Molecular characteristics of the mixed cationic/anionic collector interface probed by sum-frequency vibrational spectroscopy and molecular dynamics simulations

被引:5
作者
Zhu, Guangli [1 ,2 ]
Liu, Runzhe [3 ]
Wang, Xuming [4 ]
Miller, Jan D. [4 ]
Cao, Yijun [1 ]
机构
[1] Zhengzhou Univ, Zhongyuan Crit Met Lab, 100 Sci Ave, Zhengzhou 450001, Henan, Peoples R China
[2] Zhengzhou Univ, Henan Prov Ind Technol Res Inst Resources & Mat, 100 Sci Ave, Zhengzhou 450001, Henan, Peoples R China
[3] Yunnan Phosphate Chem Grp Co, Phosphate Resources Engn Res Branch, 403 Yongle Ave, Kunming 650113, Yunnan, Peoples R China
[4] Univ Utah, Coll Engn, Dept Mat Sci & Engn, 122 S Cent Campus Dr, 303, Salt Lake City, UT 84112 USA
基金
中国国家自然科学基金;
关键词
Mixed cationic; anionic collectors; Molecular structure; SFVS; MD simulation; AIR/WATER INTERFACE; WATER-MOLECULES; ADSORPTION MECHANISM; FLOTATION; SURFACTANTS; ORIENTATION; GENERATION; MONOLAYER; SPODUMENE; FELDSPAR;
D O I
10.1016/j.molliq.2023.122408
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
The molecular structure and orientation of collectors and water molecules on bubble surfaces in ore pulp is a fundamental phenomenon in the process of froth flotation. Considering the adsorption behavior and orientation of collectors and water molecules at the air/solution interface is of particular significance. In this study, the molecular structure and orientation of an aqueous solution of mixed dodecylamine hydrochloride (DDA) and sodium oleate (NaOL) with different molar ratios, and water molecules were examined at the air/solution interface and characterized using a combination of surface pressure measurements, sum frequency vibrational spectroscopy (SFVS) and molecular dynamics (MD) simulations. Both individual NaOL and DDA collectors were observed to be well ordered at the interface, while gauche defects appeared in some mixed collector systems. The ordering of interfacial water molecules in the presence of collectors with increasing molar ratios of NaOL to DDA is manifested by an enhancement of OH symmetric stretch from tetrahedrally coordinated water and a decreased bond disorder in the molecular arrangement or a "liquid-like" structure. In these mixed collector systems, the -COO- group from NaOL stretches deeper into water than -NH3+ groups from DDA, and Na cations originating from NaOL distribute closer to -COO- groups compared with the Cl originating from DDA to -NH3+ groups. The interfacial water in the single NaOL system is more strongly hydrogen bonded than those in the DDA and mixed collector systems. Conversely, the alignment of interfacial water molecules in the DDA system was more disrupted. These results provide a better understanding of the ordering of mixed NaOL/DDA collectors, as well as the orientation of water molecules at the air/water interface. This might therefore provide valuable insight into the relationship between the flotation phenomena and molecular characteristics of collectors at the air/water interface and should help to improve the froth flotation technology.
引用
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页数:11
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