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The Effect of Dissolved Copper and Silver on Sphalerite Dissolution in Ferric Sulphate-Sulphuric Acid Media

机译:溶解的铜和银对硫酸铁-硫酸介质中闪锌矿溶解的影响

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The dissolution rates of low-iron Santander (0.08 % Fe) and Oklahoma (0.2 % Fe) sphalerites, defined by l-(l-a)~(1/3) = kt, increase rapidly as the dissolved copper concentration of the 0.3 M Fe(SO_4)_(1.5)- 0.3 M H_2SO_4 leach solution increases from 0 to about 100 mg/L. The rates then increase slightly, or remain nearly constant, as the copper concentration rises to about 500 mg/L. Further increases in the copper concentration, to 5000 mg/L, cause the rates to decrease. For the high-iron Montauban (8.0 % Fe) and Kenabic Lake (10.4 % Fe) sphalerites, the leaching rates decrease dramatically as the Cu concentration increases from 0 to about 20 mg/L, but then essentially stabilize at a very low level for dissolved copper concentrations up to 7500 mg/L. Detailed SEM-EDX study of the reacted sphalerites detected only sphalerite and elemental sulphur. Copper sulphides were not detected, in agreement with the fact that the dissolved copper concentration remained essentially constant throughout the experiments done in the presence of the ferric sulphate oxidant. Dissolved silver concentrations in the 0 to 10 mg/L range effectively suppress the dissolution of both low-iron and high-iron sphalerite. A dissolved Ag concentration of only 1 mg/L almost entirely suppresses the leaching of low-iron sphalerites, whereas a concentration of 2 or 4 mg/L is needed to produce a similar effect for the iron-rich Montauban or Kenabic Lake sphalerites. SEM-EDX studies of the reacted low-iron and high-iron sphalerites confirmed the inhibitory effect of dissolved silver. A few particles of silver sulphide were detected on the sphalerite surfaces or embedded in sulphur globules, but there was no evidence of a continuous passivating silver sulphide film. Thus, the dissolved silver must either form an adsorbed monolayer on the sphalerite or somehow alter the electronic properties of the sphalerite surface as seems to be the situation for dissolved copper.
机译:低铁桑坦德铁(0.08%Fe)和俄克拉荷马州(0.2%Fe)闪锌矿的溶解速率(由1-(la)〜(1/3)= kt定义)随着0.3 M Fe的溶解铜浓度而迅速增加(SO_4)_(1.5)-0.3 M H_2SO_4浸出溶液从0增加到约100 mg / L。然后,随着铜浓度增加到约500 mg / L,速率会略有增加,或保持接近恒定。铜浓度进一步增加至5000 mg / L会使速率降低。对于高铁蒙托邦(铁含量为8.0%)和肯纳比克湖(铁含量为10.4%)的闪锌矿,其浸出速率随着Cu浓度从0增加到约20 mg / L而急剧下降,但随后基本上稳定在非常低的水平溶解的铜浓度高达7500 mg / L。对已反应闪锌矿的详细SEM-EDX研究仅检测到闪锌矿和元素硫。未检测到硫化铜,这与在硫酸铁氧化剂存在下进行的整个实验中溶解的铜浓度基本保持恒定这一事实是一致的。 0至10 mg / L范围内的溶解银浓度可有效抑制低铁和高铁闪锌矿的溶解。仅1 mg / L的溶解Ag浓度几乎完全抑制了低铁闪锌矿的浸出,而对于富铁的Montauban或Kenabic Lake闪锌矿,则需要2或4 mg / L的浓度才能产生类似的效果。 SEM-EDX对反应的低铁和高铁闪锌矿的研究证实了溶解银的抑制作用。在闪锌矿表面上发现了一些硫化银颗粒或嵌入了硫球中,但没有证据表明连续钝化了硫化银膜。因此,溶解的银必须要么在闪锌矿上形成吸附的单层,要么以某种方式改变闪锌矿表面的电子性能,这似乎是溶解铜的情况。

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