Adsorption of Pb(II) and Cu(II) metal ions on functionalized large-pore mesoporous silica
Autor: | J.-Y. Lee, Chia-Han Chen, Soofin Cheng, H.-Y. Li |
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Rok vydání: | 2015 |
Předmět: |
Langmuir
Environmental Engineering Aqueous solution Chemistry Metal ions in aqueous solution Inorganic chemistry chemistry.chemical_element 02 engineering and technology Mesoporous silica 010402 general chemistry 021001 nanoscience & nanotechnology 01 natural sciences Copper 0104 chemical sciences Adsorption Chemical engineering Environmental Chemistry 0210 nano-technology General Agricultural and Biological Sciences Mesoporous material Hydrophobic silica |
Zdroj: | International Journal of Environmental Science and Technology. 13:65-76 |
ISSN: | 1735-2630 1735-1472 |
DOI: | 10.1007/s13762-015-0841-y |
Popis: | Adsorption of copper and lead ions in aqueous solutions onto large-pore mesoporous silica materials functionalized with amino and mercapto groups and those with different morphologies including fiber-like, rod-like, and platelet was studied. The synthesized materials were characterized by techniques such as X-ray powder diffraction, nitrogen adsorption–desorption isotherms, scanning electron microscopy, and infrared spectra. Batch experiments were conducted to determine the adsorption processes. The equilibrium adsorption data agreed with Langmuir isotherms and revealed that four amino groups were required to form a stable surface complex with copper ions. Results indicated that initial adsorption rate onto platelet mesoporous adsorbent was rapid and faster than that of rod-like and fibrous morphologies due to its short channeling pores. Thiol-functionalized mesoporous silica adsorbents of all the morphologies have a better affinity for Pb2+ than the amino-mesoporous silica. In contrast, amino-mesoporous silica has a stronger affinity for Cu2+ compared to thiol-mesoporous silica. The optimal Pb2+ uptake on thiol-mesoporous silica was in solution with pH in 2–6, while the highest Cu2+ uptake on amino-mesoporous silica was at pH 5. |
Databáze: | OpenAIRE |
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