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An Alternative Depressant of Chalcopyrite in Cu–Mo Differential Flotation and Its Interaction Mechanism

机译:Cu-Mo差分浮选中氯偶沸石的另一种抑制剂及其相互作用机理

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摘要

Carboxymethylcellulose (CMC) is a nontoxic and biodegradable polysaccharide, which can potentially replace the frequently used hazardous depressants in Cu⁻Mo separation. However, a lack of understanding of the interaction mechanism between the CMC and the minerals has hindered its application. In the present study, it is found that 50 mg·L−1 CMC can inhibit chalcopyrite entirely in the pH range 4⁻6, while having little effect on molybdenite. The results also showed that the inhibition effect of the depressant for chalcopyrite enhanced with the increase of the degree of substitution (DS) and molecular weight (Mw) of CMC. The low DS and high Mw of CMC were detrimental to the Cu⁻Mo separation flotation. Furthermore, CMC adsorption was found to be favored by a positive zeta potential but hindered by the protonation of the carboxyl groups. An electrochemical study showed that CMC inhibited 92.9% of the electrochemical reaction sites of chalcopyrite and greatly reduced the production of hydrophobic substances. The XPS and FTIR measurements displayed that the chemisorption was mainly caused by Fe3+ on the chalcopyrite surface and the carboxyl groups in the CMC molecular structure.
机译:羧甲基纤维素(CMC)是无毒和可生物降解的多糖,其可能替代Cu 1MO分离中的经常使用的危险抑制剂。然而,缺乏对CMC和矿物质之间的相互作用机制的理解阻碍了其应用。在本研究中,发现50mg·L-1 CMC可以完全在pH范围内抑制黄铜矿,同时对钼效应不大。结果还表明,随着CMC的取代度(DS)和分子量(MW)的增加,抑制剂对黄铜矿的抑制作用增强。 CMC的低DS和高MW对Cu⁻mo分离浮选有害。此外,发现CMC吸附是通过阳性Zeta电位而受到的,但是通过羧基的质子化阻碍。电化学研究表明,CMC抑制了硫代铜矿电化学反应部位的92.9%,大大降低了疏水性物质的产生。 XPS和FTIR测量显示,化学吸附主要是由Chalcyite表面的Fe 3 +引起的CMC分子结构中的羧基。

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