Low Temperature CO Oxidation over Cobalt Catalysts Supported on Mesoporous CeO2

2013 ◽  
Vol 643 ◽  
pp. 76-82 ◽  
Author(s):  
Jun Jie Tian ◽  
Wei Na ◽  
Hua Wang ◽  
Wen Gui Gao
Keyword(s):  
Crystal Structure ◽  
Co Oxidation ◽  
Mesoporous Structure ◽  
Cobalt Catalysts ◽  
Precipitation Method ◽  
Molar Ratio ◽  
N2 Adsorption ◽  
Adsorption And Desorption ◽  
Low Temperature Co Oxidation ◽  
Temperature Programmed

Mesoporous CeO2 was first synthesized by hydrothermal method, and then used to synthesize different content of (Co3O4)x/CeO2 (x was the molar ratio of Cu and Co) by deposition-precipitation method. The fresh and doped catalysts were characterized by X-ray diffraction (XRD), N2 adsorption and desorption, H2 temperature programmed reduction (H2-TPR) and O2 temperature programmed desorption (O2-TPD) to study the crystal structure, surface area, and the mechanism of CO oxidation. The results show that: In XRD pattems, the doped cobalt amounts of samples from x=20% to x=100% have Co3O4 crystal structure. The N2 adsorption and desorption indicated the samples were mesoporous structure. Compared with other samples, the better reducibility and activity oxygen species of (Co3O4)50%/CeO2 coincided with its better catalytic activity.

Effect of TiO2 crystal structure on the catalytic performance of Co3O4/TiO2 catalyst for low-temperature CO oxidation

2014 ◽  
Vol 4 (5) ◽  
pp. 1268-1275 ◽  
Author(s):  
Jie Li ◽  
Guanzhong Lu ◽  
Guisheng Wu ◽  
Dongsen Mao ◽  
Yanglong Guo ◽  
...  
Keyword(s):  
Crystal Structure ◽  
Low Temperature ◽  
Co Oxidation ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Tio2 Catalyst ◽  
Excellent Activity ◽  
Low Temperature Co Oxidation

Co3O4 supported on TiO2 (anatase (A), rutile (R) and P25 (Degussa)) catalysts were prepared by a deposition–precipitation method. Co3O4/TiO2 (A) shows excellent activity for CO oxidation with 100% conversion at −43 °C.

scholarly journals Nanosheet-Like Ho2O3 and Sr-Ho2O3 Catalysts for Oxidative Coupling of Methane

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 388
Author(s):  
Yuqiao Fan ◽  
Changxi Miao ◽  
Yinghong Yue ◽  
Weiming Hua ◽  
Zi Gao
Keyword(s):  
Oxidative Coupling ◽  
Temperature Programmed Desorption ◽  
Oxidative Coupling Of Methane ◽  
Molar Ratio ◽  
Impregnation Method ◽  
Oxygen Species ◽  
N2 Adsorption ◽  
Basic Sites ◽  
Chemisorbed Oxygen ◽  
Temperature Programmed

In this work, Ho2O3 nanosheets were synthesized by a hydrothermal method. A series of Sr-modified Ho2O3 nanosheets (Sr-Ho2O3-NS) with a Sr/Ho molar ratio between 0.02 and 0.06 were prepared via an impregnation method. These catalysts were characterized by several techniques such as XRD, N2 adsorption, SEM, TEM, XPS, O2-TPD (temperature-programmed desorption), and CO2-TPD, and they were studied with respect to their performances in the oxidative coupling of methane (OCM). In contrast to Ho2O3 nanoparticles, Ho2O3 nanosheets display greater CH4 conversion and C2-C3 selectivity, which could be related to the preferentially exposed (222) facet on the surface of the latter catalyst. The incorporation of small amounts of Sr into Ho2O3 nanosheets leads to a higher ratio of (O− + O2−)/O2− as well as an enhanced amount of chemisorbed oxygen species and moderate basic sites, which in turn improves the OCM performance. The optimal catalytic behavior is achievable on the 0.04Sr-Ho2O3-NS catalyst with a Sr/Ho molar ratio of 0.04, which gives a 24.0% conversion of CH4 with 56.7% selectivity to C2-C3 at 650 °C. The C2-C3 yield is well correlated with the amount of moderate basic sites present on the catalysts.

Positive effects of a halloysite-supported Cu/Co catalyst fabricated by a urea-driven deposition precipitation method on the CO-SCR reaction and SO2 poisoning

2021 ◽  
Author(s):  
Wei-Jing Li ◽  
Shu Tsai ◽  
Ming-Yen Wey
Keyword(s):  
Co Oxidation ◽  
Catalytic Reduction ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Halloysite Nanotube ◽  
Co Catalyst ◽  
Reduction Of No ◽  
Co Catalysts ◽  
Positive Effects ◽  
So2 Poisoning

Cu/Co catalysts were prepared on halloysite nanotube supports by a urea-driven deposition-precipitation method for CO oxidation and the selective catalytic reduction of NO (CO-SCR). First, the Cu/NH3 molar ratio was...

The Different Morphology of Co3O4 Catalysts and Application in the Abatement of Carbon Monoxide

2021 ◽  
Vol 21 (12) ◽  
pp. 6082-6087
Author(s):  
Chih-Wei Tang ◽  
Hsiang-Yu Shih ◽  
Ruei-Ci Wu ◽  
Chih-Chia Wang ◽  
Chen-Bin Wang
Keyword(s):  
Carbon Monoxide ◽  
Catalytic Activity ◽  
Co Oxidation ◽  
Nitrogen Adsorption ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Programmed ◽  
Adsorption Desorption

The increase of harmful carbon monoxide (CO) caused by incomplete combustion can affect human health even lead to suffocation. Therefore reducing the CO discharged by vehicles or factories is urgent to improve the air quality. The spinel cobalt (II, III) oxide (Co3O4) is an active catalyst for CO abatement. In this study, we tried to fabricate dispersing Co3O4 via the dispersion-precipitation method with acetic acid, formic acid, and oxalic acid as the chelating dispersants. Then, the asprepared samples were calcined at 300 ºC for 4 h to obtain active catalysts, and assigned as Co(A), Co(F) and Co(O) respectively, the amount of the dispersants used are labeled as I (0.12 mole), II (0.03 mole) and III (0.01 mole). For comparison, another CoAP sample was prepared via alkaliinduced precipitation and calcined at 300 ºC. All samples were characterized by X-ray diffraction (XRD), temperature-programmed reduction (TPR), scanning electron microscope (SEM), and nitrogen adsorption/desorption system, and the catalytic activity focused on the CO oxidation. The influence of chelating dispersant on the performance of abatement of CO was pursued in this study. Apparently, the results showed that the chelating dispersant can influence the catalytic activity of CO abatement. An optimized ratio of dispersant can improve the performance, while excess dispersant lessens the surface area and catalytic performance. The series of Co(O) samples can easily donate the active oxygen since the labile Co–O bonding and indicated the preferential performance than both Co(A) and Co(F) samples. The nanorod Co(O)-II showed preferential for CO oxidation, T50 and T90 approached 96 and 127 ºC, respectively. Also, the favorable durability of Co(O)-II sample maintains 95% conversion still for 50 h at 130 ºC and does not emerge deactivation.

Nanosized Pt-Co Catalysts for the Preferential CO Oxidation

2006 ◽  
Vol 6 (11) ◽  
pp. 3567-3571 ◽  
Author(s):  
Eun-Yong Ko ◽  
Eun Duck Park ◽  
Kyung Won Seo ◽  
Hyun Chul Lee ◽  
Doohwan Lee ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Co Oxidation ◽  
Peak Shift ◽  
Molar Ratio ◽  
High Catalytic Activity ◽  
Preferential Co Oxidation ◽  
X Ray ◽  
Co Catalysts ◽  
Transmission Electron ◽  
Temperature Programmed

The preferential CO oxidation in the presence of excess hydrogen was studied over Pt-Co/γ-Al2O3. CO chemisorption, X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive X-ray spectrometer (EDX) and temperature programmed reduction (TPR) were conducted to characterize active catalysts. The catalytic activity for CO oxidation and methanation at low temperatures increased with the amounts of cobalt in Pt-Co/γ-Al2O3. This accompanied the TPR peak shift to lower temperatures. The optimum molar ratio between Co and Pt was determined to be 10. The co-impregnated Pt-Co/γ-Al2O3 appeared to be superior to Pt/Co/γ-Al2O3 and Co/Pt/γ-Al2O3. The reductive pretreatment at high temperature such as 773 K increased the CO2 selectivity over a wide reaction temperature. The bimetallic phase of Pt-Co seems to give rise to high catalytic activity in selective oxidation of CO in H2-rich stream.

Synthesis and catalytic application of ceria nanoparticles and ceria-SiC composites

2009 ◽  
Vol 1217 ◽  
Author(s):  
Christian Schrage ◽  
Emanuel Kockrick ◽  
Stefan Kaskel
Keyword(s):  
Precipitation Method ◽  
Molar Ratio ◽  
Ceria Nanoparticles ◽  
Soot Combustion ◽  
Temperature Programmed Oxidation ◽  
Catalytic Application ◽  
Transmission Electron ◽  
Inverse Microemulsion ◽  
Temperature Programmed ◽  
Sic Composites

AbstractThe synthesis of ceria nanoparticles using an inverse microemulsion technique and precipitation method was investigated. Ceria nanoparticles were synthesized by adding diluted ammonia to a microemulsion consisting of n-heptane, Marlophen NP5 and cerium nitrate. The micelle and particle size were adjustable in the range of 5-12nm by varying the molar ratio of water to surfactant and analyzed by dynamic light scattering (DLS), small angle X-ray scattering (SAXS) and high-resolution transmission electron microscopy (HRTEM). After isolation through precipitation, the nanoparticles were subsequently treated at 100-600 °C. The catalytic activity of particles annealed at 400 and 600 °C were tested in soot combustion reactions and characterized by temperature-programmed oxidation (TPO) indicating a size-dependant activity. To prevent the nanoparticles from aggregation, the microemulsion technique was adopted to integrate the nanoparticles homogeneously into a mesoporous SiC matrix through the use of a preceramic polymer. The obtained composite material was also tested in soot combustion reactions.

Effect of Preparation Method on Ag Modified Ti-HMS Catalyst Structure and Catalytic Oxidative Desulfurization Performance

2017 ◽  
Vol 16 (3) ◽  
Author(s):  
Fang Wang ◽  
Guangjian Wang ◽  
Liancheng Bing ◽  
Yong Wang ◽  
Aixiu Tian ◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Molecular Sieves ◽  
Oxidative Desulfurization ◽  
Mesoporous Structure ◽  
Catalytic Performance ◽  
Mesoporous Molecular Sieves ◽  
Precipitation Method ◽  
Molar Ratio ◽  
Extraction Solvent ◽  
Catalytic Oxidative Desulfurization

AbstractAg modified mesoporous molecular sieves Ti-HMS were prepared by in-situ synthesis (Ag/Ti-HMS-I), deposition-precipitation method (Ag/Ti-HMS-D) and ultrasound-assisted impregnation methods (Ag/Ti-HMS-U), respectively. The catalytic performance of catalysts in the oxidative desulfurization(ODS) of benzothiophene with hydrogen peroxide (H2O2) has been investigated. The physicochemical properties of the catalysts were characterized by XRD, SEM, BET and FT-IR techniques. Experimental results showed that the catalyst Ag/Ti-HMS-U exhibited the best catalytic activity, and this maybe because the catalyst possessed relatively good mesoporous structure and high Ag dispersion. Under the best operating condition for the catalytic oxidative desulfurization: temperature 60 °C, atmospheric pressure, 0.1 g catalysts, 8 molar ratio of hydrogen peroxide to sulfur, using acetonitrile as extraction solvent for double extraction, the sulfur content in model diesel fuel (MDF) was reduced from 800 ppm to 17 ppm with 97.8% of total sulfur after 1 h.

scholarly journals Catalytic oxidation of CO over CuO/CeO2 nanocomposites synthesized via solution combustion method: effect of fuels

2020 ◽  
Vol 59 (1) ◽  
pp. 131-143 ◽  
Author(s):  
Thanh Son Cam ◽  
Tatyana Alekseevna Vishnievskaia ◽  
Vadim Igorevich Popkov
Keyword(s):  
Low Temperature ◽  
Co Oxidation ◽  
Combustion Method ◽  
X Ray Diffraction ◽  
Solution Combustion ◽  
Solution Combustion Method ◽  
X Ray ◽  
Low Temperature Co Oxidation ◽  
Temperature Programmed ◽  
Adsorption Desorption

AbstractA series of CuO/CeO2 catalysts were successfully synthesized via solution combustion method (SCS) using different fuels and tested for CO oxidation. The catalysts were characterized by energy-dispersive X-ray analysis (EDXA), X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscope (SEM), N2 adsorption-desorption isotherms and H2 temperature-programmed reduction (H2-TPR). It was found that the used fuels strongly affected the characterization and the low-temperature reduction behavior of CuO/CeO2 catalysts. The CuO/CeO2-urea catalyst exhibited higher catalytic activity toward CO oxidation (t50=120∘C, t100=159∘C) than the 5 other synthesized catalysts. In addition, the CuO/CeO2-urea catalyst displayed high stability for CO oxidation during five cycles and water resistance. The enhanced catalytic CO oxidation of the synthesized samples can be attributed by a combination of factors, such as smaller crystallite size, higher specific surface area, larger amount of amorphous copper(II) oxide, more mesoporous and uniform spherical-like structure. These findings are worth considering in order to continue the study of the CuO/CeO2 catalyst with low-temperature CO oxidation.

scholarly journals Influence of Cr/Zr Ratio on Activity of Cr–Zr Oxide Catalysts in Non-Oxidative Propane Dehydrogenation

Crystals ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 1435
Author(s):  
Alexander Zubkov ◽  
Tatiana Bugrova ◽  
Mikhail Salaev ◽  
Grigory Mamontov
Keyword(s):  
Oxide Catalysts ◽  
Propane Dehydrogenation ◽  
Precipitation Method ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Mixed Oxide Catalysts ◽  
Uv Visible ◽  
Temperature Programmed ◽  
Co Precipitation ◽  
Adsorption Desorption

Two series of chromium–zirconium mixed oxide catalysts with different Cr/Zr molar ratio are prepared by co-precipitation method. Porous structure of the catalysts is studied by low-temperature N2 adsorption–desorption. Phase composition and chromium states in the catalysts are characterized by X-ray diffraction (XRD), UV-visible spectroscopy, and temperature-programmed reduction with hydrogen (TPR-H2). The mixed catalysts are tested in non-oxidative dehydrogenation of propane at 550 °C. The catalysts synthesized without ageing of precipitate show higher activity in propane dehydrogenation due to the higher content of reducible Cr+5/+6 species due to its stabilization on the ZrO2 surface.

Pd-Only Catalyst Modified by BaO with Co- Precipitation and Impregnation Methods towards the Methanol Fuel Emission Control

2012 ◽  
Vol 581-582 ◽  
pp. 313-316
Author(s):  
Xue Qiao Zhang ◽  
Zhi Xiang Ye ◽  
Cheng Hua Xu ◽  
Ming Zhao ◽  
Yao Qiang Chen
Keyword(s):  
Co Oxidation ◽  
Photoelectron Spectroscopy ◽  
Palladium Catalysts ◽  
Active Species ◽  
Precipitation Method ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Temperature Programmed ◽  
Co Precipitation

Barium oxide was introduced to modify Palladium catalysts supported on CeO2–ZrO2-La2O3-Al2O3 (CZLA) by impregnation and co-precipitation. methods. Various techniques, including X-ray diffraction (XRD), H2-temperature-programmed reduction (H2-TPR) and X-ray photoelectron spectroscopy (XPS), were employed to characterize the physicochemical properties of BaO-modified Pd-only catalyst. Catalytic activity for methanol, CO, C3H8 and NO conversions showed that BaO-modified catalyst prepared by impregnation method exhibited the best performance for methanol, C3H8 and NO removals, while the catalyst prepared by co-precipitation method was in favor of CO oxidation. Combined with the results of XRD, H2-TPR and XPS, it is concluded that the co-existence of PdO and Pd-O-Ce active species by impregnation played an important role in the methanol, C3H8 and NO removals, while the higher dispersion of palladium and improved reducibility were mostly favorable to the CO oxidation. The conversion of NO was co-effected by tow active species and the formation of Ba2AlLaO5 mixed oxide.

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