4.7 Article

Char reactivity and kinetics based on the dynamic char structure during gasification by CO2

期刊

FUEL PROCESSING TECHNOLOGY
卷 211, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.fuproc.2020.106583

关键词

Rapid heating TGA; Dynamic structure; Gasification reactivity; Kinetic; Activation energy

资金

  1. Natural Science Foundation of China [U1703252]
  2. NSFC-DFG [21761132032]
  3. Foundation of State Key Laboratory of Coal Conversion [J20-21-301]
  4. Bureau of International Cooperation, Chinese Academy of Sciences [122214KYSB20170020]
  5. Natural Science Foundation of Xinjiang [U1703252]

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Coal char reactivity is crucial for gasifier design and operation, and is dynamic with reaction during gasification. In-situ char reactivity increases and then decreases due to gas switch step, graphitization degree increase, and inhibition effect of minerals, while ex-situ char reactivity is initially controlled by chemical structure and later by catalytic activity of minerals. The unreaction core model (URCM) is suitable for interpreting gasification kinetics based on dynamic char structure.
Coal char reactivity is the essential for gasifier design and operation. Char structure and reactivity are dynamic with reaction during gasification. To obtain the relationship between dynamic structure and reactivity, char samples at different carbon conversion were prepared at 1223 K by a rapid heating thermogravimetric analyzer (R-TGA). The ex-situ char reactivity was investigated in TGA between 1073 and 1223 K, and was correlated with the dynamic structure. Besides of XRD and SEM results, nano-computed tomography (nano-CT) revealed the morphology of carbon matrix and minerals during gasification. Results showed that reaction rate of in-situ char significantly increased firstly and then decreased, which was attributed to the gas switch step, the increase of graphitization degree and inhibition effect of minerals. In contrast, the reactivity of ex-situ char was initially controlled by chemical structure and later by the abundant catalytic activity of minerals. The reactivity decreased slightly and then increased with increasing carbon conversion. The unreaction core model (URCM) was more suitable to interpret the gasification kinetics based on the dynamic char structure and fitting coefficient. Meanwhile, the results by iso-conversional method also supported the validity of URCM, but also indicated that the activation energy of char gasification gradually increased during in-situ gasification.

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