Simultaneous capture of SO and NO from flue gas is critical for coal-fired power generation. In this study, environmentally friendly and high-performance deep eutectic solvents based on ethylene glycol and ammonium bromide were designed to capture SO and NO simultaneously. The SO and NO absorption performances and absorption mechanisms were systematically investigated by H NMR and Fourier transform infrared (FT-IR) spectroscopy in combination with ab initio calculations using Gaussian software. The results showed that EG-TBAB DESs can absorb low concentrations of SO and NO from the flue gas simultaneously at low temperatures (≤50 °C). H NMR, FT-IR, and simulation results indicate that SO and NO are absorbed by forming EG-TBAB-SO-NO complexes, Br is the main active site for NO absorption, and NO is more active in an EG-TBAB-NO-SO complex than SO. EG-TBAB DESs exhibit outstanding regeneration capability, and absorption capacities remain unchanged after five absorption-desorption cycles. The fundamental understanding of simultaneous capture of SO and NO from this study enables DES structures to be rationally designed for efficient and low-cost desulfurization and denitrification reagents.
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http://dx.doi.org/10.1021/acsomega.2c03221 | DOI Listing |
iScience
August 2024
Ocean College, Zhejiang University, Zhoushan, Zhejiang 316021, China.
A major obstacle to exploiting industrial flue gas for microalgae cultivation is the unfavorable acidic environment. We previously identified three upregulated genes in the low-pH-adapted model diatom : ferredoxin (PtFDX), cation/proton antiporter (PtCPA), and HCO transporter (PtSCL4-2). Here, we individually overexpressed these genes in to investigate their respective roles in resisting acidic stress (pH 5.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
Key Laboratory of Groundwater Resources and Environment (Jilin University), Ministry of Education, College of New Energy and Environment, Jilin University, Changchun 130021, China. Electronic address:
As the frontier of environmental catalysis, mercury removal by deNO unit over bifunctional catalyst has emerged. However, it is fundamentally challenging to achieve simultaneous NO and mercury removal in industrial flue gas due to the commercial selective catalytic reduction (SCR) molecular sieves' lack of demercuration active centers. Herein, we demonstrate an active site in situ reconfiguration approach to enhance the oxidation of elemental mercury and immobilize divalent mercury by modified commercial SCR catalysts.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Materials Science and Engineering, Ulsan National Institute of Science and Technology (UNIST), Ulsan 44919 Republic of Korea.
The simultaneous removal reaction (SRR) is a pioneering approach for achieving the simultaneous removal of anthropogenic NO and CO pollutants through catalytic reactions. To facilitate this removal across diverse industrial fields, it is crucial to understand the trade-offs and synergies among the multiple reactions involved in the SRR process. In this study, we developed mixed metal oxide nanostructures derived from layered double hydroxides as catalysts for the SRR, achieving high catalytic conversions of 93.
View Article and Find Full Text PDFJ Environ Manage
December 2024
Key Laboratory of Energy Thermal Conversion and Control, Ministry of Education, School of Energy and Environment, Southeast University, Nanjing, 210096, PR China.
J Colloid Interface Sci
December 2024
College of Materials Science and Engineering, Xi'an University of Architecture and Technology, Xi'an 710055, PR China. Electronic address:
NH-MIL-125 with abundant porosity and specific interactions with CO molecules, has been demonstrate great potential in the field of photocatalytic CO reduction. However, conventional NH-MIL-125 and their composites much lower CO photoreduction efficiency in aerobic environments because of the O competition. To circumvent the issue, this study modifies NH-MIL-125 through crystal facet engineering to enhance its selective CO adsorption and photocatalytic efficiency in the environment of impurity CO.
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