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PROCESSING OF HIGH SILVER-GOLD ORES WITH GLYCAT~(TM) TECHNOLOGY

机译:用Glycat〜(TM)技术加工高银金矿

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Gold and silver are traditionally extracted from high silver-gold ores by cyanidation with high concentrations of cyanide in both the leaching and Merrill-Crowe metal recovery steps. Cyanide is continually consumed during the cyanidation process and additional cyanide needs to be added in order to maintain cyanide levels at the optimum leaching concentration. This paper investigates an alternative gold and silver extraction process, consisting of a cyanide-catalysed glycine leaching system, known commercially as GlyCat~(TM). The silver-gold ore used in this study contained 3.13 g/t gold and 64 g/t silver. The gold was predominantly present as native gold and the silver predominantly present as silver halides. The leaching conditions for the GlyCat~(TM) system were glycine at 7.5 g/L, ferricyanide at 1.5 g/L, with the sodium cyanide (NaCN) concentration maintained at 200 ppm for the duration of the test. Cyanidation leaching was undertaken with NaCN maintained at concentrations of 1000 ppm for the duration of the test. A level of 1000 ppm cyanidation was adopted for this study as it represents a level that would typically be employed industrially for this type of ore. The leaching rate in the GlyCat? system was found to be approximately tenfold faster than the 1000 ppm cyanidation system, with higher gold recovery after 6 hours at 98% for the GlyCat? system. Gold and silver recovery from cyanidation leaching at 1000 ppm after 48 hours were 97.1% and 80% respectively, compared to 96.7% and 75.6% respectively for the GlyCat~(TM) system for the same time period. Gold and silver recovery from cyanidation leaching at 200 ppm after 48 hours was much lower at 85.5% and 52.0% respectively. In the GlyCat~(TM) system, 0.81 kg/t of NaCN was consumed compared with 2 kg/t in the 1000 ppm cyanidation system. Lime consumption was also lower for the GlyCat~(TM) system, with 2.82 kg/t lime consumed compared to 4.3 kg/t lime for the 1000 ppm cyanidation system. Lower mercury dissolution was observed in the GlyCat~(TM) system, with 0.7% dissolved into solution, compared to 10% during the cyanidation at 1000 ppm. The concentration of free cyanide present in the final leach solution for the GlyCat~(TM) process was 175 mg/L, which was approximately 20% of the free cyanide present in the final leach from the 1000 ppm cyanidation process. The results showed that the GlyCat~(TM) leaching system achieved a similar level of gold and silver metal recovery to cyanidation at 1000 ppm, but with reduced cyanide consumption, reduced lime consumption and reduced mercury dissolution compared to the cyanidation system. Cyanidation at 200 ppm achieved significantly lower gold and silver recoveries compared to the GlyCat~(TM) leaching system.
机译:在浸出和美林群金属恢复步骤中,通过氰化物的氰化物中的高浓度氰化物从高银金矿中提取金和银。在氰化过程中不断消耗氰化物,需要添加另外的氰化物以保持氰化物水平以最佳的浸出浓度。本文研究了由氰化物催化的甘氨酸溶液浸出系统组成的替代金和银萃取过程,以商业上作为甘草〜(TM)。本研究中使用的银矿石含有3.13克/吨金,64克/吨银。黄金主要以原卤作为银卤代呈现的原生金和银。甘草〜(TM)系统的浸出条件是甘氨酸,甘氨酸在1.5g / L的1.5g / L,氰化钠(NaCN)浓度为200ppm,在试验期间保持在200ppm。在试验期间,用NaCN保持氰化浸出的NACN保持浓度为1000ppm。本研究采用了1000ppm氰化水平,因为它代表了这种水平,通常用于这种类型的矿石。糖类中的浸出率?发现系统比1000ppm氰化物系统快大约十倍,在糖酸98%后6小时后的黄金恢复较高?系统。在48小时后,从氰化浸出的金银回收浸出在48小时后分别为97.1%和80%,同时甘草〜(TM)系统分别为96.7%和75.6%。在48小时后,从氰化浸出的金银回收到200ppm,分别为85.5%和52.0%。在甘草〜(TM)系统中,在1000ppm氰化物系统中与2kg / t相比消耗0.81kg / t的NaCn。甘草〜(TM)系统也降低了石灰消耗,而含有2.82kg / t石灰,而1000 ppm氰化系统的4.3kg / t石灰相比消耗。在糖粉〜(TM)系统中观察到较低的汞溶解,溶解在溶液中的0.7%,而在1000ppm下的氰化期间的10%相比。对于糖粉〜(TM)工艺的最终浸出溶液中存在的自由氰化物的浓度为175mg / L,从1000ppm氰化过程中,最终浸出中存在的自由氰化物的20%。结果表明,甘草〜(TM)浸出系统以1000ppm的氰化物达到类似水平的金色和银金属回收,但与氰化物消耗降低,降低了石灰消耗,与氰化系统相比减少了汞溶解。与甘草〜(TM)浸出系统相比,200ppm的氰化物可显着降低金和银回收率。

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