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0000-0001-8314-6344
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UNSW Sydney
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Systems engineering | Civil engineering | Fire safety engineering | Functional materials
Publisher: MDPI AG
Date: 31-05-2021
DOI: 10.3390/MIN11060590
Abstract: Acid mine drainage (AMD) is a serious environmental issue associated with mining due to its acidic pH and potentially toxic elements (PTE) content. This study investigated the performance of the Fe-Al bimetallic particles for the treatment of combined AMD-gold processing effluents. Batch experiments were conducted in order to eliminate potentially toxic elements (including Hg, As, Cu, Pb, Ni, Zn, and Mn) from a simulated waste solution at various bimetal dosages (5, 10, and 20 g/L) and time intervals (0 to 90 min). The findings show that metal ions with greater electrode potentials than Fe and Al have higher affinities for electrons released from the bimetal. Therefore, a high removal ( %) was obtained for Hg, As, Cu, and Pb using 20 g/L bimetal in 90 min. Higher uptakes of Hg, As, Cu, and Pb than Ni, Zn, and Mn also suggest that electrochemical reduction and adsorption by Fe-Al (oxy) hydroxides as the primary and secondary removal mechanisms, respectively. The total Al3+ dissolution in the experiments with a higher bimetal content (10 and 20 g/L) were insignificant, while a high release of Fe ions was recorded for various bimetal dosages. Although the secondary Fe pollution can be considered as a drawback of using the Fe-Al bimetal, this issue can be tackled by a simple neutralization and Fe precipitation process. A rapid increase in the solution pH (initial pH 2 to in 90 min) was also observed, which means that bimetallic particles can act as a neutralizing agent in AMD treatment system and promote the precipitation of the dissolved metals. The presence of chloride ions in the system may cause akaganeite formation, which has shown a high removal capacity for PTE. Moreover, nitrate ions may affect the process by competing for the released electrons from the bimetal owing to their higher electrode potential than the metals. Finally, the Fe-Al bimetallic material showed promising results for AMD remediation by electrochemical reduction of PTE content, as well as acid-neutralization/metal precipitation.
Publisher: Elsevier BV
Date: 03-2019
DOI: 10.1016/J.CHEMOSPHERE.2018.11.053
Abstract: Acid mine/rock drainage (AMD/ARD), effluents with low pH and high concentrations of hazardous and toxic elements generated when sulfide-rich wastes are exposed to the environment, is considered as a serious environmental problem encountered by the mining and mineral processing industries around the world. Remediation options like neutralization, adsorption, ion exchange, membrane technology, biological mediation, and electrochemical approach have been developed to reduce the negative environmental impacts of AMD on ecological systems and human health. However, these techniques require the continuous supply of chemicals and energy, expensive maintenance and labor cost, and long-term monitoring of affected ecosystems until AMD generation stops. Unfortunately, the formation of AMD could persist for hundreds or even thousands of years, so these approaches are both costly and unsustainable. Recently, two alternative strategies for the management of AMD and mine tailings are gaining much attention: (1) prevention techniques, and (2) mine waste recycling. In this review, recent advances in AMD prevention techniques like oxygen barriers, utilization of bactericides, co-disposal and blending, and passivation of sulfide minerals are discussed. In addition, recycling of mine tailings as construction and geopolymer materials to reduce the amounts of wastes for disposal are introduced.
Publisher: Elsevier BV
Date: 03-2020
Publisher: Elsevier BV
Date: 06-2020
Publisher: Elsevier BV
Date: 02-2010
Publisher: Elsevier BV
Date: 12-2012
Publisher: Elsevier BV
Date: 03-2014
DOI: 10.1016/J.SCITOTENV.2013.12.029
Abstract: Sedimentary rocks excavated in Japan from road- and railway-tunnel projects contain relatively low concentrations of hazardous trace elements like boron (B), arsenic (As) and selenium (Se). However, these seemingly harmless waste rocks often produced leachates with concentrations of hazardous trace elements that exceeded the environmental standards. In this study, the leaching behaviors and release mechanisms of B, As and Se were evaluated using batch leaching experiments, sequential extraction and geochemical modeling calculations. The results showed that B was mostly partitioned with the residual/crystalline phase that is relatively stable under normal environmental conditions. In contrast, the majority of As and Se were associated with the exchangeable and organics/sulfides phases that are unstable under oxidizing conditions. Dissolution of water-soluble phases controlled the leaching of B, As and Se from these rocks in the short term, but pyrite oxidation, calcite dissolution and adsorption/desorption reactions became more important in the long term. The mobilities of these trace elements were also strongly influenced by the pH of the rock-water system. Although the leaching of Se only increased in the acidic region, those of B and As were enhanced under both acidic and alkaline conditions. Under strongly acidic conditions, the primarily release mechanism of B, As and Se was the dissolution of mineral phases that incorporated and/or adsorbed these elements. Lower concentrations of these trace elements in the circumneutral pH range could be attributed to their strong adsorption onto minerals like Al-/Fe-oxyhydroxides and clays, which are inherently present and/or precipitated in the rock-water system. The leaching of As and B increased under strongly alkaline conditions because of enhanced desorption and pyrite oxidation while that of Se remained minimal due to its adsorption onto Fe-oxyhydroxides and co-precipitation with calcite.
Publisher: MDPI AG
Date: 18-12-2021
DOI: 10.3390/MIN11121432
Abstract: The global demand for rare earth elements (REEs) is expected to increase significantly because of their importance in renewable energy and clean storage technologies, which are critical for drastic carbon dioxide emission reduction to achieve a carbon-neutral society. REE ore deposits around the world are scarce and those that have been identified but remain unexploited need to be developed to supply future demands. In this study, the Khalzan Buregtei deposit located in western Mongolia was studied with the aim of upgrading low-grade REE ore via magnetic separation techniques. The total REE content in this ore was ~6720 ppm (~3540 ppm light REE (LREE) + ~3180 ppm heavy REE (HREE)) with bastnaesite, pyrochlore, synchysite, and columbite-(Fe) identified as the main REE-bearing minerals. As the particle size fraction decreased from −4.0 + 2.0 mm to −0.5 + 0.1 mm, the recovery by dry high-intensity magnetic separation (DHIMS) increased from 20% to 70% of total rare earth oxide (TREO) while the enrichment ratio reached 2.8 from 1.3. Although effective, gangue minerals such as quartz and aluminosilicates were recovered (~22%) due most likely to insufficient liberation. Meanwhile, the wet high-intensity magnetic separation (WHIMS) could produce a magnetic concentrate with TREO recovery of ~80% and enrichment ratio of 5.5 under the following conditions: particle size fraction, −106 + 75 μm feed flow rate, 3.2 L/min magnetic induction, 0.8 T. These results indicate that combining DHIMS and WHIMS to upgrade the low-grade REE ore from the Khalzan Buregtei deposit is an effective approach.
Publisher: MDPI AG
Date: 21-06-2022
Abstract: The domestic water (DW) quality of an island province in the Philippines that experienced two major mining disasters in the 1990s was assessed and evaluated in 2021 utilizing the heavy metals pollution index (MPI), Nemerow’s pollution index (NPI), and the total carcinogenic risk (TCR) index. The island province sources its DW supply from groundwater (GW), surface water (SW), tap water (TP), and water refilling stations (WRS). This DW supply is used for drinking and cooking by the population. In situ analyses were carried out using an Olympus Vanta X-ray fluorescence spectrometer (XRF) and Accusensing Metals Analysis System (MAS) G1 and the target heavy metals and metalloids (HMM) were arsenic (As), barium (Ba), copper (Cu), iron (Fe), lead (Pb), manganese (Mn), nickel (Ni), and zinc (Zn). The carcinogenic risk was evaluated using the Monte Carlo (MC) method while a machine learning geostatistical interpolation (MLGI) technique was employed to create spatial maps of the metal concentrations and health risk indices. The MPI values calculated at all s ling locations for all water s les indicated a high pollution. Additionally, the NPI values computed at all s ling locations for all DW s les were categorized as “highly polluted”. The results showed that the health quotient indices (HQI) for As and Pb were significantly greater than 1 in all water sources, indicating a probable significant health risk (HR) to the population of the island province. Additionally, As exhibited the highest carcinogenic risk (CR), which was observed in TW s les. This accounted for 89.7% of the total CR observed in TW. Furthermore, all s ling locations exceeded the recommended maximum threshold level of 1.0 × 10−4 by the USEPA. Spatial distribution maps of the contaminant concentrations and health risks provide valuable information to households and guide local government units as well as regional and national agencies in developing strategic interventions to improve DW quality in the island province.
Publisher: MDPI AG
Date: 06-02-2023
DOI: 10.3390/MIN13020232
Abstract: The repurposing of gold (Au) mine tailings from artisanal and small-scale mining (ASGM) operations via alkali activation technology is a promising strategy for waste reduction in developing countries. Direct activation of mine tailings, however, is challenging because these materials contain relatively low aluminum (Al)-bearing minerals. In this study, palm oil fuel ash (POFA) was elucidated as a high Al-bearing waste derived-admixture for the synthesis of an ASGM tailings-based geopolymer composite. Semi-quantitative XRD analysis showed that the tailings contained quartz (SiO2) (~58%), pyrite (FeS2) (~20%) and calcite (CaCO3) (~15%) with minor to trace amounts of aluminosilicates (~7%). Substantial amounts of environmentally regulated pollutants such as mercury (Hg) (40 mg/kg), lead (Pb) (8430 mg/kg) and arsenic (As) (300 mg/kg) were also found in the tailings. SEM-EDS, XRD and ATR-FTIR results showed the successful formation of a hybrid geopolymer-CASH matrix, which improved the unconfined compressive strength (UCS) of geopolymer composites from ~5 MPa to ~7 MPa. Furthermore, POFA did not significantly affect the thermal resistivity of geopolymer composites based on thermal analysis. Finally, the TCLP results showed that the Pb leaching concentrations from ASGM tailings exceeded environmental standards (~15,000 µg/L), which was suppressed after alkali activation to 300–500 µg/L. This means that POFA addition to ASGM tailings-based geopolymer composite improved not only its applicability as backfill, pavements and bricks but also its ability to immobilize toxic elements.
Publisher: MDPI AG
Date: 02-11-2021
DOI: 10.3390/MIN11111220
Abstract: Hydrothermally altered rocks generated from underground/tunnel projects often produce acidic leachate and release heavy metals and toxic metalloids, such as arsenic (As). The adsorption layer and immobilization methods using natural adsorbents or immobilizer as reasonable countermeasures have been proposed. In this study, two sets of column experiments were conducted, of which one was focused on the laboratory columns and other on the in situ columns, to evaluate the effects of column conditions on leaching of As from excavated rocks and on adsorption or immobilization behavior of As by a river sediment (RS) as a natural adsorbent or immobilizer. A bottom adsorption layer consisting of the RS was constructed under the excavated rock layer or a mixing layer of the excavated rock and river sediment was packed in the column. The results showed that no significant trends in the adsorption and immobilization of As by the RS were observed by comparing laboratory and in situ column experiments because the experimental conditions did not influence significant change in the leachate pH which affects As adsorption or immobilization. However, As leaching concentrations of the in situ experiments were higher than those of the laboratory column experiments. In addition, the lower pH, higher Eh and higher coexisting sulfate ions of the leachate were observed for the in situ columns, compared to the results of the laboratory columns. These results indicate that the leaching concentration of As became higher in the in situ columns, resulting in higher oxidation of sulfide minerals in the rock. This may be due to the differences in conditions, such as temperature and water content, which induce the differences in the rate of oxidation of minerals contained in the rock. On the other hand, since the leachate pH affecting As adsorption or immobilization was not influenced significantly, As adsorption or immobilization effect by the RS were effective for both laboratory and in situ column experiments. These results indicate that both in situ and laboratory column experiments are useful in evaluating leaching and adsorption of As by natural adsorbents, despite the fact that the water content which directly affects the rate of oxidation is sensitive to weathering conditions.
Publisher: Elsevier BV
Date: 09-2019
Publisher: Elsevier BV
Date: 03-2021
Publisher: Springer Science and Business Media LLC
Date: 06-03-2018
DOI: 10.1007/S10661-018-6561-2
Abstract: Groundwater flow and its geochemical evolution in mines are important not only in the study of contaminant migration but also in the effective planning of excavation. The effects of groundwater on the stability of rock slopes and other mine constructions especially in limestone quarries are crucial because calcite, the major mineral component of limestone, is moderately soluble in water. In this study, evolution of groundwater in a limestone quarry located in Chichibu city was monitored to understand the geochemical processes occurring within the rock strata of the quarry and changes in the chemistry of groundwater, which suggests zones of deformations that may affect the stability of rock slopes. There are three distinct geological formations in the quarry: limestone layer, interbedded layer of limestone and slaty greenstone, and slaty greenstone layer as basement rock. Although the hydrochemical facies of all groundwater s les were Ca-HCO
Publisher: Elsevier BV
Date: 10-2019
DOI: 10.1016/J.CHEMOSPHERE.2019.06.020
Abstract: Scorodite is an important mineral not only for arsenic (As) removal from industrial wastewaters but also in the mobility and final fate of As in waste rocks, contaminated soils and sediments, and mine tailings. Because of the mineral's high As-loading capacity and stability, numerous studies have been done to understand its formation. Unfortunately, most of these studies were limited to elevated temperatures (>70 °C), so the processes involved in scorodite formation under ambient conditions remain unclear. This study provides evidence of the catalytic effects of hematite on the formation of scorodite at 25 °C in a pyrite-rich natural geologic material. Scorodite peaks were detected in the XRD patterns of the leaching residues with and without hematite, but those in the former were stronger and more pronounced than the latter. These results suggest that the formation of scorodite was catalysed by hematite, a generalisation that is further supported by strong characteristic IR absorption bands of scorodite at 819 cm
Publisher: MDPI AG
Date: 02-2022
Abstract: Coal Fly Ash (CFA) is a hazardous waste from coal-fired power plants, but has increasingly become a popular supplementary cementitious material for cement in the construction industry. As a secondary resource of REE, its main advantage lies in its fine particle size that eliminates the need for costly and energy-intensive comminution. In this study, the potential of CFA from the Philippines as a secondary REE resource was investigated by direct leaching of REEs with hydrochloric acid (HCl). The CFA s le came from a coal-fired power plant with a circulating fluidized bed combustion (CFBC) technology. For the leaching tests, the effects of HCl concentration, leaching time and leaching temperature on REE extractions were elucidate optimized via Response Surface Methodology (RSM). The RSM results showed that the optimum leaching occurred at 3M HCl, 65 °C and 270 min with extractions of Nd, Er, Eu, Tb and Dy at 70.8%, 76.34%, 88.02%, 90.01% and 73.38%, respectively. According to these results, the CFA from the Philippines is a promising secondary resource of REE and the extraction method employed was effective in achieving a relatively high REE dissolution. Moreover, the empirical model that was established accurately predicted the dissolution of REE with an accuracy of 98.20%, 96.66%, 97.09%, 98.17% and 97.78% for Nd, Er, Eu, Tb and Dy, respectively.
Publisher: Elsevier BV
Date: 2012
Publisher: Elsevier BV
Date: 2019
DOI: 10.1016/J.CHEMOSPHERE.2018.09.086
Abstract: Pyrite, a common gangue mineral in complex sulfide ores and coals, is rapidly oxidized in water by ferric ions and dissolved oxygen to form a very acidic and heavy metal-laden leachate called acid mine drainage (AMD). Carrier-microencapsulation (CME) using Ti
Publisher: Elsevier BV
Date: 04-2013
Publisher: Elsevier BV
Date: 03-2021
Publisher: Springer Science and Business Media LLC
Date: 07-05-2019
Publisher: Elsevier BV
Date: 08-2012
Publisher: MDPI AG
Date: 23-03-2022
DOI: 10.3390/MIN12040393
Abstract: Zinc plant leach residues (ZPLRs), particularly those produced using old technologies, have both economic importance as secondary raw materials and have environmental impacts because they contain hazardous heavy metals that pose risks to human health and the environment. Therefore, the extraction and recovery of these metals from ZPLRs has both economic and environmental benefits. In this study, we investigated the removal of lead (Pb) and zinc (Zn) from ZPLRs by alkaline (NaOH) leaching and the concurrent cementation of dissolved Pb and Zn using aluminum (Al) metal powder. The effects of the leaching time, NaOH concentration, solid-to-liquid ratio (S/L), and dosage of Al metal powder on the extraction of Pb and Zn were investigated. Pb and Zn removal efficiencies increased with increasing NaOH concentrations and decreasing S/Ls. The Pb and Zn removal efficiencies were 62.2% and 27.1%, respectively, when 2.5 g/50 mL (S/L) of ZPLRs were leached in a 3 M NaOH solution for 30 min. The extraction of Pb and Zn could be attributed to the partitioning of these metals in relatively more mobile phases—water-soluble, exchangeable, and carbonate phases—in ZPLRs. Around 100% of dissolved Pb and less than 2% of dissolved Zn were cemented in leaching pulp when Al metal powder was added. Minerals in the solid residues, particularly iron oxides minerals, were found to suppress the cementation of extracted Zn in leaching pulp, and when they were removed by filtration, Zn was recovered by Al metal powder via cementation.
Publisher: Elsevier BV
Date: 07-2021
Publisher: MDPI AG
Date: 23-11-2022
DOI: 10.3390/SU142315584
Abstract: Microplastics (MPs), defined as plastics with diameters between 1 and 5000 µm, are problematic pollutants in the environment, but their removal is challenging because of their minute size. One promising approach for their removal is flotation because MPs are inherently hydrophobic. However, the very small particle size of MPs lowers the probability of MPs-bubble collision and attachment that in turn affects the efficiency of the process. To address this challenge, we propose the use of agglomeration-flotation, a technique using kerosene as a bridging liquid to enlarge the particle sizes of MPs and make them amenable to flotation. In this study, the effects of kerosene dosage on particle size enlargement and floatability of six types of MPs with 100–1000 µm size fractions were investigated. The results showed that MPs with lower density compared with water could easily float in water without bubble attachment and particle agglomeration required. So, the effects of agglomeration on removal were negligible. In contrast, agglomeration using kerosene enhanced the floatability of MPs with high-density plastics. Moreover, image analysis was used to determine the agglomerated MPs’ particle size. The results indicate that kerosene could agglomerate the MPs and enhanced the removal of MPs by agglomeration-flotation.
Publisher: Elsevier BV
Date: 2020
Publisher: Elsevier BV
Date: 04-2021
Publisher: Elsevier BV
Date: 10-2021
Publisher: Elsevier BV
Date: 04-2021
Publisher: Elsevier BV
Date: 11-2017
DOI: 10.1016/J.CHEMOSPHERE.2017.07.145
Abstract: Rocks excavated in tunnel construction projects for roads and railways throughout Japan often leached out hazardous trace elements like arsenic (As) and selenium (Se) upon their exposure to the environment. In nature, the various oxyanionic species of As and Se not only coexist but also exhibit contrasting adsorption-desorption behaviors, so speciation is a crucial factor in their migration through natural geologic media. In this study, the leaching and transport of arsenite (As
Publisher: Elsevier BV
Date: 07-2019
Publisher: Elsevier BV
Date: 12-2018
Publisher: MDPI AG
Date: 29-03-2022
DOI: 10.3390/W14071070
Abstract: Without treatment, the harmful effects of acid mine drainage (AMD) lead to the destruction of surrounding ecosystems, including serious health impacts to affected communities. Active methods, like chemical neutralization, are the most widely used approach to AMD management. However, these techniques require constant inputs of energy, chemicals, and manpower, which become unsustainable in the long-term. One promising and sustainable alternative for AMD management is to use passive treatment systems with locally available and waste-derived alkalinity-generating materials. In this study, the treatment of synthetic AMD with laterite mine waste (LMW), concrete waste, and limestone in a successive process train was elucidated, and the optimal process train configuration was determined. Six full factorial analyses were performed following a constant ratio of 0.75 mL AMD/g media with a 15-min retention time. The evolution of the pH, redox potential (Eh), total dissolved solids (TDS), heavy metals concentration, and sulfates concentrations were monitored as the basis for evaluating the treatment performance of each run. LMW had the highest metal and sulfates removal, while concrete waste caused the largest pH increase. A ranking system was utilized in which each parameter was normalized based on the Philippine effluent standards (DENR Administrative Order (DAO) 2016–08 and 2021–19). Run 4 (Limestone-LMW-Concrete waste) showed the best performance, that is, the pH increased from 1.35 to 8.08 and removed 39% Fe, 94% Ni, 72% Al, and 52% sulfate. With this, the process train is more effective to treat AMD, and the order of the media in treatment is significant.
Publisher: MDPI AG
Date: 30-03-2022
DOI: 10.3390/APP12073527
Abstract: This paper presents the effects of flooding on the accumulation of manganese (Mn) in soils within proximity of the Boac and Mogpog rivers in Marinduque of The Philippines. Marinduque, an island province in the Philippines, experienced two catastrophic tailings storage facility (TSF) failures in the 1990s that released sulfide-rich tailings into the two major rivers. The Philippines experiences 21–23 typhoons every year, 11 of which pass thru Marinduque that causing inundation of floodplain areas in the province. A flood hazard map developed using LiDAR DEM was utilized for the Boac and Mogpog rivers for an accurate representation of flooding events. A portable X-ray fluorescence spectrometer (pXRF) and a Hannah multi-parameter device were used for the on-site analyses of Mn concentration and water physico-chemical properties, respectively. Spatial grid mapping with zonal statistics was employed for a comprehensive analysis of all the data collected and processed. Correlation analysis was carried out on Mn concentrations in soil and surface water, electrical conductivity (EC), total dissolved solids (TDS), pH, temperature, curve number (CN), and flood heights. The curve number indicates the runoff response characteristic of the Mogpog-Boac River basin. The results show that 40% of the total floodplain area of Boac and Mogpog were subjected to high hazards with flood heights above 1.5 m. The Mn content of soils had a statistically significant moderate positive correlation with flood height (r = 0.458) and a moderate negative correlation with pH (r = −0.438). This condition suggested that more extensive flooding promotes Mn contamination of floodplain soils in the two rivers, the source of which includes the mobilization of Mn-bearing silt, sediments, and mine drainage from the abandoned mine pits and TSFs. There is also a strong negative correlation between pH and Mn concentrations in surface water, a relationship attributed to the solubilization of Mn-bearing precipitates based on geochemical modeling results. Using Muller’s geo-accumulation index, 77.5% of the total floodplain of the two rivers was identified as “moderately contaminated” with an average Mn soil content of 3.4% by weight (34,000 mg/kg). The Mn contamination map of floodplain soils in the Mogpog and Boac rivers described in this study could guide relevant regional, national, and local government agencies in planning appropriate intervention, mitigation, remediation, and rehabilitation strategies to limit human exposure to highly contaminated areas.
Publisher: MDPI AG
Date: 20-10-2020
DOI: 10.3390/MET10101393
Abstract: Copper (Cu) has been recovered from speiss generated from top submerged lance furnace process, but it was reported that the leaching efficiency of Cu in sulfuric acid solution decreased with increasing antimony (Sb) content in the speiss. Scanning electron microscopy (SEM)–energy-dispersive X-ray spectroscopy (EDS) results indicate that Sb exists as CuSb alloy, which would retard the leaching of Cu. Therefore, hydrochloric acid leaching with aeration was performed to investigate the leaching behaviors of copper and antimony. The leaching efficiency of Cu increased with increasing agitation speed, temperature, HCl concentration, and the introduction ratio of O2, but also with decreasing pulp density. The leaching efficiency of Cu increased to more than 99% within 60 min in 1 mol/L HCl solution at 600 rpm and 90 °C with 10 g/L pulp density and 1000 cc/min O2. The leaching efficiency of Sb increased and then decreased in all 1 mol/L HCl leaching tests, and precipitate was observed in the leach solution, which was determined to be SbOCl or Sb2O3 by XRD analyses. However, in 2 mol/L–5 mol/L HCl solutions, the leaching efficiency of Sb increased to more than 95% (about 900 mg/L) and remained, so more than 2 mol/L HCl could stabilize Sb ion in the HCl solution.
Publisher: Elsevier BV
Date: 10-2019
DOI: 10.1016/J.CHEMOSPHERE.2019.05.235
Abstract: Arsenic (As) contamination of the groundwater in the Mekong Delta is a serious problem affecting millions of people who rely on this important resource for drinking and agriculture. In this study, borehole cores up to a depth of 40 m were collected in the Vietnamese-side of the delta, and the solid-phase partitioning of As with depth was investigated to understand the factors and processes controlling the release of this toxic element under oxic, acidic and reducing conditions. The results showed that in most of the sediments, substantial amounts of As are partitioned with exchangeable phases that are easily released into solution. Two borehole cores obtained between the Hau and Tien Rivers also had significantly high As partitioned with organic/sulfide phases and one of these cores had abundant As-bearing pyrite in 1-m thick peat layers. Leaching experiments in deionized (DI) water coupled with principal component analysis suggest that As release was controlled by sorption-desorption reactions with clays hyllosilicates (i.e., kaolinite, muscovite and clinochlore), proton-promoted dissolution of iron-oxyhydroxides, and oxidation of pyrite/organic matter. The mobility of As was further promoted under acidic conditions in the presence of chloride (Cl
Publisher: Elsevier BV
Date: 08-2020
Publisher: Elsevier BV
Date: 11-2020
Publisher: Elsevier BV
Date: 12-2018
DOI: 10.1016/J.SCITOTENV.2018.07.103
Abstract: Massive and ambitious underground space development projects are being undertaken by many countries around the world to decongest megacities, improve the urban landscapes, upgrade outdated transportation networks, and expand modern railway and road systems. A number of these projects, however, reported that substantial portions of the excavated debris are oftentimes naturally contaminated with hazardous elements, which are readily released in substantial amounts once exposed to the environment. These contaminated excavation debris/spoils/mucks, loosely referred to as "naturally contaminated rocks", contain various hazardous and toxic inorganic elements like arsenic (As), selenium (Se), boron (B), and heavy metals like lead (Pb), cadmium (Cd), copper (Cu), and zinc (Zn). If left untreated, these naturally contaminated rocks could pose very serious problems not only to the surrounding ecosystem but also to people living around the construction and disposal sites. Several incidents of soil and ground/surface water contamination, for ex le, have been documented due to the false assumption that excavated materials are non-hazardous because they only contain background levels of environmentally regulated elements. Naturally contaminated rocks are hazardous wastes, but they still remain largely unregulated. In fact, standard leaching tests for their evaluation and classification are not yet established. In this review, we summarized all available studies in the literature about the factors and processes crucial in the enrichment, release, and migration of the most commonly encountered hazardous and toxic elements in naturally contaminated geological materials. Although our focus is on naturally contaminated rocks, analogue systems like contaminated soils, sediments, and other hazardous wastes that have been more widely studied will also be discussed. Classification schemes and leaching tests to properly identify and regulate excavated rocks that may potentially pose environmental problems will be examined. Finally, management and mitigation strategies to limit the negative effects of these hazardous wastes are introduced.
Publisher: Elsevier BV
Date: 04-2015
DOI: 10.1016/J.JCONHYD.2015.01.003
Abstract: Sedimentary rocks of marine origin excavated from tunnel construction projects usually contain background levels of hazardous trace elements, but when exposed to the environment, they generate leachates with concentrations of arsenic (As), selenium (Se) and boron (B) exceeding the WHO guideline for drinking water. In this study, the leaching of As, Se and B was evaluated under in situ conditions at various flow patterns, particle size distributions and column thicknesses. The results showed that these trace elements were leached out of the rock via short and long term mechanisms. In the short term, all three elements were rapidly and simultaneously released due to the dissolution of soluble evaporite salts formed from entrapped sea water of the Cretaceous. After their rapid release, however, these trace elements behaved differently as a result of their contrasting adsorption affinities onto minerals like clays and Fe-oxyhydroxides, which were further influenced by the pH, presence of coexisting ions and speciation of the trace elements. Selenium was quickly and easily transported out of the columns because it was mostly present as the very mobile selenate ion (Se[VI]). In comparison, the migration of As and B was hindered by adsorption reactions onto mineral phases of the rock. Boron was initially the least mobile among the three because of its preferential adsorption onto clay minerals that was further enhanced by the slightly alkaline pH and high concentrations of Ca(2+) and Na(+). However, it was gradually re-mobilized in the latter part of the experiments because it was only weakly adsorbed via outer sphere complexation reactions. In the long term, the rock continued to release substantial amounts of As, Se and B via pyrite oxidation and adsorption/desorption reactions, which were regulated by the temperature and rainfall intensity/frequency on site.
Publisher: Elsevier BV
Date: 2020
Publisher: Springer Science and Business Media LLC
Date: 07-01-2020
Publisher: MDPI AG
Date: 08-07-2020
DOI: 10.3390/MET10070912
Abstract: Flotation is the conventional method for processing porphyry copper deposits, one of the most economically important sources of copper (Cu) worldwide. The rapidly decreasing grade of this type of Cu ore in recent years, however, presents serious problems with fine particle recovery using conventional flotation circuits. This low recovery could be attributed to the low collision efficiency of fine particles and air bubbles during flotation. To improve collision efficiency and flotation recovery, agglomeration of finely ground chalcopyrite (CuFeS2) (D50 = 3.5 μm) using emulsified oil stabilized by emulsifiers was elucidated in this study. Specifically, the effects of various types of anionic (sodium dodecyl sulfate (SDS), potassium amyl xanthate (KAX)), cationic (dodecyl amine acetate (DAA)), and non-ionic (polysorbate 20 (Tween 20)) emulsifiers on emulsified oil stability and agglomeration–flotation efficiency were investigated. When emulsifiers were added, the average size of agglomerates increased, resulting in higher Cu recovery during flotation. This dramatic improvement in flotation efficiency could be attributed to the smaller oil droplet size in emulsified oil and their higher stability in the presence of emulsifiers. The utilization of emulsifiers during agglomeration–flotation not only lowered the required agitation strength for agglomeration but also shortened the agglomeration time, both of which made the process easier to incorporate in existing flotation circuits.
Publisher: Elsevier BV
Date: 10-2022
Publisher: International Research Centre for the Management of Degraded and Mining Lands
Date: 31-12-2021
DOI: 10.15243/JDMLM.2021.082.2551
Abstract: An island province in the Philippines exposed to acid mine drainage for about 22-25 years, uncovered new discovery in selected agricultural yields. The acid mine drainage was from two open mine pits of higher elevation flowing to Boac and Mogpog River system. A total of 78 various agricultural yields s les with 234 specimens were collected and analyzed from six municipalities of Marinduque, Philippines in 2019. These agricultural yields were (A) vegetables, (B) root crops, (C) fruits, and (D) rice. Inductively Coupled Plasma – Optical Emission Spectrometry (ICP-OES) Perkin Elmer Optima 8000 with ICP multi-element standard solution IV were used to detect metals concentration in the agricultural s les. Digestion of s les followed the EPA Method 200.3. Results were compared with the WHO/FAO limit followed by the identification of yields and areas that pose risks to public health. Determination of the spatial distribution was by ArcGIS. The six municipalities i.e., Boac, Buenavista, Gasan, Mogpog, Torrijos and Sta. Cruz, were labelled as B, BV, G, M, T and S, respectively. Record showed that S le A from G contain higher metal concentration among other yields. Manganese concentration in S les A, B, and D were found to be higher than WHO/FAO limit. However, copper and zinc concentration in S le C in all municipalities exceeded the allowable limit. Elevated total chromium concentration was found in S le D collected from G, T, and S. These results would help relevant government agencies and units design strategies to mitigate the degraded agricultural lands and protect public health.
Publisher: Elsevier BV
Date: 03-2017
DOI: 10.1016/J.SCITOTENV.2016.12.050
Abstract: The oxidative dissolution of pyrite is an important process in the redox recycling of iron (Fe) and is well-known for its role in the formation of acid mine drainage (AMD), which is considered as the most serious and widespread problem after the closure of mines and mineral processing operations. Because this process requires the movement of electrons, common metal oxides in nature that have either semiconducting (e.g., hematite) or insulating (e.g., alumina) properties may have strong effects on it. In this study, changes in the electrochemical behavior of pyrite in the presence of hematite and alumina were investigated. Results showed that the formation of surface-bound species directly influenced the anodic and cathodic half-cell reactions as well as the transfer of electrons between these sites. Pyrite pretreated in the air became anodically more reactive than that pretreated in oxygenated water, but the type of oxidizing media had little effect on the cathodic half-cell reaction. The presence of hematite and alumina during pretreatment also had strong effects on the electrochemical properties of pyrite. Chrono erometry measurements suggest that hematite and alumina enhanced the anodic half-cell reaction but suppressed the cathodic half-cell reaction of pyrite oxidation. Increased anodic half-cell reaction in the presence of hematite could be attributed to electron "bridging" and catalytic effects of this mineral. In contrast, the effects of alumina on the anodic half-cell reaction were indirect and could be explained by the formation of Fe
Publisher: Elsevier BV
Date: 2020
Publisher: Elsevier BV
Date: 10-2020
Publisher: Springer Science and Business Media LLC
Date: 03-07-2019
Publisher: Universitas Gadjah Mada
Date: 02-09-2015
DOI: 10.22146/JAG.7197
Abstract: Arsenic (As) is a toxic element found in both natural and anthropogenic sources. High concentration of this element was recently uncovered in the groundwater of Sumbawa Island, Indonesia. To mitigate this problem, As adsorption potential of natural geological materials like lignite, bentonite, shale, and iron sand obtained in Indonesia were evaluated by batch experiments. Arsenic adsorption onto these materials was investigated as a function of solution pH, particle sizes of adsorbents and coexisting sulfate concentration. In addition, batch leaching experiments were performed to elucidate the stability of geogenic As present in all adsorbents at different pHs. The results showed that among these natural materials tested, lignite was the most effective adsorbent of As(V) followed by bentonite, shale and then iron sand, and that the amounts of As(III) adsorbed onto all adsorbents were lower than those of As(V).This indicates that As(III) is more mobile in comparison to As(V). The adsorption isotherms of As(III) and As(V) conformed to nonlinear types, either Langmuir or Freundlich. It was found that adsorption of As onto these natural adsorbents was pH-dependent. This could be attributed to the changes in the surface charges of the adsorbents with pH. With respect to the adsorbent particle size, the amount adsorbed somewhat increased with decreasing particle size, which could be explained by the larger surface area of the smaller particles. Acidic (pH 6) and alkaline (pH ) conditions destabilized the geogenic As content of the adsorbents, indicating that the effectiveness of these natural materials as adsorbents is greatly limited by the pH of the contaminated system. Keywords: Adsorption, arsenic, natural geological materials, particle size, pH
Publisher: Japan Institute of Metals
Date: 02-2019
Publisher: Elsevier BV
Date: 02-2017
DOI: 10.1016/J.SCITOTENV.2016.12.015
Abstract: Pyrite is one of the most common and geochemically important sulfide minerals in nature because of its role in the redox recycling of iron (Fe). It is also the primary cause of acid mine drainage (AMD) that is considered as a serious and widespread problem facing the mining and mineral processing industries. In the environment, pyrite oxidation occurs in the presence of ubiquitous metal oxides, but the roles that they play in this process remain largely unknown. This study evaluates the effects of hematite (α-Fe
Publisher: MDPI AG
Date: 27-08-2021
DOI: 10.3390/MET11091352
Abstract: The use of galvanic interactions between zero-valent aluminum (ZVAl) and activated carbon (AC) to recover gold (Au) ions is a promising technique to overcome the challenges due to the poor recovery in ammonium thiosulfate systems, but the applicability to practical Au ore processing remains elusive so far. The present study describes (1) the recovery of Au ions from low Au concentrations, which are typical concentrations used in Au ore processing and (2) an investigation into the effects of various coexisting base metal ions that can be present in pregnant ore-leached solutions. The results showed that high Au recovery (i.e., over 85%) was obtained even at low Au concentrations under the following conditions: 1:1 of 0.15 g of ZVAl and AC with 10 mL of ammonium thiosulfate solution containing 5 mg/L of Au ions at 25 °C for 1 h in an anoxic atmosphere. Selected coexisting metal ions (i.e., copper, iron, cobalt, nickel, and zinc) were studied to establish their effects on Au recovery, and the results showed that the Au recovery was enhanced (about 90%) when copper ions coexist in the solution with minimal effects from other competing base metal ions.
Publisher: Elsevier BV
Date: 08-2019
DOI: 10.1016/J.JCONHYD.2019.103502
Abstract: This paper describes the geochemistry of groundwater and its flow system in the closed Yatani mine in southern Yamagata Prefecture, Japan. The mine is located in a sulfide deposit containing pyrite and has been generating acid mine drainage (AMD). The study was intended to elucidate the formation of AMD and its flow patterns using geological, hydrological, geochemical, and isotopic techniques. The results indicate that AMD is formed by the interaction of groundwater with sulfide minerals, sand slime, and tailings back-filled into excavated mine areas. Groundwater recharge areas were identified on the mountain slope at an elevation of ~900 m. The formation of AMD in the drifts and shaft was more extensive than that in the deeper drainage levels. Principal component analysis was applied to the hydrogeochemical data to identify the causes of AMD formation. The first, second, and third principal components reveal that the increased ion concentrations in mine drainage are a result of water-mineral reactions in excavated mine areas, the contribution of groundwater in deep reductive environments, and isotopic fractionation during precipitation, respectively. A promising method of reducing AMD formation is to prevent contact between dissolved oxygen and sulfide minerals by increasing the drainage level or by filling the shallow underground excavated area with cementitious materials.
Publisher: SAGE Publications
Date: 2023
DOI: 10.1177/16094069231176340
Abstract: The rehabilitation of legacy mines continues to be a big challenge because of the difficulties in returning them to safe and stable conditions and ensuring that the mined-out areas become productive to support the economic activity of the host community. Previous efforts are often focused on purely technical and environmental aspects, leading to resistance from the local community due to their exclusion from the rehabilitation process. To address the issues associated with legacy mines and lack of participation of the community, we have developed a project, Bio ersity Positive Mining For The Net Zero Challenge (Bio + Mine), focusing on the abandoned Sto. Niño copper mine (Benguet, Philippines). The mine was closed in 1982 without a plan involving local stakeholders and leaving a significant ongoing negative legacy. Using the social-ecological-technological system framework, we will explore the intersections of the structure and functions of socio-economicdemographic, ecological, and technological data useful in devising a more inclusive mitigation strategy for the reconstruction of the supporting ecosystem. We aim to develop a site-specific system, underpinned by the local community's knowledge and practices, that can be a model for wider implementation in other legacy and active mines worldwide.
Publisher: Elsevier BV
Date: 09-2009
DOI: 10.1016/J.JHAZMAT.2009.04.049
Abstract: This paper describes the effects of pH, dissolved oxygen (DO), redox conditions, and mixing ratio of different rocks on the leaching behaviors of As and Pb from hydrothermally altered rock as well as the functional groups incorporating As and Pb in the rock. Most of As and Pb were incorporated in the residual or crystalline phase although significant amounts were also determined to be exchangeable, with carbonates and with Fe-Mn oxides. Under oxic conditions, As and Pb showed similar leaching behaviors at similar pH values, a higher mobilization in the acidic and alkaline regions and a minimum at circumneutral pH. The absence of DO restricted the oxidation of sulfide minerals that also contained significant quantities of As resulting in a lower As release under these conditions. Strongly reducing conditions favored the release of As by the reductive dissolution of Fe-Mn oxides and prevention of carbonate precipitation while the same conditions immobilized Pb because of its re-precipitation under reducing conditions. In general, depending on the pH, DO, and redox conditions, the major modes of As and Pb release from these sources could be either one or more of the following mechanisms: acid dissolution, reductive dissolution, ion exchange, desorption and sulfide oxidation processes.
Publisher: Elsevier BV
Date: 07-2019
Publisher: Elsevier BV
Date: 05-2020
Publisher: Elsevier BV
Date: 02-2014
DOI: 10.1016/J.SCITOTENV.2013.11.006
Abstract: Sedimentary rocks of marine origin excavated in tunnel projects were recently identified as potentially hazardous because they could release significant amounts of toxic trace elements when exposed to the environment. This study investigated the leaching characteristics of B, As, Se and the major coexisting ions under various conditions to identify the factors and processes controlling their evolution in the leachate. In addition, we evaluated whether the parameters of the currently used leachability test for excavated rocks were adequate. Although the leachabilities of B, As and Se similarly increased at longer contact times, only those of B and As were influenced by the mixing speed and/or liquid-to-solid ratio (L/S). The majority of trace elements dissolved in the leachate originated from the dissolution of soluble salts formed from seawater of the Cretaceous trapped during the formation of the sedimentary rocks. Moreover, the alkaline pH of the leachates could be attributed to the simultaneous dissolutions at varying degrees of the mineral components of the rocks as well as the precipitation of clay minerals. In the leaching test of excavated rocks for regulatory purposes, the best values of contact time and mixing speed should represent conditions of the highest trace element extractabilities, which in this study were found at longer contact times (>48 h) and the fastest mixing speed (200 rpm). The most appropriate L/S for the leaching test is 10 because it was around this L/S that the extractabilities and leaching concentrations of the trace elements were simultaneously observed at their highest values.
Publisher: Elsevier BV
Date: 06-2020
Publisher: Elsevier BV
Date: 11-2019
Publisher: Elsevier BV
Date: 11-2023
Publisher: MDPI AG
Date: 20-08-2021
DOI: 10.3390/MIN11080902
Abstract: Climate change is one of the most pressing problems facing humanity this century [...]
Publisher: Elsevier BV
Date: 07-2018
DOI: 10.1016/J.WASMAN.2018.04.039
Abstract: This paper describes the recovery of gold (Au) from shredder light fraction (SLF) of a recycling plant by flotation and leaching. SLF is typically sent to landfills as waste, but it still contains substantial amounts of Au, and other metals like Cu and Fe. The SLF s le used in this study contains 0.003% of Au, 12% of Cu, and 10% of Fe. Flotation results showed that over 99% of Au and 50% of combustibles were recovered in froth while most of the base metals were recovered in tailing. SEM-EDX of froth products indicates that Au floated via two mechanisms: (1) flotation of Au-plated plastic particles, and (2) agglomeration of fine Au particles together with plastic particles due to kerosene-induced hydrophobic-hydrophobic interactions followed by the flotation of these agglomerated particles. Combustibles in froth/tailing were analyzed by ATR-FTIR, and the results showed that plastics in the froth were mostly sulfonated polystyrene (PS) and acrylonitrile butadiene styrene (ABS) while those in tailing were polyurethane (PU) and polyethylene terephthalate (PET). Contact angle measurements of plastic particles suggest that PS and ABS are more hydrophobic than PU and PET. Most of the base metals in the tailing had either bent or twisted shapes because they were mostly made up of wires. In flotation, these large and heavy particles are unaffected by bubbles and simply sink. Leaching results using ammonium thiosulfate solutions showed that Au extraction increased from 33 to 51% after flotation.
Publisher: Elsevier BV
Date: 08-2021
Publisher: Elsevier BV
Date: 12-2017
DOI: 10.1016/J.CHEMOSPHERE.2017.08.088
Abstract: Predicting the fates of arsenic (As) and selenium (Se) in natural geologic media like rocks and soils necessitates the understanding of how their various oxyanionic species behave and migrate under dynamic conditions. In this study, geochemical factors and processes crucial in the leaching and transport of arsenite (As
Publisher: Elsevier BV
Date: 08-2020
Publisher: Springer Science and Business Media LLC
Date: 06-11-2018
Publisher: MDPI AG
Date: 20-04-2020
DOI: 10.3390/MET10040531
Abstract: Zinc plant leach residues (ZPLRs) contain significant amounts of metal compounds of lead (Pb), zinc (Zn), iron (Fe), etc., hence, they are considered as a secondary source of metals. On the other hand, ZPLRs are regarded as hazardous materials because they contain heavy metals that pollute the environment. Resources and environmental concerns of ZPLRs were addressed in this study by removing/recovering Pb and Zn using a concurrent dissolution and cementation technique. To cement the dissolved Pb and Zn in leaching pulp, zero-valent aluminum (ZVAl) was added during ZPLRs leaching in the hydrochloric (HCl)–sodium chloride (NaCl) solution. The resulting cemented metals were agglomerated and separated by sieving. Lead removal increased with increasing both NaCl and HCl concentrations. However, when ZVAl was added, significant Pb removal was achieved at a low concentration. Zinc was not cemented out of the pulp using ZVAl and its recovery from ZPLRs was dependent on the HCl concentration only. By applying a concurrent dissolution and cementation technique, both Pb and Zn were removed using a low concentration of NaCl, and most importantly Pb—the most toxic metal in ZPLRs—was captured and separated before the solid-liquid separation, hence, eliminating the need for extensive washing of the generated residues to remove the inherent residual solution.
Publisher: MDPI AG
Date: 30-06-2020
DOI: 10.3390/MET10070868
Abstract: Dry gravity separation using a vibrating zirconia ball bed is proposed in this study to separate aluminum (Al) and stainless steel (STS) scraps obtained from spent hard disk drive recycling. The effects of zirconia ball sizes and vibrating power (vibration litude) on the separation efficiency of Al and STS scraps were investigated. The zirconia balls moved down at the center of the vessel and rose with the wall during the vibration test. Although more STS scraps sunk than Al scraps did, the separation efficiency was not maintained because Al scraps also sunk along with balls’ movement. The separation efficiency increased to 86.6% using 1-mm zirconia balls with a 2.5-mm vibration litude at 4 min, but it decreased rapidly by ball moving. Therefore, when a ball bed of mixed sizes (2:1 ratio of 1 and 3 mm) was used and arranged, whereby the 3-mm zirconia balls were above the 1-mm ball bed, the separation efficiency increased to 100% for more than 2 min. This dramatic improvement was because the 3-mm ball bed acted as a barrier to prevent sunken STS scraps from rising, and Al scrap cannot sink through the 3-mm ball bed. These results indicate that the separation of Al and STS scraps could be achieved successfully using the dry gravity separation method.
Publisher: Elsevier BV
Date: 12-2022
Publisher: Japan Institute of Metals
Date: 10-2020
Publisher: Elsevier BV
Date: 2014
Publisher: Elsevier BV
Date: 10-2021
Publisher: Elsevier BV
Date: 05-2021
Publisher: Elsevier BV
Date: 07-2021
Publisher: Elsevier BV
Date: 08-2019
Publisher: Elsevier BV
Date: 08-2018
DOI: 10.1016/J.CHEMOSPHERE.2018.04.088
Abstract: Pyrite (FeS
Publisher: Elsevier BV
Date: 2020
Publisher: Elsevier BV
Date: 2020
Publisher: Springer Science and Business Media LLC
Date: 08-08-2020
Publisher: Springer Science and Business Media LLC
Date: 06-05-2012
Publisher: Elsevier BV
Date: 02-2018
DOI: 10.1016/J.JHAZMAT.2017.10.025
Abstract: Arsenopyrite is the most common arsenic-bearing sulfide mineral in nature, and its weathering contributes to acid mine drainage (AMD) formation and the release of toxic arsenic (As). To mitigate this problem, carrier-microencapsulation (CME) using titanium (Ti)-catechol complex (i.e., Ti-based CME) was investigated to passivate arsenopyrite by forming a protective coating. Ti
Publisher: Elsevier BV
Date: 11-2018
Publisher: MDPI AG
Date: 03-05-2022
DOI: 10.3390/MIN12050579
Abstract: Siltation is the biggest environmental challenge associated with nickel laterite mining in the Philippines. The amount of silt generated is huge and one mitigation strategy currently employed by the mining companies is the construction of siltation ponds where the bulk of the clayey- and silt-sized surface runoffs is collected. However, this poses several serious environmental hazards such as landslides due to heavy rainfall and the potential release of hazardous heavy metals. A promising approach to reduce the risks associated with long-term storage of nickel mine waste (NMW) is to employ circular economy by repurposing it for ceramic applications. While generating useful materials with economic value out of a mine waste, it will result in a reduction in volume of waste for disposal. In this study, the method employed to produce NMW-based ceramic wall and floor tiles is slip casting as it is the most appropriate method in forming tiles with complex surface features. Five formulations of NMW-based slips were made for the casting of ceramic tiles and each slip was characterized for its suitability as raw material. The results of NMW characterization show that NMW could be utilized as raw materials for both ceramic wall and floor tiles and the addition of feldspar can enhance casting and physical properties.
Publisher: SAGE Publications
Date: 30-01-2018
Publisher: Elsevier BV
Date: 11-2018
DOI: 10.1016/J.WASMAN.2018.09.041
Abstract: Ammonium thiosulfate solution is an ideal lixiviant to extract gold (Au) from electronic wastes (E-wastes) because it is non-toxic, less corrosive, and more selective than conventional cyanide or halide solutions. It was reported recently, however, that Au leaching efficiency in ammonium thiosulfate medium dramatically decreased at high solid-to-liquid ratios (S/L), even though the amounts of reagents used were in excess. To understand how this occurred, leaching experiments were conducted using printed circuit boards (PCBs) from waste mobile phones, and Au distribution in the leaching residues was examined by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX). Significant amounts of Au were found together with copper (Cu) and aluminum (Al), implying that extracted Au ions were likely re-deposited during leaching onto Cu and Al found in PCBs via cementation (i.e., reductive deposition). A more detailed elucidation of this phenomenon by cementation experiments using pure Cu and/or Al powders indicates that these metals could only recover Au ions alone via cementation at very high amounts, however, this process became more extensive when Cu and Al powders were suspended together in solution even though the amounts of the in idual metals were much lower. Electrochemical experiments (chrono erometry) in ammonium thiosulfate solutions containing Au ions using an Al working electrode also showed that Au ion cementation was dramatically enhanced when Cu powder was present in solution, and the bulk of Au was cemented on Cu powder rather than on the Al electrode. These results suggest that coexistence of Cu and Al interfered with the extraction of Au in ammonium thiosulfate medium at high S/L because of the enhanced re-deposition of extracted Au via galvanic interaction.
Publisher: Elsevier BV
Date: 12-2020
Publisher: Elsevier BV
Date: 06-2012
Start Date: 04-2024
End Date: 04-2029
Amount: $4,999,700.00
Funder: Australian Research Council
View Funded Activity