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Robert R. Seal,

Publications and source records attributed to Robert R. Seal,.

At least 19 recordsLinked to original sources

Critical minerals in mine waste

Introduction Critical minerals are commodities with vulnerable supply chains that play a vital role in supporting the United States’ economy, national defense and security, emerging technologies, and energy independence. The prosperity of our Nation depends on generating a resilient supply of domestic critical minerals; mine waste may be an untapped source of these commodities. Mine waste from centuries of legacy mining persist on the landscape and may contain critical minerals and other valuable commodities previously deemed uneconomic to recover. At modern mines, the financial viability of recovering byproduct critical minerals, which are not the primary target, may be marginal and can ultimately destine them to mine waste. Further, mine waste can be a liability for the mining company or, at legacy mines, the taxpayer because of its effect on the landscape. The U.S. Geological Survey (USGS) has several initiatives to evaluate critical mineral resources in various types of waste. This factsheet highlights studies of mine waste carried out by USGS scientists at the Geology, Energy & Minerals Science Center in collaboration with other science centers funded through the USGS Mineral Resources Program. Recovery of critical minerals from mine waste can aid in remediation efforts and increase domestic supply of vital mineral resources.

Fact Sheet↗

Using stable oxygen isotope dual-inlet isotope-ratio mass spectrometry to elucidate uranium transport and mixed 230Th/U calcite formation ages at the seminal Devils Hole, Nevada, natural laboratory

Rationale Vein calcite in Devils Hole has been precipitating continuously in oxygen-isotope equilibrium at a constant temperature for over 500 000 years, providing an unmatched δ 18 O paleoclimate time series. A substantial issue is that coeval calcite (based on matching δ 18 O values) has uranium-series ages differing by 12 000 years. Methods An unparalleled high-accuracy δ 18 O chronology series from continuously submerged calcite was used to correct the published uranium-series ages of non-continuously formed calcite in two cores, cyclically exposed by water-table decline during glacial–interglacial transitions. This method relies on the premise that the δ 18 O values of coevally precipitated calcite are identical, allowing matching calcite δ 18 O values to establish formation ages. Results Exposed calcite can have apparent ages that are 12 000 years too young due to unrecognized uranium mobility and resulting mixed ages identified in over 50 mixed uranium-series ages from previous studies. Secondary uranium in fluids, sourced from the formation or dissolution of porous carbonate deposits (folia) with high uranium-238 ( 238 U) concentrations, has migrated up to 10 mm into vein calcite. Conclusions The continuously submerged Devils Hole δ 18 O chronology is not explained by orbital forcing. Rather, this chronology represents a regional climate record in the southern Great Basin of sea-surface-temperature (SST) variations off California, variations that preceded the last and penultimate deglaciations by 5000 to approximately 10 000 years. Temporal discrepancies between the continuously submerged Devils Hole chronology and other regional δ 18 O records (e.g., the Leviathan chronology) can be explained by unrecognized cryptic, pernicious uranium mobility, leading to model estimations that may be thousands of years younger than actual ages. Consequently, paleo-moisture availability, water-table, and groundwater recharge models based on these mixed uranium-series ages are too young by as much as 12 000 years. The potential for post-formation uranium addition in subaerial cores and speleothems underscores the need for caution in uranium-series dating, highlighting δ 18 O time-series comparisons as a method for identifying mixed ages.

Nevada↗

A novel non-destructive workflow for examining germanium and co-substituents in ZnS

A suite of complementary techniques was used to examine germanium (Ge), a byproduct critical element, and co-substituent trace elements in ZnS and mine wastes from four mineral districts where germanium is, or has been, produced within the United States. This contribution establishes a comprehensive workflow for characterizing Ge and other trace elements, which captures the full heterogeneity of samples through extensive pre-characterization. This process proceeded from optical microscopy, to scanning electron microscopy and cathodoluminescence (CL) imaging, to electron microprobe analysis, prior to synchrotron-based investigations. Utilizing non-destructive techniques enabled reanalysis, which proved essential for verifying observations and validating unexpected results. In cases where the Fe content was <0.3 wt% in ZnS, cathodoluminescence imaging proved to be an efficient means to qualitatively identify trace element zonation that could then be further explored by other micro-focused techniques. Micro-focused X-ray diffraction was used to map the distribution of the non-cubic ZnS polymorph, whereas micro-focused X-ray fluorescence (μ-XRF) phase mapping distinguished between Ge 4+ hosted in primary ZnS and a weathering product, hemimorphite [Zn 4 Si 2 O 7 (OH) 2 ·H 2 O]. Microprobe data and μ-XRF maps identified spatial relationships among trace elements in ZnS and implied substitutional mechanisms, which were further explored using Ge and copper (Cu) X-ray absorption near-edge spectroscopy (XANES). Both oxidation states of Ge (4+ and 2+) were identified in ZnS along with, almost exclusively, monovalent Cu. However, the relative abundance of Ge oxidation states varied among mineral districts and, sometimes, within samples. Further, bulk XANES measurements typically agreed with micro-focused XANES (μ-XANES) spectra, but unique micro-environments were detected, highlighting the importance of complementary bulk and micro-focused measurements. Some Ge μ-XANES utilized a high energy resolution fluorescence detector, which improved spectral resolution and spectral signal-to-noise ratio. This detector opens new opportunities for exploring byproduct critical elements in complex matrices. Overall, the non-destructive workflow employed here can be extended to other byproduct critical elements to more fully understand fundamental ore enrichment processes, which have practical implications for critical element exploration, resource quantification, and extraction.

Frontiers in Earth Science↗

Geoenvironmental model for roll-type uranium deposits in the Texas Gulf Coast

Geoenvironmental models were formulated by the U.S. Geological Survey in the 1990s to describe potential environmental effects of extracting different types of ore deposits in different geologic and climatic regions. This paper presents a geoenvironmental model for roll-front (roll-type) uranium deposits in the Texas Coastal Plain. The model reviews descriptive and quantitative information derived from environmental studies and existing databases to depict existing conditions and potential environmental concerns associated with mining this deposit type. This geoenvironmental model describes how features of the deposits including host rock; ore and gangue mineralogy; geologic, hydrologic, and climatic settings; and mining methods (legacy open-pit and in situ recovery [ISR]) influence potential environmental effects from mining. Element concentrations in soil and water are compared to regulatory thresholds to depict ambient surface water and groundwater conditions. Although most open-pit operations in this region have been reclaimed, concerns remain about groundwater quality at three of the four former mills that supported former open-pit mines and are undergoing closure activities. The primary environmental concerns with ISR mining are (1) radon gas at active ISR operations, (2) radiation or contaminant leakage during production and transport of ISR resin or yellowcake, (3) uranium excursions into groundwater surrounding active ISR operations, and (4) contamination of groundwater after ISR mining. Although existing regulations attempt to address these concerns, some problems remain. Researchers suggest that reactive transport modeling and a better understanding of geology, stratigraphy, and geochemistry of ISR production areas could minimize excursions into surrounding aquifers and improve results of groundwater restoration.

Texas↗

Germanium redistribution during weathering of Zn mine wastes: Implications for environmental mobility and recovery of a critical mineral

Germanium (Ge) is a metal used in emerging energy technologies, communications, and defense, and has been deemed critical by the United States due to its essential applications and scarce supply. Germanium is recovered as a byproduct of zinc (Zn) sulfides, and mining and processing of these materials lead to waste that could act both as a source of extractable Ge and a source for exposure to humans and ecosystems. Yet the distribution, speciation, and mineral hosts of Ge in mining-impacted areas are poorly understood. The Tar Creek Superfund Site, a former Zn mining area and Ge producer, is a natural laboratory to understand the environmental behavior and economic implications of Ge in mine wastes. We studied the distribution and behavior of Ge in solid wastes at the Tar Creek Superfund Site using bulk and microanalytical techniques. In wastes at this site we find that Ge has been redistributed from its original host, sphalerite (ZnS), to the fine-grained weathering product hemimorphite (Zn4Si2O7(OH)2·H2O), which impacts germanium's mobility, bioaccessibility, and potential for recovery. We provide chemical and mineralogical evidence of this redistribution, along with an evaluation of the oxidation state and molecular-scale substitution of Ge into sphalerite, hemimorphite, and quartz. Geochemical modeling shows that hemimorphite is more stable than sphalerite in waste piles and provides a stable secondary repository for Ge. However, hemimorphite is fine-grained, and if ingested or inhaled is readily soluble, with the potential to release Ge. Lastly, we discuss other sites internationally where similar behavior may be important. This study shows that weathering can have a significant impact on the distribution, speciation, and mineral hosts of Ge in mine wastes; directly influence mobilization from waste piles and subsequent availability to humans and ecosystems; and dictate metallurgical strategies to target Ge for recovery.

Oklahoma↗

USGS Critical Minerals Review: 2021

In 2021, the U.S. Geological Survey (USGS) continued to play a central role in understanding and anticipating potential supply chain disruptions by defining and quantitatively evaluating mineral criticality. In addition, the USGS continued to evaluate new sources of domestic critical minerals by conducting mineral resource assessments, mapping and surveying regions prospective for critical minerals, re-assessing mine waste, and pursuing fundamental research in support of responsible, sustainable mining.

Mining Engineering↗

Environmental geochemistry of an epigenetic Pb-Zn-Ag deposit at the abandoned Cecilia mine, Puno region, Peru

The abandoned Cecilia Pb-Zn-Ag mine is located at the headwaters of the Lake Titicaca watershed in the Altiplano of Peru. The site is characterized by three months of high precipitation and nine months of limited precipitation. The environmental geochemical characterization of the abandoned mine was done to evaluate environmental risks at the site from mine wastes and mine drainage, and their potential for downstream impacts on water quality in Lake Titicaca. The approach included sampling of mine waste, water, and sediment. Composite mine waste samples were collected from six main piles (four tailings, two waste rock). The surface water was collected from (1) drainage from mine portals; (2) the Cecilia and Crucero rivers upstream of mine influences; (3) the impacted reach of the Cecilia River down to its confluence with the Crucero River; and (4) the Crucero River, which receives drainage from the Cecilia River. Sampling in the dry season did not identify seeps from the waste rock or tailings piles. This study documents the capacity of the site to generate acid mine drainage from the mine waste and underground workings. Mine waste has elevated concentrations of As (up to 883 mg/kg), Cu (up to 20,106 mg/kg), Pb (up to 16,716 mg/kg), and Zn (up to 11,937 mg/kg). Results for dissolved concentrations from leaching experiments on mine waste samples showed high leachability for As (0.001 to 0.95 mg/L), Cu (0.01 to 57.34 mg/L), Cd (0.001 to 1.13 mg/L), Fe (0.42 to 785 mg/L), Zn (0.01 to 91 mg/L), and Mn (0.05 to 279 mg/L) with an acidic pH (2.5 to 6.0). Water chemistry at the site varied on the basis of water type. The Cecilia and Crucero rivers had neutral pH and low concentrations of metals upstream of mine influences. In contrast, samples collected at the mine portal were highly acidic (pH 1.4 to 3.7) with high dissolved concentrations of Fe (up to 4,720 mg/L), Al (up to 400 mg/L), sulfate (up to 19,428 mg/L), As (up to 5.92 mg/L), Cd (up to 9.84 mg/L), Cu (up to 1.56 mg/L), Pb (up to 1.95 mg/L), and Zn (up to 4,065 mg/L), causing an increase in metal concentrations in the river downstream after mixing. Carbonate rocks in the watershed produce alkaline waters that neutralize acid drainage prior to its confluence with the Crucero River. Proposed remediation methods include capping mine waste to limit contact with rainwater and passive treatment of mine portal drainage.

Cecilia mine↗

Economic geology and environmental characteristics of antimony deposits

Antimony is commonly listed as a critical mineral, particularly in the United States and European Union [1]. Its criticality, or supply risk, is derived from a combination of economic vulnerability, disruption potential of supply, and trade exposure [2].Disruption potential relates a country’s ability and willingness to supply a commodity. Commodities for which supply is concentrated in the fewest countries have the greatest potential for supply disruption, trade exposure, and economic vulnerability. In 2018, approximately 61% of the world production of antimony was mined from China, followed by Russia (20%) and Tajikistan (10%) [3] (Fig. 3.1). Several reviews of antimony as a critical mineral have been recently published [4, 5]. The uses of antimony can be divided into three main categories: metal products, non-metal uses, and flame retardants [5]. Most metallic antimony use is inlead-acid batteries. Antimony trioxide (Sb 2 O 3 ) combined with halogenated com-pounds is used as a fire retardant in plastics, fabrics, and other applications. Other non-metallic uses include as a catalyst for plastics, and in the glass industry. Emerging uses include data storage and novel photovoltaic cells. Recycling of batteries represents an important reuse of antimony, but other uses of antimony do not lend themselves to recycling. This chapter describes mineral deposit types that are primary sources of antimony, and environmental effects related to their mining. Antimony can be re-covered as either a primary commodity from some deposits or as a by product commodity from some gold or silver deposits. Environmental risks associated with antimony mining include those related to mining in general, such as the acid-generating potential of solid mine waste, and some issues specific to antimony, as described below.

Book chapter↗

USGS 2020 critical minerals review

Concerns about the lack of domestic production and availability of essential mineral raw materials were a recurring theme throughout the 20th century, particularly in the periods around armed conflicts (Congressional Research Service, 2019). These concerns resulted in the designation of particular minerals as “strategic” or “critical,” terms that commonly depend on the perspective of the user, but which are generally understood to relate to mineral commodities with uses in essential applications, and which are exposed to risk of supply disruptions, with attendant implications for economic and national security interests.

Mining Engineering↗

Conceptual framework and approach for conducting a geoenvironmental assessment of undiscovered uranium resources

This report presents a novel conceptual framework and approach for conducting a geologically based environmental assessment, or geoenvironmental assessment, of undiscovered uranium resources within an area likely to contain uranium deposits. The framework is based on a source-to-receptor model that prioritizes the most likely contaminant sources, contaminant pathways, and affected environmental media for three common uranium extraction methods—open pit or underground mining with milling and in situ recovery (ISR). Data on regional geology, hydrology, and climate, as well as historical uranium mining and milling records are used to estimate the probable amounts of waste rock, tailings, wastewater, surface land disturbance, and subsurface aquifer disturbance for likely mining methods. Constituents of concern that might take the form of leachates, dust, radon, and sediments formed by chemical and physical weathering are also identified in the geoenvironmental assessment. Finally, areas where constituents of concern are likely to occur and persist in air, land, surface water, and groundwater are indicated by the potential for dispersion of dust by wind, accumulation of radon because of air stagnation, dispersion of sediments and wastewater by runoff, and infiltration of wastewater or leachates with consideration of the likely mobility of contaminants in surface water and groundwater. The geoenvironmental assessment output can be summarized in the following primary products: (1) a descriptive geoenvironmental model; (2) maps and statistics of variables that indicate the potential for constituents of concern to occur and persist in air, land, surface water, and groundwater within a tract that is geologically permissive for the occurrence of uranium; and (3) tables providing estimated or indicated quantities of waste rock, tailings, wastewater, dust, and radon emissions that could be associated with undiscovered uranium resources, if extracted, for each permissive tract. The uranium geoenvironmental assessment could help natural resource managers to prioritize and (or) identify (1) important potential contaminant pathways, (2) management practices required depending on the types of constituents that could be of concern, (3) areas for response in the event of accidental release, and (4) future directions for study. Furthermore, indicators of rock and water volumes potentially associated with an undiscovered uranium deposit may be evaluated to make quantitative comparisons of water required for uranium production or potential waste products generated during uranium extraction from areas permissive for uranium resource occurrence throughout the United States.

Scientific Investigations Report↗

Micrometer-scale characterization of solid mine waste aids in closure due diligence

Precious- and base-metal mining often occurs in deposits with high acid-generating potential, resulting in mine waste that contains metals in forms of varying bioavailability, and therefore toxicity. The solids that host these metals are often noncrystalline, nanometer to micrometer in size, or undetectable by readily available analytical techniques (e.g., X-ray diffraction). This analytical shortcoming can pose a challenge when attempting to characterize sources and natural attenuation of metals at a given site, which is a best practice to satisfy closure due diligence. Numerous case studies have shown that efforts to characterize mine waste at multiple scales, particularly the micrometer scale, often lead to a better understanding of metal distribution and potential contamination risks. This paper presents a case study that compares the use of both traditional and non-traditional techniques to identify and quantify metal hosts in sediments downstream of the abandoned mine waste piles at the Ely Copper Mine Superfund site in Vermont (USA). The contaminant present in the highest concentration in the sediments is copper, yet not all copper-bearing solids were detected with bulk X-ray diffraction (XRD). At the micrometer scale, a combination of synchrotron-based X-ray absorption spectroscopy (XAS) and an automated mineralogy (AM) system were used to identify the most abundant copper-bearing solids. Bulk XAS and AM also provided semi-quantitative abundances of these solids in the sediment. At the Ely Copper Mine, copper in stream sediments was found to be predominantly hosted in sulphide minerals downstream of a major mine waste pile, whereas upstream copper was predominantly hosted in secondary iron and manganese (oxyhydr)oxides. These copper-bearing hosts were consistent with the expected bioavailability of copper in the sediments based on laboratory toxicity tests with aquatic organisms. When the bulk of copper was present in sulphides, aquatic organisms experienced greater survival than when copper was mostly associated with secondary iron and manganese (oxyhydr)oxides. The information gained from probing the sediments at multiple scales can now be used to prioritize containment and remediation strategies. While synchrotron-based analytical techniques have proven to be invaluable in many studies of mine waste, access to these techniques is limited. In contrast, access to a scanning electron microscope that can perform AM is becoming more common, primarily for the application in mining design and mineral processing operations. More recently, the successful use of AM to characterize mine waste suggests that this technique can be equally as valuable for mine closure plans. The resolution of information obtained may go beyond what is required from a regulatory perspective, but given that the results have the potential to be more conclusive than many traditional techniques, this level of characterization may save time and money in the long run.

Vermont↗

Hydrologic balance, water quality, chemical-mass balance, and geochemical modeling of hyperalkaline ponds at Big Marsh, Chicago, Illinois, 2016–17

Hyperalkaline (pH greater than 12) ponds and groundwater exist at Big Marsh near Lake Calumet, Chicago, Illinois, a site used by the steel industry during the mid-1900s to deposit steel- and iron-making waste, in particular, slag. The hyperalkaline ponds may pose a hazard to human health and the environment. The U.S. Geological Survey (USGS), in cooperation with the Environmental Protection Agency (EPA) and in collaboration with the City of Chicago’s Park District, completed a study to evaluate the hydrologic balance, water quality, and chemical-mass balance of hyperalkaline ponds at Big Marsh and geochemical modeling used to evaluate remediation options for water quality at the site based on data collected in 2016–17. Synoptic measurements of surface-water and groundwater elevations were used to determine flow directions and to enable a preliminary estimate of the hydrologic balance for the ponds. Water-quality samples also were collected and analyzed for selected constituents including major anions and cations, nutrients, metals, and trace elements. The results of the water-quality analyses were used to develop a geochemical model to evaluate concentrations, factors affecting pH, and the state of equilibrium between surface waters and atmospheric carbon dioxide. The geochemical model was used to evaluate remediation scenarios using riprap, spillways, or active aeration. The results indicate that active aeration will decrease the pH to near 7.5 in about 8 hours, the fastest rate of the scenarios. Passive aeration, such as riprap or spillways, also can be effective at decreasing the pH in about 45 hours, but spatial obstacles limit their implementation. Seasonal variations in temperature also affect the rate of equilibration, where colder temperatures may have a lower pH than warmer temperatures and may affect the timing and frequency of remediation.

Illinois↗

Geochemical characterization of iron and steel slag and its potential to remove phosphate and neutralize acid

Iron and steel slags from legacy and modern operations in the Chicago-Gary area of Illinois and Indiana, USA, are predominantly composed of Ca (10 - 44 wt. % CaO), Fe, (0.3 - 28 wt. % FeO), and Si (10 - 44 wt. % SiO2), with generally lesser amounts of Al (< 1 15 wt. % Al2O3), Mg (2 11 wt. % MgO), and Mn (0.3 9 wt. % MnO). Mineralogy is dominated by CaMgAl silicates, FeCa oxides, Ca-carbonates, and high temperature SiO2 phases. Chromium and Mn concentrations in most samples may be environmentally significant based on comparison with generic soil contaminant guidelines. However, simulated weathering tests suggest these elements are present in generally insoluble phases making use in water treatment applications possible; generation of high pH and alkaline solutions may be an issue. As for water treatment applications, batch and flow-through experiments document effective removal of phosphate from synthetic solutions for nearly all slag samples. Air-cooled fine fractions (< 10 mm) of modern slag were most effective; other types, including modern granulated, modern air-cooled coarse fractions (> 10 mm), and legacy slag removed phosphate, but to a lesser degree. An additional water treatment application is the use of slag to neutralize acidic waters. Most slag samples are extremely alkaline and have high net neutralization potentials (NNP) (400 830 kg CaCO3/t), with the highest approximately equivalent to 80% the neutralization potential of calcite. Overall, phosphate removal capacity and NNP correlate positively with total Ca content and the dissolution of Ca minerals facilitates secondary Ca phosphate formation and consumes acid during hydrolysis. Utilizing locally available slag to treat waste or agricultural waters in this region may be a higher value alternative than use in construction, potentially offsetting restoration costs to degraded legacy areas and decreasing steel manufacturers current waste footprint.

Minerals↗

USGS critical minerals review

The United States’ supply of critical minerals has been a concern and a source of potential strategic vulnerabilities for U.S. economic and national security interests for decades (for example, see Strategic and Critical Minerals Stockpiling Act, 1939). More recently, with the rapid increase in the types of materials being used in advanced technologies (Fortier et al. 2018a), and geopolitical events surrounding the supply of rare earth elements (Ting and Seaman, 2013), among other developments, the critical minerals issue has again achieved a high level of visibility within the U.S. government (Executive Order 13817 (2017)).

Mining Engineering↗

Rare-earth elements

The rare-earth elements (REEs) are 15 elements that range in atomic number from 57 (lanthanum) to 71 (lutetium); they are commonly referred to as the “lanthanides.” Yttrium (atomic number 39) is also commonly regarded as an REE because it shares chemical and physical similarities and has affinities with the lanthanides. Although REEs are not rare in terms of average crustal abundance, the concentrated deposits of REEs are limited in number. Because of their unusual physical and chemical properties, the REEs have diverse defense, energy, industrial, and military technology applications. The glass industry is the leading consumer of REE raw materials, which are used for glass polishing and as additives that provide color and special optical properties to the glass. Lanthanum-based catalysts are used in petroleum refining, and cerium-based catalysts are used in automotive catalytic converters. The use of REEs in magnets is a rapidly increasing application. Neodymium-iron-boron magnets, which are the strongest known type of magnets, are used when space and weight are restrictions. Nickel-metal hydride batteries use anodes made of a lanthanum-based alloys. China, which has led the world production of REEs for decades, accounted for more than 90 percent of global production and supply, on average, during the past decade. Citing a need to retain its limited REE resources to meet domestic requirements as well as concerns about the environmental effects of mining, China began placing restrictions on the supply of REEs in 2010 through the imposition of quotas, licenses, and taxes. As a result, the global rare-earth industry has increased its stockpiling of REEs; explored for deposits outside of China; and promoted new efforts to conserve, recycle, and substitute for REEs. New mine production began at Mount Weld in Western Australia, and numerous other exploration and development projects noted in this chapter are ongoing throughout the world. The REE-bearing minerals are diverse and often complex in composition. At least 245 individual REE-bearing minerals are recognized; they are mainly carbonates, fluorocarbonates, and hydroxylcarbonates (n = 42); oxides (n = 59); silicates (n = 85); and phosphates (n = 26). Many of the world’s significant REE deposits occur in carbonatites, which are carbonate igneous rocks. The REEs also have a strong genetic association with alkaline magmatism. The systematic geologic and chemical processes that explain these observations are not well understood. Economic or potentially economic REE deposits have been found in (a) carbonatites, (b) peralkaline igneous systems, (c) magmatic magnetite-hematite bodies, (d) iron oxide-copper-gold (IOCG) deposits, (e) xenotime-monazite accumulations in mafic gneiss, (f) ion-absorption clay deposits, and (g) monazite-xenotime-bearing placer deposits. Carbonatites have been the world’s main source for the light REEs since the 1960s. Ion-adsorption clay deposits in southern China are the world’s primary source of the heavy REEs. Monazite-bearing placer deposits were important sources of REEs before the mid-1960s and may be again in the future. In recent years, REEs have been produced from large carbonatite bodies mined at the Mountain Pass deposit in California and, in China, at the Bayan Obo deposit in Nei Mongol Autonomous Region, the Maoniuping deposit in Sichuan Province, the Daluxiang deposit in Sichuan Province, and the Weishan deposit in Anhui Province. Alkaline igneous complexes have recently been targeted for exploration because of their enrichments in the heavy REEs. Information relevant to the environmental aspects of REE mining is limited. Little is known about the aquatic toxicity of REEs. The United States lacks drinking water standards for REEs. The concentrations of REEs in environmental media are influenced by their low abundances in crustal rocks and their limited solubility in most groundwaters and surface waters. The scarcity of sulfide minerals, including pyrite, minimizes or eliminates concerns about acid-mine drainage for carbonatite-hosted deposits and alkaline-intrusion-related REE deposits. For now, insights into environmental responses of REE mine wastes must rely on predictive models.

Professional Paper↗

Tellurium

Tellurium (Te) is a very rare element that averages only 3 parts per billion in Earth’s upper crust. It shows a close association with gold and may be present in orebodies of most gold deposit types at levels of tens to hundreds of parts per million. In large-tonnage mineral deposits, such as porphyry copper and seafloor volcanogenic massive sulfide deposits, sulfide minerals may contain hundreds of parts per million tellurium, although the orebodies likely have overall concentrations of 0.1 to 1.0 parts per million tellurium. Tellurium is presently recovered as a primary ore from only two districts in the world; these are the gold-tellurium epithermal vein deposits located adjacent to one another at Dashuigou and Majiagou (Sichuan Province) in southwestern China, and the epithermal-like mineralization at the Kankberg deposit in the Skellefteå VMS district of Västerbotten County, Sweden. Combined, these two groups of deposits account for about 15 percent (about 70 metric tons) of the annual global production of between 450 and 470 metric tons of tellurium. Most of the world’s tellurium, however, is produced as a byproduct of the mining of porphyry copper deposits. These deposits typically yield concentrations of 1 to 4 percent tellurium in the anode slimes recovered during copper refining. Present production of tellurium from the United States is solely from the anode slimes at ASARCO LLC’s copper refinery in Amarillo, Texas, and may total about 50 metric tons per year. The main uses of tellurium are in photovoltaic solar cells and as an additive to copper, lead, and steel alloys in various types of machinery. The environmental data available regarding the mining of tellurium are limited; most concerns to date have focused on the more-abundant metals present in the large-tonnage deposits from which tellurium is recovered as a byproduct. Global reserves of tellurium are estimated to be 24,000 metric tons, based on the amount of tellurium likely contained in global copper reserves and on a 50 percent recovery rate from refinery anode slimes during the commonly used electrolytic process, also known as solvent extraction-electrolytic refining. If the more economical solvent-leach process—a process that does not recover tellurium—is increasingly used in the future to recover lower grades of copper from porphyry and other large-tonnage deposits, then additional high-grade tellurium-rich gold deposits may become new primary sources for tellurium, particularly epithermal vein deposits associated with alkaline magmatism.

Professional Paper↗