A functionalized phosphonate-rich organosilica layered hybrid material (PSLM) fabricated through a mild process for heavy metal uptake
Creators
- 1. Department of Materials Science and Engineering, University of Ioannina, Ioannina 45110 (Greece)
- 2. Institute of Materials Science, NCSR "Demokritos", Ag. Paraskevi Attikis, Athens 15310 (Greece)
- 3. Laboratory of Physical Chemistry, Department of Environmental and Natural Resources Management, University of Patras, Seferi 2, Agrinio 30100 (Greece)
- 4. Regional Centre of Advanced Technologies and Materials, Faculty of Science, Department of Physical Chemistry and Experimental Physics, Palacky University, Olomouc 77146 (Czech Republic)
Description
Highlights: • Novel phosphonate-rich organosilica layered hybrid material (PSLM) fabricated through a mild xerogel process. • Surface Complexation Modeling reveals that PSLM bears 2 types of functional groups able to bind heavy metal. • Maximum metal uptake capacities were found 2.72 mmol g−1 for Cu2+, 1.67 mmol g−1 for Pb2+ and 1.00 mmol g−1 for Cd2+ at pH 7. • EPR spectroscopy reveals local coordination environment for Cu2+ ions. - Abstract: A phosphonate-rich organosilica layered hybrid material (PSLM) made of 3-(trihydroxysilyl)propyl methylphosphonate, monosodium salt, as the single silica source, has been obtained from its aqueous solution through a xerogel process and mild thermal aging. The method is simple, affording bulk quantities of powdered PSLM in a single-step. The hybrid is stable in water and possesses a high content of phosphonate groups fixed on the solid matrix. In addition, PSLM shows good thermal stability, which exceeds 300 °C in air. The material was characterized using SEM, TEM, XRD, FT-IR and TGA techniques. Potentiometric titrations show that PSLM bears high-surface density of phosphonate groups (3 mmol g−1). As a result, the material displays high metal uptake capacity for heavy metal ions such as Cu2+ (2.72 mmol g−1), Pb2+ (1.67 mmol g−1) and Cd2+ (1.00 mmol g−1) at neutral pH values e.g. the pH of natural waters. Detailed theoretical modeling using a Surface Complexation Model combined with Electron Paramagnetic Resonance (EPR) spectroscopy shows that the surface distribution of surface bound Cu2+ ions is rather homogeneous e.g. copper-binding phosphonate sites are arranged in average distances 5–8 Å
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jhazmat.2014.01.045Additional details
Identifiers
- DOI
- 10.1016/j.jhazmat.2014.01.045;
- PII
- S0304-3894(14)00069-7;
Publishing Information
- Journal Title
- Journal of Hazardous Materials
- Journal Volume
- 270
- Journal Page Range
- p. 118-126
- ISSN
- 0304-3894
- CODEN
- JHMAD9
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 46033737
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY;
- Descriptors DEI
- CADMIUM IONS; COPPER IONS; ELECTRON SPIN RESONANCE; HEAVY METALS; LEAD IONS; POTENTIOMETRY; SILICA
- Descriptors DEC
- CHARGED PARTICLES; CHEMICAL ANALYSIS; ELEMENTS; IONS; MAGNETIC RESONANCE; METALS; MINERALS; OXIDE MINERALS; QUANTITATIVE CHEMICAL ANALYSIS; RESONANCE; TITRATION; VOLUMETRIC ANALYSIS
Optional Information
- Copyright
- Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.