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Cadmium enrichment factor

Uranium is not a very rare element. It is widely disseminated in nature with estimates of its average abundance in the Earth s crust varying from 2 to 4 ppm, close to that of molybdenum, tungsten, arsenic, and beryllium, but richer than such metals as bismuth, cadmium, mercury, and silver its crustal abundance is 2.7 ppm. The economically usable tenor of uranium ore deposits is about 0.2%, and hence the concentration factor needed to form economic ore deposits is about 750. In contrast, the enrichment factors needed to form usable ore deposits of common metals such as lead and chromium are as high as 3125 and 1750, respectively. [Pg.70]

Scallops accumulate cadmium from sea water by an exceptionally high enrichment factor of 2.26 x 106. In particular, the visceral mass dried at 110 °C contains up to 2000 ppm of cadmium59). [Pg.107]

Here [Mp] and [Mr] are the metal concentrations in particulate matter and in crustal rock, respectively, and [Alp] and [Ah] are the concentrations of aluminum (or any suitable reference element) in particulate matter and crustal rock, respectively. Table 3 lists EEs for SPM or fine sediment in contrasting estuaries. Enrichment factors are close to unity for the baseline sediment and in the pristine Lena Estuary, while the greatest EE values are encountered for cadmium in the Rhine (impacted by the production of phosphate fertilizers) and the Scheldt, and for copper in Restronguet Creek (impacted by historical mining activity). The general sequence of EEs... [Pg.269]

Welz et al. [59] expanded the procedure to the determination of cadmium, cobalt, and nickel in whole blood, urine, liver, animal and plant tissues. They found that about 70% of the cadmium and 50% of the cobalt and nickel were retained in the collector. Enrichment factors of 24, 19, and 20 and enhancement factors of 52, 43, and 52 were obtained for cadmium, cobalt, and nickel, respectively, with a 40-sec coprecipitation time. Detection limits were 0.15, 1.3, and 1.5 p.g/liter, respectively, and the precision was typically around 2%. [Pg.104]

Fang and Dong [60] adapted the online coprecipitation preconcentration for ETAAS. They determined cadmium and nickel in digested whole blood. Enrichment factors of 16 and 8 were obtained for cadmium and nickel, respectively, using 20- and 40-sec precipitate collection times at a flow rate of 3 mL/min for cadmium and 2 mL/min for nickel. The detection limits were 0.003 p,g/liter for cadmium and 0.02 ng/liter for nickel. [Pg.104]

The contents of some trace elements in the continental crust, shales, soils, bituminous coals and plankton are given in Table 1.1 to provide some perspective when considering other aspects of these elements. In each of these situations, organic matter is associated with the elements to a greater or a lesser degree. This is not usually very marked with crustal rocks except shales, but may be a major factor for some elements in surface soils and coals. The data in Table 1.1 show that, for some elements, e.g. beryllium, cadmium, cobalt and molybdenum, the contents of the various reservoirs are similar, while for others, there may be enrichments relative to the crust, e.g. boron and sulfur in many shales, soils and coals, mercury, nickel and selenium in many shales, and germanium in some coals. [Pg.3]

The nuclear fuel consists of uranium, usually in the form of its oxide, U3O8 (Figure 23.12). Naturally occurring uranium contains about 0.7 percent of the uranium-235 isotope, which is too low a concentration to sustain a small-scale chain reaction. For effective operation of a light water reactor, uranium-235 must be enriched to a concentration of 3 or 4 percent. In principle, the main difference between an atomic bomb and a nuclear reactor is that the chain reaction that takes place in a nuclear reactor is kept under control at all times. The factor limiting the rate of the reaction is the number of neutrons present. This can be controlled by lowering cadmium or boron rods between the fuel elements. These rods capture neutrons according to the equations... [Pg.919]

Adsorptive stripping voltammetry (ASV) is another specialised technique where the SMDE electrode is used for reducible species and carbon paste electrodes for oxidisable ones. This allows enrichment (by factors of 100-1000) of ions at the working electrode before stripping them off for measurement this improves the detection limits. This technique is rapid, sensitive (10 "M), economical and simple for trace analysis. The basic instrumentation for stripping analysis is apotentiostat (with voltammetric analyser), electrode and recorder. While voltammetry is generally very useful for compounds that do not have a chromophore or fluorophore, stripping analysis is the best analytical tool for direct, simultaneous determination of metals of environmental concern, e.g. lead, cadmium, zinc and copper in sea water. [Pg.158]

The disadvantage factor was obtained by the so-called integral technique. Foils of a uranium-aluminum alloy of 17.5 wt% uranium that was enriched to 92.75 wt% U-235 were shaped to measure the U-235 fission rate in representative portions of the fuel and moderator volumes of a unit cell. Cadmium ratios in both fuel and moderator sections were determined with 0.051-cm cadmium covers. Various thicknesses (0.0051 to 0.066 cm) of foils were used. The foil activities were corrected for thermal self-shielding. Ih the cadmium-covered irradiations, various masses of cadmium were used and the cadmium ratios were corrected to zero cadmium mass. [Pg.143]

The threshold reaction contributions to the total fission rate can be assumed small for the AGN-201 reactor, since its moderator-to-uranium volume ratio is appreciable and its fuel is enriched with the isotope. Very fast fission is normally accounted for in the four-factor formula by the factor e, the number of neutrons produced by all fissions divided by the number produced by thermal fission. In the AGN-201, nonthermal fission is predominately resonance fission, since has finite fission cross sections at all energies. The amount of epithermal fission can be determined by a simple cadmium-ratio measurement of AGN-201-type fuel. The fission product activity of a bare and cadmium-covered fuel sample can be counted on a proportional counter after two similar irradiations in the reactor core. Their ratio will yield the amount of nonthermal fission to total fission after proper corrections for differences of sample weight, irradiation times, and, power level have been made. The final expression for power level then becomes, . . f... [Pg.158]


See other pages where Cadmium enrichment factor is mentioned: [Pg.2500]    [Pg.166]    [Pg.166]    [Pg.20]    [Pg.201]    [Pg.90]    [Pg.108]    [Pg.485]    [Pg.675]    [Pg.879]    [Pg.156]    [Pg.814]   
See also in sourсe #XX -- [ Pg.270 ]




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Enrichment factor

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