期刊
JOURNAL OF COLLOID AND INTERFACE SCIENCE
卷 430, 期 -, 页码 140-146出版社
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jcis.2014.05.046
关键词
Humic acid; Adsorption; Magnetic separation; Magnetically separable polyaniline
资金
- National Science Foundation of China [21107065]
- Natural Science Basic Research Plan in Shaanxi Province [2012JQ2003]
- Science and Technology Research and Development Program of Shaanxi Province, Xi'an [2013K13-01-07]
- State Key Laboratory Program of Pollution Control and Resources Reuse, Nanjing China [PCRRF11012]
Magnetically separable polyaniline (Fe3O4@SiO2-PANI) was prepared by in situ chemical polymerization of aniline on the surface of silica-coated Fe3O4 nanoparticles, and characterized by FTIR spectroscopy, powder X-ray diffraction, elemental analysis, transmission electron microscopy, vibrating sample magnetometry and X-ray photoelectron spectroscopy. Characterization results showed that Fe3O4@SiO2-PANI with amino groups of 1.78 mmol/g and the average diameter of 21.6 nm are superparamagnetic. Adsorption behavior of Fe3O4@SiO2-PANI nanoparticles for humic acid (HA) was investigated by batch experiments and adsorption kinetic tests. HA adsorption amount on the adsorbent decreased with increasing solution pH and the presence of Ca2+ resulted in the enhanced HA adsorption. HA adsorption on Fe3O4@SiO2-PANI could be well described by Langmuir model and the maximum adsorption amount of the adsorbent for HA at 25 degrees C was 36.36 mg/g. HA adsorption process on the adsorbent obey pseudo-second-order kinetics and the adsorption rates decrease with increasing initial HA concentration. The XPS analysis verified that HA adsorption over the adsorbent could be attributed to the surface complexation between the disassociated HA molecules and the protonated nitrogen of polyaniline on the adsorbent. HA loaded adsorbent could be magnetically separated and easily desorbed in 0.01 mol/L NaOH solution. Regeneration tests indicated that Fe3O4@SiO2-PANI could be used repeatedly. (C) 2014 Elsevier Inc. All rights reserved.
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