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The Partitioning of Arsenic, Selenium, Cadmium, and Cesium during Pulverized Coal Combustion in a 17 kW Downflow Combustor
Author(s) -
Seames Wayne S.,
Wendt Jost O. L.
Publication year - 2001
Publication title -
developments in chemical engineering and mineral processing
Language(s) - English
Resource type - Journals
eISSN - 1932-2143
pISSN - 0969-1855
DOI - 10.1002/apj.5500090303
Subject(s) - arsenic , chemistry , flue gas , cadmium , fly ash , coal combustion products , combustion , selenium , coal , combustor , pulverized coal fired boiler , volatilisation , environmental chemistry , metal , caesium , metallurgy , waste management , chemical engineering , inorganic chemistry , materials science , organic chemistry , engineering
Abstract The combustion of coal liberates arsenic, selenium, cadmium, and cesium into the environment. These toxic metals, which are discharged with the flue gas or collected with fly ash, may vaporize in the hot portions of the combustor then return to the solid phase in cooler zones of the process downstream. Understanding the mechanisms by which toxic metals partition between the vapor and solid phases is an important step for predicting and mitigating the effect of these metals upon the environment. An investigation of these partitioning mechanisms was performed. The results suggest that the dominant heterogeneous partitioning mechanism for transformation to the solid phase in the post‐combustion zone is the reaction of metal vapor on the surface or within the pores of a supermicron ash particle for the Pittsburgh seam and Illinois #6 coals but not for the Ohio blend coal. A relationship between the concentration of supermicron phase arsenic, selenium, and cadmium to calcium was also observed, suggesting the formation of As‐Ca, Se‐Ca, and Cd‐Ca reaction products. Selenium appears to be more reactive than arsenic for the formation of these calcium‐based complexes.