Sodium neutrons

Analyses of alloys or ores for hafnium by plasma emission atomic absorption spectroscopy, optical emission spectroscopy (qv), mass spectrometry (qv), x-ray spectroscopy (see X-ray technology), and neutron activation are possible without prior separation of hafnium (19). Alternatively, the combined hafnium and zirconium content can be separated from the sample by fusing the sample with sodium hydroxide, separating silica if present, and precipitating with mandelic acid from a dilute hydrochloric acid solution (20). The precipitate is ignited to oxide which is analy2ed by x-ray or emission spectroscopy to determine the relative proportion of each oxide. 

Full advantage of the neutron production by plutonium requires a fast reactor, in which neutrons remain at high energy. Cooling is provided by a hquid metal such as molten sodium or NaK, an alloy of sodium and potassium. The need for pressurization is avoided, but special care is required to prevent leaks that might result in a fire. A commonly used terminology is Hquid-metal fast-breeder reactor (LMFBR). 

Sodium is used as a heat-transfer medium in primary and secondary cooling loops of Hquid-metal fast-breeder power reactors (5,155—157). Low neutron cross section, short half-life of the radioisotopes produced, low corrosiveness, low density, low viscosity, low melting point, high boiling point, high thermal conductivity, and low pressure make sodium systems attractive for this appHcation (40). 

X-ray crystallographic analysis of the sodium thiosulfate pentahydrate [10102-17-7] crystal indicates a tetrahedral stmcture for the thiosulfate ion. The S—S bond distance is 197 pm the S—O bond distance is 148 pm (5). Neutron diffraction of a barium thiosulfate monohydrate [7787-40-8] crystal confirms the tetrahedral stmcture and bond distances for the thiosulfate ion (6). 

Properties. Most of the alloys developed to date were intended for service as fuel cladding and other stmctural components in hquid-metal-cooled fast-breeder reactors. AHoy selection was based primarily on the following criteria corrosion resistance in Hquid metals, including lithium, sodium, and NaK, and a mixture of sodium and potassium strength ductihty, including fabricabihty and neutron considerations, including low absorption of fast neutrons as well as irradiation embrittlement and dimensional-variation effects. Alloys of greatest interest include V 80, Cr 15, Ti 5... 

For the deterrnination of trace amounts of bismuth, atomic absorption spectrometry is probably the most sensitive method. A procedure involving the generation of bismuthine by the use of sodium borohydride followed by flameless atomic absorption spectrometry has been described (6). The sensitivity of this method is given as 10 pg/0.0044M, where M is an absorbance unit the precision is 6.7% for 25 pg of bismuth. The low neutron cross section of bismuth virtually rules out any deterrnination of bismuth based on neutron absorption or neutron activation. 

Let us start with the sodium atom. It has a nucleus of 11 protons, each with a + charge (and 12 neutrons with no charge at all) surrounded by 11 electrons each carrying a -charge (Fig. 4.3). 

Atomic absorption spectroscopy of VPD solutions (VPD-AAS) and instrumental neutron activation analysis (INAA) offer similar detection limits for metallic impurities with silicon substrates. The main advantage of TXRF, compared to VPD-AAS, is its multielement capability AAS is a sequential technique that requires a specific lamp to detect each element. Furthermore, the problem of blank values is of little importance with TXRF because no handling of the analytical solution is involved. On the other hand, adequately sensitive detection of sodium is possible only by using VPD-AAS. INAA is basically a bulk analysis technique, while TXRF is sensitive only to the surface. In addition, TXRF is fast, with an typical analysis time of 1000 s turn-around times for INAA are on the order of weeks. Gallium arsenide surfaces can be analyzed neither by AAS nor by INAA. 

Nickel-manganese-palladium brazes are resistant to attack by molten alkali metals and And applications in sodium-cooled turbine constructions. Their freedom from silver and other elements of high thermal neutron-capture cross-section allows them to be used in liquid-metal-cooled nuclear reactors. 

The aggregation numbers of sodium octyl, decyl, dodecyl, and tetradecyl sulfates at temperatures between 20°C and 60°C have been studied by Vass by small-angle neutron scattering [130]. Table 22 shows the aggregation numbers of some alcohol and alcohol ether sulfates. 

In a nuclear power plant, heat must be transferred from the core to the turbines without any transfer of matter. This is because fission and neutron capture generate lethal radioactive products that cannot be allowed to escape from the core. A heat-transfer fluid such as liquid sodium metal flows around the core, absorbing the heat produced by nuclear fission. This hot fluid then flows through a steam generator, where its heat energy is used to vaporize... 

To date, a few methods have been proposed for direct determination of trace iodide in seawater. The first involved the use of neutron activation analysis (NAA) [86], where iodide in seawater was concentrated by strongly basic anion-exchange column, eluted by sodium nitrate, and precipitated as palladium iodide. The second involved the use of automated electrochemical procedures [90] iodide was electrochemically oxidised to iodine and was concentrated on a carbon wool electrode. After removal of interference ions, the iodine was eluted with ascorbic acid and was determined by a polished Ag3SI electrode. The third method involved the use of cathodic stripping square wave voltammetry [92] (See Sect. 2.16.3). Iodine reacts with mercury in a one-electron process, and the sensitivity is increased remarkably by the addition of Triton X. The three methods have detection limits of 0.7 (250 ml seawater), 0.1 (50 ml), and 0.02 pg/l (10 ml), respectively, and could be applied to almost all the samples. However, NAA is not generally employed. The second electrochemical method uses an automated system but is a special apparatus just for determination of iodide. The first and third methods are time-consuming. 

Murthy and Ryan [823] used colloid flotation as a means of preconcentration prior to neutron activation analysis for arsenic, molybdenum, uranium, and vanadium. Hydrous iron (III) oxide is floated in the presence of sodium decyl sulfate with small nitrogen bubbles from 1 litre of seawater at pH 5.7. Recoveries of arsenic, molybdenum, and vanadium were better than 95%, whilst that of uranium was about 75%. 

Lieser et al. [628] studied the application of neutron activation analysis to the determination of trace elements in seawater, with particular reference to the limits of detection and reproducibility obtained for different elements when comparing various preliminary concentration techniques such as adsorption on charcoal, cellulose, and quartz, and complexing agents such as dithizone and sodium diethyldithiocarbamate. 

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