Synthetic carbons activated with phosphoric acid: I. Surface chemistry and ion binding properties
Synthetic activated carbons were prepared by phosphoric acid activation of a styrene–divinylbenzene copolymer at various temperatures in the 400–1000 °C range. The resulting carbons were characterized by elemental analysis, cation-exchange capacity measurement, infrared spectroscopy, potentiometric...
Gespeichert in:
Veröffentlicht in: | Carbon (New York) 2002-01, Vol.40 (9), p.1493-1505 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Synthetic activated carbons were prepared by phosphoric acid activation of a styrene–divinylbenzene copolymer at various temperatures in the 400–1000
°C range. The resulting carbons were characterized by elemental analysis, cation-exchange capacity measurement, infrared spectroscopy, potentiometric titration with calculation of proton affinity spectra, and copper adsorption from solution. The results indicate that the synthetic carbons obtained possess acidic character and show cation-exchange properties similar to those of oxidized carbons. However, the acidic compounds arising from treatment with phosphoric acid are tightly bound to the carbon lattice and are chemically and thermally more stable than those introduced by oxidative treatments. The largest amount of cation-exchange surface groups is introduced after activation at 800
°C. Infrared investigations showed that phosphorus compounds may be polyphosphates bound to the carbon lattice. Proton affinity distribution curves calculated from potentiometric titration experiments showed four types of surface groups on synthetic phosphoric acid activated carbons. Among them phosphorus-containing groups are the most important for the adsorption of heavy metal ions (copper) from acid solutions. Thus, carbons activated with phosphoric acid may be regarded as prospective cation-exchangers for the removal of heavy metals from water solutions. |
---|---|
ISSN: | 0008-6223 1873-3891 |
DOI: | 10.1016/S0008-6223(01)00317-7 |