Macroscale Modeling of Geochemistry Influence on Polymer and Low-Salinity Waterflooding in Carbonate Oil Reservoirs.

The enhancement of oil recovery (EOR) through low-salinity waterflooding (LSWF) and the emerging hybrid with a polymer (LSP) has proven to be effective at microscale investigations and cost-effective with ease of operation at field-scale tests. Their application in carbonate oil reservoirs, which typically occur oil-wet, presents a particularly essential capacity given that over half of the global oil reserves are hosted in carbonate formation. However, modeling the mechanisms involved to predict and evaluate the performance of low salinity-based EOR at a large scale is complex and requires the integration of geochemistry in reservoir simulation to upscale the interfacial interactions of crude oil, brine, and rock observed at the micrometer scale. This study presents an integrated approach that combines MRST's polymer model with PHREEQC geochemical modeling to simulate LSWF at the reservoir scale. Using single-phase and multiphase experimental flooding data for validation, the coupled model was shown to accurately predict effluent ionic and oil recovery profiles. The simulation of LSWF and LSP both exhibited additional tertiary oil recovery, with LSWF and LSP showing 3 and 2%, respectively, which are consistent with previously reported field and core flooding results. Furthermore, the sequential application of formation water (FW), LSWF, and LSP flooding in secondary mode showed a high increase in oil recovery, with oil recovery percentages of 61, 20, and 19%, respectively. However, the FW results were 50% lower compared to regular core flooding due to upscaling limitations. The modeling of vertical and anisotropic permeability heterogeneity effects showed a positive synergy with low-salinity floodings, resulting in a 4% drop and 3 and 1% increase in FW, LSWF, and LSP, respectively. These findings demonstrate the potential of the coupled MRST-PHREEQC model in accurately simulating hydrogeochemical interactions during LSWF/LSP at the reservoir scale, providing valuable insights for the optimization of low salinity-based EOR strategies in carbonate reservoirs.

Functional modification of mussel adhesive protein to control solubility and adhesion property.

Marine mussels produce strong underwater adhesives called mussel adhesive proteins (MAPs) that can adhere to a variety of surfaces under physiological conditions. Thus, MAPs have been investigated as a potentially sustainable alternative to conventional petrochemical-based adhesives. Recombinant MAPs would be promising for large-scale production and commercialization; however, MAPs are intrinsically adhesive, aggregative, and insoluble in water. In this study, we have developed a solubilization method for the control of MAP adhesion by fusion protein technique. Foot protein 1 (Fp1), a kind of MAP, was fused with the highly water-soluble protein, which is the C-terminal domain of ice-nucleation protein K (InaKC), separated by a protease cleaving site. The fusion protein exhibited low adhesion but high solubility and stability. Notably, Fp1 recovered its adhesive property after removal from the InaKC moiety by protease cleaving, which was evaluated and confirmed by the agglomeration of magnetite particles in water. The ability to control adhesion and agglomeration makes MAPs favorable prospects for bio-based adhesives.

Conventional and recent advances in gravity separation technologies for coal cleaning: A systematic and critical review.

"Affordable and clean energy" is enshrined in the UN Sustainable Development Goals (SDGs; #7) because of its importance in supporting the sustainable development of society. As an energy source, coal is widely used because it is abundant and its utilization for electricity and heat generation do not require complex infrastructures and technologies, which makes it ideal for the energy needs of low-income and developing countries. Coal is also essential in steel making (as coke) and cement production and will continue to be on high demand for the foreseeable future. However, coal is naturally found with impurities or gangue minerals like pyrite and quartz that could create by-products (e.g., ash) and various pollutants (e.g., CO2, NOX, SOX). To reduce the environmental impacts of coal during combustion, coal cleaning-a kind of pre-combustion clean coal technology-is essential. Gravity separation, a technique that separates particles based on their differences in density, is widely used in coal cleaning due to the simplicity of its operation, low cost, and high efficiency. In this paper, recent studies (from 2011 to 2020) related to gravity separation for coal cleaning were systematically reviewed using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A total of 1864 articles were screened after removing duplicates, and after a thorough evaluation 189 articles were reviewed and summarized. Among of conventional separation techniques, dense medium separator (DMS), particularly dense medium cyclone (DMC), is the most popular technologies studied, which could be attributed to the growing challenges of cleaning/processing fine coal-bearing materials. In recent years, most of works focused on the development of dry-type gravity technologies for coal cleaning. Finally, gravity separation challenges and future applications to address problems in environmental pollution and mitigation, waste recycling and reprocessing, circular economy, and mineral processing are discussed.

Reverse hybrid jig separation efficiency estimation of floating plastics using apparent specific gravity and concentration criterion.

We developed a technique called the reverse hybrid jig, an advanced physical separation technique that combines the principles of jig and flotation to separate floating plastics. This technique is a promising green technology that is more economical and environmentally friendly compared with the conventional flotation. Although the applicability of this technique to separate PP/PE have been reported, the index to illustrate the possibility of separation for the reverse hybrid jig is still not available. In this study, a reverse apparent concentration criterion (CC RA ) is proposed to estimate reverse hybrid jig separation efficiency. This modified concentration criterion can be calculated using the specific gravity (SG) of particle with attached bubbles called the apparent specific gravity (SG A ). To determine the volume of attached bubbles on plastic surfaces under water pulsation, a laser-assisted apparatus was used under various conditions, including plastic type, air flow rate, dosage, and type of wetting agent. The results of attached bubble volume measurements were used to calculate the SG A and CC RA . The estimated values were then compared with the results of reverse hybrid jig separation. It was found that higher CC RA resulted in better separation efficiency. In addition, an empirical linear equation for estimating the reverse hybrid jig separation efficiency is proposed.

Enhanced pyrite passivation by carrier-microencapsulation using Fe-catechol and Ti-catechol complexes.

Acid mine drainage (AMD) formation is mainly caused by the oxidation of pyrite. Carrier-microencapsulation (CME) using metal-catecholate complexes has been proposed to passivate sulfide minerals by forming surface-protective coatings on their surfaces. Among the various metal-catecholate complexes, Ti-catecholate formed stable coatings having superior acid-resistance, but a thick enough passivating film required considerable time (ca. 14 days) to grow. Meanwhile, Fe-catecholates can form Fe-oxyhydroxide coatings within 2 days, however, they are less stable than Ti-based coating. To address these drawbacks of using a single metal-complex, this study investigated the concurrent use of Fe-catechol and Ti-catechol complexes for accelerating the formation of stable passivating coating on pyrite. Compared with a single metal-complex system, the coating formation was significantly accelerated in mixed system. Linear sweep voltammetry showed the simultaneous decomposition of [Fe(cat)]+ and [Ti(cat)3]2- as the main reason for improved coating formation. Electrochemical properties of coatings formed by single and mixed complex systems, confirmed by electrochemical impedance spectroscopy and cyclic voltammetry, indicated the coating formed in the mixed system had higher resistance and more electrochemically inert than the other cases. The simultaneous use of Fe-catechol and Ti-catechol complexes enhanced pyrite passivation by accelerating metal-complex decomposition and forming more stable coating composed of Fe2TiO5.

A novel arsenic immobilization strategy via a two-step process: Arsenic concentration from dilute solution using schwertmannite and immobilization in Ca-Fe-AsO4 compounds.

Acid mine drainage (AMD) with toxic arsenic (As) is commonly generated from the tailings storage facilities (TSFs) of sulfide mines due to the presence of As-bearing sulfide minerals (e.g., arsenopyrite, realgar, orpiment, etc.). To suppress As contamination to the nearby environments, As immobilization by Ca-Fe-AsO4 compounds is considered one of the most promising techniques; however, this technique is only applicable when As concentration is high enough (>1 g/L). To immobilize As from wastewater with low As concentration (~10 mg/L), this study investigated a two-step process consisting of concentration of dilute As solution by sorption/desorption using schwertmannite (Fe8O8(OH)8-2x(SO4)x; where (1 ≤ x ≤ 1.75)) and formation of Ca-Fe-AsO4 compounds. Arsenic sorption tests indicated that As(V) was well adsorbed onto schwertmannite at pH 3 (Qmax = 116.3 mg/g), but its sorption was limited at pH 13 (Qmax = 16.1 mg/g). A dilute As solution (~11.2 mg/L As) could be concentrated by sorption with large volume of dilute As solution at pH 3 followed by desorption with small volume of eluent of which pH was 13. The formation of Ca-Fe-AsO4 compounds from As concentrate solution (2 g/L As(V)) was strongly affected by temperature and pH. At low temperature (25-50 °C), amorphous ferric arsenate was formed, while at high temperature (95 °C), yukonite (Ca2Fe3-5(AsO4)3(OH)4-10·xH2O; where x = 2-11) and johnbaumite (Ca5(AsO4)3OH) were formed at pH 8 and 12, respectively. Among the synthesized products, johnbaumite showed strongest As retention ability even under acidic (pH < 2) and alkaline (pH > 9) conditions.

Suppression of arsenopyrite oxidation by microencapsulation using ferric-catecholate complexes and phosphate.

Mineral processing, pyro- and hydrometallurgical processes of auriferous sulfide ores and porphyry copper deposits (PCDs) generate arsenopyrite-rich wastes. These wastes are disposed of into the tailings storage facilities (TSF) in which toxic arsenic (As) is leached out and acid mine drainage (AMD) is generated due to the oxidation of arsenopyrite (FeAsS). To suppress arsenopyrite oxidation, this study investigated the passivation of arsenopyrite by forming ferric phosphate (FePO4) coating on its surface using ferric-catecholate complexes and phosphate simultaneously. Ferric iron (Fe3+) and catechol form three types of complexes (mono-, bis-, and triscatecholate complexes) depending on the pH, but mono-catecholate complex (i.e.,[Fe(cat)]+) became unstable in the presence of phosphate because the chemical affinity of Fe3+-PO43- is most probably stronger than that of Fe3+-catechol in [Fe(cat)]+. When two or more catechol molecules were coordinated with Fe3+ (i.e., [Fe(cat)2]- and [Fe(cat)3]3-), however, these complexes were stable irrespective of the presence of phosphate. The treatment of arsenopyrite with [Fe(cat)2]- and phosphate could suppress its oxidation due to the formation of FePO4 coating, evidenced by SEM-EDX and XPS analyses. The mechanism of FePO4 coating formation by [Fe(cat)2]- and phosphate was confirmed by linear sweep voltammetry (LSV): (1) [Fe(cat)2]- was oxidatively decomposed and (2) the resultant product (i.e., [Fe(cat)]+) reacts with phosphate, resulting in the formation of FePO4.

Solid-phase partitioning and release-retention mechanisms of copper, lead, zinc and arsenic in soils impacted by artisanal and small-scale gold mining (ASGM) activities.

Artisanal and small-scale gold mining (ASGM) operations are major contributors to the Philippines' annual gold (Au) output (at least 60%). Unfortunately, these ASGM activities lacked adequate tailings management strategies, so contamination of the environment is prevalent. In this study, soil contamination with copper (Cu), lead (Pb), zinc (Zn) and arsenic (As) due to ASGM activities in Nabunturan, Davao de Oro, Philippines was investigated. The results showed that ASGM-impacted soils had Cu, Pb, Zn and As up to 3.6, 83, 73 and 68 times higher than background levels, respectively and were classified as 'extremely' polluted (CD = 30-228; PLI = 5.5-34.8). Minerals typically found in porphyry copper-gold ores like pyrite, chalcopyrite, malachite, galena, sphalerite and goethite were identified by XRD and SEM-EDS analyses. Furthermore, sequential extraction results indicate substantial Cu (up to 90%), Pb (up to 50%), Zn (up to 65%) and As (up to 48%) partitioned with strongly adsorbed, weak acid soluble, reducible and oxidisable fractions, which are considered as 'geochemically mobile' phases in the environment. Although very high Pb and Zn were found in ASGM-impacted soils, they were relatively immobile under oxidising conditions around pH 8.5 because of their retention via adsorption to hydrous ferric oxides (HFOs), montmorillonite and kaolinite. In contrast, Cu and As release from the historic ASGM site samples exceeded the environmental limits for Class A and Class C effluents, which could be attributed to the removal of calcite and dolomite by weathering. The enhanced desorption of As at around pH 8.5 also likely contributed to its release from these soils.

Acid mine drainage formation and arsenic mobility under strongly acidic conditions: Importance of soluble phases, iron oxyhydroxides/oxides and nature of oxidation layer on pyrite.

Acid mine drainage (AMD) formation and toxic arsenic (As) pollution are serious environmental problems encountered worldwide. In this study, we investigated the crucial roles played by common secondary mineral phases formed during the natural weathering of pyrite-bearing wastes-soluble salts (melanterite, FeSO4·7H2O) and metal oxides (hematite, Fe2O3)-on AMD formation and As mobility under acidic conditions (pH 1.5-4) prevalent in historic tailings storage facilities, pyrite-bearing rock dumps and AMD-contaminated soils and sediments. Our results using a pyrite-rich natural geological material containing arsenopyrite (FeAsS) showed that melanterite and hematite both directly-by supplying H+ and/or oxidants (Fe3+)-and indirectly-via changes in the nature of oxidation layer formed on pyrite-influenced pyrite oxidation dynamics. Based on SEM-EDS, DRIFT spectroscopy and XPS results, the oxidation layer on pyrite was mainly composed of ferric arsenate and K-Jarosite when melanterite was abundant with/without hematite but changed to Fe-oxyhydroxide/oxide and scorodite when melanterite was low and hematite was present. This study also observed the formation of a mechanically 'strong' coating on pyrite that suppressed the mineral's oxidation. Finally, As mobility under acidic conditions was limited by its precipitation as ferric arsenate, scorodite, or a Fe/Al arsenate phase, including its strong adsorption to Fe-oxyhydroxides/oxides.

Carrier-microencapsulation of arsenopyrite using Al-catecholate complex: nature of oxidation products, effects on anodic and cathodic reactions, and coating stability under simulated weathering conditions.

Mining activities often generate large amounts of sulfide-rich wastes containing arsenopyrite (FeAsS), which when dissolved releases toxic arsenic (As) and generates acid mine drainage (AMD) that are both disastrous to the environment. To suppress arsenopyrite dissolution, a technique that selectively coats sulfide minerals with a protective layer of Al-oxyhydroxide called Al-based carrier-microencapsulation (CME) was developed. Although a previous study of the authors showed that Al-based CME could significantly limit arsenopyrite dissolution, nature of the coating formed on arsenopyrite, including its electrochemical properties, is still not well understood. Moreover, stability of the coating once exposed to weathering conditions remains unclear. Better understanding of these important issues would greatly improve Al-based CME especially in its application to real mine wastes. In this study, nature of the coating formed by Al-based CME was investigated using SEM-EDX, DRIFTS and XPS while the electrochemical properties of the coating were evaluated by cyclic voltammetry and chronoamperometry. Meanwhile, stability of the coating was elucidated using consecutive batch leaching experiments and weathering cell tests. SEM-EDX, DRIFTS and XPS results indicate that the protective coating formed on arsenopyrite by Al-based CME was mainly composed of bayerite (α-Al(OH)3), gibbsite (γ-Al(OH)3), and boehmite (γ-AlO(OH)). These Al-based coatings, which have insulating properties, made arsenopyrite less electrochemically active. The coatings also limited the extent of both the anodic and cathodic half-cell reactions of arsenopyrite oxidation that suppressed As release and acid generation. Weathering cell tests indicated that the oxidation of CME-treated arsenopyrite was effectively limited until about 15 days but after this, it started to gradually progress with time due to the increasing acidity of the system where Al-based coatings became unstable. Nonetheless, CME-treated arsenopyrite was less oxidized based on the released amounts of Fe, As and S suppressed by 80, 60 and 70%, respectively, compared with the one treated with control.

Improved pyrolysis behavior of ammonium polyphosphate-melamine-expandable (APP-MEL-EG) intumescent fire retardant coating system using ceria and dolomite as additives for I-beam steel application.

This study describes the effects of ceria (CeO2) and dolomite [CaMg(CO3)2] additives on the pyrolysis behavior and fire resistive property of conventional intumescent flame retardant (IFR) coating system for I-beam steel substrate called ammonium polyphosphate-melamine-expandable graphite (APP-MEL-EG) system. The fire resistance of various formulations was evaluated using the standard vertical Bunsen burner fire test. Thermogravimetric analysis (TGA) was used to understand the degradation of coating formulations. Observations by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) demonstrated that significant amounts of additives favored the formation of homogeneous compacted char structures, which were predominantly composed of carbon (C), phosphorus (P) and oxygen (O). These three main components of the char were also found to be in various binding combinations with other lighter elements like nitrogen (N) and hydrogen (H) as illustrated by the attenuated total reflectance Fourier transform infrared (ATR-FTIR) spectroscopy results. X-ray photoelectron spectroscopy (XPS) further suggest that polyethylene([(CH2-C2H2-CH2)n-]) free radicals were abundant on the char surface for the two best formulations and the binding energy of this radical promoted the formation of aromatic carbon chains that enhanced the char's thermal stability. This means that the selection of appropriate additives and combinations of flame-retardant ingredients could significantly change the morphology of the char layer and improve its thermal stability during fire exposure.

Hematite-catalysed scorodite formation as a novel arsenic immobilisation strategy under ambient conditions.

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-1 (As-O bending vibration), 785 and 725 cm-1 (As-O stretching vibrations), and 2990 cm-1 (OH-vibration) as well as the distinct XPS binding energies of Fe(III)-As (709.7 eV), As(V)-O (44.8, 44.31 and 43.7 eV), O2- (530.5 eV) and coordinated water (531.3 eV) in scorodite. This phenomenon could be attributed to three possible mechanisms: (1) more rapid precipitation promoted by the "seeding" effect of hematite particles, (2) additional supply of Fe3+ from hematite dissolution under acidic conditions, and (3) enhanced oxidations of Fe2+ to Fe3+ and As(III) to As(V) on the surface of hematite.

Suppressive effects of ferric-catecholate complexes on pyrite oxidation.

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 Ti4+, Si4+, and Al3+ was reported as a promising new approach to prevent pyrite oxidation by forming a passivating barrier on the pyrite surface. In CME, the presence of Fe3+-catecholate complexes is unavoidable but their effects on pyrite oxidation remain unclear. In this study, the effects of Fe3+-catecholate complexes on pyrite oxidation were investigated. Formations of mono-, bis-, and tris-catecholate complexes of Fe3+ were verified by UV-Vis spectrophotometry and their speciation with pH was consistent with thermodynamic considerations. Linear sweep voltammetry was conducted to evaluate the redox properties of Fe3+-catecholate complexes, and the results indicate that ligands in the three complexes were sequentially oxidized until Fe3+ is released. Coating formation on pyrite was confirmed after treatment with mono- and bis-catecholate complexes. Results of SEM-EDX and ATR-FTIR indicate that the coating is composed primarily of iron oxyhydroxide phases. The results of leaching experiments showed that pyrite oxidation was suppressed by Fe3+-catecholate complexes via two mechanisms: (1) electron donating effects of the complexes, and (2) formation of a protective coating on pyrite. The results provide not only a better understanding of the effects of Fe3+-catecholate complexes on pyrite oxidation but also some possible applications of Fe3+-based CME such as the suppression of pyrite oxidation to prevent AMD formation and depression of pyrite floatability in mineral processing.

A review of recent strategies for acid mine drainage prevention and mine tailings recycling.

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.

Interference of coexisting copper and aluminum on the ammonium thiosulfate leaching of gold from printed circuit boards of waste mobile phones.

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 individual metals were much lower. Electrochemical experiments (chronoamperometry) 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.

Arsenic, selenium, boron, lead, cadmium, copper, and zinc in naturally contaminated rocks: A review of their sources, modes of enrichment, mechanisms of release, and mitigation strategies.

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 example, 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.

Gold recovery from shredder light fraction of E-waste recycling plant by flotation-ammonium thiosulfate leaching.

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 sample 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.

Simultaneous suppression of acid mine drainage formation and arsenic release by Carrier-microencapsulation using aluminum-catecholate complexes.

Pyrite (FeS2), the most common sulfide mineral in nature, plays an important role in the formation of acid mine drainage (AMD), one of the most serious environmental problems after the closure of mines and mineral processing operations. Likewise, arsenopyrite (FeAsS) is an important sulfide mineral because its dissolution releases toxic arsenic (As) into the environment. To mitigate the serious environmental problems caused by pyrite and arsenopyrite, this study investigated carrier-microencapsulation (CME) using Al-catecholate complexes, a technique that selectively forms protective coatings on the surfaces of sulfide minerals, by electrochemical techniques and batch leaching experiments coupled with surface sensitive characterization techniques. Cyclic voltammetry (CV) of Al-catecholate complexes (mono-, bis-, tris-catecholate) suggest that these three species could be oxidatively decomposed in this order: [Al(cat)3]3-→[Al(cat)2]-→[Al(cat)]+→Al3+, and these reactions were irreversible. Among these three species, [Al(cat)]+ was the most effective in suppressing pyrite and arsenopyrite oxidations because it requires less steps for complete decomposition than the other two complexes. Analyses of CME treated minerals by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) indicated that they were covered with Al-oxyhydroxide (γ-AlO(OH)), which became more extensive at higher [Al(cat)]+ concentrations. In addition, this coating was stable even at relatively high applied potentials that simulated surface oxidizing conditions. Based on these results, a detailed mechanism of Al-based CME is proposed: (1) adsorption of [Al(cat)]+ on the surface of mineral, (2) oxidative decomposition of [Al(cat)]+ and release of "free" Al3+, and (3) precipitation and formation of Al-oxyhydroxide coating.

Suppression of the release of arsenic from arsenopyrite by carrier-microencapsulation using Ti-catechol complex.

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. Ti4+ ion dissolved in sulfuric acid and catechol were used to successfully synthesize Ti(IV) tris-catecholate complex, [Ti(Cat)3]2-, which was stable in the pH range of 5-12. Electrochemical studies on the redox properties of this complex indicate that its oxidative decomposition was a one-step, irreversible process. The leaching of As from arsenopyrite was suppressed by CME treatment using the synthesized Ti-catechol complex. Scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) indicate that this suppression was primarily due to the formation of an anatase (ß-TiO2)-containing coating. Based on these results, a detailed 4-step mechanism to explain the decomposition of [Ti(Cat)3]2- and formation of TiO2 coating in Ti-based CME is proposed: (1) adsorption, (2) partial oxidation-intermediate formation, (3) non electrochemical dissociation, and (4) hydrolysis-precipitation.