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Sulfur, abundance deposition

Pyrite is the most abundant of the metal sulfides. Eor many years, until the Erasch process was developed, pyrite was the main source of sulfur and, for much of the first half of the twentieth century, comprised over 50% of world sulfur production. Pyrite reserves are distributed throughout the world and known deposits have been mined in about 30 countries. Possibly the largest pyrite reserves in the world are located in southern Spain, Portugal, and the CIS. Large deposits are also in Canada, Cypms, Einland, Italy, Japan, Norway, South Africa, Sweden, Turkey, the United States, and Yugoslavia. However, the three main regional producers of pyrites continue to be Western Europe Eastern Europe, including the CIS and China. [Pg.119]

Atomic masses calculated in this manner, using data obtained with a mass spectrometer can in principle be precise to seven or eight significant figures. The accuracy of tabulated atomic masses is limited mostly by variations in natural abundances. Sulfur is an interesting case in point. It consists largely of two isotopes, fiS and fgS. The abundance of sulfur-34 varies from about 4.18% in sulfur deposits in Texas and Louisiana to 4.34% in volcanic sulfur from Italy. This leads to an uncertainty of 0.006 amu in the atomic mass of sulfur. [Pg.53]

Figure 1.109. Sulfur isotopic compositions of Neogene Au-Ag vein-type and disseminated-type deposits. Sulfur isotopic compositions on the samples from the Yatani deposits (Sample No. YT26 from Zn-Pb vein S S = -)-3.3%o), and HS72050305-YT1, YT24 and NS-3 from Au-Ag vein (average S S = +3.3%c)) by Shikazono and Shimazaki (1985) are also plotted. Base-metal rich implies the sample containing abundant sulfide minerals but no Ag-Au minerals from base-metal rich deposits and also from Ginguro-type deposits (Shikazono, 1987b). Figure 1.109. Sulfur isotopic compositions of Neogene Au-Ag vein-type and disseminated-type deposits. Sulfur isotopic compositions on the samples from the Yatani deposits (Sample No. YT26 from Zn-Pb vein S S = -)-3.3%o), and HS72050305-YT1, YT24 and NS-3 from Au-Ag vein (average S S = +3.3%c)) by Shikazono and Shimazaki (1985) are also plotted. Base-metal rich implies the sample containing abundant sulfide minerals but no Ag-Au minerals from base-metal rich deposits and also from Ginguro-type deposits (Shikazono, 1987b).
The ash of peat forming plant species contains a predominant amount of silicon. This element is particularly abundant in the Sphagnum, where its content achieves 36% by ash weight. Iron and aluminum are the next abundant. The first is accumulated during the peat formation process. The accumulation of calcium and potash is more pronounced than sodium, and the sulfur content is also remarkable. A large amount of mechanically admixed mineral particles (40-80% by ash weight) is found in mosses. This is due to the deposition of fine dispersed mineral material from snowmelting waters and atmosphere dust deposition (Table 1). [Pg.129]

Most of these are relatively common and some are common indeed. For example, silicon and aluminum are the second and third most abundant elements in the Earth s crust. The rarest of these elements, selenium, is twice as abundant as silver and 20 times more abundant than gold, and it is relatively easy to obtain because it often occurs in sulfur deposits. [Pg.86]

Substituted and condensed thiophenes and thiophenols are usually the most abundant sulfur-containing compounds in refined fuels. These compounds are known to react with oxygen to form peroxides and eventually result in color bodies and gumlike fuel deposits. The reaction of thiophenol with a free-radical compound and oxygen is shown below ... [Pg.117]


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