Recovery and Refining of Au by Gold-Cyanide Ion Biosorption Using Animal Fibrous Proteins

Author(s):  
Shin-ichi Ishikawa ◽  
Kyozo Suyama
2002 ◽  
Vol 56 (9) ◽  
pp. 1147-1151 ◽  
Author(s):  
Keunchang Cho ◽  
Yong Soon Jang ◽  
Myoung-Seon Gong ◽  
Kwan Kim ◽  
Sang-Woo Joo

Raman spectra of silver and gold cyanide complexes have been investigated in order to determine the speciation of aqueous plating solutions. We have examined the ionic species in the concentration ranges of 0.003 ∼ 0.5 M for the metals and 0.1 ∼ 2.5 M for the cyanide ion. When the initial concentration of [Ag(CN)2]− was below ∼0.1 M, [Ag(CN)4]3– did not appear prominent even at high CN−/Ag(I) ratios of 3 ∼ 10, differing from the case of previous infrared measurements. Concentrations of the metal cyanide complexes and CN− ion as low as 0.001 ∼ 0.01 M could be determined with an error of less than ∼3% from the analysis of Raman peak areas.


1979 ◽  
Vol 99 (3) ◽  
pp. 341-346 ◽  
Author(s):  
Maria Beŀtowska-Brzezinska ◽  
Edward Dutkiewicz ◽  
Wojciech Ŀawicki

2013 ◽  
Vol 825 ◽  
pp. 270-273 ◽  
Author(s):  
Gayathri Natrajan ◽  
Yen Peng Ting

Rapid technological advancement and the relatively short life time of electronic goods have resulted in an alarming growth rate of electronic waste which often contains significant quantities of toxic and precious metals. Compared to conventional chemical recovery methods, bioleaching has been shown to be an environmentally friendly process for metal extraction. In this work, gold bioleaching from electronic scrap material (ESM) was examined using batch cultures of the bacterium Chromobacterium violaceum which produces cyanide as a secondary metabolite. Gold was bioleached via gold cyanide complexation. The ESM was pretreated using nitric acid to dissolve the base metals (mainly copper) in order to reduce competition for the cyanide ion from other metals present in ESM. ESM was added to the bacterial culture after it reached maximum cyanide production during early stationary phase. Spent medium bioleaching using bacterial cell- free metabolites showed a higher gold recovery of 18%, compared to that of two-step bioleaching of 11% at 0.5% w/v pulp density of ESM. Gold bioleaching was further enhanced to 30% when the pH of the spent medium was increased to shift the equilibrium in favor of cyanide ions production. Spent medium bioleaching of pretreated ESM yield a higher gold recovery compared to two-step bioleaching at a pulp density of 0.5% w/v.


1985 ◽  
Vol 24 (2) ◽  
pp. 236-238 ◽  
Author(s):  
Henry H. Law ◽  
Wilson L. Wilson ◽  
N. Elise Gabriel

2017 ◽  
Vol 120 (3) ◽  
pp. 303-322
Author(s):  
D. Pienaar ◽  
B.M. Guy ◽  
C. Pienaar ◽  
K.S. Viljoen

Abstract Mineralogical and textural variability of ores from different sources commonly leads to processing inefficiencies, particularly when a processing plant is designed to treat ore from a single source (i.e. ore of a relatively uniform composition). The bulk of the Witwatersrand ore in the Klerksdorp goldfield, processed at the AngloGold Ashanti Great Noligwa treatment plant, is derived from the Vaal Reef (>90%), with a comparatively small contribution obtained from the Crystalkop Reef (or C-Reef). Despite the uneven contribution, it is of critical importance to ensure that the processing parameters are optimized for the treatment of both the Vaal and C-Reefs. This paper serves to document the results of a geometallurgical study of the C-Reef at the Great Noligwa gold mine in the Klerksdorp goldfield of South Africa, with the primary aim of assessing the suitability of the processing parameters that are in use at the Great Noligwa plant. The paper also draws comparisons between the C-Reef and the Vaal Reef A-facies (Vaal Reef) and attempts to explain minor differences in the recovery of gold and uranium from these two sources. Three samples of the C-Reef were collected in-situ from the underground operations at Great Noligwa mine for mineralogical analyses and metallurgical tests. Laboratory-scale leach tests for gold (cyanide) and uranium (sulphuric acid) were carried out using dissolution conditions similar to that in use at the Great Noligwa plant, followed by further diagnostic leaching in the case of gold. The gold in the ore was found to be readily leachable with recoveries ranging from 95% to 97% (as opposed to 89% to 93% for the Vaal Reef). Additional recoveries were achieved in the presence of excess cyanide (96% to 98%). The recovery of uranium varied between 72% and 76% (as opposed to 30% to 64% for the Vaal Reef), which is substantially higher than predicted, given the amount of brannerite in the ore, which is generally regarded as refractory. Thus, the higher uranium recoveries from the C-Reef imply that a proportion of the uranium was recovered by the partial dissolution of brannerite. As the Vaal Reef contain high amounts of chlorite (3% to 8%), which is an important acid consumer, it is considered likely that this could have reduced the effectiveness of the H2SO4 leach in the case of the ore of the Vaal Reef. Since the gold and uranium recoveries from the C-Reef were higher than the recoveries from the Vaal Reef, the results demonstrate that the processing parameters used for treatment of the Vaal Reef are equally suited to the treatment of the C-Reef. Moreover, small processing modifications, such as increased milling and leach retention times, may well increase the recovery of gold (particularly when e.g. coarse gold, or unexposed gold, is present).


Author(s):  
Mahesh Gosi ◽  
Nagaraju Marepu ◽  
Yeturu Sunandamma

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