Thermal stability is crucial for maintaining the efficient performance and low regeneration energy of biphasic absorbents, while the synergistic degradation reactions and condition fluctuations could significantly influence the thermal degradation process of biphasic solutions. In this research, a typical amide-based biphasic absorbent diethylenetriamine(DETA)/diethanolamine(DEA)/N, N-dimethylacetamide(DMAC) with low regeneration energy, was applied in a thermal degradation investigation. The thermal stability of active amine in DETA/DEA/DMAC was superior to 30 wt% MEA, 7 M DETA solution, and other biphasic absorbents, with a 19.9 % lower amine degradation ratio compared to 7 M DETA. The primary thermal degradation products in DETA/DEA/DMAC with and without CO2 were analyzed using Cation Ion Chromatography (IC) and 13C Nuclear Magnetic Resonance (NMR). A series of synergistic reactions between DETA and DMAC, with DMAC being an inducer, was revealed in thermal degradation of DETA/DEA/DMAC, leading to accelerated DETA degradation and DEA formation. Various operational conditions including CO2 loading and degradation temperature were considered to build a systemic impact mechanism on thermal degradation for biphasic absorbents. Before phase separation, CO2 absorption and increasing temperature significantly exacerbated DETA degradation. However, phase separation behavior was found to effectively prevent the synergistic degradation reactions in the solution, leading to a 27.4 % reduction in the DETA degradation ratio of the aqueous phase after phase separation. Moreover, it achieved a 24.1 % reduction of the DETA degradation ratio caused by rising temperature in the solution after phase separation. Therefore, it is essential to ensure the completion of phase separation for biphasic solvents before entering the stripper in applications. After thermal degradation, the regeneration rate and cyclic capacity of DETA/DEA/DMAC were strengthened, which was 84.9 % and 63.3 % higher than that of 30 wt% MEA, respectively.
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