A new nano-sorbent for fast and efficient removal of heavy metals from aqueous solutions based on modification of magnetic mesoporous silica nanospheres
Creators
- 1. School of Chemistry, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of)
- 2. Department of Chemistry, Alzahra University, Tehran (Iran, Islamic Republic of)
- 3. Center of Excellence in Electrochemistry, School of Chemistry, College of Science, University of Tehran, Tehran (Iran, Islamic Republic of)
- 4. Biosensor Research Center, Endocrinology and Metabolism Molecular-Cellular Sciences Institute, Tehran University of Medical Sciences, Tehran (Iran, Islamic Republic of)
Description
Highlights: • Magnetic mesoporous silica nanospheres were functionalized with bis(3-triethoxysilylpropyl)tetrasulfide. • The functionalized mesoporous silica nanospheres had high surface areas. • High removal efficiencies of Hg(II), Pd(II), and Pb(II) were achieved with MSCMNPs-S4. • The MSCMNPs-S4 nanospheres show a good regeneration and reusability performance after five-cycle regenerations. - Abstract: In the present study, a new and efficient nanosorbent for the fast removal of heavy metal ions was prepared. The proposed nanosorbent was fabricated using Fe3O4 magnetic core shelled by mesoporous silica, and cetyltrimethylammonium bromide (CTAB) as surfactant template through a sol-gel process. The magnetic nanomaterial was further modified with bis(3-triethoxysilylpropyl)tetrasulfide (MSCMNPs-S4). The final nanosphers were characterized by FT-IR, XRD, TGA, BET, SEM, TEM, DLS, VSM, EDX, and UV–Vis. The potential of the resultant mesoporous magnetite nanomaterials was investigated as a convenient and effective adsorbent for the removal of toxic heavy metal ions from aqueous solutions in a batch system. The effect of essential parameters on the removal efficiency including initial pH of sample solution, adsorbent amount, metal ion concentration, contact time and type and quantity of the eluent on the adsorption characteristics of the MSCMNPs-S4 were studied. Under the optimized conditions, the proposed nanosorbent exhibited high adsorption capacity of 303.03, 256.41 and 270.27 mg g−1 and maximum removal percentages of 98.8%, 96.4%, 95.7% for Hg(II), Pd(II) and Pb(II) ions, respectively. The mechanism of the adsorbtion was found to be in good agreement with the Langmuir isotherm model. Furthermore, the reusability investigation indicated that the MSCMNPs-S4 could be used frequently at least for five cycles without any significant loss in its performance.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jmmm.2017.05.065Additional details
Identifiers
- DOI
- 10.1016/j.jmmm.2017.05.065;
- PII
- S0304885317303323;
Publishing Information
- Journal Title
- Journal of Magnetism and Magnetic Materials
- Journal Volume
- 441
- Journal Page Range
- p. 193-203
- ISSN
- 0304-8853
- CODEN
- JMMMDC
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 51055539
- Subject category
- S36: MATERIALS SCIENCE;
- Descriptors DEI
- ABSORPTION SPECTROSCOPY; ADSORBENTS; AMMONIUM COMPOUNDS; AQUEOUS SOLUTIONS; EFFICIENCY; FERRITES; FOURIER TRANSFORM SPECTROMETERS; HEAVY IONS; HEAVY METALS; MAGNET CORES; MAGNETIC CORES; MAGNETIZATION; NANOSTRUCTURES; REMOVAL; SCANNING ELECTRON MICROSCOPY; SILICA; SOL-GEL PROCESS; SURFACE AREA; THERMAL GRAVIMETRIC ANALYSIS; X-RAY DIFFRACTION
- Descriptors DEC
- CHARGED PARTICLES; CHEMICAL ANALYSIS; COHERENT SCATTERING; DIFFRACTION; DISPERSIONS; ELECTRON MICROSCOPY; ELEMENTS; FERRIMAGNETIC MATERIALS; GRAVIMETRIC ANALYSIS; HOMOGENEOUS MIXTURES; IONS; IRON COMPOUNDS; MAGNETIC MATERIALS; MAGNETIC STORAGE DEVICES; MATERIALS; MEASURING INSTRUMENTS; MEMORY DEVICES; METALS; MICROSCOPY; MINERALS; MIXTURES; OXIDE MINERALS; OXYGEN COMPOUNDS; QUANTITATIVE CHEMICAL ANALYSIS; SCATTERING; SOLUTIONS; SPECTROMETERS; SPECTROSCOPY; SURFACE PROPERTIES; THERMAL ANALYSIS; TRANSITION ELEMENT COMPOUNDS
Optional Information
- Notes
- © 2017 Elsevier B.V. All rights reserved.