4.8 Article

Reduction of energy requirement of CO2 desorption from a rich CO2-loaded MEA solution by using solid acid catalysts

期刊

APPLIED ENERGY
卷 202, 期 -, 页码 673-684

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.apenergy.2017.05.135

关键词

Energy reduction; Solvent regeneration; Catalyst-aided CO2 desorption; Catalytic reaction mechanism; Properties of the catalyst

资金

  1. National Natural Science Foundation of China (NSFC) [21536003, 21476064, U1362112, 21376067, 51521006]
  2. National Key Technology R&D Program (MOST) [2014BAC18B04]
  3. Innovative Research Team Development Plan (MOE) [IRT1238]
  4. Specialized Research Fund for the Doctoral Program of Higher Education (MOE) [20130161110025]
  5. China Scholarship Council [201606135004]
  6. China Outstanding Engineer Training Plan for Students of Chemical Engineering & Technology in Hunan University (MOE) [2011-40]

向作者/读者索取更多资源

In this work, the regeneration of rich CO2-loaded monoethanolamine (MEA) solvent with two catalysts (e.g. SAPO-34 and SO42-/TiO2) was investigated in order to reduce the energy requirement for solvent regeneration. The regeneration behavior with and without catalyst of a 5M MEA solution with an initial CO2 loading of 0.5 mol CO2/mol amine at 96 degrees C was studied to compare their CO2 desorption rate and heat duties. The results show that the two solid acid catalysts can reduce the heat duty for solvent regeneration and increase the CO2 desorption rate in comparison with blank test. The mechanism of CO2 desorption with catalyst in 5M MEA was proposed based on the result of catalyst characterization (e.g. N-2 absorption/desorption experiment, Py-IR, NH3-TPD, FT-IR and XRD) to better understand the desorption process. The results indicate that SAPO-34 with the higher joint value of Br phi nsted/Lewis acid sites ratio (B/L) and rnesopore surface area (MSA) shows the faster CO2 desorption rate and lower heat duty than SO4/TiO2. Based on the experimental results, the addition of solid acid catalysts into amine solution could be considered as one of choices to reduce the heat duty for CO2 desorption from CO2-loaded amine solvent. (C) 2017 Elsevier Ltd. All rights reserved.

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