Mercury stability of byproducts from wet flue gas desulfurization devices

摘要

Mercury released from wet flue gas desulfurization (WFGD) devices can be inhibited by additives that can transfer mercury to its solid phase. However, the use of additives increases the mercury content in desulfurization gypsum, and the mercury is released again during the calcination process. In this study, NaHS, 2,4,6-trimercaptotiazine, trisodium salt nonahydrate (Na-3(C3N3S3)center dot 9H(2)O, or TMT) and sodium dithiocarbamate (DTCR) were used as additives to control mercury emissions in simulated WFGD devices. Then, different calcination methods were adopted to study mercury release behaviors from calcination process. The transformation of mercury compound species on gypsum was also investigated to explain its behavior during calcination. The result showed that the mercury content in the solid phase increased significantly in the presence of additives. Among three additives, simulated desulfurization slurry with TMT had the highest trapping efficiency over mercury. The mercury thermal stability in gypsum increased in the order of using DTCR, TMT and NaHS. Due to the migration of mercury to the solid phase and the stronger thermal stability of resultants, the residual content of mercury in gypsum with additives after calcination were higher than that without additives. In general, using TMT coupled with slow-speed calcination had the best effect on controlling mercury contamination from WFGD slurry and WFGD byproducts. Moreover, it was verified by temperature programmed decomposition experiments that, after using NaHS, TMT and DTCR, the mercury compound in the gypsum was mainly in the form of HgS, Hg-3(TMT)(2), Hg(DTCR)(2), respectively, which explained the mercury release behaviors during calcination. (C) 2016 Elsevier Ltd. All rights reserved.