TY - JOUR
ID - 10.1016/j.jes.2021.09.033
TI - Elemental mercury (Hg0) removal from coal syngas using magnetic tea-biochar: Experimental and theoretical insights
AU - Fazeel Abid
AU - Adnan Raza Altaf
AU - Yusuf G. Adewuyi
AU - Haipeng Teng
AU - Gang Liu
VL - 34
IS - 12
PB -
SP - 150
EP - 161
PY -
JF - Journal of Environmental Sciences
JA - J. Environ. Sci.
UR - http://www.jesc.ac.cn/jesc_en/ch/reader/view_abstract.aspx?file_no=S1001074221004071&flag=1
KW - Corresponding authors.;Mercury removal;Waste management;Citric acid;Ultrasound;Coal gasification;TPD analysis
AB - Mercury is ranked 3rd as a global pollutant because of its long persistence in the environment. Approximately 65% of its anthropogenic emission (Hg0) to the atmosphere is from coal-thermal power plants. Thus, the Hg0 emission control from coal-thermal power plants is inevitable. Therefore, multiple sorbent materials were synthesized using a one-step pyrolysis method to capture the Hg0 from simulated coal syngas. Results showed, the Hg0 removal performance of the sorbents increased by the citric acid/ultrasonic application. T5CUF0.3 demonstrated the highest Hg0 capturing performance with an adsorption capacity of 106.81 µg/g within 60 min at 200 °C under complex simulated syngas mixture (20% CO, 20% H2, 10 ppmV HCl, 6% H2O, and 400 ppmV H2S). The Hg0 removal mechanism was proposed, revealing that the chemisorption governs the Hg0 removal process. Besides, the active Hg0 removal performance is attributed to the high dispersion of valence Fe3O4 and lattice oxygen (α) contents over the T5CUF0.3 surface. In addition, the temperature programmed desorption (TPD) and XPS analysis confirmed that H2S/HCl gases generate active sites over the sorbent surface, facilitating high Hg0 adsorption from syngas. This work represented a facile and practical pathway for utilizing cheap and eco-friendly tea waste to control the Hg0 emission.
ER -