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Arsenic illustration

The amount of HEU that becomes avadable for civdian use through the 1990s and into the twenty-first century depends on the number of warheads removed from nuclear arsenals and the amount of HEU in the weapons complex that is already outside of the warheads, ie, materials stockpdes and spent naval reactor fuels. An illustrative example of the potential amounts of weapons-grade materials released from dismanded nuclear weapons is presented in Table 7 (36). Using the data in Table 7, a reduction in the number of warheads in nuclear arsenals of the United States and Russia to 5000 warheads for each country results in a surplus of 1140 t of HEU. This inventory of HEU is equivalent to 205,200 t of natural uranium metal, or approximately 3.5 times the 1993 annual demand for natural uranium equivalent. [Pg.188]

The SNMS instrumentation that has been most extensively applied and evaluated has been of the electron-gas type, combining ion bombardment by a separate ion beam and by direct plasma-ion bombardment, coupled with postionization by a low-pressure RF plasma. The direct bombardment electron-gas SNMS (or SNMSd) adds a distinctly different capability to the arsenal of thin-film analytical techniques, providing not only matrbe-independent quantitation, but also the excellent depth resolution available from low-energy sputterii. It is from the application of SNMSd that most of the illustrations below are selected. Little is lost in this restriction, since applications of SNMS using the separate bombardment option have been very limited to date. [Pg.575]

To illustrate case a, ii we may refer to the reduction of chlorate by arsenious acid induced by different 1-equivalent oxidizing reagents. The effect of the oxidizing agent is to form arsenic(IV). Chlorate will be reduced by arsenic(IV) which is a stronger reducing agent than arsenic(III). [Pg.515]

Tao et al. [658] have described a procedure in which antimony and arsenic were generated as hydrides and irradiated with ultraviolet light. The broad continuous emission bands were observed in the ranges about 240-750 nm and 220 - 720 nm, and the detection limits were 0.6 ng and 9.0 ng for antimony and arsenic, respectively. Some characteristics of the photoluminescence phenomenon were made clear from spectroscopic observations. The method was successfully applied to the determination of antimony in river water and seawater. The apparatus used in this technique is illustrated in Fig. 5.16. [Pg.236]

Illustrations provided by James Palmer, Pine Bluff Arsenal. [Pg.182]

In this work, the column performances were examined by supplying 1 mM of arsenic species, which corresponds to 75 ppm of arsenic. Such a high level arsenic is rarely found in surface water. Since the highest concentration levels of arsenic in well water of Ganges Delta are ca. 2 ppm. Thus, the removal of arsenic form dilute arsenite solutions was tested. Figure 5 illustratively shows the results. [Pg.48]

Fig. 12.4 illustrates the complex interactions induced by the presence of silica between reaction temperature, sulphuric acid acidity and the apparent level of phosphorus found. By careful control of acid concentration and reaction temperature, interference by silica can be minimized. Arsenic, germanium and bismuth would interfere in the method but not at the low levels normally encountered in sediment in water samples. [Pg.336]

This deposit is located in the north-east of Russia and belongs to a gold-arsenic type of low-sulphide formation (Abramson et al, 1980). It lies within a carbonaceous terrigenous rock of Triassic age and is associated with a dome-shaped uplift in a node of intersecting faults of various directions. The ore bodies consist of zones of silicification and kaolinization with veinlet-disseminated sulphide mineralisation. Gold is present in the form of finely-dispersed dissemination in arsenopyrite and pyrite. As an example. Figure 1 illustrates the distribution of Au and Mn in connection with commercial ore... [Pg.103]

It was found that the platinum(II) complexes of these ligands were of two types. All isomers form compounds of the t)rpe PtBr2 (arsine) 2, some of which are illustrated in Fig. 5. In these compounds, coordination to the platinum is effected through the arsenic atom alone. In addition, the ortho isomers of both arsines form 1 1 complexes with platinum(II) bromide in which the ligand is bidentate. Both the arsenic atom and the double bond are coordinated to the platinum as shown in Fig. 6. [Pg.9]

To illustrate how improvised explosives are often related to historically rejected formulations a sampling of the anarchist literature will be utilized. The small cross section examined will consist of Guerrilla s Arsenal (GA) [8], Improvised Munitions Black Book Vol. 1 (BB1) [9], Ragnar s Homemade Detonators (RHD) [10], and FMX The Revised Black Book (FMX) [11], It should be stressed that this small cross section examined represents only a fraction of the readily available information accessible through the Internet. These examples are utilized solely to show the overlap of historical explosive formulations and current terrorist recipes. More examples of current-day usage of these improvised materials will be included in the next sections of this chapter. [Pg.50]

The intermetallic phase [26] Na2Tl illustrates a simple application of the Zintl-Klemm concept to a group 13 metal cluster. Complete electron transfer from Na to T1 leads to the (Na" )2Tl formulation. The Tl dianion is isoelectronic with group 15 elements and thus should form similar tetrahedral structures with six two-center two-electron bonds along the edges of the tetrahedron. Indeed, the Tl anions in the Na2Tl phase form Tl4 tetrahedra, similar to the isoelectronic P4 and As4 units in white phosphorus and yellow arsenic. [Pg.4]

There is sometimes ambiguity as to which nearest neighbours to assign to the local coordination polyhedron. This is illustrated by the two different puckered layer structure types which are displayed by the most stable polymorphs of phosphorus and arsenic respectively. They may both be thought of as resulting from the breaking of three bonds about each atom on a simple cubic lattice as shown in Fig. 1.5. The layers then distort Black... [Pg.7]

The 8-N rule states that the number of bonds (or local coordination, x) equals 8 minus the number of the periodic group. This rule is illustrated in Fig. 1.2 where we see that for N — 7 the halogens take dimeric structure types with x = 1, for N = 6 the chalcogenides selenium and tellurium take helical chain structures with x = 2, for N = 5 the pnictides arsenic, antimony, and bismuth take a puckered layer structure with x = 3, and for N = 4 the semiconductors... [Pg.208]

The arsenal of antibacterials available for the treatment of infectious diseases has expanded exponentially since then. Currently, as illustrated in Fig. 1, the repertoire includes the (J-lactams (e.g. 3) sulfa drugs (e.g. 4) macrolides (e.g. 5, erythromycin A), nitrofuran drugs (e.g. 6, furazolidone), and many aminoglycosides. [Pg.75]


See other pages where Arsenic illustration is mentioned: [Pg.858]    [Pg.96]    [Pg.20]    [Pg.70]    [Pg.563]    [Pg.10]    [Pg.52]    [Pg.321]    [Pg.285]    [Pg.64]    [Pg.210]    [Pg.39]    [Pg.339]    [Pg.18]    [Pg.21]    [Pg.139]    [Pg.931]    [Pg.55]    [Pg.11]    [Pg.65]    [Pg.26]    [Pg.546]    [Pg.132]    [Pg.24]    [Pg.122]    [Pg.436]    [Pg.196]    [Pg.391]    [Pg.246]    [Pg.5]    [Pg.170]    [Pg.24]    [Pg.92]    [Pg.254]    [Pg.70]    [Pg.148]    [Pg.392]   
See also in sourсe #XX -- [ Pg.702 ]




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