Hierarchically structured polyacrylonitrile nanofiber mat as highly efficient lead adsorbent for water treatment

被引:82
|
作者
Luo, Chao
Wang, Jianqiang
Jia, Peng
Liu, Yuxuan
An, Junhu
Cao, Bing [1 ]
Pan, Kai
机构
[1] Beijing Univ Chem Technol, Key Lab Carbon Fiber & Funct Polymers, Minist Educ, Beijing 100029, Peoples R China
基金
中国国家自然科学基金;
关键词
Hierarchical nanofiber; Adsorption; MnO2; Pb(II) removal; HEAVY-METAL IONS; AQUEOUS-SOLUTION; ADSORPTION BEHAVIOR; HEXAVALENT CHROMIUM; CARBON NANOTUBES; REMOVAL; COMPOSITE; COPPER(II); MECHANISM; SORPTION;
D O I
10.1016/j.cej.2014.09.116
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Hierarchical nanofiber mat (polyacrylonitrile/polypyrrole/manganese dioxide, PAN/PPy/MnO2) was prepared by electrospinning and followed by in situ polymerization of pyrrole monomer, and subsequently treated with KMnO4 solution to deposit MnO2. The obtained nanofiber mats were used as adsorbent for Pb(II) removal from aqueous solution. Fourier transform infrared (FTIR) results confirmed the presence of polypyrrole (PPy) and manganese dioxide (MnO2) layers on the surface of PAN nanofiber. The morphology and structure of the PAN/PPy/MnO2 nanofiber mat were studied by scanning electron microscopy (SEM) and transmission electron microscope (TEM). The hierarchical structures can be clearly seen from the SEM and TEM results. Thermo-gravimetric analysis (TGA) results showed that MnO2 accounts for about 9.25 wt.% in the PAN/PPy/MnO2 nanofiber. Adsorption results indicated that the adsorption performance for Pb(II) increased as the initial solution pH increased. The adsorption equilibrium reached within 120 min, and the process can be better described using the pseudo-second-order model. Isotherm data fitted well to the Langmuir isotherm model. Thermodynamic study revealed that the adsorption process is endothermic and spontaneous in nature. Desorption results showed that the adsorption performance can remain up to 80% after 5 times usage. The adsorption mechanism was also studied by XPS. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:775 / 784
页数:10
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