Kupfer ist ein für die Ernährung aller Lebewesen essentielles Element, das jedoch bei einem extremen Überangebot zu toxischen Wirkungen führen kann. Der mittlere Cu-Gehalt der Gesteine der oberen kontinentalen Erdkruste (Clarkewert) beträgt 14 mg/kg. Analog zu Chrom und Nickel ist es vor allem in basischen Gesteinen angereichert (Diabase, Basalte, Metabasite). Die mittleren Cu-Gehalte (Mediane) der sächsischen Haupt-gesteinstypen reichen von 2 bis 67 mg/kg, der regionale Clarke des Erzgebirges/Vogtlandes beträgt 23 mg/kg. Geogene Cu-Anreicherungen sind vor allem im Erzgebirge über den hier weit verbreiteten Mineralisationen zu finden. Chalkopyrit (Kupferkies) ist nahezu in allen Mineralassoziationen als sog. Durchläufermineral verbreitet. Starke anthropogene Cu-Einträge werden vor allem durch die Buntmetallurgie verursacht. Durch die vielfältige Verwendung von Cu, u. a. in der Elektrotechnik, als Legierungsmetall, Rohrleitungsmaterial und Regenrinnen, wird das Element auch verstärkt in das Abwasser eingetragen. Für unbelastete Böden gelten Cu-Gehalte von 2 bis 40 mg/kg als normal. Die regionale Verteilung der Cu-Gehalte im Oberboden wird vor allem durch den geogenen Anteil der Substrate bestimmt. Auf Grund der erhöhten Cu-Gehalte der im Vogtland weit verbreiteten Diabase (58 mg/kg), der punktförmig auftretenden tertiären Basaltoide (60 mg/kg) und der lokal eingelagerten Amphibolite (46 mg/kg) des metamorphen Grundgebirges, kommt es zu anomal hohen Cu-Gehalten in den Verwitterungsböden über den genannten Festgesteinen. Durch eine verstärkte Lössbeeinflussung (mit relativ niedrigen Cu-Gehalten von ca. 12 mg/kg), kann es über Cu-reichen Substraten, je nach Lössanteil, zu einem "Verdünnungseffekt" kommen (z. B. über den Monzonitoiden bei Meißen). Extrem niedrige Cu-Konzentrationen sind in den Verwitterungsböden über sauren Magmatiten (Granit von Ei-benstock, Teplice-Rhyolith), Metagranitoiden (Erzgebirgs-Zentralzone), Sandsteinen (Elbsandstein- und Zittauer Gebirge) und bei Bodengesellschaften aus periglaziären sandigen Decksedimenten in Nordsachsen zu beobachten. Bedeutende regionale Anomalien befinden sich vor allem im Freiberger Raum, dem wichtigsten früheren Standort des Bergbaus und der Verhüttung polymetallischer Erze. Die anthropogenen Einträge sind aber i. W. auf die unmittelbare Umgebung der Hüttenstandorte beschränkt. Dabei kommt es zu Überlagerung mit geogenen Anteilen im Boden, die in ursächlichem Zusammenhang mit der Verbreitung von Kupferkies führenden Mineralassoziationen stehen. Analoge Verhältnisse finden sich, wenn auch in abgeschwächter Form, im Raum Schneeberg - Schwarzenberg - Annaberg-Buchholz - Marienberg. Besonders hohe Cu-Gehalte weisen die Auenböden der Freiberger Mulde auf. Nach Eintritt der Freiberger Mulde in das Freiberger Bergbau- und Hüttenrevier kommt es zu einer nachhaltigen stofflichen Belastung der Auenböden, die über die Aue der Vereinigten Mulde bis an die nördliche Landesgrenze reicht. Erhöhte Cu-Gehalte, jedoch auf deutlich niedrigerem Niveau, treten auch in den Auenböden der Zwickauer Mulde auf, wo sich im Einzugsgebiet die polymetallischen Vererzungen des Westerzgebirges befinden. Infolge der beschriebenen geogenen und anthropogenen Prozesse werden in den Auenböden der Freiberger und der Vereinigten Mulde die Maßnahmenwerte der Bundes-Bodenschutz- und Altlastenverordnung (BBodSchV) für Grünlandnutzung (Schafhaltung) teilweise überschritten.
Arsen ist ein zu den Halbmetallen zählendes, ubiquitäres und toxisch wirkendes Element. Es kommt in der Natur weit verbreitet in verschiedenen Mineralisationen als Arsensulfid bzw. -oxid und als Kupfer-, Nickel- und Eisenarsenat vor. Der durchschnittliche As-Gehalt der Gesteine der oberen kontinentalen Erdkruste (Clarkewert) beträgt 2 mg/kg. In der Fachliteratur werden As-Gehalte 20 mg/kg als Normalgehalte beschrieben, wobei die mittleren Gehalte etwa 5 mg/kg betragen. Unter den toxisch wirkenden Elementen kommt dem Arsen auf Grund seiner großflächigen Verbreitung erhöhter Gehalte in sächsischen Böden eine besondere Bedeutung zu. Die Ursachen sind zweifellos in der geochemisch-metallogenetischen Spezialisierung der Fichtelgebirgisch Erzgebirgischen Antiklinalzone zu suchen. Der flächenbezogene mittlere As-Gehalt der Hauptgesteinstypen (petrogeochemische Komponente) beträgt ca. 13 mg/kg. Eine besondere Bedeutung erlangt im Erzgebirge die chalkogene Komponente. Neben der Elementanreicherung in der Vererzung selbst, die Gegenstand des Bergbaus war, kam es darüber hinaus zu einer großflächigen Beeinflussung der Nebengesteine bzw. deren Verwitterungsprodukte (primäre und sekundäre geochemische Aureole). Bei der anthropogenen Beeinflussung der natürlichen Böden sind vor allem die Erzaufbereitungsanlagen und die Emissionen der Buntmetallhütten zu nennen. Während in den Oberböden Nord- und in Teilen Mittelsachsens niedrige Gehalte dominieren (As-arme periglaziäre sandige bis lehmige Substrate; Löss), kommt es in den Verwitterungsböden über Festgesteinen infolge der höheren petrogenen As-Komponente zu einer relativen Anreicherung. Bedeutende regionale Anomalien befinden sich vor allem im Freiberger Raum (Osterzgebirge), dem bedeutendsten Standort des Bergbaus und der Verhüttung polymetallischer Erze, sowie im Westerzgebirge (Raum Aue - Ehrenfriedersdorf). Die große Extensität und Intensität der Verbreitung von As-Mineralen in den polymetallischen-, Zinn-Wolfram- und Bi-Co-Ni-Ag-U-Erzformationen sowie ihre Verhüttung führten zu großflächigen geogenen und anthropogenen Anreicherungen. Getrennt werden beide Bereiche durch die Nordwest-Südost streichende Flöha-Zone, einem Bereich, in dem kaum Erzmineralisationen auftreten und somit die chalkogene Komponente nur selten entwickelt ist. Großflächig erhöhte As-Gehalte in Böden der Vorerzgebirgssenke (Zwickau - Chemnitz) sind auf die geochemisch spezialisierten Rotliegendsedimente (u. a. Abtragungsprodukte des Erzgebirges) zurückzuführen. Besonders hohe As-Gehalte sind in den Auenböden der Freiberger Mulde, Zschopau, Zwickauer Mulde und der Vereinigten Mulde verbreitet. Durch den geologischen Prozess der Abtragung von Böden aus den erzgebirgischen Lagerstättengebieten sowie anthropogenen Einträgen durch die Erzaufbereitung und Hüttenindustrie, kommt es bei Ablagerung der Flusssedimente und Schwebanteile in den Überflutungsbereichen zu einer ständigen As-Anreicherung in den Auenböden. Infolge der beschrieben geogenen und anthropogenen Prozesse werden im Erzgebirge und in den Auenböden des Muldensystems die Prüf- und Maßnahmenwerte der Bundes-Bodenschutz- und Altlastenverordnung (BBodSchV) für Arsen z. T. flächenhaft überschritten.
technologyComment of gold mine operation and refining (SE): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. ORE AND WASTE HAULAGE: The haul trucks transport the ore to various areas for processing. The grade and type of ore determine the processing method used. Higher-grade ores are taken to a mill. Lower grade ores are taken to leach pads. Some ores may be stockpiled for later processing. HEAP LEACHING: The ore is crushed or placed directly on lined leach pads where a dilute cyanide solution is applied to the surface of the heap. The solution percolates down through the ore, where it leaches the gold and flows to a central collection location. The solution is recovered in this closed system. The pregnant leach solution is fed to electrowinning cells and undergoes the same steps as described below from Electro-winning. ORE PROCESSING: Milling: The ore is fed into a series of grinding mills where steel balls grind the ore to a fine slurry or powder. Oxidization and leaching: Some types of ore require further processing before gold is recovered. In this case, the slurry is pressure-oxidized in an autoclave before going to the leaching tanks or a dry powder is fed through a roaster in which it is oxidized using heat before being sent to the leaching tanks as a slurry. The slurry is thickened and runs through a series of leaching tanks. The gold in the slurry adheres to carbon in the tanks. Stripping: The carbon is then moved into a stripping vessel where the gold is removed from the carbon by pumping a hot caustic solution through the carbon. The carbon is later recycled. Electro-winning: The gold-bearing solution is pumped through electro-winning cells or through a zinc precipitation circuit where the gold is recovered from the solution. Smelting: The gold is then melted in a furnace at about 1’064°C and poured into moulds, creating doré bars. Doré bars are unrefined gold bullion bars containing between 60% and 95% gold. References: Newmont (2004) How gold is mined. Newmont. Retrieved from http://www.newmont.com/en/gold/howmined/index.asp technologyComment of gold production (US): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. UNDERGROUND MINING: Some ore bodies are more economically mined underground. In this case, a tunnel called an adit or a shaft is dug into the earth. Sort tunnels leading from the adit or shaft, called stopes, are dug to access the ore. The surface containing the ore, called a face, is drilled and loaded with explosives. Following blasting, the broken ore is loaded onto electric trucks and taken to the surface. Once mining is completed in a particular stope, it is backfilled with a cement compound. BENEFICIATION: Bald Mountain Mines: The ore treatment method is based on conventional heap leaching technology followed by carbon absorption. The loaded carbon is stripped and refined in the newly commissioned refinery on site. Water is supplied by wells located on the mine property. Grid power was brought to Bald Mountain Mine in 1996. For this purpose, one 27-kilometre 69 KVA power line was constructed from the Alligator Ridge Mine substation to the grid. Golden Sunlight Mines: The ore treatment plant is based on conventional carbon-in-pulp technology, with the addition of a Sand Tailings Retreatment (STR) gold recovery plant to recover gold that would otherwise be lost to tailings. The STR circuit removes the heavier gold bearing pyrite from the sand portion of the tailings by gravity separation. The gold is refined into doré at the mine. Tailing from the mill is discharged to an impoundment area where the solids are allowed to settle so the water can be reused. A cyanide recovery/destruction process was commissioned in 1998. It eliminates the hazard posed to wildlife at the tailings impoundment by lowering cyanide concentrations below 20 mg/l. Fresh water for ore processing, dust suppression, and fire control is supplied from the Jefferson Slough, which is an old natural channel of the Jefferson River. Ore processing also uses water pumped from the tailings impoundment. Pit water is treated in a facility located in the mill complex prior to disposal or for use in dust control. Drinking water is made available by filtering fresh water through an on-site treatment plant. Electric power is provided from a substation at the south property boundary. North-Western Energy supplies electricity the substation. Small diesel generators are used for emergency lighting. A natural gas pipeline supplies gas for heating buildings, a crusher, air scrubber, boiler, carbon reactivation kiln, and refining furnaces. Cortez Mine: Three different metallurgical processes are employed for the recovery of gold. The process used for a particular ore is determined based on grade and metallurgical character of that ore. Lower grade oxide ore is heap leached, while higher-grade non-refractory ore is treated in a conventional mill using cyanidation and a carbon-in-leach (“CIL”) process. When carbonaceous ore is processed by Barrick, it is first dry ground, and then oxidized in a circulating fluid bed roaster, followed by CIL recovery. In 2002 a new leach pad and process plant was commissioned; this plant is capable of processing 164 million tonnes of heap leach ore over the life of the asset. Heap leach ore production is hauled directly to heap leach pads for gold recovery. Water for process use is supplied from the open pit dewatering system. Approximately 90 litres per second of the pit dewatering volume is diverted for plant use. Electric power is supplied by Sierra Pacific Power Company (“SPPC”) through a 73 kilometre, 120 kV transmission line. A long-term agreement is in place with SPPC to provide power through the regulated power system. The average power requirement of the mine is about 160 GWh/year. REFINING: Wohlwill electrolysis. It is assumed that the gold doré-bars from both mines undergo the treatment of Wohlwill electrolysis. This process uses an electrolyte containing 2.5 mol/l of HCl and 2 mol/l of HAuCl4 acid. Electrolysis is carried out with agitation at 65 – 75 °C. The raw gold is intro-duced as cast anode plates. The cathodes, on which the pure gold is deposited, were for many years made of fine gold of 0.25 mm thickness. These have now largely been replaced by sheet titanium or tantalum cathodes, from which the thick layer of fine gold can be peeled off. In a typical electrolysis cell, gold anodes weighing 12 kg and having dimensions 280×230×12 mm (0.138 m2 surface) are used. Opposite to them are conductively connected cathode plates, arranged by two or three on a support rail. One cell normally contains five or six cathode units and four or five anodes. The maximum cell voltage [V] is 1.5 V and the maximum anodic current density [A] 1500 A/m2. The South African Rand refinery gives a specific gold production rate of 0.2 kg per hour Wohlwill electrolysis. Assuming a current efficiency of 95% the energy consumption is [V] x [A] / 0.2 [kg/h] = 1.63 kWh per kg gold refined. No emissions are assumed because of the purity and the high value of the material processed. The resulting sludge contains the PGM present in the electric scrap and is sold for further processing. OTHER MINES: Information about the technology used in the remaining mines is described in the References. WATER EMISSIONS: Water effluents are discharged into rivers. References: Auerswald D. A. and Radcliffe P. H. (2005) Process technology development at Rand Refinery. In: Minerals Engineering, 18(8), pp. 748-753, Online-Version under: http://dx.doi.org/10.1016/j.mineng.2005.03.011. Newmont (2004) How gold is mined. Newmont. Retrieved from http://www.newmont.com/en/gold/howmined/index.asp Renner H., Schlamp G., Hollmann D., Lüschow H. M., Rothaut J., Knödler A., Hecht C., Schlott M., Drieselmann R., Peter C. and Schiele R. (2002) Gold, Gold Alloys, and Gold Compounds. In: Ullmann's Encyclopedia of Industrial Chemistry. Online version, posting date: September 15, 2000 Edition. Wiley-Interscience, Online-Version under: http://dx.doi.org/10.1002/14356007.a12_ 499. Barrick (2006b) Environment: Performance Tables from http://www.barrick. com/Default.aspx?SectionID=8906c4bd-4ee4-4f15-bf1b-565e357c01e1& LanguageId=1 Newmont (2005b) Now & Beyond: Sustainability Reports. Newmont Mining Corporation. Retrieved from http://www.newmont.com/en/social/reporting/ index.asp technologyComment of gold production (CA): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. UNDERGROUND MINING: Some ore bodies are more economically mined underground. In this case, a tunnel called an adit or a shaft is dug into the earth. Sort tunnels leading from the adit or shaft, called stopes, are dug to access the ore. The surface containing the ore, called a face, is drilled and loaded with explosives. Following blasting, the broken ore is loaded onto electric trucks and taken to the surface. Once mining is completed in a particular stope, it is backfilled with a cement compound. ORE AND WASTE HAULAGE: The haul trucks transport the ore to various areas for processing. The grade and type of ore determine the processing method used. Higher-grade ores are taken to a mill. Lower grade ores are taken to leach pads. Some ores may be stockpiled for later processing. BENEFICIATION: In the Porcupine Mines, gold is recovered using a combination of gravity concentration, milling and cyanidation techniques. The milling process consists of primary crushing, secondary crushing, rod/ball mill grinding, gravity concentration, cyanide leaching, carbon-in-pulp gold recovery, stripping, electrowinning and refining. In the Campbell Mine, the ore from the mine, after crushing and grinding, is processed by gravity separation, flotation, pressure oxidation, cyanidation and carbon-in-pulp process followed by electro-winning and gold refining to doré on site. The Musselwhite Mine uses gravity separation, carbon in pulp, electro¬winning and gold refining to doré on site. REFINING: Wohlwill electrolysis. It is assumed that the gold doré-bars from both mines undergo the treatment of Wohlwill electrolysis. This process uses an electrolyte containing 2.5 mol/l of HCl and 2 mol/l of HAuCl4 acid. Electrolysis is carried out with agitation at 65 – 75 °C. The raw gold is intro-duced as cast anode plates. The cathodes, on which the pure gold is deposited, were for many years made of fine gold of 0.25 mm thickness. These have now largely been replaced by sheet titanium or tantalum cathodes, from which the thick layer of fine gold can be peeled off. In a typical electrolysis cell, gold anodes weighing 12 kg and having dimensions 280×230×12 mm (0.138 m2 surface) are used. Opposite to them are conductively connected cathode plates, arranged by two or three on a support rail. One cell normally contains five or six cathode units and four or five anodes. The maximum cell voltage [V] is 1.5 V and the maximum anodic current density [A] 1500 A/m2. The South African Rand refinery gives a specific gold production rate of 0.2 kg per hour Wohlwill electrolysis. Assuming a current efficiency of 95% the energy consumption is [V] x [A] / 0.2 [kg/h] = 1.63 kWh per kg gold refined. No emissions are assumed because of the purity and the high value of the material processed. The resulting sludge contains the PGM present in the electric scrap and is sold for further processing. WATER EMISSIONS: Effluents are discharged into the ocean. REFERENCES: Newmont (2004) How gold is mined. Newmont. Retrieved from http://www.newmont.com/en/gold/howmined/index.asp Renner H., Schlamp G., Hollmann D., Lüschow H. M., Rothaut J., Knödler A., Hecht C., Schlott M., Drieselmann R., Peter C. and Schiele R. (2002) Gold, Gold Alloys, and Gold Compounds. In: Ullmann's Encyclopedia of Industrial Chemistry. Online version, posting date: September 15, 2000 Edition. Wiley-Interscience, Online-Version under: http://dx.doi.org/10.1002/14356007.a12_ 499. Auerswald D. A. and Radcliffe P. H. (2005) Process technology development at Rand Refinery. In: Minerals Engineering, 18(8), pp. 748-753, Online-Version under: http://dx.doi.org/10.1016/j.mineng.2005.03.011. technologyComment of gold production (AU): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. UNDERGROUND MINING: Some ore bodies are more economically mined underground. In this case, a tunnel called an adit or a shaft is dug into the earth. Sort tunnels leading from the adit or shaft, called stopes, are dug to access the ore. The surface containing the ore, called a face, is drilled and loaded with explosives. Following blasting, the broken ore is loaded onto electric trucks and taken to the surface. Once mining is completed in a particular stope, it is backfilled with a cement compound. ORE AND WASTE HAULAGE: The haul trucks transport the ore to various areas for processing. The grade and type of ore determine the processing method used. Higher-grade ores are taken to a mill. Lower grade ores are taken to leach pads. Some ores may be stockpiled for later processing. LEACHING: The ore is crushed or placed directly on lined leach pads where a dilute cyanide solution is applied to the surface of the heap. The solution percolates down through the ore, where it leaches the gold and flows to a central collection location. The solution is recovered in this closed system. The pregnant leach solution is fed to electrowinning cells and undergoes the same steps as described below from Electro-winning. ORE PROCESSING: Milling: The ore is fed into a series of grinding mills where steel balls grind the ore to a fine slurry or powder. Oxidization and leaching: Some types of ore require further processing before gold is recovered. In this case, the slurry is pressure-oxidized in an autoclave before going to the leaching tanks or a dry powder is fed through a roaster in which it is oxidized using heat before being sent to the leaching tanks as a slurry. The slurry is thickened and runs through a series of leaching tanks. The gold in the slurry adheres to carbon in the tanks. Stripping: The carbon is then moved into a stripping vessel where the gold is removed from the carbon by pumping a hot caustic solution through the carbon. The carbon is later recycled. Electro-winning: The gold-bearing solution is pumped through electro-winning cells or through a zinc precipitation circuit where the gold is recovered from the solution. Smelting: The gold is then melted in a furnace at about 1’064°C and poured into moulds, creating doré bars. Doré bars are unrefined gold bullion bars containing between 60% and 95% gold. REFINING: Wohlwill electrolysis. It is assumed that the gold doré-bars from both mines undergo the treatment of Wohlwill electrolysis. This process uses an electrolyte containing 2.5 mol/l of HCl and 2 mol/l of HAuCl4 acid. Electrolysis is carried out with agitation at 65 – 75 °C. The raw gold is intro-duced as cast anode plates. The cathodes, on which the pure gold is deposited, were for many years made of fine gold of 0.25 mm thickness. These have now largely been replaced by sheet titanium or tantalum cathodes, from which the thick layer of fine gold can be peeled off. In a typical electrolysis cell, gold anodes weighing 12 kg and having dimensions 280×230×12 mm (0.138 m2 surface) are used. Opposite to them are conductively connected cathode plates, arranged by two or three on a support rail. One cell normally contains five or six cathode units and four or five anodes. The maximum cell voltage [V] is 1.5 V and the maximum anodic current density [A] 1500 A/m2. The South African Rand refinery gives a specific gold production rate of 0.2 kg per hour Wohlwill electrolysis. Assuming a current efficiency of 95% the energy consumption is [V] x [A] / 0.2 [kg/h] = 1.63 kWh per kg gold refined. No emissions are assumed because of the purity and the high value of the material processed. The resulting sludge contains the PGM present in the electric scrap and is sold for further processing. WATER EMISSIONS: Water effluents are discharged into rivers. REFERENCES: Newmont (2004) How gold is mined. Newmont. Retrieved from http://www.newmont.com/en/gold/howmined/index.asp Renner H., Schlamp G., Hollmann D., Lüschow H. M., Rothaut J., Knödler A., Hecht C., Schlott M., Drieselmann R., Peter C. and Schiele R. (2002) Gold, Gold Alloys, and Gold Compounds. In: Ullmann's Encyclopedia of Industrial Chemistry. Online version, posting date: September 15, 2000 Edition. Wiley-Interscience, Online-Version under: http://dx.doi.org/10.1002/14356007.a12_ 499. Auerswald D. A. and Radcliffe P. H. (2005) Process technology development at Rand Refinery. In: Minerals Engineering, 18(8), pp. 748-753, Online-Version under: http://dx.doi.org/10.1016/j.mineng.2005.03.011. technologyComment of gold production (TZ): The mining of ore from open pit and underground mines is considered. technologyComment of gold refinery operation (ZA): REFINING: The refinery, which provides a same day refining service, employs the widely used Miller Chlorination Process to upgrade the gold bullion it receives from mines to at least 99.50% fine gold, the minimum standard required for gold sold on the world bullion markets. It also employs the world’s leading silver refining technology. To further refine gold and silver to 99.99% the cost-effective once-through Wohlwill electrolytic refining process is used. MILLER CHLORINATION PROCESS: This is a pyrometallurgical process whereby gold dore is heated in furnace crucibles. The process is able to separate gold from impurities by using chlorine gas which is added to the crucibles once the gold is molten. Chlorine gas does not react with gold but will combine with silver and base metals to form chlorides. Once the chlorides have formed they float to the surface as slag or escape as volatile gases. The surface melt and the fumes containing the impurities are collected and further refined to extract the gold and silver. This process can take up to 90 minutes produces gold which is at least 99.5% pure with silver being the main remaining component. This gold can be cast into bars as 99.5% gold purity meets the minimum London Good Delivery. However some customers such as jewellers and other industrial end users require gold that is almost 100% pure, so further refining is necessary. In this case, gold using the Miller process is cast into anodes which are then sent to an electrolytic plant. The final product is 99.99% pure gold sponge that can then be melted to produce various end products suited to the needs of the customer. WOHLWILL PROCESS - The electrolytic method of gold refining was first developed by Dr. Emil Wohlwill of Norddeutsche Affinerie in Hamburg in 1874. Dr. Wohlwill’s process is based on the solubility of gold but the insolubility of silver in an electrolyte solution of gold chloride (AuCl3) in hydrochloric acid. Figure below provide the overview of the refining process (source Rand Refinery Brochure) imageUrlTagReplace7f46a8e2-2df0-4cf4-99a8-2878640be562 Emissions includes also HCl to air: 7.48e-03 Calculated from rand refinery scrubber and baghouse emmission values Metal concentrators, Emmision report 2016 http://www.environmentalconsultants.co.za/wp-content/uploads/2016/11/Appendix-D1.pdf technologyComment of gold refinery operation (RoW): REFINING: The refinery, which provides a same day refining service, employs the widely used Miller Chlorination Process to upgrade the gold bullion it receives from mines to at least 99.50% fine gold, the minimum standard required for gold sold on the world bullion markets. It also employs the world’s leading silver refining technology. To further refine gold and silver to 99.99% the cost-effective once-through Wohlwill electrolytic refining process is used. MILLER CHLORINATION PROCESS: This is a pyrometallurgical process whereby gold dore is heated in furnace crucibles. The process is able to separate gold from impurities by using chlorine gas which is added to the crucibles once the gold is molten. Chlorine gas does not react with gold but will combine with silver and base metals to form chlorides. Once the chlorides have formed they float to the surface as slag or escape as volatile gases. The surface melt and the fumes containing the impurities are collected and further refined to extract the gold and silver. This process can take up to 90 minutes produces gold which is at least 99.5% pure with silver being the main remaining component. This gold can be cast into bars as 99.5% gold purity meets the minimum London Good Delivery. However some customers such as jewellers and other industrial end users require gold that is almost 100% pure, so further refining is necessary. In this case, gold using the Miller process is cast into anodes which are then sent to an electrolytic plant. The final product is 99.99% pure gold sponge that can then be melted to produce various end products suited to the needs of the customer. WOHLWILL PROCESS - The electrolytic method of gold refining was first developed by Dr. Emil Wohlwill of Norddeutsche Affinerie in Hamburg in 1874. Dr. Wohlwill’s process is based on the solubility of gold but the insolubility of silver in an electrolyte solution of gold chloride (AuCl3) in hydrochloric acid. Figure below provide the overview of the refining process (source Rand Refinery Brochure) imageUrlTagReplace7f46a8e2-2df0-4cf4-99a8-2878640be562 Emissions includes also HCl to air: 7.48e-03 Calculated from rand refinery scrubber and baghouse emmission values Metal concentrators, Emmision report 2016 http://www.environmentalconsultants.co.za/wp-content/uploads/2016/11/Appendix-D1.pdf technologyComment of gold-silver mine operation with refinery (PG): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. ORE AND WASTE HAULAGE: The haul trucks transport the ore to various areas for processing. The grade and type of ore determine the processing method used. Higher-grade ores are taken to a mill. Lower grade ores are taken to leach pads. Some ores may be stockpiled for later processing. HEAP LEACHING: The recovery processes of the Misima Mine are cyanide leach and carbon in pulp (CIP). The ore is crushed or placed directly on lined leach pads where a dilute cyanide solution is applied to the surface of the heap. The solution percolates down through the ore, where it leaches the gold and flows to a central collection location. The solution is recovered in this closed system. The pregnant leach solution is fed to electrowinning cells and undergoes the same steps as described below from Electro-winning. ORE PROCESSING: Milling: The ore is fed into a series of grinding mills where steel balls grind the ore to a fine slurry or powder. Oxidization and leaching: The recovery process in the Porgera Mine is pressure oxidation and cyanide leach. The slurry is pressure-oxidized in an autoclave before going to the leaching tanks or a dry powder is fed through a roaster in which it is oxidized using heat before being sent to the leaching tanks as a slurry. The slurry is thickened and runs through a series of leaching tanks. The gold in the slurry adheres to carbon in the tanks. Stripping: The carbon is then moved into a stripping vessel where the gold is removed from the carbon by pumping a hot caustic solution through the carbon. The carbon is later recycled. Electro-winning: The gold-bearing solution is pumped through electro-winning cells or through a zinc precipitation circuit where the gold is recovered from the solution. Smelting: The gold is then melted in a furnace at about 1’064°C and poured into moulds, creating doré bars. Doré bars are unrefined gold bullion bars containing between 60% and 95% gold. WATER SUPPLY: For Misima Mine, process water is supplied from pit dewatering bores and in-pit water. Potable water is sourced from boreholes in the coastal limestone. For Porgera Mine, the main water supply of the mine is the Waile Creek Dam, located approximately 7 kilometres from the mine. The reservoir has a capacity of approximately 717, 000 m3 of water. Water for the grinding circuit is also extracted from Kogai Creek, which is located adjacent to the grinding circuit. The mine operates four water treatment plants for potable water and five sewage treatment plants. ENERGY SUPPLY: For Misima Mine, electricity is produced by the mine on site or with own power generators, from diesel and heavy fuel oil. For Porgera Mine, electricity is produced by the mine on site. Assumed with Mobius / Wohlwill electrolysis. Porgera's principal source of power is supplied by a 73-kilometre transmission line from the gas fired and PJV-owned Hides Power Station. The station has a total output of 62 megawatts (“MW”). A back up diesel power station is located at the mine and has an output of 13MW. The average power requirement of the mine is about 60 MW. For both Misima and Porgera Mines, an 18 MW diesel fired power station supplies electrical power. Diesel was used in the station due to the unavailability of previously supplied heavy fuel oil. technologyComment of gold-silver mine operation with refinery (CA-QC): One of the modelled mine is an open-pit mine and the two others are underground. technologyComment of gold-silver mine operation with refinery (RoW): The mining of ore from open pit mines is considered. technologyComment of platinum group metal, extraction and refinery operations (ZA): The ores from the different ore bodies are processed in concentrators where a PGM concentrate is produced with a tailing by product. The PGM base metal concentrate product from the different concentrators processing the different ores are blended during the smelting phase to balance the sulphur content in the final matte product. Smelter operators also carry out toll smelting from third part concentrators. The smelter product is send to the Base metal refinery where the PGMs are separated from the Base Metals. Precious metal refinery is carried out on PGM concentrate from the Base metal refinery to split the PGMs into individual metal products. Water analyses measurements for Anglo Platinum obtained from literature (Slatter et.al, 2009). Mudd, G., 2010. Platinum group metals: a unique case study in the sustainability of mineral resources, in: The 4th International Platinum Conference, Platinum in Transition “Boom or Bust.” Water share between MC and EC from Mudd (2010). Mudd, G., 2010. Platinum group metals: a unique case study in the sustainability of mineral resources, in: The 4th International Platinum Conference, Platinum in Transition “Boom or Bust.” technologyComment of primary zinc production from concentrate (RoW): The technological representativeness of this dataset is considered to be high as smelting methods for zinc are consistent in all regions. Refined zinc produced pyro-metallurgically represents less than 5% of global zinc production and less than 2% of this dataset. Electrometallurgical Smelting The main unit processes for electrometallurgical zinc smelting are roasting, leaching, purification, electrolysis, and melting. In both electrometallurgical and pyro-metallurgical zinc production routes, the first step is to remove the sulfur from the concentrate. Roasting or sintering achieves this. The concentrate is heated in a furnace with operating temperature above 900 °C (exothermic, autogenous process) to convert the zinc sulfide to calcine (zinc oxide). Simultaneously, sulfur reacts with oxygen to produce sulfur dioxide, which is subsequently converted to sulfuric acid in acid plants, usually located with zinc-smelting facilities. During the leaching process, the calcine is dissolved in dilute sulfuric acid solution (re-circulated back from the electrolysis cells) to produce aqueous zinc sulfate solution. The iron impurities dissolve as well and are precipitated out as jarosite or goethite in the presence of calcine and possibly ammonia. Jarosite and goethite are usually disposed of in tailing ponds. Adding zinc dust to the zinc sulfate solution facilitates purification. The purification of leachate leads to precipitation of cadmium, copper, and cobalt as metals. In electrolysis, the purified solution is electrolyzed between lead alloy anodes and aluminum cathodes. The high-purity zinc deposited on aluminum cathodes is stripped off, dried, melted, and cast into SHG zinc ingots (99.99 % zinc). Pyro-metallurgical Smelting The pyro-metallurgical smelting process is based on the reduction of zinc and lead oxides into metal with carbon in an imperial smelting furnace. The sinter, along with pre-heated coke, is charged from the top of the furnace and injected from below with pre-heated air. This ensures that temperature in the center of the furnace remains in the range of 1000-1500 °C. The coke is converted to carbon monoxide, and zinc and lead oxides are reduced to metallic zinc and lead. The liquid lead bullion is collected at the bottom of the furnace along with other metal impurities (copper, silver, and gold). Zinc in vapor form is collected from the top of the furnace along with other gases. Zinc vapor is then condensed into liquid zinc. The lead and cadmium impurities in zinc bullion are removed through a distillation process. The imperial smelting process is an energy-intensive process and produces zinc of lower purity than the electrometallurgical process. technologyComment of processing of anode slime from electrorefining of copper, anode (GLO): Based on typical current technology. Anode slime treatment by pressure leaching and top blown rotary converter. Production of Silver by Möbius Electrolysis, Gold by Wohlwill electrolysis, copper telluride cement and crude selenium to further processing. technologyComment of silver-gold mine operation with refinery (CL): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. BENEFICIATION: The processing plant consists of primary crushing, a pre-crushing circuit, (semi autogenous ball mill crushing) grinding, leaching, filtering and washing, Merrill-Crowe plant and doré refinery. The Merrill-Crowe metal recovery circuit is better than a carbon-in-pulp system for the high-grade silver material. Tailings are filtered to recover excess water as well as residual cyanide and metals. A dry tailings disposal system was preferred to a conventional wet tailings impoundment because of site-specific environmental considerations. technologyComment of silver-gold mine operation with refinery (RoW): Refinement is estimated with electrolysis-data. technologyComment of treatment of precious metal from electronics scrap, in anode slime, precious metal extraction (SE, RoW): Anode slime treatment by pressure leaching and top blown rotary converter. Production of Silver by Möbius Electrolysis, Gold by Wohlwill electrolysis, Palladium to further processing
technologyComment of iron ore beneficiation (IN): Milling and mechanical sorting. Average iron yield is 65% . The process so developed basically involves crushing, classification, processing of lumps, fines and slimes separately to produce concentrate suitable as lump and sinter fines and for pellet making. The quality is essentially defined as Fe contents, Level of SiO2 and Al2O3 contamination. The process aims at maximizing Fe recovery by subjecting the rejects/tailings generated from coarser size processing to fine size reduction and subsequent processing to recover iron values. technologyComment of iron ore beneficiation (RoW): Milling and mechanical sorting. Average iron yield is 84%. technologyComment of iron ore mine operation and beneficiation (CA-QC): Milling and mechanical sorting. Average iron yield is 75%. Specific data were collected on one of the two production site in Quebec. According to the documentation available, the technologies of the 2 mines seems similar. Uncertainity has been adjusted accordingly. technologyComment of niobium mine operation and beneficiation, from pyrochlore ore (BR, RoW): Open-pit mining is applied and hydraulic excavators are used to extract the ore with different grades, which is transported to stockpiles awaiting homogenization through earth-moving equipment in order to attain the same concentration. Conveyor belts (3.5 km) are utilized to transport the homogenized ore to the concentration unit. Initially, the ore passes through a jaw crusher and moves to the ball mills, where the pyrochlore grains (1 mm average diameter) are reduced to diameters less than 0.104 mm. In the ball mills, recycled water is added in order to i) granulate the concentrate and ii) remove the gas from the sintering unit. The granulated ore undergoes i) magnetic separation, where magnetite is removed and is sold as a coproduct and ii) desliming in order to remove fractions smaller than 5μm by utilizing cyclones. Then the ore enters the flotation process - last stage of the beneficiation process – where the pyrochlore particles come into contact with flotation chemicals (hydrochloric & fluorosilic acid, triethylamene and lime), thereby removing the solid fractions and producing pyrochlore concentrate and barite as a coproduct which is also sold. The produced concentrate contains 55% Nb2O5 and 11% water and moves to the sintering unit, via tubes or is transported in bags while the separated and unused minerals enter the tailings dam. In the sintering unit, the pyrochlore concentrate undergoes pelletizing, sintering, crushing and classification. These units not only accumulate the material but are also responsible for removing sulfur and water from the concentrate. Then the concentrate enters the dephosphorization unit, where phosphorus and lead are removed from the concentrate. The removal of sulphur and phosphorus have to be executed because of the local pyrochlore ore composition. Then the concentrate undergoes a carbothermic reduction by using charcoal and petroleum coke, producing a refined concentrate, 63% Nb2O5 and tailings with high lead content that are disposed in the tailings dam again. technologyComment of rare earth element mine operation and beneficiation, bastnaesite and monazite ore (CN-NM): Firstly, open pit, mining (drilling and blasting) is performed in order to obtain the iron ore and a minor quantity of rare earth ores (5−6 % rare earth oxide equivalent). Then, a two-step beneficiation process is applied to produce the REO concentrate. In the first step, ball milling and magnetic separation is used for the isolation of the iron ore. In the second step, the resulting REO tailing (containing monazite and bastnasite), is processed to get a 50% REO equivalent concentrate via flotation. technologyComment of rare earth oxides production, from rare earth oxide concentrate, 70% REO (CN-SC): This dataset refers to the separation (hydrochloric acid leaching) and refining (metallothermic reduction) process used in order to produce high-purity rare earth oxides (REO) from REO concentrate, 70% beneficiated. ''The concentrate is calcined at temperatures up to 600ºC to oxidize carbonaceous material. Then HCl leaching, alkaline treatment, and second HCl leaching is performed to produce a relatively pure rare earth chloride (95% REO). Hydrochloric acid leaching in Sichuan is capable of separating and recovering the majority of cerium oxide (CeO) in a short process. For this dataset, the entire quantity of Ce (50% cerium dioxide [CeO2]/REO) is assumed to be produced here as CeO2 with a grade of 98% REO. Foreground carbon dioxide CO2 emissions were calculated from chemical reactions of calcining beneficiated ores. Then metallothermic reduction produces the purest rare earth metals (99.99%) and is most common for heavy rare earths. The metals volatilize, are collected, and then condensed at temperatures of 300 to 400°C (Chinese Ministryof Environmental Protection 2009).'' Source: Lee, J. C. K., & Wen, Z. (2017). Rare Earths from Mines to Metals: Comparing Environmental Impacts from China's Main Production Pathways. Journal of Industrial Ecology, 21(5), 1277-1290. doi:10.1111/jiec.12491 technologyComment of scandium oxide production, from rare earth tailings (CN-NM): See general comment. technologyComment of vanadium-titanomagnetite mine operation and beneficiation (CN): Natural rutile resources are scarce in China. For that reason, the production of titanium stems from high-grade titanium slag, the production of which includes 2 processes: i) ore mining & dressing process and ii) titanium slag smelting process. During the ore mining and dressing process, ilmenite concentrate (47.82% TiO2) is produced through high-intensity magnetic separation of the middling ore, which is previously produced as a byproduct during the magnetic separation sub-process of the vanadium titano-magnetite ore. During the titanium slag smelting process, the produced ilmenite concentrate from the ore mining & dressing process is mixed with petroleum coke as the reducing agent and pitch as the bonding agent. Afterwards it enters the electric arc furnace, where it is smelted, separating iron from the ilmenite concentrate and obtaining high-grade titanium slag.
Die Hg-Konzentration in der oberen kontinentalen Kruste beträgt 0,06 mg/kg. Für unbelastete Böden gelten Hg-Gehalte von 0,02 bis 0,5 mg/kg als normal. Die regionale Verbreitung erhöhter Hg-Gehalte in den sächsischen Böden kann nur unter Vorbehalt geogenen und anthropogenen Ursachen und Einflüssen zugeordnet werden, da der Kenntnisstand zur Hg-Verteilung in Gesteinen und Böden, im Vergleich zu anderen Schwermetallen, relativ gering ist. Der Hg-Gehalt im mineralischen Oberboden ist gegenüber dem des Unterbodens deutlich erhöht, was auf einen verstärkten ubiquitären atmosphärischen Eintrag hinweist. Die Ausgangsgesteine der Bodenbildung unterscheiden sich in Sachsen hinsichtlich ihres lithogenen Hg-Gehalts nicht wesentlich. Die von jüngeren Lockergesteinen bedeckten nördlichen und westlichen Landesteile haben etwas geringere Hg-Gehalte als die metamorphen Gesteine des Erzgebirges/Vogtlandes. Schwache geogene Hg-Anreicherungen sind nur aus den silurischen Alaun- und Kieselschiefern sowie den tertiären Basalten bekannt, die jedoch aufgrund ihrer geringen flächenhaften Verbreitung im Untersuchungsmaßstab dieser Arbeiten nur bedingt wirksam werden. Weiterhin weisen die Böden über den Ton- und Schluffschiefern des Ordoviziums des West-erzgebirges und Vogtlandes leicht erhöhte natürliche Hg-Gehalte gegenüber den sich anschließenden Glimmerschiefern und Gneisen auf. Hg-führende Mineralisationen (Zinnober /HgS), die in Sachsen jedoch keine größere Bedeutung besitzen, können lokal zu zusätzlichen geogenen Hg-Anreicherungen führen. Anthropogene Hg-Einträge in den Boden erfolgen hauptsächlich durch Emissionen von Großfeuerungs- (Kohle, Gas) und Müllverbrennungsanlagen, durch Erzverhüttung, Farben und Pharmazeutika. In aquatische Systeme wird Hg vor allem durch industrielle Abwässer von Chlor-Alkali-Elektrolysen und der holz- und metallverarbeitenden Industrie eingetragen. Auf landwirtschaftlich genutzten Böden erfolgte in der Vergangenheit der Eintrag über Hg-haltige Fungizide als Saatgutbeizmittel für Getreide. Auch mit dem Ausbringen von Klärschlämmen und kompostierten Siedlungsabfällen gelangte Hg in die Böden. Bei einem insgesamt relativ niedrigen Grundniveau treten erhöhte Hg-Gehalte in Sachsen vor allem im Raum Freiberg auf. Diese Anomalie wurde durch die Jahrhunderte währende Betriebszeit der Amalgamierwerke und Hüttenanlagen verursacht. Verstärkte Hg-Akkumulationen sind ebenfalls in den Auenböden der Elbe, der Freiberger und Vereinigten Mulde zu beobachten, die durch Hg-haltige industrielle und kommunale Abwässer bedingt sind. Das ehemalige Amalgamierwerk Halsbrücke und der Hüttenstandort in Muldenhütten bei Freiberg liegen in unmittelbarer Nähe der Freiberger Mulde und haben durch die jahrhundertelange Emissionsbelastung sicherlich noch heute einen Anteil an der Hg-Belastung der Auenböden der Freiberger und Vereinigten Mulde bis Eilenburg. Quecksilber ist ein starkes Gift für Tier und Mensch. Die gemessenen Hg-Gehalte sind für den Wirkungspfad Boden - Mensch kaum relevant, da der Prüfwert nach BBodSchV für eine direkte Aufnahme bei 10 mg/kg liegt und nur sehr selten erreicht wird. Der Prüfwert für den Pfad Boden - Pflanze (Acker- und Gartenbau) beträgt 5 mg/kg. Für eine Grünlandnutzung gilt als Maßnahmenwert 2 mg/kg.
From 1946 – 1990, i.e. from shortly after the end of World War II and the rise of the cold war until the German reunification, there had been extensive uranium mining both in Saxony and Thuringia, which formed the southern parts of the former German Democratic Republic. Mining activities started in Saxony in the Ore Mountains (German: Erzgebirge). Mining was conducted by a Soviet, since 1954 by a Soviet- German Incorporated Company named Wismut. It is estimated that about 400,000 persons may have worked in this time period with the company, most of them underground or in uranium ore processing facilities. In the early years, exposure to radiation and dust was particularly high for underground workers. After introduction of several ventilation measures and wet drilling from 1955 onwards, the levels of exposures to the various agents steadily decreased. After German reunification, it was decided by the German Federal Ministry for the Environment to save health data that were stored in different places, but which together formed the Wismut Health Data Archives. Based on parts of the information kept in different places by different bodies, a cohort of 64,311 former Wismut employees could be established. The objective of the cohort study was to examine the long-term health effects of chronic exposure to radiation, dust and arsenic as well as their combined effects. Particular focus should be given to the outcome lung cancer, but also to extrapulmonary cancers, cardiovascular and respiratory diseases. This report gives a comprehensive overview on the background of the study, its objectives, material and methods employed so far for data analysis, information on how the cohort was established and which data are available, and descriptive results. All data referred to in this report are based on the cohort's second follow-up for the years 1946 – 2003.
The BAT reference document (BREF) entitled 'Non-Ferrous Metals Industries' forms part of a series presenting the results of an exchange of information between EU Member States, the industries concerned, non-governmental organisations promoting environmental protection, and the Commission, to draw up, review and, where necessary, update BAT reference documents as required by Article 13(1) of the Directive 2010/75/EU on industrial emissions. This document is published by the European Commission pursuant to Article 13(6) of the Directive. This BREF for 'Non-Ferrous Metals Industries' concerns the activities specified in Sections 2 and 6.8 of Annex I to Directive 2010/75/EU, namely: - 2.1: Metal ore (including sulphide ore) roasting or sintering; - 2.5: Processing of non-ferrous metals: (a) production of non-ferrous crude metals from ore, concentrates or secondary raw materials by metallurgical, chemical or electrolytic processes; (b) melting, including the alloyage, of non-ferrous metals, including recovered products and operation of non-ferrous metal foundries, with a melting capacity exceeding 4 tonnes per day for lead and cadmium or 20 tonnes per day for all other metals; - 6.8: Production of carbon (hard-burnt coal) or electrographite by means of incineration or graphitisation. This document also covers: - the production of zinc oxide from fumes during the production of other metals; - the production of nickel compounds from liquors during the production of a metal; - the production of silicon-calcium (CaSi) and silicon (Si) in the same furnace as the production of ferro-silicon; - the production of aluminium oxide from bauxite prior to the production of primary aluminium, where this is an integral part of the production of the metal; - the recycling of aluminium salt slag. Important issues for the implementation of Directive 2010/75/EU in the non-ferrous metals industries are the emissions to air of dust, metals, organic compounds (which can result in the formation of PCDD/F) and sulphur dioxide; diffuse air emissions; emissions to water of metals (e.g. Hg, Cd, Cu, Pb, Zn); resource efficiency; and the prevention of emissions to soil and groundwater. This BREF contains 12 chapters. Chapters 1 and 2 provide general information on the non-ferrous metals industry and on the common industrial processes and techniques used within the whole sector. Chapters 3, 4, 5, 6, 7, 8, 9 and 10 correspond to the following specific production sectors: copper, aluminium, lead and/or tin, zinc and/or cadmium, precious metals, ferro-alloys, nickel and/or cobalt, and carbon and graphite. For each specific production sector, these eight chapters provide information and data concerning the applied processes and techniques; the environmental performance of installations in terms of current emissions, consumption of raw materials, water and energy, and generation of waste; the techniques to prevent or, where this is not practicable, to reduce the environmental impact of operating installations in these sectors that were considered in determining the BAT; and the emerging techniques as defined in Article 3(14) of the Directive. Chapter 11 presents the BAT conclusions as defined in Article 3(12) of the Directive. Chapter 12 is dedicated to concluding remarks and recommendations for future work. Quelle: BAT-Merkblatt JRC 107041
technologyComment of gold mine operation and refining (SE): OPEN PIT MINING: The ore is mined in four steps: drilling, blasting, loading and hauling. In the case of a surface mine, a pattern of holes is drilled in the pit and filled with explosives. The explosives are detonated in order to break up the ground so large shovels or front-end loaders can load it into haul trucks. ORE AND WASTE HAULAGE: The haul trucks transport the ore to various areas for processing. The grade and type of ore determine the processing method used. Higher-grade ores are taken to a mill. Lower grade ores are taken to leach pads. Some ores may be stockpiled for later processing. HEAP LEACHING: The ore is crushed or placed directly on lined leach pads where a dilute cyanide solution is applied to the surface of the heap. The solution percolates down through the ore, where it leaches the gold and flows to a central collection location. The solution is recovered in this closed system. The pregnant leach solution is fed to electrowinning cells and undergoes the same steps as described below from Electro-winning. ORE PROCESSING: Milling: The ore is fed into a series of grinding mills where steel balls grind the ore to a fine slurry or powder. Oxidization and leaching: Some types of ore require further processing before gold is recovered. In this case, the slurry is pressure-oxidized in an autoclave before going to the leaching tanks or a dry powder is fed through a roaster in which it is oxidized using heat before being sent to the leaching tanks as a slurry. The slurry is thickened and runs through a series of leaching tanks. The gold in the slurry adheres to carbon in the tanks. Stripping: The carbon is then moved into a stripping vessel where the gold is removed from the carbon by pumping a hot caustic solution through the carbon. The carbon is later recycled. Electro-winning: The gold-bearing solution is pumped through electro-winning cells or through a zinc precipitation circuit where the gold is recovered from the solution. Smelting: The gold is then melted in a furnace at about 1’064°C and poured into moulds, creating doré bars. Doré bars are unrefined gold bullion bars containing between 60% and 95% gold. References: Newmont (2004) How gold is mined. Newmont. Retrieved from http://www.newmont.com/en/gold/howmined/index.asp technologyComment of primary lead production from concentrate (GLO): There are two basic pyrometallurgical processes available for the production of lead from lead or mixed lead-zinc-sulphide concentrates: sinter oxidation / blast furnace reduction route or Direct Smelting Reduction Processes. Both processes are followed by a refining step to produce the final product with the required purity, and may also be used for concentrates mixed with secondary raw materials. SINTER OXIDATION / BLAST FURNACE REDUCTION: The sinter oxidation / blast furnace reduction involves two steps: 1) A sintering oxidative roast to remove sulphur with production of PbO; and 2) Blast furnace reduction of the sinter product. The objective of sintering lead concentrates is to remove as much sulphur as possible from the galena and the accompanying iron, zinc, and copper sulphides, while producing lump agglomerate with appropriate properties for subsequent reduction in the blast furnace (a type of a shaft furnace). As raw material feed, lead concentrates are blended with recycled sinter fines, secondary material and other process materials and pelletised in rotating drums. Pellets are fed onto sinter machine and ignited. The burning pellets are conveyed over a series of wind-boxes through which air is blown. Sulphur is oxidised to sulphur dioxide and the reaction generates enough heat to fuse and agglomerate the pellets. Sinter is charged to the blast furnace with metallurgical coke. Air and/or oxygen enriched air is injected and reacts with the coke to produce carbon monoxide. This generates sufficient heat to melt the charge. The gangue content of the furnace charge combines with the added fluxes or reagents to form a slag. For smelting bulk lead-zinc-concentrates and secondary material, frequently the Imperial Smelting Furnace is used. Here, hot sinter and pre-heated coke as well as hot briquettes are charged. Hot air is injected. The reduction of the metal oxides not only produces lead and slag but also zinc, which is volatile at the furnace operating temperature and passes out of the ISF with the furnace off-gases. The gases also contain some cadmium and lead. The furnace gases pass through a splash condenser in which a shower of molten lead quenches them and the metals are absorbed into the liquid lead, the zinc is refined by distillation. DIRECT SMELTING REDUCTION: The Direct Smelting Reduction Process does not carry out the sintering stage separately. Lead sulphide concentrates and secondary materials are charged directly to a furnace and are then melted and oxidised. Sulphur dioxide is formed and is collected, cleaned and converted to sulphuric acid. Carbon (coke or gas) and fluxing agents are added to the molten charge and lead oxide is reduced to lead, a slag is formed. Some zinc and cadmium are “fumed” off in the furnace, their oxides are captured in the abatement plant and recovered. Several processes are used for direct smelting of lead concentrates and some secondary material to produce crude lead and slag. Bath smelting processes are used: the ISA Smelt/Ausmelt furnaces (sometimes in combination with blast furnaces), Kaldo (TBRC) and QSL integrated processes are used in EU and Worldwide. The Kivcet integrated process is also used and is a flash smelting process. The ISA Smelt/Ausmelt furnaces and the QSL take moist, pelletised feed and the Kaldo and Kivcet use dried feed. REFINING: Lead bullion may contain varying amounts of copper, silver, bismuth, antimony, arsenic and tin. Lead recovered from secondary sources may contain similar impurities, but generally antimony and calcium dominate. There are two methods of refining crude lead: electrolytic refining and pyrometallurgical refining. Electrolytic refining uses anodes of de-copperised lead bullion and starter cathodes of pure lead. This is a high-cost process and is used infrequently. A pyrometallurgical refinery consists of a series of kettles, which are indirectly heated by oil or gas. Over a series of separation processes impurities and metal values are separated from the lead bouillon. Overall waste: The production of metals is related to the generation of several by-products, residues and wastes, which are also listed in the European Waste Catalogue (Council Decision 94/3/EEC). The ISF or direct smelting furnaces also are significant sources of solid slag. This slag has been subjected to high temperatures and generally contains low levels of leachable metals, consequently it may be used in construction. Solid residues also arise as the result of the treatment of liquid effluents. The main waste stream is gypsum waste (CaSO4) and metal hydroxides that are produced at the wastewater neutralisation plant. These wastes are considered to be a cross-media effect of these treatment techniques but many are recycled to pyrometallurgical process to recover the metals. Dust or sludge from the treatment of gases are used as raw materials for the production of other metals such as Ge, Ga, In and As, etc or can be returned to the smelter or into the leach circuit for the recovery of lead and zinc. Hg/Se residues arise at the pre-treatment of mercury or selenium streams from the gas cleaning stage. This solid waste stream amounts to approximately 40 - 120 t/y in a typical plant. Hg and Se can be recovered from these residues depending on the market for these metals. Overall emissions: The main emissions to air from zinc and lead production are sulphur dioxide, other sulphur compounds and acid mists; nitrogen oxides and other nitrogen compounds, metals and their compounds; dust; VOC and dioxins. Other pollutants are considered to be of negligible importance for the industry, partly because they are not present in the production process and partly because they are immediately neutralised (e.g. chlorine) or occur in very low concentrations. Emissions are to a large extent bound to dust (except cadmium, arsenic and mercury that can be present in the vapour phase). Metals and their compounds and materials in suspension are the main pollutants emitted to water. The metals concerned are Zn, Cd, Pb, Hg, Se, Cu, Ni, As, Co and Cr. Other significant substances are fluorides, chlorides and sulphates. Wastewater from the gas cleaning of the smelter and fluid-bed roasting stages are the most important sources. References: Sutherland C. A., Milner E. F., Kerby R. C., Teindl H. and Melin A. (1997) Lead. In: Ullmann's encyclopedia of industrial chemistry (ed. Anonymous). 5th edition on CD-ROM Edition. Wiley & Sons, London. IPPC (2001) Integrated Pollution Prevention and Control (IPPC); Reference Document on Best Available Techniques in the Non Ferrous Metals Industries. European Commission. Retrieved from http://www.jrc.es/pub/english.cgi/ 0/733169 technologyComment of primary zinc production from concentrate (RoW): The technological representativeness of this dataset is considered to be high as smelting methods for zinc are consistent in all regions. Refined zinc produced pyro-metallurgically represents less than 5% of global zinc production and less than 2% of this dataset. Electrometallurgical Smelting The main unit processes for electrometallurgical zinc smelting are roasting, leaching, purification, electrolysis, and melting. In both electrometallurgical and pyro-metallurgical zinc production routes, the first step is to remove the sulfur from the concentrate. Roasting or sintering achieves this. The concentrate is heated in a furnace with operating temperature above 900 °C (exothermic, autogenous process) to convert the zinc sulfide to calcine (zinc oxide). Simultaneously, sulfur reacts with oxygen to produce sulfur dioxide, which is subsequently converted to sulfuric acid in acid plants, usually located with zinc-smelting facilities. During the leaching process, the calcine is dissolved in dilute sulfuric acid solution (re-circulated back from the electrolysis cells) to produce aqueous zinc sulfate solution. The iron impurities dissolve as well and are precipitated out as jarosite or goethite in the presence of calcine and possibly ammonia. Jarosite and goethite are usually disposed of in tailing ponds. Adding zinc dust to the zinc sulfate solution facilitates purification. The purification of leachate leads to precipitation of cadmium, copper, and cobalt as metals. In electrolysis, the purified solution is electrolyzed between lead alloy anodes and aluminum cathodes. The high-purity zinc deposited on aluminum cathodes is stripped off, dried, melted, and cast into SHG zinc ingots (99.99 % zinc). Pyro-metallurgical Smelting The pyro-metallurgical smelting process is based on the reduction of zinc and lead oxides into metal with carbon in an imperial smelting furnace. The sinter, along with pre-heated coke, is charged from the top of the furnace and injected from below with pre-heated air. This ensures that temperature in the center of the furnace remains in the range of 1000-1500 °C. The coke is converted to carbon monoxide, and zinc and lead oxides are reduced to metallic zinc and lead. The liquid lead bullion is collected at the bottom of the furnace along with other metal impurities (copper, silver, and gold). Zinc in vapor form is collected from the top of the furnace along with other gases. Zinc vapor is then condensed into liquid zinc. The lead and cadmium impurities in zinc bullion are removed through a distillation process. The imperial smelting process is an energy-intensive process and produces zinc of lower purity than the electrometallurgical process. technologyComment of treatment of electronics scrap, metals recovery in copper smelter (SE, RoW): Conversion of Copper in a Kaldo Converter and treatment in converter aisle. technologyComment of treatment of scrap lead acid battery, remelting (RoW): The referred operation uses a shaft furnace with post combustion, which is the usual technology for secondary smelters. technologyComment of treatment of scrap lead acid battery, remelting (RER): The referred operation uses a shaft furnace with post combustion, which is the usual technology for secondary smelters. Typically this technology produces 5000 t / a sulphuric acid (15% concentration), 25’000 t lead bullion (98% Pb), 1200 t / a slags (1% Pb) and 3000 t / a raw lead matte (10% Pb) to be shipped to primary smelters. Overall Pb yield is typically 98.8% at the plant level and 99.8% after reworking the matte. The operation treats junk batteries and plates but also lead cable sheathing, drosses and sludges, leaded glass and balancing weights. From this feed it manufactures mainly antimonial lead up to 10% Sb, calcium-aluminium lead alloys with or without tin and soft lead with low and high copper content. All these products are the result of a refining and alloying step to meet the compliance with the designations desired. The following by products are reused in the process: fine dust, slag, and sulfuric acid. References: Quirijnen L. (1999) How to implement efficient local lead-acid battery recycling. In: Journal of Power Sources, 78(1-2), pp. 267-269.
technologyComment of cobalt production (GLO): Cobalt, as a co-product of nickel and copper production, is obtained using a wide range of technologies. The initial life cycle stage covers the mining of the ore through underground or open cast methods. The ore is further processed in beneficiation to produce a concentrate and/or raffinate solution. Metal selection and further concentration is initiated in primary extraction, which may involve calcining, smelting, high pressure leaching, and other processes. The final product is obtained through further refining, which may involve processes such as re-leaching, selective solvent / solution extraction, selective precipitation, electrowinning, and other treatments. Transport is reported separately and consists of only the internal movements of materials / intermediates, and not the movement of final product. Due to its intrinsic value, cobalt has a high recycling rate. However, much of this recycling takes place downstream through the recycling of alloy scrap into new alloy, or goes into the cobalt chemical sector as an intermediate requiring additional refinement. Secondary production, ie production from the recycling of cobalt-containing wastes, is considered in this study in so far as it occurs as part of the participating companies’ production. This was shown to be of very limited significance (less than 1% of cobalt inputs). The secondary materials used for producing cobalt are modelled as entering the system free of environmental burden. technologyComment of natural gas production (CA-AB): Canadian data completed with german data. The uncertainty has been adjusted accordingly. Data used in original data contains no information on technology. technologyComment of natural gas production (DE): Data in environmental report contains no information on technology. technologyComment of natural gas production (RoW): The data describes an average onshore technology for natural gas to 13% out of combined oil gas production. Natural gas is assumed to 20% sour. Leakage in exploitation is estimated at 0.38% and production 0.12%. It is further assumed that about 30% of the produced water is discharged in surface water. Water emissions are differentiated between combined oil and gas production and gas production. technologyComment of natural gas production (RU): The data describes an average onshore technology for natural gas with a share of 4% out of combined oil gas production and 96% from mere natural gas production. Natural gas is assumed to 20% sour. It is assumed that about 30% of the produced water is discharged in surface water. Water emissions are differentiated between combined oil and gas production and gas production. technologyComment of natural gas production (US): US data (NREL) for emissions completed with german data. Emissions from NREL include combined production (petroleumm and gas) and off-shore production. The uncertainty has been adjusted accordingly. Data used in original data contains no information on technology. technologyComment of petroleum refinery operation (CH): Average data for the used technology. technologyComment of primary zinc production from concentrate (RoW): The technological representativeness of this dataset is considered to be high as smelting methods for zinc are consistent in all regions. Refined zinc produced pyro-metallurgically represents less than 5% of global zinc production and less than 2% of this dataset. Electrometallurgical Smelting The main unit processes for electrometallurgical zinc smelting are roasting, leaching, purification, electrolysis, and melting. In both electrometallurgical and pyro-metallurgical zinc production routes, the first step is to remove the sulfur from the concentrate. Roasting or sintering achieves this. The concentrate is heated in a furnace with operating temperature above 900 °C (exothermic, autogenous process) to convert the zinc sulfide to calcine (zinc oxide). Simultaneously, sulfur reacts with oxygen to produce sulfur dioxide, which is subsequently converted to sulfuric acid in acid plants, usually located with zinc-smelting facilities. During the leaching process, the calcine is dissolved in dilute sulfuric acid solution (re-circulated back from the electrolysis cells) to produce aqueous zinc sulfate solution. The iron impurities dissolve as well and are precipitated out as jarosite or goethite in the presence of calcine and possibly ammonia. Jarosite and goethite are usually disposed of in tailing ponds. Adding zinc dust to the zinc sulfate solution facilitates purification. The purification of leachate leads to precipitation of cadmium, copper, and cobalt as metals. In electrolysis, the purified solution is electrolyzed between lead alloy anodes and aluminum cathodes. The high-purity zinc deposited on aluminum cathodes is stripped off, dried, melted, and cast into SHG zinc ingots (99.99 % zinc). Pyro-metallurgical Smelting The pyro-metallurgical smelting process is based on the reduction of zinc and lead oxides into metal with carbon in an imperial smelting furnace. The sinter, along with pre-heated coke, is charged from the top of the furnace and injected from below with pre-heated air. This ensures that temperature in the center of the furnace remains in the range of 1000-1500 °C. The coke is converted to carbon monoxide, and zinc and lead oxides are reduced to metallic zinc and lead. The liquid lead bullion is collected at the bottom of the furnace along with other metal impurities (copper, silver, and gold). Zinc in vapor form is collected from the top of the furnace along with other gases. Zinc vapor is then condensed into liquid zinc. The lead and cadmium impurities in zinc bullion are removed through a distillation process. The imperial smelting process is an energy-intensive process and produces zinc of lower purity than the electrometallurgical process. technologyComment of rare earth oxides production, from rare earth oxide concentrate, 70% REO (CN-SC): This dataset refers to the separation (hydrochloric acid leaching) and refining (metallothermic reduction) process used in order to produce high-purity rare earth oxides (REO) from REO concentrate, 70% beneficiated. ''The concentrate is calcined at temperatures up to 600ºC to oxidize carbonaceous material. Then HCl leaching, alkaline treatment, and second HCl leaching is performed to produce a relatively pure rare earth chloride (95% REO). Hydrochloric acid leaching in Sichuan is capable of separating and recovering the majority of cerium oxide (CeO) in a short process. For this dataset, the entire quantity of Ce (50% cerium dioxide [CeO2]/REO) is assumed to be produced here as CeO2 with a grade of 98% REO. Foreground carbon dioxide CO2 emissions were calculated from chemical reactions of calcining beneficiated ores. Then metallothermic reduction produces the purest rare earth metals (99.99%) and is most common for heavy rare earths. The metals volatilize, are collected, and then condensed at temperatures of 300 to 400°C (Chinese Ministryof Environmental Protection 2009).'' Source: Lee, J. C. K., & Wen, Z. (2017). Rare Earths from Mines to Metals: Comparing Environmental Impacts from China's Main Production Pathways. Journal of Industrial Ecology, 21(5), 1277-1290. doi:10.1111/jiec.12491 technologyComment of scandium oxide production, from rare earth tailings (CN-NM): See general comment. technologyComment of sulfur production, petroleum refinery operation (Europe without Switzerland): The technology level in Europe applied here represents a weighted average of BREF types II (62%), III (29%), IV (9%) refineries; API 35; sulfur content 1.03%. technologyComment of sulfur production, petroleum refinery operation (PE): The technology represents BREF type II refinery; API 25; sulfur content 0.51% technologyComment of sulfur production, petroleum refinery operation (BR): The technology represents BREF type II refinery; API 25; sulfur content 0.57% technologyComment of sulfur production, petroleum refinery operation (ZA): The technology represents a weighted average of BREF types II and III refineries; API 35; sulfur content 0.7% technologyComment of sulfur production, petroleum refinery operation (CO): The technology represents a weighted average of BREF types II and IV refineries; API 35; sulfur content 0.56% technologyComment of sulfur production, petroleum refinery operation (IN): The technology represents a weighted average of BREF types II and IV refineries; API 35; sulfur content 1.39% technologyComment of sulfur production, petroleum refinery operation (RoW): This dataset represents the prevailing technology level in Europe, this is a weighted average of BREF complexity types II (62%), III (29%), IV (9%) refineries (see BREF document, European Commission, 2015); API 35; sulfur content 1.03%. Reference(s): European Commission (2015) Best Available Techniques (BAT) Reference Document (BREF) for the Refining of Mineral Oil and Gas, Industrial Emissions Directive 2010/75/EU Integrated Pollution Prevention and control, accessible online at http://eippcb.jrc.ec.europa.eu/reference/BREF/REF_BREF_2015.pdf, February 2019 technologyComment of synthetic fuel production, from coal, high temperature Fisher-Tropsch operations (ZA): SECUNDA SYNFUEL OPERATIONS: Secunda Synfuels Operations operates the world’s only commercial coal-based synthetic fuels manufacturing facility of its kind, producing synthesis gas (syngas) through coal gasification and natural gas reforming. They make use of their proprietary technology to convert syngas into synthetic fuel components, pipeline gas and chemical feedstock for the downstream production of solvents, polymers, comonomers and other chemicals. Primary internal customers are Sasol Chemicals Operations, Sasol Exploration and Production International and other chemical companies. Carbon is produced for the recarburiser, aluminium, electrode and cathodic production markets. Secunda Synfuels Operations receives coal from five mines in Mpumalanga (see figure attached). After being crushed, the coal is blended to obtain an even quality distribution. Electricity is generated by both steam and gas and used to gasify the coal at a temperature of 1300°C. This produces syngas from which two types of reactor - circulating fluidised bed and Sasol Advanced SynthoTM reactors – produce components for making synthetic fuels as well as a number of downstream chemicals. Gas water and tar oil streams emanating from the gasification process are refined to produce ammonia and various grades of coke respectively. imageUrlTagReplacea79dc0c2-0dda-47ec-94e0-6f076bc8cdb6 SECUNDA CHEMICAL OPERATIONS: The Secunda Chemicals Operations hub forms part of the Southern African Operations and is the consolidation of all the chemical operating facilities in Secunda, along with Site Services activities. The Secunda Chemicals hub produces a diverse range of products that include industrial explosives, fertilisers; polypropylene, ethylene and propylene; solvents (acetone, methyl ethyl ketone (MEK), ethanol, n-Propanol, iso-propanol, SABUTOL-TM, PROPYLOL-TM, mixed C3 and C4 alcohols, mixed C5 and C6 alcohols, High Purity Ethanol, and Ethyl Acetate) as well as the co-monomers, 1-hexene, 1-pentene and 1-octene and detergent alcohol (SafolTM).
technologyComment of cobalt production (GLO): Cobalt, as a co-product of nickel and copper production, is obtained using a wide range of technologies. The initial life cycle stage covers the mining of the ore through underground or open cast methods. The ore is further processed in beneficiation to produce a concentrate and/or raffinate solution. Metal selection and further concentration is initiated in primary extraction, which may involve calcining, smelting, high pressure leaching, and other processes. The final product is obtained through further refining, which may involve processes such as re-leaching, selective solvent / solution extraction, selective precipitation, electrowinning, and other treatments. Transport is reported separately and consists of only the internal movements of materials / intermediates, and not the movement of final product. Due to its intrinsic value, cobalt has a high recycling rate. However, much of this recycling takes place downstream through the recycling of alloy scrap into new alloy, or goes into the cobalt chemical sector as an intermediate requiring additional refinement. Secondary production, ie production from the recycling of cobalt-containing wastes, is considered in this study in so far as it occurs as part of the participating companies’ production. This was shown to be of very limited significance (less than 1% of cobalt inputs). The secondary materials used for producing cobalt are modelled as entering the system free of environmental burden. technologyComment of platinum group metal mine operation, ore with high palladium content (RU): imageUrlTagReplace6250302f-4c86-4605-a56f-03197a7811f2 technologyComment of platinum group metal, extraction and refinery operations (ZA): The ores from the different ore bodies are processed in concentrators where a PGM concentrate is produced with a tailing by product. The PGM base metal concentrate product from the different concentrators processing the different ores are blended during the smelting phase to balance the sulphur content in the final matte product. Smelter operators also carry out toll smelting from third part concentrators. The smelter product is send to the Base metal refinery where the PGMs are separated from the Base Metals. Precious metal refinery is carried out on PGM concentrate from the Base metal refinery to split the PGMs into individual metal products. Water analyses measurements for Anglo Platinum obtained from literature (Slatter et.al, 2009). Mudd, G., 2010. Platinum group metals: a unique case study in the sustainability of mineral resources, in: The 4th International Platinum Conference, Platinum in Transition “Boom or Bust.” Water share between MC and EC from Mudd (2010). Mudd, G., 2010. Platinum group metals: a unique case study in the sustainability of mineral resources, in: The 4th International Platinum Conference, Platinum in Transition “Boom or Bust.” technologyComment of processing of nickel-rich materials (GLO): Based on typical current technology. technologyComment of smelting and refining of nickel concentrate, 16% Ni (GLO): Extrapolated from a typical technology for smelting and refining of nickel ore. MINING: 95% of sulphidic nickel ores are mined underground in depths between 200m and 1800m, the ore is transferred to the beneficiation. Widening of the tunnels is mainly done by blasting. The overburden – material, which does not contain PGM-bearing ore – is deposed off-site and is partially refilled into the tunnels. Emissions: The major emissions are due to mineral born pollutants in the effluents. The underground mining operations generate roughly 80 % of the dust emissions from open pit operations, since the major dust sources do not take place underground. Rain percolate through overburden and accounts to metal emissions to groundwater. Waste: Overburden is deposed close to the mine. Acid rock drainage occurs over a long period of time. BENEFICIATION: After mining, the ore is first ground. In a next step it is subjected to gravity concentration to separate the metallic particles from the PGM-bearing minerals. After this first concentration step, flotation is carried out to remove the gangue from the sulphidic minerals. For neutralisation lime is added. In the flotation several organic chemicals are used as collector, frother, activator, depressor and flocculant. Sometimes cyanide is used as depressant for pyrite. Tailings usually are led to tailing heaps or ponds. As a result, nickel concentrates containing 7 - 25% Ni are produced. Emissions: Ore handling and processing produce large amounts of dust, containing PM10 and several metals from the ore itself. Flotation produce effluents containing several organic agents used. Some of these chemicals evaporate and account for VOC emissions to air. Namely xanthates decompose hydrolytically to release carbon disulphide. Tailings effluent contains additional sulphuric acid from acid rock drainage. Waste: Tailings are deposed as piles and in ponds. Acid rock drainage occurs over a long period of time. METALLURGY AND REFINING: There are many different process possibilities to win the metal. The chosen process depends on the composition of the ore, the local costs of energy carrier and the local legislation. Basically two different types can be distinguished: the hydrometallurgical and the pyrometallurgical process, which paired up with the refining processes, make up five major production routes (See Tab.1). All this routes are covered, aggregated according to their market share in 1994. imageUrlTagReplace00ebef53-ae97-400f-a602-7405e896cb76 Pyrometallurgy. The pyrometallurgical treatment of nickel concentrates includes three types of unit operation: roasting, smelting, and converting. In the roasting step sulphur is driven off as sulphur dioxide and part of the iron is oxidised. In smelting, the roaster product is melted with a siliceous flux which combines with the oxidised iron to produce two immiscible phases, a liquid silicate slag which can be discarded, and a solution of molten sulphides which contains the metal values. In the converting operation on the sulphide melt, more sulphur is driven off as sulphur dioxide, and the remaining iron is oxidised and fluxed for removal as silicate slag, leaving a high-grade nickel – copper sulphide matte. In several modern operations the roasting step has been eliminated, and the nickel sulphide concentrate is treated directly in the smelter. Hydrometallurgy: Several hydrometallurgical processes are in commercial operation for the treatment of nickel – copper mattes to produce separate nickel and copper products. In addition, the hydrometal-lurgical process developed by Sherritt Gordon in the early 1950s for the direct treatment of nickel sulphide concentrates, as an alternative to smelting, is still commercially viable and competitive, despite very significant improvements in the economics and energy efficiency of nickel smelting technology. In a typical hydrometallurgical process, the concentrate or matte is first leached in a sulphate or chloride solution to dissolve nickel, cobalt, and some of the copper, while the sulphide is oxidised to insoluble elemental sulphur or soluble sulphate. Frequently, leaching is carried out in a two-stage countercurrent system so that the matte can be used to partially purify the solution, for example, by precipitating copper by cementation. In this way a nickel – copper matte can be treated in a two-stage leach process to produce a copper-free nickel sulphate or nickel chloride solution, and a leach residue enriched in copper. Refining: In many applications, high-purity nickel is essential and Class I nickel products, which include electrolytic cathode, carbonyl powder, and hydrogen-reduced powder, are made by a variety of refining processes. The carbonyl refining process uses the property of nickel to form volatile nickel-carbonyl compounds from which elemental nickel subsides to form granules. Electrolytic nickel refineries treat cast raw nickel anodes in a electrolyte. Under current the anode dissolves and pure nickel deposits on the cathode. This electrorefining process is obsolete because of high energy demand and the necessity of building the crude nickel anode by reduction with coke. It is still practised in Russia. Most refineries recover electrolytic nickel by direct electrowinning from purified solutions produced by the leaching of nickel or nickel – copper mattes. Some companies recover refined nickel powder from purified ammoniacal solution by reduction with hydrogen. Emissions: In all of the metallurgical steps, sulphur dioxide is emitted to air. Recovery of sulphur dioxide is only economic for high concentrated off-gas. Given that In the beneficiation step, considerable amounts of lime are added to the ore for pH-stabilisation, lime forms later flux in the metallurgical step, and decomposes into CO2 to form calcite. Dust carry over from the roasting, smelting and converting processes. Particulate emissions to the air consist of metals and thus are often returned to the leaching process after treatment. Chlorine is used in some leaching stages and is produced during the subsequent electrolysis of chloride solution. The chlorine evolved is collected and re-used in the leach stage. The presence of chlorine in wastewater can lead to the formation of organic chlorine compounds (AOX) if solvents etc. are also present in a mixed wastewater. VOCs can be emitted from the solvent extraction stages. A variety of solvents are used an they contain various complexing agents to form complexes with the desired metal that are soluble in the organic layer. Metals and their compounds and substances in suspension are the main pollutants emitted to water. The metals concerned are Cu, Ni, Co, As and Cr. Other significant substances are chlorides and sulphates. Wastewater from wet gas cleaning (if used) of the different metallurgical stages are the most important sources. The leaching stages are usually operated on a closed circuit and drainage systems, and are therefore regarded as minor sources. In the refining step, the combustion of sulphur leads to emissions of SO2. Nitrogen oxides are produced in significant amounts during acid digestion using nitric acid. Chlorine and HCl can be formed during a number of digestion, electrolytic and purification processes. Chlorine is used extensively in the Miller process and in the dissolution stages using hydrochloric acid and chlorine mixtrues respectively. Dust and metals are generally emitted from incinerators and furnaces. VOC can be emitted from solvent extraction processes, while organic compounds, namely dioxins, can be emitted from smelting stages resulting from the poor combustion of oil and plastic in the feed material. All these emissions are subject to abatement technologies and controlling. Large quantities of effluents contain amounts of metals and organic substances. Waste: Regarding the metallurgical step, several co-products, residues and wastes, which are listed in the European Waste Catalogue, are generated. Some of the process specific residues can be reused or recovered in preliminary process steps (e. g. dross, filter dust) or construction (e. g. cleaned slag). Residues also arise from the treatment of liquid effluents, the main residue being gypsum waste and metal hydroxides from the wastewater neutralisation plant. These residuals have to be disposed, usually in lined ponds. In the refining step, quantities of solid residuals are also generated, which are mostly recycled within the process or sent to other specialists to recover any precious metals. Final residues generally comprise hydroxide filter cakes (ironhydroxide, 60% water, cat I industrial waste). References: Kerfoot D. G. E. (1997) Nickel. In: Ullmann's encyclopedia of industrial chemis-try (ed. Anonymous). 5th edition on CD-ROM Edition. Wiley & Sons, London. technologyComment of smelting and refining of nickel concentrate, 7% Ni (CN): The nickel concentrate (6.78% beneficiated - product of the mining and beneficiation processes) undergoes drying, melting in flash furnace and converting to produce high nickel matte. The nickel matte undergoes grinding-floating separation and is refined through anode plate casting and electrolysis in order to produce electrolytic nickel 99.98% pure. Deng, S. Y., & Gong, X. Z. (2018). Life Cycle Assessment of Nickel Production in China. Materials Science Forum, 913, 1004-1010. doi:10.4028/www.scientific.net/MSF.913.1004 technologyComment of treatment of metal part of electronics scrap, in copper, anode, by electrolytic refining (SE, RoW): Production of cathode copper by electrolytic refining.
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