2-Methylol-12-crown-4 ether immobilized PolyHIPEs toward recovery of lithium(i)

被引:42
作者
Huang, Wei [1 ]
Liu, Shucheng [1 ]
Liu, Jinxin [1 ]
Zhang, Wenli [1 ]
Pan, Jianming [1 ,2 ]
机构
[1] Jiangsu Univ, Sch Chem & Chem Engn, Zhenjiang 212013, Peoples R China
[2] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
中国国家自然科学基金;
关键词
IMPRINTED POLYMERS; SOLVENT-EXTRACTION; CARBON NANOTUBES; PICKERING HIPES; LI+ ADSORBENTS; CROWN-ETHERS; RATIO BRINE; ION-SIEVES; ADSORPTION; CHEMISTRY;
D O I
10.1039/c8nj01961d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A facile strategy to fabricate crown ether (2-methylol-12-crown-4, 2M12C4) immobilized porous polymers (PGMA-CE) was reported toward lithium(i) (Li+) recovery. Macroporous polymer foam (polymeric glycidyl methacrylate, PGMA) with abundant epoxy groups was firstly prepared as a support using a high internal phase emulsion (HIPE) template. And then 2M12C4 was covalently attached onto the surface of PGMA to endow the PGMA-CE with good stability and high selectivity. PGMA-CE was characterized by SEM, FT-IR, XPS, and C-13 NMR spectroscopy, and its porous structure and the successful introduction of 2M12C4 were confirmed. In batch mode experiments under optimum conditions, PGMA-CE exhibited fast adsorption kinetics (the equilibrium time was 3.0 h), and the kinetics data were well described using a pseudo-second-order model. A Langmuir-type monolayer adsorption was investigated, and the calculated maximum equilibrium adsorption capacity was 3.15 mg g(-1). In addition, PGMA-CE displayed excellent selectivity for Li+ in the presence of multiple interfering ions (Na+, K+, Mg+, and Ca2+), and the selective separation factors () were above 4.75. Regeneration analysis showed that the adsorption capacity of PGMA-CE toward Li+ after five cycles was 91.8% of the first cycle.
引用
收藏
页码:16814 / 16822
页数:9
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