The history of its dissociation is connected with that of the class, viz.
In neutral, and still more in acid solutions, the dissociation of the indicator is practically nothing, and the liquid is colourless.
The specific rotation also varies with the concentration; this is due to the dissociation of complex molecules into simpler ones, a view confirmed by cryoscopic measurements.
There he remained for thirteen years, and it was during this period that he devised his well-known method for determining vapour densities, and carried out his experiments on the dissociation of the halogens.
Boric acid (q.v.) being only a weak acid, its salts readily undergo hydrolytic dissociation in aqueous solution, and this property can be readily shown with a concentrated aqueous solution of borax, for by adding litmus and then just sufficient acetic acid to turn the litmus red, the addition of a large volume of water to the solution changes the colour back to blue again.
They are yellowish-red solids, which behave as weak bases, their salts undergoing hydrolytic dissociation in aqueous solution.
These colour changes are connected with a dissociation of the molecules.
Sulphuretted hydrogen, H 2 S, a compound first examined by C. 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.
The Chemistry of the Sun (1887) is an elaborate treatise on solar spectroscopy based on the hypothesis of elemental dissociation through the intensity of solar heat.
The result of this treatment is that the comparatively heavy oils undergo dissociation, as shown by the experiments of Thorpe and Young, into specifically lighter hydrocarbons of lower boiling points, and the yield of kerosene from ordinary crude petroleum may thus be greatly increased.
The primary products of the dissociation of albumins are the albumoses, characterized by not being coagulable by heat, more soluble than the albumins, having a far less complex composition, and capable of being " salted (7) out " by certain salts, and the peptones, similar to albumoses but not capable of being " salted out "; moreover, peptones are less complex than albumoses.
(I) In very dilute solutions of simple substances, where only one kind of dissociation is possible and the dissociation of the ions is complete, the number of pressure-producing particles necessary to produce the observed osmotic effects should be equal to the number of ions given by a molecule of the salt as shown by its electrical properties.
(2) As the concentration of the solutions increases, the ionization as measured electrically and the dissociation as measured osmotically might decrease more or less together, though, since the thermodynamic theory only holds when the solution is so dilute that the dissolved particles are beyond each other's sphere of action, there is much doubt whether this second relation is valid through any appreciable range of concentration.
In simple substances like potassium chloride it seems evident that one kind of dissociation only is possible.
It is possible that in complicated organic substances we might have two kinds of dissociation, electrical and non-electrical, occurring simultaneously, while the possibility of the association of molecules accompanied by the electrical dissociation of some of them into new parts should not be overlooked.
The dissociation theory was originally suggested by the osmotic pressure relations.
The ratios of the coagulative powers can thus be calculated to be i: x: x 2, and putting x =32 we get I: 32: 1024, a satisfactory agreement with the numbers observed.4 The question of the application of the dissociation theory to the case of fused salts remains.
While it seems clear that the conduction in this case is carried on by ions similar to those of solutions, since Faraday's laws apply equally to both, it does not follow necessarily that semi-permanent dissociation is the only way to explain the phenomena.
The evidence in favour of dissociation in the case of solutions does not apply to fused salts, and it is possible that, in their case, a series of molecular interchanges, somewhat like Grotthus's chain, may represent the mechanism of conduction.
In the case of substances like ammonia and acetic acid, where the dissociation is very small, I - a is nearly equal to unity, and only varies slowly with dilution.
Van 't Hoff's formula is equivalent to taking the frequency of dissociation as proportional to the square of the concentration of the molecules, and the frequency of recombination as proportional to the cube of the concentration of the ions.
The two solutions, then, will so act on each other when mixed that they become isohydric. Let us suppose that we have one very active acid like hydrochloric, in which dissociation is nearly complete, another like acetic, in which it is very small.
The dissociation theory gives an immediate explanation of the fact that, in general, no heat-change occurs when two neutral salt solutions are mixed.
Since the salts, both before and after mixture, exist mainly as dissociated ions, it is obvious that large thermal effects can only appear when the state of dissociation of the products is very different from that of the reagents.
Let us consider the case of the neutralization of a base by an acid in the light of the dissociation theory.
C. Jones, The Theory of Electrolytic Dissociation (New York, 1900); N.
Diseases of the latter kind are especially interesting, as in them we see that parts of the nervous structure, separated in space, may nevertheless be associated in function; for instance, wasting of a group of muscles associated in function may depend on a set of central degenerations concurring in parts whose connexion, in spite of dissociation in space, we thus perceive.
On the other hand, they are much weaker bases than the aliphatic amines, their salts undergoing hydrolytic dissociation in aqueous solution.
There must be considerable dissociation of molecules, and as a first approximation it may be taken that of io molecules of most of the components about 9 (or in the case of magnesium sulphate 5) have been separated into their ions, and that it is only during slow concentration as in a natural saline that the ions combine to produce the various salts in the proportions set out in the above table.
This takes place when in the manufacture of the carbide the material is kept too long in contact with the arc, since this overheating causes the dissociation of some of the calcium carbide and the solution of metallic calcium in the remainder.
DISSOCIATION, a separation or dispersal, the opposite of association.
Electrolytic or ionic dissociation is the separation of a substance in solution into ions.
Carbon dioxide dissociates, when strongly heated, into carbon monoxide and oxygen, the reaction being a balanced action; the extent of dissociation for varying temperatures and pressures has been calculated by H.
The alkali and alkaline earth cyanides are soluble in water and in alcohol, and their aqueous solution, owing to hydrolytic dissociation, possesses an alkaline character.
In many of these cases the observed facts might perhaps be explained by dissociation, the undissociated compound producing no marked effect on the spectra.
It is one of the "weak" acids, its dissociation constant being only 0.0 8 169 (J.
From the osmotic side also, then, electrolytic dissociation is indicated, and indeed, it was from this side that the idea was first suggested by S.
It was soon discovered that the faculty of inducing dissociation possessed by the current might now be utilized with some hope of pecuniary success, but as electrolytic currents are of lower voltage than those required in electric furnaces, molten alumina again became impossible.
The operation is essentially a dissociation of alumina into aluminium, which collects at the cathode, and into oxygen, which combines with the anodes to form carbon monoxide, the latter escaping and being burnt to carbon dioxide outside.
The dissociation of the hybrid element in a plant must be obviated by careful selection.
All thallium compounds volatile or liable to dissociation at the temperature of the flame of a Bunsen lamp impart to such flame an intense green colour.
For strong solutions the discrepancies from Raoult's law often become very large, even if dissociation is allowed for.
Vapour density determinations indicate that dissociation occurs when the vapour is heated above the boiling point.
The theory of the ionization of salts in solution has raised much discussion amongst chemists, but the general fact is certain that electricity only moves through liquids in association with matter, and simultaneously involves chemical dissociation of molecular groups.
From 1865 onwards he treated this question in several papers, and in particular maintained the dissociation of vapour of chloral hydrate, in opposition to H.
Ostwald, among other chemists, in support of the hypothesis of electrolytic dissociation in solutions.
It boils at 290°, forming a colourless vapour which just about the boiling-point corresponds in density to tetratomic molecules, P4; at 1500° to 1700°, however, Biltz and Meyer detected dissociation into P2 molecules.
It does not dissociate on heating as do the pentachloride and pentabromide, thus indicating the existence of pentavalent phosphorus in a gaseous compound; dissociation, however, into the trifluoride and free fluorine may be brought about by induction sparks of 150 to 200 mm.
It sublimes when heated, but under pressure it melts at 148°, giving a normal vapour density, but on further heating it dissociates into the trichloride and chlorine; this dissociation may be retarded by vapourizing in an atmosphere of chlorine.
Vapour density determinations at 448° indicate a partial dissociation of the double molecule Fe2Cl6I on stronger heating it splits into ferrous chloride and chlorine.
Deviation from this rule indicates molecular dissociation or association.
The dissociation theory refers this to the action of electric charges carried by the free ions.
In order that there should be no change in the states of dissociation on mixing, it is necessary, therefore, that the concentration of the hydrogen ions should be the same in each separate solution.
In the case of weaker acids, the dissociation of which is less complete, divergences from this constant value will occur, for some of the molecules have to be separated into their ions.
Compound bodies, we now know, have their own spectra, and only when dissociation occurs can the compound show the rays characteristic of the element: this perhaps was to be expected, but it came as a surprise and was not readily believed, that elements, as a rule, possess more than one spectrum according to the physical conditions under which they become luminous.
In every solid body there is a continual atomic dissociation, the result of which is that mixed up with the atoms of chemical matter composing them we have a greater or less percentage of free electrons.
Wharfinger states that in chlorosis the specific action of iron is only obtained by administering those inorganic preparations which give a reaction with the ordinary reagents; the iron ions in a state of dissociation act as a catalytic agent, destroying the hypothetical toxin which is the cause of chlorosis.