TY - JOUR
T1 - PCDD/F formation from oxy-PAH precursors in waste incinerator flyash
AU - Hajizadeh, Yaghoub
AU - Onwudili, Jude A.
AU - Williams, Paul T.
PY - 2011/12/1
Y1 - 2011/12/1
N2 - The yield of PCDD/F in relation to the presence of oxygenated PAH in model waste incinerator flyash has been investigated in a fixed bed laboratory scale reactor. Experiments were undertaken by thermal treatment of the model flyash at 250 and 350°C under a simulated flue gas stream for 2. h. After reaction, the PCDD/F content of the reacted flyash and the PCDD/F released into the exhaust gas, and subsequently trapped by XAD-II resin in a down-stream condensation system were analyzed. The PAHs investigated were, dibenzofuran and benzo[b]naphtho[2,3-d]furan and were spiked onto the model flyash as reactant precursors for PCDD/F formation. The results showed significant formation of furans from both of the PAH investigated, however except from some highly chlorinated dioxin congeners, the formation of dioxins was not so common. Benzonaphthofuran was significantly more reactive than dibenzofuran in PCDD/F formation, in spite of the fact that dibenzofuran is structurally more similar to that of PCDD/F. Thus, there was no clear attribution between the chemical structure of PAH used and the formation of PCDD/F. There were considerable differences between the yields of PCDD/F congeners in the gaseous species and those in the reacted flyash under the same operational conditions. The concentration of PCDD/Fs was reduced at the higher reaction temperature of 350°C; however, the higher temperature resulted in the majority of the PCDD/F formed on the flyash being released into the gas phase.
AB - The yield of PCDD/F in relation to the presence of oxygenated PAH in model waste incinerator flyash has been investigated in a fixed bed laboratory scale reactor. Experiments were undertaken by thermal treatment of the model flyash at 250 and 350°C under a simulated flue gas stream for 2. h. After reaction, the PCDD/F content of the reacted flyash and the PCDD/F released into the exhaust gas, and subsequently trapped by XAD-II resin in a down-stream condensation system were analyzed. The PAHs investigated were, dibenzofuran and benzo[b]naphtho[2,3-d]furan and were spiked onto the model flyash as reactant precursors for PCDD/F formation. The results showed significant formation of furans from both of the PAH investigated, however except from some highly chlorinated dioxin congeners, the formation of dioxins was not so common. Benzonaphthofuran was significantly more reactive than dibenzofuran in PCDD/F formation, in spite of the fact that dibenzofuran is structurally more similar to that of PCDD/F. Thus, there was no clear attribution between the chemical structure of PAH used and the formation of PCDD/F. There were considerable differences between the yields of PCDD/F congeners in the gaseous species and those in the reacted flyash under the same operational conditions. The concentration of PCDD/Fs was reduced at the higher reaction temperature of 350°C; however, the higher temperature resulted in the majority of the PCDD/F formed on the flyash being released into the gas phase.
KW - Flyash
KW - Incineration
KW - PAH
KW - PCDD/F
UR - http://www.scopus.com/inward/record.url?scp=84855760450&partnerID=8YFLogxK
UR - https://www.sciencedirect.com/science/article/pii/S0045653511009490?via%3Dihub
U2 - 10.1016/j.chemosphere.2011.07.078
DO - 10.1016/j.chemosphere.2011.07.078
M3 - Article
C2 - 22024099
AN - SCOPUS:84855760450
SN - 0045-6535
VL - 85
SP - 1672
EP - 1681
JO - Chemosphere
JF - Chemosphere
IS - 11
ER -