4.7 Article

Template-free synthesis of hybrid silica nanoparticle with functionalized mesostructure for efficient methylene blue removal

Journal

MATERIALS & DESIGN
Volume 201, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.matdes.2021.109494

Keywords

Hybrid silica; Mesoporous silica nanoparticles; Co-condensation; Phosphonic acid; Methylene blue adsorption

Funding

  1. Swiss National Science Foundation (SNSF) [206021_150638/1]

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A simple one-pot synthesis process was developed to prepare functionalized mesostructured silica nanoparticles (MSNP) with high surface area. The novel MSNP demonstrated excellent adsorption performance for cationic pollutants like methylene blue, and showed easy regeneration and recyclability in acidic medium.
A simple one-pot synthesis process for functionalized mesostructured silica nanoparticles (MSNP) is reported. The novel process demonstrated the possibility to achieve MSNP with a surface area up to 501 m(2).g(-1) using a phosphonate based nonsilane precursor such as N, N'-bis[4,6-bis(diethylphosphono)-1,3,5-triazin-yl]-1,2-diaminoethane (ED). MSNP obtained by using 20 mol% of ED achieved a surface area of 80 m(2).g(-1) and increasing the ED content to 30 mol% resulted in a surface area of 501 m(2).g(-1). Zeta potential of novel MSNPs (-65.5 and 70.0 mV) were much higher than the nanoparticle (NP) prepared from only TEOS (-49 mV), indicating the presence of a large number of -SiOH and phosphonic acid surface functional groups, as confirmed by Fourier-transform infrared spectroscopy (FT-IR) and Nuclear magnetic resonance (NMR) analysis. The functionalized MSNPs were used as an adsorbent for the removal of cationic pollutants like methylene blue (MB). The MSNP with the highest porosity displayed favorable MB adsorption behavior with similar to 380 mg.g(-1) of MB adsorption capacity. Facile regeneration in an acidic medium (similar to pH 4.5) with easy recyclability (10 cycles) confirmed the practical applicability of this novel functionalized MSNPs. (C) 2021 The Author(s). Published by Elsevier Ltd.

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