4.7 Article

Fast co-pyrolysis of lignin with spent bleaching clay into monocyclic aromatic hydrocarbons over a novel low-cost composite catalyst

Journal

Publisher

ELSEVIER
DOI: 10.1016/j.jaap.2022.105748

Keywords

Lignin; Spent bleaching clay; Catalytic co -pyrolysis; Monocyclic aromatic hydrocarbons; Coke

Funding

  1. National Key R & D Program of China
  2. National Natural Science Foundation of China
  3. National Natural Science Foundation of Shandong
  4. Guangdong Provincial Key Laboratory of New and Renewable Energy Research and Development
  5. [2019YFD1100602]
  6. [52176192]
  7. [52130610]
  8. [ZR2021ME035]
  9. [ZR2021QE132]
  10. [E239kf0701]

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This study successfully improved the anti-coking performance of HZSM-5 by using CSBC as a binder, while increasing the selectivity for MAHs. After 3 reaction-regeneration cycles, the catalytic activity of CSHZ11 for MAHs was 71.11 % of fresh catalyst. The research demonstrates the feasibility of using binder modification to enhance the anti-coking performance of HZSM-5 and provides a reference for the integrated utilization of SBC and lignin.
Improving the anti-coking performance of catalyst during lignin-catalyzed pyrolysis without affecting the selectivity of the monocyclic aromatic hydrocarbons (MAHs) is a challenge. In this paper, a low-cost composite catalyst (CSHZ) was prepared using calcined spent bleaching clay (CSBC) as a binder for HZSM-5 to resolve the issue. In order to evaluate the performance of the composite catalyst, an ex-situ fast catalytic co-pyrolysis experiment was performed in a fixed-bed reaction system with lignin and spent bleaching clay (SBC) as raw materials. The impacts of the temperature, CSBC-to-HZSM-5 ratios, raw material-to-catalyst ratios, and cycle -regeneration times on MAHs distribution, are then studied. The selectivity of CSHZ11 (CSBS-to-HZSM-5 ratio of 1:1) for MAHs in bio-oil reached 78.02 % at 550 celcius and the raw material-to-catalyst ratio of 1:1, which exceeded those of HZSM-5 alone by 19.12 %. After 3 reaction-regeneration cycles, the catalytic activity of CSHZ11 for MAHs was 71.11 % of fresh catalyst. The characterization (TEM, Py-IR, TGA, etc.) of the catalysts (fresh and discarded) revealed that the addition of CSBC regulated the acidity and pore channels of HZSM-5 and inhibited the formation of catalyst graphite-like coke. This study demonstrates the feasibility of using binder modification to improve the anti-coking performance of HZSM-5. It also serves as a reference for the integrated utilization of SBC and lignin.

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