Mono- to Octachlorinated Polychlorinated Dibenzo-p-dioxin and Dibenzofuran Emissions from Sintering Plants Synergistically Controlled by the Desulfurization Process.

Abstract

The influence of desulfurization systems in sintering plants on polychlorinated dibenzo-p-dioxin and dibenzofuran (PCDD/F) concentrations, profiles, and emission factors was studied. Mono- to tri-CDD/Fs and tetra- to octa-CDD/F concentrations were 4.4 ± 2.3 and 10.5 ± 8.3 ng m(-3), respectively, at the inlets and 0.87 ± 0.48 and 0.47 ± 0.22 ng m(-3), respectively, after desulfurization. The toxic equivalents (TEQs) were 0.95 ± 0.093 and 0.51 ± 0.040 ng of I-TEQ m(-3) at the inlets and after desulfurization, respectively. The congener profiles and homologue distributions were dominated by 2-MoCDF and MoCDF, respectively. The PCDD/F removal efficiencies achieved by desulfurization increased as the chlorination level increased. The PCDD/Fs became adsorbed to gypsum. Annual mono- to tri-CDD/Fs PCDD/F and TEQ (tetra- to octa-CDD/F) emission factors for flue gas and gypsum between 2003 and 2012 were determined. The total amounts of mono- to tri-CDD/Fs emitted in flue gas and gypsum between 2003 and 2012 were 10.7 and 10.2 kg, respectively. The total TEQs emitted in flue gas and gypsum between 2003 and 2012 were estimated to be 15486 and 1878 g of I-TEQ, respectively. PCDD/Fs adsorbed to gypsum are not effectively eliminated. The PCDD/F concentrations increased as the fly ash surface area increased moving through the electrostatic precipitator stages.