The influence of flue gas components and activated carbon injection on mercury capture of municipal solid waste incineration in China

被引:81
|
作者
Li, Guoliang
Wu, Qingru
Wang, Shuxiao [1 ]
Li, Zhijian
Liang, Hongyan
Tang, Yi
Zhao, Minjiang
Chen, Lei
Liu, Kaiyun
Wang, Fengyang
机构
[1] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China
基金
美国国家科学基金会;
关键词
Mercury removal; Municipal solid waste incineration; Flue gas; Activated carbon; ELEMENTAL MERCURY; COAL-COMBUSTION; FLY-ASH; CATALYTIC-OXIDATION; EMISSION FACTORS; LOW-TEMPERATURE; BIO-CHARS; REMOVAL; ADSORPTION; SO2;
D O I
10.1016/j.cej.2017.05.099
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
This study investigates the influence of flue gas components and original/modified activated carbon (AC) injection on mercury removal to obtain a suitable mercury removal method for typical municipal solid waste (MSW) incineration plants in China. The field test was conducted to research the mercury emission characteristics of a typical plant. The result shows that the mercury concentration of before and after air pollution control devices (APCDs) is 91.28 +/- 47.98 and 25.67 +/- 18.13 mu gm(-3), respectively, and the average mercury removal efficiency is 71.9%. Based on actual APCDs condition, the flue gas components (O-2, SO2, HCl and NO), fly ash, activated carbon and NH4Cl-modfied AC were used to further remove the mercury of flue gas. The O-2 and HCl slightly promoted mercury removal while the SO2 and NO addition decreased mercury concentration from 50 mu gm(-3) to 35.8 and 13.7 mu gm(-3), respectively. The increase of AC injection amount failed to decrease emission concentration to desired value and imposed heavy financial burden to plants. The method of 2.5 wt% Cl-modified AC addition reduced mercury concentration to below 5 mu gm(-3) in various flue gas condition and did not need to change any existing APCDs or operating parameters, which was considered as the optimal method for mercury removal in MSW incineration. Reaction mechanism of SO2, NO and Cl-modified AC was explored by TPD, XPS and in situ Diffuse Reflectance Fourier Transform (DRIFT). The SO2 and NO formed effective active groups of SO3-M and NO2-M, and their reaction mechanism follows Langmiur-Hinshelwood mechanism and Eley-Rideal mechanism, respectively. The Cl modification effectiveness was ascribed to C-Cl group formation. (C) 2017 Published by Elsevier B.V.
引用
收藏
页码:561 / 569
页数:9
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