Abstract
The application of activated carbons has become a commonly used emission control protocol for the removal or adsorption of persistent organic pollutants from the flue gas streams of waste incinerators. In this study, the 2378-substituted PCDD/F removal efficiency of three types of activated carbons derived from the pyrolysis of refuse derived fuel, textile waste and scrap tyre was investigated and compared with that of a commercial carbon. Experiments were carried out in a laboratory scale fixed-bed reactor under a simulated flue gas at 275°C with a reaction period of four days. The PCDD/F in the solid matrices and exhaust gas, were analyzed using gas chromatography coupled with a triple quadrupole mass spectrometer. In the absence of activated carbon adsorbent, there was a significant increase in the concentration of toxic PCDD/F produced in the reacted flyash, reaching up to 6.6 times higher than in the raw flyash. In addition, there was a substantial release of PCDD/F into the gas phase, which was found in the flue gas trapping system. By application of the different commercial, refuse derived fuel, textile and tyre activated carbons the total PCDD/F toxic equivalent removal efficiencies in the exhaust gas stream were 58%, 57%, 64% and 52%, respectively. In general, the removal of the PCDDs was much higher with an average of 85% compared to PCDFs at 41%. Analysis of the reacted activated carbons showed that there was some formation of PCDD/F, for instance, a total of 60.6μg I-TEQ kg-1 toxic PCDD/F was formed in the refuse derived fuel activated carbon compared to 34μg I-TEQ kg-1 in the commercial activated carbon. The activated carbons derived from the pyrolysis of waste, therefore, showed good potential as a control material for PCDD/F emissions in waste incinerator flue gases.
| Original language | English |
|---|---|
| Pages (from-to) | 1194-1201 |
| Number of pages | 8 |
| Journal | Waste Management |
| Volume | 31 |
| Issue number | 6 |
| DOIs | |
| Publication status | Published - 1 Jun 2011 |
Funding
The authors would like to thank the UK Engineering & Physical Sciences Research Council for support for this work via Grant No. EP/F021615/1. The support of Isfahan University of Medical Sciences in Iran via PhD scholarship is gratefully acknowledged. The authors would also like to thank Dr. Adrian Cunliffe and Simon Lloyd for their assistance with the analytical work, and Ed Woodhouse for the construction of the reactor.
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