Search Documents

By J. S. Jacobi

Treating copper ores by heap-leaching and similar hydrometallurgical means is a time-honored practice, which was well known even in the 19th century. Later the method lost ground to better ore dressing processes, particularly selective. flotation. More recently there has been a distinct reversion to leaching techniques, particularly for scavenging operations in old mining stopes, in connection with LPF systems, irrigation of tailings dumps and similar situations. These hydrometallurgical techniques will gain further ground because processing is simple and permits better extraction of copper, particularly from low-grade or partly oxidized ores. In the lixiviation of primary ores at some major operations, copper-bearing liquors may undergo re-circulation in heap-leaching arrangements or the ores may be subjected to systematic percolation treatment. The liquors resulting from this source usually are quite strong (above 10 gpl copper) and copper would normally be reclaimed by electrowinning or cementation. These processes fall out- side the scope of this paper which is concerned with recovery of copper from weak 1iquor.s containing from 0.1 to about 3 gpl copper.

Jan 9, 1963

Copper entering a lead ,smelter in concentrate or from other sources is recoVered as matte and speiss which contain appreciable quantities of lead. The matte and speiss are usually sold to copper smelters to recover the copper content and also any gold and silver in these products, but the value of the lead is largely lost. Some copper plants pay for portion of the lead content, but regarded as a means of recovering lead it is more costly and less efficient than if the lead were recovered at the lead smelter.Because of the value of this lead loss, the metallurgy of copper recovery has assumed greater importance in recent years owing to the rise on the price of lead.Two processes are in use today to produce matte and speiss, namely the iron matte process and the soda matte process developed by the American Smelting and Refining Co. 1 in D.S.A. The latter process is characterised by a higher copper to lead ratio than the older iron matting process.The following analyses are typical of matte and speiss produced at Broken Hill Associated Smelters, by both processes, although the soda matte process is still in a developmental stage and experience indicates that matte and speiss of lower lead tenor can be produced under favourable conditions.

Jan 1, 1951

By Chao Li, Shi Sun, Hongxu Li, Jiaqi Fan, Liangtian Wei

Aiming at the recovery of copper from smelting slag, a flotation approach was studied. It was found that this slag composed of fine particles with complex association and distribution, in which bornite was the main copper-bearing mineral after a detailed mineralogy analysis via polarizing microscope, SEM and XRD. Consequently, flotation was attempted to recycle Cu in slag containing copper sulphide components. Three key factors affecting flotation were ascertained, namely, grinding fineness, the collector and the pH value, while the recovery of Cu estimated by ICP and XRF. Copper concentrate grading at 14.47 with 79.66% Cu recovery was obtained, in the condition of the grinding fineness of −0.074 mm and the proportion of 80%, reagent dosages of 50 g/t for butyl xanthate and a pH value of 10 adjusted using Na2CO3.

Mar 1, 2017

By D. R. George

Preliminary research has identified several organic and aqueous solutions that are effective absorbents for SO, from simulated smelter gas containing 0.3 to 2% SO2. These SO2 loaded solutions are also compatible to the reaction of H2S and SO2 to precipitate a readily filtered elemental sulfur. The economic removal of SO2 and production of elemental sulfur from stack gases discharged by base- metal smelters is a challenging goal. The magnitude of this task is illustrated by the estimate that about 3.5 million tons of SO2 are discharged to the atmosphere by smelters annually in the U.S. The SO2 concentration of the gases ranges from about 0.5 to more than 3%. As the sulfur content of SO2 is 50% a potential production of 1,750,000 tons of sulfur per year is indicated.

Jan 1, 1970

By R. W. Bruce, K. W. Downes

"IntroductionSULPHUR production in Canada from all sources for the year 1953 amounted to about 375,000 tons. Except for 16,000 tons of elemental sulphur derived from natural gas, this production was in the form of by-product pyrites, liquid sulphur dioxide, and sulphuric acid. In the same year, Canadian industry imported 359,000 tons of elemental sulphur from the United States. The cost, including transportation charges, to Canadian consuming plants ranged from $35.00 to $45.00 per long ton, depending upon location.Although most of the sulphur consumed is used in the oxidized form it is often most convenient to buy sulphur in the elemental form, and convert it to sulphur dioxide or sulphuric acid in situ as required. This is because elemental sulphur is easily shipped and stored, weighs only half as much as an equivalent quantity of sulphur dioxide and one-third as much as the corresponding quantity of sulphuric acid, and is readily converted to these forms in a sulphur burner. A process, therefore, which could economically recover elemental sulphur from sulphide ores would be most attractive.Since the turn of the century, notable improvements have been made in extractive metallurgy, but until recently only limited attention has been paid to the possibilities of elemental sulphur recovery. This has been due to the plentiful supplies of cheaply mined Frasch sulphur which have been available on the world markets."

Jan 1, 1955

By A. M. Abouzeid, S. Chander, D. W. Fuerstenau

Today numerous ores contain valuable minerals in finely disseminated form; and although the recovery of these fine mineral particles is generally exceedingly difficult, diminishing raw material resources necessitates the recovery of such mineral values. In many systems, the efficiency of recovering fine particles is still extremely low and often fine particles must be discarded as slimes. However, in recent years, various advances have taken place in the recovery of mineral particles in the very fine size range. In this paper, the background and performance of a number of processes for fine particle processing and separation are reviewed and discussed, particularly from the point of view of how fine particle recovery might be improved.

Jan 1, 1979

By Keith Sarbutt, I. Jackman

The recovery of gold from a high grade telluride/sulphide flotation concentrate was investigated. Conventional cyanidation resulted in very slow rates of gold extraction. Historically, the refractory nature of tellurides has been overcome by fine grinding, the use of excess lime and long leach times. In some instances, pre­oxidation of the tellurides has also been necessary, to render the gold soluble in cyanide solutions. The former conditions did improve the rate of gold extraction from the present sample, but final recovery was still unacceptable. Chemical oxidation of the tellurides and leaching with oxygen improved gold recovery further. However, it was found that simple modifications to the cyanidation conditions overcame the detrimental effects of the complex chemistry involved in leaching a telluride concentrate. The incorporation of a solution change, or the application of a carbon-in-leach procedure increased the recovery of gold to over 97 percent in 96 hours. In every case, leaching was enhanced by the addition of lead salts.

Jan 1, 1990

By J. B. Hiskey, X. H. Jiang

The extraction of gold from chloride solutions by ion exchange is examined. It is shown that at initial gold concentrations between 1 - 5 ppm, 20 g/l C1- and pH 5, the kinetics of loading on weak base resins are slightly slower than those observed with activated charcoal. Equilibrium loading of auric chloride varies considerably as a function of pH from one resin to another. For all of the resins studied, nearly complete gold extraction was achieved between pH 2 and pH 6.5. Sodium hypochlorite was found to exhibit a slight effect on the equilibrium loading of gold chloride.

Jan 1, 1990

By P. D. Kondos, J. R. Goode

Given the global inventory of low grade and refractory gold deposits, processes that could turn these challenged deposits into mines are of considerable interest. Such gold deposits have low value and potentially high operating costs and so they pose special challenges for the mining engineer and metallurgist. Conventionally, refractory gold ores have been processed by whole ore pressure oxidation and roasting, or flotation followed by roasting, pressure oxidation or bio-oxidation of the concentrate. Halide-based processes have recently been developed that might be applied to concentrates. Low grade refractory gold ores have been processed using heap bio-oxidation followed by cyanide heap leaching or milling. Other processes are emerging. Barrick has completed an inventory of emerging technologies (1). A summary of the current status of these developments will be presented with the view that, with additional development, some of these technologies or a combination thereof may unlock the value of these deposits.

Jan 1, 2005

Ion exchange resins are an attractive alternative to activated carbon in both column and resin-in-pulp processes for the recovery of gold from cyanide solution. Resins are widely used for this purpose in the Soviet Union apparently in preference to activated carbons.A wide range of resins are available and the high level of resin technology is demon-strated in the resin processes used to recover uranium.The anionic gold complex, Au(CN) 2 , is selectively adsorbed onto weak and strong base resins. However other anionic cyanide complexes, cyanide ions and other anions from the process water are also adsorbed onto resin sites. Resin selectively for gold is not as high as it is for activated carbons. As a result similar gold loading capacities are obtained for resins and carbons when used in plant liquors.

Jan 1, 1984

By R. J. Davidson, B. Strong

The piloting and eventual large-scale operation of fixed-bed carbon columns for the recovery of gold from plant effluents is described. A fixed-bed carbon pilot plant comprising three adsorption columns was used for the recovery of gold from clarified plant effluent at the Vaal Reefs Exploration and Mining Company (West Division). The effluent ,which contained 0,1 toO,S g/t of gold and less than 10 g/t of free cyanide, was adjusted to pH 8 prior to use. Daily acid treatment of the carbon circuit with 3 per cent hydrochloric acid was shown to have a most significant effect on increasing the gold adsorption. The acid treatment involved a plant downtime of only I to 2 minutes per day. High loadings of gold (up to 30 k g/t) and copper (up to 75 k g/t) were obtained on the leading column, while the gold recoveries averaged 98 per cent over 17 weeks of continuous operation. The subsequent elution of loaded carbon in a pilot elution column indicated the use of abnormally high amounts of the pretreatment reagent (caustic soda and cyanide) used in gold elution. This was attributed to the high loading of copper on the carbon. However, the elution of both the gold and the copper at 110°C with demineralized water as the eluant was satisfactory. In a similar large-scale operation, three fixed-bed carbon columns each containing 4,5 t of carbon were used to treat 80 to 120 t/h of plant effluent with a gold concentration of about 0,15 g/t. Gold loadings of 5 to 6 k g/t were obtained regularly, while the gold recovery averaged 97 per cent over a 12-month period. The capital cost of the plant was recovered in 2 to 3 months. The evidence presented strongly suggests that copper plays a significant role in the adsorption and elution of gold under the prescribed conditions, and in the subsequent precipitation of gold following acidification of the eluates. The formation of a highly insoluble gold-copper complex produced under acid conditions appears to explain many of the observations made in the investigation.

Jan 1, 1983

By R. J. Davidson, W. D. Douglas, J. A. Tumilty

SYNOPSIS Two pilot plants operating on different types of carbon were used to generate steady-state adsorption data in the treatment of gold-plant solutions of high and low tenor. A pilot plant comprising three 4 m long columns and using 3 mm extruded activated carbon was used to treat pregnant solutions with a gold concentration of 5 to 8 g/t at pH 10 to 11,5. Column influent was pumped at a super¬ficial flow velocity of 0,5 m/min while the carbon was moved daily so as to effect gold loadings on the carbon of 5 to 10 k /t. With a carbon-bed depth of 12 m, an adsorption efficiency of 99,9 per cent was obtained in a bed depth of 9 m, which was subsequently reduced to 8 m when the depth of the carbon bed was reduced to 8 m. This improvement in efficiency was attributed to the reduced residence time of the carbon from 12 to 8 days. A corresponding decrease in adsorbed silica indicated that some silica fouling of the carbon had occurred. A second pilot plant, comprising a single column 6 m in length and using coconut-shell carbon of 1,0 to 2,4 mm, treated a solution with a gold concentration of 0,7 g/t at pH 8,0. Feed solution was pumped at a superficial flow velocity of 1,0 m/min while carbon was moved every 8 hours to give gold loadings of more than 5 kg/t. An adsorp¬tion efficiency of 99,5 per cent was indicated at steady state. Intermittent washing of the column with dilute hydrochloric acid was shown to have a beneficial effect on the gold adsorption and to reduce the pressure drop across the column. Intermittent washing with dilute sulphuric acid indicated that there had been some passivation of the car¬bon during the treatment of a solution with a gold concentration of only 0,2 g/t. Compared with other adsorption systems, the countercurrent moving bed appears to offer significant advantages in terms of metallurgical efficiency and capital investment. The inability normally associated with moving-bed systems to treat solutions containing suspended solids may be overcome to a degree by the use of relatively coarse extrud¬ed carbon.

Jan 1, 1985

By J. P. R. deVilliers

A procedure is described whereby gold-containing calcined concentrates and leach residues from refractory gold ores are smelted with carbon to form a small amount of metal. The gold is liberated upon smelting, and is collected in the molten metallic phase, which is easily separable from the slag. The metallic phase consists of approximately 1 to 15 per cent (by mass) of the material after smelting, and the gold content is generally upgraded by a factor of greater than 6 compared with that of the original roasted material. Recoveries better than 95% have routinely been achieved. The quenched metal contains predominant Fe-Ni alloy, as well as minor Fe sulphides and Cu-Fe sulphides. Trace amounts of Fe-Ni arsenide and Au-Cu alloy are also present. The gold content of the metallic phase can be increased further by oxidation of the hot metal in the presence of silica or slag. This will reduce the amount of metal, and will concentrate the gold in a smaller volume. The metallic phase can then be treated hydrometallurgically to recover the nickel and the gold.

Jan 1, 1989

By L. P. Hendriks

Consolidated Murchison, the only antimony producer in South Africa, is situated in the northeastern part of Transvaal. Phalaborwa, an important copper/phosphate mining town is situated about 60 km to the east of Consolidated Murchison, on the border of the Kruger National Park. The mine is jointly controlled by Johannesburg Consolidated Investment Co. Ltd. (JCI) and Anglovaal Limited.

Jan 1, 1998

Refractory gold ores have been the subject of intensive metallurgical study in order to achieve more efficient recovery of contained values and at the same time to minimise environmental impact. Considerable innovative gold processing technology was introduced in New Zealand last century, the most notable being the first successful commercialisation of the cyanidation process by the Crown Mines Company at Karangahake in 1889. The Karangahake gold-silver deposit was second only +to the Waihi Martha mine in total bullion production from the region with active mining from 1882 until about 1920 and sporadic production between 1930 and 1944. Reevaluation at Karangahake with associated metallurgical testing has continued since that time becoming particularly active in the last decade as a result of increasing gold prices. Gold processing technology is reviewed and results of some recent test work are presented and discussed in the context of Karangahake history and future development possibilities. This work confirms the variability and complexity of the Karangahake deposit both mineralogically and metallurgically and suggests flotation followed by new and innovative smelting is the most appropriate processing route for the recovery of gold from the high grade ore which could be produced from the Karangahake workings in moderate tonnages.

Jan 1, 1993

By R. M. Enick

A novel liquid-liquid separation for the recovery of free or liberated gold from mixtures of fine particles was evaluated. The separation, conducted at ambient temperature and a pressure of about 1000 psi a, was based on the difference in wettability of precious metals and minerals. Contact angle results indicated that in the presence of water and liquid CO2, gold, platinum and silver had intermediate wettability. Minerals such as quartz and magnetite, however, were hydrophilic. Therefore fine gold particles. -325 mesh, that were mixed with water and liquid CO2 dispersed in the CO2 or agglomerated at the H2O-CO2 interface while the minerals tended to remain in the aqueous phase. Best results were obtained when these fine gold particles were liberated, were not agglomerated in slimes, were not adhering to minerals, and were not coated with minerals.

Jan 1, 1998

By Y. Wang, E. Forssberg

Wet magnetic separation methods for the recovery of hematite and chromite fines and ultrafines were investigated. These methods included wet high-intensity and high-gradient magnetic separation, carrier or "piggy-hack" magnetic separation, magnetic field-induced aggregation and magnetic seeding. This investigation indicated that wet magnetic separation is more efficient for fines and ultrafines. This investigation also indicated that other methods can be used to enhance the particle aggregation and/or the magnetic response. The magnetic behavior of these minerals with respect to the magnetizing field, temperature and particle size is also presented.

Jan 1, 1995

By Y. Wang

Wet magnetic separation methods for recovering hematite and chromite fines and ultrafines are investigated in this paper. These methods include wet high intensity and high gradient magnetic separations, carrier or "piggy-back" magnetic method, magnetic field-induced aggregation and magnetic seeding. This investigation indicates that wet magnetic separation is more efficient for fines and ultrafines whereas other methods can be used to enhance the particle aggregation and/or the magnetic response. The magnetic behaviour of these minerals with respect to magnetizing field, particle size and temperature is also presented.

Jan 1, 1993

By R. T. Um, W. K. Tolley, J. C. Stauter

A hydrometallurgical process for the recovery of lead from sulfide concentrates is presented The process combines the unit operations of selective dry chlormation, brine leaching and fused salt electrolysis as key steps An overview of the chemistry involved in the process 1s discussed as it pertains to overall recovery.

Jan 1, 1981

By Thomas Gliick, Jianming Lu, David Dreisinger

"The recovery of manganese from the Boleo project of Baja Mining is via an acid oxidation and acid reduction process in seawater. Manganese as manganese dioxide is leached into solution as manganese sulphate with the addition of sulphur dioxide gas as a reductant and then precipitated as a manganese carbonate. The use of the manganese carbonate intermediate to produce electrolytic manganese metal (EMM) has been extensively studied. The manganese carbonate can be used in place of natural (MnC03) or reduced ores (MnO) of manganese as a feed to the EMM plant. Manganese carbonate can be dissolved in spent electrolyte from manganese plating, followed by purification using ammonium sulphide precipitation of minor elements and then electrowinning in a selenium free process. The results of small cell testing of manganese electrowinning are reported.IntroductionThe Boleo Project of Baja Mining is a greenfields development currently under construction approximately 5 km north of the town of Santa Rosalia, Baja California Sur, Mexico. The Boleo property is held by the Mexican company, Minera y Metalurgica del Boleo S.A. de C. V. (MMB). MMB is owned 70% by Baja Mining Corp. and 30% by a consortium of Korean companies consisting of KORES - Korea Resources Corporation, LS Nikko Copper, Hyundai Hysco, SK Networks and lljin Copper.The Boleo deposit has Measured and Indicated resources of264.7 million tonnes grading 1.50% copper equivalent (CuEq) & Inferred resources of 159.9 million tonnes grading 1.15% CuEq. The calculation of copper equivalent is based on a combination of metal prices and predicted metallurgical recoveries (Table I). The metallurgical recoveries have been confined by extensive bench and pilot plant testing. Proven and probable reserves are available at Boleo to provide for more than a 30 year mine life. Initially, 25 years of mine life and 23 years of process plant operation have been scheduled in the February 2010 Technical Report Update (www.sedar.com)"

Jan 1, 2012