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Experimental study on char nitrogen conversion characteristics during char combustion process in pressurized O2/CO2/H2O atmosphere

Pressurized oxy-fuel combustion is an advanced CO₂ capture technology with potential applications in coal-fired power generation. In this study, the conversion behavior of char-nitrogen under pressurized oxy-fuel combustion conditions was investigated using a horizontal furnace across a pressure ran...

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Bibliographic Details
Published in:Energy (Oxford) 2024-12, Vol.313, p.133874, Article 133874
Main Authors: Bai, Chenxi, Li, Yukai, Chen, Kun, Zhang, Wenda, Xu, Sicong, Zhao, Yijun, Sun, Shaozeng, Feng, Dongdong
Format: Article
Language:English
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Summary:Pressurized oxy-fuel combustion is an advanced CO₂ capture technology with potential applications in coal-fired power generation. In this study, the conversion behavior of char-nitrogen under pressurized oxy-fuel combustion conditions was investigated using a horizontal furnace across a pressure range of 0.1–1.3 MPa in an O₂/CO₂/H₂O atmosphere. The influences of pressure, gas composition, and residence time on nitrogen conversion were examined, and key factors affecting nitrogen transformation pathways were identified. Results indicated that elevated pressures favored NH₃ formation while inhibiting the formation of NO and NO₂, particularly at pressures above 0.7 MPa. Under pressurized conditions (0.7/1.3 MPa), increasing the O₂/CO₂ ratio further suppressed the conversion of char-N to NO, a contrast to behavior observed at atmospheric pressure. X-ray photoelectron spectroscopy analysis revealed a preferential consumption of nitrogen species, such as pyridinic and pyrrolic nitrogen, with pressurization enhancing the depletion of protonated nitrogen. Furthermore, an increased O₂/CO₂ ratio promoted the conversion of nitrogen oxides and other nitrogenous forms. [Display omitted] •Char-N conversion in O₂/CO₂/H₂O atmosphere was investigated under 0.1–1.3 MPa.•Increased pressure promoted NH₃ formation while reducing NO and NO₂ production.•Pressure impacted nitrogen functional group transformations on char surfaces.
ISSN:0360-5442
DOI:10.1016/j.energy.2024.133874