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Acid-forming oxides

After firing, restoring the bomb pressure to atmospheric pressure too rapidly may result in the loss of oxides of sulfur and nitrogen. A correction must be made to the gross calorific value for the amounts of these acid-forming oxides produced in the bomb. Their loss results in a high calorific value. The pressure of the bomb must be restored very slowly to prevent this. [Pg.135]

Of the perchlorates A[C104] naturally no polynuclear complex ions are conceivable in fact two tetrahedra, C1207, here form the neutral acid-forming oxide. [Pg.70]

Solid acid-forming oxides give positively charged clouds. [Pg.315]

Silica belongs to the class of acid-forming oxides, and the silicic acid corresponding to the oxide Si02 must have the formula H SiOf or Si(OH) , as is seen from a conparison of the hydrides of the four groups of tire non-metalUc dements. [Pg.573]

Hydride complexes react with a variety of acids. Strong acids usually result in salts, while weak acids form oxidative addition products. In the latter case, reductive elimination of dihydrogen may follow, affording a convenient route for introducing conjugate bases X such as C CR, SiRa, acac (aceylacetonate), SPh, and OCOR into the coordination sphere of the metal ... [Pg.23]

H0S(0)200S(0)20H. Dibasic acid formed as salts by electrolysis of sulphates at low temperatures and high current density. The acid and persulphates are strong oxidizing agents ( "[S20a] to S04 -t-2 01 volts in acid) but the reactions are often slow. Compare permonosulphuric acid. [Pg.301]

Racemic acid, ( )-tartaric acid, is a compound of the two active forms. M.p. 273 C (with IHjO), m.p. 205°C (anhydrous). Less soluble in water than (-t-)-tartaric acid. Formed, together with mesotartaric acid, by boiling (4-)-tartaric acid with 30% NaOH solution, or by oxidation of fumaric acid. Potassium hydrogen racemate is very insoluble. [Pg.385]

Arsenic dissolves in concentrated nitric acid forming arsenicfV) acid, H3ASO4, but in dilute nitric acid and concentrated sulphuric acid the main product is the arsenic(III) acid, HjAsOj. The more metallic element, antimony, dissolves to form the (III) oxide Sb O, with moderately concentrated nitric acid, but the (V) oxide Sb205 (structure unknown) with the more concentrated acid. Bismuth, however, forms the salt bismulh(lll) nitrate Bi(N03)3. 5H,0. [Pg.212]

The more noble metals (for example copper, mercury and silver) can form oxides, and exhibit variable oxidation state in such compounds (for example CU2O, CuO), but it is not easy to prepare such oxides by direct action of oxygen on the metal, and elevated temperatures are necessary. Moreover, in the case of silver and mercury, loss of oxygen from the oxide by heating is easy. The oxidesare, however, basic (for example Ag20 - Ag, CuO - Cu in acids). [Pg.286]

The other more electronegative elements are non-metals and form oxides which are entirely covalent and usually acidic. For example, sulphur yields the oxides SO2 and SO3, dissolving in bases to form the ions SO3 and SO4" respectively. A few non-metallic oxides are often described as neutral (for example carbon monoxide and dinitrogen oxide) because no directly related acid anion is known to exist. [Pg.286]

Manganese(IV) oxide is a dark-brown solid, insoluble in water and dilute acids. Its catalytic decomposition of potassium chlor-ate(V) and hydrogen peroxide has already been mentioned. It dissolves slowly in alkalis to form manganates(lW), but the constitution of these is uncertain. It dissolves in ice-cold concentrated hydrochloric acid forming the complex octahedral hexachloromangan-ate(IV) ion ... [Pg.387]

Pyronines. Pyronines are diphenylmethane derivatives synthesized by the condensation of y -dialkylarninophenols with formaldehyde, followed by oxidation of tiie xantiiene detivative (12) to the coiiesponding xanthydiol (13) which in the presence of acid forms the dye (14). If R is methyl, the dye produced is... [Pg.399]

Ketene can be obtained by reaction of carbon oxides with ethylene (53). Because ketene combines readily with acetic acid, forming anhydride, this route may have practical appHcations. Litde is known about the engineering possibiHties of these reactions. [Pg.78]

Dry chlorine has a great affinity for absorbing moisture, and wet chlorine is extremely corrosive, attacking most common materials except HasteUoy C, titanium, and tantalum. These metals are protected from attack by the acids formed by chlorine hydrolysis because of surface oxide films on the metal. Tantalum is the preferred constmction material for service with wet and dry chlorine. Wet chlorine gas is handled under pressure using fiberglass-reinforced plastics. Rubber-lined steel is suitable for wet chlorine gas handling up to 100°C. At low pressures and low temperatures PVC, chlorinated PVC, and reinforced polyester resins are also used. Polytetrafluoroethylene (PTFE), poly(vinyhdene fluoride) (PVDE), and... [Pg.510]

Cellulose nitrate also has widespread use as an adhesive and coating material. Whereas stabilizers are added to products, eg, sodium carbonate as a neutralizer, many conservators are hesitant to use cellulose nitrate materials because of the inherent instabiUty and the dangers to the object from nitric acid, formed when the nitric oxide combines with moisture. [Pg.427]

Oxides and hydroxides react with HCl to form a salt and water as in a simple acid—base reaction. However, reactions with low solubiHty or insoluble oxides and hydroxides is complex and the rate is dependent on many factors similar to those for reactions with metals. Oxidizing agents such as H2O2, H2SeO, and V2O3 react with aqueous hydrochloric acid, forming water and chlorine. [Pg.444]

Glycohc acid also undergoes reduction or hydrogenation with certain metals to form acetic acid, and oxidation by hydrogen peroxide ia the presence of ferrous salts to form glyoxylic acid [298-12A], HCOCOOH, and ia the presence of ferric salts ia neutral solution to form oxaHc acid, HOOCCOOH formic acid, HCOOH and Hberate CO2 and H2O. These reduction and oxidation reactions are not commercially significant. [Pg.516]

Acid Oxidation. Reactions of lead with acid and alkaUes are varied. Nitric acid, the best solvent for lead, forms lead nitrate acetic acid forms soluble lead acetate in the presence of oxygen sulfuric acid forms insoluble lead sulfate. Sulfuric acid is stored in containers with chemical or acid-grade lead. Lead dissolves slowly in HCl, but in the presence of aqueous alkaUes forms soluble plumbites and plumbates. [Pg.33]


See other pages where Acid-forming oxides is mentioned: [Pg.405]    [Pg.153]    [Pg.98]    [Pg.234]    [Pg.181]    [Pg.61]    [Pg.84]    [Pg.112]    [Pg.300]    [Pg.308]    [Pg.236]    [Pg.486]    [Pg.405]    [Pg.153]    [Pg.98]    [Pg.234]    [Pg.181]    [Pg.61]    [Pg.84]    [Pg.112]    [Pg.300]    [Pg.308]    [Pg.236]    [Pg.486]    [Pg.101]    [Pg.131]    [Pg.184]    [Pg.315]    [Pg.328]    [Pg.378]    [Pg.395]    [Pg.414]    [Pg.241]    [Pg.285]    [Pg.450]    [Pg.119]    [Pg.241]    [Pg.343]    [Pg.243]    [Pg.361]    [Pg.522]    [Pg.524]    [Pg.511]   
See also in sourсe #XX -- [ Pg.528 ]




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Acid-forming oxidation processe

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