scholarly journals CO Oxidation over Metal Oxide (La2O3, Fe2O3, PrO2, Sm2O3, and MnO2) Doped CuO-Based Catalysts Supported on Mesoporous Ce0.8Zr0.2O2 with Intensified Low-Temperature Activity

Catalysts ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 724 ◽  
Author(s):  
Yan Cui ◽  
Leilei Xu ◽  
Mindong Chen ◽  
Chufei Lv ◽  
Xinbo Lian ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Metal Oxide ◽  
Metal Oxides ◽  
Co Oxidation ◽  
Active Sites ◽  
Earth Metal ◽  
High Dispersion ◽  
Impregnation Method ◽  
X Ray

CuO-based catalysts are usually used for CO oxidation owing to their low cost and excellent catalytic activities. In this study, a series of metal oxide (La2O3, Fe2O3, PrO2, Sm2O3, and MnO2)-doped CuO-based catalysts with mesoporous Ce0.8Zr0.2O2 support were simply prepared by the incipient impregnation method and used directly as catalysts for CO catalytic oxidation. These mesoporous catalysts were systematically characterized by X-ray powder diffraction (XRD), N2 physisorption, transmission electron microscopy (TEM), energy-dispersed spectroscopy (EDS) mapping, X-ray photoelectron spectroscopy (XPS), and H2 temperature programmed reduction (H2-TPR). It was found that the CuO and the dopants were highly dispersed among the mesoporous framework via the incipient impregnation method, and the strong metal framework interaction had been formed. The effects of the types of the dopants and the loading amounts of the dopants on the low-temperature catalytic performances were carefully studied. It was concluded that doped transition metal oxides could regulate the oxygen mobility and reduction ability of catalysts, further improving the catalytic activity. It was also found that the high dispersion of rare earth metal oxides (PrO2, Sm2O3) was able to prevent the thermal sintering and aggregation of CuO-based catalysts during the process of calcination. In addition, their presence also evidently improved the reducibility and significantly reduced the particle size of the CuO active sites for CO oxidation. The results demonstrated that the 15CuO-3Fe2O3/M-Ce80Zr20 catalyst with 3 wt. % of Fe2O3 showed the best low-temperature catalytic activity toward CO oxidation. Overall, the present Fe2O3-doped CuO-based catalysts with mesoporous nanocrystalline Ce0.8Zr0.2O2 solid solution as support were considered a promising series of catalysts for low-temperature CO oxidation.

scholarly journals Catalytic activity of nanostructured Au: Scale effects versus bimetallic/bifunctional effects in low-temperature CO oxidation on nanoporous Au

2013 ◽  
Vol 4 ◽  
pp. 111-128 ◽  
Author(s):  
Lu-Cun Wang ◽  
Yi Zhong ◽  
Haijun Jin ◽  
Daniel Widmann ◽  
Jörg Weissmüller ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Co Oxidation ◽  
Surface Area ◽  
Photoelectron Spectroscopy ◽  
Scale Effects ◽  
Structural Parameters ◽  
Kinetic Measurements ◽  
X Ray ◽  
Low Temperature Co Oxidation

The catalytic properties of nanostructured Au and their physical origin were investigated by using the low-temperature CO oxidation as a test reaction. In order to distinguish between structural effects (structure–activity correlations) and bimetallic/bifunctional effects, unsupported nanoporous gold (NPG) samples prepared from different Au alloys (AuAg, AuCu) by selective leaching of a less noble metal (Ag, Cu) were employed, whose structure (surface area, ligament size) as well as their residual amount of the second metal were systematically varied by applying different potentials for dealloying. The structural and chemical properties before and after 1000 min reaction were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The catalytic behavior was evaluated by kinetic measurements in a conventional microreactor and by dynamic measurements in a temporal analysis of products (TAP) reactor. The data reveal a clear influence of the surface contents of residual Ag and Cu species on both O2 activation and catalytic activity, while correlations between activity and structural parameters such as surface area or ligament/crystallite size are less evident. Consequences for the mechanistic understanding and the role of the nanostructure in these NPG catalysts are discussed.

scholarly journals Sulfur resistance of Ce-Mn/TiO 2 catalysts for low-temperature NH 3 –SCR

2018 ◽  
Vol 5 (3) ◽  
pp. 171846 ◽  
Author(s):  
Quan Xu ◽  
Wenjing Yang ◽  
Shitong Cui ◽  
Jason Street ◽  
Yan Luo
Keyword(s):  
Low Temperature ◽  
Photoelectron Spectroscopy ◽  
Conversion Rate ◽  
Active Sites ◽  
Sol Gel ◽  
Textural Properties ◽  
Catalyst Loading ◽  
Impregnation Method ◽  
No Conversion ◽  
X Ray

Ce-Mn/TiO 2 catalyst prepared using a simple impregnation method demonstrated a better low-temperature selective catalytic reduction of NO with NH 3 (NH 3 –SCR) activity in comparison with the sol-gel method. The Ce-Mn/TiO 2 catalyst loading with 20% Ce had the best low-temperature activity and achieved a NO conversion rate higher than 90% at 140–260°C with a 99.7% NO conversion rate at 180°C. The Ce-Mn/TiO 2 catalyst only had a 6% NO conversion rate decrease after 100 ppm of SO 2 was added to the stream. When SO 2 was removed from the stream, the catalyst was able to recover completely. The crystal structure, morphology, textural properties and valence state of the metals involving the novel catalysts were investigated using X-ray diffraction, N 2 adsorption and desorption analysis, X-ray photoelectron spectroscopy, scanning electron microscopy and energy dispersive spectroscopy, respectively. The decrease of NH 3 –SCR performance in the presence of 100 ppm SO 2 was due to the decrease of the surface area, change of the pore structure, the decrease of Ce 4+ and Mn 4+ concentration and the formation of the sulfur phase chemicals which blocked the active sites and changed the valence status of the elements.

scholarly journals Effect of Ce Addition on Adsorption and Oxidation of NO over MnO x /Al2O3

2021 ◽  
Vol 2021 ◽  
pp. 1-8
Author(s):  
Chunhui Mou ◽  
Hui Li ◽  
Ning Dong ◽  
Shien Hui ◽  
Denghui Wang
Keyword(s):  
Catalytic Activity ◽  
Catalytic Oxidation ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Catalyst Surface ◽  
Fixed Bed ◽  
No Oxidation ◽  
Impregnation Method ◽  
X Ray ◽  
Oxidation Of No

The MnO x /Al2O3 catalysts with different Ce content doping were prepared by an ultrasonic impregnation method, and the catalytic activity for NO oxidation removal was tested in a fixed-bed quartz tube furnace. Simultaneously, the catalysts were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), full-automatic physical-chemical adsorption instrument, and field emission scanning electron microscope (FESEM) to analyze the effect of Ce addition on the adsorption capacity and catalytic activity. Experimental results validated that the activity of the MnO x /Al2O3 catalyst was greatly promoted with Ce addition. According to the characterization results, it could be concluded that Ce doping led to significant changes in the crystalline phase on the catalyst surface, which increased the relative content of surface lattice oxygen and promoted the catalytic oxidation of NO. By observing the physical properties of the surface and analyzing the surface elements of the catalyst, it could be inferred that a manganese-cerium solid solution was formed on the surface of Mn0.4Ce0.05/Al. Moreover, Ce addition increased the catalyst pore size, which enhanced the adsorption and contact of NO and O2 with the active sites on the catalyst surface, and reduced the resistance of the reactants during internal diffusion. All these variations assigned to Mn0.4Ce0.05/Al were favorable for the catalytic oxidation of NO.

Structural/Texture Evolution During Facile Substitution of Ni into ZSM-5 Nanostructure vs. its Impregnation Dispersion Used in Selective Transformation of Methanol to Ethylene and Propylene

2020 ◽  
Vol 23 ◽  
Author(s):  
Parisa Sadeghpour ◽  
Mohammad Haghighi ◽  
Mehrdad Esmaeili
Keyword(s):  
High Temperature ◽  
Physicochemical Properties ◽  
Active Sites ◽  
Catalytic Performance ◽  
Fixed Bed Reactor ◽  
Light Olefins ◽  
Isomorphous Substitution ◽  
Impregnation Method ◽  
Hydrothermal Temperature ◽  
X Ray

Aim and Objective: Effect of two different modification methods for introducing Ni into ZSM-5 framework was investigated under high temperature synthesis conditions. The nickel successfully introduced into the MFI structures at different crystallization conditions to enhance the physicochemical properties and catalytic performance. Materials and Methods: A series of impregnated Ni/ZSM-5 and isomorphous substituted NiZSM-5 nanostructure catalysts were prepared hydrothermally at different high temperatures and within short times. X-ray diffraction (XRD), Field emission scanning electron microscopy (FESEM), Energy dispersive X-ray (EDX), Brunner, Emmett and Teller-Barrett, Joyner and Halenda (BET-BJH), Fourier transform infrared (FTIR) and Temperature-programmed desorption of ammonia (TPDNH3) were applied to investigate the physicochemical properties. Results: Although all the catalysts showed pure silica MFI–type nanosheets and coffin-like morphology, using the isomorphous substitution for Ni incorporation into the ZSM-5 framework led to the formation of materials with lower crystallinity, higher pore volume and stronger acidity compared to using impregnation method. Moreover, it was found that raising the hydrothermal temperature increased the crystallinity and enhanced more uniform incorporation of Ni atoms in the crystalline structure of catalysts. TPD-NH3 analysis demonstrated that high crystallization temperature and short crystallization time of NiZSM-5(350-0.5) resulted in fewer weak acid sites and medium acid strength. The MTO catalytic performance was tested in a fixed bed reactor at 460ºC and GHSV=10500 cm3 /gcat.h. A slightly different reaction pathway was proposed for the production of light olefins over impregnated Ni/ZSM-5 catalysts based on the role of NiO species. The enhanced methanol conversion for isomorphous substituted NiZSM-5 catalysts could be related to the most accessible active sites located inside the pores. Conclusion: The impregnated Ni/ZSM-5 catalyst prepared at low hydrothermal temperature showed the best catalytic performance, while the isomorphous substituted NiZSM-5 prepared at high temperature was found to be the active molecular sieve regarding the stability performance.

scholarly journals CO Oxidation Efficiency and Hysteresis Behavior over Mesoporous Pd/SiO2 Catalyst

Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 131 ◽  
Author(s):  
Rola Mohammad Al Soubaihi ◽  
Khaled Mohammad Saoud ◽  
Myo Tay Zar Myint ◽  
Mats A. Göthelid ◽  
Joydeep Dutta
Keyword(s):  
Carbon Monoxide ◽  
Catalytic Activity ◽  
Co Oxidation ◽  
Active Sites ◽  
Bond Activation ◽  
Dissociative Adsorption ◽  
High Catalytic Activity ◽  
Good Catalytic Activity ◽  
Pretreatment Conditions ◽  
Oxidation Efficiency

Carbon monoxide (CO) oxidation is considered an important reaction in heterogeneous industrial catalysis and has been extensively studied. Pd supported on SiO2 aerogel catalysts exhibit good catalytic activity toward this reaction owing to their CO bond activation capability and thermal stability. Pd/SiO2 catalysts were investigated using carbon monoxide (CO) oxidation as a model reaction. The catalyst becomes active, and the conversion increases after the temperature reaches the ignition temperature (Tig). A normal hysteresis in carbon monoxide (CO) oxidation has been observed, where the catalysts continue to exhibit high catalytic activity (CO conversion remains at 100%) during the extinction even at temperatures lower than Tig. The catalyst was characterized using BET, TEM, XPS, TGA-DSC, and FTIR. In this work, the influence of pretreatment conditions and stability of the active sites on the catalytic activity and hysteresis is presented. The CO oxidation on the Pd/SiO2 catalyst has been attributed to the dissociative adsorption of molecular oxygen and the activation of the C-O bond, followed by diffusion of adsorbates at Tig to form CO2. Whereas, the hysteresis has been explained by the enhanced stability of the active site caused by thermal effects, pretreatment conditions, Pd-SiO2 support interaction, and PdO formation and decomposition.

Property of Cu2O-CuO/ZSM-5 nanocomposite and degradation process of azo dye AO7 without sacrificial agent (H2O2)

2016 ◽  
Vol 73 (11) ◽  
pp. 2747-2753 ◽  
Author(s):  
Wusong Kong ◽  
Hongxia Qu ◽  
Peng Chen ◽  
Weihua Ma ◽  
Huifang Xie
Keyword(s):  
Catalytic Activity ◽  
Aqueous Solutions ◽  
Photoelectron Spectroscopy ◽  
Oxygen Demand ◽  
Operating Conditions ◽  
Surface Element ◽  
Impregnation Method ◽  
X Ray ◽  
Initial Ph ◽  
Sacrificial Agent

In this study, Cu2O-CuO/ZSM-5 nanocomposite was synthesized by the impregnation method, and its catalytic performance for the destruction of AO7 in aqueous solutions was investigated. The morphology, structure and surface element valence state of Cu2O-CuO/ZSM-5 were characterized by transmission electron microscopy, X-ray diffraction and X-ray photoelectron spectroscopy. The operating conditions on the degradation of AO7 by Cu2O-CuO/ZSM-5, such as initial pH values, concentration of AO7 and catalyst dosage were investigated and optimized. The results showed that the sample had good catalytic activity for destruction of AO7 in the absence of a sacrificial agent (e.g. H2O2): it could degrade 91% AO7 in 140 min at 25 °C and was not restricted by the initial pH of the AO7 aqueous solutions. Cu2O-CuO/ZSM-5 exhibited stable catalytic activity with little loss after three successive runs. The total organic carbon and chemical oxygen demand removal efficiencies increased rapidly to 69.36% and 67.3% after 120 min of treatment by Cu2O-CuO/ZSM-5, respectively.

MOF-derived metal oxide composite Mn2Co1Ox/CN for efficient formaldehyde oxidation at low temperature

2019 ◽  
Vol 9 (20) ◽  
pp. 5845-5854 ◽  
Author(s):  
Xi Wang ◽  
Jiawei Ying ◽  
Yuliang Mai ◽  
Junjie Zhang ◽  
Jiazhi Chen ◽  
...  
Keyword(s):  
Catalytic Activity ◽  
Low Temperature ◽  
Metal Oxide ◽  
Low Temperature Oxidation ◽  
Carbon Catalyst ◽  
Temperature Oxidation ◽  
Oxide Composite ◽  
Formaldehyde Oxidation

A novel MOF-derived MnCoOx nanoparticles embedded in porous N-doped carbon catalyst exhibits excellent catalytic activity for the low-temperature oxidation of formaldehyde.

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