This
study is based on a 300 MW coal-fired power plant cocombusting
2% of MSW, focusing on the emission characteristics and formation
pathway of polychlorinated dibenzo-p-dioxins and
dibenzofurans (PCDD/Fs). Data from two scenarios, including the cocombustion
test (CCT) and normal operation conditions (NOCs), are comprehensively
analyzed, indicating that the TEQ concentration of PCDD/Fs increases
by 12.69% during cocombustion but still satisfied the national emission
limits. The purification efficiencies of toxic PCCD/Fs in CCT and
NOC are 41.28 and 28.33%, respectively. Following this, major air
pollutant emissions could also satisfy the national standard and even
meet the zero-emission requirement. For flue gas in both CCT and NOC,
1,2,3,4,6,7,8-HpCDD, OCDD, 2,3,4,6,7,8-HxCDF, and 1,2,3,4,6,7,8-HpCDF
are the main contributors to 2,3,7,8-PCDD/Fs on the mass concentration
level, while OCDD and OCDF dominate in fly ash. The major difference
is that the CCT condition has a higher fraction of 1,2,3,4,6,7,8-HpCDD,
OCDD, and lower contents of 2,3,4,6,7,8-HxCDF to NOC. Furthermore,
the distribution of integral 136 PCDD/F congeners also show infinite
variation between CCT and NOC, but with a huge gap in the quantity
of different isomers. However, cocombustion affects the potential
formation routes, as PCDD/Fs from de novo synthesis
and DD chlorination dominate the formation pathways in NOC. In contrast,
PCDD/Fs from the CP-route of precursor synthesis are mostly occupied
under NOCs, possibly due to the incineration deterioration caused
by MSW that generates more precursors. Additionally, there is little
correlation with a mutual Pearson correlation coefficient (R
2) of 0.2474 between HCl and PCDD/Fs in the
flue gas, indicating the lessened influence of high-temperature gaseous
synthesis by imported MSW.