Perovskites with flexible structures and excellent redox properties have attracted considerable attention in industry, and their denitration activities can be further improved with metal substitution. In order to investigate the effect of Ce and Cu substitution on the physicochemical properties of perovskite in NH-SCR system, a series of La Ce Mn Cu O ( = 0, 0.1, = 0, 0.05, 0.1, 0.2, 0.4) catalysts were prepared by citrate sol-gel method and employed for NO removal in the simulated flue gas, and the physical and chemical properties of the catalysts were studied using XRD, SEM, BET, XPS, DRIFT characterizations. The Ce substitution on A-site cation of LaMnO can improve the denitration activity of the perovskite catalyst, and LaCeMnO displays NO conversion of 86.7% at 350 °C. The characterization results indicate that the high denitration activity of LaCeMnO is mainly attributed to the larger surface area, which contributes to the adsorption of NH and NO. Besides, the appropriate Cu substitution on B-site cation of LaCeMnO can further improve the denitration activity of perovskite catalyst, and LaCeMnCuO displays the NO conversion of 91.8% at 350 °C. Although the specific surface area of LaCeMnCuO is lower than LaCeMnO, the Cu active sites and the Ce contents are more developed, making many reaction units formed on the catalyst surface and redox properties of catalyst improved. In addition, strong metal interaction (Ce + Mn + Cu ↔ Ce + Mn/Mn + Cu) and high concentrations of chemical adsorbed oxygen and lattice oxygen both strengthen the redox reaction on catalyst surface, thus contributing to the better denitration activity of LaCeMnCuO. Therefore, appropriate cerium and copper substitution will markedly improve the denitration activity of La-Mn perovskite catalyst. We also reasonably conclude a multiple reaction mechanism during NH-SCR denitration process basing on DRIFT results, which includes the Eley-Rideal mechanism and Langmuir-Hinshelwood mechanism.
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http://dx.doi.org/10.1039/d2ra04085a | DOI Listing |
Acta Pharmacol Sin
January 2025
Department of Anatomy and Convergence Medical Science, College of Medicine, Institute of Medical Science, Tyrosine Peptide Multiuse Research Group, Anti-aging Bio Cell Factory Regional Leading Research Center, Gyeongsang National University, Jinju, Gyeongnam, Republic of Korea.
Glutamine synthetase (GS) plays a crucial role in the homeostasis of the glutamate-glutamine cycle in the brain. Hypoactive GS causes depressive behaviors. Under chronic stress, GS has no change in expression, but its activity is decreased due to nitration of tyrosine (Tyr).
View Article and Find Full Text PDFChem Asian J
November 2024
State Key Joint Laboratory of Environment Simulation and Pollution Control, School of Environment, Tsinghua University, 100084, Beijing, P. R. China.
A series of x Cu-TiO obtained from the sol-gel method were tested for NH selective catalytic oxidation (NH-SCO). Its performance was higher than that of supported Cu/TiO-Im and solvent-free Cu/TiO-SF. The catalyst exhibits better water resistance at 300 °C.
View Article and Find Full Text PDFJ Hazard Mater
November 2024
Key Laboratory of Functional Inorganic Material Chemistry, Ministry of Education of the People's Republic of China, School of Chemistry and Materials, Heilongjiang University, No.74 Xuefu Road, Harbin 150080, PR China. Electronic address:
The MnNbTiO (a = 0.6-0.9) catalysts for NH selective catalytic reduction denitration were prepared using the co-precipitation method.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
State Key Laboratory of Coal Conversion, Institute of Coal Chemistry, Chinese Academy of Sciences, Taiyuan 030001, PR China; University of Chinese Academy of Sciences, Beijing 100049, PR China. Electronic address:
Nitrogen oxides (NO) and volatile organic compounds (VOCs) are the main pollutants in flue gas, and the synergistic removal of NO and VOCs in the presence of SO is still a challenge. In this work, the microstructure of NiMnO-CeO catalysts and the distribution of sulfur-containing substances were studied to reveal the inactivation mechanism of sulfur poisoning. NO conversion could reach more than 80 % at 100-250 °C, and CH conversion could achieve 90 % at 210 °C in the synergistic reaction on NiMnO-CeO catalyst, which has dual active sites with propane oxidation and SCR reactions carried out at Mn and Ni sites, respectively.
View Article and Find Full Text PDFJ Colloid Interface Sci
February 2025
School of Energy and Environmental Engineering, University of Science and Technology Beijing, Beijing 100083, China; Beijing Key Laboratory of Resource-oriented Treatment of Industrial Pollutants, Beijing 100083, China. Electronic address:
In the selective catalytic reduction of NOx by NH (NH-SCR), conventional Mn-based denitration catalysts often suffered from susceptibility to poisoning by alkali and alkaline earth metals, this paper presented an innovative self-protected Chlorella@Mn denitration catalyst. Remarkably, in the presence of high concentrations (2 wt%) of alkali and alkaline earth metal oxides, the Chlorella@Mn catalyst sustained a NOx conversion exceeding 96 % at 175 °C. At an even higher concentration (4 wt%), NOx conversion above 90 % at 175 °C, surface analysis revealed that POMn sites acted as sacrificial sites, binding to the alkali and alkaline earth metals, the Chlorella@Mn catalyst surface naturally carried a spectrum of acidic species (such as SO, PO, SiO), proficient in capturing alkali/alkaline earth metal effectively, elements such as S, P, and Si formed bonds with K, Na, Ca, and Mg.
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