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Reducing Energy Penalty of CO_2 Capture Using Fe Promoted SO_4~(2-)/ZrO_2/MCM-41 Catalyst

机译:铁促进的SO_4〜(2-)/ ZrO_2 / MCM-41催化剂降低CO_2捕集的能量损失

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摘要

The high energy consumption of CO2-loaded solvent regeneration is the biggest impediment for the real application of the amine-based CO2 capture process. To lower the energy requirement, three Fe promoted SO42-/ZrO2 supported on MCM-41 (SZMF) catalysts with different iron oxide content (5%, 10%, and 15%) were synthesized and applied for the rich monoethanolamine solution regeneration process at 98 degrees C. Results reveal that the use of SZMF hugely enhanced the CO2 desorption performances (i.e., desorption factor) by 260-388% and reduced the heat duty by about 28-40%, which is better than most of the reported catalysts for this purpose. The eminent catalytic activities of SZMF are related to their enhanced ratio of Bronsted to Lewis acid sites, weak acid sites, basic sites, and high dispersed Fe3+ species. Meanwhile, the addition of SZMF for CO2 desorption shows a promotional effect on its CO2 absorption performance, and SZMF presents an excellent cyclic stability. A possible mechanism is suggested for the SZMF catalyzed CO2 desorption process. Results of this work may provide direction for future research and rational design of more efficient catalysts for this potential catalyst-aided CO2 desorption technology.
机译:负载有CO2的溶剂再生的高能耗是胺基CO2捕集工艺实际应用的最大障碍。为了降低能量需求,合成了三种负载在具有不同氧化铁含量(5%,10%和15%)的MCM-41(SZMF)催化剂上的Fe促进的SO42- / ZrO2,并用于富氧单乙醇胺溶液的再生工艺。 98摄氏度。结果表明,使用SZMF可使CO2解吸性能(即解吸系数)大大提高260-388%,热负荷降低约28-40%,这比大多数报道的催化剂要好。这个目的。 SZMF的显着催化活性与其提高的布朗斯台德与路易斯酸位点,弱酸位点,碱性位点和高分散的Fe3 +物种的比率有关。同时,添加SZMF用于CO2解吸对CO2吸收性能显示出促进作用,并且SZMF具有出色的循环稳定性。建议一种可能的机制用于SZMF催化的CO2解吸过程。这项工作的结果可能为该潜在的催化剂辅助的CO2解吸技术的未来研究和合理设计更有效的催化剂提供指导。

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  • 来源
    《Environmental Science & Technology》 |2019年第10期|6094-6102|共9页
  • 作者单位

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, Peoples R China;

    Hunan Univ, Joint Int Ctr Capture & Storage iCCS CO2, Prov Hunan Key Lab Cost Effect Utilizat Fossil Fu, Coll Chem & Chem Engn, Changsha 410082, Hunan, 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);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 04:24:32

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