Minerals Report - International Seabed Authority

Minerals Report - International Seabed Authority Minerals Report - International Seabed Authority

05.02.2013 Views

3.4. Chemical Composition All USGS chemical data in this report (Table 6) are normalized to zero percent hygroscopic water because that adsorbed water varies markedly depending on analytical conditions. Hygroscopic water can vary up to 30 weight percent (%) and thereby affects the contents of all other elements. Compositions normalized for hygroscopic water can be more meaningfully compared and also more closely represent the grade of the potential ore. Unfortunately, water contents are not provided in many published reports, so we were unable to correct compiled data listed in Table 6. Mean chemical compositions are provided for crusts that occur in the areas marked on Fig. 6, which correspond to the different columns in Table 6. Hydrogenetic Fe-Mn crusts generally have iron/manganese ratios between 0.4 and 1.2, most commonly 0.7 ± 0.2, whereas mixed hydrogenetic and hydrothermal crusts and continental margin hydrogenetic crusts have ratios between 1 and 3, mostly 1.3-1.8 (from data used to compile Table 6). Cobalt is the metal with the greatest economic potential in crusts and ranges from about 0.05-1.7% (500-17,000 parts per million, ppm) in individual bulk crusts and averages between 0.19% and 0.74% (1900-7400 ppm) for various parts of the global ocean (Table 6). Cobalt is also considered the element most characteristic of hydrogenetic precipitation in crusts (64) and is considered to maintain a constant flux from seawater to Fe-Mn crusts (65), regardless of water depth. Nickel and platinum are also considered of economic importance and range up to 1.1% and 1.3 ppm respectively for individual bulk crusts. Platinum ranges up to 3 ppm for individual crust layers (66). Elements most strongly enriched over abyssal Fe-Mn nodules include iron, cobalt, platinum, lead, arsenic, bismuth, bromine, vanadium, phosphorus, calcium, titanium, strontium, tellurium, and REEs, whereas nodules are more enriched in copper, nickel, zinc, lithium, aluminium, potassium (only Pacific crusts), and cadmium. Fe-Mn crusts are enriched over seawater in all elements except bromine, chlorine, and sodium; enrichments over seawater between 108 and 10 10 times include bismuth, cobalt, manganese, titanium, iron, tellurium, lead, and thorium, and between 106 and 108 times include tin, hafnium, zirconium, aluminium, yttrium, scandium, thallium, nickel, calcium, niobium, indium, copper, germanium, zinc, tungsten, and tantalum. Crusts are enriched over lithospheric concentrations about five thousand times for INTERNATIONAL SEABED AUTHORITY 210

tellurium and a hundred to five hundred times for molybdenum, thallium, antimony, cobalt, manganese, bismuth, arsenic, selenium, and lead. Crusts may have an economic potential not only for cobalt, nickel, manganese, and platinum, but also for titanium, cerium, tellurium, thallium, zirconium, and phosphorus. Elements in crusts have different origins and are associated with different crust mineral phases (67). Generally elements are associated with five phases in crusts, δ-MnO2, iron oxyhydroxide, detrital (aluminosilicate), CFA, and residual biogenic phases. Manganese, cobalt, nickel, cadmium, and molybdenum are invariably associated with the δ-MnO2 phase. In addition, in more than 40% of the regions studied, lead, vanadium, zinc, sodium, calcium, strontium, magnesium, and titanium are also associated with that phase. Iron and arsenic are most commonly the only elements associated with the iron oxyhydroxide phase, although less commonly vanadium, copper, lead, yttrium, phosphorus, chromium, beryllium, strontium, titanium, and cerium have also been reported to be associated with that phase. The detrital phase always includes silicon, aluminium, and potassium, and commonly also titanium, chromium, magnesium, iron, sodium, and copper. The CFA phase invariably includes calcium, phosphorus, and carbon dioxide, and also commonly strontium and yttrium; molybdenum, barium, cerium, and zinc may also be associated with the CFA phase in some regions. The residual biogenic phase includes barium, strontium, cerium, copper, vanadium, calcium, and magnesium, and in some regions also iron, arsenic, sodium, molybdenum, yttrium, phosphorus, carbon dioxide, lead, titanium, and nickel. Iron is the most widely distributed element and occurs intermixed in the δ-MnO2 phase; is the main constituent in the iron oxyhydroxide phase; occurs in the detrital phase in minerals such as pyroxene, amphibole, smectite, magnetite, and spinel; and is in the residual biogenic phase. The strength of correlations between iron and other elements depends on the relative abundance of iron in the various phases (68). The CFA phase only occurs in thick crusts because the inner layers of those crusts have been phosphatized. In thin crusts or the surface scrapes of thick crusts, calcium, phosphorus, and carbon dioxide are associated with the δ-MnO2 and/or residual biogenic phases. CFA associated elements as well as platinum, rhodium, and iridium generally increase with increasing crust thickness. In contrast, cobalt and INTERNATIONAL SEABED AUTHORITY 211

tellurium and a hundred to five hundred times for molybdenum, thallium,<br />

antimony, cobalt, manganese, bismuth, arsenic, selenium, and lead. Crusts<br />

may have an economic potential not only for cobalt, nickel, manganese, and<br />

platinum, but also for titanium, cerium, tellurium, thallium, zirconium, and<br />

phosphorus.<br />

Elements in crusts have different origins and are associated with<br />

different crust mineral phases (67). Generally elements are associated with<br />

five phases in crusts, δ-MnO2, iron oxyhydroxide, detrital (aluminosilicate),<br />

CFA, and residual biogenic phases. Manganese, cobalt, nickel, cadmium, and<br />

molybdenum are invariably associated with the δ-MnO2 phase. In addition,<br />

in more than 40% of the regions studied, lead, vanadium, zinc, sodium,<br />

calcium, strontium, magnesium, and titanium are also associated with that<br />

phase. Iron and arsenic are most commonly the only elements associated with<br />

the iron oxyhydroxide phase, although less commonly vanadium, copper,<br />

lead, yttrium, phosphorus, chromium, beryllium, strontium, titanium, and<br />

cerium have also been reported to be associated with that phase. The detrital<br />

phase always includes silicon, aluminium, and potassium, and commonly also<br />

titanium, chromium, magnesium, iron, sodium, and copper. The CFA phase<br />

invariably includes calcium, phosphorus, and carbon dioxide, and also<br />

commonly strontium and yttrium; molybdenum, barium, cerium, and zinc<br />

may also be associated with the CFA phase in some regions. The residual<br />

biogenic phase includes barium, strontium, cerium, copper, vanadium,<br />

calcium, and magnesium, and in some regions also iron, arsenic, sodium,<br />

molybdenum, yttrium, phosphorus, carbon dioxide, lead, titanium, and<br />

nickel. Iron is the most widely distributed element and occurs intermixed in<br />

the δ-MnO2 phase; is the main constituent in the iron oxyhydroxide phase;<br />

occurs in the detrital phase in minerals such as pyroxene, amphibole, smectite,<br />

magnetite, and spinel; and is in the residual biogenic phase. The strength of<br />

correlations between iron and other elements depends on the relative<br />

abundance of iron in the various phases (68). The CFA phase only occurs in<br />

thick crusts because the inner layers of those crusts have been phosphatized.<br />

In thin crusts or the surface scrapes of thick crusts, calcium, phosphorus, and<br />

carbon dioxide are associated with the δ-MnO2 and/or residual biogenic<br />

phases. CFA associated elements as well as platinum, rhodium, and iridium<br />

generally increase with increasing crust thickness. In contrast, cobalt and<br />

INTERNATIONAL SEABED AUTHORITY 211

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