Cooley's Cyclopaedia of Practical Receipts Volume Ii Part 2

Other methods of obtaining it from Chilian nitre consist in treating the mother-liquors left after the salt has been crystallised out with sulphurous acid, until the separated iodine begins to redissolve. Nitrous acid has also been subst.i.tuted for sulphurous. The iodine so procured is purified by sublimation, whilst that which remains in the residual saline matter is removed by treatment with chlorine.

_Prop._ Iodine is usually met with under the form of semi-crystalline lumps having a semi-metallic l.u.s.tre, or in micaceous, friable scales, somewhat resembling plumbago or gunpowder. By carefully conducted sublimation, or by the slow evaporation of its solution in hydriodic acid, it may be obtained in rhombic plates an inch long. It has a greyish-black colour, a hot acrid taste, and a disagreeable odour not much unlike that of chlorine. It fuses at 225 into a deep-brown liquid, volatilises slowly at ordinary temperatures, boils at 347, forming a magnificent violet-coloured vapour, when mixed with water it rapidly rises with the steam at 212 Fahr. It dissolves in about 7000 parts of water, and freely in alcohol, ether, solutions of the iodides, liquid hydriodic acid, chloroform, petroleum, bisulphide of carbon, &c. Most of these solutions have the brown colour of liquid iodine, but some (particularly those formed by the last three solvents named above) have the beautiful violet colour of the vapour. It bleaches like chlorine, only more feebly. Iodine has an extensive range of affinity; with the metals it forms compounds termed iodides, of which several are used in medicine. Its princ.i.p.al compounds with oxygen are the iodic and periodic anhydrides. Sp. gr. 4946 to 4948. According to Debaugne, the addition of syrup of orange peel or tannin to water greatly increases its power of dissolving iodine. 2 gr. of the latter will enable 6 fl. oz. of water to take 10 gr. of iodine. A knowledge of these facts may prove useful to the pharmaceutist.

_Pur._ It is entirely soluble in rectified spirit, and in a solution of iodide of pota.s.sium. On applying heat to it, it first liquefies, and then (wholly) sublimes in violet-coloured vapour. The iodine of commerce is usually that of the first sublimation, and generally contains from 12% to 20% of water. Some of the foreign iodine, prepared by precipitation with chlorine, without subsequent sublimation, even contains 1-4th part of water, and has a dead leaden-grey colour, and evolves a sensible odour of chlorine. Coal, plumbago, oxide of manganese, crude antimony, and charcoal, are also frequently mixed with iodine to increase its weight.

Water may be detected by the loss of weight it suffers when exposed to strong pressure between bibulous paper; or more accurately by drying it in the manner directed below,--chlorine may be detected by the odour, and the other substances mentioned above, by their insolubility in rectified spirit and in a solution of iodide of pota.s.sium. Before use as a medicine it should be dried by being placed in a shallow basin, of earthenware, in a small confined s.p.a.ce of air, with 10 or 12 times its weight of fresh-burnt lime, till it scarcely adheres to the side of a dry bottle, or else prepared from the commercial iodine as follows:--Place it in a deep circular porcelain capsule, and having covered it accurately with a gla.s.s matra.s.s filled with cold water, apply a water heat to the capsule for 20 minutes, and then allow the whole to cool; should the sublimate attached to the bottom of the matra.s.s include acicular prism of a white colour, and a pungent odour, it must be sc.r.a.ped off with a gla.s.s rod, and rejected; the apparatus is then to be again exposed to a gentle and steady heat until the whole of the iodine has sublimed; the sublimate is, lastly, to be collected from the bottom of the matra.s.s, and at once enclosed in a stoppered bottle.

_Tests._ Free iodine may be recognised by the violet colour of its vapour, by its imparting a violet colour to bisulphide of carbon, and by its striking a blue colour with starch. The latter test is so delicate, that water containing only 1/450000th part of iodine acquires a perceptible blue tinge on the addition of starch. Free iodine may be eliminated from solutions of iodides by chlorine, nitric acid, concentrated sulphuric acid and peroxide of manganese, and may be made evident by adding starch-paste.

This reagent serves to detect minute traces of iodine in insoluble as well as in soluble compounds of that element. The substance under examination is mixed in a retort with concentrated nitric acid, and a strip of white cotton cloth moistened with a solution of starch suspended from the stopper; in a few hours the cloth will become coloured blue if the most minute trace of iodine be present. By mixing the liquid containing the iodine with the starch and acid, and lightly pouring thereon a small quant.i.ty of aqueous chlorine, a very visible blue zone will be developed at the line of contact, even in very dilute solutions.

Iodides give a pale yellowish precipitate with nitrate of silver, scarcely soluble in ammonia, and insoluble in dilute nitric acid; a bright yellow one with acetate of lead; and a scarlet one with bichloride of mercury.

This distinguishes them from the iodates which give white precipitates with the same reagents. In solutions of alkaline iodides, chloride of palladium produces a black precipitate.

_Estim._ The proportion of free iodine in a mixture may be estimated: by separating it by heat, and collecting and weighing the sublimate; by solution in rectified spirit, adding water, and collecting the resulting precipitate, which must then be dried and weighed; by dissolving it in a solution of iodide of pota.s.sium, and then adding a standard solution of hyposulphite of sodium, until the whole of the free iodine is taken up, and the mixture no longer strikes a blue colour with starch. 248 gr. of the hyposulphite are necessary to absorb 127 gr. of free iodine;[2] by comparing the tint of a solution prepared by chloroform with that of a standard solution containing a known quant.i.ty of iodine, as in Crum's process for estimating chlorine.

[Footnote 2: For details of this and other methods of accurately determining the per-centage of iodine, free or combined, the reader is referred to Sutton's "Systematic Handbook of Volumetric a.n.a.lysis."]

_Uses, &c._ Iodine is chiefly used as a medicine, a chemical test, and in photography. Until within the last year it was largely used in the manufacture of the green coal-tar colours; these latter are now chiefly made from anthracene. In small doses it appears to be both alterative and tonic, rapidly diffusing itself through the body, and exerting a stimulating action on the organs of secretion. It is also said to be diuretic, and in some cases to have produced diaph.o.r.esis and salivation.

Iodine has been exhibited in the following diseases, as well as in most others depending on an imperfect action of the absorbents, or accompanied by induration or enlargement of individual glands or organs:--_Internally_, in bronchocele, goitre, Derbyshire neck, scrofula, ovarian tumours, enlargement or induration of the lymphatic, prostate, and parotid glands, amenorrha, leucorrha, diseases of the muco-genital tissues, phthisis, chronic nervous diseases, lepra, psoriasis, chronic rheumatism, dropsies, hydrocele, &c.:--_Externally_, in scrofula, numerous skin diseases, (especially the scaly), erysipelas, diseased joints, chilblains, burns, scalds, various wounds, to check ulceration, to promote absorption, &c.--_Dose_, 1/2 gr. dissolved in spirit, or in water by means of an equal weight of iodide of pota.s.sium. It is seldom exhibited alone, being usually combined with the last-named substance, which, in fact, is now generally preferred by pract.i.tioners. It is applied externally in the form of ointment, solution, or tincture.

=Iodine, Bro'mides of.= Bromine and iodine unite rapidly by mere mixture.

By careful distillation a red vapour is obtained, which, on cooling, condenses into red crystals, of a form resembling fern leaves. This is said to be the protobromide (IBr). By adding more bromine, these crystals are converted into a fluid, said to be a pentabromide (IBr_{5}).

=Iodine, Chlo"rides of.= When dry chlorine is pa.s.sed over dry iodine, at common temperatures, heat is evolved, and a yellow solid terchloride (ICl_{3}) results when the iodine is fully saturated, and an orange-red liquid protochloride (ICl) when the iodine is in excess. They both absorb moisture in the air, are volatile, and very soluble in water.

=Iodine and Hydrogen.= HYDRIODIC ACID, HI. _Syn._ IODHYDRIC ACID; ACIDUM HYDRIODIc.u.m, L. An acid compound of iodine and hydrogen. _Prep._ 1.

(GASEOUS).--_a._ Into a gla.s.s tube, closed at one end, introduce a little iodine, then a small quant.i.ty of roughly powdered gla.s.s moistened with water, next a few small fragments of phosphorus, and upon this some more gla.s.s; this order (iodine, gla.s.s, phosphorus, gla.s.s) is to be repeated until the tube is one half or two thirds filled; a cork and delivery tube are then to be fitted, a gentle heat applied, and the gas collected by 'downward displacement' or over mercury. If the gas be pa.s.sed into water a solution of hydriodic acid will be obtained.

_Obs._ Hydriodic acid gas can only be retained a short time over mercury, owing to its action on that metal.

_b._ Pour a little water over some pentiodide of phosphorus, previously put into a gla.s.s retort, apply a gentle heat, and collect the gas as before.

_c._ Heat together in a retort water, iodide of pota.s.sium, iodine, and phosphorus, and collect the gas as in _b_.

_d._ Place pure iodide of barium in a retort, and decompose it with sulphuric acid.

2. (SOLUTION OF HYDRIODIC ACID.)--_a._ The gas prepared by either of the above methods pa.s.sed into cold distilled water.

_b._ Iodine, in fine powder, is suspended in water, and a stream of sulphuretted hydrogen pa.s.sed through the mixture as long as sulphur is deposited, or until it becomes colourless. The liquid is then gently heated, to expel the excess of sulphuretted hydrogen, and either decanted or filtered. A cheap and excellent process.

_c._ (MEDICINAL HYDRIODIC ACID.) Dr Buchanan.--Tartaric acid, 264 gr.; pure iodide of pota.s.sium, 330 gr.; dissolve each separately in 1-1/2 fl.

oz. of water; mix the solutions, and when the precipitate has settled decant the clear liquid, and add a sufficiency of water to make it up to 6-1/4 fl. oz. The liquid retains a little acid tartrate of pota.s.sium in solution, but this does not interfere with its medicinal properties. This preparation "possesses all the therapeutic powers of iodine without its irritating properties." (Pereira.)--_Dose_, 1/2 to 1 fl. dr., gradually increased to 2 or 3 fl. dr., twice or thrice daily.

_Prop., &c._ Gaseous hydriodic acid is colourless, fumes in the air, is very soluble in water, and has a density of about 44. Liquid hydriodic acid, when strong, is very liable to decompose, and should be kept in well-stoppered bottles. Both the gas and the solution are decomposed by pota.s.sium, zinc, iron, and other metals, with the evolution of hydrogen and the formation of salts called iodides.

IODIZED COTTON WOOL. (Mehu.) _Prep._ Finely powdered iodine (5 to 10 per cent.) is strewn upon loose cotton wool in such a manner that the gla.s.s jar in which this operation is performed contains alternate layers of cotton wool and iodine. The mixture is gently heated in the open jar on a water bath to expel the air; when this is accomplished the jar is closed and the application of heat continued for about two hours, during which the iodine vapour thoroughly penetrates the wool, imparting to it a yellow colour.

=IODO'FORM.= CHI_{3}. _Syn._ IODOFORMUM, L. A solid, yellow, crystallisable substance, obtained by the action of iodine on alcohol.

_Prep._ 1. An alcoholic solution of potash is added to tincture of iodine, carefully avoiding excess; the whole is then gently evaporated to dryness, the residuum is washed with water, and then dissolved in alcohol; the alcoholic solution yields crystals by evaporation.

2. (Paris Pharmaceutical Society.) Pure carbonate of potash, 2 parts; alcohol (84) 5 parts; distilled water, 15 parts. The potash, water, alcohol, and the iodine reduced to powder are placed together in a flask, and the whole heated in a water bath until the decoloration of the liquid.

Another 1/2 part of iodine is then added and heat again applied, and the addition of the element is repeated until the liquid remains slightly brown coloured. It is then decolorised by the addition of one or two drops of caustic potash solution, and upon cooling crystals of iodoform are obtained.

These are collected upon a filter, washed lightly with cold distilled water, then dried upon blotting paper and enclosed in well-stoppered bottle.

By the evaporation of the mother liquor iodide of pota.s.sium is obtained.

_Prop., &c._ Nearly insoluble in water; freely soluble in alcohol; the solution is decomposed by caustic pota.s.sa into formic acid and iodide of pota.s.sa.--_Dose_, 1/2 gr. to 3 gr. Medicinal applications, the same as those of iodine itself.

=IPECACUAN'HA.= _Syn._ (IPECACUANHA, L.; IPECACUHAN, E., B. P.) RADIX IPECACUANHae, IPECACUANHA (Ph. L. E. & D.), L. The dried root of _Cephaelis Ipecacuanha_, or the true ipecacuanha plant, one of the _Cinchonaceae_.

"Ashy coloured, tortuous, very much cracked, and marked in rings with deep fissures, having an acrid, aromatic, bitterish taste." (Ph. L.) It occurs in pieces 3 or 4 inches long, and about the size of a writing quill.--_Dose._ As an emetic, 10 to 20 gr., a.s.sisted by the copious use of warm water; as a nauseant, 1 to 3 gr.; as an expectorant and sudorific, 1/2 to 1 gr. It is undoubtedly the safest and most useful medicine of its cla.s.s. It has recently been highly recommended in dyspepsia, combined with other bitters or aperients. Almond meal is sometimes used as an adulterant in ipecacuanha powder.

The following is Bucholz's a.n.a.lysis of ipecacuanha root:--

Emetic extractive (emetina) 413 Soft resin 243 Wax 075 Gum 2517 Starch 900 Woody fibre 1080 Bitter extractive 1012 Sugar 200 Extractive, gum and starch } extracted by potash } 3480 Loss 080 ------ 10000

The annexed process for the determination of the emetina in ipecacuanha is by Zenoffsky:--Take 15 grammes of the root, mix with 15 drops of dilute sulphuric acid, and so much of 85 per cent. alcohol that the volume shall be 155 c.c. Digest 24 hours, filter, measure 100 c.c. of the filtrate, evaporate the alcohol, and add a deci-normal solution of iodo-hydrargyrate of pota.s.sium until no more reaction takes place. The number of c.c. of the reagent used multiplied by 00189 (1/10000th of an equivalent of emetine) gives the amount of emetine in the 10 grammes of root to which the 100 c.c. of liquid corresponds. The deci-normal solution of iodo-hydrargyrate of pota.s.sium is made by dissolving 13546 grammes of mercuric chloride and 498 grammes of pota.s.sium iodide in water, and making up to 1 litre.

Quant.i.tative determination showed that one c.c. of such a solution corresponds to 00189 gramme of emetine. To perform the volumetric estimation, the standard solution is added to the liquid containing the alkaloid, until no more turbidity is produced. To determine the end of the reaction, filter a few drops on to a watch-gla.s.s (placed on black glazed paper) and touch with a gla.s.s rod previously moistened with the standard solution. To prevent loss both filter and filtrate should be returned to the liquor.

=IRID'IUM.= Ir. A rare metal discovered by Descotils in 1803, and by Tennant in 1804, in the black powder left in dissolving crude platinum.

This powder is an alloy of iridium with osmium. The metal is also found native and nearly pure amongst the Uralian platinum ores.

_Prep._ The native alloy of iridium and osmium remaining after dissolving crude platinum in aqua regia is reduced to powder, mixed with an equal weight of dry chloride of sodium, and heated to redness in a gla.s.s tube, through which a stream of moist chloride gas is transmitted. The further extremity of the tube is connected with a receiver containing liquor of ammonia. Chloride of iridium and chloride of osmium are produced; the former remains in combination with the chloride of sodium; the latter, being volatile, is carried forward into the receiver, where it is decomposed into osmic and hydrochloric acids, which combine with the ammonia. The contents of the tube, when cold, are treated with water to dissolve out the double chloride of iridium and sodium; the solution thus formed is mixed with an excess of carbonate of sodium, and evaporated to dryness. The residue is ignited in a crucible, boiled with water, and dried; it then consists of a mixture of sesquioxide of iron and a combination of oxide of iridium with sodium hydrate. It is reduced by hydrogen at a high temperature, and treated successively with water and strong hydrochloric acid, which remove the alkali and the iron, leaving metallic iridium in a divided state. By strong pressure and exposure to a welding heat, a certain degree of compactness may be given to the product.

_Prop., &c._ Brittle, white, very hard, only fusible by the strongest heat of Deville's gas furnace. In its pure state it is not acted upon by any of the acids, but it is oxidised by fusion and nitre, and by ignition to redness in the air. An ingot of iridium, weighing 27-3/4 oz., melted by Deville's process, was displayed in Messrs Johnson and Matthey's case at the International Exhibition of 1862. An alloy of iridium and osmium (artificial or native) has been employed for tipping the nibs of gold pens (everlasting pens).

=Iridium, Chlo'rides of.= DICHLORIDE. IrCl_{2}. An olive-green powder formed by transmitting chlorine over powdered iridium, heated to a dull red, or by digesting the hydrated protoxide in hydrochloric acid.

SESQUICHLORIDE, Ir_{2}Cl_{6}, obtained by calcining iridium with nitrate of pota.s.sium, digesting in nitric acid, washing with water, and solution in hydrochloric acid. TETRACHLORIDE, IrCl_{4}, obtained in solution by adding hydrofluosilicic acid to the tetrachloride of iridium and pota.s.sium (formed when chloride is pa.s.sed over a heated mixture of iridium and chloride of pota.s.sium). HEXACHLORIDE, IrCl_{6}, obtained in combination with pota.s.sium by heating iridium with nitrate of pota.s.sium, dissolving in aqua regia, and evaporating to dryness.

=Iridium, Ox'ides of.= MONOXIDE, IrO, prepared by adding pota.s.sium hydrate to the hexachloride of iridium, and digesting the precipitate in an acid.

It is a heavy black powder, insoluble in acid. SESQUIOXIDE, Ir_{2}O_{3}, is best prepared by fusing in a silver crucible a mixture of carbonate of pota.s.sium and the double chloride of iridium and pota.s.sium, and boiling the product in water. Bluish-black TRIOXIDE, IrO_{3}, is produced when carbonate of pota.s.sium is gently heated with hexachloride of iridium. A greyish-yellow hydrate, containing alkali.

=IRITIS.= A very dangerous disease of the eye, producing inflammation in the iris or coloured circle which surrounds the pupil. Iritis is frequently produced by rheumatism, as well as by scrofula and gout, and often places the sight in great peril.

The symptoms are pains around the ball of the eye and on the brow, which increase at night, cloudiness of the cornea, difficulty, and inequality of contraction in the pupil, change of colour in the iris, frequently disturbed vision, and much pain in and watering from the eye when the patient is placed in the light, particularly a strong light.

We have described the princ.i.p.al symptoms of this serious disorder in order that any one affected by them may at once seek the a.s.sistance of a skilful surgeon or oculist.

=I'RON.= Fe. _Syn._ FERRUM, L.; FER, Fr.; EISEN, Ger. The history of this most important metal extends to the remote past. The discovery of an iron rod in one of the a.s.syrian bronzes brought to England by Mr Layard established the interesting fact that this metal was known and commonly employed, where strength was required, nearly 3000 years ago. Rust of iron and scales of iron were used as medicines at a period equally remote.

_Sources._ Iron in a metallic state (native iron) is of very rare occurrence; but it invariably enters into the composition of meteorites.

Combined with oxygen and other elements, as iron ores, it occurs in nearly every part of the earth. These ores may be divided into the oxides and the carbonates. The oxides may be again divided into four distinct cla.s.ses, viz.--(1) Magnetic iron ore, consisting of 31% protoxide and 69% sesquioxide, with an insignificant proportion of silica; (2) specular iron, or iron glance, composed of the sesquioxide, with a small admixture of magnetic oxide; (3) red haemat.i.te, consisting of the sesquioxide nearly in a state of purity; and (4) brown haemat.i.te, the hydrated sesquioxide of iron. The carbonates are princ.i.p.ally two, viz.--(5) spathose iron, the protocarbonate of iron in a sparry condition, and (6) clay ironstone or black band ironstone, which consists of the protocarbonates a.s.sociated with clay and carbonaceous matter.

Swedish iron is made almost entirely from No. 1, which occurs in ma.s.sive beds at Arendahl and Dannemora, in Sweden. This iron is of great purity, being perfectly free from sulphur and phosphorus. The t.i.taniferous iron sand found at Taranaki, in New Zealand, consists almost entirely of No. 1 and the metal t.i.tanium. No. 2 found princ.i.p.ally in the island of Elba, in the form of rhombohedral crystals. The micaceous iron ore found in small quant.i.ties in Wales and Lancashire has nearly the same composition, but crystallises in brilliant plates. No. 3 occurs in radiated fibrous ma.s.ses in different parts of the world. It is found in large quant.i.ties in Wales and Lancashire, some of the specimens from the latter locality containing nearly 99% of the sesquioxide. It makes excellent iron. No. 4 occurs in reddish-brown ma.s.ses of a botryoidal form. It is a valuable ore, and is found in England, Wales, and Scotland. No. 5 is found chiefly at Siegen, in Prussia. No. 6 is the princ.i.p.al ore of the Staffordshire and Scotch iron districts, where it occurs in great abundance, a.s.sociated with the fuel and the flux required for smelting it. Iron is contained in plants, and forms an essential component of the blood of the higher animals.

_Prep., &c._ Iron is only prepared on the large scale, and an account of the manufacture would be out of place here. Those requiring detailed information must consult the elaborate works of Percy, Hunt, Fairbairn, Phillips, and other metallurgists.

Pure iron may be prepared by introducing fine iron wire, cut small, 4 parts, and black oxide of iron, 1 part, into a Hessian crucible; covering with a mixture of white sand, lime, and carbonate of pota.s.sium (in the proportions used for gla.s.s-making); and, after applying a closely fitting cover, exposing the crucible to a very high degree of heat. A b.u.t.ton of pure metal is thus obtained, the traces of carbon and silicon present in the wire having been removed by the oxygen of the black oxide.