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<br />Pege 5 <br />The tdlowing sections d the paper torus on the chemistry, performance, appiicatlons, and economics of <br />the cyanide recovery from sdutions end slurries, wRh emphasis on the cyanide recovery system proposed <br />for the Gdden Cross Mine. <br />PROCESS DESCRIPTION AND CHEMISTRY - <br />Cyanide recovery processes utilize the vdatUlty of HCN at a lowered pH (I.e. Figure 2) to strip tree <br />from sdution or slurry and recover h In usable form (I.e. NaCN or Ca(CN),). The vdatilRy of tree rr <br />cyanide (HCN) Is related to fts Henry's_l~~+CAnstant, which Is affected by several factors Including v <br />Is Iiauid film limfted. and <br />to <br />psi are required to create t <br />_. __.~.____._.Y, <br />There are several factors which affect the rate and extent of HCN removal Irom slurries or sdutions through <br />air stripping. These (actors Incude: <br />1. The pH of the soution <br />2. The form of cyanide <br />3. The concentration of cyanide <br />4. The temperature of the slurry or solution <br />5. The pressure maintained within the recovery system <br />6. The air to liquid ratio <br />7. The mechanical dispersion equipment <br />8. The viscosity of the sdutlon or siurry <br />9. The liquid tc air contact period <br />A great deal of Information is available regarding the effects of these design parameters on the recovery of <br />cyanide Irom clarHied sdutions, but limfted data is available concerning the treatment of taiings slurries. <br />The current cyanide recovery processes are upgraded versions of the original Mills Crewe Process <br />previously discussed. A schematic of the generalized cyanide recovery process is presented on Figure 3. <br />._ The process is conducted In three stages. The first stage known as acidification Invdves lowering of the ~ ~ <br />~' ~ waster nH In rha range of tS-8.5 with the use of concentrated mineral acid. The acid employed most <br />commonly Is sulfuric acid, due to fts relatively low cost and ease of availability. In addition, the handling, <br />storage, and feeding of sulfuric acki Is quite common in industry: -The potential problems associated with <br />sulfuric acid Include an Increase in sulfate and total dissdved solids concentrations and the potential for;. <br />precipitation of calcium sulfate or gypsum In oversaturated sdutions. The pH'of the sdutlon or slurry is - <br />_ , ..monitored In-situ continuously. The aciditiratloasten must tie endosed to oreyent escape of HCN gas and -- <br />requires about 10 to 20 minutes to complete. The reduction of HCN during the acidification step Is about I <br />t0 to 15 percent of the total cyanide concentration. <br />In accordance wfth the stability of the particular complexes <br />recovered. For the recovery of free cyanide from <br />and Zn(CN),I. 8 DH In the range of 4.5 to 8.5 Is employed. For recovery of weak add Clssoclable~wAU) <br />cyanide, the pH is lowered to about 4.0. For rernoyai of Iron complexed~anlde the pH Is_ lowered to_ less <br />than P.0.-ln this case, an Insduble metal Iron cyanide complex forms, and precipitates from solution. The <br />es approach Is to utilize a near neutral or basic pH when possible to minimize precipitation Problems and <br />an Increase in total dissdved solids. _ - -- - <br />From the ackificatlon stage, the acidified solution or slurry containing HGN passes Into the cyanide stripping <br />or vdatillzat(on stage, which consists Of either open or packed to•.vers, a series of complete rnfx reactors, <br />