definition
Any salt of hydrochloric acid, such as sodium chloride, or any binary compound of chlorine and another element or radical
Iridium sesquichloride, IrC1 31 is obtained when one of the corresponding double chlorides is heated with concentrated sulphuric acid, the mixture being then thrown into water.
It forms double chlorides with the alkaline chlorides.
Two chlorides of copper are known, one a highly coloured substance, the other quite white.
They are soluble in water and give characteristic precipitates with platinic and auric chlorides, and with potassium ferrocyanide.
The salts of all the metals of this group usually crystallize well, the chlorides and nitrates dissolve readily in water, whilst the carbonates, phosphates and sulphates are either very sparingly soluble or are insoluble in water.
The cotton bollworm (Chlorides obsoleta, also known as Heliothis armiger) is a caterpillar.
Numerous double chlorides are known, e.g.
For example, compounds of oxygen are oxides, of chlorine, chlorides, and so on.
The action of these acids on many metals was also studied; Glauber obtained zinc, stannic, arsenious and cuprous chlorides by dissolving the metals in hydrochloric acid, compounds hitherto obtained by heating the metals with corrosive sublimate, and consequently supposed to contain mercury.
For this purpose the cold solution is treated with hydrochloric acid, which precipitates lead, silver and mercurous salts as chlorides.
In the second group, we may notice the application of litmus, methyl orange or phenolphthalein in alkalimetry, when the acid or alkaline character of the solution commands the colour which it exhibits; starch paste, which forms a blue compound with free iodine in iodometry; potassium chromate, which forms red silver chromate after all the hydrochloric acid is precipitated in solutions of chlorides; and in the estimation of ferric compounds by potassium bichromate, the indicator, potassium ferricyanide, is placed in drops on a porcelain plate, and the end of the reaction is shown by the absence of a blue coloration when a drop of the test solution is brought into contact with it.
The N-derivatives are prepared by the action of alkyl halides and acid chlorides on potassium pyrrol.
Soon afterwards, William Cruickshank decomposed the magnesium, sodium and ammonium chlorides, and precipitated silver and copper from their solutions - an observation which led to the process of electroplating.
Of other lead minerals we may mention the basic sulphate lanarkite, PbO PbSO 4; leadhillite, PbSO 4.3PbCO 3; the basic chlorides matlockite, PbO PbC12j and mendipite, PbC1 2.2PbO; the chloro-phosphate pyromorphite, PbC12.3Pb3(P04)2, the chloro-arsenate mimetesite, PbC12.3Pb3(As04)2; the molybdate wulfenite, PbMoO 4; the chromate crocoite or crocoisite, PbCrO 4; the tungstate stolzite, PbW04.
It combines with alkaline chlorides - potassium, rubidium and caesium - to form crystalline plumbichlorides; it also forms a crystalline compound with quinoline.
It forms double salts with metallic chlorides and with the hydrochlorides of organic bases.
It combines readily with alkaline and other chlorides to form double salts, e.g.
Now differences in the amount of crystalloids cause alteration in osmotic pressure while the proteid content affects it but little; and of the crystalloids the chlorides appear to be those most liable to variation.
Widal, Lemierre and other French observers have noted a diminution in the excretion of chlorides in nephritis associated with oedema; Widal and Javal found that a chloride-free diet caused diminution in the oedema and a chloride containing diet an increase of oedema.
Some other observers, however, have not got such good results with a chloride-free diet, and Marishler, Scheel, Limbecx, Dreser and others, dispute Widal's hypothesis of a retention of chlorides as being the cause of oedema, in the case of renal dropsy at all events; they assert that the chlorides are held back in order to keep the osmotic pressure of the fluid, which they assume to have been effused, equal to that of the blood and tissues.
When heated with the alkali and alkaline earth metals it yields silicon and the corresponding metallic chlorides.
Aqueous Sulphuric or Hydrochloric Acid readily dissolves groups I and 2, with evolution of hydrogen and formation of chlorides or sulphates.
Aqua Regia, a mixture of nitric and hydrochloric acids, converts all metals (even gold, the "king of metals," whence the name) into chlorides, except only rhodium, iridium and ruthenium, which, when pure, are not attacked.
Chlorine.-All metals, when treated with chlorine gas at the proper temperatures, pass into chlorides.
Iron, for instance, is converted first into FeC1 21 ultimately into FeCl 3, which practically means a mixture of the two chlorides, or pure FeC1 3 as a final product.
Of the several products, the chlorides of gold and platinum (AuC13 and PtC1 4) are the only ones which when heated beyond their temperature of formation dissociate into metal and chlorine.
Somewhat less volatile than the last-named group are the chlorides (MC1 2) of barium, strontium and calcium.
Metallic chlorides, as a class, are readily soluble in water.
The chlorides AsC1 3, SbC1 3, BiC1 3, are at once decomposed by (liquid) water, with formation of oxide (As203) or oxychlorides (SbOC1, BiOCI) and hydrochloric acid.
The chlorides MgC1 21 A1C13, CrC1 3, FeC1 3, suffer a similar decomposition when evaporated with water in the heat.
All chlorides, except those of silver and mercury (and, of course, those of gold and platinum), are oxidized by steam at high temperatures, with elimination of hydrochloric acid.
Those substituted in the benzene nucleus are obtained by condensing two molecules of a substituted benzyl and benzal chlorides.
The diortho and dipara dinitro compounds result from the action of alcoholic potash on orthoand para-nitrobenzyl chlorides.
They are all strong bases, readily forming salts with the mineral acids and double salts with the chlorides of gold, platinum and mercury.
It is obvious that, with suitable methods and apparatus, the electrolysis of alkaline chlorides may be made to yield chlorine, hypochlorites (bleaching liquors), chlorates or caustic alkali, but that great care must be exercised if any of these products is to be obtained pure and with economy.
The same inventor has patented the application of electrolysed chlorides to the purification of starch by the oxidation of less stable organic bodies, to the bleaching of oils, and to the purification of coal gas, spirit and other substances.
His system for the disinfection of sewage and similar matter by the electrolysis of chlorides, or of sea-water, has been tried, but for the most part abandoned on the score of expense.
In solution minute quantities of gold may be detected by the formation of " purple of Cassius," a bluish-purple precipitate thrown down by a mixture of ferric and stannous chlorides.
The potassium salt is obtained by crystallizing equivalent quantities of potassium and auric chlorides.
The bromides and iodides resemble the chlorides.
Salt is added in the roasting to convert any lime, magnesia or lead which may be present, into the corresponding chlorides.
The second process depends upon the fact that, if chlorine be led into the molten alloy, the base metals and the silver are converted into chlorides.
The solution of metallic chlorides or sulphates so obtained is precipitated by iron, the metallic bismuth filtered, washed with water, pressed in canvas bags, and finally fused in graphite crucibles, the surface being protected by a layer of charcoal.
Bismuth dioxide, BiO or Bi 2 O 2, is said to be formed by the limited oxidation of the metal, and as a brown precipitate by adding mixed solutions of bismuth and stannous chlorides to a solution of caustic potash.
Two chlorides are known, the dichloride, TeC121 and the tetrachloride, TeCl 4.
The great similarity between the salts of the ocean and the gaseous products of volcanic eruptions at the present time, rich in chlorides and sulphates of all kinds, is a strong argument for the ocean having been salt from the beginning.
Besides the determination of salinity by titration of the chlorides, the method of determination by the specific gravity of the sea-water is still often used.
This residue consists of sodium, potassium and lithium chlorides, with small quantities of caesium and rubidium chlorides.
The platino-chlorides are reduced by hydrogen, and the caesium and rubidium chlorides extracted by water.
Many double chlorides are known, and may be prepared by mixing solutions of the two components in the requisite proportions.