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Minerals oxide

Fig. 10. Relationship between the lEP and the floatabiUty of a typical oxide mineral (Goethite Fe202 At pH > pH p the 2eta potential has a... Fig. 10. Relationship between the lEP and the floatabiUty of a typical oxide mineral (Goethite Fe202 At pH > pH p the 2eta potential has a...
Pyrolusite is a black, opaque mineral with a metallic luster and is frequendy soft enough to soil the fingers. Most varieties contain several percent water. Pyrolusite is usually a secondary mineral formed by the oxidation of other manganese minerals. Romanechite, a newer name for what was once known as psilomelane [12322-95-1] (now a group name) (7), is an oxide of variable composition, usually containing several percent water. It is a hard, black amorphous material with a dull luster and commonly found ia the massive form. When free of other oxide minerals, romanechite can be identified readily by its superior hardness and lack of crystallinity. [Pg.487]

Copper ore minerals maybe classified as primary, secondary, oxidized, and native copper. Primaryrninerals were concentrated in ore bodies by hydrothermal processes secondary minerals formed when copper sulfide deposits exposed at the surface were leached by weathering and groundwater, and the copper reprecipitated near the water table (see Metallurgy, extractive). The important copper minerals are Hsted in Table 1. Of the sulfide ores, bornite, chalcopyrite, and tetrahedrite—teimantite are primary minerals and coveUite, chalcocite, and digenite are more commonly secondary minerals. The oxide minerals, such as chrysocoUa, malachite, and azurite, were formed by oxidation of surface sulfides. Native copper is usually found in the oxidized zone. However, the principal native copper deposits in Michigan are considered primary (5). [Pg.192]

Uranium, too, is widely distributed and, since it probably crystallized late in the formation of igneous rocks, tends to be scattered in the faults of older rocks. Some concentration by leaching and subsequent re-precipitation has produced a large number of oxide minerals of which the most important are pitchblende or uraninite, U3O8, and camotite, K2(U02)2(V04)2.3H20. However, even these are usually dispersed so that typical ores contain only about 0.1% U, and many of the more readily exploited deposits are nearing exhaustion. The principal sources are Canada, Africa and countries of the former USSR. [Pg.1255]

Stauffer TB, MacIntyre WG. 1986. Sorption of low-polarity organic compounds on oxide minerals and aquifer material. Environ Toxicol Chem 5 949-955. [Pg.291]

Otsu, H. and Harada, H. (1963) On the modes of occurrence of hydrothermal iron oxide minerals in Green Tuff region. Japan. Geol Surv. Bull, 14, 579-590 (in Japanese). [Pg.282]

Spinels. There are limited experimental data on uranium and thorium partitioning between magnetite and melt (Nielsen et al. 1994 Blundy and Brooker 2003). Both studies find U and Th to be moderately incompatible. Blundy and Brooker s results for a hydrous dacitic melt at 1 GPa and 1025°C give Du and D h. of approximately 0.004. The accuracy of these values is compromised by the very low concentrations in the crystals and the lack of suitable SIMS secondary standards for these elements in oxide minerals. Nonetheless, these values are within the range of Djh of magnetites at atmospheric pressure 0.003-0.025 (Nielsen et al. 1994). It is difficult to place these values within the context of the lattice strain model, firstly because there are so few systematic experimental studies of trace element partitioning into oxides and secondly because of the compositional diversity of the spinels and their complex intersite cation ordering. [Pg.112]

Minerals belonging to the category of insoluble oxide and silicate minerals are many in number. Insoluble oxide minerals include those superficially oxidized and those of oxide type. The former category comprises mainly superficially oxidized sulfide minerals, including metals such as aluminum, tin, manganese, and iron which are won from their oxidic sources. As far as silicate minerals are concerned, there can be a ready reference to several metals such as beryllium, lithium, titanium, zirconium, and niobium which are known for their occurrence as (or are associated with) complex silicates in relatively low-grade deposits. [Pg.192]

Flotation is certainly the major separation method based on the surface chemistry of mineral particles. It is, however, not the only method. Selective flocculation and agglomeration may be mentioned as other methods used commercially to a limited extent. The former is for hematite, while the latter is for coal and finely divided metallic oxide minerals. Both processes use the same principles as described for flotation to obtain selectivity. In selective flocculation, polymeric flocculants are used. The flocculants selectively adsorb on the hematite, and the hematite floes form and settle readily. Thereby separation from the sili-... [Pg.211]

In addition to pure oxides, oxidic minerals and ores also can be converted to metal chlorides. Examples include minerals such as zircon, bastnasite, monazite, ilmenite, etc. [Pg.402]

The reagents useful for the fluorination of ores and compounds include flurosilicates, elemental fluorine, hydrogen fluoride, and alkali hydrogen fluorides. Their use is illustrated for fluorination of oxides and oxidic minerals. [Pg.412]

The present description pertaining to copper refers to solvent extraction of copper at the Bluebird Mine, Miami. When the plant became operational in the first quarter of 1968 it used L1X 64, but L1X 64N was introduced in to its operation from late 1968. The ore consists of the oxidized minerals, chrysocolla and lesser amounts of azurite and malachite. A heap leaching process is adopted for this copper resource. Heap-leached copper solution is subjected to solvent extraction operation, the extractant being a solution of 7-8% L1X 64N incorporated in kerosene diluent. The extraction process flowsheet is shown in Figure 5.20. The extraction equilibrium diagram portrayed in Figure 5.21 (A) shows the condi-... [Pg.524]

The (compositionally) simplest mineral class comprises the native elements, that is, those elements, either metals or nonmetals that occur naturally in the native state, uncombined with others. Native gold, silver, and copper, for example, are metals that naturally occur in a ductile and malleable condition, while carbon - in the form of either graphite or diamond -and sulfur are examples of nonmetallic native elements. Next in compositional complexity are the binary minerals composed of two elements a metal or nonmetallic element combined with oxygen in the oxides, with a halogen - either fluorine, chlorine bromine, or iodine - in the halides, or sulfur, in the sulfides. The oxide minerals, for example, are solids that occur either in a somewhat hard, dense, and compact form in mineral ores and in rocks, or as relatively soft, unconsolidated sediments that melt at moderate to... [Pg.36]

Table 1.2 Diagnostic criteria for iron oxide minerals. [Pg.55]

Oxide minerals, e.g. Fe3+ ions and carbonate and seawater contents Deep zones of metals and very reduced minerals in the mantle Some parts of the atmosphere 03, N2/02 All such chemicals are thermodynamically unstable in the absence of air relative to C02, CH4 and H20 and in air all are unstable relative to C02 and H20 but all have considerable kinetic stability... [Pg.417]

Harvey, T. J. Yen, W. T. Paterson, J. G. Selective zinc extraction from complex copper-zinc sulfide concentrates by pressure oxidation. Miner. Eng. 1992, 5, 975-992. [Pg.800]


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Acid mine drainage, sulfide mineral oxidation

Adsorbent mineral oxides

Adsorption chelates oxide minerals

Adsorption oxide minerals

Aqueous surface chemistry of oxides and complex oxide minerals

Arsenite-containing minerals oxidation

Auto-inhibition of oxide mineral

Auto-inhibition of oxide mineral reductive capacity toward

Clay minerals ruthenium oxide support

Complex oxide minerals, aqueous

Complex oxide minerals, aqueous surface chemistry

Contents Oxide Minerals

Differential thermal analysis oxide minerals

Dissolution kinetics minerals, oxides

EDTA oxide mineral reductive capacity

Factors influencing the oxidation of arsenic-bearing sulfide minerals

Fe oxide minerals

Fingerprinting mineral deposit types using iron-oxide chemistry Application to till from Thompson, Manitoba, Canada

Ion Binding to Oxide Minerals

Iron oxidizing bacteria, mineral oxidation

Major Oxides and Oxide Minerals

Major oxide minerals

Manganese oxide minerals formed

Manganese oxide minerals formed environments

Metal oxide minerals

Metal oxides mineral processing

Mineral oxidants

Mineral oxidants

Mineral oxidation, iron oxidizing bacterial

Mineral sulfide-oxidizing acidophilic

Mineral sulfide-oxidizing acidophilic bacteria

Mineralization partial oxidation products

Mineralization, by oxidation

Minerals complex oxide

Minerals nickel oxide

Minerals oxidation

Minerals oxidation

Minerals oxide-type

Minerals titanium oxide

Minerals zinc oxide

Mn oxide minerals

Nitrogen dioxide mineral oxides, reactions with

Organic-surface interactions, oxide minerals

Oxidation metallic mineral deposits

Oxidation of mineral oils

Oxidation of minerals

Oxidation of sulfide minerals

Oxidation polymerization reactions mineral surfaces

Oxidation primary minerals

Oxidation reactions, mineral

Oxidation reactions, mineral surfaces

Oxidations mineral formation

Oxide mineral reductive capacity

Oxide minerals origin

Oxide minerals, aqueous surface

Oxide minerals, thermal analysis

Phenol oxidation mineralization

Sulfide minerals oxidation

Synthetic Oxides Versus Minerals

Thermal Analysis Curves of Oxide Minerals

Uranium minerals oxide hydrates

Uranium minerals uranyl oxide hydrates

Zinc oxide mineralizers

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