4.7 Article

Reduction-oxidation kinetics of three different iron oxide phases for CO2 activation to CO

期刊

FUEL
卷 202, 期 -, 页码 547-555

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.fuel.2017.04.076

关键词

Kinetics; Redox reaction; Iron ores; CO2 activation; Chemical looping process

资金

  1. National Research Foundation of Korea (NRF) grant - Korea government [NRF-2016M3D3A1A01913253, NRF-2014R1A1A2053532]
  2. Korea Institute of Energy Technology Evaluation and Planning (KETEP) [20132010201750]
  3. Industrial Strategic Technology Development Program of the Korea Evaluation Institute of Industrial Technology - Ministry of Trade, Industry and Energy (MOTIE, Korea) [10045068]
  4. R&D Center for Valuable Recycling (Global-Top R&D Program) of the Ministry of Environment of Korea [RE201606017]
  5. Korea Evaluation Institute of Industrial Technology (KEIT) [20132010201750] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The reduction-oxidation characteristics and proper kinetic models of three different iron ores having respective main phases of FeOOH, Fe3O4, and Fe2O3 were investigated using an isothermal method. A proposed kinetic model was well satisfied to explain the experimental data for CO2 activation to CO with a high accuracy. The kinetic data of the different phases of iron ores for its reduction by H-2 and for the oxidation by CO2 were relatively well described by a simple three-dimensional diffusion model of Jander equation. Activation energies of three different iron ores with the phase of FeOOH, Fe2O3, and Fe3O4 for the oxidation by CO2 were found to be 42, 25, and 12 kJ/mol, respectively. Iron ore having a FeOOH phase exhibited a higher redox property by showing a large amount of CO generation through CO2 activation with an activation energy of 42 kJ/mol and a rate constant of 0.0065 min(-1). The superior activities on the FeOOH were mainly attributed to a large surface area with medium grain size of FeOOH crystallites by forming a thermodynamically stable Fe3O4 phase on the outer surfaces even under the reductionoxidation reaction cycle. (C) 2017 Elsevier Ltd. All rights reserved.

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