Oxides basic

Thus, ihe strongly basic oxide ion attacks the weakly acidic SiOj in a molten salt as solvent (p. 187 ... 

Lead(II) oxide is the most basic oxide formed by a Group IV element. It dissolves easily in acids to give lead(II) salts but it also dissolves slowly in alkalis to give hydroxoplumbates(II) and must, therefore, be classed as an amphoteric oxide, for example ... 

Nitrogen is unusual in forming so many oxides. The acidity of the Group V oxides falls from phosphorus, whose oxides are acidic, through arsenic and antimony whose oxides are amphoteric, to the basic oxide ofbismuth. This change is in accordance with the change from the non-metallic element, phosphorus, to the essentially metallic element, bismuth. The +5 oxides are found, in each case, to be more acidic than the corresponding + 3 oxides. 

Sulphur trioxide unites exothermically with basic oxides to give sulphates, for example... 

Meta.1 Conta.mina.nts and Ash. Alkali metals form basic oxides that are very reactive toward acidic species such as the acid gases, siHcates, and alurninates. These form stable salts with acid gases if the off-gas contains such gases. Sodium, the most common of these metals, prefers to form chlorides ahead of sulfates. Sodium carbonate only forms in the absence of haHdes and sulfur oxides, SO. There usually is too Htde NO present to form nitrates (see Sodium compounds). 

Alkali metal haHdes can be volatile at incineration temperatures. Rapid quenching of volatile salts results in the formation of a submicrometer aerosol which must be removed or else exhaust stack opacity is likely to exceed allowed limits. Sulfates have low volatiHty and should end up in the ash. Alkaline earths also form basic oxides. Calcium is the most common and sulfates are formed ahead of haHdes. Calcium carbonate is not stable at incineration temperatures (see Calcium compounds). Transition metals are more likely to form an oxide ash. Iron (qv), for example, forms ferric oxide in preference to haHdes, sulfates, or carbonates. SiHca and alumina form complexes with the basic oxides, eg, alkaH metals, alkaline earths, and some transition-metal oxidation states, in the ash. 

Acidic Properties. As a typical acid, it reacts readily with alkaUes, basic oxides, and carbonates to form salts. The largest iadustrial appHcation of nitric acid is the reaction with ammonia to produce ammonium nitrate. However, because of its oxidising nature, nitric acid does not always behave as a typical acid. Bases having metallic radicals ia a reduced state (eg, ferrous and staimous hydroxide becoming ferric and stannic salts) are oxidized by nitric acid. Except for magnesium and manganese ia very dilute acid, nitric acid does not Hberate hydrogen upon reaction with metals. 

Basic oxides of metals such as Co, Mn, Fe, and Cu catalyze the decomposition of chlorate by lowering the decomposition temperature. Consequendy, less fuel is needed and the reaction continues at a lower temperature. Cobalt metal, which forms the basic oxide in situ, lowers the decomposition of pure sodium chlorate from 478 to 280°C while serving as fuel (6,7). Composition of a cobalt-fueled system, compared with an iron-fueled system, is 90 wt % NaClO, 4 wt % Co, and 6 wt % glass fiber vs 86% NaClO, 4% Fe, 6% glass fiber, and 4% BaO. Initiation of the former is at 270°C, compared to 370°C for the iron-fueled candle. Cobalt hydroxide produces a more pronounced lowering of the decomposition temperature than the metal alone, although the water produced by decomposition of the hydroxide to form the oxide is thought to increase chlorine contaminate levels. Alkaline earths and transition-metal ferrates also have catalytic activity and improve chlorine retention (8). 

The acidic character of siUca is shown by its reaction with a large number of basic oxides to form siUcates. The phase relations of numerous oxide systems involving siUca have been summarized (23). Reactions of siUca at elevated temperatures with alkaU and alkaline-earth carbonates result in the displacement of the more volatile acid, CO2, and the formation of the corresponding siUcates. Similar reactions occur with a number of nitrates and sulfates. Sihca at high temperature in the presence of sulfides gives thiosiUcates or siUcon disulfide, SiS2. 

Fused basic salts and basic oxides react with vitreous siUca at elevated temperatures. Reaction with alkaline-earth oxides takes place at approximately 900°C. Hahdes tend to dissolve vitreous siUca at high temperatures fluorides are the most reactive (95). Dry halogen gases do not react with vitreous siUca below 300°C. Hydrogen fluoride, however, readily attacks vitreous siUca. 

Bismuth trioxide is practically insoluble in water it is definitely a basic oxide and hence dissolves in acids to form salts. Acidic properties are just barely detectable, eg, its solubiUty slightly increases with increasing base concentration, presumably because of the formation of bismuthate(III) ions, such as Bi(OH) g and related species. 

Ash fusion characteristics are important in ash deposition in boilers. Ash deposition occurring on the furnace walls is termed slagging, whereas accumulation on the superheater and other tubes is termed fouling. A variety of empirical indexes have been developed (60,61) to relate fouling and slagging to the ash chemical composition through parameters such as acidic and basic oxides content, sodium, calcium and magnesium, and sulfur. 

SnO and hydrous tin(II) oxide are amphoteric, dissolving readily in aqueous acids to give Sn" or its complexes, and in alkalis to give the pyramidal Sn(OH)3 at intermediate values of pH, condensed basic oxide-hydroxide species form, e.g. [(OH)2SnOSn(OH)2] and [Sn3(OH)4] +, etc. Analytically, the hydrous oxide frequently has a composition close to 3Sn0.H20 and an X-ray study shows it to... 

Oppenauer oxidation of the enol ether (34) affords the corresponding 17 ketone (37) (the enol ether is stable to the basic oxidation conditions). This ketone affords the corresponding 17a-ethynyl compound on reaction with metal acetylides. Hydrolysis of the enol ether under mild conditions leads directly... 

These melts are very acidic so that basic oxides such as NiO and CoO would be strongly attacked, and as Rapp showed, addition of NaVO, to Na2S04 shifts the solubility minimum to more basic values while raising its absolute value. Thus the acidic oxides Cr20 AI2O3 and particularly SiOj would be expected to be more resistant to this type of attack. 

The attack of most glasses in water and acid is diffusion controlled and the thickness of the porous layer formed on the glass surface consequently depends on the square root of the time. There is ample evidence that the diffusion of alkali ions and basic oxides is thermally activated, suggesting that diffusion occurs either through small pores or through a compact body. The reacted zone is porous and can be further modified by attack and dissolution, if alkali is still present, or by further polymerisation. Consolidation of the structure generally requires thermal treatment. 

As an acidic oxide, SiOj is resistant to attack by other acidic oxides, but has a tendency towards fluxing by basic oxides. An indication of the likelihood of reaction can be obtained by reference to the appropriate binary phase equilibrium diagram. The lowest temperature for liquid formation in silica-oxide binary systems is shown below ... 

The second group is the group of oxyfluorides that are derived from ferroelectric oxides by means of fluorine-oxygen substitution. The basic oxides are usually perovskite, tetragonal tungsten bronze, pyrochlore, lithium tantalate etc. [400]. 

Silicon is the second most abundant element in the earth s crust. It occurs in sand as the dioxide Si02 and as complex silicate derivatives arising from combinations of the acidic oxide Si02 with various basic oxides such as CaO, MgO, and K20. The clays, micas, and granite, which make up most soils and rocks, are silicates. All have low solubility in water and they are difficult to dissolve, even in strong acids. Silicon is not found in the elemental state in nature. 

Because all of the alkaline earth oxides react with water to form basic hydroxides, they are called basic oxides. The reactions and their heats are as follows ... 

All elements in the s block are reactive metals that form basic oxides. The p-block elements tend to gain electrons to complete dosed shells they range from metals through metalloids to nonmetals. 

A basic oxide is an oxide that reacts with water to form a Bronsted base, as in the reaction... 

Basic oxides are ionic compounds, such as CaO, that also react with acids to give a salt and water. For instance, magnesium oxide, a basic oxide, reacts with hydrochloric acid ... 

Metals typically form basic oxides and nonmetals typically form acidic oxides, but what about the elements that lie on the diagonal frontier between the metals and nonmetals Along this frontier from beryllium to polonium, metallic character blends into nonmetallic character, and the oxides of these elements have both acidic and basic character (Fig. 10.7). Substances that react with both acids and bases are classified as amphoteric, from the Greek word for both. For example, aluminum oxide, A1203, is amphoteric. It reacts with acids ... 

Metals form basic oxides, nonmetals form acidic oxides the elements on a diagonal line from beryllium to polonium and several d-block metals form amphoteric oxides. 

The valence electron configuration of the atoms of the Group 2 elements is ns1. The second ionization energy is low enough to be recovered from the lattice enthalpy (Fig. 14.18). Flence, the Group 2 elements occur with an oxidation number of +2, as the cation M2+, in all their compounds. Apart from a tendency toward nonmetallic character in beryllium, the elements have all the chemical characteristics of metals, such as forming basic oxides and hydroxides. 

Galvanized containers should therefore not be used for transporting alkalis. Cadmium, which is lower down the group and is more metallic, has a more basic oxide. 

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