Potential Hazards of Brominated Carbon Sorbents for Mercury Emission Control

被引:84
作者
Bisson, Teresa M. [1 ]
Xu, Zhenghe [1 ,2 ]
机构
[1] Univ Alberta, ECERF, Dept Chem & Mat Engn, Edmonton, AB T6G 2V4, Canada
[2] Tsinghua Univ, Inst Nucl & New Energy Technol, Beijing 1000084, Peoples R China
基金
中国国家自然科学基金; 加拿大自然科学与工程研究理事会;
关键词
ACTIVATED CARBON; BIOMASS ASH; STABILITY;
D O I
10.1021/es5052793
中图分类号
X [环境科学、安全科学];
学科分类号
083001 [环境科学];
摘要
Mercury is a toxic air pollutant, emitted from the combustion of coal. Activated Carbon (AC) or other carbon sorbent (CS) injection into coal combustion flue gases can remove elemental mercury through an adsorption process. Recently, a brominated CS with biomass ash as the carbon source (Br-Ash) was developed as an alternative for costly AC-based sorbent for mercury capture. After mercury capture, these sorbents are disposed in landfill, and the stability of bromine and captured mercury is of paramount importance. The objective of this study is to determine the fate of mercury and bromine from Br-Ash and brominated AC after their service. Mercury and bromine leaching tests were conducted using the standard toxicity characteristic leaching procedure (TCLP). The mercury was found to be stable on both the BrAsh and commercial brominated AC sorbents, while the bromine leached into the aqueous phase considerably. Mercury pulse injection tests on the sorbent material after leaching indicate that both sorbents retain significant mercury capture capability even after the majority of bromine was removed. Testing of the Br-Ash sorbent over a wider range of pH and liquid:solid ratios resulted in leaching of <5% of mercury adsorbed on the Br-Ash. XPS analysis indicated more organically bound Br and less metalBr bonds after leaching.
引用
收藏
页码:2496 / 2502
页数:7
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