کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
4409058 | 1307461 | 2013 | 7 صفحه PDF | دانلود رایگان |

• Multiwalled carbon nanotubes are immobilized in electrospun nanofibrous membrane.
• Addition of MWCNTs increases specific surface area and tensile strength of ENFMs.
• MWCNTs-ENFMs show faster sorption rate and higher sorption capacity for PFOS.
• Solution pH affects surface property and sorption efficiency of MWCNTs-ENFMs.
• Sorption mechanisms mainly include hydrophobic and electrostatic interactions.
Multi-walled carbon nanotube-filled electrospun nanofibrous membranes (MWCNT-ENFMs) were prepared by electrospinning. The addition of MWCNTs (0.5 wt.% vs. ENFMs) doubled the specific surface area and tensile strength of the ENFMs. The MWCNT-ENFMs were used to adsorb perfluorooctane sulfonate (PFOS) in aqueous solutions. The sorption kinetics results showed that the sorption rate of PFOS onto the MWCNT-ENFMs was much higher than the sorption rate of PFOS onto the pure ENFMs control, and the pseudo-second-order model (PSOM) described the sorption kinetics well. The sorption isotherms indicated that the sorption capacity of the MWCNT-ENFMs for PFOS (16.29 ± 0.26 μmol g−1) increased approximately 18 times, compared with the pure ENFMs (0.92 ± 0.06 μmol g−1). Moreover, the solution pH significantly affected the sorption efficiency and sorption mechanism. The MWCNT-ENFMs were negatively charged from pH 2.0–10.0, but the electrostatic repulsion between the MWCNT-ENFMs and PFOS was overcome by the hydrophobic interactions between PFOS and the MWCNTs or nanofibers. The strong hydrophobic interactions between PFOS and the MWCNTs played a dominant role in the sorption process. For the pure ENFMs, the electrostatic repulsion was conquered by the hydrophobic interactions between PFOS and the nanofibers at pH > 3.1. In addition to the hydrophobic interactions, an electrostatic attraction between PFOS and the pure ENFMs was involved in the sorption process at pH < 3.1.
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Journal: Chemosphere - Volume 93, Issue 8, November 2013, Pages 1593–1599