Efficient Gallium Recovery from Aqueous Solutions Using Polyacrylonitrile Nanofibers Loaded with D2EHPA

被引:5
作者
Segala, Bibiane Nardes [1 ]
Wenzel, Bruno Munchen [2 ]
Power, Nicholas P. [3 ]
Krishnamurthy, Satheesh [4 ]
Bertuol, Daniel Assumpcao [1 ]
Tanabe, Eduardo Hiromitsu [1 ]
机构
[1] Fed Univ St Maria UFSM, Chem Engn Dept, Environm Proc Lab LAPAM, BR-97105900 Santa Maria, RS, Brazil
[2] Fed Univ Fronteira Sur UFFS, Postgrad Program Environm & Sustainable Technol, BR-97900000 Cerro Largo, Brazil
[3] Open Univ, Sch Life Hlth & Chem Sci, Milton Keynes MK7 6AA, England
[4] Open Univ, Sch Engn & Innovat, Milton Keynes MK7 6AA, England
关键词
centrifugal spinning; Di-(2-ethylhexyl) phosphoric acid; polyacrylonitrile nanofibers; gallium; adsorption; desorption; SOLID-PHASE EXTRACTION; PHOSPHORIC-ACID; ADSORPTION; REMOVAL; SEPARATION; GA(III); IONS; COMPOSITE; INDIUM; CONTAMINANTS;
D O I
10.3390/met13091545
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Centrifugal spinning was utilized in producing polyacrylonitrile (PAN) nanofibers loaded with extractant di-(2-ethylhexyl) phosphoric acid (D2EHPA) for efficient adsorption recovery of gallium from aqueous solutions. The adsorption experimental data were best fitted by a pseudo-second-order kinetic model and the BET equilibrium isotherm model. Optimal adsorption performance by the PAN/D2EHPA nanofibers exhibited an adsorption capacity of 33.13 mg g-1 for the recovery of gallium at pH 2.5 and 55 degrees C. The thermodynamic parameters demonstrated that adsorption was endothermic, spontaneous, and favorable. The stability and reusability of the nanofibers was assessed, demonstrating retention of structural and functional integrity for the nanofibers over five cycles of an adsorption/desorption process, whilst retaining adsorption efficiency. The results demonstrate that PAN/D2EHPA nanofibers have excellent potential for utilization in an efficient adsorption process for gallium recovery, offering significant positive environmental impact over conventional liquid-liquid extraction methods.
引用
收藏
页数:19
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