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Gold cyanidation (also known as the cyanide process or the MacArthur-Forrest process) is a hydrometallurgical technique for extracting gold from low-grade ore by converting the gold to a water-soluble coordination complex. It is the most commonly used leaching process for gold extraction.[1]

Production of reagents for mineral processing to recover gold, copper, zinc and silver represents approximately 13% of cyanide consumption globally, with the remaining 87% of cyanide used in other industrial processes such as plastics, adhesives, and pesticides.[2] Due to the highly poisonous nature of cyanide, the process may be considered controversial and its usage is banned in a small number of countries and territories.


In 1783, Carl Wilhelm Scheele discovered that gold dissolved in aqueous solutions of cyanide. Through the work of Bagration (1844), Elsner (1846), and Faraday (1847), it was determined that each atom of gold required two cyanide ions, i.e. the stoichiometry of the soluble compound.

Industrial process[edit]

John Stewart MacArthur developed the cyanide process for gold extraction in 1887.

The expansion of gold mining in the Rand of South Africa began to slow down in the 1880s, as the new deposits being found tended to pyritic ore. The gold could not be extracted from this compound with any of the then available chemical processes or technologies.[3]In 1887, John Stewart MacArthur, working in collaboration with brothers Robert and William Forrest for the Tennant Company in Glasgow, Scotland, developed the MacArthur-Forrest process for the extraction of gold ores. Several patents were issued in the same year.[4] By suspending the crushed ore in a cyanide solution, a separation of up to 96 percent pure gold was achieved.[5]The process was first used on the Rand in 1890 and, despite operational imperfections, led to a boom of investment as larger gold mines were opened up.[6][3]

By 1891, Nebraska pharmacist Gilbert S. Peyton had refined the process at his Mercur Mine in Utah, 'the first mining plant in the United States to make a commercial success of the cyanide process on gold ores.'[7][8] In 1896, Bodländer confirmed that oxygen was necessary for the process, something that had been doubted by MacArthur, and discovered that hydrogen peroxide was formed as an intermediate.[6]Around 1900, the American metallurgist Charles Washington Merrill (1869-1956) and his engineer Thomas Bennett Crowe improved the treatment of the cyanide leachate, by using vacuum and zinc dust. Their process is the Merrill–Crowe process.[9]

Chemical reactions[edit]

Ball-and-stick model of the aurocyanide or dicyanoaurate(I) complex anion, [Au(CN)2].[10]
Cyanide leaching 'heap' at a gold mining operation near Elko, Nevada

The chemical reaction for the dissolution of gold, the 'Elsner Equation', follows:

4 Au(s) + 8 NaCN(aq) + O2(g) + 2H2O(l)→ 4 Na[Au(CN)2](aq) + 4 NaOH(aq)

In this redox process, oxygen removes, via a two-step reaction, one electron from each gold atom to form the complex Au(CN)


The ore is comminuted using grinding machinery. Depending on the ore, it is sometimes further concentrated by froth flotation or by centrifugal (gravity) concentration. Water is added to produce a slurry or pulp. The basic ore slurry can be combined with a solution of sodium cyanide or potassium cyanide; many operations use calcium cyanide, which is more cost effective.

To prevent the creation of toxic hydrogen cyanide during processing, slaked lime (calcium hydroxide) or soda (sodium hydroxide) is added to the extracting solution to ensure that the acidity during cyanidation is maintained over pH 10.5 - strongly basic.Lead nitrate can improve gold leaching speed and quantity recovered, particularly in processing partially oxidized ores

Effect of dissolved oxygen[edit]

Oxygen is one of the reagents consumed during cyanidation, and a deficiency in dissolved oxygen slows leaching rate. Air or pure oxygen gas can be purged through the pulp to maximize the dissolved oxygen concentration. Intimate oxygen-pulp contactors are used to increase the partial pressure of the oxygen in contact with the solution, thus raising the dissolved oxygen concentration much higher than the saturation level at atmospheric pressure. Oxygen can also be added by dosing the pulp with hydrogen peroxide solution.

Pre-aeration and ore washing[edit]

In some ores, particularly those that are partially sulfidized, aeration (prior to the introduction of cyanide) of the ore in water at high pH can render elements such as iron and sulfur less reactive to cyanide, therefore making the gold cyanidation process more efficient. Specifically, the oxidation of iron to iron (III) oxide and subsequent precipitation as iron hydroxide minimizes loss of cyanide from the formation of ferrous cyanide complexes. The oxidation of sulfur compounds to sulfate ions avoids the consumption of cyanide to thiocyanate (SCN) byproduct.

Recovery of gold from cyanide solutions[edit]

In order of decreasing economic efficiency, the common processes for recovery of the solubilized gold from solution are (certain processes may be precluded from use by technical factors):

Cyanide remediation processes[edit]

The cyanide that remain in tails streams from gold plants is potentially hazardous. Therefore, some operations process the cyanide-containing waste streams in a detoxification step. This step lowers the concentrations of these cyanide compounds. The INCO-licensed process and the Caro's acid process oxidise the cyanide to cyanate, which is not as toxic as the cyanide ion, and which can then react to form carbonates and ammonia:[citation needed]

+ [O] → OCN
+ 2 H
+ NH

The Inco process can typically lower cyanide concentrations to below 50 mg/L, whereas the Caro's acid process can lower cyanide levels to between 10 and 50 mg/L, with the lower concentrations achievable in solution streams rather than slurries. Caro's acid – peroxomonosulfuric acid (H2SO5) - converts cyanide to cyanate. Cyanate then hydrolyses to ammonium and carbonate ions. The Caro's acid process is able to achieve discharge levels of WAD below 50 mg/L, which is generally suitable for discharge to tailings. Hydrogen peroxide and basic chlorination can also be used to oxidize cyanide, although these approaches are less common.

Over 90 mines worldwide now use an Inco SO2/air detoxification circuit to convert cyanide to the much less toxic cyanate before waste is discharged to a tailings pond. Typically, this process blows compressed air through the tailings while adding sodium metabisulfite, which releases SO2. Lime is used to maintain the pH at around 8.5, and copper sulfate is added as a catalyst if there is insufficient copper in the ore extract. This procedure can reduce concentrations of 'Weak Acid Dissociable' (WAD) cyanide to below the 10 ppm mandated by the EU's Mining Waste Directive. This level compares to the 66-81 ppm free cyanide and 500-1000 ppm total cyanide in the pond at Baia Mare.[12] Remaining free cyanide degrades in the pond, while cyanate ions hydrolyse to ammonium. Studies show that residual cyanide trapped in the gold-mine tailings causes persistent release of toxic metals (e.g. mercury ) into the groundwater and surface water systems.[13][14]

Effects on the environment[edit]

Sodium cyanide drum at the abandoned Chemung Mine in Masonic, California

Despite being used in 90% of gold production:[15] gold cyanidation is controversial due to the toxic nature of cyanide. Although aqueous solutions of cyanide degrade rapidly in sunlight, the less-toxic products, such as cyanates and thiocyanates, may persist for some years. The famous disasters have killed few people — humans can be warned not to drink or go near polluted water, but cyanide spills can have a devastating effect on rivers, sometimes killing everything for several miles downstream. The cyanide is soon washed out of river systems and, as long as organisms can migrate from unpolluted areas upstream, affected areas can soon be repopulated. According to Romanian authorities, in the Someș river below Baia Mare, the plankton returned to 60% of normal within 16 days of the spill; the numbers were not confirmed by Hungary or Yugoslavia.[12]Famous cyanide spills include:

1985-91SummitvilleUSLeakage from leach pad
1980s-presentOk TediPapua New GuineaUnrestrained waste discharge
1995OmaiGuyanaCollapse of tailings dam
1998KumtorKyrgyzstanTruck drove over bridge
2000Baia MareRomaniaCollapse of containment dam (see 2000 Baia Mare cyanide spill)
2000TolukumaPapua New GuineaHelicopter dropped crate into rainforest[16]
2018San DimasMexicoTruck leaked 200 liters of cyanide solution into the Piaxtla River in Durango[17]

Such spills have prompted fierce protests at new mines that involve use of cyanide, such as Roşia Montană in Romania, Lake Cowal in Australia, Pascua Lama in Chile, and Bukit Koman in Malaysia.

Alternatives to cyanide[edit]

Although cyanide is cheap, effective, and biodegradable, its high toxicity has led to new methods for extracting gold using less toxic reagents. Other extractants have been examined including thiosulfate (S2O32−), thiourea (SC(NH2)2), iodine/iodide, ammonia, liquid mercury and alpha-cyclodextrin. Challenges include reagent cost and the efficiency of gold recovery. Thiourea has been implemented commercially for ores containing stibnite.[18]

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The US states of Montana[19] and Wisconsin,[20] the Czech Republic,[21]Hungary,[22] have banned cyanide mining. The European Commission rejected a proposal for such a ban, noting that existing regulations (see below) provide adequate environmental and health protection.[23] Several attempts to ban gold cyanidation in Romania were rejected by the Romanian Parliament. There are currently protests in Romania calling for a ban on the use of cyanide in mining (see 2013 Romanian protests against the Roșia Montană Project).

In the EU, industrial use of hazardous chemicals is controlled by the so-called Seveso II Directive (Directive 96/82/EC,[24] which replaced the original Seveso Directive (82/501/EEC[25] brought in after the 1976 dioxin disaster. 'Free cyanide and any compound capable of releasing free cyanide in solution' are further controlled by being on List I of the Groundwater Directive (Directive 80/68/EEC)[26] which bans any discharge of a size which might cause deterioration in the quality of the groundwater at the time or in the future. The Groundwater Directive was largely replaced in 2000 by the Water Framework Directive (2000/60/EC).[27]

Visual studio for mac resx. In response to the 2000 Baia Mare cyanide spill, the European Parliament and the Council adopted Directive 2006/21/EC on the management of waste from extractive industries.[28] Article 13(6) requires 'the concentration of weak acid dissociable cyanide in the pond is reduced to the lowest possible level using best available techniques', and at most all mines started after 1 May 2008 may not discharge waste containing over 10ppm WAD cyanide, mines built or permitted before that date are allowed no more than 50ppm initially, dropping to 25ppm in 2013 and 10ppm by 2018.

Under Article 14, companies must also put in place financial guarantees to ensure clean-up after the mine has finished. This in particular may affect smaller companies wanting to build gold mines in the EU, as they are less likely to have the financial strength to give these kinds of guarantees.

The industry has come up with a voluntary 'Cyanide Code'[29] that aims to reduce environmental impacts with third party audits of a company's cyanide management.


  1. ^Rubo, Andreas; Kellens, Raf; Reddy, Jay; Steier, Norbert; Hasenpusch, Wolfgang (2006). 'Alkali Metal Cyanides'. Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.i01_i01. ISBN978-3527306732.
  2. ^Barrick Gold - Facts About CyanideArchived 2010-09-20 at the Wayback Machine
  3. ^ abGray, J. A.; McLachlen, J. (Jun 1933). 'A history of the introduction of the MacArthur-Forrest cyanide process to the Witwatersrand goldfields'. Journal of the Southern African Institute of Mining and Metallurgy. 33 (12): 375–397. hdl:10520/AJA0038223X_5033.
  4. ^us US403202, MacArthur, John Stewart; William Forrest & Robert Forrest Robert, 'Process of Obtaining Gold and Silver from Ores', issued 1889-05-14
  5. ^'Methods to recover Gold II'. 2013-05-14.
  6. ^ abHabashi, Fathi Recent Advances in Gold MetallurgyArchived 2008-03-30 at the Wayback Machine
  7. ^The alumni quarterly and fortnightly notes. University of Illinois. January 1, 1921. Retrieved May 1, 2016.
  8. ^'Mercur, UT'. Retrieved May 1, 2016.
  9. ^Adams, Mike D. (2005-12-02). Advances in Gold Ore Processing. Elsevier. pp. XXXVII–XLII. ISBN978-0-444-51730-2. ISSN0167-4528.
  10. ^Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd Edn.), Oxford:Butterworth-Heinemann. ISBN0-7506-3365-4.
  11. ^(Web Archive) Technical Bulletin, https://web.archive.org/web/20091023235047/http://www.multimix.com.au/DOCUMENTS/Technical%20Bulletin1.PDF
  12. ^ abUNEP/OCHA Environment Unit 'UN assessment mission - Cyanide Spill at Baia Mare, March 2000'
  13. ^Maprani, Antu C.; Al, Tom A.; MacQuarrie, Kerry T.; Dalziel, John A.; Shaw, Sean A.; Yeats, Phillip A. (2005). 'Determination of Mercury Evasion in a Contaminated Headwater Stream'. Environmental Science & Technology. 39 (6): 1679–1687. Bibcode:2005EnST..39.1679M. doi:10.1021/es048962j.
  14. ^Al, Tom A.; Leybourne, Matthew I.; Maprani, Antu C.; MacQuarrie, Kerry T.; Dalziel, John A.; Fox, Don; Yeats, Phillip A. (2006). 'Effects of acid-sulfate weathering and cyanide-containing gold tailings on the transport and fate of mercury and other metals in Gossan Creek: Murray Brook mine, New Brunswick, Canada'. Applied Geochemistry. 21 (11): 1969–1985. Bibcode:2006ApGC..21.1969A. doi:10.1016/j.apgeochem.2006.08.013.
  15. ^'Long Term persistence of cyanide species in mine waste environments', B. Yarar, Colorado School of Mines, Tailings and Mine Waste '02, Swets & Zeitlinger ISBN90-5809-353-0, pp. 197 (Google Books)
  16. ^BBC News BBC: 'Cyanide seeps into PNG rivers' March 23, 2000.
  17. ^Wilson, T.E. La politica es la politica: 'After cyanide spill, can First Majestic clean up its act?' April 21, 2018.
  18. ^La Brooy, S.R.; Linge, H.G.; Walker, G.S. (1994). 'Review of gold extraction from ores'. Minerals Engineering. 7 (10): 1213–1241. doi:10.1016/0892-6875(94)90114-7.
  19. ^The Citizens Initiative banning of cyanide mining in the State of Montana, USArchived October 21, 2007, at the Wayback Machine
  20. ^2001 Senate Bill 160 regarding the use of cyanide in mining.
  21. ^'Czech Senate bans use of cyanide in gold mining'. Nl.newsbank.com. 2000-08-10. Retrieved 2013-01-03.
  22. ^Zöld siker: törvényi tilalom a cianidos bányászatra!Archived July 21, 2011, at the Wayback Machine
  23. ^International Mining - European Commission rejects proposed ban on using cyanide in extractive industry, July, 2010
  24. ^Council Directive 96/82/EC of 9 December 1996 on the control of major-accident hazards involving dangerous substances. For the modifications see the consolidated version.
  25. ^Council Directive 82/501/EEC of 24 June 1982 on the major-accident hazards of certain industrial activities. Not in force.
  26. ^Council Directive 80/68/EEC of 17 December 1979 on the protection of groundwater against pollution caused by certain dangerous substances. Not in force.
  27. ^Directive 2000/60/EC of the European Parliament and of the Council of 23 October 2000 establishing a framework for Community action in the field of water policy (the Water Framework Directive). For the modifications see the consolidated version.
  28. ^Directive 2006/21/EC of the European Parliament and of the Council of 15 March 2006 on the management of waste from extractive industries. For the modifications see the consolidated version.
  29. ^ICMI www.cyanidecode.org International Cyanide Management Code For The Manufacture, Transport and Use of Cyanide In The Production of Gold

External links[edit]

Wikimedia Commons has media related to Gold mining.
  • Yestech A different commercial method that does not use toxic cyanide
  • Cyanide Uncertainties (PDF)
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