Efficient separation of sulfide minerals using a heterocyclic collector by regulating strong and weak interactions

IF 9 1区 工程技术 Q1 ENGINEERING, CHEMICAL Separation and Purification Technology Pub Date : 2025-03-16 DOI:10.1016/j.seppur.2025.132526
Lin Yang , Xin Jin , Zhitao Feng , Shihong Xu , Feng Xie , Wei Sun , Wanjia Zhang , Zhiyong Gao
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Abstract

Galena is the primary source of lead (Pb), and its efficient utilization is hindered by associated minerals such as sphalerite and pyrite. Flotation is the main method used for their separation, requiring the development of efficient flotation reagents, particularly collectors. In this work, a novel galena collector, 5-mercapto-3-phenyl-1,3,4-thiadiazole-2(3H)-thione (YC-2), was designed and synthesized to selectively float galena from sphalerite and pyrite. By regulating both strong (coordination) and weak (hydrogen bonding) interactions between YC-2 molecules and the surfaces of the sulfide minerals, the energy and spatial matching degrees in adsorption were enhanced. The flotation tests indicate that YC-2 can efficiently and greenly separate galena from sphalerite and pyrite under natural pulp pH (∼8), demonstrating strong collecting ability and high selectivity. Zeta potential, XPS analysis, and DFT calculations confirm that YC-2 selectively adsorbs on galena by forming N–Pb–S bonds, rather than on sphalerite or pyrite. As pH increases, the electrostatic repulsion between YC-2 and the sulfide minerals gradually strengthens, attributed to the increased negative charge of the coordination groups in YC-2 and more negative zeta potentials on the sulfide mineral surfaces. At pH 8, electrostatic repulsion reaches its optimal level, maximizing galena selectivity. In terms of energy matching, strong interactions are regulated by incorporating a xanthate skeleton into an azacycle, while YC-2 is constructed with lower molecular polarity, fewer ionic bonds, and higher selectivity. Regarding spatial matching, weak interactions are regulated by increasing spatial hindrance, enhancing YC-2 selectivity due to differences in the hydration layers of sulfide minerals. Water molecules loosely adsorb on galena mainly via S···H hydrogen bonds, but tightly adsorb on sphalerite and pyrite mainly via Zn–O/Fe–O bonds. Due to desolvation, YC-2 preferentially adsorbs on galena over sphalerite and pyrite. In conclusion, YC-2 exhibits enhanced flotation performance, achieving efficient and green separation of galena from complex sulfide ores, with industrial application potential.

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利用杂环捕收剂通过调节强弱相互作用有效分离硫化矿物
方铅矿是铅的主要来源,伴生矿物如闪锌矿和黄铁矿阻碍了其有效利用。浮选是它们分离的主要方法,这就要求开发高效的浮选试剂,特别是捕收剂。本文设计并合成了一种新型方铅矿捕收剂——5-巯基-3-苯基-1,3,4-噻二唑-2(3H)-硫酮(YC-2),用于从闪锌矿和黄铁矿中选择性浮选方铅矿。通过调节YC-2分子与硫化物矿物表面的强(配位)和弱(氢键)相互作用,增强了吸附的能量和空间匹配度。浮选试验表明,在自然矿浆pH(~ 8)条件下,YC-2能高效、绿色地分离方铅矿、闪锌矿和黄铁矿,表现出较强的捕收能力和较高的选择性。Zeta电位、XPS分析和DFT计算证实,YC-2通过形成N-Pb-S键选择性吸附在方铅矿上,而不是在闪锌矿或黄铁矿上。随着pH的增加,YC-2与硫化矿物之间的静电斥力逐渐增强,这是由于YC-2中配位基团的负电荷增加,硫化矿物表面的负zeta电位增加。在pH值为8时,静电斥力达到最佳水平,最大化方铅矿的选择性。在能量匹配方面,强相互作用通过将黄原药骨架纳入氮杂环来调节,而YC-2具有较低的分子极性,较少的离子键和较高的选择性。在空间匹配方面,由于硫化矿物水化层的差异,弱相互作用通过增加空间阻碍来调节,增强了YC-2的选择性。水分子主要通过S··H氢键在方铅矿上松散吸附,而主要通过Zn-O / Fe-O键在闪锌矿和黄铁矿上紧密吸附。由于溶解作用,YC-2优先吸附方铅矿,而非闪锌矿和黄铁矿。综上所述,YC-2浮选性能较好,实现了方铅矿从复杂硫化矿石中高效、绿色分离,具有工业应用潜力。
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来源期刊
Separation and Purification Technology
Separation and Purification Technology 工程技术-工程:化工
CiteScore
14.00
自引率
12.80%
发文量
2347
审稿时长
43 days
期刊介绍: Separation and Purification Technology is a premier journal committed to sharing innovative methods for separation and purification in chemical and environmental engineering, encompassing both homogeneous solutions and heterogeneous mixtures. Our scope includes the separation and/or purification of liquids, vapors, and gases, as well as carbon capture and separation techniques. However, it's important to note that methods solely intended for analytical purposes are not within the scope of the journal. Additionally, disciplines such as soil science, polymer science, and metallurgy fall outside the purview of Separation and Purification Technology. Join us in advancing the field of separation and purification methods for sustainable solutions in chemical and environmental engineering.
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