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See also:OXYGEN (See also:symbol 0, atomic See also:weight 16) , a non-metallic chemical See also:element . It was apparently first obtained in 1727 by See also:Stephen See also:Hales by strongly See also:heating minium, but he does' not seem to have recognized that he had obtained a new element, and the first published description of its properties was due to J . See also:Priestley in 1774, who obtained the See also:gas by igniting mercuric See also:oxide, and gave it the name " dephlogisticated See also:air." . K . W . See also:Scheele, working independently, also announced in 1775 the See also:discovery of this element which he called " empyreal air " (Crells' Annalen, 1785, 2, pp . 229, 291) . A . L . See also:Lavoisier repeated Priestley's experiments and named the gas " See also:oxygen " (from Gr . 6Ebs, sour, yevvhw, I produce) to denote that in a large number of cases, the products formed by the See also:combustion of substances in the gas were of an See also:acid See also:character . Oxygen occurs naturally as one of the See also:chief constituents of the See also:atmosphere, and in See also:combination with other elements it is found in very large quantities; it constitutes approximately eight-ninths by See also:weight of See also:water and nearly one-See also:half by weight of the rocks composing the See also:earth's crust . It is also disengaged by growing vegetation, See also:plants possessing the See also:power of absorbing See also:carbon dioxide, assimilating the carbon and rejecting the oxygen . Oxygen may be prepared by heating mercuric oxide; by strongly heating See also:manganese dioxide and many other peroxides; by heating the oxides of See also:precious metals; and by heating many oxy-acids and oxy-salts to high temperatures, for example, nitric acid, sulphuric acid, See also:nitre, See also:lead nitrate, See also:zinc sulphate, See also:potassium chlorate, &c . Potassium chlorate is generally used and the reaction is accelerated and carried out at a See also:lower temperature by previously mixing the See also:salt with about one-third of its weight of manganese dioxide, which acts as a catalytic See also:agent . The actual decomposition of the chlorate is not settled definitely; the following equations give the results obtained by P . F . See also:Frankland and See also:Dingwall (Chem . See also:News, 1887, 55, p . 67):—at a moderate See also:heat: 8KC103= 5KC1O4+3KC1+2O2, succeeded by the following reactions as the temperature increases: 2KC103=KC1O4+KC1+02 and 2KC103=2KC1+3O2 (see also F . Teed, ibid., 1887, 55, p . 91; H . N . See also:Warren, ibid., 1888, 58, p . 247; W . H . Sodeau, Proc . Chem . See also:Soc., 1901, 17, p . 149) . It may also be obtained by heating manganese dioxide or potassium bichromate or potassium permanganate with sulphuric acid; by the See also:action of See also:cobalt salts or manganese dioxide on a See also:solution of See also:bleaching See also:powder (Th . Fleitmann, See also:Ann., 1865, 134, p . 64); by the action of a ferrous or manganous salt with a salt of cobalt, See also:nickel or See also:copper on bleaching powder (G . F . See also:Jaubert, Ger. pat . 157171); by passing See also:chlorine into See also:milk of See also:lime (C . Winkler, Jour. prakt . Chem., 1866, 98, p . 340); by the action of chlorine on See also:steam at a See also:bright red heat; by the decomposition of See also:hydrogen peroxide by bleaching powder, manganese dioxide, potassium ferricyanide in alkaline solution, or potassium permanganate in acid solution; by heating See also:barium peroxide with an aqueous solution of potassium ferricyanide (G . Kassner, Zeit. angew . Chem., 189o, p . 448) BaO2+2K3Fe(CN)6=Ba[FeK3(CN)s]2+02; by the decomposition of See also:sodium and potassium peroxides with a solution of potassium permanganate in the presence of a trace of nickel salts (G . F . Jaubert, Comptes rendus, 1902, 134, P . 778) . Numerous methods have been devised-for the manufacture of oxygen . The more important See also:ate as follows: by decomposing strongly heated sulphuric acid in the presence of a contact substance; by heating an intimate mixture of one See also:part of sodium nitrate with two parts of zinc oxide (T . H . See also:Pepper, Dingler's Jour., 1863, 167, p . 39): 2ZnO+4NaNO3= 2Zn(ONa)2+2N2+502; by the use of cuprous chloride which when mixed with See also:clay and See also:sand, moistened with water and heated in a current of air at 100-200° C. yields an oxychloride, which latter yields oxygen when heated to 400° C (A . See also:Mallet, Comptes rendus, 1867, 64, p . 226; 1868, 66, p . 349); by the See also:electrolysis of solutions of sodium hydroxide, using nickel electrodes; by heating See also:calcium plumbate (obtained from litharge and calcium carbonate) in a current of carbon dioxide (G . Kassner, Monit . Scient., 189o, pp . 503, 614); and from air by the See also:process of Tessie du Motay (Ding . Jour., 1870,196, p . 230), in which air is See also:drawn over a heated mixture of manganese dioxide and sodium hydroxide, the sodium manganate so formed being then heated to about 450° C. in a current of steam, the following reversible reaction taking See also:place: 4NaOH+2MnOs+ 02--_42Na2MnO4+2H2O . Oxygen is largely prepared by See also:Brin's process (Mem. soc. See also:des Ingen. civ., 1881, p . 45o) in which barium monoxide is heated in a current of air, forming the dioxide, which when the retorts are exhausted yields up oxygen and leaves a See also:residue of monoxide; but this method is now being superseded, its place being taken by the fractional See also:distillation of liquid air (The Times, Engin . Suppl., See also:April 14, 1909, p . 13) as carried out by the Linde method (Eng . Pat . 14111; 1902) . Oxygen is a colourless, odourless and tasteless gas . It is somewhat heavier than air, its specific gravity being 1.10523 (A . Leduc, Comptes rendus, 1896, 123, p . 8o5) . It is slightly soluble in water and more so in See also:alcohol . It also dissolves quite readily in some molten metals, especially See also:silver . Oxygen does not See also:burn, but is the greatest supporter of combustion known, nearly all the other elements combining with it under suitable conditions (cf . OXIDE) . These reactions, however, do not take place if the substances are absolutely dry . Thus H . B . See also:Baker (Proc . Chem . Soc., 1902, 18, p . 40) has shown that perfectly dry oxygen and hydrogen will not combine even at a temperature of loco° C . It is the only gas capable of supporting respiration . For the properties of liquid oxygen see LIQUID GASES . It is found, more especially in the See also:case of organic compounds, that if a substance which oxidizes readily at See also:ordinary temperature be mixed with another which is not capable of such oxidation, then both are oxidized simultaneously, the amount of oxygen used being shared equally between them; or in some cases when the substance is spontaneously oxidized an See also:equivalent amount of oxygen is converted into See also:ozone or hydrogen peroxide . This phenomenon was first noticed by C . F . See also:Schonbein (Jour. prakt . Chem., 1858–1868), who found that on oxidizing lead in the presence of sulphuric acid, the same quantity of oxygen is used to See also:form lead oxide as is converted into hydrogen peroxide . In a similar manner M . Traube (Ber., 1882–1893) found that when zinc is oxidized in presence of water equivalent quantities of zinc hydroxide and hydrogen peroxide are formed at first, thus: Zn+See also:H2O+02=ZnO+H2O2, followed by ZnO+H2O=Zn(OH)i,Zn+H202=Zn(OH)2 . The oxygen uniting with the substance undergoing oxidation is generally known as See also:bound oxygen," whilst that which is transformed into ozone or hydrogen peroxide is usually called " active oxygen." C . Engler (Ber., 1897, 3o, p . 1669) calls the substance which undergoes oxidation the " autoxidizer " and the substance which unites with the active oxygen the " acceptor "; in the oxidation of metals he expresses results as: M+02=MO2, followed by MO2–~M•O+O, and if water be See also:present, O+H2O = H2O2 . Various theories have been See also:developed in See also:order to See also:account for these phenomena . Schonbein (loc. cit.) assumed that the ordinary oxygen See also:molecule is decomposed into two parts which carry See also:electrical charges of opposite kinds, the one with the See also:positive See also:charge being called " antozone " and the other carrying the negative charge being called " ozone," one variety being preferentially used up by the oxidizing See also:compound or element and the other for the secondary reaction . J . H . See also:Van't Hoff (Zeit. phys . Chem., 1895, 16, p . 411) is of the See also:opinion that the oxygen molecule is to a certain extent ionized and that the ions of one See also:kind are preferably used by the oxidizing compound . Traube (loc. cit.), on the other See also:hand, concludes that the oxygen molecule enters into action as a whole and that on the oxidation of metals, hydrogen peroxide and the oxide of the See also:metal are the See also:primary products of the reaction . A . See also:Bach (Comptes rendus, 1897, 124, p . 2) considers that the first See also:stage in the reaction consists in the See also:production of a peroxide which then interacts with water to form hydrogen peroxide (see also W . Manchot, Ann., 1901, 314, p . 177; 1902, 325, p . 95) . Oxygen is a member of the See also:sixth See also:group in the periodic See also:classification, and consequently possesses a maximum See also:valency of six . In most cases it behaves as a divalent element, but it may also be quadrivalent . A. v . See also:Baeyer and V . Villiger (Ber., 1901, 34, pp . 2679, 3612) showed that many organic compounds (See also:ethers, See also:alcohols, See also:aldehydes, See also:ketones, &c.) behave towards acids, particularly the more complex acids, very much like bases and yield crystallized salts in which quadrivalent oxygen must be assumed as the basic element . These salts are considered to be derived from the hypothetical See also:base OH3.OH, oxonium, hydroxide (compare sulphonium salts) . Further see J . See also:Schmidt, " Ober See also:die basischen Eigenschaften des Sauerstoffs " (See also:Berlin, 1904) . Baeyer and Villiger assume for the configuration of the salts of carbonyl compounds the arrangement > C : 0 <1c, whilst J . W . See also:Bruhl and P . W . See also:Walden point out from the physico-chemical standpoint that in water and hydrogen peroxide the oxygen See also:atom is probably quadrivalent . The atomic weight of oxygen is now generally taken as 16, and as such is used as the See also:standard by which the atomic weights of the other elements are determined, owing to the fact that most elements combine with oxygen more readily than with hydrogen (see ELEMENT) . Oxygen is widely used in medical practice as well as in See also:surgery . Inhalations of the gas are of service in See also:pneumonia, See also:bronchitis, See also:heart disease, See also:asthma, angina and other conditions accompanied by cyanosis and dyspnoea . They often avert See also:death from See also:asphyxia, or render the end less distressing . Oxygen is also administered in See also:chloroform poisoning, and in threatened death from the inhalation of See also:coal gas or nitrous oxides . It is of value in See also:cyanide and See also:opium poisoning and in the resuscitation of the apparently drowned . The mode of See also:administration is by an inhaler attached to an inhalation bag, which serves to break the force with which the oxygen issues from the cylinders in which it is sold in a compressed form . It can be administered pure or mixed with air as required . If given in too See also:great quantity a temporary See also:condition of See also:apnoea (cessation of breathing) is produced, the See also:blood being fully charged with the gas . Oxygen may be applied locally as a disinfectant to foul and diseased surfaces by the use of the peroxide of hydrogen, which readily parts with its oxygen; a solution of hydrogen peroxide therefore forms a valuable spray in See also:diphtheria, See also:tonsillitis, laryngeal See also:tuberculosis and ozaena . It can also be used with See also:advantage in inoperable uterine See also:cancer, See also:favus and See also:lupus, and as an injection in gonorrhoea and suppurative conditions of the See also:ear . It relieves the See also:pain of See also:wasp and See also:bee stings . Internally hydrogen peroxide is used in various diseased conditions of the gastro-intestinal See also:tract, such as See also:dyspepsia, See also:diarrhoea and enteric See also:fever . The B.P. preparation Liquor Hydrogenii Peroxidi dose z to 2 drs. is synonymous with the Aqua Hydrogenii Dioxidi of the U.S.P. and the ten-See also:volume solution termed eau oxygenee in See also:France . It is customary to use oxygen in combination with chlorofarm, or nitrous oxide in order to produce insensibility to pain (see ANAESTHETICS) . |
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