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Carbonate content

Fuel switch. The choice of fuel used in furnaces and steam boilers has a major effect on the gaseous utility waste from products of combustion. For example, a switch from coal to natural gas in a steam boiler can lead to a reduction in carbon dioxide emissions of typically 40 percent for the same heat released. This results from the lower carbon content of natural gas. In addition, it is likely that a switch from coal to natural gas also will lead to a considerable reduction in both SO, and NO, emissions, as we shall discuss later. [Pg.293]

Fuel switch. Fuel switch from, say, coal to natural gas reduces the CO2 emissions for the same heat release because of the lower carbon content of natural gas. [Pg.306]

The student will doubtless be aware of the fact that methyl, ethyl, n-propyl and iso propyl alcohols are completely miscible with water. The solubilities of the higher aloohols decrease progressively as the carbon content increases. The solubilities of all types of alcohols with five carbon atoms or more are quite small. For the isomeric butyl alcohols the solubilities (g. per 100 g. of water at 20°) are n-butyl, 8 iso-butyl, 23 scc.-butyl, 13 ierl.-butyl, completely miscible. [Pg.260]

The lower members have remarkably disagreeable odours, but the offensive odour diminishes with increasing carbon content until it almost disappears at about CioH2i SH, n-dodecyl (lauryl) mercaptan. [Pg.496]

The glycidic esters are of interest primarily because upon hydrolysis aud decarboxylation they aflFord aldehydes (if ClCHjCOOEt is used) or ketones (if substituted chloroacetic esters- ClCHRCOOEt are employed) having a higher carbon content than the original aldehyde or ketone. Thus (I) gives o-phenyl-propionaldehyde or hydratropaldehyde (II) ... [Pg.906]

Group I. This includes the lower members of the various homologous series (4-5 atoms in a normal chain) that contain oxygen and/or nitrogen in their structures they are soluble iu water because of their low carbon content. If the compound is soluble in both water and ether, it would also be soluble in other solvents so that further solubility tests are generally unnecessary the test with sodium bicarbonate solution should, however, be performed (see Section XI,6). [Pg.1053]

Burning of any hydrocarbon (fossil fuel) or, for that matter, any organic material converts its carbon content to carbon dioxide and its hydrogen to water. Because power plants and other industries emit large amounts of carbon dioxide, they contribute to the so-called greenhouse warming effect on our planet, which causes significant en-... [Pg.215]

Esters can participate m hydrogen bonds with substances that contain hydroxyl groups (water alcohols carboxylic acids) This confers some measure of water solubil ity on low molecular weight esters methyl acetate for example dissolves m water to the extent of 33 g/100 mL Water solubility decreases as the carbon content of the ester increases Fats and oils the glycerol esters of long chain carboxylic acids are practically insoluble m water... [Pg.846]

The chemical characteristics of biomass vary over a broad range because of the many different types of species. Table 8 compares the typical analyses and energy contents of land- and water-based biomass, ie, wood, grass, kelp, and water hyacinth, and waste biomass, ie, manure, urban refuse, and primary sewage sludge, with those of cellulose, peat, and bituminous coal. Pure cellulose, a representative primary photosynthetic product, has a carbon content of... [Pg.13]

Most of the renewable carbon sources Hsted in Table 8 have carbon contents near this value. When adjusted for moisture and ash contents, it is seen that with the exception of the sludge sample, the carbon contents are slightly higher than that of cellulose, but span a relatively narrow range. [Pg.14]

Fuel economy is measured usiag a carbon balance method calculation. The carbon content of the exhaust is calculated by adding up the carbon monoxide (qv), carbon dioxide (qv), and unbumed hydrocarbons (qv) concentrations. Then usiag the percent carbon ia the fuel, a volumetric fuel economy is calculated. If the heating value of the fuel is known, an energy specific fuel economy ia units such as km/MJ can be calculated as well. [Pg.189]

Carbon content is usually about 0.15% but may be higher in bolting steels and hot-work die steels. Molybdenum content is usually between 0.5 and 1.5% it increases creep—mpture strength and prevents temper embrittlement at the higher chromium contents. In the modified steels, siUcon is added to improve oxidation resistance, titanium and vanadium to stabilize the carbides to higher temperatures, and nickel to reduce notch sensitivity. Most of the chromium—molybdenum steels are used in the aimealed or in the normalized and tempered condition some of the modified grades have better properties in the quench and tempered condition. [Pg.117]

Cmde products from organic-based processes contain organic impurities which affect color, odor, surface tension, and stabiUty, and ate normally pretreated to reduce the carbon content before final purification and concentration by various distillation methods. [Pg.478]

The carbon content of DRI depends primarily on the direct reduction process used and the way the process is operated. Carbon content can be adjusted within limits by operating changes within the DR process. Most steelmakers prefer slightly more carbon than is required to balance the remaining FeO in the DRI. DRI from gas-based processes typically contains 1 to 2.5% carbon, mostly in the form of cementite [12169-32-3] Fe C. DRI containing approximately 6 to 7% carbon in the form of cementite is called iron carbide. DRI from coal-based, rotary-kiln processes contains very low (ca 0.5%) levels of carbon. [Pg.425]

In the past, all grades of refined ferromanganese were made by various modifications of multistep silicon reduction processes. Depending on the carbon content desired in the product, a manganese ore and lime mixture was allowed to react with the silicon in silicomanganese or low carbon silicomanganese in an open, electric-arc furnace. The equilibrium reaction is... [Pg.494]

Austenitic steels that are used for nonmagnetic and cryogenic appHcations have lower carbon content than Hadfteld steels and range in composition from 15 to 29% manganese (30). [Pg.496]

Fig. 5. Schematic illustiation of the inciease in caibon content with caibutizing time. The maximum caibon content at the surface is given by the saturation value, (a) Phase diagram (b) plot of carbon content under the surface where the arrow represents increasing time at temperature (9). Fig. 5. Schematic illustiation of the inciease in caibon content with caibutizing time. The maximum caibon content at the surface is given by the saturation value, (a) Phase diagram (b) plot of carbon content under the surface where the arrow represents increasing time at temperature (9).
If the gas has the correct composition, the carbon content at the surface increases to the saturation value, ie, the solubiUty limit of carbon in austenite (Fig. 2), which is a function of temperature. Continued addition of carbon to the surface increases the carbon content curve. The surface content is maintained at this saturation value (9) (Fig. 5). The gas carburizing process is controlled by three factors (/) the thermodynamics of the gas reactions which determine the equiUbrium carbon content at the surface (2) the kinetics of the chemical reactions which deposit the carbon and (J) the diffusion of carbon into the austenite. [Pg.213]

The temperature dependence of K is weU known experimentally. At a given temperature, if the composition of the gas is fixed, then equiUbrium carbon content is fixed. This composition is sometimes referred to as the carbon potential. [Pg.213]

The relationship between the gas composition, austenite carbon content, and temperature is known. For example, a gas in equiUbrium with austenite containing 0.8% C must have the partial pressure ratio / Pco ) comprised of only CO and CO2, then the sum of the partial... [Pg.213]

Many commercial gases are generated by burning hydrocarbons (qv) eg, natural gas or propanes, in air (see Gas, natural Liquified petroleum gas). The combustion process, especially the amount of air used, determines the gas composition. For a given fuel-to-air ratio, the gas composition can be used to determine the water vapor content required to achieve a desired equiUbrium carbon content of the austenite (see Combustiontechnology). [Pg.213]

The equihbrium carbon content of austenite also depends on the alloy content, eg, Cr or Ni of the steel. A given gas composition equiUbrates with a carbon content of the austenite which is different for a plain carbon steel than for an alloy steel. [Pg.213]

Diffusion of Carbon. When carbon atoms are deposited on the surface of the austenite, these atoms locate in the interstices between the iron atoms. As a result of natural vibrations the carbon atoms rapidly move from one site to another, statistically moving away from the surface. Carbon atoms continue to be deposited on the surface, so that a carbon gradient builds up, as shown schematically in Figure 5. When the carbon content of the surface attains the equihbrium value, this value is maintained at the surface if the kinetics of the gas reactions are sufficient to produce carbon atoms at least as fast as the atoms diffuse away from the surface into the interior of the sample. [Pg.213]

The maximum surface carbon content is usually set by the gas composition via the equiUbtium constant. If the gas reaction kinetics deposit carbon at a rate which carmot be equaled by the diffusion of carbon into the steel, then the surface value may be less than the possible equiUbtium value. [Pg.214]

In some cases, the carbon profile may not provide the necessary hardness or other properties. For example, if the carbon content is too high, quenching to room temperature may not produce all martensite at the surface because the high carbon content places the martensite finish temperature, Mj below room temperature. This results in the presence of soft retained austenite, and a low surface hardness. Conversion to martensite by subzero cooling to below the temperature can increase the hardness (Fig. 6) (12). [Pg.214]

Fig. 6. (a) The effect of sub2ero cooling on the hardness gradient in a carburized and quenched 3312 steel where (e) is oil quenched from 925 to 20°C and ( ) is cooled to -195°C. The initial quench to 20°C does not convert all of the austenite to martensite because the high carbon content in the surface region lowers the temperature below 20°C. Subsequent cooling to -195°C converts most of the retained austenite to martensite, raising the hardness, (b) The... [Pg.214]

Addition of niobium to austenitic stainless steels inhibits intergranular corrosion by forming niobium carbide with the carbon that is present in the steel. Without the niobium addition, chromium precipitates as a chromium carbide film at the grain boundaries and thus depletes the adjacent areas of chromium and reduces the corrosion resistance. An amount of niobium equal to 10 times the carbon content is necessary to prevent precipitation of the chromium carbide. [Pg.26]

Carbonate Decomposition. The carbonate content of Green River oil shale is high (see Table 4). In addition, the northern portion of the Piceance Creek basin contains significant quantities of the carbonate minerals nahcoUte and dawsonite. The decomposition of these minerals is endothermic and occurs at ca 600—750°C for dolomite, 600—900°C for calcite, 350—400°C for dawsonite, and 100—120°C for nahcohte. Kinetics of these reactions have been studied (19). Carbon dioxide, a product of decomposition, dilutes the off-gases produced from retorting processes at the above decomposition temperatures. [Pg.347]

A flame-ionization, total hydrocarbon analyzer determines the THC, and the total carbon content is calculated as methane. Other methods include catalytic combustion to carbon dioxide, which may be deterrnined by a sensitive infrared detector of the nondispersive type. Hydrocarbons other than methane and acetylene are present only in minute quantities and generally are inert in most appHcations. [Pg.480]

Physical Properties. Some physical properties of alkyl hydroperoxides (in order of increasing carbon content) are Hsted in Table 1 (44). Descriptions of hydroperoxides are given in the chemical Hterature (1,4—6,10,28,43,45). [Pg.102]


See other pages where Carbonate content is mentioned: [Pg.36]    [Pg.187]    [Pg.392]    [Pg.1046]    [Pg.132]    [Pg.130]    [Pg.14]    [Pg.78]    [Pg.346]    [Pg.123]    [Pg.427]    [Pg.71]    [Pg.163]    [Pg.490]    [Pg.213]    [Pg.213]    [Pg.214]    [Pg.217]    [Pg.360]    [Pg.5]    [Pg.161]   
See also in sourсe #XX -- [ Pg.154 ]




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