Issue 40, 2013

Magnetic mesoporous silica hybrid nanoparticles for highly selective boron adsorption

Abstract

Novel core–shell magnetic mesoporous silica hybrid nanoparticles were synthesized and functionalized further with a glycidol reagent to produce boron-specific cis-diol, chelating functional derivatives. The resulting core–shell hybrid nanoparticles were found to be a better alternative to the existing boron adsorbents that had been modified with large molecular weight saccharide moieties and polymer functionalities. The magnetic mesoporous silica hybrid nanoparticles had a surface area, diameter, pore size, and saturation magnetization of 629 m2 g−1, 200–300 nm, 2.5 nm, and 33.25 emu g−1, respectively. The glycidol-modified nanoparticles with cis-diol functional groups showed high adsorption affinity and excellent selectivity towards boron in an aqueous solution, even in the presence of competitive metal ions (Ni2+, Cu2+, Cr2+ and Fe2+) and sulphates and chlorides of Na+, K+, Ca2+ and Mg2+ ions. Adsorption equilibrium could be established within 15–20 min, and the level of boron adsorption was 2.37 mmol g−1, which is much higher than the values previously reported for other boron adsorbent materials. The synthesized magnetic mesoporous silica hybrid nanoparticles showed approximately 97% boron removal capacity from a H3BO3 solution (100 mg L−1), and the used adsorbent particles could be separated easily from the aqueous suspensions by an external magnetic field. The adsorbent could be used repeatedly after a simple acid treatment (0.1 M HCl) and regenerated by an aqueous ammonia solution (3% NH3·H2O).

Graphical abstract: Magnetic mesoporous silica hybrid nanoparticles for highly selective boron adsorption

Supplementary files

Additions and corrections

Article information

Article type
Paper
Submitted
01 Jul 2013
Accepted
13 Aug 2013
First published
14 Aug 2013

J. Mater. Chem. A, 2013,1, 12485-12496

Magnetic mesoporous silica hybrid nanoparticles for highly selective boron adsorption

M. S. Moorthy, D. Seo, H. Song, S. S. Park and C. Ha, J. Mater. Chem. A, 2013, 1, 12485 DOI: 10.1039/C3TA12553J

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