With growing environmental and occupational safety concerns over the use of cyanide in gold processing, more acceptable alternatives are receiving increased interest. The most promising of the possible alternatives is thiosulfate. However, as activated carbon is not an effective substrate for the adsorption of the gold thiosulfate complex, the thiosulfate process lacks a proven in-pulp method for recovering dissolved gold. Anion exchange resins offer a possible route for in-pulp recovery. This thesis describes work aimed at evaluating the effectiveness of commercially available anion exchange resins for the recovery of gold from thiosulfate leach liquors and pulps.ududIt was found that Strong-base resins are superior at accommodating the gold thiosulfate complex compared to Weak-base resins, which means Strong-base resins have a greater capacity to compete with other anions in leach solutions. Strong-base resins were therefore the preferred choice of resin for recovery of gold from thiosulfate leach solutions and pulps. Work with a selected commercial Strong-base resin showed that competing polythionates (particularly tri- and tetrathionate) lower the maximum possible loading of gold but that gold is selectively recovered over other base-metal anions in typical leach solutions. From kinetic experiments, it was found that competing polythionates did not affect the initial rate of loading of gold but displaced the loaded gold at long times. Thus it would be important to minimise the contact time of the resin with the pulp.ududEquilibrium loading isotherms of gold in the presence of competing anions could be analysed by treating the ion exchange reaction as a simple chemical reaction. However, a stoichiometry and equilibrium quotient which does not follow that normally used for anion exchange, was required to describe the experimental data. A single value for the equilibrium constant also cannot be used to describe the data over the range of concentrations for a given competing anion. The order of selectivity of the anions for the anion exchange resin could be explained by the difference in structure and the charge of each anion.ududThe rate of loading of gold is controlled by mass transport in the aqueous phase in the presence of weakly competing anions such as sulfate and thiosulfate. An attempt was made to describe the more complex loading curves obtained in the presence of stronger competing anions such as sulfite, trithionate and tetrathionate in which it was found that the loading of gold increased to a maximum before declining to a lower equilibrium value. The difference in the rate of loading between the macroporous and gel anion exchange resins was explained by the difference in the location of their functional groups.ududOperation of a small-scale resin-in-pulp plant showed that gold could be recovered from a leach pulp to yield loadings of gold of up to 6000 mg L-1 and loadings of copper below 100 mg L-1. Under ideal conditions, the gold concentration in the barren pulp could contain less than 0.01 mg L-1. Throughout the trial it was shown that loaded copper would be displaced by gold which would result in the loading of copper falling from 2000 mg L-1 in the last stage to lower than 100 mg L-1 on the resin in the first stage. It was observed that some of the dissolved gold precipitated or adsorbed on the solids during leaching. Some of this adsorbed gold was found to be recovered by the anion exchange resins that would have reported to the tails if a solid/liquid separation method was employed.ududGold was efficiently eluted with a nitrate solution and the two-step elution process using aerated ammonia followed by nitrate effectively stripped all the copper and gold from the resin. This process was found not to materially affect the equilibrium gold concentration on the resin after eight cycles, thus allowing the resin to be recycled without the need for regeneration. Electrochemical studies showed that the gold thiosulfate complex was reduced on stainless steel from a nitrate solution. Conventional electrowinning could therefore be used to recover the gold from the eluant.
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机译:随着人们越来越关注在金加工中使用氰化物的环境和职业安全问题,越来越多的可接受的替代品受到越来越多的关注。最有希望的替代方法是硫代硫酸盐。然而,由于活性炭不是吸附硫代硫酸金络合物的有效底物,因此硫代硫酸盐工艺缺乏用于回收溶解金的成熟纸浆法。阴离子交换树脂为纸浆中回收提供了一条可能的途径。本论文描述了旨在评估可商购获得的阴离子交换树脂从硫代硫酸盐浸出液和纸浆中回收金的有效性的工作。 ud ud发现,与弱电相比,强碱树脂在容纳硫代硫酸金络合物方面具有优势。碱树脂,这意味着强碱树脂在沥滤溶液中具有与其他阴离子竞争的更大能力。因此,强碱树脂是从硫代硫酸盐浸出液和纸浆中回收金的首选树脂选择。使用选定的商业强碱树脂进行的研究表明,竞争的多硫酸盐(尤其是三硫酸盐和四硫酸盐)降低了金的最大可能负载量,但是在典型的浸出溶液中,金被选择性地回收了其他贱金属阴离子。从动力学实验中发现,竞争的多硫酸盐不会影响金的初始加载速率,但是会长时间置换加载的金。因此,重要的是使树脂与纸浆的接触时间最短。 ud ud在存在竞争性阴离子的情况下,金的平衡负载等温线可以通过将离子交换反应视为简单的化学反应来进行分析。然而,描述实验数据需要不符合通常用于阴离子交换的化学计量和平衡商。平衡常数的单个值也不能用于描述给定竞争阴离子的浓度范围内的数据。阴离子对阴离子交换树脂的选择性顺序可以通过结构和每个阴离子的电荷差异来解释。 ud ud在弱离子存在下,金的负载率受水相中的质量传输控制。竞争性阴离子,例如硫酸根和硫代硫酸根。试图描述在更强的竞争性阴离子(如亚硫酸根,三硫酸根和四硫酸根)存在下获得的更复杂的负载曲线,其中发现金的负载在下降到较低的平衡值之前增加到最大值。大孔阴离子交换树脂和凝胶阴离子交换树脂之间的负载率差异可以通过其官能团位置的差异来解释。 ud ud小规模纸浆树脂制浆工厂的运营表明,可以从中回收金一种浸出矿浆,以产生高达6000 mg L-1的金含量和低于100 mg L-1的铜含量。在理想条件下,贫浆中金的含量可能少于0.01 mg L-1。在整个试验过程中,结果表明,负载的铜将被金置换,这将导致铜的负载量从最后阶段的2000 mg L-1下降到第一阶段树脂中的100 mg L-1以下。观察到在浸出过程中一些溶解的金沉淀或吸附在固体上。发现某些吸附的金是通过阴离子交换树脂回收的,如果采用固/液分离方法,这些阴离子交换树脂会在尾巴上报告。 ud ud金用硝酸盐溶液有效洗脱,并分两步洗脱使用充气氨水和硝酸盐可以有效地从树脂中去除所有铜和金。发现该方法在八个循环后不会对树脂上的平衡金浓度产生实质性影响,从而使树脂可以循环使用而无需再生。电化学研究表明,从硝酸盐溶液中还原了不锈钢上的硫代硫酸金络合物。因此,常规的电解提取可以用于从洗脱液中回收金。
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