Simultaneous removal of 3d transition metals from multi-component solutions by activated carbons from co-mingled wastes

The main purpose of the present work was to study the simultaneous removal of 3d transition metals from multi-component solutions by novel porous material obtained from carbon-containing liquid and solid waste. The activated carbon was prepared from co-mingled natural organic waste: 25% sunflower hu...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Separation and purification technology 2008-05, Vol.60 (3), p.264-271
Hauptverfasser: Lyubchik, Svetlana B., Lyubchik, Andrej I., Lygina, Elena S., Lyubchik, Sergej I., Makarova, Tatiana L., Vital, Joaquim, Rego, Ana M.B. do, Fonseca, Isabel M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The main purpose of the present work was to study the simultaneous removal of 3d transition metals from multi-component solutions by novel porous material obtained from carbon-containing liquid and solid waste. The activated carbon was prepared from co-mingled natural organic waste: 25% sunflower husks, 50% petroleum waste and 25% low-grade bituminous coal. The porous carbon material was obtained via stages of pre-oxidation with binary eutectic Na/K carbonates (in order to avoid melting and coke formation), followed by “step by step” carbonization at 100–400 °C in an inert atmosphere and activation with steam at 850 °C. The adsorption of the 3d transition metals: copper (II), cobalt (III), nickel (II), iron (III), and chromium (III), on novel activated carbons has been investigated using multi-component model solutions. Experiments have been carried out on the thermodynamics of the simultaneous adsorption of the 3d transition metals in a static mode. The total metal removal combines the process of metal hydroxide precipitation in the solution with the metal cation adsorption on negatively charged carbon surface in a single operation unit. The carbon/metals interaction at the surface of spent adsorbents is discussed.
ISSN:1383-5866
1873-3794
DOI:10.1016/j.seppur.2007.08.020