4.7 Article

Copper modified activated coke for mercury removal from coal-fired flue gas

期刊

CHEMICAL ENGINEERING JOURNAL
卷 286, 期 -, 页码 585-593

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2015.10.107

关键词

Activated coke; Metal modification; Copper; Mercury; Flue gas

资金

  1. Program for New Century Excellent Talents in University [NCET-12-0776]
  2. Fundamental Research Funds for the Central Universities [FRF-TP-13-041]

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A series of copper modified activated coke were prepared by an impregnation method to evaluate their efficiency of mercury removal in a simulated coal-fired flue gas. Effect of factors (including active component, copper loading value, calcinations temperature, reaction temperature and partial flue gas components) were studied. Results showed that the efficiency of raw coke could be enhanced by HNO3 pretreatment its dual functions of dirty cleaning and surface functional group modifying. The sample with 8% Cu loading value and 300 degrees C calcination for 3 h was found to be the optimal material for mercury removal, achieving around 73% average efficiency at 120 degrees C. Meanwhile, the increase of reaction temperature would enhance the removal efficiency when it was below 160 degrees C, but had a negative effect with further increase. Besides, experimental results also revealed that 02 and NO all had a positive effect on mercury removal. Various means (SEM, MIR, BET, XRD, TGA) in this work were used to characterize samples. Results indicated that copper modification could change surface functional groups of activated coke, while calcination temperature would have an impact on the species of decomposition product. Cu(NO3)(2) would decompose into CuO at lower calcination temperature, while partly into Cu2O at higher temperature. Moreover, the BET results revealed that metal modification broadened pore distribution of AC, which favored mercury removal. The two peaks in TG curve could be ascribed to elemental mercury (Hg) and HgO, which testified that the mechanism of mercury removal over CuO/AC-H was the combination of adsorption and catalytic oxidation. (C) 2015 Elsevier B.V. All rights reserved.

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