Adsorptive removal of humic acid from aqueous solution on polyaniline/attapulgite composite

► PANI was successfully incorporated onto the surface of ATP clay. ► ATP–PANI showed high adsorption capacity for HA dependent on pH and ionic strength. ► The adsorbent can be regenerated in alkaline solution and used repeatedly. ► Electrostatic interaction played an important role in the enhanced H...

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Veröffentlicht in:Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2011-09, Vol.173 (1), p.171-177
Hauptverfasser: Wang, Jiahong, Han, Xiaojing, Ma, Hongrui, Ji, Yanfen, Bi, Lijuan
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container_title Chemical engineering journal (Lausanne, Switzerland : 1996)
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Han, Xiaojing
Ma, Hongrui
Ji, Yanfen
Bi, Lijuan
description ► PANI was successfully incorporated onto the surface of ATP clay. ► ATP–PANI showed high adsorption capacity for HA dependent on pH and ionic strength. ► The adsorbent can be regenerated in alkaline solution and used repeatedly. ► Electrostatic interaction played an important role in the enhanced HA adsorption. Polyaniline/attapulgite composite (ATP–PANI) was prepared by in situ chemical oxidation and characterized by FITR, XRD, and TEM. Characterized results showed that polyaniline (PANI) was successfully encapsulated on the surface of attapulgite (ATP). Humic acid (HA) adsorption onto ATP–PANI was investigated by batch experiments and adsorption kinetic tests. In contrast with the low HA adsorption amount on ATP, substantially enhanced HA adsorption onto ATP–PANI was observed. Adsorption isotherms of HA can be well described by Langmuir model and the maximum adsorption amounts were found to be 43.01, 52.91, 61.35 mg/g at 15, 25, and 35 °C, respectively. HA adsorption increased with rise in temperature indicating of an endothermic process of HA adsorption onto ATP–PANI. Pseudo-second order kinetic equation can fit HA adsorption very well and the adsorption rate decreased with increasing initial HA concentration. HA adsorption decreased monotonously with increasing solution pH. Co-existed cations (Na +, K +, Ca 2+) in aqueous solution improved HA adsorption amount on ATP–PANI, and the augment of HA adsorption amount was order as Ca 2+ > K + > Na +. Results of HA adsorption onto ATP–PANI showed that the electrostatic interaction between amine and imine groups of the adsorbents and HA molecules in solution may account for the enhanced HA adsorption. The HA molecules adsorbed on ATP–PANI can be effectively desorbed in 2 M NaOH solution, and regenerated adsorbent can be repeatedly used in the subsequently four adsorption-regeneration cycles with little loss of HA adsorption amount.
doi_str_mv 10.1016/j.cej.2011.07.065
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Polyaniline/attapulgite composite (ATP–PANI) was prepared by in situ chemical oxidation and characterized by FITR, XRD, and TEM. Characterized results showed that polyaniline (PANI) was successfully encapsulated on the surface of attapulgite (ATP). Humic acid (HA) adsorption onto ATP–PANI was investigated by batch experiments and adsorption kinetic tests. In contrast with the low HA adsorption amount on ATP, substantially enhanced HA adsorption onto ATP–PANI was observed. Adsorption isotherms of HA can be well described by Langmuir model and the maximum adsorption amounts were found to be 43.01, 52.91, 61.35 mg/g at 15, 25, and 35 °C, respectively. HA adsorption increased with rise in temperature indicating of an endothermic process of HA adsorption onto ATP–PANI. Pseudo-second order kinetic equation can fit HA adsorption very well and the adsorption rate decreased with increasing initial HA concentration. HA adsorption decreased monotonously with increasing solution pH. Co-existed cations (Na +, K +, Ca 2+) in aqueous solution improved HA adsorption amount on ATP–PANI, and the augment of HA adsorption amount was order as Ca 2+ &gt; K + &gt; Na +. Results of HA adsorption onto ATP–PANI showed that the electrostatic interaction between amine and imine groups of the adsorbents and HA molecules in solution may account for the enhanced HA adsorption. 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Polyaniline/attapulgite composite (ATP–PANI) was prepared by in situ chemical oxidation and characterized by FITR, XRD, and TEM. Characterized results showed that polyaniline (PANI) was successfully encapsulated on the surface of attapulgite (ATP). Humic acid (HA) adsorption onto ATP–PANI was investigated by batch experiments and adsorption kinetic tests. In contrast with the low HA adsorption amount on ATP, substantially enhanced HA adsorption onto ATP–PANI was observed. Adsorption isotherms of HA can be well described by Langmuir model and the maximum adsorption amounts were found to be 43.01, 52.91, 61.35 mg/g at 15, 25, and 35 °C, respectively. HA adsorption increased with rise in temperature indicating of an endothermic process of HA adsorption onto ATP–PANI. Pseudo-second order kinetic equation can fit HA adsorption very well and the adsorption rate decreased with increasing initial HA concentration. HA adsorption decreased monotonously with increasing solution pH. 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subjects Adsorbents
Adsorption
Applied sciences
ATP
Chemical engineering
Desorption
Exact sciences and technology
Humic acid
Humic acids
Hydroxyapatite
Mathematical models
Polyaniline/attapulgite composite
Polyanilines
Reactors
Surface chemistry
title Adsorptive removal of humic acid from aqueous solution on polyaniline/attapulgite composite
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