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SULPHUR

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Originally appearing in Volume V26, Page 65 of the 1911 Encyclopedia Britannica.
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SULPHUR  [See also:

symbol S, atomic See also:weight 32•o7 (0=16)1, a non-metallic chemical See also:element, known from very remote times and regarded by the alchemists, on See also:account of its inflammable nature, as the principle of See also:combustion; it is also known as See also:brimstone (q.v.) . The element occurs widely and abundantly distributed in nature both in the See also:free See also:state and in See also:combination . Free or native sulphur, known also as " virgin sulphur," occurs in connexion with volcanoes and in certain stratified rocks in several modes, viz. as crystals, and as stalactitic, encrusting, reniform, massive, earthy and occasionally pulverulent forms as " sulphur See also:meal." It seems rather doubtful whether the unstable See also:monoclinic modification of sulphur (0–sulphur) is ever found in a native state . The crystals belong to the orthorhombic See also:system, and have usually a pyramidal See also:habit (fig.), but may be sphenoidal or See also:tabular . Twins are rare . The cleavage is imperfect, but there is a well-marked conchoidal fracture . The hardness ranges from about I to 2, and the sp.gr. from 1.9 to 2.1 . Crystals of sulphur are transparent or translucent and highly refractive with strong birefringence; they have a resinous or slightly adamantine lustre, and See also:present the characteristic sulphur-yellow See also:colour . Impurities render the See also:mineral See also:grey, greenish or red-dish, bituminous See also:matter being often present in the massive varieties . Sulphur containing See also:selenium, such as occurs in the isle of Vulcano in the Lipari Isles, may be See also:orange-red; and a similar colour is seen in sulphur which contains See also:arsenic sulphide, such as that from La See also:Solfatara near See also:Naples . The presence of See also:tellurium in native sulphur is rare, but is known in certain specimens from See also:Japan . Volcanic sulphur usually occurs as a sublimate around or on the walls of the vents, and has probably been formed in many cases by the interaction of sulphur dioxide and See also:hydrogen sulphide .

Sub-limed sulphur also results from the spontaneous combustion of See also:

coal seams containing See also:pyrites . Deposits of sulphur are frequently formed by the decomposition of hydrogen sulphide, on exposure to the See also:atmosphere: hence natural sulphureous See also:waters, especially hot springs, readily See also:deposit sulphur . The reduction of sulphates to sulphides by means of organic matter, probably through the agency of sulphur-bacteria, may also indirectly furnish sulphur, and hence it is frequently found in deposits of See also:gypsum . Free sulphur may also result from the decomposition of pyrites, as in pyritic shales and lignites, or from the alteration of See also:galena: thus crystals of sulphur occur, with anglesite, in cavities in galena at Monteponi near See also:Iglesias in See also:Sardinia; whilst the pyrites of Rio Tinto in See also:Spain sometimes yield sulphur on weathering . It should be noted that the oxidation of sulphur itself by atmospheric See also:influence may give rise to sulphuric See also:acid, which in the presence of See also:limestone will See also:form gypsum: thus the sulphur-deposits of See also:Sicily suffer alteration of this See also:kind, and have their outcrop marked by a See also:pale earthy gypseous See also:rock called briscale . Some of the most important deposits of sulphur in the See also:world are worked in Sicily, chiefly in the provinces of See also:Caltanisetta and See also:Girgenti, as at Racalmuto and Cattolica; and to a less extent in the provinces of See also:Catania, See also:Palermo (Lercara) and See also:Trapani (Gibellina) . The sulphur occurs in See also:Miocene marls and limestone, associated with gypsum, See also:celestine, See also:aragonite and See also:calcite . It was formerly believed that the sulphur had a volcanic origin, but it is now generally held that it has eitherbeen reduced from gypsum by organic agencies, or more probably deposited from sulphur-bearing waters . Liquid occasion-ally enclosed in the sulphur and gypsum has been found by O . Silvestri and by C . A . H .

Sjogren to contain salts like those of sulphur-springs . An important See also:

zone of sulphur-bearing Miocene rocks occurs on the See also:east See also:side of the See also:Apennines, constituting a See also:great See also:part of the See also:province of Forli and part of See also:Pesaro . See also:Cesena and Perticara are well-known localities in this See also:district, the latter yielding crystals coated with See also:asphalt . Sulphur is occasionally found crystallized in See also:Carrara See also:marble; and the mineral occurs also in See also:Calabria . See also:Fine crystals occur at Conil near See also:Cadiz; whilst in the province of See also:Teruel in See also:Aragon, sulphur in a compact form replaces fresh-See also:water shells and plant-remains, suggesting its origin from sulphur-springs . Nodular forms of sulphur occur in Miocene marls near Radoboj in Croatia, and near Swoszowic, See also:south of See also:Cracow . See also:Russia possesses large deposits of sulphur in See also:Daghestan in See also:Transcaucasia, and in the Transcaspian See also:steppes . Important deposits of sulphur are worked at several localities in Japan, especially at the Kosaka mine in the province of Rikuchiu, and at Yatsukoda-See also:yama, in the province of See also:Mutsu . Sulphur is worked in See also:Chile and See also:Peru . A See also:complete See also:list of localities for sulphur would include all the volcanic regions of the world . In the See also:United States, sulphur occurs in the following states, in many of which the mineral has been worked: See also:Louisiana (q.v.), See also:Utah, See also:Colorado, See also:California, See also:Nevada, See also:Alaska, See also:Ida-ho, See also:Texas and See also:Wyoming . The See also:Rabbit Hole sulphur-mines are in Nevada, and a great deposit in Utah occurs at See also:Cove See also:Creek, See also:Beaver See also:county .

In the See also:

British Islands native sulphur is only a mineralogical rarity, but it occurs in the Carboniferous Limestone of Oughterard in Co . See also:Galway, See also:Ireland.' In combination the element chiefly occurs as metallic sulphides and sulphates . The former are of great commercial importance, being, in most cases, valuable ores, e.g. See also:copper pyrites (copper), galena (See also:lead), See also:blende (See also:zinc), See also:cinnabar (See also:mercury), &c . Of the sulphates we See also:notice gypsum and See also:anhydrite (See also:calcium), See also:barytes (See also:barium) and kieserite (See also:magnesium) . Gaseous compounds, e.g. sulphur dioxide and sulphuretted hydrogen, are present in volcanic exhalations (see See also:VOLCANO) and in many mineral waters . The element also occurs in the See also:animal and See also:vegetable kingdoms . It is present in See also:hair and See also:wool, and ,in albuminous bodies; and is also a constituent of certain vegetable See also:oils, such as the oils of See also:garlic and See also:mustard . There is, in addition, a See also:series of bacteria which decompose sulphureous compounds and utilize the element thus liberated in their See also:protoplasm (see See also:BACTERIOLOGY) . Extraction.—As quarried or See also:mined free sulphur is always contaminated with limestone, gypsum, See also:clay, &c.; the principle underlying its extraction from these impurities is one of See also:simple liquation, i.e. the element is melted, either by the See also:heat of its own combustion or other means, and runs off from the earthy See also:residue . In the simplest and crudest method, as practised in Sicily, a See also:mass of the ore is placed in a hole in the ground and fired; after a See also:time the heat melts a part of the sulphur which runs down to the bottom of the hole and is then ladled out . This exceptionally wasteful See also:process, in which only one-third of the sulphur is recovered, has been improved by conducting the See also:fusion in a sort of See also:kiln . A semicircular or semi-elliptical See also:pit (calcarone) about 33 ft. in See also:diameter and 8 ft. deep is dug into the slope of a See also:hill, and the sides are coated with a See also:wall of See also:stone .

The See also:

sole consists of two halves slanting against each other, the See also:line of intersection forming a descending See also:gutter which runs to the outlet . This outlet having been closed by small stones and sulphate of See also:lime See also:cement, the pit is filled with sulphur ore, which is heaped up considerably beyond the edge of the pit and covered with a layer of burnt-out ore . In See also:building up the heap a number of narrow See also:vertical passages are See also:left to afford a See also:draught for the See also:fire . The ore is kindled from above and the fire so regulated (by making or unmaking See also:air-holes in the covering) that, by the heat produced 1 References.—A very full See also:article (" Zolfo ") by G . Aichino, of the See also:Geological Survey of See also:Italy, will be found in the Enciclopedia delle erte e industrie (See also:Turin, 1898) . This includes a full bibliography . See also J . F . See also:Kemp in See also:Rothwell's Mineral See also:Industry (1893), vol. ii.; Jules Brunfaut, De l'Exploitation See also:des soufres (2nd ed., 1874) ; Georgio See also:Spezia, Sull' origine del solfo See also:nei giacementi solfiferi della Sicilia (Turin, 1892) . For See also:Japanese sulphur see T . Wada, Minerals of Japan (See also:Tokyo, 1904) . by the combustion of the least sufficient quantity of sulphur, the See also:rest is liquefied .

The molten sulphur accumulates on the sole, whence it is from time to time run out into a square stone receptacle, from which it is ladled into See also:

damp See also:poplar-See also:wood moulds and so brought into the shape of truncated cones weighing See also:Ito to 130 lb each . These cakes are sent out into See also:commerce . A calcarone with a capacity of 28,256 cub. ft. See also:burns for about two months, and yields about 200 tons of sulphur . The yield is about 50% . The immense volumes of sulphurous acid evolved give rise to many complaints; all the See also:minor pits suspend See also:work during the summer to avoid destruction of the crops . A calcarone that is to be used all the See also:year See also:round must be at least 220 yds. from any inhabited See also:place and i t_o yds. from any See also:field under cultivation . More efficient is the Gill kiln which uses See also:coke as a See also:fuel . The kiln consists of two (or more) connected cells which are both charged with the ore . The first See also:cell is heated and the products of combustion are led into the second cell where they give up part of their heat to the contained ore, so that by the time the first cell is exhausted the mass in the second cell is at a sufficiently high temperature to ignite spontaneously when air is admitted . Other methods have been employed, but with varying commercial success . For example, in the Gritti and Orlando processes the ore is charged into retorts and the fusion effected by superheated See also:steam, the sulphur being run off as usual; or as was suggested by R . E .

Bollman in 1867 the ore may be extracted by See also:

carbon bisulphide . Crude sulphur, as obtained from kilns, contains about 3% of earthy impurities, and consequently needs refining . The following apparatus (invented originally by See also:Michel of See also:Marseilles and improved subsequently by others) enables the manufacturer to produce either of two forms of " refined " sulphur which commerce demands . It consists of a large stone chamber which communicates directly with two slightly slanting tubular retorts of See also:iron . The retorts are charged with molten sulphur from an upper See also:reservoir, which is kept at the requisite temperature by means of the lost heat of the See also:retort fires . The chamber has a safety value at the See also:top of its vault, which is so balanced that the least surplus pressure from within sends it up . The first puff of sulphur vapour which enters the chamber takes fire and converts the air of the chamber into a mixture of See also:nitrogen and sulphur dioxide . The next following instalments of vapour, getting diffused throughout a large mass of relatively See also:cold See also:gas, condense into a kind of " See also:snow," known in commerce and valued as " See also:flowers of sulphur " (flares sulphuris) . By conducting the See also:distillation slowly, so that the temperature within the chamber remains at a sufficiently See also:low degree, it is possible to obtain the whole of the product in the form of " flowers." If compact (" See also:roll ") sulphur is wanted the distillation is made to go on at the quickest admissible See also:rate . The temperature of the interior of the chamber soon rises to more than the fusing-point of sulphur (113° C.), and the distillate accumulates at the bottom as a liquid, which is tapped off from time to time to be See also:cast into the customary form of rods . The Louisiana deposits are worked by a process devised by Merman Frasch in 1891 . It consists in sinking a See also:bore-hole, after the manner of a See also:petroleum well, and letting in four pipes centrally arranged, the See also:outer See also:pipe being 10 in. in diameter, the next 6 in., the next 3 in. and the innermost i in .

The operation consists in forcing down the 3-in. pipe superheated steam at 330° F. to melt the sulphur . Compressed air is now driven down the I-in. pipe and bubbles into the melted sulphur and water; the specific gravity of which is greatly diminished, so that it rises to the See also:

surface through the outer pipes; it is then run off to settling tanks . The sulphur so obtained is 98% pure . In some places sulphur is extracted from iron pyrites by one of two methods . The pyrites is subjected to dry distillation from out of iron or fire-clay tubular retorts at a See also:bright red heat . One-third of the sulphur is volatilized—3FeSs = Fe3S4 + 2S—and obtained as a distillate . The second method is analogous to the calcarone method of liquation: the ore is placed in a limekiln-Iike See also:furnace over a mass of kindled fuel to start a partial combustion of the mineral, and the process is so regulated that, by the heat generated, the unburnt part is decomposed with elimination of sulphur, which collects in the molten state on an inverted roof-shaped sole below the furnace and is thence conducted into a cistern . Such pyrites sulphur is usually contaminated with arsenic, and consequently is of less value than Sicilian sulphur, which is characteristically free from this impurity . Large quantities are also recovered from See also:alkali See also:waste (see A1,See also:KALI MANUFACTURE): another source is the spent See also:oxide of gas manufacture (see GAS) . The substance known as " See also:milk of sulphur " (See also:lac sulphuris) is very finely divided sulphur produced by the following, or some analogous, chemical process . One part of quicklime is slaked with 6 parts of water, and the See also:paste produced diluted with 24 parts of water: 2.3 parts of flowers of sulphur are added; and the whole is boiled for about an See also:hour or longer, when the sulphur dissolves . The mixed See also:solution of poivsulphides and thiosulphate of calcium thus produced is clarified, diluted largely, and then mixed with enough of pure dilute hydrochloric acid to produce a feebly alkaline mixture when sulphur is precipitated .

The addition of more acid would produce an additional See also:

supply of sulphur (by the See also:action of the H2S2O3 on the dissolved H2S) ; but this thiosulphate sulphur is yellow and compact, while the polysulphide part has the desired qualities,forming an extremely fine, almost See also:white, See also:powder . The precipitate is washed, collected, and dried at a very moderate heat . Properties.—Sulphur exists in several allotropic modifications, but before considering these systematically we will See also:deal with the properties of See also:ordinary (or rhombic) sulphur . Commercial sulphur forms yellow crystals which melt at 113° and See also:boil at 444.53° C. under ordinary pressure (H . L . Callendar, Chem . See also:News, 1891, 63, p . 1); just above the boiling point the vapour is orange-yellow, but on continued See also:heating it darkens, being deep red at 5oo° ; at higher temperatures it lightens, becoming See also:straw-yellow at 65o° . These colour changes are connected with a See also:dissociation of the molecules . At 524° See also:Dumas deduced the structure Ss from vapour-See also:density determinations, whilst for the range 86o° to 1040°; Sainte-Claire Deville and Troost deduced the See also:formula S2 . Biltz (Be"., 1888, 21, p . 2013; 1901, 34, p .

2490) showed that the vapour density decreased with the temperature, and also depended on the pressure . G . Preuner and W . Schupp (Zeit. phys . Chem., 1909, 69, p . 157), in a study of the dissociation isotherms over 300°–85o°, detected molecules of S8, Ss and S2, whilst S, appears to exist below pressures of 30 mm . Boiling and freezing-point determinations of the molecular weight in solution indicate the formula S8 . The density of solid sulphur is 2.062 to 2.070, and the specific heat 0.1712; it is a See also:

bad conductor of See also:electricity and becomes negatively electrified on See also:friction . It ignites in air at 363° and in See also:oxygen at 275–280° (H . See also:Moissan, Compt. rend., 1903, 137, p . 547), burning with a characteristic See also:blue See also:flame and forming much sulphur dioxide, recognized by its pungent odour . At the same time a little trioxide is formed, and, according to Hempel (Ber., 1890, 23, p .

1455), See also:

half the sulphur is converted into this oxide if the combustion be carried out in oxygen at a pressure of 40 to 50 atmospheres . • Sulphur also combines directly with most of the elements to form sulphides . The atomic weight was determined by See also:Berzelius, See also:Erdmann and Marchand, Dumas and See also:Stas . See also:Thomsen (Zeit. phys . Chem., 1894, 13, p . 726) obtained the value 32.0606 . Allotropic Modifications.—Sulphur assumes crystalline, amor- phous and (possibly) colloidal forms . Historically the most important are the rhombic (S°) and monoclinic (Sp) forms, discussed by E . See also:Mitscherlich in 1822 (see See also:Ann. chim. phys., 1823, 24, p . 264) . The transformations of these two forms are discussed in See also:CHEMISTRY: See also:Physical . Rhombic sulphur may be obtained artificially by slowly crystallizing a solution of sulphur in carbon bisulphide, or, better, by exposing See also:pyridine saturated with sulphuretted hydrogen to atmospheric oxidation (See also:Ahrens, Ber., 1890, 23, p .

2708) . It is insoluble in water,' but readily soluble in carbon bisulphide, sulphur chloride and oil of See also:

turpentine . The See also:common monoclinic variety is obtained by allowing a crust to form over molten sulphur by partially cooling it, and then breaking the crust and pouring off the still liquid portion, whereupon the interior of the See also:vessel will be found coated with See also:long needles of this variety . Like S. it is soluble in carbon bisulphide . Three other monoclinic forms have been described . By acting upon a solution of See also:sodium hyposulphite with See also:potassium bisulphate, Gernez (Compt. rend.; 1884, 98, p . 144) obtained a form which he termed nacre (or pearly) sulphur; the same modification was obtained by See also:Sabatier (ibid., 1885, 100, p . 1346) on shaking hydrogen persulphide with See also:alcohol or See also:ether . It is readily transformed into rhombic sulphur . Another form, mixed with the variety just described, is obtained by adding 3 to 4 volumes of alcohol to a solution of ammonium sulphide saturated with sulphur and exposing the mixture to air at about 5° . See also:Engel's monoclinic form (Compt. rend., 1891, 112, p . 866) is obtained by mixing a solution of sodium hyposulphite with See also:double its See also:volume of hydrochloric acid, filtering and extracting with See also:chloroform; the See also:extract yielding the variety on evaporation .

A triclinic form is claimed to be obtained by See also:

Friedel (See also:Bull. See also:soc. chim., 1879, 32, p . 14) on subliming ordinary sulphur . ' It is a common practice of keepers of See also:dogs to place a piece of roll sulphur in the animal's water but this serves no useful purpose owing to this See also:property . Amorphous sulphur or Sy exists in two forms, one soluble in carbon bisulphide, the other insoluble . Milk of sulphur (see above), obtained by decomposing a polysulphide with an acid, contains both forms . The insoluble variety may also be obtained by decomposing sulphur chloride with water and by other re-actions . It gradually transforms itself into rhombic sulphur . The colloidal sulphur, Ss, described by Debus as a product of the interaction of sulphuretted hydrogen and sulphur dioxide in aqueous solution, is regarded by See also:Spring (Rec. See also:tray. chim., 1906, 25, p . 253) as a See also:hydrate of the formula S8•See also:H2O . The " blue sulphur," described by Orloff, has been investigated by See also:Paterno and Mazzucchelli (Abs . Journ . Chem .

Soc., 1907, ii . 451) . Molten Sulphur.—Several interesting phenomena are witnessed when sulphur is heated above its melting point . The solid melts to a pale yellow liquid which on continued heating gradually darkens and becomes more viscous, the maximum viscosity occurring at 180°, the product being dark red in colour . This See also:

change is associated with a change in the spectrum (N . See also:Lockyer) . On continuing the heating, the viscosity diminishes while the colour remains the same . If the viscous variety be rapidly cooled, or the more highly heated mass be poured into water, an elastic substance is obtained, termed plastic sulphur . This substance, however, on See also:standing becomes brittle . The See also:character of molten sulphur has been mainly elucidated by the researches of A . See also:Smith and his collaborators . Smith (Abs .

Journ . Chem . Soc., 1907, ii . 20, 451, 757) regards molten sulphur as a mixture of two isomers SA and Ss in dynamic See also:

equilibrium, SA being See also:light in colour and See also:mobile, and Ss dark and viscous . At low temperatures SA predominates, but as the temperature is raised S;A increases; the transformation, however, is retarded by some f _.ses, e.g. sulphur dioxide and hydrochloric acid, and accelerated by others, e.g. See also:ammonia . The solid derived from SA is crystalline and soluble in carbon bisulphide, that from Ss is amorphous and insoluble . As to the formation of precipitated sulphur, Smith considers that the element first separates in the liquid SN, See also:condition, which is transformed into Sa and finally into Ss; the insoluble (in carbon bisulphide) forms arise when little of the Ss has been transformed; whilst the soluble consist mainly of S . Similar views are adopted by H . Erdmann (Ann., 1928, 362, p . 133), but he regards Sµ as the polymer S3, analogous to See also:ozone 03; Smith, however, regards Ss as S8 . Compounds . Sulphuretted hydrogen, H2S, a See also:compound first examined by C .

See also:

Scheele, may be obtained by heating sulphur in a current of hydrogen, combination taking place between 200° C. and 358° C., and being complete at the latter temperature, dissociation taking place above this temperature (M . Bodenstein, Zeit. phys . Chem., 1899, 29, p . 315) ; by heating some metallic sulphides in a current of hydrogen; by the action of acids on various metallic sulphides (ferrous suiphide and dilute sulphuric acid being most generally employed) ; by the action of sulphur on heated See also:paraffin See also:wax or See also:vaseline, or by heating a solution of magnesium sulphydrate . It is also produced during the putrefaction of organic substances containing sulphur and is found among the products obtained in the destructive distillation of coal . To obtain pure sulphuretted hydrogen the method generally adopted consists in decomposing precipitated See also:antimony sulphide with concentrated hydrochloric acid . As an alternative, H . Moissan (Comp. rend., 1903, 137, p . 363) condenses the gas by means of liquid air and fractionates the product . Sulphuretted hydrogen is a colourless gas possessing an extremely offensive odour . It acts as a strong See also:poison . It burns with a pale blue flame, forming sulphur dioxide and water .

It is moderately soluble in water, the solution possessing a faintly acid reaction . This solution is not very See also:

stable, since on exposure to air it slowly oxidizes and becomes turbid owing to the See also:gradual precipitation of sulphur . The gas is much more soluble in alcohol . It forms a hydrate of See also:composition H2S•7H,0 . (De Forcrand, Comp'. rend., 1888, 106, p . 1357.} The gas may be liquefied by a pressure of about 17 atmospheres, the liquid so obtained boiling at -61.8° C.; and by further cooling it yields a solid, the melting point of which is given by various observers as -82° to -86° C . (see Ladenburg, See also:Bet., 1900, 33, p . 637) . It is decomposed by the See also:halogens, with liberation of sulphur . Concentrated sulphuric acid also decomposes it: H2SO4+H2S=2H20+SO2+S . It combines with many metals to form sulphides, and also decomposes many metallic salts with consequent See also:production of sulphides, a property which renders itextremely useful in chemical See also:analysis . It is frequently used as a reducing See also:agent: in acid solutions it reduces ferric to ferrous salts, arsenates to arsenites, permanganates to manganous salts, &c., whilst in alkaline solution it converts many organic nitro compounds into the corresponding amino derivatives .

Oxidizing agents rapidly attack sulphuretted hydrogen, the See also:

primary products of the reaction being water and sulphur . By the action of dilute hydrochloric acid on metallic polysulphides, an oily product is obtained which C . L . Berthollet considered to be H3S6 . L . See also:Thenard, on the other See also:hand, favoured the formula H2S2 . It was also examined by W . See also:Ramsay (Journ . Chem . Soc., 1874, 12, p . 857) . See also:Hofmann, who obtained it by saturating an alcoholic solution of ammonium sulphide with sulphur and mixing the product with an alcoholic solution of See also:strychnine, considered the resulting product to be H2S3; while P .

Sabatier by fractionating the crude product in vacuo obtained an oil which boiled between 60° and 85° C. and possessed the composition H4S5 . Several halogen compounds of sulphur are known, the most stable of which is sulphur fluoride, SF6, which was first prepared by H . Moissan and See also:

Lebeau (See also:Comet. rend., 1900, 130, p . 865) by fractionally distilling the product formed in the See also:direct action of See also:fluorine on sulphur . It is tasteless, colourless and odourless gas, which is exceedingly stable and inert . It may be condensed and yields a solid which melts at -55° C . Sulphuretted hydrogen decomposes it with formation of hydrofluoric acid and liberation of sulphur . Sulphur chloride, S2C12, is obtained as a by-product in the manufacture of carbon tetrachloride from carbon bisulphide and See also:chlorine, and may also be prepared on the small See also:scale by distilling sulphur in a chlorine gas, or by the action of sulphur on sulphuryl chloride in the presence of See also:aluminium chloride (0 . See also:Ruff) . It is an See also:amber-coloured, fuming liquid possessing a very unpleasant irritating See also:smell . It boils at 139° C. and is solid at -8o° C . It is soluble in carbon bisulphide and in See also:benzene .

Phoenix-squares

It is gradually decomposed by water: 2S2C12 + 3H2O = 4HC1 -i- 2S + H2S2O3, the thiosulphuric acid produced in the primary reaction gradually decomposing into water, sulphur and sulphur dioxide . Sulphur chloride dissolves sulphur with great readiness and is consequently used largely for vulcanizing See also:

rubber; it also dissolves chlorine . The chloride SC1, according to the investigations of 0 . Ruff and See also:Fischer (See also:Bee., 1903, 36, p . 418) did not appear to exist, but E . See also:Beckmann (Zeit. phys . Chem., 1909, 42, p . 1839) obtained it by distilling the product of the interaction of chlorine and S2C12 at low pressures . The tetrachloride, SCl4, is formed by saturating S2Cl2 with chlorine at -22° C . (See also:Michaelis, Ann., 1873, 170, p . I) . It is a yellowish-See also: