scholarly journals Purification of fuel ethanol engine exhaust with platinum-loaded Ce0.5Zr0.5O2 catalyst

2019 ◽  
Vol 9 ◽  
pp. 184798041988667
Author(s):  
Fei Zhao ◽  
Chunyu Wang ◽  
Xianjing Liu ◽  
Qingyue Luo ◽  
Ling Zhu
Keyword(s):  
Catalytic Performance ◽  
Fuel Ethanol ◽  
Photoelectron Spectra ◽  
Exhaust Gas ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Engine Exhaust ◽  
X Ray ◽  
Temperature Programmed ◽  
Three Way Catalyst

This work aimed at exploring a new kind of purification catalysts for fuel ethanol engine exhaust. Platinum loaded on Ce0.5Zr0.5O2 was prepared by impregnation method and characterized by X-ray diffraction, Brunner–Emmet–Teller measurements (BET), temperature-programmed reduction of hydrogen, scanning electron microscope, and X-ray photoelectron spectra. The three-way catalyst platinum/ceria–zirconia/fw is prepared with the paste ball mill coating technique. And the catalytic performance is evaluated under simulated fuel ethanol engine exhaust gas condition. The catalysts not only show excellent low-temperature performances and several-way catalytic activities for carbon monoxide, hydrocarbons, nitrogen oxides, and acetaldehyde but also have better high-temperature resistance. The addition of sulfur dioxide to feedstream degrades the performances of the catalysts.

scholarly journals Applicability of V2O5-WO3/TiO2 Catalysts for the SCR Denitrification of Alumina Calcining Flue Gas

Catalysts ◽  
2019 ◽  
Vol 9 (3) ◽  
pp. 220 ◽  
Author(s):  
Ruliang Ning ◽  
Li Chen ◽  
Erwei Li ◽  
Xiaolong Liu ◽  
Tingyu Zhu
Keyword(s):  
Flue Gas ◽  
Photoelectron Spectroscopy ◽  
Catalytic Performance ◽  
Inhibitory Effect ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
So2 Resistance ◽  
Temperature Programmed ◽  
Diffuse Reflectance Infrared

V2O5-WO3/TiO2 catalysts with different V2O5 and WO3 loadings were prepared by the impregnation method. H2O and SO2 resistance of the catalysts under high H2O concentration (30 vol.%) was studied. Influence of various basic metal oxides, such as Al2O3, CaO, Na2O, and K2O on the catalytic performance was studied and compared. It is revealed that the inhibitory effect is in the sequence of K > Na > Ca > Al, which is consistent with their alkalinity. X-ray diffraction (XRD), N2 physisorption (BET), temperature-programmed desorption of NH3 (NH3-TPD), H2-temperature programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) were carried out, and the results were well-correlated with the catalytic studies.

scholarly journals Influence of Sulfur-Containing Sodium Salt Poisoned V2O5–WO3/TiO2 Catalysts on SO2–SO3 Conversion and NO Removal

Catalysts ◽  
2018 ◽  
Vol 8 (11) ◽  
pp. 541 ◽  
Author(s):  
Haiping Xiao ◽  
Chaozong Dou ◽  
Hao Shi ◽  
Jinlin Ge ◽  
Li Cai
Keyword(s):  
Photoelectron Spectroscopy ◽  
No Reduction ◽  
Catalytic Performance ◽  
Acid Sites ◽  
Impregnation Method ◽  
So2 Oxidation ◽  
Sodium Salts ◽  
X Ray ◽  
Temperature Programmed ◽  
Physical Features

A series of poisoned catalysts with various forms and contents of sodium salts (Na2SO4 and Na2S2O7) were prepared using the wet impregnation method. The influence of sodium salts poisoned catalysts on SO2 oxidation and NO reduction was investigated. The chemical and physical features of the catalysts were characterized via NH3-temperature programmed desorption (NH3-TPD), H2-temperature programmed reduction (H2-TPR), X-ray photoelectron spectroscopy (XPS), Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), and Fourier Transform Infrared Spectroscopy (FT-IR). The results showed that sodium salts poisoned catalysts led to a decrease in the denitration efficiency. The 3.6% Na2SO4 poisoned catalyst was the most severely deactivated with denitration efficiency of only 50.97% at 350 °C. The introduction of SO42− and S2O72− created new Brønsted acid sites, which facilitated the adsorption of NH3 and NO reduction. The sodium salts poisoned catalysts significantly increased the conversion of SO2–SO3. 3.6%Na2S2O7 poisoned catalyst had the strongest effect on SO2 oxidation and the catalyst achieved a maximum SO2–SO3-conversion of 1.44% at 410 °C. Characterization results showed sodium salts poisoned catalysts consumed the active ingredient and lowered the V4+/V5+ ratio, which suppressed catalytic performance. However, they increased the content of chemically adsorbed oxygen and the strength of V5+=O bonds, which promoted SO2 oxidation.

scholarly journals Generalized Methodology for Inserting Metal Heteroatoms into the Layered Zeolite Precursor RUB-36 by Interlayer Expansion

Crystals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 530 ◽  
Author(s):  
Chaoqun Bian ◽  
Xiao Wang ◽  
Lan Yu ◽  
Fen Zhang ◽  
Jie Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
Zeolite Sample ◽  
X Ray ◽  
Inductively Coupled ◽  
Temperature Programmed ◽  
First Time ◽  
N2 Sorption

The incorporation of metal heteroatoms into zeolites is an effective modification strategy for enhancing their catalytic performance. Herein, for the first time we report a generalized methodology for inserting metal heteroatoms (such as Sn, Fe, Zn, and Co) into the layered zeolite precursor RUB-36 via interlayer expansion by using the corresponding metal acetylacetate salt. Through this generalized methodology, Sn-JHP-1, Fe-JHP-1, Zn-JHP-1 and Co-JHP-1 zeolites could be successfully prepared by the reaction of RUB-36 and corresponding metal acetylacetate salt at 180 °C for 24 h in the presence of HCl solution. As a typical example, Sn-JHP-1 and calcined Sn-JHP-1 (Sn-JHP-2) zeolite is well characterized by the X-ray diffraction (XRD), diffuse reflectance ultraviolet-visible (UV-Vis), inductively coupled plasma (ICP), N2 sorption, temperature-programmed-desorption of ammonia (NH3-TPD) and X-ray photoelectron spectroscopy (XPS) techniques, which confirm the expansion of adjacent interlayers and thus the incorporation of isolated Sn sites within the zeolite structure. Notably, the obtained Sn-JHP-2 zeolite sample shows enhanced catalytic performance in the conversion of glucose to levulinic acid (LA) reaction.

Preparation and Catalytic Performance of Ti(SO4)2/γ-Al2O3 Catalysts for Oligomerization of 1-Butene

2013 ◽  
Vol 634-638 ◽  
pp. 696-700
Author(s):  
Lin Jiu Xiao ◽  
Peng Li ◽  
Yong Gang Sheng
Keyword(s):  
Heat Treatment ◽  
Physicochemical Properties ◽  
Heat Treatment Temperature ◽  
Catalytic Performance ◽  
Treatment Temperature ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Isothermal Adsorption ◽  
X Ray ◽  
Adsorption Desorption

A series of Ti(SO4)2/γ-Al2O3 catalysts were prepared by impregnation method and the catalytic performance of these catalysts in 1-butene oligomerization was investigated. The heat treatment temperature played great influences on the catalytic performance of these catalysts in the oligomerization. 90.1 wt.% conversion of 1-butene and 92.2 wt.% selectivity of dimers were obtained on Ti(SO4)2/γ-Al2O3(450) catalyst at 80 °C, 1.0 Mpa and LHSV=0.6 h−1. The heat treatment temperature determined the crystallinity of TiOSO4 and specific surface area of these catalysts, which affected the catalytic performance of these catalysts in 1-butene oligomerization. In addition, the physicochemical properties of these catalysts were comparatively characterized by powder X-ray diffraction (XRD), N2 isothermal adsorption-desorption techniques.

Preparation and Characterization of Cu Loaded TiO2 Nanotube Arrays and their Photocatalytic Activity

2011 ◽  
Vol 364 ◽  
pp. 377-381 ◽  
Author(s):  
Syazwani Mohd Zaki ◽  
Srimala Sreekantan
Keyword(s):  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Anatase Phase ◽  
Average Diameter ◽  
Photoelectron Spectra ◽  
Nanotube Arrays ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Wet Impregnation ◽  
X Ray

This paper described the preparation of Cu loaded TiO₂ nanotube arrays. Firstly, TiO₂ nanotube arrays were formed by anodization. Afterwards, the formed nanotube arrays were incorporated with Cu by wet impregnation method. The soaking time and concentration were varied to obtain an optimum set of parameter for Cu incorporation in TiO₂ nanotubes. After anodization, all samples were annealed at 400°C for 4 hours to obtain anatase phase. The nanotube arrays were characterized by field emission scanning electron microscopy (FESEM), x-ray diffraction (XRD) and x-ray photoelectron spectra (XPS). An average diameter 63.02 nm and length 12.15µm were obtained for TiO₂ nanotubes. The photocatalytic activity of these nanotubes were investigated with methyl orange (MO) and the TiO₂ nanotube prepared in 0.01M of Cu (NO₃)₂ solution within 3 hours demonstrates the highest photocatalytic activity with 83.6% degradation of methyl orange. Keywords: copper doping, wet impregnation, photocatalytic activity

Catalytic Activity of Bimetallic Cu-Ag/MgO-SiO2 Toward the Conversion of Ethanol to 1,3-Butadiene

2016 ◽  
Vol 14 (5) ◽  
pp. 945-954 ◽  
Author(s):  
Anamol Tripathi ◽  
Kajornsak Faungnawakij ◽  
Apirat Laobuthee ◽  
Suttichai Assabumrungrat ◽  
Navadol Laosiripojna
Keyword(s):  
Chemical Properties ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Monometallic Catalysts ◽  
Reaction Test ◽  
Spent Catalysts ◽  
Temperature Programmed ◽  
Preparation Techniques ◽  
Microwave Assisted Method

Abstract In the present work, the catalytic conversion of ethanol to 1,3-butadiene (1,3-BD) was studied over monometallic of Cu and Ag, and bimetallic Cu-Ag supported on MgO-SiO2 (with MgO/SiO2 ratio of 2.0) under the temperature range from 250 to 325 °C. All catalysts were prepared by 4 different techniques including (i) conventional impregnation, (ii) microwave-assisted method, (iii) polyvinyl alcohol/sodium borohydride (PVA/NaBH4) assisted method, and (iv) benzoxaxine-assisted method to elucidate the effect of catalyst preparation method on their catalytic performance. All fresh and spent catalysts were also characterized by X-ray diffraction (XRD), N2 adsorption and Temperature-programmed reduction (TPR) techniques to understand the relation between their physical/chemical properties and catalytic performance. From the reaction test, it was found that 5 %Ag/MgO-SiO2 showed greater activity towards 1,3-BD production than 5 %Cu/MgO-SiO2; nevertheless, higher deactivation after 6 h of operation was observed from 5 %Ag/MgO-SiO2. Importantly, this study revealed that bimetallic 2.5 %Cu-2.5 %Ag/MgO-SiO2 enhanced significantly higher activity and stability towards the reaction than monometallic catalysts. In addition, 2.5 %Cu-2.5 %Ag/MgO-SiO2 prepared by benzoxaxine-assisted method enhanced significantly higher reaction activity and stability than other preparation techniques, from which 1,3-BD yield of 46.40 % after 6 h of operation can be achieved. From the characterization, the good activity of this catalyst is mainly due to the dispersion improvement of metal over MgO-SiO2 support.

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.

Preparation and Ultra-Deep Hydrorefining Performance of Ni-P/Al2O3-ZrO2 Catalysts

2011 ◽  
Vol 236-238 ◽  
pp. 724-727
Author(s):  
Feng Li ◽  
Hua Song ◽  
Hua Yang Zhang
Keyword(s):  
Chemical Precipitation ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Thiophene Hydrodesulfurization ◽  
Composite Oxides ◽  
Temperature Programmed ◽  
Supported Ni

A series of Al2O3-ZrO2 (AZ-X) composite oxides with different ZrO2 contents were prepared by a chemical precipitation method. Ni-P/AZ-X catalysts were prepared by temperature-programmed reduction. The supports and catalysts were extensively characterized by X-ray diffraction (XRD) and BET. The effects of support composition and P/Ni molar ratios on the catalytic performance of the catalysts were investigated by thiophene hydrodesulfurization (HDS) and pyridine hydrodenitrogenation (HDN). In comparison with Al2O3, Al2O3-ZrO2 (20 wt% ZrO2) composite oxide supported Ni-P catalyst exhibited higher activity and the activities of HDS and HDN increased by 7.5 % and 11.1 %, respectively. Studies of Ni-P/AZ-X catalysts with varying initial P/Ni molar ratios indicated that oxidic precursors with molar ratios of P/Ni = 2/1 yielded catalyst containing phase-pure Ni2P which exhibited optimal activity.

Effect of zinc introduction on catalytic performance of ZSM-5 in conversion of methanol to light olefins

2014 ◽  
Vol 68 (9) ◽  
Author(s):  
Su-Hong Zhang ◽  
Zhi-Xian Gao ◽  
Shao-Jun Qing ◽  
Sheng-Yu Liu ◽  
Yan Qiao
Keyword(s):  
Methanol Conversion ◽  
Catalytic Performance ◽  
Light Olefins ◽  
Acidic Property ◽  
X Ray Diffraction ◽  
Light Olefin ◽  
X Ray ◽  
Olefin Conversion ◽  
Methanol To Olefin ◽  
Temperature Programmed

AbstractThe effect of Zn on the catalytic performance of ZSM-5 in the methanol-to-olefin conversion was investigated. The samples were characterised by X-ray diffraction, N2 adsorption, FTIR, temperature-programmed desorption of ammonia and water, and Py-IR. The experimental results revealed Znmodified ZSM-5 to show a lower selectivity to light olefin at the higher reaction temperature of 520°C but a higher selectivity to light olefin at lower temperatures. As a comparison, the catalytic performance of Ca-modified ZSM-5 for the methanol conversion is also given. From the above results, it is concluded that Zn may play another role in the methanol conversion in addition to tuning the surface acidic property after modification.

Microstructural of Cr/MWCNT Composites and its Catalysis in Synthesis of Biodiesel

2012 ◽  
Vol 455-456 ◽  
pp. 1053-1059
Author(s):  
Xue Hai Fan ◽  
Guo Min Xiao
Keyword(s):  
Electron Microscopy ◽  
Potassium Dichromate ◽  
Catalytic Performance ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Multi Walled Carbon Nanotubes ◽  
Ft Ir ◽  
Walled Carbon Nanotubes

Multi-walled carbon nanotubes (MWCNTs), potassium dichromate (K2Cr2O7) and sulphuric acid were used for the preparation of Cr/MWCNT composite by impregnation method. The composites were comprehensively characterized by transmission electron microscopy （TEM），energy dispersive X-ray analysis (EDX), infrared spectroscopy (FT-IR), X-ray diffraction (XRD) and thermal gravity analysis (TGA). Due to its unique electrical and structural properties, this composite was applied to the synthesis of biodiesel (FAME) as a catalyst, showing effectively catalytic performance.

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