Combined catalytic oxidation and activated carbon adsorption of dioxins

A mechanical mixture of lignite‐based activated carbon (AC) and V2O5‐TiO2‐catalyst (CAT) is applied to destroy gas‐phase polychlorinated dibenzo‐p‐dioxins and dibenzofurans (PCDD/Fs) at high concentration (9.8 ng I‐TEQ Nm−3). Even at low temperature (160°C), the mix of AC/CAT shows high removal effi...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Environmental progress 2015-03, Vol.34 (2), p.346-350
Hauptverfasser: Ji, Shasha, Yu, Mingfeng, Ren, Yong, Buekens, Alfons, Lu, Shengyong, Cen, Kefa, Li, Xiaodong
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:A mechanical mixture of lignite‐based activated carbon (AC) and V2O5‐TiO2‐catalyst (CAT) is applied to destroy gas‐phase polychlorinated dibenzo‐p‐dioxins and dibenzofurans (PCDD/Fs) at high concentration (9.8 ng I‐TEQ Nm−3). Even at low temperature (160°C), the mix of AC/CAT shows high removal efficiency (RE) and destruction efficiency (DE). Varying the proportions of catalyst to AC has slight effect only on the DE‐value, but the RE‐value augments with rising ratio of AC, benefiting from enhanced adsorption on AC. When temperature is 160°C and the proportion of AC and CAT is 3:2, with oxygen concentration rising from 0 to 20%, the DE‐value even amplifies from 27 to 82%, by conversion of V4+OX into higher oxides. In the presence of ozone, PCDD/Fs are further broken down and the DE‐values of high‐chlorinated congeners surge. In the presence of ozone, AC breaks down to black brown flock, which contains more than 50 wt % carbons. Both reducing the content of AC and increasing the reaction temperature restrain the production of flock. The best condition occurred at 200°C in the presence of ozone with the DE of 98%, when the proportion of AC and CAT is 1:1. © 2014 American Institute of Chemical Engineers Environ Prog, 34: 346–350, 2015
ISSN:1944-7442
1944-7450
DOI:10.1002/ep.11990