Thenard in 1808 by heating boron trioxide with potassium, in an iron tube.
By strongly heating a mixture of boron trioxide and aluminium, protected from the air by a layer of charcoal, F.
Boron hydride has probably never been isolated in the pure condition; on heating boron trioxide with magnesium filings, a magnesium boride Mg 3 B 2 is obtained, and if this be decomposed with dilute hydrochloric acid a very evil-smelling gas, consisting of a mixture of hydrogen and boron hydride, is obtained.
This mixture burns with a green flame forming boron trioxide; whilst boron is deposited on passing the gas mixture through a hot tube, or on depressing a cold surface in the gas flame.
Thenard and is best obtained by heating a mixture of the trioxide and fluorspar with concentrated sulphuric acid.
Boron chloride BC1 3 results when amorphous boron is heated in chlorine gas, or more readily, on passing a stream of chlorine over a heated mixture of boron trioxide and charcoal, the volatile product being condensed in a tube surrounded by a freezing mixture.
It can also be prepared by heating borimide B2(NH)31 or by heating boron trioxide with a metallic cyanide.
Boron sulphide B 2 S 3 can be obtained by the direct union of the two elements at a white heat or from the tri-iodide and sulphur at 44 0 ° C., but is most conveniently prepared by heating a mixture of the trioxide and carbon in a stream of carbon bisulphide vapour.
Boron trioxide B203 is the only known oxide of boron; and may be prepared by heating amorphous boron in oxygen, or better, by strongly igniting boric acid.
2 2 a latter case with the formation of a blue solution which on heating, becomes colourless, molybdenum trioxide being formed with the liberation of sulphur dioxide.
Molybdenum combines with oxygen to form many oxides, the most important of which are: the monoxide, MoO.n (H 2 O), the sesquioxide, M0203, the dioxide, MoO 2, and the trioxide, MoO 3.
Molybdenum sesquioxide, Mo 2 O 3, a black mass insoluble in acids, is formed by heating the corresponding hydroxide in vacuo, or by digesting the trioxide with zinc and hydrochloric acid.
Molybdenum trioxide, Mo03, is prepared by oxidizing the metal or the sulphide by heating them in air, or with nitric acid.
Molybdenum trioxide, like chromium trioxide, is an acidic oxide, and forms salts known as molybdates.
Molybdenum disulphide, MoS 2, is found as the mineral molybdenite, and may be prepared by heating the trioxide with sulphur or sulphuretted hydrogen.
Dumas (Ann., 1860, 113, p. 32), by converting the trioxide into the metal, obtained the value 95.65.
At the same time a little trioxide is formed, and, according to Hempel (Ber., 1890, 2 3, p. 1 455), half the sulphur is converted into this oxide if the combustion be carried out in oxygen at a pressure of 40 to 50 atmospheres.
Four oxides of sulphur a.re known, namely sulphur dioxide, S02, sulphur trioxide, S03, sulphur sesquioxide, S203, and persulphuric anhydride, S 2 0 7.
Thionyl chloride, SOC1 21 may be obtained by the action of phosphorus pentachloride on sodium sulphite; by the action of sulphur trioxide on sulphur dichloride at 75 -80° C. (Journ.
Sulphur trioxide, SO 3, mentioned by Basil Valentine in the 15th century, was obtained by N.
Soc., 1856, 7, p. 11) by the direct union of sulphur trioxide with hydrochloric acid gas, may also be obtained by distilling concentrated sulphuric acid with phosphorus oxychloride: 2H 2 SO 4 +POC1 3 =2SO 2 C1.
Disulphuryl chloride, S 2 O 5 C1 2, corresponding to pyrosulphuric acid, is obtained by the action of sulphur trioxide on sulphur dichloride, phosphorus oxychloride, sulphuryl chloride or dry sodium chloride: 650 3- + 2POC1 3 = P 2 O 5 + 3S 2 O 5 C1 2; S2C12+ 5503 = S 2 0 5 C1 2 + 550 2; SO 3 + SO 2 C1 2 = S 2 0 5 C1 2; 2NaC1 + 3SO 3 = S 2 0 5 C1 2 -1 Na 2 SO 4.
Sulphur sesquioxide, S203, is formed by adding well-dried flowers of sulphur to melted sulphur trioxide at about 12-15° C. The sulphur dissolves in the form of blue drops which sink in the liquid and finally solidify in blue-green crystalline crusts.
Persulphuric anhydride, S207, is a thick viscous liquid obtained by the action of the silent discharge upon a mixture of sulphur trioxide and oxygen.
It is decomposed readily into sulphur trioxide and oxygen when heated.
For example take the oxides of nitrogen, N 2 0, NO, N 2 0 3, NO 2, N 2 0 5; these are known respectively as nitrous oxide, nitric oxide, nitrogen trioxide, nitrogen peroxide and nitrogen pentoxide.
The term allotropy has also been applied to inorganic compounds, identical in composition, but assuming different crystallographic forms. Mercuric oxide, sulphide and iodide; arsenic trioxide; titanium dioxide and silicon dioxide may be cited as examples.
Nitrous oxide, N 2 0, nitric oxide, NO, nitrogen trioxide, N203, nitrogen peroxide, N02, and nitrogen pentoxide, N205, whilst three oxyacids of nitrogen are known: hyponitrous acid, H2N202, nitrous acid, HN02, and nitric acid, HNO 3 (q.v.).
Nitrogen trioxide, N203, was first mentioned by J.
Soc., 18 9 0, 5, p. 59 o), by distilling arsenious oxide with nitric acid and cooling the distillate, obtained a green liquid which consisted of nitrogen trioxide and peroxide in varying proportions, and concluded that the trioxide could not be obtained pure.
Soc., 1907, 91, p. 1862) obtained nitrogen trioxide in the gaseous form by volatilizing the liquid under special conditions.
In small works the cupellation is finished in one furnace, and the resulting low-grade silver fined in a plumbago crucible, either by overheating in the presence of air, or by the addition of silver sulphate to the melted silver, when air or sulphur trioxide and oxygen oxidize the impurities.
By fusing litharge with boron trioxide, glasses of a composition varying with the proportions of the mixture are obtained; some of these are used in the manufacture of glass.
Three oxides of columbium are certainly known, namely the dioxide, Cb202, the tetroxide, Cb 2 0 4, and the pentoxide, Cb 2 0 5, whilst a fourth oxide, columbium trioxide, Cb203, has been described by E.
A hydrated tin trioxide, Sn03, was obtained by Spring by adding barium dioxide to a solution of stannous chloride and hydrochloric acid; the solution is dialysed, and the colloidal solution is evaporated to form a white mass of 2Sn03 H20.
In recent practice some sulphin trioxide, or fuming sulphuric acid, is added, so that the mixture of acids contains less than I% of water.
Titanium trioxide, T103, is obtained as a yellow precipitate by dropping the chloride into alcohol, adding hydrogen peroxide, and finally ammonium carbonate or potash.
When shaken with potash and air it undergoes autoxidation, hydrogen peroxide being formed first, which converts the trioxide into the dioxide and possibly pertitanic acid.
In the last case it becomes coated with a greyish-black layer of an oxide (dioxide (?)), at a red heat the layer consists of the trioxide (B1203), and is yellow or green in the case of pure bismuth, and violet or blue if impure; at a bright red heat it burns with a bluish flame to the trioxide.
Bismuth forms four oxides, of which the trioxide, B1203, is the most important.
Bismuth tetroxide, Bi 2 O 4, sometimes termed bismuth bismuthate, is obtained by melting bismuth trioxide with potash, or by igniting bismuth trioxide with potash and potassium chlorate.
It is also formed by oxidizing bismuth trioxide suspended in caustic potash with chlorine, the pentoxide being formed simultaneously; oxidation and potassium ferricyanide simply gives the tetroxide (Hauser and Vanino, Zeit.
It combines directly with sulphur trioxide to form a complex of composition TeC1 4.2SO 3.
Two oxides of the element are definitely known, viz., the dioxide, Te02, and the trioxide, Te03, whilst a monoxide, TeO, has also been described.
The trioxide is an orangecoloured solid which is formed when telluric acid is strongly heated.
Tantalum pentoxide, Ta205, is a white amorphous infusible powder, or it may be crystallized by strongly heating, or by fusing with boron trioxide or microcosmic salt.
It is insoluble in acids and exists in several hydrated forms. The osmiates, corresponding to the unknown trioxide 0503, are red or green coloured salts; the solutions are only stable in the presence of excess of caustic alkali; on boiling an aqueous solution of the potassium salt it decomposes readily, forming a black precipitate of osmic acid, H20s04.
Sodium trioxide, Na 2 O 31 is said to be formed from an excess of oxygen and a solution of sodammonium in liquid ammonia.
It Is Also Formed When Sulphur Trioxide Reacts With Carbon Bisulphide At 100° C., Cs2 3S03 =Cos 4So 2, And By The Decomposition Of Ethyl Potassium Thiocarbonate With Hydrochloric Acid, Co(0C2115)Sk Hc1= Cos Kc1 C 2 H 5 Oh.
Chromium forms three series of compounds, namely the chromous salts corresponding to CrO, chromous oxide, chromic salts, corresponding to Cr203, chromium sesquioxide, and the chromates corresponding to Cr0,, chromium trioxide or chromic anhydride.
Various other oxides of chromium, intermediate in composition between the sesquioxide and trioxide, have been described, namely chromium dioxide, Cr203 Cr03, and the oxide Cr03.2Cr203.
The sesquioxide, Cr 2 0 3, occurs native, and can be artificially obtained in several different ways, e.g., by igniting the corresponding hydroxide, or chromium trioxide, or ammonium bichromate, or by passing the vapours of chromium oxychloride through a red-hot tube, or by ignition of mercurous chromate.
Chromium trioxide, Cr03, is obtained by adding concentrated sulphuric acid to a cold saturated solution of potassium bichromate, when it separates in long red needles; the mother liquor is drained off and the crystals are washed with concentrated nitric acid, the excess of which is removed by means of a current of dry air.
Chromic sulphide, Cr2S3, results on heating chromium and sulphur or on strongly heating the trioxide in a current of sulphuretted hydrogen; it forms a dark green crystalline powder, and on ignition gives the sesquioxide.
BORIC ACID, or Boracic Acid, H 3 B0 3, an acid obtained by dissolving boron trioxide in water.
The acid on being heated to Ioo° C. loses water and is converted into metaboric acid, HBO 3 i at 140° C., pyroboric acid, H 2 B 4 0 7, is produced; at still higher temperatures, boron trioxide is formed.