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Experiment and Simulation of the Non-Catalytic Reforming of Biomass Gasification Producer Gas for Syngas Production

Yongbin Wang, Guoqiang Cao (), Zhongren Ba, Hao Cheng, Donghai Hu, Jonas Baltrusaitis, Chunyu Li, Jiantao Zhao () and Yitian Fang
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Yongbin Wang: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Guoqiang Cao: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Zhongren Ba: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Hao Cheng: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Donghai Hu: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Jonas Baltrusaitis: Department of Chemical and Biomolecular Engineering, Lehigh University, B336 Iacocca Hall, 111 Research Drive, Bethlehem, PA 18015, USA
Chunyu Li: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Jiantao Zhao: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China
Yitian Fang: State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, China

Energies, 2025, vol. 18, issue 11, 1-19

Abstract: Among biomass gasification syngas cleaning methods, non-catalytic reforming emerges as a sustainable and high-efficiency alternative. This study employed integrated experimental analysis and kinetic modeling to examine non-catalytic reforming processes of biomass-derived producer gas utilizing a synthetic tar mixture containing representative model compounds: naphthalene (C 10 H 8 ), toluene (C 7 H 8 ), benzene (C 6 H 6 ), and phenol (C 6 H 5 OH). The experiments were conducted using a high-temperature fixed-bed reactor under varying temperatures (1100–1500 °C) and equivalence ratios (ERs, 0.10–0.30). The results obtained from the experiment, namely the measured mole concentration of H 2 , CO, CH 4 , CO 2 , H 2 O, soot, and tar suggested that both reactor temperature and O 2 content had an important effect. Increasing the temperature significantly promotes the formation of H 2 and CO. At 1500 °C and a residence time of 0.01 s, the product gas achieved CO and H 2 concentrations of 28.02% and 34.35%, respectively, while CH 4 , tar, and soot were almost entirely converted. Conversely, the addition of O 2 reduces the concentrations of H 2 and CO. Increasing ER from 0.10 to 0.20 could reduce CO from 22.25% to 16.11%, and H 2 from 13.81% to 10.54%, respectively. Experimental results were used to derive a kinetic model to accurately describe the non-catalytic reforming of producer gas. Furthermore, the maximum of the Root Mean Square Error (RMSE) and the Relative Root Mean Square Error (RRMSE) between the model predictions and experimental data are 2.42% and 11.01%, respectively. In particular, according to the kinetic model, the temperature increases predominantly accelerated endothermic reactions, including the Boudouard reaction, water gas reaction, and CH 4 steam reforming, thereby significantly enhancing CO and H 2 production. Simultaneously, O 2 content primarily influenced carbon monoxide oxidation, hydrogen oxidation, and partial carbon oxidation.

Keywords: non-catalytic reforming; biomass gasification producer gas; kinetic model; sensitivity analysis; reaction pathway (search for similar items in EconPapers)
JEL-codes: Q Q0 Q4 Q40 Q41 Q42 Q43 Q47 Q48 Q49 (search for similar items in EconPapers)
Date: 2025
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