Novel PVA/MOF Nanofibres: Fabrication, Evaluation and Adsorption of Lead Ions from Aqueous Solution
Plain polyvinyl alcohol (PVA) nanofibres and novel polyvinyl alcohol benzene tetracarboxylate nanofibres incorporated with strontium, lanthanum and antimony ((PVA/Sr-TBC), (PVA/La-TBC) and (PVA/Sb-TBC)), respectively, where TBC is benzene 1,2,4,5-tetracarboxylate adsorbents, were fabricated by elect...
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Published in | Nanoscale research letters Vol. 11; no. 1; pp. 414 - 13 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Springer US
01.12.2016
Springer Nature B.V |
Subjects | |
Online Access | Get full text |
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Summary: | Plain polyvinyl alcohol (PVA) nanofibres and novel polyvinyl alcohol benzene tetracarboxylate nanofibres incorporated with strontium, lanthanum and antimony ((PVA/Sr-TBC), (PVA/La-TBC) and (PVA/Sb-TBC)), respectively, where TBC is benzene 1,2,4,5-tetracarboxylate adsorbents, were fabricated by electrospinning. The as-prepared electrospun nanofibres were characterized by scanning electron microscope (SEM), Fourier transform infrared (FTIR) and thermogravimetric analysis (TGA). Only plain PVA nanofibres followed the Freundlich isotherm with a correlation coefficient of 0.9814, while novel nanofibres (PVA/Sb-TBC, PVA/Sr-TBC and PVA/La-TBC) followed the Langmuir isotherm with correlation coefficients of 0.9999, 0.9994 and 0.9947, respectively. The sorption process of all nanofibres followed a pseudo second-order kinetic model. Adsorption capacity of novel nanofibres was twofold and more compared to that of plain PVA nanofibres. The thermodynamic studies: apparent enthalpy (Δ
H
°) and entropy (Δ
S
°), showed that the adsorption of Pb(II) onto nanofibres was spontaneous and exothermic. The novel nanofibres exhibited higher potential removal of Pb(II) ions than plain PVA nanofibres. Ubiquitous cations adsorption test was also investigated and studied. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1931-7573 1556-276X |
DOI: | 10.1186/s11671-016-1631-2 |