Novel Homogeneous and Mesoporous MnOx-Doped Ceria Nanosheets as Catalysts for Low-Temperature Selective Catalytic Reduction

2019 ◽  
Vol 72 (9) ◽  
pp. 657
Author(s):  
Yan Yue ◽  
Yanhua Wang ◽  
Jun Ling ◽  
Weilin Sun ◽  
Zhiquan Shen
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
Bet Surface Area ◽  
Homogeneous Distribution ◽  
X Ray Diffraction ◽  
X Ray ◽  
Co Precipitation ◽  
Scr Of Nox

The development of a catalyst for the selective catalytic reduction (SCR) of NOx is essential for purifying air and the denitration of coal-burning exhaust. Herein, we prepare novel MnOx-CeO2 nanosheets with porous structures by a homogeneous coordination precipitation (HCP) method which exhibit a high NO removal efficiency above 90% in the SCR reaction at low temperature (150–240°C). The MnOx-CeO2(HCP) catalysts have a higher Brunauer–Emmett–Teller (BET) surface area and more homogeneous distribution of Mnx+ in the CeO2 lattice than those prepared by co-precipitation and precursor mixture combustion methods according to BET, X-ray diffraction, scanning electron microscopy, energy dispersive spectroscopy, and X-ray photoelectron spectroscopy characterizations. Together with a higher ratio of Mn4+, Ce3+, and Oα, the above properties are responsible for the high catalytic performances of MnOx-CeO2(HCP) in the SCR of NOx.

scholarly journals Nanosized V-Ce Oxides Supported on TiO2 as a Superior Catalyst for the Selective Catalytic Reduction of NO

Catalysts ◽  
2020 ◽  
Vol 10 (2) ◽  
pp. 202
Author(s):  
Long Lu ◽  
Xueman Wang ◽  
Chunhua Hu ◽  
Ying Liu ◽  
Xiongbo Chen ◽  
...  
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Redox Capacity ◽  
Scr Of No ◽  
Temperature Programmed

Nanosized V-Ce oxides supported on TiO2 (VCT) were prepared and utilized in the low-temperature selective catalytic reduction (SCR) of NO with NH3. Compared with the other V-Ce oxides-based catalysts supported on Al2O3, ZrO2, and ZSM-5, VCT showed the best SCR activity in a low-temperature range. The NOx conversion of 90% could be achieved at 220 °C. Characterizations including X-ray diffraction (XRD), scanning election micrograph (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), temperature-programmed desorption with NH3 (NH3-TPD), and temperature-programmed reduction with H2 (H2-TPR) showed that V1.05Ce1/TiO2 exhibited a good dispersion of V2O5, enrichment of surface Ce3+ and chemical-absorbed oxygen, and excellent redox capacity and acidity, which resulted in the best SCR performance at low temperature.

scholarly journals Precursor Effect on Mn-Fe-Ce/TiO2 Catalysts for Selective Catalytic Reduction of NO with NH3 at Low Temperatures

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 259
Author(s):  
Siva Sankar Reddy Putluru ◽  
Leonhard Schill ◽  
Anker Degn Jensen ◽  
Bernard Siret ◽  
Frank Tabaries ◽  
...  
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
Reduction Of No ◽  
X Ray ◽  
Nh3 Scr ◽  
Fast Scr ◽  
Oxide Phases ◽  
Temperature Programmed

Preparation of Mn/TiO2, Mn-Fe/TiO2, and Mn-Fe-Ce/TiO2 by the deposition-precipitation (DP) method can afford very active catalysts for low-temperature NH3-SCR (selective catalytic reduction of NO with NH3). The effect of precursor choice (nitrate vs. acetate) of Mn, Fe, and Ce on the physiochemical properties including thermal stability and the resulting SCR activity were investigated. The resulting materials were characterized by N2-Physisorption, XRD (Powder X-ray diffraction), XPS (X-ray photoelectron spectroscopy), H2-TPR (temperature-programmed reduction with hydrogen), and the oxidation of NO to NO2 measured at 300 °C. Among all the prepared catalysts 5MnAce/Ti, 25Mn0.75AceFe0.25Nit/Ti, and 25Mn0.75AceFe0.20NitCe0.05Ace/Ti showed superior SCR activity at low temperature. The superior activity of the latter two materials is likely attributable to the presence of amorphous active metal oxide phases (manganese-, iron- and cerium-oxide) and the ease of the reduction of metal oxides on TiO2. Enhanced ability to convert NO to NO2, which can promote fast-SCR like pathways, could be another reason. Cerium was found to stabilize amorphous manganese oxide phases when exposed to high temperatures.

Research of SO2 Resistance of MnOx Catalyst Modified by Ce for Low Temperature SCR with NH3

2011 ◽  
Vol 356-360 ◽  
pp. 529-532 ◽  
Author(s):  
Yan Wang ◽  
Liu Yang ◽  
Wei Ping Liao ◽  
Fei Wang
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Area Measurement ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Thermal Gravimetry ◽  
Surface Area Measurement ◽  
Low Temperature Scr

Two catalysts, MnOx and ceria modified MnOx were prepared by deposition-precipitation method and used for low-temperature selective catalytic reduction (SCR) with NH3in the presence of SO2. The catalysts were characterized by X-ray diffraction (XRD), surface area measurement (BET) and thermal gravimetry analysis(TG). The deactivation of MnOx and MnOx-CeO2by SO2was observed during SCR process. It was found that the resistance to SO2could be greatly enhanced for Ce modified MnOx. It was because that the formation of Mn(SO4)x was prevented and the depositions of (NH4)2SO4and NH4HSO4were significantly inhibited with the doping of ceria.

scholarly journals Preparation of Quasi-MIL-101(Cr) Loaded Ceria Catalysts for the Selective Catalytic Reduction of NOx at Low Temperature

Catalysts ◽  
2020 ◽  
Vol 10 (1) ◽  
pp. 140 ◽  
Author(s):  
Min Lu ◽  
Haili Hou ◽  
Chuanying Wei ◽  
Xiaohui Guan ◽  
Wei Wei ◽  
...  
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
Great Influence ◽  
X Ray ◽  
Nh3 Scr ◽  
Transmission Electron ◽  
Ir Transmission ◽  
Ceria Catalysts

At present, the development of novel catalysts with high activity Selective Catalytic Reduction (SCR) reaction at the low temperature is still a challenge. In this work, the authors prepare CeO2/quasi-MIL-101 catalysts with various amounts of deposited ceria by a double-solvent method, which are characterized by X-ray diffraction (XRD), Fourier Transform infrared spectroscopy (FT-IR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and so on. The results show that the increase of Ce content has a great influence on the catalytic property of the catalyst. The introduction of Ce can promote the conversion between Cr3+ and Cr5+ and increase the proportion of lattice oxygen, which improves the activity of the catalyst. However, the catalyst will be peroxidized when the content of Ce is too high, resulting in the decline of the catalytic activity. This experiment indicates that CeO2/quasi-MIL-101 plays a significant role in the NH3-SCR process at the low temperature when the loading of Ce is 0.5%. This work has proved the potential of this kind of material in NH3-SCR process at the low temperature, providing help for subsequent studies.

Selective catalytic reduction of NO by Co-Mn based nanocatalysts

2021 ◽  
Vol 0 (0) ◽  
Author(s):  
Vahid Zabihi ◽  
Mohammad Hasan Eikani ◽  
Mehdi Ardjmand ◽  
Seyed Mahdi Latifi ◽  
Alireza Salehirad
Keyword(s):  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Energy Dispersive ◽  
Diffraction Field ◽  
X Ray Diffraction ◽  
X Ray ◽  
Analysis Techniques ◽  
Acidic Sites ◽  
Temperature Window ◽  
Temperature Programmed

Abstract One of the most significant aspects in selective catalytic reduction (SCR) of nitrogen oxides (NOx) is developing suitable catalysts by which the process occurs in a favorable way. At the present work SCR reaction by ammonia (NH3-SCR) was conducted using Co-Mn spinel and its composite with Fe-Mn spinel, as nanocatalysts. The nanocatalysts were fabricated through liquid routes and then their physicochemical properties such as phase composition, degree of agglomeration, particle size distribution, specific surface area and also surface acidic sites have been investigated by X-ray diffraction, Field Emission Scanning Electron Microscope, Energy-dispersive X-ray spectroscopy, energy dispersive spectroscopy mapping, Brunauer–Emmett–Teller, temperature-programmed reduction (H2-TPR) and temperature-programmed desorption of ammonia (NH3-TPD) analysis techniques. The catalytic activity tests in a temperature window of 150–400 °C and gas hourly space velocities of 10,000, 18,000 and 30,000 h−1 revealed that almost in all studied conditions, CoMn2O4/FeMn2O4 nanocomposite exhibited better performance in SCR reaction than CoMn2O4 spinel.

scholarly journals Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Solid Solutions ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation ◽  
Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

Vanadium-doped titania-pillared montmorillonite clay as a catalyst for selective catalytic reduction of NO by ammonia

Clay Minerals ◽  
1997 ◽  
Vol 32 (4) ◽  
pp. 665-672 ◽  
Author(s):  
K. Bahranowski ◽  
J. Janas ◽  
T. Machej ◽  
E. M. Serwicka ◽  
L. A. Vartikian
Keyword(s):  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Catalytic Performance ◽  
Pillared Clay ◽  
Area Measurement ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
Reduction Of No ◽  
Pillared Montmorillonite ◽  
Doped Titania

AbstractA series of V-doped titania-pillared clay catalysts, characterized by ICP-AES chemical analysis, X-ray diffraction, BET surface area measurement, and ESR spectroscopy, have been tested in the selective catalytic reduction of NO by NH3. An ESR analysis shows that V dopant is anchored to the titania pillars. Vanadyl species with differing degrees of in-plane V-O π-covalent bonding are produced depending on the method of sample preparation. Polymeric V species appear as the V content is increased. Catalytic performance of these systems depends on the method of preparation and on the V content. The best catalyst, converting 90-100% NO in the temperature range 523-623 K, is obtained by exchange of pillared montmorillonite with vanadyl ions, at an extent of exchange below the level where significant amounts of polymeric V species appear. The co-pillared catalyst, containing vanadyl centres characterized by a higher degree of in-plane ncovalent bonding (according to ESR), is less selective than the exchanged samples.

scholarly journals Microwave-assisted preparation of ZnS and ZnSe nanocrystals with different morphologies for photodegradation process of organic dyes

2019 ◽  
Author(s):  
Katarzyna Matras-Postolek ◽  
A. Zaba ◽  
S. Sovinska ◽  
D. Bogdal
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Organic Dyes ◽  
Zinc Sulphide ◽  
Conventional Heating ◽  
Bet Surface Area ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Vis Spectroscopy

Zinc sulphide (ZnS) and zinc selenide (ZnSe) and manganese-doped and un-doped with different morphologies from 1D do 3D microflowers were successfully fabricated in only a few minutes by solvothermal reactions under microwave irradiation. In order to compare the effect of microwave heating on the properties of obtained  nanocrystals, additionally the synthesis under conventional heating was conducted additionally in similar conditions. The obtained nanocrystals were systematically characterized in terms of structural and optical properties using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), diffuse reflectance UV-Vis spectroscopy (DR UV-Vis), Fourier-transform infrared spectroscopy (FT-IR), photoluminescence spectroscopy (PL), X-ray photoelectron spectroscopy (XPS) and Brunauer-Emmett-Teller (BET) surface area analysis. The photocatalytic activity of ZnSe, ZnS, ZnS:Mn and ZnSe:Mn nanocrystals with different morphologies was evaluated by the degradation of methyl orange (MO) and Rhodamine 6G (R6G), respectively. The results show that Mn doped NCs samples had higher coefficient of degradation of organic dyes under ultraviolet irradiation (UV).

scholarly journals Mechanism and Performance of the SCR of NO with NH3 over Sulfated Sintered Ore Catalyst

Catalysts ◽  
2019 ◽  
Vol 9 (1) ◽  
pp. 90 ◽  
Author(s):  
Wangsheng Chen ◽  
Fali Hu ◽  
Linbo Qin ◽  
Jun Han ◽  
Bo Zhao ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
Nox Reduction ◽  
Space Velocity ◽  
Acid Sites ◽  
X Ray Diffraction ◽  
X Ray ◽  
Diffuse Reflectance Infrared Spectroscopy ◽  
And Performance ◽  
Diffuse Reflectance Infrared

A sulfated sintered ore catalyst (SSOC) was prepared to improve the denitration performance of the sintered ore catalyst (SOC). The catalysts were characterized by X-ray Fluorescence Spectrometry (XRF), Brunauer–Emmett–Teller (BET) analyzer, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance infrared spectroscopy (DRIFTS) to understand the NH3-selective catalytic reduction (SCR) reaction mechanism. Moreover, the denitration performance and stability of SSOC were also investigated. The experimental results indicated that there were more Brønsted acid sites at the surface of SSOC after the treatment by sulfuric acid, which lead to the enhancement of the adsorption capacity of NH3 and NO. Meanwhile, Lewis acid sites were also observed at the SSOC surface. The reaction between −NH2, NH 4 + and NO (E-R mechanism) and the reaction of the coordinated ammonia with the adsorbed NO2 (L-H mechanism) were attributed to NOx reduction. The maximum denitration efficiency over the SSOC, which was about 92%, occurred at 300 °C, with a 1.0 NH3/NO ratio, and 5000 h−1 gas hourly space velocity (GHSV).

Coating Iron Oxides on Kaolinite for the Adsorption of Fluoride

2012 ◽  
Vol 479-481 ◽  
pp. 250-254
Author(s):  
Wen Jun Xiang
Keyword(s):  
Iron Oxides ◽  
Freundlich Isotherm ◽  
Zero Point ◽  
Bet Surface Area ◽  
Maximum Adsorption Capacity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Fluoride Adsorption ◽  
Adsorption Data ◽  
Co Precipitation

Iron oxides-coated kaolinite (Fe-Kaolinite) was prepared by co-precipitation and indentified using X-ray diffraction (XRD). Moreover, the surface properties and fluoride adsorption characteristics of Fe-Kaolinite were investigated and compared with those of kaolinite. Compared to kaolinite, the BET surface area and surface fractal dimension of Fe-Kaolinite increased significantly. The pH at zero point of charge (pHZPC) of kaolinite and Fe-Kaolinite was 3.16 and 6.24, respectively. In the suspensions of pH 6.0, the fitted maximum adsorption capacity (qmax) for fluoride of kaolinite and Fe-Kaolinite was 1.32 and 5.86 mg/g, respectively. The adsorption data for fluoride by Fe-Kaolinite could be fitted using Freundlich isotherm (R2 =0.987), and Langmuir isotherm was very suitable for describing the fluoride adsorption of kaolinite (R2 =0.991).

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