Version 2 2019-01-23, 14:18Version 2 2019-01-23, 14:18
Version 1 2019-01-17, 15:49Version 1 2019-01-17, 15:49
journal contribution
posted on 2019-01-08, 00:00authored byYanbiao Liu, Peng Wu, Fuqiang Liu, Fang Li, Xiaoqiang An, Jianshe Liu, Zhiwei Wang, Chensi Shen, Wolfgang Sand
Herein,
we rationally designed a dual-functional electroactive
filter system for simultaneous detoxification and sequestration of
Sb(III). Binder-free and nanoscale TiO2-modified carbon
nanotube (CNT) filters were fabricated. Upon application of an external
electrical field, in situ transformation of Sb(III) to less toxic
Sb(V) can be achieved, which is further sequestered by TiO2. Sb(III) removal kinetics and capacity increase with applied voltage
and flow rate. This can be explained by the synergistic effects of
the filter’s flow-through design, electrochemical reactivity,
small pore size, and increased number of exposed sorption sites. STEM
characterization confirms that Sb were mainly sequestered by TiO2. XPS, AFS, and XAFS results verify that the Sb(III) conversion
process was accelerated by the electrical field. The proposed electroactive
filter technology works effectively across a wide pH range. The presence
of sulfate, chloride, and carbonate ions negligibly inhibited Sb(III)
removal. Exhausted TiO2–CNT filters can be effectively
regenerated using NaOH solution. At 2 V, 100 μg/L Sb(III)-spiked
tap water generated ∼1600 bed volumes of effluent with >90%
efficiency. Density functional theory calculations suggest that the
adsorption energy of Sb(III) onto TiO2 increases (from
−3.81 eV to −4.18 eV) and Sb(III) becomes more positively
charged upon application of an electrical field.