School of Environmental Science and Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
School of Chemistry and Chemical Engineering, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, China.
Environ Sci Technol. 2020 Apr 21;54(8):5249-5257. doi: 10.1021/acs.est.9b07524. Epub 2020 Apr 8.
A novel, atomically dispersed carbon-based sorbent was synthesized by anchoring manganese atoms with N atoms for the capture of gaseous elemental Hg (Hg). Oxygen atoms were also introduced into the synthesis process to adjust the oxidizing ability of the Mn atoms. High-valence Mn (Mn) anchored by the O and N atoms (Mn-O/N-C) in the carbon-based materials provided more exposed active sites. The mercury removal efficiency of the composite exceeded 99%. The composite with a Mn loading of 0.9 wt % exhibited high affinity for Hg, and the capacity for Hg adsorption within 275 min at room temperature reached 16.95 mg·g. The Mn utilization was ∼56.61%, which is much larger than that of reported Mn-based oxide sorbents. The atomic-level distribution of Mn was well evidenced by aberration-corrected high-angle annular darkfield scanning transmission electron microscopy. Density functional theory calculations were conducted to evaluate the energy for adsorption of Hg on Mn-O/N-C. The results indicated that the amount of N and O atoms in the Mn coordination environment determined the Hg adsorption energy, and the presence of five optimized Mn adsorption structures in Mn-O/N-C was confirmed by Hg temperature-programmed desorption analysis. These materials may be utilized for mercury removal from disposal sites with high concentrations of mercury, broken mercury-containing lamps, or mercurial thermometers. The strategy of atomic dispersion during synthesis of the materials and adjusting the oxidizing ability in the single-atom strategy may be helpful for the development of environmentally benign functional materials.
一种新型的原子分散碳基吸附剂通过将锰原子与 N 原子锚定用于捕获气态元素汞 (Hg) 而合成。氧原子也被引入到合成过程中,以调节 Mn 原子的氧化能力。高化合价的 Mn(Mn)被碳基材料中的 O 和 N 原子(Mn-O/N-C)锚定,提供了更多暴露的活性位点。该复合材料的汞去除效率超过 99%。在 0.9wt%的 Mn 负载下,该复合材料对 Hg 具有高亲和力,在室温下 275 分钟内的 Hg 吸附容量达到 16.95mg·g。Mn 的利用率约为 56.61%,远高于已报道的基于 Mn 的氧化物吸附剂。高角度环形暗场扫描透射电子显微镜的像差校正证实了 Mn 的原子级分布。通过密度泛函理论计算评估了 Hg 在 Mn-O/N-C 上的吸附能。结果表明,Mn 配位环境中的 N 和 O 原子数量决定了 Hg 的吸附能,通过 Hg 程序升温脱附分析证实了 Mn-O/N-C 中存在五种优化的 Mn 吸附结构。这些材料可用于从高浓度汞处置地点、破碎的含汞灯或汞温度计中去除汞。在材料合成过程中采用原子分散策略和在单原子策略中调节氧化能力的策略可能有助于开发环境友好型功能材料。