scholarly journals Selective Catalytic Reduction of NO with NH3 over Ce-W-Ti Oxide Catalysts Prepared by Solvent Combustion Method

2018 ◽  
Vol 8 (12) ◽  
pp. 2430 ◽  
Author(s):  
Xinbo Zhu ◽  
Yaolin Wang ◽  
Yu Huang ◽  
Yuxiang Cai
Keyword(s):  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Space Velocity ◽  
Combustion Method ◽  
Catalytic Performance ◽  
Solution Combustion ◽  
X Ray ◽  
Nh3 Scr ◽  
Scr Of No ◽  
Temperature Programmed

In this work, a series of Ce-W-Ti catalysts were synthesized using a solution combustion method for the selective catalytic reduction (SCR) of NO with NH3 at low temperatures. The reaction performance of NH3-SCR of NO was significantly improved over the Ce-W-Ti catalysts compared to Ce0.4Ti and W0.4Ti catalysts, while Ce0.2W0.2Ti showed the best activity among all the samples. The Ce0.2W0.2Ti catalyst exhibited over 90% removal of NO and 100% N2 selectivity in the temperature range of 250–400 °C at a gas hourly space velocity (GHSV) of 120,000 mL·g−1·h−1. The Ce-W-Ti catalysts were characterized using N2 adsorption-desorption, X-ray diffraction, X-ray photoelectron spectrometry and temperature programmed desorption of NH3 to establish the structure-activity relationships of the Ce-W-Ti catalysts. The excellent catalytic performance of the Ce0.2W0.2Ti catalyst could be associated with the larger specific surface area, highly dispersed Ce and W species, increased amount of surface adsorbed oxygen (Oads) and enhanced total acidity on the catalyst surfaces.

scholarly journals Novel Preparation of Cu and Fe Zirconia Supported Catalysts for Selective Catalytic Reduction of NO with NH3

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 55
Author(s):  
Katarzyna Świrk ◽  
Ye Wang ◽  
Changwei Hu ◽  
Li Li ◽  
Patrick Da Costa ◽  
...  
Keyword(s):  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Supported Catalysts ◽  
Catalytic Performance ◽  
Experimental Conditions ◽  
One Pot ◽  
Nh3 Scr ◽  
Scr Of No ◽  
Temperature Programmed ◽  
Stationary Sources

Copper and iron promoted ZrO2 catalysts were prepared by one-pot synthesis using urea. The studied catalysts were characterized by XRD, N2 physisorption, XPS, temperature-programmed desorption of NH3 (NH3-TPD), and tested by the selective catalytic reduction by ammonia (NH3-SCR) of NO in the absence and presence of water vapor, under the experimental conditions representative of exhaust gases from stationary sources. The influence of SO2 on catalytic performance was also investigated. Among the studied catalysts, the Fe-Zr sample showed the most promising results in NH3-SCR, being active and highly selective to N2. The addition of SO2 markedly improved NO and NH3 conversions during NH3-SCR in the presence of H2O. The improvement in acidic surface properties is believed to be the cause.

scholarly journals Effect of Organic Assistant on the Performance of Ceria-Based Catalysts for the Selective Catalytic Reduction of NO with Ammonia

Catalysts ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 357 ◽  
Author(s):  
Huang ◽  
Li ◽  
Qiu ◽  
Chen ◽  
Cheng ◽  
...  
Keyword(s):  
Selective Catalytic Reduction ◽  
Ball Milling ◽  
Catalytic Reduction ◽  
Temperature Programmed Desorption ◽  
Milling Process ◽  
X Ray ◽  
Ball Milling Process ◽  
Nh3 Scr ◽  
Temperature Programmed ◽  
Catalytic Performances

In the present study, a series of CeO2/TiO2 catalysts were fabricated by dry ball milling method in the absence and presence of organic assistants, and their catalytic performances for the selective catalytic reduction (SCR) of NO by NH3 were investigated. It was found that the addition of organic assistants in the ball milling process and the calcining ambience exerted a significant influence on the catalytic performances of CeO2/TiO2 catalysts. The nitrogen sorption isotherm measurement (BET), powder X-ray diffraction (XRD), Raman spectra, high-resolution transmission electron microscopy (HR-TEM), hydrogen temperature-programmed reduction (H2-TPR), ammonia temperature-programmed desorption (NH3-TPD), sulfur dioxide temperature-programmed desorption (SO2-TPD), thermogravimetric analysis (TG), Fourier transform infrared (FT-IR) and X-ray photoelectron spectra (XPS) characterizations showed that the introduction of citric acid in the ball milling process could significantly change the decomposition process of the precursor mixture, which can lead to improved dispersion and reducibility of cerium species, surface acidity as well as the surface microstructure, all which were responsible for the high low temperature activity of CeTi-C-N in an NH3-SCR reaction. In contrast, the addition of sucrose in the milling process showed an inhibitory effect on the catalytic performance of CeO2/TiO2 catalyst in an NH3-SCR reaction, possibly due to the decrease of the crystallinity of the TiO2 support and the carbon residue covering the active sites.

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.

Effect of the Addition of In to Co/HMCM-49 Catalyst for the Selective Catalytic Reduction of NO Under Lean-burn Conditions

2010 ◽  
Vol 224 (06) ◽  
pp. 907-920 ◽  
Author(s):  
Fei Li ◽  
Dehai Xiao ◽  
Jing Li ◽  
Xiangguang Yang
Keyword(s):  
Selective Catalytic Reduction ◽  
Wide Temperature Range ◽  
Catalytic Reduction ◽  
Temperature Programmed Desorption ◽  
X Ray Diffraction ◽  
Lean Burn ◽  
Reduction Of No ◽  
X Ray ◽  
Scr Of No ◽  
Temperature Programmed

AbstractSelective catalytic reduction (SCR) of NO with propane using bimetals (3Co2Ce, 3Co2Sr, 3Co2Sn and 3Co2In) loaded on HMCM-49 zeolite was studied under lean-burn condition. Only 3Co2In/HMCM-49 exhibited higher deNOx activity in a wide temperature range. The catalysts were characterized by N2-adsoption, X-ray diffraction (XRD), temperature-programmed surface reactions (TPSR) and temperature-programmed desorption (TPD) of NO. TPSR and TPD results exhibited that the addition of In inhibited the oxidation ability of Co on 3Co2In/HMCM-49 catalyst, but enhanced NOx adsorption.

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.

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.

Time-resolved in situ DRIFTS study on NH3–SCR of NO on CeO2/TiO2 catalyst

2022 ◽  
Author(s):  
Jie Yang ◽  
Shan Ren ◽  
Mingming Wang ◽  
Zhicaho Chen ◽  
Lin Chen ◽  
...  
Keyword(s):  
Nitrogen Oxides ◽  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Time Resolved ◽  
In Situ Drifts ◽  
Tio2 Catalyst ◽  
Nh3 Scr ◽  
Scr Of No

Ce–Ti catalysts were considered as promising replacement for V–Ti based catalysts for selective catalytic reduction (SCR) of nitrogen oxides (NO and NO2) with NH3. In this work, CeO2/TiO2 catalyst was...

Novel Fe–Ce–Ti catalyst with remarkable performance for the selective catalytic reduction of NOx by NH3

2016 ◽  
Vol 6 (17) ◽  
pp. 6688-6696 ◽  
Author(s):  
Zhiming Liu ◽  
Yuxian Liu ◽  
Biaohua Chen ◽  
Tianle Zhu ◽  
Lingling Ma
Keyword(s):  
Selective Catalytic Reduction ◽  
Catalytic Reduction ◽  
Catalytic Performance ◽  
Redox Cycle ◽  
Reaction Intermediates ◽  
Scr Of No ◽  
Reduction Of Nox

The redox cycle (Ce4+ + Fe2+ ↔ Ce3+ + Fe3+) over the Fe–Ce–Ti catalyst contributes to the activation of NOx and NH3 and thus the formation of reaction intermediates, leading to the high catalytic performance for the NH3-SCR of NOx.

scholarly journals A CeO2/ZrO2-TiO2 Catalyst for the Selective Catalytic Reduction of NOx with NH3

Catalysts ◽  
2018 ◽  
Vol 8 (12) ◽  
pp. 592 ◽  
Author(s):  
Wenpo Shan ◽  
Yang Geng ◽  
Yan Zhang ◽  
Zhihua Lian ◽  
Hong He
Keyword(s):  
Selective Catalytic Reduction ◽  
Ph Value ◽  
Catalytic Reduction ◽  
Space Velocity ◽  
Catalytic Performance ◽  
Excellent Activity ◽  
Reduction Of Nox ◽  
High Space ◽  
Catalytic Performances ◽  
High Space Velocity

In this study, CeZr0.5TiaOx (with a = 0, 1, 2, 5, 10) catalysts were prepared by a stepwise precipitation approach for the selective catalytic reduction of NOx with NH3. When Ti was added, all of the Ce-Zr-Ti oxide catalysts showed much better catalytic performances than the CeZr0.5Ox. Particularly, the CeZr0.5Ti2Ox catalyst showed excellent activity for broad temperature range under high space velocity condition. Through the control of pH value and precipitation time during preparation, the function of the CeZr0.5Ti2Ox catalyst could be controlled and the structure with highly dispersed CeO2 (with redox functions) on the surface of ZrO2-TiO2 (with acidic functions) could be obtained. Characterizations revealed that the superior catalytic performance of the catalyst is associated with its outstanding redox properties and adsorption/activation functions for the reactants.

Studies on the Preparation and DeNOx Performance of MnxOy/CNTs Catalyst for Low-Temperature Selective Catalytic Reduction

2013 ◽  
Vol 798-799 ◽  
pp. 231-234 ◽  
Author(s):  
Bing Nan Ren ◽  
Qiao Wen Yang
Keyword(s):  
Low Temperature ◽  
Selective Catalytic Reduction ◽  
Oxide Catalyst ◽  
Catalytic Reduction ◽  
Space Velocity ◽  
Impregnation Method ◽  
Active Components ◽  
Reaction Conditions ◽  
No Conversion ◽  
Scr Of No

The metal oxide catalyst was prepared by loading MnxOyon carbon nanotubes (CNTs) with impregnation method. Then the catalyst was characterized by BET, TEM and XPS, and the catalytic activity of the catalyst for selective catalytic reduction (SCR) of NO at low-temperature was investigated. The results showed that the species of active components loaded on the catalyst were MnO2and Mn2O3. The NO conversion was improved with reduction temperature increase under 250°C, increased slowly over 250°C. The O2content had an outstanding effect on NO conversion of catalysts at a low concentration range. Once the oxygen content was enhanced over 5%, there was no significant increase in the NO conversion. With the increasing of space velocity, the NO conversion rate was decreased under the reaction conditions.

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