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作 者:付鹏[1,2] 李解[1] 李保卫[1] 王介良[1,2] 赵婧雯[2] 胡庆成[1] Fu Peng Li Jie Li Baowei Wang Jieliang Zhao Jingwen Hu Qingcheng(Key Laboratory of Integrated Exploitation of Bayan Obo Multi-Metal Resources, Inner Mongolia University of Sci- ence and Technology, Baotou 014010, China Mining Research Institute, Inner Mongolia University of Science and Technology, Baotou 014010, China)
机构地区:[1]内蒙古科技大学白云鄂博矿多金属资源综合利用重点实验室,内蒙古包头014010 [2]内蒙古科技大学矿业研究院,内蒙古包头014010
出 处:《稀有金属》2017年第7期792-798,共7页Chinese Journal of Rare Metals
基 金:内蒙古自然科学基金项目(2015MS0559;2014MS0521)资助
摘 要:通过黄铁矿纯矿物浮选实验、紫外分光光度计(UV-Vis)分析、Zeta电位测定和傅里叶变换红外光谱(FT-IR)分析研究了工业回水中超标离子(NH+4,Mg^(2+),Ca^(2+),F-)对黄铁矿浮选的作用机制。结果表明,回水中NH_4^+可以提高矿物表面的电位,扩大黄铁矿浮选的pH值范围,红外光谱表明其能促进黄铁矿与黄药发生化学吸附,且矿物表面黄药吸附量随着NH+4的增加而增加,经NH_4^+活化后,黄铁矿浮选回收率提高15.5%。而回水中Ca^(2+),Mg^(2+),F-会抑制黄铁矿对黄药的吸附,浮选回收率平均下降10%。其中,Ca^(2+),Mg^(2+)在黄铁矿表面易形成亲水膜,阻碍黄铁矿对黄药的表面吸附;Zeta电位测试发现F-吸附在矿物表面导致矿物表面带负电,与同为阴离子的黄原酸根离子形成竞争吸附,减少了黄原酸盐在黄铁矿表面的吸附量,降低了其可浮性。The action mechanism of over proof ions ( NH4 , Mg2 + , Ca2 + , F- ) in industry backwater to flotation of pyrite was inves- tigated by pure mineral flotation tests, ultraviolet visual ( UV-Vis ) spectrophotometer, Zeta potential and Fourier transform infrared spectroscopy (FT-IR) spectra measurements. The results showed that NH4 in backwater made the potential of mineral surface increase and extended the range of pH values of pyrite flotation. FT-IR spectra results showed that NH4 also made xanthate chemisorb on pyrite surface, and adsorption quantity increased with NH/concentration increasing. The flotation recovery rate increased by 15.5% after ac- tivation of NH4 . While Mg2 + , Ca2 + and F - in backwater inhibited the adsorption of xanthate on pyrite surface, the flotation recovery rate decreased by 10% on average. Mg2+ and Ca2+ easily formed hydrophilic membranes on pyrite surface to hinder xanthate adsorp- tion; F- adsorption on mineral surface could make mineral surface be negatively charged, which was found by Zeta potential test, and thus formed a competitive adsorption between xanthate ion and F , both being anions, and reduced xanthate adsorption on pyrite sur- face, so floatability of pyrite decreased.
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