Search

Environmentally friendly pretreatment of double refractory gold ores (DRGO) to improve gold recovery without emitting pollutant gas is challenging. Sequential biotreatment, including iron-oxidizing microorganisms to decompose sulfides, followed by the enzymatic decomposition of carbonaceous matter, was recently developed. The effect of acid washing by 1 M HCl for 24 h between two bioprocesses was evaluated using a real double refractory gold ore from the Syama mines, Mali, which includes 24 g/t of Au and 5.27 wt% of carbon with a relatively higher graphitic degree. The addition of the acid washing process significantly improved gold recovery by cyanidation to yield to 84.9 ± 0.7% from 64.4 ± 9.2% (n = 2). The positive effects of acid washing can be explained by chemical alteration of carbonaceous matter to facilitate the accessibility for lignin peroxidase (LiP) and manganese peroxidase (MnP) in cell-free spent medium (CFSM), although the agglomeration was enhanced by an acid attack to structural Fe(III) in clay minerals. Sequential treatment of DRGO basically consists of the oxidative dissolution of sulfides and the degradation of carbonaceous matter prior to the extraction of gold; however, the details should be modified depending on the elemental and mineralogical compositions and the graphitic degree of carbonaceous matter.

Sequential treatment was applied to carbonaceous Au-Ag-bearing ore concentrate to maximize the Au and Ag recovery. In the preliminary test, the present carbonaceous ore had well liberated and exposed type of gold grains, which are not refractory, but included mainly three types of Ag presented as electrum, hessite (Ag2Te) and Ag-bearing other minerals. Au recovery was ∼100% without any treatment, meanwhile Ag recovery was only 33.3%. The sequential treatment comprises two oxidation steps: (a) mixed culture of iron- and sulfur-oxidizing microorganisms at pH 1.2, followed by (b) cell-free spent medium (CFSM) at pH 4.0 from a white rot-fungus, Phanerochaete chrysosporium, which includes lignin-degrading enzymes. As a result, Ag recovery was 55.5% after the first step and greatly improved to ∼100%, including the dissolved Ag+ concentration in the first step of acid treatment. Although the acidophilic iron-oxidizing microorganisms were inhibited by dissolved Ag+ and Cd2+ ions, the strong acidic conditions dissolved hessite and Ag-bearing oxide minerals. However, the remaining carbonaceous matter acted to sorb Ag(CN)2− in cyanidation, causing the recovery loss. In the next step the lignin-degrading enzymes degraded carbonaceous matter in the ore. This step is necessary to avoid the adsorption of Ag(CN)2− on graphitic carbonaceous matter, leading a mostly perfect recovery of the remaining Ag in the solid residues, without necessity of alkaline washing. The sequential treatment including enzymatic lignin-degrading process was also effective in carbonaceous silver ore avoiding the emission of air pollutants.

Several efforts are made to find various green alternatives for carbonaceous matter (CM) degradation in carbonaceous gold ores. The deleterious effect of CM is observed during cyanidation, where CM adsorbs Au(CN)2- behaving like activated carbon, an effect called pre-robbing. Thus, biotechnological approaches like enzyme degradation of CM to reduce Au(CN)2- adsorption are currently being studied. In the present work, the potential of CM degradation and gold preg-robbing reduction by laccase-mediator system (LMS) oxidation was evaluated using powder activated carbon (PAC) as CM surrogate material through model experiments. Based upon gas chromatography-mass spectrometry (GC-MS) analysis of extracted by-products from bio-treated PAC, LMS treatment after seven days physically and chemically altered the surface of PAC by the reduction of specific surface area and pore volume, the disruption of aromatic moieties into aliphatic compounds, and the formation of oxygen-containing functional groups. Subsequently, under the studied condition, the adsorption capacity of Au(CN)2- on the surface-degraded PAC was dramatically decreased from 46 μmol/g to 7.36 μmol/g. The present findings provide a new outlook of an alternative pre-treatment process of carbonaceous gold ore in mineral processing.

Carbonaceous matter in refractory gold ore is known to be one of the primary causes of gold recovery loss. Model experiments were conducted to simulate the bio-modification of carbonaceous matter using powdered activated carbon (PAC) as a surrogate and cell-free spent medium (CFSM) of Phanerochaete chrysosporium. The CFSM was used because of the lignin peroxidase and manganese peroxidase secreted by the microbe during its incubation. In the present work, an investigation was conducted to determine the physical and chemical alterations in PAC after enzymatic treatment and its effect on Au(CN)2− uptake. Characterization of the solid residues of PAC by 13C NMR and N2 adsorption after bio-modification revealed that the treatment had decomposed poly-aromatic carbons into aliphatic carbons and also reduced the specific surface area from 1430 m2/g to 697 m2/g in 14 days. As a result, Au(CN)2− uptake decreased from 100% (0.048 mmol/g) to 43% within 12 h primarily due to the enzyme treatment and adsorption of CFSM components. It further decreased to 26% due to surface passivation by bio-chemicals derived from CFSM and/or decomposed aliphatic hydrocarbons from aromatic carbons between 7 days and 14 days. These findings may contribute to efforts to decrease preg-robbing in hydrometallurgical processing of refractory gold ores.

The detailed mechanism behind the bio-decomposition of carbonaceous matter in refractroy goold ore byPhanerocheate chrysosporiumto facilitate improved cyanidation of gold is as yet undersdtood. To gain a better understanding of this mechanism, the present work model experiments using powdery activated carbon (PAC) and cell-free extracts ofP.chrysosporiumto simulate and focus on the biotransformation of carbonaceous matters in refractory gold ores. The results of solid characterization using SEM and XRD indicated a more non-uniform surface and smaller crystal sizes for PAC treaded with cell-free extracts for 72 hours. The significant decomposition of aromatic compounds into aliphatic compounds were observed in13C-NMR and FTIR results for the high ratio of cell-free extract volume to mass of PAC. This results support the theory that one of the fundamental mechanisms behind the bio-decomposition process is aromatic bond cleavage by biomolecules produced byP.chrysosporium.