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Dioxide dissolution

The aqueous solution is safe to handle, the dissolution being essentially physical. On standing in sunlight the solution slowly decomposes to a mixture of acids. In alkaline solution a mixture of chlorate(lll), CIO2, and chlorate(V), CIO J, ions is rapidly produced. Chlorine dioxide is paramagnetic, the molecule containing an odd electron and having a structure very like that of NOj (p. 231). [Pg.335]

Niobium Dioxide Fluoride. Niobium dioxide fluoride, Nb02F, is formed on dissolution of niobium pentoxide in 48 wt % aqueous hydrofluoric acid, evaporation of the solution to dryness, and heating to 250°C. [Pg.27]

Titanium Silicides. The titanium—silicon system includes Ti Si, Ti Si, TiSi, and TiSi (154). Physical properties are summarized in Table 18. Direct synthesis by heating the elements in vacuo or in a protective atmosphere is possible. In the latter case, it is convenient to use titanium hydride instead of titanium metal. Other preparative methods include high temperature electrolysis of molten salt baths containing titanium dioxide and alkalifluorosiUcate (155) reaction of TiCl, SiCl, and H2 at ca 1150°C, using appropriate reactant quantities for both TiSi and TiSi2 (156) and, for Ti Si, reaction between titanium dioxide and calcium siUcide at ca 1200°C, followed by dissolution of excess lime and calcium siUcate in acetic acid. [Pg.132]

The analytical chemistry of titanium has been reviewed (179—181). Titanium ores can be dissolved by fusion with potassium pyrosulfate, followed by dissolution of the cooled melt in dilute sulfuric acid. For some ores, even if all of the titanium is dissolved, a small amount of residue may still remain. If a hiU analysis is required, the residue may be treated by moistening with sulfuric and hydrofluoric acids and evaporating, to remove siUca, and then fused in a sodium carbonate—borate mixture. Alternatively, fusion in sodium carbonate—borate mixture can be used for ores and a boiling mixture of concentrated sulfuric acid and ammonium sulfate for titanium dioxide pigments. For trace-element deterrninations, the preferred method is dissolution in a mixture of hydrofluoric and hydrochloric acids. [Pg.134]

Neutralizing Amines. Neutralizing amines are used to neutralize the acid (H" ) generated by the dissolution of carbon dioxide or other acidic process contaminants in the condensate. These amines hydrolyze when added to water and generate the hydroxide ions required for neutralization ... [Pg.265]

Total carbon in beryUium is determined by combustion of the sample, along with an accelerator mixture of tin, iron, and copper, in a stream of oxygen (15,16). The evolved carbon dioxide is usuaUy measured by infrared absorption spectrometry. BeryUium carbide can be determined without interference from graphitic carbon by dissolution of the sample in a strong base. BeryUium carbide is converted to methane, which can be determined directly by gas chromatography. Alternatively, the evolved methane can be oxidized to carbon dioxide, which is determined gravimetricaUy (16). [Pg.69]

Thus for non-ferrous metals, SO is consumed in the corrosion reactions whereas in the rusting of iron and steel it is believed that ferrous sulphate is hydrolysed to form oxides and that the sulphuric acid is regenerated. Sulphur dioxide thus acts as a catalyst such that one SOj" ion can catalyse the dissolution of more than 100 atoms of iron before it is removed by leaching, spalling of rust or the formation of basic sulphate. These reactions can be summarised as follows ... [Pg.343]

Dissolution Some waters continuously dissolve appreciable amounts of copper . Factors that favour this action are high free carbon dioxide, chloride and sulphate contents, low hardness, and increase of temperature. The trouble is therefore most prevalent in hot, soft, acid waters. The corrosion is general and the resulting thinning is so slight that the useful life of the pipe or component is virtually unaffected (unless impingement attack... [Pg.700]

The effect of pH on the corrosion of zinc has already been mentioned (p. 4.170). In the range of pH values from 5 -5 to 12, zinc is quite stable, and since most natural waters come within this range little difficulty is encountered in respect of pH. The pH does, however, affect the scale-forming properties of hard water (see Section 2.3 for a discussion of the Langelier index). If the pH is below the value at which the water is in equilibrium with calcium carbonate, the calcium carbonate will tend to dissolve rather than form a scale. The same effect is produced in the presence of considerable amounts of carbon dioxide, which also favours the dissolution of calcium carbonate. In addition, it is important to note that small amounts of metallic impurities (particularly copper) in the water can cause quite severe corrosion, and as little as 0-05 p.p.m. of copper in a domestic water system can be a source of considerable trouble with galvanised tanks and pipes. [Pg.819]

Complete dissolution of plutonium residues, especially high temperature calcined plutonium dioxide contained in residues such as incinerator ash, continues to cause problems, despite continued research since the Manhattan Project (9). Methods to improve the Rocky Flats system include the use of additives (e.g., cerium) and electrochemistry, other solvents (HCl-SnCl2) as well as high-temperature fusion methods (10). High pressure dissolution, HF preleaching, fluorination, and other methods are being investigated. [Pg.372]

The pentafluorophenylcopper tetramer is usually analytically pure as isolated and melts at 200° with decomposition. If any significant decomposition occurs during the final drying, the product can be purified by dissolution in ether, filtration to remove copper metal, and precipitation by addition of hexane. It can also be recrystallized from benzene. When kept in a sealed container under nitrogen at room temperature, pentafluorophenyl copper tetramer appears to be stable for reasonable periods. It can be stored indefinitely at -78° under an atmosphere of carbon dioxide. [Pg.64]

Nanoparticles of the semicondnctor titanium dioxide have also been spread as mono-layers [164]. Nanoparticles of TiOi were formed by the arrested hydrolysis of titanium iso-propoxide. A very small amount of water was mixed with a chloroform/isopropanol solution of titanium isopropoxide with the surfactant hexadecyltrimethylammonium bromide (CTAB) and a catalyst. The particles produced were 1.8-2.2 nm in diameter. The stabilized particles were spread as monolayers. Successive cycles of II-A isotherms exhibited smaller areas for the initial pressnre rise, attributed to dissolution of excess surfactant into the subphase. And BAM observation showed the solid state of the films at 50 mN m was featureless and bright collapse then appeared as a series of stripes across the image. The area per particle determined from the isotherms decreased when sols were subjected to a heat treatment prior to spreading. This effect was believed to arise from a modification to the particle surface that made surfactant adsorption less favorable. [Pg.89]

Lj + G —> L2 Absorption of gases in water Dissolution of gases like hydrogen chloride, ammonia and carbon dioxide in water... [Pg.310]

The dissolution of porous minerals, the combustion of porous carbon, the reaction between porous carbon and carbon dioxide, and the formation of nickel carbonyl from pure nickel are some examples of fluid-solid reactions where the reactant solid is porous and where no solid reaction product is formed. A reaction of this type can be represented as... [Pg.333]

The presentation finally descends on the very last of the listed chemical precipitation processes, and this pertains to precipitation implemented by carbonate anions (CO-). The dissolution of carbon dioxide takes place with the formation of the weak diabasic acid, H2C03. The overall dissociation of this acid (dissociation constant, KD) is represented by ... [Pg.539]

Sodium bicarbonate tablets are administered in increments of 325 and 650 mg tablets. A 650 mg tablet of sodium bicarbonate contains 7.7 mEq (7.7 mmol) each of sodium and bicarbonate. Sodium retention associated with sodium bicarbonate can cause volume overload, which can exacerbate hypertension and chronic heart failure. Patient tolerability of sodium bicarbonate is low because of carbon dioxide production in the GI tract that occurs during dissolution. [Pg.392]

Amino-(122, R = H) gave 3-acetamido-2-quinoxalinecarbonitrile 1,4-dioxide (122, R = Ac) (excess neat Ac20, reflux to dissolution 80%).1012... [Pg.279]

FIGURE 44 Weathering. A weathered sandstone column. Calcite (composed of calcium carbonate) is dissolved by rain and groundwater (see Textbox 73). When stone in which calcite is a main component as, for example, sandstone, limestone, and marble, is in contact with water for long periods of time, it is weathered and partly or entirely dissolved. Pollutants such as sulfur dioxide are fundamental in accelerating the weathering and dissolution process. When sulfur dioxide, for example, dissolves in rainwater, it forms sulfuric acid, a strong acid that, at ambient temperatures, rapidly dissolves calcium carbonate. [Pg.234]


See other pages where Dioxide dissolution is mentioned: [Pg.499]    [Pg.500]    [Pg.200]    [Pg.354]    [Pg.174]    [Pg.202]    [Pg.240]    [Pg.112]    [Pg.198]    [Pg.134]    [Pg.102]    [Pg.2205]    [Pg.265]    [Pg.265]    [Pg.1015]    [Pg.347]    [Pg.729]    [Pg.242]    [Pg.152]    [Pg.5]    [Pg.200]    [Pg.730]    [Pg.555]    [Pg.713]    [Pg.99]    [Pg.105]    [Pg.25]    [Pg.118]    [Pg.139]    [Pg.492]    [Pg.248]    [Pg.446]    [Pg.447]   
See also in sourсe #XX -- [ Pg.507 , Pg.511 , Pg.512 ]




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Dissolution of carbon dioxide

Dissolution plutonium dioxide

Uranium dioxide dissolution

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