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

机译:使用Fe促销SO_4〜(2 - )/ ZRO_2 / MCM-41催化剂来减少CO_2捕获的能量惩罚

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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:CO2负载溶剂再生的高能耗是基于胺类的CO2捕获过程的实际应用最大的障碍。为了降低能量要求,合成了三种促进了在MCM-41(SZMF)催化剂上的SO42- / ZrO 2,其具有不同的氧化铁含量(5%,10%和15%)并施加富含单乙醇胺溶液再生过程98℃。结果表明,使用SZMF的使用较大地增强了二氧化碳解吸性能(即解吸因子)260-388%并将热占58-40%降低,这优于大多数报告的催化剂这个目的。 SZMF的显着催化活性与其增强的富朗酸盐酸盐位点,弱酸位点,碱性位点和高分散的Fe3 +物种有关。同时,对二氧化碳解吸的SZMF的添加显示了对其CO 2吸收性能的促进作用,并且SZMF具有优异的循环稳定性。提出了SZMF催化的CO2解吸过程的可能机制。这项工作的结果可以为该潜在催化剂辅助二氧化碳解吸技术提供更有效的催化剂的未来研究和理性设计方向。

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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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