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在不同气体成分存在下,药用残渣生物炭去除元素汞。

Removal of element mercury by medicine residue derived biochars in presence of various gas compositions.

机构信息

School of Energy and Environmental Engineering, Hebei University of Technology, Tianjin 300401, China; College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.

School of Energy and Environmental Engineering, Hebei University of Technology, Tianjin 300401, China; College of Environmental Science and Engineering, Nankai University, Tianjin 300071, China.

出版信息

J Hazard Mater. 2015 Nov 15;298:162-9. doi: 10.1016/j.jhazmat.2015.05.031. Epub 2015 May 21.

Abstract

Pyrolyzed biochars from an industrial medicinal residue waste were modified by microwave activation and NH4Cl impregnation. Mercury adsorption of different modified biochars was investigated in a quartz fixed-bed reactor. The results indicated that both physisorption and chemisorption of Hg(0) occurred on the surface of M6WN5 which was modified both microwave and 5wt.% NH4Cl loading, and exothermic chemisorption process was a dominant route for Hg(0) removal. Microwave activation improved pore properties and NH4Cl impregnation introduced good active sites for biochars. The presence of NO and O2 increased Hg(0) adsorption whereas H2O inhibited Hg(0) adsorption greatly. A converse effect of SO2 was observed on Hg(0) removal, namely, low concentration of SO2 promoted Hg(0) removal obviously whereas high concentration of SO2 suppressed Hg(0) removal. The Hg(0) removal by M6WN5 was mainly due to the reaction of the C−Cl with Hg(0) to form HgCl2, and the active state of C−Cl(*) groups might be an intermediate group in this process. Thermodynamic analysis showed that mercury adsorption by the biochars was exothermic process and apparent adsorption energy was 43.3 kJ/mol in the range of chemisorption. In spite of low specific surface area, M6WN5 proved to be a promising Hg(0) sorbent in flue gas when compared with other sorbents.

摘要

工业药用残渣废料热解生物炭经微波活化和 NH4Cl 浸渍改性。在石英固定床反应器中研究了不同改性生物炭对汞的吸附性能。结果表明,在经过微波和 5wt.% NH4Cl 负载双重改性的 M6WN5 表面上,Hg(0)的吸附既有物理吸附又有化学吸附,而放热的化学吸附过程是 Hg(0)去除的主要途径。微波活化改善了生物炭的孔性能,NH4Cl 浸渍则引入了良好的活性位。NO 和 O2 的存在会增加 Hg(0)的吸附,而 H2O 则会极大地抑制 Hg(0)的吸附。SO2 对 Hg(0)去除的影响则相反,即低浓度的 SO2 明显促进 Hg(0)的去除,而高浓度的 SO2 则抑制 Hg(0)的去除。M6WN5 去除 Hg(0)主要是由于 C−Cl 与 Hg(0)反应生成 HgCl2,而 C−Cl(*)基团的活性状态可能是该过程中的中间基团。热力学分析表明,生物炭对汞的吸附是放热过程,在化学吸附范围内的表观吸附能为 43.3 kJ/mol。尽管比表面积较低,但与其他吸附剂相比,M6WN5 被证明是一种很有前途的烟气 Hg(0)吸附剂。

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