8. (LINNÆUS' REMEDY.) Hydrochloric acid, 1 oz.; water, 11 oz. As No. 3.

9. (MORTON'S LINIMENT.) Calomel and camphor, of each 1 dr.; spermaceti

ointment, 4 dr.; oil of turpentine and cocoa-nut oil, of each 2 dr. As No.

5.

10. (WAHLER'S OINTMENT.) Black oxide of iron, bole, and oil of turpentine,

of each 1 dr.; resin cerate, 1 oz. For broken chilblains. We have found a

mixture of equal parts of calamine cerate and resin cerate answer quite as

well. See CERATE, OINTMENT.

11. (RUSSIAN REMEDY.) The rind of perfectly ripe cucumbers dried, with the

soft parts attached. For use they are placed with the inner side,

previously soaked in warm water, over the soft parts. (Med. Zeitung.)

12. (RHEIN.) Dissolve 1 _oz._ of tannin in a pint of water, and 74 grains

of iodine in 1-3/4 _oz._ of spirit of wine; the solutions are then mixed,

and enough water added to make the whole up to 2-1/2 pints. In applying

it, which is best done at bedtime, the mixture is gently warmed over a

slow fire; the affected part is dipped into it while still cold, and

retained in it till the liquid, on being stirred, feels uncomfortably hot.

The vessel is then withdrawn from the fire, and the affected part dried

over it. The vessel must be of earthenware or porcelain, and care must be

taken not to use too much iodine, especially when abrasions are present.

13. (L'UNION MÉDICALE.) Oxide of zinc, 2 parts; tannic acid, 1 part;

glycerin, 10 parts; balsam of Peru, 8 parts; camphor, 4 parts.

14. (SWEDIAUR'S PASTE.) Bitter almonds, 8 oz.; honey, 6 oz.; powdered

camphor and flour of mustard, of each 1/2 oz.; burnt alum and olibanum, of

each 1/2 oz.; yolks of 3 eggs; beat to a paste. To be applied night and

morning.

15. (VANCE'S CREAM.) Ointment of nitrate of mercury, 1 oz.; camphor, 1

dr.; oil of turpentine, 2 dr.; oil of olives, 4 dr.; mix well together. To

be applied by gentle friction 2 or 3 times daily.

_Obs._ All the preceding preparations are intended for chilblains before

they break. The liniments of ammonia, camphor, opium, soap, and

turpentine, as well as the compound camphor liniment of the British

Pharmacop[oe]ia, are also excellent preparations for the same purposes.

=CHIL'DREN (Care of).= See INFANCY.

=Children (Diseases of).= See the respective heads, and DISEASES.

=CHIL'LIES.= See CAPSICUM, PEPPERS.

=CHIM'NEYS= were not introduced into England until the reign of Queen

Elizabeth, and for a considerable period the principles of their

construction were ill-understood. When the air inside and outside a

chimney is at the same temperature, an equilibrium exists; there is no

draught in the chimney, because the downward tendency of that within is

counteracted by the upward pressure of that without. Let a fire be kindled

in the grate; hot air is evolved, the chimney is heated, the air it

contains suffers expansion, and a portion is expelled. The chimney now

contains a smaller weight of air than it did before; the external and

internal columns no longer equibalance each other, the warmer and lighter

air is forced upwards from below, and its place is occupied by cold, and

consequently heavier air. If the fire continues to burn, and the chimney

retains its temperature, the second portion of air is disposed of like the

first, and the ascending current continues, so long as the sides of the

chimney are hotter than the surrounding air. Should the reverse happen to

be the case, as sometimes occurs from sudden atmospheric changes, the

column of air within the chimney rapidly contracts in volume, the

deficiency is filled up from without, the column of air becomes heavier

than one of a corresponding height on the outside of it, or in the

apartment, and, obeying the common laws of gravitation, it falls out of

the throat of the chimney or fire-place just as a heavy body sinks in

water, and has its place occupied by air from above. In this way a

descending current, of more or less intensity and duration, is

established, and, if there is a fire in the grate, the chimney "smokes,"

or, if the grate is empty, perhaps the smoke from neighbouring chimneys

finds its way into our apartments. By the judicious arrangement of the

fire-place, and the throat and flue of a chimney, an upward current may be

constantly ensured so long as there is a fire in the grate, or the air of

the apartment is warmer than the external atmosphere.

Count Rumford was the first who scientifically investigated the

construction of chimneys. He showed that more heat is obtained from the

fire by reflection when the coverings are placed in an oblique position.

He also directed that the fire itself should be kept as near to the hearth

as possible, and that the throat of the chimney should be constructed much

narrower than was then the practice, in order to prevent the escape of so

much heated air as happened with wide throats. By contracting the open

part of the fire-place immediately over the fire, as by lessening the

width of the hobs, or by bringing the throat of the chimney closer to the

fire, and by contracting the throat of the chimney itself, within certain

limits, any desired amount of draught may be obtained. When the space

above the fuel is too small, the throat too near the burning fuel, or the

throat itself too contracted, the draught of a common chimney is often too

strong, and much fuel and heat is wasted. When the reverse is the case,

the draught is commonly too languid, the fire draws badly, a portion of

the smoke escapes into the room, and all the usual annoyances of a smoky

chimney are suffered. By a proper attention to these conditions a common

fire-place may be adapted for the combustion of bituminous or easy burning

coal, or of anthracite, and varieties of coal that require a considerable

draught. It may even be converted into a wind furnace; whilst the

inconvenience of smoky chimneys may be always avoided, and, when existing,

easily cured. This is presuming, however, that a sufficient supply of air

exists in front of the fire-place (_i.e._ in the apartment), not only for

the combustion of the fuel, but also for the upward current of the

chimney. Many chimneys smoke simply from the apartment being so

ill-ventilated that the supply here alluded to is not provided. It may be

further stated, as a rule, that the greater the length of a chimney the

stronger will be the draught. Hence, the chimneys of the upper rooms of a

house often smoke, whilst the fires in the rooms beneath them burn

pleasantly and vigorously. Such cases are commonly relieved by a

chimney-pot or cowl, of which numerous varieties are now before the

public. The more crooked or tortuous the course of a chimney the less

likely is it to be affected by eddies and gusts of wind from neighbouring

buildings or hills. See FIRE, GRATE, SMOKE PREVENTION, STOVE.

=CHI'NA.= In the purchase of china, glass, and earthenware, care should be

taken to select those patterns which in case of breakage can be the most

readily matched. Peculiar or rare patterns should be avoided, for if any

such be broken, it will generally be found very difficult and expensive,

and frequently impossible, to replace them.

China, glass, and earthenware, when very dirty, are best cleaned with

finely powdered fuller's earth and warm water, followed by rinsing in

clean water. A little clean soft soap may be added to the water instead of

fuller's earth. See PACKING, PORCELAIN.

=CHIN'OIDINE.= See QUINOIDINE.

=CHINOLINE BLUE.= See CYANINE.

=CHINTZ (to Wash).= Boil 2 lbs. of rice in two gallons of water till soft;

and pour the mixture into a tub; let it stand until it attains a warmth

generally used for coloured linens; then put the chintz in it, and wash it

with the rice instead of soap, until all the dirt has disappeared. Next

boil another 2 lb. of rice, as above, in another two gallons of water, but

strain the rice from the water, and mix it in warm water. Wash the chintz

in this till quite clean, and afterwards rinse it in the water the rice

was boiled in. This will answer the same end as starch, as no wet will

affect it, as it will be stiff while it is worn. If a gown, it must be

taken to pieces; and when dried, it must be hung as smooth as possible,

after which it must be dry-rubbed with a smooth stone, but no iron must be

used.

=CHIRETTA.= CHIRATA. The entire plant (_Ophelia chirata_) is employed in

medicine. Northern India. The plant is pulled up by the root when the

flowers begin to decay, and the capsules are formed. The dried plant,

sometimes with, but more commonly without, the root, is the form in which

the chiretta is generally met with in commerce. The whole plant is

intensely bitter, but is without odour. In its physiological action it

bears a great resemblance to gentian. Instead of a constipating, it

appears to possess a slightly relaxing effect. It is an excellent

stomachic and carminative, and is said to diminish the tendency to

acidity, and to be of great service in the dyspepsia accompanying gout. No

vegetable alkaloid has been obtained from it. If given in powder, the dose

of chiretta is twenty grains. It is, however, more generally given in the

form of an infusion or tincture (which _see_).

=CHI'TIN.= This name has been given to the hard, insoluble matter forming

the shells and elytra of insects. It is obtained by boiling the elytra of

the cockchafer with water, alcohol, ether, acetic acid, and alkalies.

=CHIT'TICK'S REMEDY.= Dr Chittick's remedy for stone consisted of a fixed

alkali, administered in veal broth. (Paris.)

=CHLORAL.= C_{2}HCl_{3}O. A peculiar liquid first obtained by Liebig, by

the action of chlorine on alcohol. The name was intended to express its

origin from chlorine and alcohol.

_Prep._ (Liebig.) Anhydrous alcohol is placed in a tubulated retort, and

dry chlorine gas passed through it, at first in the cold, but afterwards

with the application of a gentle heat, until the chlorine passes unchanged

through the liquor on raising it to the boiling temperature; on cooling,

the whole forms a crystalline mass of what was at one time thought to be

chloral hydrate, but which subsequent researches have shown to be chloral

alcoholate; this is melted by a gentle heat, and agitated with three times

its volume of oil of vitriol; on increasing the heat a little, an oily

stratum of impure chloral rises to the surface. It is purified by boiling

it for some time (to drive off free hydrochloric acid and alcohol), next

distilling it with an equal volume of oil of vitriol; and lastly,

rectifying it from some powdered quick-lime, the process being stopped as

soon as the surface of the lime becomes dry.

_Prop., &c._ Chloral is an oily liquid, possessing an ethereal smell; it

is soluble in alcohol, ether, and water; with a small quantity of the

latter it rapidly changes into a semi-solid crystalline mass (chloral

hydrate), which is soluble in a larger quantity of water; boils at 201°;

sp. gr. 1·502. It is decomposed by the caustic earths and alkalies. By age

it is converted into a white, solid, translucent substance (insoluble

chloral), which is reconverted by heat and by sulphuric acid into ordinary

chloral.

_Obs._ In operating as above the chlorine is most conveniently introduced

by a tube inserted into the tubulature of the retort, and a long tube,

bent upwards, should be connected with the beak to convey away the

hydrochloric acid gas extricated, and to allow the volatilised alcohol and

chloral to condense, and flow back into the retort.

=Chloral, Camphorated.= Hydrate of chloral and camphor, equal parts. Rub

them together in a warm mortar until they liquefy. It forms clear mixtures

with oil of turpentine and chloroform, but not with solution of ammonia.

It is a counter-irritant, and applied externally it has been found to give

relief in rheumatic pains and neuralgia. It should be painted on the

affected part with a camel's-hair brush.

=Chloral, Hydrate.= C_{2}HCl_{3}O. Aq. _Syn._ HYDRATE OF CHLORAL. _Prep._

"Pass dry chlorine gas, for several days, through absolute alcohol, sp.

gr. 0·795, until it becomes a thick viscid liquid of sp. gr. 1·57. At the

beginning of the operation the alcohol is well cooled to prevent

inflammation and explosion, but towards the end of the operation the

alcohol is heated nearly to the boiling point. The resulting liquid, which

after a day or two solidifies to a mass of crude chloral hydrate, is

agitated with four times its bulk of concentrated sulphuric acid, and the

anhydrous chloral which floats on the surface is separated and purified by

fractional distillation. The purified anhydrous chloral is placed in a

still, mixed with 11 per cent. of water, and distilled over chalk to

remove any hydrochloric acid that may be present; the resulting solid

distillate is then fused and poured out into shallow vessels to cast into

cakes." (Squire.) The purest chloral hydrate is said to be that which has

been crystallised two or three times out of pure bisulphide of

carbon.--_Prop._ White opaque solid, having a pungent odour resembling

that of a ripe melon. Soluble in water, glycerin, and alcohol. Gradually

volatilises in the air, and may be distilled without decomposition. From

100 gr. dissolved in 1/2 fl. oz. of water, well shaken with 1 fl. oz. of

solution of potash (B. P.), and allowed to stand for several hours, at

least 46 grain-measures of chloroform should separate.

Chloral hydrate may be obtained in crystals by mixing the cake with about

half its bulk of chloroform, and putting aside in a cool place. When the

crystallisation is complete (which is generally in about 8 or 10 days) the

crystals are freed from the mother liquor by a centrifugal machine, and

afterwards dried at a gentle heat. The mother liquor may be utilised for

future crystallisations.

_Uses._ An excellent sedative, antispasmodic, hypnotic, anodyne. It has

done good service in hypochondriacal and other nervous affections, as well

as in the insomnia of the insane, and of dipsomaniacs; also in asthma,

hooping-cough, and scarlet fever. It has also the reputation of being an

efficient preventive of sea-sickness, especially on short voyages, such as

crossing the channel, which can be accomplished during the sleep

occasioned by the agent.--_Dose_, from 10 to 60 gr.

It was introduced into medical practice by Dr Liebreich, of Berlin.

Immense quantities are imported into this country from Germany.

=CHLORALUM.= An impure aqueous solution of chloride of aluminum, sp. gr.

1·15, 1 fl. oz. of the liquid contains 75 grains of anhydrous chloride.

Introduced by Professor Gamgee as an antiseptic and disinfectant, for

which purposes it is recommended to dilute the article as sold with four

times its bulk of water.

=CHLO''RATE.= _Syn._ HYPEROXYMU''RIATE[dagger], CHLO''RAS, L. A compound

in which the hydrogen of chloric acid, HClO_{3}, is replaced by a metal or

other basic radical, _e.g._ KClO_{3}, chlorate of potassium. Chlorates may

be prepared by dissolving the hydrate or oxide in chloric acid, and

crystallising. The alkaline chlorates, however, are made by passing

chlorine into solutions of the hydrate or carbonate of potassium or

sodium, boiling the resulting liquid, and separating the chlorate from the

chloride, which is also formed by crystallisation. They are very similar

to the nitrates, both in their general properties and composition. They

are all decomposed at a red heat, metallic chlorides being formed and

oxygen gas given off. Like the nitrates, they deflagrate with inflammable

substances, but with greater facility and violence. A mixture of this kind

will detonate with a slight blow or friction. All the chlorates are

soluble in water.

_Char., Tests, &c._ The chlorates are known by their deflagrating when

placed on red-hot charcoal. By evolving a yellow gas when treated with

concentrated sulphuric acid, in the cold, which gas also communicates to

the liquid a red or yellow tinge. By evolving oxygen gas when heated alone

in a test-tube. This test is not characteristic, unless carried a stage

further, by dissolving the residual chloride out of the tube, and adding

to the filtered solution a few drops of nitrate of silver; then the

formation of a white precipitate, insoluble in nitric acid, will show that

the salt treated was a chlorate, and not a nitrate. Pure chlorates give no

precipitate with nitrate of silver.

=CHLORHY'DRIC ACID.= See HYDROCHLORIC ACID.

=CHLO''RIC ACID.= HClO_{3}. _Syn._ HYPEROXYMURIAT'IC ACID; ACIDUM

CHLO''RICUM, L. An acid discovered by Chenevix, but first obtained in a

separate form by Gay-Lussac.

=CHLO''RIDE= (-[)i]d). _Syn._ CHLO''RURET[dagger]; CHLORI'DUM, L. A

chemical compound of chlorine with a metal or other basic radical, _e.g._

NaCl, chloride of sodium; C_{2}H_{5}Cl, chloride of ethyl.

_Prep._ The majority of the metallic chlorides may be made by simply

dissolving the metal or its carbonate, oxide, or hydrate, in hydrochloric

acid (previously diluted with about twice its weight of water), and

evaporating and crystallising the solution in the usual manner. Zinc,

cadmium, iron, nickel, cobalt, and tin, dissolve readily in hydrochloric

acid; copper only in strong boiling acid; silver, mercury, and gold, not

at all. The insoluble chlorides, as those of silver and mercury, may be

readily prepared by precipitating any of their corresponding soluble salts

with hydrochloric acid, or a soluble chloride, such as common salt.

Anhydrous chlorides are generally prepared by the direct action of

chlorine on the bases.

_Char., Tests, &c._ Most of the metallic chlorides are soluble in water.

Many fuse when heated, and volatilise unchanged, but others are completely

or partially decomposed at a red heat. All, with the exception of those of

the alkali and earth metals, are decomposed at a red heat in a current of

hydrogen. They are recognised by the following reactions:--1. Heated with

a little peroxide of manganese and sulphuric acid, chlorine is evolved,

and easily detected by its colour, smell, and bleaching properties:--2.

The soluble chlorides may be readily detected by their solutions, slightly

acidulated with nitric acid, giving with a solution of nitrate of silver a

white, curdy precipitate (chloride of silver), insoluble in nitric acid,

freely soluble in liquor of ammonia, and blackened by the light:--3. The

insoluble chlorides may be tested by digesting them in a little liquor of

potassa, when a solution of chloride of potassium will be formed, which

may be treated as just directed (2); or the chloride may be dissolved in

nitric acid, and tested with nitrate of silver as before.

=CHLORIM'ETRY.= See CHLOROMETRY.

=CHLORINA'TED LIME.= See LIME.

=CHLORINA'TED SO'DA.= See SODIUM.

=CHLO''RINE.= _Syn._ CHLORIN'IUM, L.; CHLORE, Fr.; CHLOR, Ger. An

elementary substance discovered by Scheele in 1774, and at first supposed

to be a compound body. In 1809 MM. Gay-Lussac and Thénard suggested the

probability of it being a simple substance; but it was reserved for Sir H.

Davy, shortly afterwards, to demonstrate the truth of the suggestion of

these foreign chemists.

_Nat. Hist._ It exists in nature chiefly in the form of chloride of

sodium, which constitutes rock salt when deposited in inland beds, sea

salt when dissolved in masses of water. The sea also contains chlorides of

potassium, calcium, and magnesium. It is a constituent of several

well-known minerals. It has been met with in the air of volcanic

districts, combined with hydrogen, as hydrochloric acid.

_Prep._ Strong hydrochloric acid is poured on half of its weight of

finely-powdered peroxide of manganese, previously placed in a glass flask

or retort; chlorine gas is immediately evolved, even in the cold, but much

more rapidly on the application of a gentle heat, and is collected in

clean, dry bottles by displacement. The tube conducting the gas is so

arranged as to reach to the bottom of the bottle, and the chlorine, being

heavier than the air, displaces the latter without mixing with it. The

bottle is known to be full by the gas, easily perceived by its green

colour, overflowing the top of the vessel. The bottle is then closed up

with an accurately fitting stopper, previously greased, and an empty one

put in its place, which is subsequently treated in like manner. To free

the gas entirely from hydrochloric acid it is passed through a wash bottle

containing a small quantity of water; and to render it quite dry it is

passed over fused chloride of calcium. When the presence of moisture is no

object chlorine may be collected over warm water, or, what is better, a

saturated solution of common salt, in the pneumatic trough. The mercurial

trough cannot be employed, as the chlorine rapidly acts upon the metal,

and becomes absorbed.

_Commercial._--From oil of vitriol and water, of each 7 parts, cautiously

mixed, and allowed to cool; chloride of sodium (common salt), 4 parts,

mixed intimately with peroxide of manganese, 3 parts. The dilute acid is

placed in a retort or other generating vessel, and the powder added. The

gas comes off slowly at first, but the application of a gentle heat causes

it to rush forth in large quantities. Of late years, owing to the general

demand for bleaching agents, numerous new methods and suggestions for

obtaining chlorine have been patented, of which the following are the most

important.

1. Elliott. By this method the reconversion of the chloride of manganese

to peroxide was attempted as follows:--The manganese residues left in the

still are first heated to dryness. They are then roasted in a current of

steam, the result being the formation of hydrochloric acid (which is

condensed), and a residue consisting of a mixture of protoxide and

peroxide of manganese.

2. Gatty. In this process the manganese residues, after evaporation to a

suitable consistence, are mixed with nitrate of soda, and the nitrate of

manganese and chloride of sodium formed, when dried, are strongly heated

in an iron retort, the fumes of nitric acid which come off being employed

in the manufacture of sulphuric acid. The residue in the retort,

consisting of peroxide of manganese, being lixiviated, yields the peroxide

in a pure state:

Mn(NO_{3})_{2} + 2(NaCl) + O_{2} = MnO_{2} + 2NaCl + 2(NO_{3}).

3. Hoffman. This process consisted in the regeneration of the manganese by

means of soda waste. In this process the chloride of manganese is, by the

addition of the yellow ley obtained from the lixiviation of soda waste,

converted into sulphide of manganese. The precipitate so obtained consists

of

Sulphide of manganese 55·00

Sulphur 40·00

Protoxide of manganese 5

------

100·00

This is dried and then calcined, the sulphurous acid evolved being

conducted into the sulphuric acid chamber.

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