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Inhibition mechanism of Ca2+, Mg2+ and Fe3+ in fine cassiterite flotation using octanohydroxamic acid

机译:Ca2 +,Mg2 +和Fe3 +在辛酸异羟肟酸微细锡石浮选中的抑制机理

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摘要

The existence of metal ions should not be ignored in both hydrometallurgy and flotation. In this study, the effects of Ca2+, Mg2+ and Fe3+ on the flotation performance of cassiterite using octanohydroxamic acid (OHA) as the collector were investigated by micro-flotation tests, X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, contact angle, zeta ( ζ ) potential measurements and atomic force microscopy (AFM) imaging. The results of the flotation and contact angle experiments showed that the addition of Ca2+, Mg2+ and Fe3+ significantly decreased both the recovery and contact angle of cassiterite with pH ranged from 6.0 to 12.0 in the presence of OHA collector. ζ- Potential measurements, solution chemistry analysis and FTIR measurements indicated that the flotation recovery of the cassiterite declined due to the CaOH+, MgOH+ and Fe(OH)3 sites on the cassiterite surface. XPS results indicated that the chemisorption of OHA and calcium ions on the cassiterite surface finally changed its chemical properties. The AFM images also revealed that new species Fe(OH)3 of Fe3+ formed and adsorbed on the cassiterite surface at pH 9.0. The adsorption of Fe(OH)3 reduced the adsorption of OHA on the cassiterite surface, thus the hydrophobicity of cassiterite was deteriorated.
机译:在湿法冶金和浮选中均不应忽略金属离子的存在。本研究中,Ca 2 + ,Mg 2 + 和Fe 3 + 对使用辛基异羟肟酸(OHA)浮选锡石的性能的影响通过微浮选测试,X射线光电子能谱(XPS),傅里叶变换红外(FTIR)光谱,接触角,ζ(ζ)电势测量和原子力显微镜(AFM)成像研究了作为集电极的材料。浮选和接触角实验结果表明,Ca 2 + ,Mg 2 + 和Fe 3 + 的添加均显着降低了在OHA捕收剂存在下,pH值从6.0到12.0的锡石回收率和接触角。 ζ-电位测量,溶液化学分析和FTIR测量表明,由于CaOH + ,MgOH + 和Fe(OH)在锡石表面上有3 个位点。 XPS结果表明,OHA和钙离子在锡石表面的化学吸附作用最终改变了其化学性质。原子力显微镜图像还显示,新的Fe 3 + 物种Fe(OH) 3 在pH 9.0下形成并吸附在锡石表面。 Fe(OH) 3 的吸附减少了OHA在锡石表面上的吸附,从而降低了锡石的疏水性。

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