl iodide and sodium hydroxide in dimethyl sulfoxide solution. This procedure should be equally applicable to the preparation of estradiol da-methyl ether derivatives. 

A mixture of 200 parts of p-chlorophenol, 1,000 parts of acetone and 360 parts of sodium hydroxide pellets is heated under reflux and 240 parts of chloroform are gradually added at such a rate that the mixture continues to reflux without further application of heat. 

A mixture of 198 grams of 2,4,5-trichlorophenol and 1B.B grams of paraformaldehyde was heated to 65°C and well stirred. 65 grams of oleum 20% was added dropwise and the addition was So regulated that the temperature increased, without the application of external heat, until it reached 135°C at the end of the acid addition, which took 10 to 15 minutes. The contents of the reaction vessel were stirred for 2 minutes more and then allowed to run into a solution of 100 grams of sodium hydroxide in 1,000 cc of water. 

While a metal or alloy may be selected largely on the basis of its mechanical or physical properties, the fact remains that there are very few applications where the effect of the interaction of a metal with its environment can be completely ignored, although the importance of this interaction will be of varying significance according to circumstances for example, the slow uniform wastage of steel of massive cross section (such as railway lines or sleepers) is of far less importance than the rapid perforation of a buried steel pipe or the sudden failure of a vital stressed steel component in sodium hydroxide solution. 

The theoretical aspects of molybdenum s corrosion behaviour are complex and there is as yet no clear cut, generally applicable picture. There are, however, a large number of literature references which include data on polarisation, passivation and potential of molybdenum under widely assorted conditions. The electrode potential of molybdenum depends on its surface condition. For example, some tests showed an of -t-0-66V when the molybdenum was passivated by treatment with concentrated chromic acid and —0-74 V after activation by cathodic treatment in sodium hydroxide. 

Niobium like tantalum relies for its corrosion resistance on a highly adherent passive oxide film it is however not as resistant as tantalum in the more aggressive media. In no case reported in the literature is niobium inert to corrosives that attack tantalum. Niobium has not therefore been used extensively for corrosion resistant applications and little information is available on its performance in service conditions. It is more susceptible than tantalum to embrittlement by hydrogen and to corrosion by many aqueous corrodants. Although it is possible to prevent hydrogen embrittlement of niobium under some conditions by contacting it with platinum the method does not seem to be broadly effective. Niobium is attacked at room temperature by hydrofluoric acid and at 100°C by concentrated hydrochloric, sulphuric and phosphoric acids. It is embrittled by sodium hydroxide presumably as the result of hydrogen absorption and it is not suited for use with sodium sulphide. 

The trend in architectural applications has been towards more matt finishes, and the sodium hydroxide-based etchants used frequently contain additives such as sodium nitrate or nitrite or sodium fluoride. Chelating agents such as gluconates, heptonates or sorbitol are added to complex the aluminium produced, and other additives such as sulphides may be present in the etchant to complex zinc dissolved from the alloy, and allow it to be used continuously without dumping ... 

The theory of titrations between weak acids and strong bases is dealt with in Section 10.13, and is usually applicable to both monoprotic and polyprotic acids (Section 10.16). But for determinations carried out in aqueous solutions it is not normally possible to differentiate easily between the end points for the individual carboxylic acid groups in diprotic acids, such as succinic acid, as the dissociation constants are too close together. In these cases the end points for titrations with sodium hydroxide correspond to neutralisation of all the acidic groups. As some organic acids can be obtained in very high states of purity, sufficiently sharp end points can be obtained to justify their use as standards, e.g. benzoic acid and succinic acid (Section 10.28). The titration procedure described in this section can be used to determine the relative molecular mass (R.M.M.) of a pure carboxylic acid (if the number of acidic groups is known) or the purity of an acid of known R.M.M. 

An interesting application of these results is to the direct quantitative separation of copper and cadmium. The copper is first deposited in acid solution the solution is then made slightly alkaline with pure aqueous sodium hydroxide, potassium cyanide is added until the initial precipitate just re-dissolves, and the cadmium is deposited electrolytically. 

Both hot and cold processes are employed, although the hot process, which takes place at or above 212 °F (100 °C), is usually preferred for boiler FW applications, because it produces water of lower hardness levels and usually a lower silica content as well. Also, less lime is needed because the carbon dioxide with which it would normally react is driven off at the higher temperatures. Sometimes caustic soda (sodium hydroxide) is used in place of soda, depending on the alkalinity of the water and the chemical costs however, irrespective of the process or chemicals used, the major precipitants are always calcium carbonate and magnesium hydroxide. 

Alkalinity boost chemistries typically are based on adjunct products containing primarily potassium hydroxide (for maximum solubility) or sodium hydroxide (for lowest cost), although sodium carbonate is still used in certain limited applications. These adjuncts may also contain (in almost any combination) smaller percentages of tannins, sodium ligonsulfonate, phosphate or polymers. 

In the case of carbamate pesticides the chromatogram is heated to 150 °C for 20 min after the application of the reagent. Spraying later with a solution of 2 N sodium hydroxide solution to improve the color contrast is recommended [15]. Occasionally a small amount of iron(III) chloride is added to the reagent [13]. 

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