Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, School of Energy and Environment, Southeast University, Nanjing, Jiangsu 210096, China.
Key Laboratory of Energy Thermal Conversion and Control of Ministry of Education, School of Energy and Environment, Southeast University, Nanjing, Jiangsu 210096, China.
Sci Total Environ. 2019 Mar 15;656:937-945. doi: 10.1016/j.scitotenv.2018.11.460. Epub 2018 Nov 30.
Accurate mercury speciation measurements are critical for developing methods for mercury removal from flue gas, but the lack of reliable adsorbents has made Hg selective retention challenging. Calcium oxide (CaO) loaded on porous support is promising for HgCl selective adsorption because of its porosity and alkaline nature. The main hypothesis investigated in this paper is if the capacity of CaO sorbent for HgCl selective adsorption is attributed to its basic sites, then this will be drastically impacted by the calcium precursors. We synthesized a suite of CaO/SiO sorbents from different precursors, including hydrated calcium oxide (CaO-HS), calcium nitrate tetrahydrate (CaO-NS), and calcium acetate monohydrate (CaO-AcS), to investigate their performance on HgCl selective adsorption in a fixed-bed reactor. Compared with CaO-HS and CaO-NS, CaO-AcS was demonstrated to have the strongest affinity for HgCl and almost complete breakthrough for Hg. Advanced porosity and surface basicity of CaO-AcS were confirmed by characterization analysis. CaO (001) and CaO (011) facet as well as surface defects that have different unsaturated O sites were observed using the high resolution transmission electron microscope (HRTEM). Combined theoretical and experimental methods were used to study the interaction mechanisms between HgCl and basic sites on CaO-AcS surfaces. Density functional theory (DFT) calculations indicated all CaO surfaces weakly interact with Hg, while four robust bonding states of HgCl were predicted on different basic sites with the intensity in increasing order: Monodentate < Tridendate < Bidentate < Bridging. This was consistent with HgCl-TPD experiments that demonstrated that the four HgCl adsorption configurations on CaO-AcS were attributed to different unsaturated O sites. The findings in this work highlight the application potential of CaO-AcS for gaseous Hg sampling and measurement from coal-fired flue gas.
准确的汞形态测量对于开发从烟道气中去除汞的方法至关重要,但缺乏可靠的吸附剂使得汞的选择性保留具有挑战性。负载在多孔载体上的氧化钙(CaO)因其多孔性和碱性而有望用于 HgCl 选择性吸附。本文的主要假设是,如果 CaO 吸附剂对 HgCl 选择性吸附的能力归因于其碱性位,则这些碱性位将受到钙前体的极大影响。我们从不同的前体制备了一系列 CaO/SiO 吸附剂,包括水合氧化钙(CaO-HS)、四水硝酸钙(CaO-NS)和一水醋酸钙(CaO-AcS),以研究它们在固定床反应器中对 HgCl 选择性吸附的性能。与 CaO-HS 和 CaO-NS 相比,CaO-AcS 被证明对 HgCl 具有最强的亲和力,几乎完全穿透 Hg。通过特征分析证实了 CaO-AcS 的先进孔隙率和表面碱性。使用高分辨率透射电子显微镜(HRTEM)观察到 CaO(001)和 CaO(011)晶面以及具有不同不饱和 O 位的表面缺陷。结合理论和实验方法研究了 HgCl 与 CaO-AcS 表面碱性位之间的相互作用机制。密度泛函理论(DFT)计算表明,所有 CaO 表面与 Hg 相互作用较弱,而在不同的碱性位上预测了四种稳定的 HgCl 键合态,强度依次增加:单齿配位<三齿配位<双齿配位<桥接配位。这与 HgCl-TPD 实验一致,表明 CaO-AcS 上的四种 HgCl 吸附构型归因于不同的不饱和 O 位。这项工作的结果突出了 CaO-AcS 在从燃煤烟道气中进行气态 Hg 采样和测量方面的应用潜力。