田孟杰

特聘副教授 硕士生导师

入职时间:2020-05-15

所在单位:资源加工与生物工程学院

职务:无

学历:博士研究生毕业

办公地点:中南大学和平楼

性别:男

联系方式:190708480@qq.com

学位:博士学位

在职信息:在职

主要任职:无

其他任职:无

毕业院校:中南大学

曾获荣誉:

2020-09-01  当选:  2020年度中国有色金属学会优秀博士学位论文奖

   
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Selective flotation separation of cassiterite and calcite through using cinnamohydroxamic acid as the collector and Pb2+ as the activator

发布时间:2023-03-29

点击次数:

影响因子:5.518

DOI码:10.1016/j.colsurfa.2023.131262

所属单位:中南大学

发表刊物:Colloids and Surfaces A: Physicochemical and Engineering Aspects

关键字:Cassiterite; Calcite; Flotation; Cinnamohydroxamic acid; Pb2+; Activation.

摘要:This study employs cinnamohydroxamic acid (CHA) as the collector in the flotation separation of cassiterite/calcite. Pb2+ ion is used as the activator to improve the collecting ability of CHA. This reagent system consisting of CHA collector and Pb2+ activator can achieve a higher recovery of cassiterite of ∼90% than that of calcite of ∼30%. A greater increase of 27.74% in C atomic concentration on the Pb2+-treated cassiterite surface than that of 15.21% on the Pb2+-treated calcite surface after the treatment with CHA indicates a higher adsorption amount of CHA on the Pb2+-treated cassiterite surface than that on the Pb2+-treated calcite surface, which results in its stronger ability to collect the Pb2+-activated cassiterite particles compared to the Pb2+-activated calcite particles. The treatment with CHA results in a smaller shift of ∼20 mV in the zeta potential of the Pb2+-treated cassiterite particles than that of ∼45 mV in the zeta potential of the Pb2+-treated calcite particles, which is in contradiction with the results of the X-ray photoelectron spectroscopic tests. A novel activation mechanism of Pb2+ ion for CHA flotation of cassiterite is proposed to account for this paradoxical observation. The formation of the Pb-CHA complexes is this activation mechanism of Pb2+ ion.

论文类型:期刊论文

通讯作者:田孟杰

学科门类:工学

一级学科:矿业工程

文献类型:J

卷号:666

是否译文:

发表时间:2023-03-11

收录刊物:SCI

附件:

  • Selective-flotation-separation-of-cassiterite-and-calcite.pdf

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