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Mercaptobenzothiazole collector adsorption on Cu sulfide ore minerals

机译:巯基苯并噻唑捕收剂对硫化铜矿石矿物的吸附

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The species adsorbed on Cu sulfide ore minerals from near neutral or alkaline solutions of the flotation collector 2-mercaptobenzothiazole (MBT) have been established by X-ray photoelectron spectroscopy (XPS). Previous XPS studies of the species adsorbed on chalcocite from very dilute solutions were extended to adsorption on air-exposed Cu metal, cuprite, chalcocite, covellite, cubanite, chalcopyrite, bornite and pyrite from more concentrated solutions to simulate processing of variably oxidised ores and slug addition of collector under plant conditions. It was found that even in alkaline solutions, HMBT adsorbed in addition to molecular CuMBT, (MBT)(2) and chemisorbed MBT on Cu metal, Cu-I oxide or Cu sulfide minerals. For all Cu-containing surfaces conditioned in a collector solution of concentration higher than 10(-5) M, adsorbed molecular (multilayer) CuMBT remained a minor species within the pH range investigated. For substantial collector coverage, when the concentration of adsorbed HMBT and (MBT)(2) exceeded that of chemisorbed MBT and adsorbed CuMBT, the surface was not obviously hydrophobic. Neither a Cu nor Fe surface oxide layer was predominantly removed by the collector, but MBT chemisorption involved direct interaction with surface Cu atoms rather than via intermediate 0 atoms. There was strong evidence for a Cu-N interaction in bulk CuMBT, and hence in MBT chemisorbed on surface Cu atoms, in addition to the principal interaction through the MBT exocyclic S atom. It was concluded that adsorption of some multilayer MBT species on Cu sulfide ore minerals can be deleterious, and this should be taken into account when variably oxidised ores are being processed. (C) 2016 Elsevier B.V. All rights reserved.
机译:已通过X射线光电子能谱(XPS)确定了从浮选捕收剂2-巯基苯并噻唑(MBT)的接近中性或碱性溶液吸附在硫化铜矿石矿物上的物种。以前对XPS的研究是从非常稀的溶液吸附到球晶石上的物质扩展到在更浓的溶液中对空气暴露的铜金属,铜矿,黄铜矿,陨石,堇青石,黄铜矿,褐铁矿和黄铁矿的吸附,以模拟可变氧化矿石和块状的加工。在工厂条件下添加收集器。结果发现,即使在碱性溶液中,HMBT不仅会吸附分子CuMBT,(MBT)(2),而且还会吸附化学吸附的MBT到Cu金属,Cu-1氧化物或Cu硫化物矿物上。对于所有浓度高于10(-5)M的集流体溶液中的含Cu表面,在研究的pH范围内,吸附的分子(多层)CuMBT仍为次要物种。对于大量的捕集剂覆盖,当吸附的HMBT和(MBT)(2)的浓度超过化学吸附的MBT和CuMBT的吸附浓度时,表面并不明显疏水。铜和铁的表面氧化物层都没有被集电极主要去除,但是MBT化学吸附涉及与表面铜原子的直接相互作用,而不是通过中间的0原子。有强有力的证据表明,除了通过MBT外环S原子的主要相互作用之外,本体CuMBT中还有Cu-N相互作用,因此在化学吸附在表面Cu原子上的MBT中。结论是,硫化铜矿石矿物上某些多层MBT物种的吸附可能有害,在处理各种氧化矿石时应考虑到这一点。 (C)2016 Elsevier B.V.保留所有权利。

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