Low temperature degradation of polychlorinated dibenzo-p-dioxins and dibenzofurans over a VOx-CeOx/TiO2 catalyst with addition of ozone

Copyright © 2018 Elsevier Ltd. All rights reserved.

Bibliographische Detailangaben
Veröffentlicht in:Waste management (New York, N.Y.). - 1999. - 76(2018) vom: 05. Juni, Seite 555-565
1. Verfasser: Zhan, Ming-Xiu (VerfasserIn)
Weitere Verfasser: Yu, Ming-Feng, Zhang, Guangxue, Chen, Tong, Li, Xiao-Dong, Buekens, Alfons
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2018
Zugriff auf das übergeordnete Werk:Waste management (New York, N.Y.)
Schlagworte:Journal Article Degradation mechanism MSWI Ozone PCDD/Fs VO(x)-CeO(x)/TiO(2) Benzofurans Dibenzofurans, Polychlorinated Polychlorinated Dibenzodioxins titanium dioxide mehr... 15FIX9V2JP 66H7ZZK23N Titanium D1JT611TNE
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245 1 0 |a Low temperature degradation of polychlorinated dibenzo-p-dioxins and dibenzofurans over a VOx-CeOx/TiO2 catalyst with addition of ozone 
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520 |a In order to find a catalyst to destroy polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/Fs) with high efficiency, a homemade VOx-CeOx/TiO2 catalyst was prepared, and then tested in the flue gas of a waste incinerator at temperatures of 180-240 °C. The results shows the best removal efficiency (93.4%) was attained already at 200 °C, yet degradation efficiency further raised with temperature, until 240 °C. Ozone (500 ppm) was also introduced into the system to increase the activity of catalyst, and removal efficiency of PCDD/Fs increased further to 97.4% and 98.8% at 200 and 240 °C, respectively. In addition, a lab-scale reaction system was installed to study the degradation mechanism of PCDD/Fs. Octa-chlorinated dibenzo-p-dioxin (OCDD) was selected as the study object due to the most stable structure and maximum chlorine atom number. The intermediate products resulting from the conversion of OCDD were monitored using gas chromatography/mass spectrometry and Fourier transform infrared spectroscopy and a possible reaction pathway was proposed. Dechlorination persists until the complete conversion of OCDD. Oxidation decomposes OCDD-molecules mainly into organic substances having one, two or more benzene rings, yet also alkanes, cycloalkanes and heterocompounds of sulphur, nitrogen, and halogens appear. However, more work is still needed to fit those trace products into mechanistic schemes 
650 4 |a Journal Article 
650 4 |a Degradation mechanism 
650 4 |a MSWI 
650 4 |a Ozone 
650 4 |a PCDD/Fs 
650 4 |a VO(x)-CeO(x)/TiO(2) 
650 7 |a Benzofurans  |2 NLM 
650 7 |a Dibenzofurans, Polychlorinated  |2 NLM 
650 7 |a Polychlorinated Dibenzodioxins  |2 NLM 
650 7 |a titanium dioxide  |2 NLM 
650 7 |a 15FIX9V2JP  |2 NLM 
650 7 |a Ozone  |2 NLM 
650 7 |a 66H7ZZK23N  |2 NLM 
650 7 |a Titanium  |2 NLM 
650 7 |a D1JT611TNE  |2 NLM 
700 1 |a Yu, Ming-Feng  |e verfasserin  |4 aut 
700 1 |a Zhang, Guangxue  |e verfasserin  |4 aut 
700 1 |a Chen, Tong  |e verfasserin  |4 aut 
700 1 |a Li, Xiao-Dong  |e verfasserin  |4 aut 
700 1 |a Buekens, Alfons  |e verfasserin  |4 aut 
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773 1 8 |g volume:76  |g year:2018  |g day:05  |g month:06  |g pages:555-565 
856 4 0 |u http://dx.doi.org/10.1016/j.wasman.2018.02.049  |3 Volltext 
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