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Fe-based ceramic nanocomposite membranes fabricated via e-spinning and vacuum filtration for Cd2+ ions removal.

Authors :
Wu, Jie
Xue, Songbai
Bridges, Denzel
Yu, Yongchao
Zhang, Linyue
Pooran, Joshi
Hill, Curtis
Wu, Jayne
Hu, Anming
Source :
Chemosphere. Sep2019, Vol. 230, p527-535. 9p.
Publication Year :
2019

Abstract

In this work, vacuum filtered and polymer mixed e-spinning membranes (ESPMs) made from or doped with Fe-based nanomaterials were successfully fabricated to remove Cd2+ ions from a neutral aqueous solution. The used Fe-based nanomaterials including FeOOH precursor Nanowires (NWs), α-Fe 2 O 3 NWs and Fe 3 O 4 nanoparticles (NPs) were synthesized by elevating the hydrothermal reaction temperature from 250 °C to 500 °C or doing post-heating treatment. The adsorption results showed that vacuum filtered membranes (VFMs) overall performed a better Cd2+ ions removal behavior than e-spinning ones. Among them, VFM made from Fe 3 O 4 NPs has the highest adsorption capacity (qt) with the adsorption amount of Cd2+ ions reaching about 29.3 mg/g within only 2 min due to the high specific surface area of NPs. Models of pseudo-first-order, pseudo-second-order and intraparticle diffusion were used to study the kinetics of Cd2+ ions removal process, and a high correlation coefficient (R2) of 0.99 was obtained when pseudo-second-order model was used. It was calculated that the equilibrium rate constant of VFM made from Fe 3 O 4 NPs has reached about 0.28 g mg−1 min−1, much smaller than those of other membranes, which indicated a high Cd2+ ions removal efficiency. • Vacuum filtered and polymer mixed e-spinning membranes (VFMs; ESPMs) were successfully fabricated. • VFMs had a higher Cd2+ ions removal efficiency than ESPMs. • Pseudo-second-order model can best satisfy the adsorption process for VFMs and ESPS. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00456535
Volume :
230
Database :
Academic Search Index
Journal :
Chemosphere
Publication Type :
Academic Journal
Accession number :
136713190
Full Text :
https://doi.org/10.1016/j.chemosphere.2019.05.084