Cu(I)/Cu(II) mixed-valence surface complexes of S-[(2-hydroxyamino)-2-oxoethyl]-N,N-dibutyldithiocarbamate: Hydrophobic mechanism to malachite flotation

被引:115
作者
Liu, Sheng [1 ]
Zhong, Hong [1 ]
Liu, Guangyi [1 ]
Xu, Zhenghe [2 ]
机构
[1] Cent S Univ, Sch Chem & Chem Engn, Changsha 410083, Hunan, Peoples R China
[2] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 2V4, Canada
基金
国家高技术研究发展计划(863计划); 中国国家自然科学基金;
关键词
S-[(2-hydroxyamino)-2-oxoethyl]-N; N-dibutyldithiocarbamate; Malachite; Flotation mechanism; Cu(I)/Cu(II) mixed-valence surface complexes; ToF-SIMS; N-OCTANOHYDROXAMATE; ADSORPTION MECHANISM; HYDROXAMIC ACID; TOF-SIMS; SPECTROSCOPIC CHARACTERIZATION; ETHOXYCARBONYL THIOUREA; CHELATING-AGENTS; AQUEOUS-SOLUTION; COPPER SURFACES; CHALCOPYRITE;
D O I
10.1016/j.jcis.2017.10.063
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Hypothesis: Hydroxamate and sulfhydryl surfactants are effective collectors for flotation of copper minerals. The combination application of hydroxamate and sulfhydryl collectors has been proved to be an effective approach for improving the flotation recovery of non-sulfide copper minerals. A surfactant owing both hydroxamate and dithiocarbamate groups might exhibit strong affinity to non-sulfide copper minerals through double sites adsorption, rendering an enhanced hydrophobization to non-sulfide copper minerals flotation. Experiments: The flotation performance of S-[(2-hydroxyamino)-2-oxoethyl]- N,N-dibutyldithiocarbamate (HABTC) to malachite, calcite and quartz were first evaluated through systematic micro-flotation experiments. HABTC's hydrophobic mechanism to malachite was further investigated and analyzed by zeta potential, Fourier transform infrared spectroscopy (FTIR), time-of-flight secondary ion mass spectrometry (ToF-SIMS) and X-ray photoelectron spectroscopy (XPS). Findings: The micro-flotation results demonstrated HABTC was an excellent collector for malachite flotation and exhibited favorable selectivity for flotation separation of malachite from quartz or calcite under pH 8.5-103. Zeta potential and FTIR implied that HABTC might bond with the surface copper atoms of malachite, with releasing the Fr ions of its hydroxamate group into pulp. ToF-SIMS provided clear evidences that the Cu-hydroxamate and Cu-dithiocarbamate groups were formed on malachite surfaces after HABTC adsorption. XPS revealed that Cu(l)/Cu(II) mixed -valence surface complexes of HABTC anchored on malachite through formation of Cu(l) S and Cu(II)-O bonds, accompanying with reduction of partial surface Cu(II) to Cu(I). The Cu(I)/Cu(II) mixed -valence double chelating character and "chair"-shape N,N-dibutyldithiocarbamate hydrophobic group, resulting in an enhanced affinity and hydrophobization of HABTC to malachite flotation. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:701 / 712
页数:12
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