Hierarchically porous NiAl-LDH nanoparticles as highly efficient adsorbent for p-nitrophenol from water
•Hierarchically porous LDH was prepared via surfactant-assisted hydrothermal route.•LDH showed high specific surface areas and interlayer hydrophobic property.•LDH nanoparticles exhibited strong affinity towards p-nitrophenol in water. Nickel aluminum layered double hydroxides (LDHs) fabricated via...
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Published in | Applied surface science Vol. 349; pp. 897 - 903 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
15.09.2015
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Subjects | |
Online Access | Get full text |
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Summary: | •Hierarchically porous LDH was prepared via surfactant-assisted hydrothermal route.•LDH showed high specific surface areas and interlayer hydrophobic property.•LDH nanoparticles exhibited strong affinity towards p-nitrophenol in water.
Nickel aluminum layered double hydroxides (LDHs) fabricated via sodium citrate (SC) assistant hydrothermal route were evaluated for removing p-nitrophenol from aqueous solutions. The characterization results indicate that the NiAl-LDHs nanoparticles have well-ordered layer structure with highly crystalline nature. The NiAl-LDH possessed hierarchically porous nanoarchitectures with high surface area (108.7m2/g) and great pore volume (0.41cm3/g). Meanwhile, interlamellar spacing of NiAl-LDH was increased to 0.73nm, demonstrating that the citric acid ion was intercalated into NiAl-LDH in vertical alignment. The morphology of NiAl-LDH changed from a series of disordered growth hexagon nanosheets to the flower-like microspheres with modification of variable sodium citrate. The adsorption isotherms of p-nitrophenol on NiAl-LDHs obey the Langmuir equation. It is worthy to note that the NiAl-LDH modified by sodium citrate with the addition of 2.316g exhibits excellent adsorption performance with the maximum p-nitrophenol adsorption capacity of 77.7mg/g. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2015.05.041 |