The existence of double salts, and the observations of L.
The insoluble salts are rose-red or violet in colour.
A large number of cobalt compounds are known, of which the empirical composition represents them as salts of cobalt to which one or more molecules of ammonia have been added.
In addition, certain inorganic salts, particularly certain compounds of potassium, are apparently necessary, but they seem to take no part in the chemical changes which take place.
The independence of the two is suggested by the fact that fungi can live, thrive and grow in nutritive media which contain carbohydrates together with certain salts of ammonia, but which are free from proteids.
This acid cannot be isolated in the free condition, but many of its salts are known.
FULMINIC ACID, Hcno or H 2 C 2 N 2 0 2, an organic acid isomeric with cyanic and cyanuric acids; its salts, termed fulminates, are very explosive and are much employed as detonators.
The pungent smelling salts snapped her out of the in-between place.
It dissolves in acids forming cobaltous salts, and on exposure to air it rapidly absorbs oxygen, turning brown in colour.
This hydroxide is soluble in well cooled acids, forming solutions which contain cobaltic salts, one of the most stable of which is the acetate.
The barium and magnesium salts of this acid are formed when baryta and magnesia are fused with cobalt sesquioxide.
The cobaltous salts are formed when the metal, cobaltous oxide, hydroxide or carbonate, are dissolved in acids, or, in the case of the insoluble salts, by precipitation.
The soluble salts are, when in the hydrated condition, also red, but in the anhydrous condition are blue.
They are precipitated from their alkaline solutions as cobalt sulphide by sulphuretted hydrogen, but this precipitation is prevented by the presence of citric and tartaric acids; similarly the presence of ammonium salts hinders their precipitation by caustic alkalis.
The hexammine salts are formed by the oxidizing action of air on dilute ammoniacal solutions of cobaltous salts, especially in presence of a large excess of ammonium chloride.
The pentammine purpureo-salts are formed from the luteo-salts by loss of ammonia, or from an air slowly oxidized ammoniacal cobalt salt solution, the precipitated luteosalt being filtered off and the filtrate boiled with concentrated acids.
They are formed by the action of nitrous fumes on ammoniacal solutions of cobaltous salts, or purpureo-salts, or by the mutual reaction of chlorpurpureosalts and alkaline nitrites.
The pentammine roseo-salts can be obtained from the action of concentrated acids, in the cold, on airoxidized solutions of cobaltous salts.
Cobalt salts may be readily detected by the formation of the black sulphide, in alkaline solution, and by the blue colour they produce when fused with borax.
It is monobasic and yields salts which only crystallize with great difficulty; when liberated, from these salts by a mineral acid it forms a syrupy nonvolatile mass.
After the vigorous reaction has ceased and all the sodium has been used up, the mass is thrown into dilute hydrochloric acid, when the soluble sodium salts go into solution, and the insoluble boron remains as a brown powder, which may by filtered off and dried.
They are yellowish-red solids, which behave as weak bases, their salts undergoing hydrolytic dissociation in aqueous solution.
For the phenazonium salts see Safranine.
The free acid, which is obtained by treating the salts with acids, is an oily liquid smelling like prussic acid; it is very explosive, and the vapour is poisonous to about the same degree as that of prussic acid.
Ratz (Monats., 1905, 26, p. 1241) obtained the value [a] D = - 16 9.54° at 20°; its salts are dextro-rotatory.
In 1826 he described the prismatically-coloured films of metal, known as Nobili's' rings, deposited electrolytically from solutions of lead and other salts when the anode is a polished iron plate and the cathode is a fine wire placed vertically above it.
The bark, very dark externally, is an excellent tanning substance; the inner layers form the quercitron of commerce, used by dyers for communicating to fabrics various tints of yellow, and, with iron salts, yielding a series of brown and drab hues; the colouring property depends on a crystalline principle called quercitrin, of which it should contain about 8%.
Solutions of yttria salts in their behaviour to reagents are not unlike those of zirconia.
Davy on the decomposition of the solutions of salts by the voltaic current were turned to account in the water voltameter telegraph of Sdmmering and the modification of it proposed by Schweigger, and in a similar method proposed by Coxe, in which a solution of salts was substituted for water.
It is a basic oxide, dissolving readily in acids, with the formation of salts, somewhat analogous to those of zinc.
Cadmium sulphide, CdS, occurs naturally as greenockite (q.v.), and can be artificially prepared by passing sulphuretted hydrogen through acid solutions of soluble cadmium salts, when it is precipitated as a pale yellow amorphous solid.
Cadmium salts can be recognized by the brown incrustation which is formed when they are heated on charcoal in the oxidizing flame of the blowpipe; and also by the yellow precipitate formed when sulphuretted hydrogen is passed though their acidified solutions.
Molybdenum trioxide, like chromium trioxide, is an acidic oxide, and forms salts known as molybdates.
Chiefly, they provide a number of channels, penetrating every part of the leaf, along which water and dissolved salts are conveyed to, and elaborated food-substances from, the mesophyll cells.
They possess a delicate Laticiferous layer of protoplasm, with numerous small nuclei lining Tissue the walls, while the interior of the tube (corresponding with the cell-vacuole) contains a fluid called latex, consisting of an emulsion of fine granules and drops of very various substances suspended in a watery medium in which various other substances (salts, sugars, rubber-producers, tannins, alkaloids and various enzymes) are dissolved.
Deficiency of nutritive salts, especially nitrates and phosphates; the presence of poisonous salts of iron, copper, &c., or (in the soil about the roots of trees in towns) of coal-gas and so forth.
The damping off of seedlingsand in saturated soils not only are the roots and root-hairs killed by asphyxiation, but the whole course of soil fermentation is altered, and it takes time to sweeten such by draining, because not only must the noxious bodies be gradually washed out and the lost salts restored, but the balance of suitable bacterial and fungal life must be restored.
Mineral salts, especially calcium carbonate, often rich in acidic humous compounds, and characterized by oak and birch woods, siliceous pasture, and heaths with much acidic humus in the sandy soil.
Habitats rich in mineral salts, especially calcium carbonate, poor in acidic humous compounds, and characterized by ash woods, beech woods, and calcareous pasture.
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