β-Amino-hydroxamate surfactants: Preparation, and adsorption mechanism in bastnaesite flotation

被引:42
|
作者
Qi, Jing [1 ]
Fan, Hongli [1 ]
Liu, Guangyi [1 ]
机构
[1] Cent South Univ, Coll Chem & Chem Engn, Changsha 410083, Peoples R China
基金
中国国家自然科学基金;
关键词
Bastnaesite; beta-Amino-hydroxamic acid; Flotation; Adsorption mechanism; AZA-MICHAEL REACTION; RARE-EARTH-OXIDES; AMINOHYDROXAMIC ACIDS; SODIUM OLEATE; SPECTROSCOPIC CHARACTERIZATION; HYDROPHOBIC MECHANISM; SELECTIVE FLOTATION; CONJUGATE ADDITION; CHEMISTRY; COMPLEXES;
D O I
10.1016/j.seppur.2020.116634
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
beta-Amino-hydroxamate surfactants including N-(3-(dodecylamino)) hydroxamic acid (DAHA), N-(3-(octylamino)) hydroxamic acid (OAHA) and N-(3-(hexylamino)) hydroxamic acid (HAHA) were synthesized and firstly used as flotation collectors in bastnaesite flotation. Micro-flotation results indicated that DAHA, OAHA and HAHA displayed strong collecting affinity toward bastnaesite. And HAHA floated out 92.4% bastnaesite and 37.1% calcite from their artificially mixed minerals, inferring its excellent flotation selectivity toward bastnaesite versus calcite. The existence of HAHA elevated the zeta potential of bastnaesite, while had a slight effect on calcite. The entropy change Delta S, enthalpy change Delta H, free energy change Delta G (298 K) and activation energy E-a for bastnaesite adsorption of HAHA were 317.36 J.mol(-1).K-1, 74.53 kJ.mol(-1) 20.04 kJ.mol(-1) and 13.20 kJ.mol(-1), respectively, deducing an endothermic-spontaneous chemisorption process. FTIR and XPS recommended that HAHA chelated with surface Ce atom(s) to form five-membered hydroxamate-(O,O)-Ce complexes. And the amino group of HAHA facilitated its adsorption onto bastnaesite surfaces, thereby accelerated to generate surface complexes, resulting in a significant intensification toward bastnaesite flotation recovery.
引用
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页数:10
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