Academic literature on the topic 'Cyanide leaching'

To explore the relationship between total cyanide and easily liberatable cyanide in cyanide tailings and its impact on the environment, the leaching and release characteristics of total cyanide and easily liberatable cyanide in a tailings pond were studied using a dynamic leaching experiment, and a dynamic model was established. The results show that the release concentration of total cyanide in cyanide tailings is higher than that of easily liberatable cyanide. With the increase in leaching time, the release of cyanide is more sensitive to leaching intensity. The first-order kinetic, second-order kinetic, modified Elovich, double constant, and parabolic diffusion equations were used to fit the cumulative release of cyanide. According to the kinetic results of cyanide cumulative release, in addition to the first-order kinetic equation, the other four equations revealed good fitting for the cyanide leaching process, which shows that cyanide released under simulated rainwater leaching was not simply via surface diffusion, but controlled by multiple factors.

This study reached a gold ore which contain 3.83g/t gold, to investigate the available gold recover methods, direct cyanide leaching test and “biooxidation-cyanide” leaching process were utilized after enrich gold by flotation. When regrinding the flotation concentrate to 95% -325mm, the leaching rate of “biooxidation-cyanide” leaching reached 94.47%, compare with direct leaching, the leaching rate increased almost 67%. Obviously bacterium oxidation is a useful pretreatment for gold leaching.

HAT type cyanide leaching stirring tank increases gas-liquid mass transfer area to increase leaching speed through changing inflation mode. This article introduces the industrial experiment study situation of HAT6065 cyanide leaching stirring tank with the results show that slurry stirred and suspended evenly without delamination, which can adapt to the condition of high concentration of sulfur, iron and arsenic elements. The leaching rate of HAT6065 cyanide leaching stirring tank is about 6.61% higher than that of conventional cyanide stirring tank.

The conventional cyanide leaching process is used to extract gold from a high copper gold concentrate. Because the copper associated minerals consume sodium cyanide in large quantities, the cost of the reagents is high and the economic benefit is not ideal. At the same time, a large number of cyanide tail slag are produced, which brings a series of environmental problems. In order to solve the environmental problems caused by excessive sodium cyanide consumption and cyanogen slag, the feasibility of leaching gold by thiosulfate in copper ammonia system was studied. The gold leaching rate of thiosulfate was increased to more than 90% by using the direct thiosulfate leaching process and pretreatment thiosulfate leaching process, which was close to the gold leaching index of sodium cyanide at the production site.

The gold ore which contained 4.73 g/t Au was selected from carlin-type gold deposits in Guizhou. Three experiments on the gold ore were carried out. They were direct cyanide leaching, oxidizing roasting-cyanide leaching and flotation-oxidizing roasting-cyanide leaching. The experiments revealed that with the third process, ideal production index were obtained. The optimum conditions were confirmed: combined collector ammonium dibutyl dithiophosphate dosage was 60 g/t and butyl xanthate dosage was 120 g/t. Sodium cyanide dosage was 7000 g/t. As a result, we obtained satisfying selecting targets: The grade of gold was 42.0 g/t in the flotation concentrate. The gold leaching rate was up to 96.18%, and gold recovery was 88.23% after cyanide leaching. It was of important effect on decreasing resources waste and reducing environment pollution to research the project.

Nowadays, there are many gold leaching processes, and the dominant one is cyanidation, but the virulence of cyanidation seriously endangers the environment and human health. In order to reduce environmental pollution and improve the recovery rate of gold, metallurgical workers put forward a variety of new gold leaching methods, which can be roughly divided into two types: one is to develop pretreatment technology on the basis of traditional cyanidation method; The other is non-cyanide leaching of gold. Based on the existing Non-Cyanide leaching technology, this paper puts forward the process innovation of Non-Cyanide leaching technology, thiourea method and dilute nitric acid pre-oxidation treatment process. The thiourea non-cyanide leaching system was investigated. According to the leaching situation of gold and silver in raw ore, the innovative scheme of gold and silver leaching technology was selected. Compared with other treatment methods, thiourea method and dilute nitric acid pre-oxidation treatment technology overcome the danger of high pressure, and the nitrogen oxide gas produced in the dilute nitric acid oxidation process can be recycled, which basically does not pollute the environment.

Abstract The leaching of valuable metals from mineral ores is the basis of several extractive economies around the world, but the strategies employed often need to rely on dangerous compounds such as cyanides. Due to the complex nature of most ores, leaching processes are slow and have a low efficiency in noble metal extraction, which is usually improved by fine-milling the mineral. In this manuscript, we consider this strategy, demonstrating that it may increase the amount of silver leaching, but at the expense of a higher consumption of cyanide, which renders the process inefficient (only 2% of consumed cyanide is employed to complex silver). The increase in the yield of the desired product without the smarter use of dangerous compounds is shown as a paradigm of the need to insert green chemistry principles in industrial processes. We further present the result of two potential strategies for greener mineral processing: the use of ultrasound to eliminate passivating layers formed during the leaching process and the use of chemical pretreatments to eliminate possible sources of passivation. These strategies can increase the amount of silver extraction and simultaneously increase the efficiency in cyanide consumption. The convenience of these pretreatments in the framework of the green chemistry principles, as well as the challenges towards their implementation at industrial scale, is discussed.

The gold ore is oxidized ores, and it is not suitable for flotation separation. The cyanide leaching is used for the recovery of gold. Experimental studies of cyanidation leaching for a oxidized gold ore were carried out. The factors that influence leaching such as grinding size, sodium cyanide quantity, pulp density, extraction time and segmentation leaching were conducted. And experiment pretreatment test with the copper ion which influences leaching. The results demonstrated that the good index of leaching rate 90.11% could be reach.

A theoretical substantiation of an environmentally friendly technology for extracting gold from mineral raw materials is presented. In terms of an alternative to conventional cyanide, the authors propose chlorine-bearing derivatives of organic isocyanuric acid (C3H3N3O3). In the studied process, this reagent combines the roles of a long-acting oxidant and complexing agent due to the resulting Cl– ion. For experimental purposes, the rotating disc technique was applied. Experimental results were evaluated by measuring the concentration of gold in solutions using the atomic adsorption method. The theoretical characteristics of gold dissolution using the proposed reagent were studied. In order to evaluate the applicability of the revealed regularities for practical purposes, comparative indicators for leaching gold from the ore of the Byn’govskoye deposit (Sverdlovsk Oblast) using the proposed reagent, cyanide and CYCAD cyanide substitute (China) were evaluated. The dependence of the gold disc dissolution rate on temperature, as well as leaching reagent and hydrochloric acid concentrations, were studied. In disc sample experiments, the exponential dependence of the dissolution rate on the concentration of the studied reagent was established. In this case, the maximum intensity of the process is achieved at a concentration higher than 50 g/dm3. The optimum acidity level comprises 0.3–0.4 g ion/dm3 of hydrochloric acid. Despite an increase in temperature being shown to accelerate the dissolution process, this appears to be technologically unjustified. Under optimal conditions, the gold disc dissolution rate reaches 0.5•10-3 g ion/(cm2•min), which is approximately one hundred times higher than during the dissolution by the cyanic solutions in conventional modes. Close gold extraction values were achieved in the solutions of cyanides and chlorine-bearing derivatives of isocyanuric acid during the leaching of gold from the ore under the comparable conditions. For CYCAD solutions, the same indicator is two times lower. The results of the performed studies demonstrate the high dissolution rate of gold using the proposed reagent along with the technological possibility of leaching gold from ores using this environmentally friendly reagent.

Rest potential measurements, cyclic voltammetry, linear sweep voltammetry and constant potential coulometry were used to determine the electrochemical response of arsenopyrite in the absence and in the presence of cyanide and to determine its dissolution chemistry. Surface oxidation of arsenopyrite is proposed to proceed by a two-step reaction sequence. FeOOH, H₂AsO₃⁻, and Sᵒ, are produced in the initial step. Oxidation of Sᵒ to SO₄²⁻, and H₂AsO₃⁻ to HAsO₄²⁻ account for the second step. Coulometric results confirmed that 14 electrons are involved in the overall reaction. The implications of these results on the cyanidation of arsenical gold-bearing concentrates were also investigated. The response of four different concentrates to various cyanidation techniques was examined. Alkaline pressure oxidation in 1 M NaOH, at 200°C and under 500 psi of oxygen overpressure followed by conventional cyanidation resulted in 81% gold extraction from a concentrate that yielded only 2% gold extraction after direct cyanidation.

Thesis (PhD)--Stellenbosch University, 2015.
ENGLISH ABSTRACT: In order to exploit lower grade and complex platinum group metal resources, cheaper and more efficient alternatives to the conventional mill-float-smelt-refine route are being sought. Leaching of platinum and palladium with cyanide has been proposed a number of times as a promising precious group metals (PGM) process option, and although platinum extractions are problematic, progress into the understanding of cyanide leaching of PGM containing ore and concentrate has been made. The platinum and palladium leaching will typically take place at elevated temperatures, which can range from 55°C on heaps to 180°C in autoclaves, with a better degree of leaching occurring with higher temperatures. Although this process for Pt and Pd extraction is a promising process option, research regarding the feasibility of the subsequent upgrading and recovery of the pregnant PGM leach solution, however, has been lacking. Since the carrier-phase extraction of gold using activated carbon offers significant advantages over other processes in terms of simplicity, the high pre-concentration factor, rapid phase separation, and relatively low capital and operating costs, activated carbon was deemed the most suitable sorbent for a Pt and Pd adsorption and stripping process. Very little is published on the adsorption of PGM cyanides onto activated carbon and when the effect of impurities such as base metals and thiocyanate together with a suitable elution method, are considered, no information could be found in the open literature. This study was launched and in general it was found that the activated carbon process does seem to be a viable process consideration for the upgrading of PGMs in a cyanide leach stream. Adsorption rates for dilute PGM solutions (0.15mg/L Pt, 0.38 mg/L Pd, 0.1 mg/L Au) in a stirred vessel indicated a high rate of adsorption within the first 60 minutes (giving more than 98% recovery of precious metals). A comparison of the Pt isotherm (25°C) to Au isotherms from literature indicated a similar loading capacity, while that of Pd was found to be significantly lower. In common with most diffusion controlled processes, an increase in the adsorption rate of platinum, palladium and gold cyanide with an increase in temperature was observed, while experiments with consecutive contacts of the PGM cyanide solution onto the activated carbon revealed that with an increase in temperature, the amount of PGMs that were adsorbed, decreased with each loading. In the absence of free cyanide and base metals, it was found that after 4 consecutive contacts, 99% of the total amount of platinum and palladium adsorbed at 25°C, compared to 85% of the platinum and 83% of the palladium at 50°C. No difference could be seen between the adsorption of gold cyanide at 25 and 50°C after 4 contacts. It has also been established that the detrimental effect of free cyanide on the adsorption of PGMs will increase as the temperature increases. The detrimental effect of the presence of Cu and Ni was found to depend on the amount of these base metals adsorbed, which in turn will depend on the cyanide concentration and the solution temperature. Adsorption of Pt and Pd has been found to be significantly more affected by temperature, cyanide and base metals than the adsorption of gold and needs to be carefully taken into consideration with the design of a PGM adsorption circuit to ensure sufficient Pt and Pd recovery. It is therefore highly likely that an activated carbon recovery process for Pt and Pd cyanide will not be as robust as the gold CIS (carbon-in-solution) process, which is considered to be one of its main advantages. The feasibility of eluting platinum and palladium cyanide complexes from activated carbon was investigated. It was found that platinum and palladium elute from activated carbon almost to completion in 4 to 5 bed volumes (BV) at 80°C, while the elution of gold at this temperature is slow, with a significant amount of gold (≈ 55 %) still to be eluted after 16 bed volumes. An increase in Pt and Pd elution kinetics was demonstrated with an increase in temperature with 99% recovery achieved at 4 BVs with an elution temperature of 95°C. Cyanide pre-treatment has been found to have a large influence on PGM elution. The effect of the NaCN concentration shows an increase in the recovery of Pt, Pd and Au as the cyanide increases from 0 to 2 %, after which the recovery starts decreasing again as the NaCN concentration increases from 2 to 4%. The NaOH concentration was also found to affect the PGM recovery and at 0% NaCN, an increase in the recovery is seen, while at a higher cyanide concentration (2 and 3% NaCN) a decrease in the PGM recovery occurs when the NaOH concentration is increased from 0.22% to 1.65%. A general decrease in Pt, Pd and Au recovery was seen as the ionic strength of the elution water increased and is consistent with literature on Au elution. The effect of a hydrochloric acid pre-treatment, which forms part of the process to remove calcium build-up from the activated carbon, was investigated, and for all the cases the Pt and Pd recovery increased when an acid pre-treatment was performed, compared to no acid pre-treatment. In none of the cases did any of the Pt, Pd or Au elute with the acid or the following rinsing water. The acid pre-treatment performed at 70°C removed a significant 64% to 75% of the Ni present and an additional 9.1% to 10.5% in the following rinsing water step. In the presence of copper cyanide, the elution order has been found to be copper, palladium, platinum and gold, which is the opposite order of adsorption preference. The cyanide pre-treatment has also been found to have a major influence on the elution of Cu and can be explained by the difference in the absorbance strength between the different copper cyanide complexes. The presence of Cu did not have a negative effect on the elution of the PGMs at strong pre-treatment (2% NaCN and 0.55% NaOH) conditions, but at weak pre-treatment conditions (0% NaCN) the recovery of Pt and Pd was reduced by between 10 and 18% after 5 BVs when Cu was present. The presence of 100 mg/L KSCN salt added to the leach solution during the adsorption stage, reduces the elution recovery of the PGMs at 4 BVs from 90% for Pt and Pd, when not present, to approximately 70% when present. The addition of the additional K+ ions reduced the recovery by less that 4% at 4 BV, which indicates that the possible formation of a PGM bonding with thiocyanate ([Pt(SCN)4]2- and [Pd(SCN)4]2-), which adsorb onto carbon, but doesn’t adsorb with water, cannot be ruled out completely. A maximum amount of 0.15% for Pt, 0.28% Pd and 0.6% Au was found to report to the pre-treatment solution at 25°C. For higher pre-treatment temperatures, the amount of Pt and Pd reporting to the pre-treatment solution increased significantly to approximately 8% at 80°C, while the increase in gold was marginal to 0.8% at 80°C. For the higher loading on the activated carbon (7000 mg/kg Pt and Pd), which is expected to be a better representation of plant conditions, 0.07% Pt, 0.11% Pd and 0.12% Au reported to the pre-treatment solution. The PGMs reporting to the pre-treatment solution is attributed to the distribution of the PGMs on the carbon particle, and even though very small, a certain amount of these PGMs would readily desorb or wash off the carbon. It has thus been established here that the stripping of adsorbed platinum cyanide complexes from activated carbon consists of a two step batch process, which involves the pre-treatment of the metal-loaded activated carbon with a relatively strong sodium cyanide and sodium hydroxide solution, prior to the elution step with de-ionized water at 80°C. Through the development of a mathematical model to describe this process, it was found that the rate of release of the platinum ions is governed by the amount of platinum and sodium on the activated carbon and the concentrations of these ions in the bulk of the liquid. This is mathematically described by a modified Freundlich isotherm equation and the mass transfer diffusion equation. The dependency of the platinum elution rate on the sodium concentration on the activated carbon, as suggested by gold related literature (Van Der Merwe and Van Deventer, 1990, Stange, 1990), is confirmed. Furthermore it has been found that the rate of platinum elution interchangeably depends on the equilibrium of the Pt ions at the carbon-liquid interface and the mass transfer of these Pt ions from the interface to the bulk liquid. As both of these rate-limiting factors were found to depend on the sodium concentration, the dominant platinum elution rate limiting factor shifts as the sodium concentrations change as the elution progresses. Four main time periods are used to simplify and to describe this process. The benefits of fundamentally understanding this process can ultimately lead to improved elution, better process control, shorter elution times, smaller elution columns or assist in the development of a continuous elution process.
AFRIKAANSE OPSOMMING: Nuwe prosesse om komplekse laer graad waardevolle metaal ertse te onwikkel in plaas van die konventionele maal-flotasie-smelt-raffineer proses word tans ondersoek. Loging van platinum en palladium met sianied is verskeie kere al voorgestel as n belowende proses opsie en alhoewel die ekstraksie van platinum nog 'n probleem is, is vordering al gemaak om die logings proses beter te verstaan. Die loging van platinum en palladium met sianied sal tipies plaasvind by hoër temperature wat kan wissel van 55°C in n hoop logins proses tot 180°C onder druk. Beter loging vind plaas soos wat die temperatuur styg. Alhoewel hierdie proses belowend is, is daar nog geen navorsing beskikbaar t.o.v die volgende stap in die proses wat die opgradering van die logings oplossing behels. Aangesien die gebruik van geaktiveerde koolstof in die goud industrie baie voordele inhou soos die eenvoudigheid van die proses, hoë opgraderings faktor, relatiewe vinnige adsorpsie en lae kapitaal en operationele kostes, mag hierdie tegnologie ook geskik wees vir Pt en Pd. Baie min is gepubliseer oor die adsorpsie van waardevolle metale (PGMs) met geaktiveerde koolstof en wanneer die effek van onsuiwerhede soos basis metale en thiosianied saam met n afstropings metode in ag geneem word, kon geen informasie in the literatuur gvind word nie. Hierdie studie is dus geloots en in die algemeen is daar bevind dat die geaktiveerde koolstof metode wel n geskikte oplossing bied vir die opgradering van PGMs in 'n sianied logings stroom. Adsorpsie snelheid vir verdunde PGM oplossings (0.15mg/L Pt, 0.38 mg/L Pd, 0.1 mg/L Au) in bekers wat geroer is, was vinnig vir die eerste 60 minutte (98% herwinning van die PGMs) en 'n vergelyking tussen die Pt adsorpsie isoterm en gepubliseerde Au isoterms wys op n relatiewe soorgelyke ladings kapasiteit. Die isotherm van Pd was egter laer. Soortgelyk aan meeste diffusie beheerde prosesse, het 'n verhoging van temperatuur gelei tot vinniger adsorpsie snelhede vir Pt, Pd en Au. Indien oplossings egter herhaaldelik met dieselfde koolstof in kontak gebring word, is bevind dat met 'n verhoging in temperatuur, die totale hoeveelheid PGMs wat absorbeer, met elke kontak verminder. In die afwesigheid van sianied en enige basis metale, het die totale hoeveelheid Pt en Pd wat geabsobeer is na 4 opeenvolgende kontake verminder van 99% by 25°C tot 85% adsorpsie van Pt en 83% Pd by 50°C. Daar was geen veskil tussen die adsorpsie van Au by 25°C en 50°C na 4 kontakte nie. Dit is ook vasgestel dat die negatiewe effek van vrye sianied in die oplossing, groter word soos wat die temperatuur verhoog. Die negatiewe effek van die teenwoordigheid van Cu en Ni, hang af van die hoeveelheid van hierdie metale wat absorbeer word wat weer bepaal word deur die sianied konsentrasie asook die temperatuur van die oplossing. Die mate waar in Pt en Pd ge-absorbeer word deur koolstof, word aansienlik meer beïnvloed deur temperatuur, sianied konsentrasie en die teenwoordigheid van basis metale as wat die adsorpsie van Au beïnvloed word. Met die ontwerp van n PGM adsorpsie proses, sal dit sterk in aanmerking geneem moet word, om seker te maak dat so min as moontlik Pt en Pd verlore gaan. Dit wys ook dat 'n geaktiveerde koolstof proses vir Pt en Pd, nie so onvatbaar vir proses veranderings sal wees soos wat die Au proses is nie, wat as een van die groot voordele van die Au proses beskou word. Die afstropery van die Pt en Pd sianied komplekse is ondersoek en gevind dat by 80°C, amper al die Pt en Pd binne 4 to 5 bed volumes (BV) van die geaktiveerde koolstof gestroop kan word. Die afstropery van Au by hierdie temperatuur is stadig en sowat 55% van die Au bly nog oor op die koolstof na 16 BVs. Die snelheid waarteen die Pt en Pd afgestroop word verhoog indien die temperatuur verhoog word en by 95°C is 99% van die Pt en Pd herwin na 4 BVs. Voorafbehandeling van die gelaaide koolstof met sianied, het 'n groot uitwerking op die PGM afstroping. Soos wat die NaCN konsentrasie verhoog word vanaf 0 tot by 2%, verhoog die PGM herwinning maar daal ook weer indien die NaCN konsentrasie verder verhoog word vanaf 2% tot by 4%. Die NaOH konsentrasie het ook n invloed gehad. By 0% NaCN, het die PGM herwinning verhoog soos wat die NaOH konsentrasie verhoog is maar by hoër sianied konsentrasies van 2 en 3%, is n daling in die herwinning waargeneem soos wat die NaOH verhoog is vanaf 0.22% tot by 1.65%. N algemene daling in die Pt, Pd and Au herwinning is waargeneem soos wat die ioniese sterkte van die stropings water toegeneem het. Dit stem ooreen met gepubliseerde navorsing oor die afstroping van Au. Om kalsium van die geaktiveerde koolstof te verwyder, word die koolstof vooraf met soutsuur gewas. Hierdie stap is vir Pt en Pd ondersoek en daar is bevind dat vir al die gevalle, die herwinning hoër was wanneer die gelaaide koolstof met soutsuur behandel is teenoor geen behandeling nie. In geen van die gevalle, is Pt, Pd of Au saam met die soutsuur of die daaropvolgende was water afgestroop nie. Voorafbehandeling met soutsuur teen 70°C lei wel daartoe dat tussen 64 en 75% Ni afgestroop word saam met die soutsuur en n verdere 9.1 to 10.5% saam met die daaropvolgende was water. In die teenwoordigheid van koper sianied, word Cu eerste afgestroop met Pd, Pt en dan Au wat daarop volg. Dit is presies die teenoorgestelde orde waarin die metale geabsorbeer word. Die voorafbehandeling met sianied, het ook 'n beduidende effek op die stroping van Cu. Dit kan verduidelik kan word aan die hand van die verskillende koper sianied komplekse wat vorm wat elkeen 'n verskillende affiniteit het vir adsorpsie. Wanneer 2% NaCN en 0.6% NaOH in die vooraf behandeling stap gebruik word, het die teenwoordigheid van koper geen negatiewe invloed op die afstroping van die PGMs gehad nie maar die herwinning is wel met 10% en 18% verlaag by 5 BVs wanneer geen sianied in die voorafbehandeling stap gebruik is nie. Wanneer 100 mg/L KSCN sout by die adsorpsie stap gevoeg word, daal die herwinning van die PGMs in die stropings stap van 90% tot 70% by 4 BVs. Die addisionel K+ katione verminder die herwinning met slegs 4% by 4 BVs wat beteken dat die vorming van adisionele komplekse soos [Pt(SCN)4]2- en [Pd(SCN)4]2-, wat nie op die normale metode afgestroop kan word, 'n moontlikheid mag wees. N maksimum van 0.15% vir Pt, 0.28% Pd en 0.6% Au word in die vooraf behandelings stap af gestroop. Indien die temperatuur van hierdie stap verhoog word na 80°C, verhoog die hoeveelheid Pt en Pd wat na hierdie stroom raporteer na 'n beduidende 8% tewyl Au basies onveranderd bly by 0.8%. Vir geaktiveerde koolstof wat hoër gelaai is (7000 mg/Kg Pt en Pd) en dus 'n beter verteenwoordiging van aanleg kondisies is, het 0.07% Pt, 0.11% Pd en 0.12% Au raporteer na die vooraf behandelings stap. Dit word toegeskryf aan die verspreiding van die PGMs op die koolstof wat hoofsaaklik op die oppervlakte voorkom en alhoewel die hoeveelheid klein is, word 'n sekere hoeveelheid slegs afgewas. Dit is dus vasgestel hier, dat die afstroping van Pt 'n twee stap proses is. Die eerste stap is die voorabehandeling van die koolstof met 'n sianied oplossing en daarna volg die afstroping van die Pt met suiwer water teen ongeveer 80°C. Met die ontwikkeling van n wiskundige model, is bevind dat die snelheid waarteen die Pt afgestroop word, beïnvloed word deur die hoeveelheid Pt en Na wat op die koolstof oppervlakte is, asook die konsentrasies van die metale in die vloeistof. Dit word wiskundig beskryf deur n gemodifiseerde Freundlich isotherm vergelyking asook deur die massa diffusie vergelyking. Die Pt afstropings snelheid wat afhanklik is van die Na konsentrasie kan vergelyk word met die afstroping snelheid van Au wat ook afhanklik is van die Na konsentrasie (Van Der Merwe and Van Deventer, 1990, Stange, 1990). Verder is bevind dat die snelheid van Pt stroping afhanklik is van beide die ewewig van Pt ione by die koolstof-vloeistof grens asook die massa beweging van Pt ione van die koolstof-vloeistof grens na die vloeistof. Beide hierdie snelheids bepalende faktore word bepaal deur die Na konsentrasie en skuif soos wat die Na konsentrasie verander soos wat die afstroping plaasvind. Vier hoof tyd periodes word gebruik om hierdie verskynsel te verduidelik. Deur die proses fundamenteel te verstaan, kan uiteindelik lei tot 'n beter proses, beter beheer, korter afstropings tye, kleiner toerusting of die ontwikkeling van 'n kontinue proses.

Nowadays, keeping mining and the environment sustainable is a major concern all over the world. Using toxic chemicals such as cyanide and mercury in the gold leaching process is one of the main factors that need to be considered in terms of the environment. Finding alternative lixiviants is one solution that would decrease the uses of these toxic chemicals. Thiosulfate is one of the most promising alternative substitutes to cyanide kinetically and environmentally.Gold leaching in thiosulfate solutions was evaluated environmentally and kinetically in different ways: (1) applying a closed system to leach gold (2) evaluating the environmental and metallurgical optimum thiosulfate leaching characteristics for pure gold and pure silver and gold silver alloys (4, 8, 20 and 50 wt % silver), (3) studying the electrochemical behavior of gold, silver, and gold/silver alloys (4) optimizing the leaching conditions of gold ore samples supplied from Centamin Egypt Limited Company, (5) finally, studying the ability of thiosulfate solutions to dissolve mercury and evaluating gold, copper, and mercury recovery from ion-exchange resins.The study showed that the leaching rate of gold and silver in the closed vessel was greater than that obtained in the open vessel by 30% and 45% respectively. To avoid the losses of ammonia a closed leaching system is recommended. Gold and silver leaching in thiosulfate solution is preferable kinetically and environmentally if conducted in a closed vessel system.The effect silver alloyed with gold was evaluated and the result showed that the dissolution rate of pure gold is higher than that form 4 and 8 wt% Ag alloys. And the dissolution rate of gold from 20 and 50% silver alloys is more than that obtained for pure gold. The silver dissolution rate is sensitive to copper(II) concentration being 1.67 x 10-5 mol.m-2.s-1 at an initial copper(II) concentration of 1.25 mM and 6.6x10-5 mol.m-2.s-1 at an initial copper(II) concentration of 10 mM. Silver dissolution is more sensitive to ammonia than gold.From the electrochemical study on gold/silver alloys, it was found that an increase in silver in the alloy results in an increase of the current density from both gold and silver oxidation in thiosulfate solutions in the range of potentials 0.242- 0.542 V. Also, it was found that in thiosulfate solutions containing thiourea, the oxidation current of gold/silver alloys decreased and the oxidation current from pure gold after the standard potential for gold oxidation (150 mV) is higher than the total oxidation current from gold-silver alloys.Leaching of a selected gold ore using thiosulfate solutions for 24 hours suggested the optimum conditions to leach the ore to be 0.2 – 0.4 M thiosulfate, 400 mM NH3, 10 -20 mM Cu(II), 30 ºC, 300 rpm, no air supplied, solid/liquid ratio 20%, and mean particle size of < -106 μm.Finally, the study showed that mercury dissolves in thiosulfate solutions as it dissolves in cyanide. Mercury dissolves in thiosulfate solutions in the order: HgS2