Abstract

The high temperature reduction (HTR) of flue gas divalent mercury to elemental mercury is the core technology for the mercury continuous emission monitoring system (Hg-CEMS). In this work, the high temperature reduction of HgCl2 to Hg0 was systematically investigated. The results show that HgCl2 can entirely decompose to Hg0 at 800 °C, but Cl, ClO, Cl2, and HCl can easily oxidize Hg0 at low temperature. A new efficient alkaline dechlorination agent for eliminating these Cl species was proposed firstly. The dechlorination agent can efficiently capture the HCl, Cl, and ClO but fail to completely adsorb Cl2. Consequently, a scheme was created that a pair of dechlorination agents were filled in inlet and outlet of the HTR furnace respectively. It features that the upper layer removes HCl and prevents the generation of Cl2 because HCl is the precursor of Cl2, and the lower layer adsorbs the Cl and ClO generated by the HTR process. The feasibility of the method was successfully verified in both a fixed-bed reactor and a Hg-CEMS pretreatment device. DFT calculation indicates that the adsorption of Cl, ClO, and HCl on CaO falls into the category of strong chemisorption while Cl2 is weakly chemisorbed.

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