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HYDROLYSIS (Gr. 6Swp, water, Anew, to...

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Originally appearing in Volume V14, Page 115 of the 1911 Encyclopedia Britannica.
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HYDROLYSIS (Gr. 6Swp, See also:water, Anew, to loosen)  , in See also:chemistry, a decomposition brought about by See also:water after the manner shown in the See also:equation R•X-{-H'OH=R•H+X•OH . See also:Modern See also:research' has proved that such reactions are not occasioned by water acting as See also:H2O, but really by its ions (hydrions and hydroxidions), for the velocity is proportional (in accordance with the See also:law of chemical See also:mass See also:action) to the concentration of these ions . This fact explains the so-called " catalytic " action of acids and bases in decomposing such compounds as the See also:esters . The See also:term " saponification " (See also:Lat. See also:sago, See also:soap) has the same meaning, but it is more properly restricted to the See also:hydrolysis of the fats, i.e. glyceryl esters of organic acids, into See also:glycerin and a soap (see CHEMICAL ACTION) . in small quantities to a See also:cold dilute See also:solution of the See also:acid . It is catalyst; for example, formic, glygollic, lactic, tartaric, malic, necessary that it should be as pure as possible since the commercial product usually contains traces of ferric, manganic and See also:aluminium oxides, together with some See also:silica . To purify the See also:oxide, it is dissolved in dilute hydrochloric acid until the acid is neatly neutralized, the solution is cooled, filtered, and baryta water is added until a faint permanent See also:white 'precipitate of hydrated See also:barium peroxide appears; the solution is now filtered, and a concentrated solution of baryta water is added to the filtrate, when a crystalline •precipitate of hydrated barium peroxide, BaO28•H2O, is thrown down . This is filtered off and well washed with water . The above methods give a dilute aqueous solution of See also:hydrogen peroxide, which may be concentrated somewhat by evaporation over sulphuric acid in vacua . H, P . See also:Talbot and H . R .

See also:

Moody (Jour . Anal . Chem., 1892, 6,p . 65o) prepared a more concentrated solution from the commercial product, by the addition of a 1o% solution of See also:alcohol and baryta water . The solution is filtered, and the barium precipitated by sulphuric acid . The alcohol is removed by See also:distillation in vacua, and by further concentration in vacuo a solution may be obtained which evolves 58o volumes of See also:oxygen . R . Wolffenstein (Ber., 1894, 27, p . 2307) prepared practically anhydrous hydrogen peroxide (containing 99•a% 11202) by first removing all traces of dust, heavy metals and ' See also:alkali from the commercial 3% solution . The solution is then concentrated in an open basis on the water-See also:bath until it contains 48% H202 . The liquid so obtained is extracted with See also:ether and the ethereal solution distilled under diminished pressure, and finally purified by repeated distillations . W .

Staedel (Zeit. f: avegew, Chem:, 1902, 15, p . 642) has described solid hydrogen peroxide, obtained by freezing concentrated solutions . Hydrogen peroxide is also found as 'a product in many chemical actions, being formed when See also:

carbon monoxide and See also:cyanogen See also:burn in See also:air (H . B . See also:Dixon); by passing air through solutions of strong bases in the presence of such metals as do not react with the bases to liberate hydrogen; by shaking See also:zinc See also:amalgam with alcoholic sulphuric acid and air (M . Traube, Ber., ' 1582, 1 5, p . 659); in the oxidation of zinc, See also:lead and See also:copper in presence of water, and in the See also:electrolysis of sulphuric acid of such strength that it contains two molecules of water to one See also:molecule of sulphuric acid (M . See also:Berthelot, Comptes rendus, 1878; ' 86, P . 71)• The anhydrous hydrogen peroxide obtained by Wolffenstein boils at 84-85°C . (68 mm.); its specific gravity is 1.4996 (1.5° C.) . It is very explosive (W . See also:Spring, Zeit. anorg .

Phoenix-squares

Chem.; 1895, 8, p . 424) . The See also:

explosion See also:risk seems to be most marked in the preparations which have been extracted with ether previous to distillation, and J . W . Briihl (Ber., 1895, 28, p . 2847) is of See also:opinion that a very unstable, more highly oxidized product is produced in small quantity in the See also:process . The solid variety prepared by Staedel forms colourless, prismatic crystals which melt at -2° C.; it is decomposed with explosive violence by See also:platinum sponge, and traces of See also:manganese dioxide . , The dilute aqueous solution is very unstable, giving up oxygen readily, and decomposing with explosive violence at See also:loo° C . An aqueous solution containing more than 1.5% hydrogen peroxide reacts slightly acid . To-wards lupetidin [See also:ace dimethyl piperidine, C5H9N(See also:CH3)21 hydrogen peroxide acts as a dibasic acid (A . Marcuse and R . Wolffenstein, Ber., 1901, 34, p .

2430; see also G . Bredig, Zeit . Electrochem., 1901, 7, p . 622) . Cryoscopic determinations of its molecular See also:

weight show that it is H202 . [G . See also:Carrara, Rend. See also:delta Accad . dei Lincei, 1892 (5), 1, ii. p . 19; W . R . Orndorff and J . White, Amer .

Chem . Journ., 1893, 15, p . 347.] Hydrogen peroxide behaves very frequently as a powerful oxidizing See also:

agent; thus lead sulphide is converted into lead sulphate in presence of a dilute aqueous solution of the peroxide, the hydroxides of the alkaline See also:earth metals are converted into peroxides of the type MO2BH20, See also:titanium, dioxide is converted into the trioxide, See also:iodine is liberated from See also:potassium iodide, and nitriles(in alkaline solution) are converted into acid-amides (B .

End of Article: HYDROLYSIS (Gr. 6Swp, water, Anew, to loosen)
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