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Minor elements in Arkansas bauxite

A study of the minor elements in Arkansas bauxite has revealed some striking relationships between their concentration in the parent nepheline syenite rocks as compared with their concentration in the bauxite . The ratios of concentration, in general, follow a pattern predicted by Gold-schmidt (3),2 based upon the ionic radius and ionic charge of each element present. In the Arkansas deposits, Mg, Ca, Ba, La, and Sr were depleted during the change from nepheline syenite to bauxite . The average concentration of Pb remained the same in the samples tested. Y, Mn, Be, V, Sc, Ti, and Zr were concentrated, but not as much as Al; while Mo, Nb (Cb), Ga, Cu, and Cr were concentrated more than Al.' Niobium (columbium) apparently is found in sufficient quantities to warrant search for methods to extract it commercially as a by-product of alumina plants.

Arkansas↗

Supergene and hydrothermal dispersion of heavy metals in wall rocks near ore bodies, Tintic district, Utah

Part I, T. S. Lovering. Preliminary work in the Tintic district , Utah , determined the relative distance of migration of ore metals in moist carbonate and silicic wall rocks near ore , and in ground water having a very sluggish circulation through mineralized ground. The analyses of efflorescences in the Tintic Standard mine openings at suitable localities indicated that under the conditions existing during the past 25 years lead has not moved perceptibly; gold has migrated only a few inches; copper has moved a few score feet at most and only in acid solutions; and zinc has traveled hundreds of feet, but not as far as some silver. Silver may travel far in the oxidized zone, but if it comes in contact with sulfides its migration is quickly halted. The chief chemical factors that influence the migration of metals in supergene solutions are the hydrogen ion concentration (pH) of hydrolysis of the metal ion, the solubility of sulfates of the metals , and the position of the metals in Schuermann's series if the solutions are in contact with sulfides for a considerable time.

Utah↗

A field method for the determination of titanium in rocks

About 4 mg of rock powder measured with a scoop is fused with potassium bisulfate in a test tube. Tiron is added to the cool melt and the mixture is dissolved in a buffer solution. Sodium dithionite is added and the approximate concentration of TiO 2 is determined by comparing the resulting yellow solution with permanent standards, which are simple to prepare.The results obtained by this field method for TiO 2 on 72 rock samples of various types are compared with those obtained by laboratory methods.

Economic Geology↗

Reconnaissance of superficial phosphate deposit near Minas, Uruguay

The phosphate deposit in Uruguay described here is of interest primarily because it is believed to be a superficial deposit that resulted from the action of guano on volcanic rock. Even though some of the rock contains as much as 30 per cent P206, it is unavailable as a source of fertilizer because the phosphate is combined with aluminum and iron as variscite and strengite, and possibly other equally insoluble minerals. © 1953 Society of Economic Geologists, Inc.

Economic Geology↗

Metamorphic differentiates in the blackbird mining district, Lemhi County, Idaho

Quartz pods and quartz veins devoid of economic minerals occur in the cobalt-copper mineralized Blackbird mining district in Lemhi County , Idaho . These barren quartz bodies are found in regionally and thermally metamorphosed rocks of the Yellowjacket formation (Belt series) of Pre-cambrian age and are believed to be derived from the enclosing quartz-biotite and quartz-biotite-garnet-chloritoid schists by metamorphic differentiation. Other rocks that possibly are products of metamorphic differentiation are discussed. Two zones of regional metamorphism are recognized, a biotite zone and a garnet zone. Contact metamorphism associated with the granitic intrusive rocks of the Idaho batholith is recognized adjacent to the batholith.

Idaho↗

Sedimentary facies of iron-formation

The sedimentary iron -formations of Precambrian age in the Lake Superior region can be divided on the basis of the dominant original iron mineral into four principal facies : sulfide, carbonate, oxide, and silicate. As chemical sediments, these rocks reflect certain aspects of the chemistry of the depositional environments. The major control, at least for the sulfide, carbonate, and oxide types, probably was the oxidation potential. The evidence indicates that deposition took place in restricted basins, which were separated from the open sea by thresholds that inhibited free circulation and permitted development of abnormalities in oxidation potential and water composition. The sporadic distribution of metamorphism and of later oxidation permits description of the primary facies on the basis of unoxidized, essentially unmetamorphosed material. The sulfide facies is represented by black slates in which pyrite may make up as much as 40 percent of the rock. The free-carbon content of these rocks typically ranges from 5 to 15 percent, indicating that ultra-stagnant conditions prevailed during deposition. Locally, the pyritic rocks contain layers of iron -rich carbonate. The carbonate facies consists, in its purer form, of interbedded iron -rich carbonate and chert. It is a product of an environment in which oxygen concentration was sufficiently high to destroy most of the organic material but not high enough to permit formation of ferric compounds. The oxide facies is found as two principal types, one characterized by magnetite and the other by hematite. Both minerals appear to be of primary origin. The magnetite-banded rock is one of the dominant lithologies in the region; it consists typically of magnetite interlayered with chert, carbonate, or iron silicate, or combinations of the three. Its mineralogy and association suggest origin under weakly oxidizing to moderately reducing conditions, but the mode of precipitation of magnetite is not clearly understood. The hematite-banded rocks consist of finely crystalline hematite interlayered with chert or jasper. Oolitic structure is common. This facies doubtless accumulated in a strongly oxidizing, probably near-shore, environment similar to that in which younger hema-titic ironstones such as the Clinton oolite were deposited. The silicate facies contains one or more of the hydrous ferrous silicates (greenalite, minnesotaite, stilpnomelane, chlorite) as a major constituent. Granule structure, similar to that of glauconite, is typical of some varieties; others are nongranular and finely laminated. The most common association of the silicate rocks is with either carbonate- or magnetite-bearing rocks, which suggests that the optimum conditions for deposition ranged from slightly oxidizing to slightly reducing. The relationship between the iron -rich rocks and volcanism, stressed by many authors, is considered by the writer to be structural, not chemical: in the Lake Superior region both iron -deposition and volcanism are believed to be related to geosynclinal development during Huronian time. In Michigan, the lower Huronian rocks are iron -poor quartzite and dolomite-typical "stable-shelf" deposits; much of the upper Huronian consists of iron -poor graywacke and slate with associated volcanic rocks -a typical "geosynclinal" assemblage. Thus the iron -rich beds of the middle Huronian and lower part of the upper Huronian were deposited during a transitional stage in structural history. The major environmental requirement for deposition of iron - formation is the closed or restricted basin; this requirement coincides in time with what would be a normal stage in evolution of the geosyncline: namely, structural development of offshore buckles or swells that subsequently develop into island arcs characterized by volcanism.

Lake Superior↗

Copper cities copper deposit, Globe-Miami district, Arizona

The Copper Cities copper deposit in the Globe - Miami district , Arizona , is now in process of development. It is of the "porphyry" type and occurs in a body of quartz monzonite that has been intruded by smaller masses of granite porphyry. The hypogene sulfides are pyrite, chalcopyrite, and a very little molybdenite. Pyritic mineralization extends over a large area of which only a small portion contains an appreciable amount of chalcopyrite. The outcrop of the copper -bearing rock, roughly 1,800 feet square, is bounded on the west, north, and east sides by fault zones. The south boundary is gradational. The pyrite to chalcopyrite ratio of the protore increases rapidly with depth, whereas the copper content decreases but slightly. The ore body is a shallow chalcocite zone formed by supergene enrichment. Bodies of granite porphyry within the copper -bearing area were not as strongly mineralized by hypogene solutions as the quartz monzonite, and in them the chalcocite zone is thin, undoubtedly because the granite porphyry is less pervious to ground water than the quartz monzonite.

Arizona↗

The White Pine copper deposit, Ontonagon County, Michigan

Copper, largely in the mineral chalcocite, is found in the lowermost beds of the Nonesuch shale over many square miles near White Pine, Ontonagon County, Mich. The Nonesuch shale, of late Keweenawan age, is about 600 feet thick and is composed largely of gray siltstone. It overlies 2,300 to 5,500 feet of red sandstones and conglomerates, the Copper Harbor conglomerate. This formation, in turn, overlies the middle Keweenawan Portage Lake lava series, in which occur the famous native-copper deposits of the south shore of Lake Superior. The White Pine mine is 45 to 70 miles west-southwest of the principal native copper mines.The copper-bearing beds at White Pine are primarily in the lower 20to 25 feet of the Nonesuch shale. This cupriferous zone is divided in local usage into four stratigraphic units, which are, in ascending order, the lower sandstone (the uppermost bed of the Copper Harbor conglomerate), the parting shale, the upper sandstone, and the upper shale. The sequence of beds is almost identical in the upper and parting shales, suggesting cyclic sedimentation. This sequence and the distribution of sedimentary facies are attributed to two submergences, separated by an emergence, of a deltaic area.Practically all the copper occurs in the upper and parting shales, except in a small area near the White Pine fault where it is abundant in the upper and lower sandstones. It is present in five different layers in amounts that average from 1 to 3 percent. The total amount of copper in each bed is generally higher where the bed is thick, and thickness, in turn, seems to be greatest in areas that were hollows away from the main channel or channels of the ancient delta. Copper content of the shale beds typically decreases as their sand content increases. The extent of individual copper-bearing beds 1 to 3 feet thick is measurable in square miles.The local occurrence of copper in the upper and lower sandstone beds can be reasonably explained as the result of hydrothermal transportation from the White Pine fault up the dip of the relatively permeable sandstone to the crest of an adjacent anticline. Distribution of copper in the parting and upper shales, on the other hand, seems to be completely independent of local structure, faults, and rock permeability. For the area as a whole the control is lithologic and stratigraphic. Probably the copper was dropped into or precipitated within the original mud; it may conceivably have replaced with exquisite detail something else that was so deposited.

Michigan↗

The occurrence of cobalt and nickel in the Silver Summit Mine, Coeur d'Alene district, Idaho

Cobalt and nickel of possible commercial interest have been discovered in the Silver Summit mine, Coeur d'Alene district, Idaho. Assay data indicate that an ore shoot contained about 0.40 percent cobalt and about 1.0 percent nickel in addition to the copper and rich silver ores. The cobalt-nickel mineral gersdorffite occurs in tetrahedrite-siderite veins. Gersdorffite is widespread in small amounts and appears to have been the first of the "ore shoot" minerals. The known occurrence of either cobalt bloom or gersdorffite in other properties of the Coeur d'Alene district Silver Belt suggests that other ore shoots may exist that contain commercial quantities of cobalt and nickel.

Idaho↗

Geochemistry and mineralogy of a uraniferous lignite [South Dakota]

Detailed studies have been carried out on a uraniferous lignite from the Mendenhall strip mine, Harding County, S. Dak. By means of heavy-liquid separations, a mineral-free concentrate of the lignite was obtained that contained 13.8 percent ash and 0.31 percent uranium in the ash. The minerals (gypsum 69 percent, jarosite 10 percent, quartz 2 percent, kaolinite and clay minerals 19 percent, and calcite trace) contain only 7 percent of the uranium in the original coal, indicating an association of the uranium with the organic components of the lignite.Batch extractions show that 88.5 percent of the uranium can be extracted from the lignite by two consecutive treatments with boiling 1 N hydrochloric acid. Continuous extraction with hot 6 N hydrochloric acid removes 98.6 percent of the uranium.Columns of coal were treated with water, 1 N hydrochloric acid, 6 N hydrochloric acid, and a solution of lanthanum nitrate. The experiment with lanthanum nitrate indicated that only 1.2 percent of the uranium in the coal is held by ion exchange. The elutriation experiments showed that the uranium is held in the coal as an organo-uranium compound or complex that is soluble at a pH of less than 2.18.A geochemical mechanism by which the uranium may have been introduced into and retained by the lignite is discussed.

South Dakota↗

Comments on minor elements in pyrrhotite [Idaho]

The cobalt and nickel content of pyrrhotite from the Highland-Surprise mine, Coeur d'Alene district, Idaho, was determined by spectrographic methods. The Co and Ni values fall within the ranges of values found by other investigators. Comparison of the distribution of Co and Ni in the Highland-Surprise ore shoot with the distribution of these elements in the Silberberges, Germany, and Noranda, Canada, ore shoots suggests that caution must be used in the determination of relative temperature conditions in ore shoots by means of studies of minor elements, principally because it seems likely that equilibrium concentrations are commonly absent.

Idaho↗

The lead-zinc veins of the chilete mining district in northern Peru

Lead-zinc-silver veins in the Chilete mining district in the Department of Cajamarca in northern Peru have been worked sporadically since the 17th century, but the greatest activity dates only from 1951. The ore deposits are in a thick section of andesitic volcanic rocks that overlie with marked unconformity a sequence of Cretaceous limestone, shale, and quartz-ite. The volcanic rocks form a gently north-dipping block of apparently simple structure. The Chilete deposits are quartz-sulfide veins consisting essentially of sphalerite, pyrite, and galena in a gangue of quartz and silici-fied and pyritized andesite. Wall rocks are calcitized, chloritized, pyrit-ized, and sericitized. The veins were formed by fissure filling, breccia filling, and replacement. Veins strike either northwest or east-northeast and dip steeply. They range from a few centimeters to 4 m in width and the longest has a strike length of about 1,700 m. The veins are eut by a number of post-mineral strike-slip faults of small displacement. Thicker sections of the principal northwest-striking vein, Murcielago, tend to occur where the strike swings slightly to the north. Vein intersections are not favorable loci for ore deposition, and several intersections seem to be dis-tinctly unfavorable. Ail the veins have roughly the same combined content of lead and zinc at ail levels, but the proportion of zinc to lead increases notably at the lowest levels of exploration, 200-250 m below the outerops. © 1955 Society of Economic Gelogists, Inc.

Economic Geology↗

Is Carbon dioxide an ore-forming fluid under shallow-earth conditions?

A review of some of the physical-chemical properties of CO 2 and of the system CO 2 --H 2 O indicates that under some shallow-earth conditions CO 2 can exist as a separate phase with a density approximately that of water. The effect of dissolved neutral or acid salts on the solubility of CO 2 in H 2 O is not large. Carbonates, oxides, and silicates, through reactions with a CO 2 -saturated water phase, will eventually cause the disappearance of a CO 2 phase. The prevalence of CO 2 in the earth's crust is attested by its abundance in natural gases and fluid inclusions in minerals. Some of the characteristics of uranium ores of the Colorado Plateau are not incompatible with the assumption that deposition was from a fluid CO 2 phase.

Economic Geology↗

Geochemistry and mineralogy of a uraniferous sub bituminous coal

A sample of subbituminous uraniferous coal from the Red Desert, Sweetwater County, Wyo., has been studied mineralogically. The coal contains gypsum (6 percent), kaolinite (1 percent), quartz (0.3 percent), calcite (trace), and limonite (trace). This suite of minerals and the absence of pyrite show that the coal has been subjected to weathering and oxidation. No uranium minerals have been found; mechanical fractionation has indicated that the uranium is associated with the organic constituents of the coal. The minerals that have been isolated contain 0.0006 percent uranium, a content that is to be expected for nonuraniferous sedimentary rocks. The organic components of the coal contain approximately 0.002 percent uranium. On the basis of material-balance calculations, the organic components carry 98 percent of the uranium in the coal. Batch extraction of the Wyoming coal with 6 N hydrochloric acid leads to the solution of almost 90 percent of its uranium. Recovery of uranium is independent of the particle size of the coal between - 4 and - 20 mesh, and is accompanied by the solution of approximately 70 percent of the inorganic constituents (ash) of the coal. The extract contains, together with uranium, a concentration of several elements such as manganese, cerium, and vanadium that are present in the coal. Fischer assays of this weathered coal from the Red Desert indicate a yield of 16.7 gallons of tar per ton. Yields of both tar and char are about 15 percent lower if the coal is first treated with 6 N hydrochloric acid to extract the uranium. It is suggested that uranium was introduced into the coal by means of ground water carrying soluble alkaline or alkaline-earth uranyl carbonate complexes. The mineral schroeckingerite-a similar complex-is found near this subbituminous coal in the Red Desert of Wyoming. These complexes, which are unstable in acid medium, release the uranyl ion (U02++), which may then react with organic constituents of the coal to form ionic uranyl-organic compounds that are insoluble above a pH of about 2.2. Preliminary data indicate that the uranium is associated with various humic components of the coal. The distribution of uranium among the components of the subbituminous coal from Wyoming is similar to the distribution in a lignite from South Dakota. There is no indication that uranium was introduced into or retained by the two coals by appreciably different geochemical processes. © 1955 Society of Economic Geologists, Inc.

Wyoming↗