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Black oxide, definition

There can be little doubt that black oxide of manganese is the mineral here referred to though the description is not definite. [Pg.253]

The method of oxidation is essentially that of Russigd The product obtained is slightly but definitely better than that produced at a lower temperature, or by adding the sulfuric acid to the dichromate solution, or by using ferric clrloride as in A). These latter procedures give the same yield, but the product is less pure and contains a black, ether-soluble impurity which must be washed out carefully after crystallization from ether. [Pg.70]

For iridium the position is reversed. This time it is the black dioxide, Ir02, with the rutile structure (p. 961), which is the only definitely established oxide. It is obtained by heating the metal in oxygen or by dehydrating the precipitate produced when alkali is added to an aqueous solution of [IrCl6] . Contamination either by unreacted metal or by alkali is, however, difficult to avoid. The other oxide, Ir203, is said to be... [Pg.1118]

The consolidated titanate waste pellets are similar in appearance to their glass counterparts, i.e., both are dense, black and apparently homogeneous. Microscopic analyses, however, reveal important differences between these two waste forms. While little definitive work has been done with glassy waste forms, it is apparent that several readily soluble oxide particulates of various nuclides are simply encapsulated in the glass matrix. The titanate waste form has undergone extensive analyses which includes optical microscopy, x-ray, scanning electron microscopy, microprobe, and transmission electron microscopy (l ) The samples of titanate examined were prepared by pressure sintering and consisted of material from a fully loaded titanate column. Zeolite and silicon additions were also present in the samples. [Pg.139]

Bismuth(III) oxide, Bi O is the compound produced by heating the metal, or its carbonate, in air. It is definitely a basic oxide, dissolving readily 111 acid solutions, and unlike the arsenic or antimony compounds, not amphiprotic in solution, although it forms stoichiometric addition compounds on heating with oxides of a number of other metals. It exists in three modifications, white rhombohedral, yellow rhombohedral, and gray-black cubical, Bismuth(II) oxide. BiO, has been produced by heating die basic oxalate. [Pg.238]

The electrophilic attack of nitric oxide on a bent nitrosyl is now realized to be the path by which hyponitrite-bridged Co species are formed. Reaction (93) was known since the time of Werner (217), but the black and red isomers of [Co(NO)(NH3)5]2+ obtained from this reaction defied definitive characterization for many years. It has now been established that the black isomer is a mononuclear, octahedral complex of Co(III) and NO- (218) while the red isomer is a hyponitrite bridged system containing two Co(III) ions (219). [Pg.151]

Silver sulphide, Ag2S.—The sulphide occurs in nature as argentite, and also in combination with many other sulphides. It is formed by direct synthesis from its elements at ordinary temperatures,7 and also by immersion of the metal in solutions of alkali-metal poly sulphides. It can be prepared in cubic crystals by passing sulphur-vapour over heated silver, or by the action of hydrogen trisulphide, H2S3, on silver oxide. It is the only definite compound produced by fusion of mixtures of silver and sulphur in different proportions.9 The black, amorphous form is precipitated by the action of hydrogen sulphide or a soluble sulphide on a solution of a silver salt. It is also produced by the action of hydrogen sulphide on metallic silver, a reversible reaction.10... [Pg.312]

Uranium Pentoxide, U2O5.—The existence of this oxide is not definitely established. It has been described as the black product obtained when a uranium salt of a volatile acid is strongly ignited in air when uranyl sulphate, (U02)S04.3H20, is rapidly heated when ammonium diuranate, (NH4)2U207-6H20, is heated in a carbon crucible and when a solution of uranyl nitrate is electrolysed. [Pg.302]

In the formation of valuable oxygen-containing compounds by the controlled or partial oxidation of hydrocarbons, such as benzene, two factors are of great importance, i.e., temperature and type of catahst. Other factors such as composition of hydrocarbon-air mixture and time of contact are also important. All of these factors are intimately related to each other and the successful operation of the process depends upon the control of each of them. It was early found that if mixtures of benzene apor and air in excess of tliat necessary for complete combustion were passed through heated tubes of such non-catalytic materials as iron, silica, aluminum, etc., and the temperature allowed to rise at will, only complete combustion products could be obtained, and no intermediate oxidation products could be isolated. On the other hand, if such mixtures of benzene vapor and air were passed over a catalyst such as platinum black, complete combustion also occurred but at a temperature far below that necessary in the empty tube made of non-catalytic material. However, only very small amounts of intermediate products could be obtained with such an active catalyst even when the temperatures were carefully controlled or the time of contact made very short. It is difficult to form any definite idea as to the temperatures which were actually attained by the reacting gases in most of the early experiments reported in the literature. Lack of uniformity in construction of reaction chambers, in displacement of cata-... [Pg.379]


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See also in sourсe #XX -- [ Pg.233 ]




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