資源・素材 & EARTH 2017(札幌)

講演情報(2017年8月24日付)

企画講演(Special Session)

EARTH

2017年9月28日(木) 08:45 〜 11:45 第8会場 C310 (C棟3階/Fl.3.,Build. C)

司会(Chairman):Chompunoot Wiraseranee (Mitsubishi Materials Corporation), Liu Hui (Central South University), Jonghyun Lee (Chungnam National University), Liyuan Chai (Central South University)

11:30 〜 11:45

[3801-11-11] Synthesis, Characterization and Performance of Ceria-based Nanomaterial for Elemental Mercury Removal

Chaofang Li1, Xingyao Li1, Libiao Liu1, ○Weichun Yang1,2 (1. Central South University, 2. Chinese National Engineering Research Center for Control & Treatment of Heavy Metal Pollution)

司会(Chairman):Jonghyun Lee(Chungnam National University), Liyuan Chai (Central South University)

キーワード:Ceria-based , Nanomaterial, Elemental Mercury Removal

Nano-ceria material is widely applied for catalysis due to its excellent redox ability. Pure ceria and ceria-based nanomaterials doped with cobalt(Co), copper(Cu), iron(Fe) were synthesized by a one-step hydrothermal method in this paper. XRD, SEM,TEM, nitrogen adsorption-desorption were employed for material characterization. Their performances on elemental mercury removal were studied and the mechanism of Hg0 oxidation was discovered. The XRD patterns and TEM images of Co-CeO2 under different reaction time show that Ce(OH)CO3 is regarded as eventual reaction precursor of Co-CeO2 and CeO2 is gotten after calcination. The formation mechanism assembling-dissolving-nucleation-reassembling is proposed for Co-CeO2 with lamellar structure. Hg0 oxidation performance of the four materials ranks in the order of Co-CeO2>Cu-CeO2>Fe- CeO2> CeO2 and Hg0 removal efficiency of Co-CeO2 in pure N2 is as high as 98%.On the other hand, Co-CeO2 exhibits 100% Hg0 removal efficiency in the temperature of 200OCor 300OCand the superficial velocity 150000 h-1 or 300000h-1 in atmosphere of N2+ 4%O2. Moreover, Hg0 oxidation is considered to be associated with oxygen vacancy and active oxygen concentration, which can be proved by the results of Raman andH2-TPR. Therefore, the Mars-Maessen mechanism is assumed to account for Hg0 catalytic oxidation.

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