Journal of Environmental Chemical Engineering
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2025
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IF 7.2
Shuya Rui,Na Liu,Lingwei Ren,Yang Liu,Zian Liu,Binghui Wu,Hua Pan,Zhiping Ye
Traditional Mn-Ce catalysts for selective catalytic reduction (SCR) of NO with CO (CO-SCR) in iron and steel flue gases are often hindered by competitive adsorption of NO and CO, which compromises catalytic efficiency. In this study, we present a Ni-doped Mn-Ce catalyst that overcomes these challenges, achieving 96 % NO conversion, 98 % N 2 selectivity, and 44 % CO conversion at 175 °C. Comprehensive characterization of the catalyst reveals that Ni doping significantly enhances Mn-Ce interactions, boosting oxygen vacancy density and promoting efficient redox cycling between Mn 3 + /Mn 4+ and Ce 3+ /Ce 4+ . Diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) confirms preferential NO adsorption at oxygen vacancy sites, minimizing CO-NO competition and stabilizing the Langmuir-Hinshelwood mechanism, where both gases co-adsorb and react at oxygen-rich vacancies. Mechanistic insights suggest that Ni facilitates electron transfer, weakening the N–O bond in NO and accelerating its dissociation, resulting in faster NO reduction. This study establishes Ni doping as a promising strategy for improving the low-temperature performance of Mn-Ce-based CO-SCR catalysts, paving the way for more efficient catalytic systems.
研究领域:
催化化学
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环境科学
✓ 已验证
产品关联
DOI
高影响因子
Reaction Kinetics Mechanisms and Catalysis
·
2018
·Vol. 124
·期 2
·587-601
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IF 1.515
Wang Tao,Zhang Xinyu,Liu Jun,Liu Hanzi,Sun Baomin
NO conversion using dielectric barrier discharge (DBD) plasma with different catalysts was investigated. Cu/TiO 2 , Cu/Al 2 O 3 , Cu/ZSM-5, Cu/CNTs and Cu/AC catalysts were prepared by incipient wetness impregnation with 4 wt% Cu loaded. BET, SEM, XRD, XPS, H 2 -TPR, NH 3 -TPD were used to measure and evaluate various catalysts. Compared with the plasma only process, the combination of plasma with different catalysts significant improved the NO conversion rate. The highest NO conversion rate of 76% could be achieved with Cu/ZSM-5 catalyst at the energy density of 184 J/L. The results indicate that Cu species over the support ZSM-5 can produce high concentrations of CuO, largest specific surface area, largest amounts of acidity and lowest reduction temperature (209 °C), these factors conducive to plasma-catalyst reaction. Besides, Cu/TiO 2 and Cu/Al 2 O 3 catalysts exhibited excellent NO conversion at the low energy density because of the low thermal stability. After plasma-catalyst reaction, the reducibility of CuO and Cu 2 O over supports decreased and the peak position of acid sites shifted to lower temperature.
研究领域:
环境科学
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催化化学
✓ 已验证
DOI
高影响因子
PLASMA SCIENCE & TECHNOLOGY
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2017
·Vol. 19
·期 11
·115504
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IF 0.83
Xu CAO,Weixuan ZHAO,Renxi ZHANG,Huiqi HOU,Shanping CHEN,Ruina ZHANG
This paper discusses the conversion of nitric oxide (NO) with a low-temperature plasma induced by a catalytic packed-bed dielectric barrier discharge (DBD) reactor. Alumina oxide (Al2O3), glass (SiO2) and zirconium oxide (ZrO2), three different spherical packed materials of the same size, were each present in the DBD reactor. The NO conversion under varying input voltage and specific energy density, and the effects of catalysts (titanium dioxide (TiO2) and manganese oxide (MnOx) coated on Al2O3) on NO conversion were investigated. The experimental results showed that NO conversion was greatly enhanced in the presence of packed materials in the reactor, and the catalytic packed bed of MnOx/Al2O3 showed better performance than that of TiO2/Al2O3. The surface and crystal structures of the materials and catalysts were characterized through scanning electron microscopy analysis. The final products were clearly observed by a Fourier transform infrared spectrometer and provided a better understanding of NO conversion.
研究领域:
环境科学
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化学工程
✓ 已验证
DOI
高影响因子
JOURNAL OF SOLID STATE CHEMISTRY
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2023
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IF 3.3
Yuting Hu,Ting Cheng,Zhaozhong Jiang,Kai Qin,Han He,Chengzhu Zhu
Fe-MIL-101-NH 2 was prepared by solvothermal method with ferric nitrate and 2-Aminoterephthalic Acid (DBC-NH 2 ), and Fe-MIL-101-NH 2 as precursor was calcined to prepare α-Fe 2 O 3 catalyst. The optimum synthesis condition and the NO conversion efficiency of α-Fe 2 O 3 were systematically investigated, and its crystallinity, micro-morphology and surface acidity were characterized. The results showed that α-Fe 2 O 3 over calcination at 400 °C for 1 h had excellent catalytic activity, SO 2 tolerance, water resistance, and stability. When an initial NO concentration of 500 ppm, the gas hourly space velocity (GHSV) of 35000 h −1 , and a reaction temperature of 350 °C, the NO conversion efficiency of α-Fe 2 O 3 remained above 90 %. The crystal structure of the catalyst was α-Fe 2 O 3 which retained the original octahedral morphology of Fe-MIL-101-NH 2 and increased a lot of new pores, leading to more abundant Lewis acid sites for promoting NO conversion efficiency.
研究领域:
材料科学
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环境科学
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化学工程
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING & TECHNOLOGY
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2023
·Vol. 46
·期 10
·2217-2225
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IF 2.1
Shuangshuang Lv,Xianlong Zhang,Haoyang Dong,Shi Jin,Xinyu Wang
Manganese-antimony composite oxide catalysts were prepared for use in low-temperature selective catalytic reduction of flue gas, by adopting the strategy of passivation to regulate the valence state of the active component and control catalytic activity. Activity evaluation results found that MnSb 0.36 O y delivered 80 % NO conversion in the presence of SO 2 at 200 °C, and nearly 90 % conversion at 250 °C. Doping with Sb changed the surface micromorphology, resulting in a perforated porousness layered foam with a porous structure of tens of nanometers, which was conducive to molecular mass transfer of the reaction gas. Doping with Sb regulated the valence state of the active MnO x component, which diminished catalytic oxidation of SO 2 , thus promoting catalyst stability and limiting the toxic effect of SO 2 .
研究领域:
环境科学
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催化化学
✓ 已验证
产品关联
DOI
高影响因子
Frontiers in Chemistry
·
2024
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IF 3.8
An Sufeng,Wang Peng,Wang Kuanling,Wang Xuehai,Li Baozhong,Guo Xinwen
The M/SSZ-39 catalysts (M = In, Co, Cu, Fe) with different metal species and metal loadings were synthesized using the wet impregnation method on a small-pore SSZ-39 molecular sieve. X-ray diffraction (XRD), transmission electron microscopy (TEM), nitrogen adsorption-dehydrogenation and hydrogen temperature program reduction (H2-TPR) were employed to characterize the effects of various metal components and metal loadings on the performance of CH4 selective catalytic reduction of NO reaction (CH4-SCR). The characterization results showed that the In/SSZ-39 catalyst exhibited significantly higher catalytic activity compared to the Cu-, Co-, and Fe/SSZ-39 catalysts, suggesting that indium (In) is a more suitable active ingredient for the CH4-SCR reaction. The xIn/SSZ-39 (x = 1, 2, 3, x represents the In loadings of 1.0 wt%, 2.0 wt% and 3.0 wt%) catalysts, with different In loadings, all present excellent CH4-SCR performance. By varying the In loadings, the type of In species present in the catalyst can be regulated, thus enhancing DeNOx activity and CH4 selectivity in the CH4-SCR reaction. At a low temperature of 400 °C and a low CH4/NO feed ratio (CH4/NO = 1), the 3In/SSZ-39 catalyst, featuring highly active InOx clusters, achieves the best low-temperature CH4-SCR performance, with a high NO conversion rate of up to 90% and a CH4 selectivity of up to 74.2%.
研究领域:
环境科学
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催化化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2025
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IF 13.2
Yuerui Ma,Peng Chen,Jiazhen Liao,Xing’an Dong,Wenjie He,Wendong Zhang
Selective photocatalytic oxidation of NO to nitrate (NO 3 – ) over toxic NO 2 remains challenging due to low selectivity and inefficient charge migration in existing systems. This study introduces Fe 3+ as an electron acceptor beneath a Bi 4 TaO 8 Cl/Bi 2 O 2 CO 3 heterojunction to precisely regulate electron pathways and promote targeted hydroxyl radical ( • OH) generation. Combined experimental and DFT analyses reveal Fe 3+ ’s dual role: enhancing interfacial electron transfer and activating H 2 O at surface sites to form • OH. The optimized heterojunction achieves 68.19 % NO conversion with minimal NO 2 selectivity (10.98 %). ESR and ROS quenching confirm Fe 3+ -driven electron migration enriches surface holes, boosting H 2 O adsorption and • OH production (2.76-fold increase). The strong oxidation capacity of • OH suppresses NO 2 formation, favoring complete NO oxidation to NO 3 – . This work provides a strategic approach for selective NO removal by electron-pathway engineering, advancing the design of eco-friendly photocatalysts for air pollution control.
研究领域:
环境化学
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光催化
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材料科学
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化学工程
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大气污染控制
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2019
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IF 14.229
Xin Wang,Baofang Jin,Ruixue Feng,Wei Liu,Duan Weng,Xiaodong Wu,Shuang Liu
In this work, tandem oxygen delivery systems were built by coating cube-like Co 3 O 4 with Ag/CeO 2 , which exhibited high soot oxidation activity that overwhelmed the Fe 2 O 3 -based catalysts. The results of TPR and activity tests indicated that a large amount of Co 3 O 4 lattice oxygen could be transferred into O x − with the assistance of Ag/CeO 2 . These active oxygen species accelerated the oxidation of soot and NO at low temperature. Furthermore, the Co 3 O 4 -CeO 2 synergy facilitated Co 3+ → Co 2+ transformation during reactions, resulting in boosted NO conversion and thereby NO 2 -assisted soot combustion at mild and high temperatures. Given the Ag/Co 3 O 4 @CeO 2 -type catalysts were low-cost, hydrothermally stable and could be fabricated via co-precipitation methods easily, they were highly promising for application in both gasoline and diesel particulate filters.
研究领域:
催化
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环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
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2022
·
IF 24.319
Qiuhui Zhu,Reshalaiti Hailili,Yue Xin,Yingtang Zhou,Yu Huang,Xinzhu Pang,Ke Zhang,Peter K.J. Robertson,Detlef W. Bahnemann,Chuanyi Wang
Developing full-spectrum responsive and efficient photocatalysts is still an important challenge in the field of photocatalytic treatment of trace environmental pollutants. Herein, full-spectrum Bi@Bi 2 Ti 2 O 7 with rich-oxygen vacancies (OVs) were fabricated via a one-pot hydrothermal method. The optimized composite photocatalyst exhibited a photocatalytic efficiency of 79 %, more than doubled higher than that of its counterpart, Bi 2 Ti 2 O 7 (31.79 %), for removing ppb-level NO under visible-near infrared (Vis-NIR) irradiation. The enhanced photocatalytic performance was attributed to the co-effect of Bi and OVs reveal by control experiments and theoretical calculations, which not only benefited the adsorption and photocatalytic activation of NO but broadened light absorption to near infrared region. Furthermore, the adsorption and photocatalytic conversion pathway of NO was explored by in situ DRIFTS, suggesting that NO + as intermediate species is crucial to improve the selectivity of NO converting to nitrate. This work provides a new perspective of constructing full-spectrum-driven photocatalysts for environment remediation.
研究领域:
环境科学
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材料科学
·
光催化
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF CATALYSIS
·
2024
·
IF 6.5
Yuxi Meng,Shaomian Liu,Yixi Wang,Wenqing Xu,Jiajian Gao,Sansan Yu,Fabing Su,Tingyu Zhu
Selective catalytic reduction of NO using CO (CO-SCR) is a promising technology for the purification of NO in the flue gas. However, the presence of O 2 significantly inhibits the activity of the CO-SCR catalyst. Herein, we synthesize a hollow Mn-doped CeO 2 @Co 3 O 4 catalyst (Mn-CeO 2 @Co 3 O 4 ), which achieved 82% NO conversion, 100% CO conversion, and 78% N 2 selectivity under 5 vol% O 2 at 200 °C, superior to those of CeO 2 @Co 3 O 4 and Co 3 O 4 @CeO 2 catalysts. The characterization results indicate that the strong electronic interaction at the heterointerfaces between Co 3 O 4 and CeO 2 plays a crucial role in promoting selective adsorption of NO. Furthermore, the Mn doping into the Co 3 O 4 lattice of the catalyst facilitates the conversion of N 2 O intermediates, thereby enhancing the overall activity. This research provides a new strategy for the design and synthesis of CO-SCR catalysts.
研究领域:
催化
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环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
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