沸石咪唑盐骨架
水溶液
Zeta电位
咪唑酯
砷
X射线光电子能谱
朗缪尔吸附模型
傅里叶变换红外光谱
吸附
吸附
化学工程
纳米颗粒
化学
无机化学
材料科学
核化学
金属有机骨架
纳米技术
有机化学
工程类
作者
Meipeng Jian,Bao Liu,Gaosheng Zhang,Ruiping Liu,Xiwang Zhang
标识
DOI:10.1016/j.colsurfa.2014.10.023
摘要
In this study, zeolitic imidazolate framework-8 (ZIF-8) nanosorbent was successfully synthesized via a facile method at room temperature. The ZIF-8 nanoparticles were characterized by nitrogen sorption, powder X-ray diffraction, field emission scanning electron microscope, transmission electron microscopy and Zeta potential. The synthesized ZIF-8 nanoparticles exhibited a high surface area of 1063.5 m2/g and were of 200–400 nm in particle size. The kinetic and isotherm data of arsenic adsorption on ZIF-8 were well fitted by pseudo-second-order and Langmuir models, respectively. The maximal adsorption capacities of As(III) and As(V) were of 49.49 and 60.03 mg/g, respectively, at T = 25 °C and pH 7.0. The ZIP-8 nanoparticles were stable at neutral and basic conditions. However, large amounts of Zn2+ were released into water from the sorbent at acidic condition, which dramatically hindered the adsorption of arsenic. SO42− and NO3− had no significant effect on the arsenic adsorption while the adsorption was significantly inhibited by PO43− and CO32−. X-ray photoelectron spectroscopy and Fourier transform infrared spectroscopy analysis revealed that electrostatic attraction and hydroxyl and amine groups on ZIF-8 surface played vital roles in the adsorption process.
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