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MnCeOx
JOURNAL OF MATERIALS RESEARCH · 2018 ·Vol. 33 ·期 16 ·2414-2422 · IF 1.495

Promotional effect of Ba additives on MnCeOx/TiO2 catalysts for NH3-SCR of NO at low temperature

Youchun Pan,Yuesong Shen,Qijie Jin,Shemin Zhu

A series of Ba-modified MnCeOx/TiO2 catalysts were prepared by a wet impregnation method and tested for selective catalytic reduction (SCR) of NO with NH3 at low temperature. The results showed that Ba additives obviously improved the catalytic performance of the MnCeOx/TiO2 catalyst for NH3-SCR, and the BaMnCeOx/TiO2 catalyst with 3 wt% BaO exhibited the optimal catalytic performance. Moreover, the introduction of Ba also improved the resistances toward water vapor and SO2 of catalysts. The N2 adsorption, H2-TPR, and X-ray photoelectron spectroscopy results showed that the addition of Ba increased the specific surface area, redox properties, and concentrations of surface Mn4+ and chemisorbed oxygen of catalysts. Furthermore, NH3-TPD and NO-TPD were used to investigate the absorption of NH3 and NO on the catalyst. The results revealed that although the introduction of Ba significantly promoted the adsorption of NO, it also inhibited the adsorption of NH3. Consequently, the catalytic performance of MnCeOx/TiO2 was greatly improved with the Ba additives.

研究领域: 催化化学 · 环境科学
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CHEMICAL ENGINEERING SCIENCE · 2024 · IF 4.1

M-MnCeOX derived from MOF for low temperature selective catalytic reduction of NOX by NH3: Experiments and mechanisms

Yuting Hu,Minghu Zhao,Bo Du,Ting Cheng,Zhaozhong Jiang,Kai Qin,Chengzhu Zhu

A series of M-MnCeO X catalysts using MOF (Metal-organic Framework) were prepared to apply for NH 3 -SCR (Selective Catalytic Reduction) of NO X . The effects of Mn/Ce molar ratio, calcination temperature and its activity including catalytic activity, H 2 O/SO 2 resistance and stability were systematically investigated. The results showed that under the Mn/Ce molar ratio of 1 and calcination temperature of 400 ℃, the catalyst exhibited excellent catalytic activity, H 2 O/SO 2 resistance, and stability. When the concentration of NO was 500 ppm, the gas spatiotemporal velocity (GHSV) was 36,000 h −1 , and the reaction temperature was 100 ℃, the NO conversion efficiency of M-MnCeO X exceeded 90.0 %. Added 200 ppm SO 2 and 3 vol% H 2 O simultaneously, the NO conversion efficiency was close to 80.0 %. By analyzing the physicochemical properties of the catalyst, M-MnCeO X had a large specific surface area, numerous acidic sites, and excellent redox properties. According to density functional theory (DFT), the NH 3 /NO adsorption energy of M-MnCeO X were −2.35 and −2.40 eV, exhibiting lower than a single MOF-derivative, promoting the adsorption of NH 3 or NO. The reaction mechanism on the M-MnCeO X catalyst followed the E-R and L-H mechanisms by In situ DRIFTS.

研究领域: 环境催化 · 材料科学
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2025 · IF 9.7

Investigation of Cu-doped MnCeOx in PTFE catalytic fiber for synergistic removal of CB and NO at low temperature

Shengyong Lu,Xuanhao Guo,Manting Chen,Guanjie Wang,Juan Qiu,Jiaming Ding,Minghui Tang,Zhengdong Han,Yaqi Peng,Jianhua Yan

The synergistic removal of multiple pollutants from flue gas has attracted growing interest in recent years. In this study, Cu-doped MnCeO x catalysts were synthesized via an impregnation method and integrated into PTFE fibers using a split-film process to enable the simultaneous removal of chlorobenzene (CB) and nitrogen oxide (NO). Among the catalysts tested, Mn 2 Ce 1 Cu 0.6 O x exhibited the highest performance, achieving 90 % CB degradation and 100 % NO conversion at 180 °C. The PTFE-based catalytic fibers also demonstrated excellent removal efficiency, reaching 83.7 % for dioxins at the same temperature. A possible reaction mechanism is proposed in which the NH 3 -SCR process facilitates CB oxidation by generating reactive intermediates. Cu doping was found to enhance the density of acid sites and promote the ring-opening of CB, thereby suppressing chlorine accumulation and improving catalyst stability. These findings provide valuable insights for the development and optimization of catalytic bag filters for the efficient, synergistic removal of multiple pollutants from industrial emissions.

研究领域: 环境科学 · 催化材料 · 污染控制
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APPLIED CATALYSIS A-GENERAL · 2022 · IF 5.723

Metal-organic frameworks templated micropore-enriched defective MnCeOx for low temperature chlorobenzene oxidation

Tong Chen,Rong Wang,Chen Sun,Debao Kong,Shengyong Lu,Xiaodong Li

In this study, a series of metal-organic frameworks (MOFs) derived binary porous MnCeO x catalysts were synthesized via solvothermal method for chlorobenzene (CB) oxidation . Compared with the catalysts from co-precipitation and sol-gel method, Mn1Ce1-MOF catalyst presented the best performance with T 90% at 242 °C and highest CO x yield of 94.6% at 400 °C, owing to its micropore-enriched structure, higher lattice oxygen ratio and better surface reducibility. The HCl selectivity of Mn1Ce1-MOF reached 91.3% at 400 °C. The gaseous byproducts over Mn1Ce1-MOF catalyst were identified and the degradation pathway of CB was proposed. The catalytic activity of Mn1Ce1-MOF catalyst at 300 °C could stabilize over 75% for 40 h. The oxidation of Mn 3+ and chlorine species adsorption were considered to be the main reasons for the catalyst inactivation. This work provides a highly-efficient MOFs templated porous metal oxide for tail gas purification.

研究领域: 催化 · 环境化学 · 材料科学
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RESEARCH ON CHEMICAL INTERMEDIATES · 2022 ·Vol. 48 ·期 6 ·2627-2640 · IF 3.134

Co-doped MnCeOx/ZrO2 catalysts for low temperature selective catalytic reduction of NO

Wang Guangying,Liang Yan,Song Jian,Xu Kui,Pan Youchun,Xu Xiaolong,Zhao Yu

Co-doped MnCeO x /ZrO 2 catalysts were synthesized by impregnation method and their low temperature deNOx performance were evaluated. The physicochemical properties of the catalysts were studied. The results showed that the doped Co could promote the deNOx performance of MnCeO x /ZrO 2 significantly, and the doped catalyst with the Co/Mn molar ratio of 1:2 possessed the best catalytic performance. Compared with pure MnCeO x /ZrO 2 catalyst, the deNOx efficiency of the optimal 1Co 2 MnCeO x /ZrO 2 was higher to 93% at 100 °C, improved nearly by 17%. The complete removal of NO was achieved at the temperature range of 120–250 °C. The promoted catalytic performance of Co-doped MnCeO x /ZrO 2 catalyst was mainly attributed to the improvement of the catalyst support structure and surface acidity by Co. The catalytic reaction of NO with NH 3 over 1Co2MnCeO x /ZrO 2 catalyst follows both Eley–Rideal mechanism and Langmiur–Hinshelwood mechanism.

研究领域: 催化 · 环境科学 · 材料科学
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