TY - JOUR
T1 - Endogenous CO2-assisted regeneration of biomass pyrolysis volatiles with dry reforming over NiFe2O4@SBA‑15
AU - Sun, Zhongshun
AU - Yang, Yujing
AU - Liu, Gen
AU - Huang, Huili
AU - Cheng, Chunyu
AU - Yang, Bolun
AU - Song, Chen
AU - Wu, Zhiqiang
N1 - Publisher Copyright:
© 2026 Elsevier Ltd.
PY - 2027/2
Y1 - 2027/2
N2 - Endogenous CO2 in biomass pyrolysis volatiles is commonly treated as a diluent, although it could potentially participate in oxygen-carrier regeneration and carbon reutilization. In this work, a coupled strategy integrating endogenous CO2-assisted regeneration with chemical looping dry reforming of biomass pyrolysis volatiles was investigated. The objective was to determine whether endogenous CO2 could be converted from a limiting component into a reactive carbon source under realistic reducing atmospheres containing CH4, H2, and CO. Thermodynamic analysis showed that methane dry reforming became favorable above 650 °C, while kinetic fitting indicated that the kinetic behavior over the reduced Ni0.36Fe0.64 phase was consistent with an MvK-type contribution with an Ea of 83.66 kJ·mol−1. In situ DRIFTS and XRD results revealed that CO2 activation proceeded through a hydrogen-assisted formate route and a direct carbonate route, and that the coexisting H2/CO atmosphere suppressed surface oxidative reconstruction, shifting the active structure from a Ni-Fe3O4 interfacial state to a more reduced NiFe3-rich alloy state. This structural evolution weakened CO2 activation but favored syngas formation under strongly reducing conditions. At the process level, staged regeneration with endogenous CO2 increases syngas production by 13.99% and achieves a lattice oxygen recovery rate of 45.75%. Light volatiles do not significantly increase syngas production, and the lattice oxygen recovery rate drops to about 20%; the H2/CO in the volatiles has an inhibitory effect on oxygen carrier regeneration. The enhanced syngas production in Process 4 should be attributed to the combined effect of endogenous CO2 utilization and exogenous biomethane-assisted DRM, increasing syngas yield by 34% and reduced CO2 emissions by 10.5%. These results suggest that endogenous CO2 can be repurposed as a reactive species for oxygen-carrier regeneration and syngas coproduction, providing a feasible route for improving carbon utilization and syngas production from biomass pyrolysis volatiles.
AB - Endogenous CO2 in biomass pyrolysis volatiles is commonly treated as a diluent, although it could potentially participate in oxygen-carrier regeneration and carbon reutilization. In this work, a coupled strategy integrating endogenous CO2-assisted regeneration with chemical looping dry reforming of biomass pyrolysis volatiles was investigated. The objective was to determine whether endogenous CO2 could be converted from a limiting component into a reactive carbon source under realistic reducing atmospheres containing CH4, H2, and CO. Thermodynamic analysis showed that methane dry reforming became favorable above 650 °C, while kinetic fitting indicated that the kinetic behavior over the reduced Ni0.36Fe0.64 phase was consistent with an MvK-type contribution with an Ea of 83.66 kJ·mol−1. In situ DRIFTS and XRD results revealed that CO2 activation proceeded through a hydrogen-assisted formate route and a direct carbonate route, and that the coexisting H2/CO atmosphere suppressed surface oxidative reconstruction, shifting the active structure from a Ni-Fe3O4 interfacial state to a more reduced NiFe3-rich alloy state. This structural evolution weakened CO2 activation but favored syngas formation under strongly reducing conditions. At the process level, staged regeneration with endogenous CO2 increases syngas production by 13.99% and achieves a lattice oxygen recovery rate of 45.75%. Light volatiles do not significantly increase syngas production, and the lattice oxygen recovery rate drops to about 20%; the H2/CO in the volatiles has an inhibitory effect on oxygen carrier regeneration. The enhanced syngas production in Process 4 should be attributed to the combined effect of endogenous CO2 utilization and exogenous biomethane-assisted DRM, increasing syngas yield by 34% and reduced CO2 emissions by 10.5%. These results suggest that endogenous CO2 can be repurposed as a reactive species for oxygen-carrier regeneration and syngas coproduction, providing a feasible route for improving carbon utilization and syngas production from biomass pyrolysis volatiles.
KW - Chemical looping dry reforming
KW - Endogenous CO utilization
KW - Oxygen-carrier regeneration
KW - Syngas
UR - https://www.scopus.com/pages/publications/105044573849
U2 - 10.1016/j.fuel.2026.140689
DO - 10.1016/j.fuel.2026.140689
M3 - 文章
AN - SCOPUS:105044573849
SN - 0016-2361
VL - 429
JO - Fuel
JF - Fuel
M1 - 140689
ER -