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Mechanistic investigation on the Hg0 elimination ability of MnOx–CeOx nanorod adsorbents: effects of Mn/Ce molar ratio
Waste Disposal & Sustainable Energy Pub Date : 2024-01-22 , DOI: 10.1007/s42768-023-00181-z
Shujie Gao , Xiaoxiang Wang , Yaolin Wang , Kai Zhu , Changxing Hu , Dong Ye

Mercury pollution is created by coal combustion processes in multi-component systems. Adsorbent injection was identified as a potential strategy for capturing Hg0 from waste gases, with adsorbents serving as the primary component. The hydrothermal approach was used to synthesize a series of MnOx–CeOx nanorod adsorbents with varying Mn/Ce molar ratios to maximize the Hg0 capture capabilities. Virgin CeOx had weak Hg0 elimination activity; <8% Hg0 removal efficiency was obtained from 150 °C to 250 °C. With the addition of MnOx, the amount of surface acid sites and the relative concentration of Mn4+ increased. This ensured the sufficient adsorption and oxidation of Hg0 while overcoming the limitations of restricted adsorbate-adsorbent interactions caused by the lower surface area, endowing MnOx–CeOx with increased Hg0 removal capacity. When the molar ratio of Mn/Ce reached 6/4, the adsorbent’s Hg0 removal efficiency remained over 92% at 150 °C and 200 °C. As the molar ratio of Mn/Ce grew, the adsorbent’s Hg0 elimination capacity declined due to decreased surface area, weakened acidity, and decreased activity of Mn4+; <75% Hg0 removal efficiency was reached between 150 °C and 250 °C for virgin MnOx. Throughout the overall Hg0 elimination reactions, Mn4+ and Oα were in charge of oxidizing Hg0 to HgO, with Ce4+ acting as a promoter to aid in the regeneration of Mn4+. Because of its limited adaptability to flue gas components, further optimization of the MnOx–CeOx nanorod adsorbent is required.

Graphical abstract



中文翻译:

MnOx-CeOx纳米棒吸附剂消除Hg0能力的机理研究:Mn/Ce摩尔比的影响

汞污染是由多组分系统中的煤炭燃烧过程产生的。吸附剂注入被认为是从废气中捕获 Hg 0的潜在策略,其中吸附剂是主要成分。采用水热法合成了一系列具有不同Mn/Ce摩尔比的MnO x –CeO x纳米棒吸附剂,以最大限度地提高Hg 0捕获能力。原始CeO x具有弱的Hg 0消除活性;从 150 °C 到 250 °C,获得了<8% Hg 0去除效率。随着MnO x的添加,表面酸位点的数量和Mn 4+的相对浓度增加。这确保了Hg 0的充分吸附和氧化,同时克服了表面积较低导致的吸附质-吸附剂相互作用受限的限制,赋予MnO x –CeO x增加的Hg 0去除能力。当Mn/Ce摩尔比达到6/4时,吸附剂在150℃和200℃下对Hg 0的去除率均保持在92%以上。随着Mn/Ce摩尔比的增大,吸附剂表面积减小,酸性减弱,Mn 4+活性降低,去除Hg 0能力下降;对于原始 MnO x ,在 150 °C 至 250 °C 之间达到<75% Hg 0去除效率。在整个Hg 0消除反应中,Mn 4+和O α负责将Hg 0氧化为HgO,Ce 4+充当促进剂以帮助Mn 4+的再生。由于MnO x –CeO x纳米棒吸附剂对烟气成分的适应性有限,需要进一步优化。

图形概要

更新日期:2024-01-22
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