The changes in functional groups during in situ co-pyrolysis of tar-rich coal with wheat straw were systematically examined using synchrotron diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) coupled with thermogravimetric analysis (TGA). Dynamic changes in C=C, C-O, and C-O-C groups were monitored and assessed across 50–500 °C, complemented by thermogravimetric analysis to assess synergistic effects. It revealed that co-pyrolysis significantly alters the thermal cracking pathways of oxygenated structures, reducing the overall onset temperature by approximately 150 °C. Specifically, instead of maintaining thermal stability, co-pyrolysis promoted early structural aromatization and advanced the C=O decomposition onset by 50 °C compared to coal, achieving a remarkable functional group cleavage rate of 47%. Additionally, the C=C formation temperature was advanced by 150 °C. Furthermore, co-pyrolysis effectively suppressed the secondary structural transformations observed in biomass by limiting the relative accumulation of C–O–C structures to merely a 5% increase, compared to a 52% surge in wheat straw. Interestingly, while DRIFTS confirms facilitated localized bond cleavage and deoxygenation, TGA reveals a macroscopic negative synergy regarding overall weight loss. These findings provide profound insights into the complex radical interactions during co-conversion, offering a crucial theoretical basis for optimizing coal–biomass co-pyrolysis technologies.
Xu et al. (Sat,) studied this question.