Classifiers, leaching

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). 

Continuous Percolators Coarse sohds are also leached by percolation in moving-bed equipment, including single-deck and nmlti-deck rake classifiers, bucket-elevator contactors, and horizontal-belt conveyors. 

The coverage thus far has provided an account of the usefulness of phase rule to classify equilibria and to establish the number of independent variables or degrees or of freedom available in a specific situation. In the following paragraphs the equilibria used in mass transfer are analyzed in terms of phase rule in the case of leaching, drying and crystallisation. 

RCRA was passed to manage nonhazardous and hazardous wastes and underground storage tanks, with an emphasis placed on the recovery of reusable materials as an alternative to their disposal. This act introduced the concept of the separate management of hazardous and nonhazardous wastes, and defined procedures to identify whether a waste is hazardous or nonhazardous. A waste exhibits the characteristic of toxicity, classified as a hazardous material, if the concentration of any of 39 selected analytes in the Toxicity Characteristic Leaching Procedure (TCLP) extract exceed regulatory action levels. 

A recent and extremely important development lies in the application of the technique of liquid extraction to metallurgical processes. The successful development of methods for the purification of uranium fuel and for the recovery of spent fuel elements in the nuclear power industry by extraction methods, mainly based on packed, including pulsed, columns as discussed in Section 13.5 has led to their application to other metallurgical processes. Of these, the recovery of copper from acid leach liquors and subsequent electro-winning from these liquors is the most extensive, although further applications to nickel and other metals are being developed. In many of these processes, some form of chemical complex is formed between the solute and the solvent so that the kinetics of the process become important. The extraction operation may be either a physical operation, as discussed previously, or a chemical operation. Chemical operations have been classified by Hanson(1) as follows ... 

The ability of activated carbon to absorb gold and silver from solution has been commercially exploited since the beginning of the 1970s [46,47] and the techniques used can be classified in (i) carbon in pulp (CIP) (ii) carbon in leach (CIL) and (iii) carbon in column (CIC) [46,47]. 

In a study (Boyle, et al., 1981) conducted by the American Foundrymen s Society (AFS) in conjunction with the University of Wisconsin and the USEPA, leaching tests were conducted on cupola emission control dusts and sludges from 21 different foundries. This study concluded that 9 out of the 21 foundries generated emission control residuals which would be considered as a hazardous waste on the basis of EP Toxicity for lead. Two other foundries generated emission control residuals which would be classified as hazardous on the basis of EP Toxicity for cadmium. Concentrations in the EP Toxicity Test for the 21 foundries ranged from less than 0.6 mg/1 to 130 mg/1. The mean lead... 

The data shows an immediate decrease (the difference between untreated and 0 hours after treatment) in the TCLP leachable metals concentration for all seven metals. This indicated that the metals were bound immediately upon being treated. There would be no threat for contaminant leaching during the period it took for the CHEMFIX product to physically solidify. In addition, the TCLP leachable metal concentrations of those samples that were not allowed to cure (0 hours after treatment) all passed the TCLP regulatory limits. Therefore immediately after treatment the material can be classified as non-hazardous. 

A mobility ranking based on soil thin-layer chromatography fstlci is used to classify the herbicide leaching poiential of various herbicides. Tile... 

Hazardousness Having a hazardous property. A chemical, procedure, or event that creates a substantial threat to human health and life. The United States Environment Protection Agency (US EPA) classifies hazardous wastes by four characteristics, including corrosivity (very alkaline (basic) (pH > 12) or acidic (pH 2) wastes), ignitability, toxicity, and reactivity (40 Code of Federal Regulations 261.20-261.24) (see Appendix E compare with toxicity characteristic and toxicity characteristic leaching procedure, TCLP). 

The metals of most concern are the heavy metals, especially cadmium, lead, and mercury. Although it is a metalloid with characteristics of both metals and nonmetals, arsenic is commonly classified as a heavy metal for a discussion of its toxicity. Though not particularly toxic, zinc is abundant and may reach toxic levels in some cases. For example, zinc accumulates in sewage sludge and crop productivity has been lowered on land fertilized with sludge because of zinc accumulation. Copper may be toxic to plants. Aluminum, a natural constituent of soil, may be leached from soil by polluted acidic rainwater and reach levels that are toxic to plants. Other metals that may be of concern because of their toxicides include chromium, cobalt, iron, nickel, and vanadium. Radium, a radioactive alpha particle-emitting metal, can be very toxic at even very low levels in water or food. 

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