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Study on the Elemental Mercury Adsorption Characteristics and Mechanism of Iron-Based Modified Biochar Materials

机译:铁基改性生物炭材料中元素汞的吸附特性及机理研究

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摘要

To provide a theoretical basis for the development of future mercury removal methods, two types of biochars modified by the coprecipitation method were investigated: undoped iron-based biochars modified with FeCl3 and iron-based biochars doped with Cu and Mn from CuSO4, Mn(CH3COO)(2), and KMnO4. The crystal phase compositions, pyrolysis characteristics, pore structures, microscopic morphologies, elemental speciations, and functional groups of the modified biochars were characterized. The adsorption mechanism was further explored by temperature-programmed desorption (TPD). The results showed that the mercury adsorption of the modified biochars was significantly enhanced. The mercury adsorption performances first increased and then weakened with increased loading. The modification decreased the graphitization degree. Spinel structure solid solutions of MnFe2O4 and CuFe2O4 were formed in the modified biochars, generating many cation vacancies on the biochar surface. After biochar modification, the pore structures and the contents of carbonyl, carboxyl, and metal hydroxyl functional groups were significantly increased. The removal of Hg-0 by modified biochar is the result of a combination of adsorption and oxidation. The modification process significantly promotes the chemical adsorption of Hg-0. Functional groups, lattice oxygen, chemisorbed oxygen, halogen components, and metal oxides or ions on the sorbent surface all play roles in the oxidation of the adsorbed HG(0). Fe2O3 and CuO (MnO2 and Fe2O3) double metal oxides have a synergistic effect on the removal of Hg-0.
机译:为了为未来除汞方法的发展提供理论基础,研究了两种通过共沉淀法改性的生物炭:未掺杂的FeCl3改性的铁基生物炭和掺杂有CuSO4,Mn(CH3COO)的Cu和Mn的铁基生物炭。 )(2)和KMnO4。表征了改性生物炭的晶相组成,热解特性,孔结构,微观形貌,元素形态和官能团。通过程序升温脱附(TPD)进一步探索了吸附机理。结果表明,改性生物炭对汞的吸附明显增强。汞吸附性能首先增加,然后随着负载增加而减弱。改性降低了石墨化程度。在改性生物炭中形成了MnFe2O4和CuFe2O4的尖晶石结构固溶体,在生物炭表面产生许多阳离子空位。生物炭改性后,孔结构和羰基,羧基和金属羟基官能团的含量显着增加。通过改性生物炭去除Hg-0是吸附和氧化相结合的结果。改性过程显着促进了Hg-0的化学吸附。官能团,晶格氧,化学吸附的氧,卤素组分以及吸附剂表面上的金属氧化物或离子都在吸附的HG(0)的氧化中起作用。 Fe2O3和CuO(MnO2和Fe2O3)双金属氧化物对Hg-0的去除具有协同作用。

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  • 来源
    《Energy & fuels》 |2018年第12期|12554-12566|共13页
  • 作者单位

    Taiyuan Univ Technol, Coll Elect & Power Engn, Taiyuan 030024, Shanxi, Peoples R China;

    Taiyuan Univ Technol, Coll Elect & Power Engn, Taiyuan 030024, Shanxi, Peoples R China;

    Taiyuan Univ Technol, Coll Elect & Power Engn, Taiyuan 030024, Shanxi, Peoples R China;

    Taiyuan Univ Technol, Coll Elect & Power Engn, Taiyuan 030024, Shanxi, Peoples R China;

    Taiyuan Univ Technol, Coll Elect & Power Engn, Taiyuan 030024, Shanxi, Peoples R China;

    Nanjing Normal Univ, Sch Energy & Mech Engn, Nanjing 210042, Jiangsu, Peoples R China;

    Taiyuan Univ Technol, Coll Elect & Power Engn, Taiyuan 030024, Shanxi, Peoples R China;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 04:13:58

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