scholarly journals CO2 Methanation of Biogas over 20 wt% Ni-Mg-Al Catalyst: on the Effect of N2, CH4, and O2 on CO2 Conversion Rate

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1201
Author(s):  
Danbee Han ◽  
Yunji Kim ◽  
Hyunseung Byun ◽  
Wonjun Cho ◽  
Youngsoon Baek
Keyword(s):  
Reaction Temperature ◽  
Photoelectron Spectroscopy ◽  
Conversion Rate ◽  
Space Velocity ◽  
Molar Ratio ◽  
Co2 Conversion ◽  
X Ray Diffraction ◽  
Co2 Methanation ◽  
X Ray ◽  
Ch4 Production

Biogas contains more than 40% CO2 that can be removed to produce high quality CH4. Recently, CH4 production from CO2 methanation has been reported in several studies. In this study, CO2 methanation of biogas was performed over a 20 wt% Ni-Mg-Al catalyst, and the effects of CO2 conversion rate and CH4 selectivity were investigated as a function of CH4, O2, H2O, and N2 compositions of the biogas. At a gas hourly space velocity (GHSV) of 30,000 h−1, the CO2 conversion rate was ~79.3% with a CH4 selectivity of 95%. In addition, the effects of the reaction temperature (200–450 °C), GHSV (21,000–50,000 h−1), and H2/CO2 molar ratio (3–5) on the CO2 conversion rate and CH4 selectivity over the 20 wt% Ni-Mg-Al catalyst were evaluated. The characteristics of the catalyst were analyzed using Brunauer–Emmett–Teller surface area analysis, X-ray diffraction, X-ray photoelectron spectroscopy, and scanning electron microscopy. The catalyst was stable for approximately 200 h at a GHSV of 30,000 h−1 and a reaction temperature of 350 °C. CO2 conversion and CH4 selectivity were maintained at 75% and 93%, respectively, and the catalyst was therefore concluded to exhibit stable activity.

scholarly journals CO2 Methanation of Biogas Over 20 wt% Ni-Mg-Al Catalyst: On the Effect of N2, CH4, and O2 on CO2 Conversion Rate

2020 ◽  
Author(s):  
Danbee Han ◽  
Yunji Kim ◽  
Hyunseung Byun ◽  
Wonjun Cho ◽  
Youngsoon Baek
Keyword(s):  
Reaction Temperature ◽  
Photoelectron Spectroscopy ◽  
Conversion Rate ◽  
Space Velocity ◽  
Bet Surface Area ◽  
Molar Ratio ◽  
Co2 Conversion ◽  
Co2 Methanation ◽  
X Ray ◽  
Ch4 Production

Biogas contains more than 40% CO2 that can be removed to produce high quality CH4. Recently, CH4 production from CO2 methanation has been reported in several studies. In this study, CO2 methanation of biogas was performed over a 20 wt% Ni-Mg-Al catalyst, and the effects of CO2 conversion rate and CH4 selectivity were investigated as a function of CH4, O2, H2O, and N2 compositions of the biogas. At a gas hourly space velocity (GHSV) of 30,000/h, the CO2 conversion rate was ~79.3% with a CH4 selectivity of 95%. In addition, the effects of the reaction temperature (200–450 °C), GHSV (21,000–50,000/h), and H2/CO2 molar ratio (3–5) on the CO2 conversion rate and CH4 selectivity over the 20 wt% Ni-Mg-Al catalyst were evaluated. The characteristics of the catalyst were analyzed using Brunauer-Emmett-Teller (BET) surface area analysis, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and scanning electron microscopy (SEM). The catalyst was stable for approximately 200 h at a GHSV of 30,000/h and a reaction temperature of 350 °C. CO2 conversion and CH4 selectivity were maintained at 75% and 93%, respectively, and the catalyst was therefore concluded to exhibit stable activity.

scholarly journals Photocatalytic Reduction of CO2 to Methanol Using a Copper-Zirconia Imidazolate Framework

Catalysts ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 346
Author(s):  
Sonam Goyal ◽  
Maizatul Shima Shaharun ◽  
Ganaga Suriya Jayabal ◽  
Chong Fai Kait ◽  
Bawadi Abdullah ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Catalyst Support ◽  
Oxidation Potential ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Molar Ratios ◽  
Optimum Parameters ◽  
Reduction Of Co2 ◽  
Enhanced Yield

A set of novel photocatalysts, i.e., copper-zirconia imidazolate (CuZrIm) frameworks, were synthesized using different zirconia molar ratios (i.e., 0.5, 1, and 1.5 mmol). The photoreduction process of CO2 to methanol in a continuous-flow stirred photoreactor at pressure and temperature of 1 atm and 25 °C, respectively, was studied. The physicochemical properties of the synthesized catalysts were studied using X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and photoluminescence (PL) spectroscopy. The highest methanol activity of 818.59 µmol/L.g was recorded when the CuZrIm1 catalyst with Cu/Zr/Im/NH4OH molar ratio of 2:1:4:2 (mmol/mmol/mmol/M) was employed. The enhanced yield is attributed to the presence of Cu2+ oxidation state and the uniformly dispersed active metals. The response surface methodology (RSM) was used to optimize the reaction parameters. The predicted results agreed well with the experimental ones with the correlation coefficient (R2) of 0.99. The optimization results showed that the highest methanol activity of 1054 µmol/L.g was recorded when the optimum parameters were employed, i.e., stirring rate (540 rpm), intensity of light (275 W/m2) and photocatalyst loading (1.3 g/L). The redox potential value for the CuZrIm1 shows that the reduction potential is −1.70 V and the oxidation potential is +1.28 V for the photoreduction of CO2 to methanol. The current work has established the potential utilization of the imidazolate framework as catalyst support for the photoreduction of CO2 to methanol.

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).

scholarly journals Effect of cerium content on textural and hydrodesulfurization performance for dibenzothiophene over a bulk Ni2P catalyst

2019 ◽  
Vol 44 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Yunwu Yu ◽  
Lianjie Liang ◽  
Changwei Xu ◽  
Yubo Dai ◽  
Wenhao Pan ◽  
...  
Keyword(s):  
Crystallite Size ◽  
Photoelectron Spectroscopy ◽  
Space Velocity ◽  
X Ray Diffraction ◽  
Reaction Conditions ◽  
X Ray ◽  
Weight Hourly Space Velocity ◽  
Cerium Content ◽  
Adsorption Desorption ◽  
Hydrodesulfurization Activity

A series of ceria promoted Ni2P catalysts were prepared and evaluated in dibenzothiophene hydrodesulfurization steam. These catalysts were characterized by X-ray diffraction, N2 adsorption–desorption, CO chemisorptions, and X-ray photoelectron spectroscopy. The results showed that the addition of ceria into the bulk Ni2P catalyst was conducive to the formation of the Ni2P phase and contributed to a higher surface area, leading to a better dispersion and smaller crystallite size of Ni2P particles. The CexNi2P catalysts showed higher dibenzothiophene hydrodesulfurization activity than Ni2P catalyst and the Ce0.09Ni2P catalyst showed the highest dibenzothiophene hydrodesulfurization activity. The Ce0.09Ni2P catalyst showed a dibenzothiophene hydrodesulfurization conversion of 94.5% at the reaction conditions of 320°C, 4.0 MPa, a H2/oil ratio of 500 (V/V), and a weight hourly space velocity of 8.0 h−1. The dibenzothiophene was mainly transformed through desulfurization pathway.

scholarly journals Experimental Study on CO2 Methanation over Ni/Al2O3, Ru/Al2O3, and Ru-Ni/Al2O3 Catalysts

Catalysts ◽  
2020 ◽  
Vol 10 (10) ◽  
pp. 1112 ◽  
Author(s):  
Rei-Yu Chein ◽  
Chih-Chang Wang
Keyword(s):  
Space Velocity ◽  
Molar Ratio ◽  
Ni Catalyst ◽  
Co2 Conversion ◽  
Co2 Methanation ◽  
Temperature Changes ◽  
Good Thermal Stability ◽  
Reverse Water Gas Shift ◽  
Optimum Reaction ◽  
Shift Reaction

CO2 methanation is recognized as one of the best technologies for storing intermittent renewable energy in the form of CH4. In this study, CO2 methanation performance is investigated using Ni/Al2O3, Ru/Al2O3, and Ru-Ni/Al2O3 as the catalysts under conditions of atmospheric pressure, a molar ratio of H2/CO2 = 5, and a space velocity of 5835 h−1. For reaction temperatures ranging from 250 to 550 °C, it was found that the optimum reaction temperature is 400 °C for all catalysts studied. At this temperature, the maximum values of CO2 conversion, H2 efficiency, and CH4 yield and lowest CO yield can be obtained. With temperatures higher than 400 °C, reverse CO2 methanation results in CO2 conversion and CH4 yield decreases with increased temperature, while CO is formed due to reverse water-gas shift reaction. The experimental results showed that CO2 methanation performance at low temperatures can be enhanced greatly using the bimetallic Ru-Ni catalyst compared with the monometallic Ru or Ni catalyst. Under ascending-descending temperature changes between 250 °C and 550 °C, good thermal stability is obtained from Ru-Ni/Al2O3 catalyst. About a 3% decrease in CO2 conversion is found after three continuous cycles (74 h) test.

Synthesis, Characterization and Photocatalytic Activity of Nb-Doped TiO2 Nanoparticles

2012 ◽  
Vol 455-456 ◽  
pp. 110-114 ◽  
Author(s):  
Xuan Dong Li ◽  
Xi Jiang Han ◽  
Wen Ying Wang ◽  
Xiao Hong Liu ◽  
Yan Wang ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Photocatalytic Activity ◽  
Methyl Orange ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Doped Tio2 ◽  
X Ray ◽  
Vis Spectroscopy

Nb-doped TiO2 powders with different concentrations of Nb have been synthesized by a sol-gel method and characterized by a series of technologies including X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS) and UV-vis spectroscopy. The photocatalytic activity of Nb-doped TiO2 is evaluated by degradation efficiency of methyl orange in aqueous solution. The results indicate that the photocatalytic activity of Nb-doped TiO2 synthesized with a Nb/Ti molar ratio of 5% is higher than that of TiO2 under the visible light.

Stoichiometric Controlling of Spark Plasma Sintered Boron-Carbon Ceramics

2009 ◽  
Vol 66 ◽  
pp. 25-28 ◽  
Author(s):  
Song Zhang ◽  
Chuan Bin Wang ◽  
Qiang Shen ◽  
Lian Meng Zhang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Measurement Data ◽  
Atomic Ratio ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Plasma Sintering ◽  
Spark Plasma ◽  
Carbon Ceramic ◽  
Boron Carbon

A group of boron-carbon ceramic material was in-situ synthesized and densified simultaneously via Spark Plasma Sintering (SPS) technique from carbon and boron element powders with different molar ratio. The phase structures of samples with different B/C molar ratio were characterized by X-ray Diffraction (XRD). The B/C atomic ratio of the sintered materials was calculated from X-ray photoelectron spectroscopy (XPS) measurement data. Meanwhile, the chemical analysis (CA) method had also been taken to verify the B/C atomic ratio. Finally, the experience equation had been obtained to control the B/C atomic ratio of sintered samples.

Characteristics and Properties of Absorption Materials for Mercury Removal at High Temperature

2017 ◽  
Vol 730 ◽  
pp. 185-189
Author(s):  
Han Wen Cheng ◽  
Ching Tsung Yu
Keyword(s):  
Operating Temperature ◽  
Space Velocity ◽  
Mercury Removal ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Surface Areas ◽  
Electron Detection ◽  
Metal Ratio ◽  
Structure Analyzer

In this study, some metal-M/aluminum carbonate absorption materials with molar ratio of M:Al=3:1 were manufactured. There was Cu–Al, Mn–Al, Fe–Al three kinds of sorbents synthesized by co-precipitate method. The physicochemical structures during mercury removal were analyzed by a surface area and pore structure analyzer (BET), an X-ray diffraction (XRD), a scanning electron microscope coupled with an electron detection scanning (SEM/EDS), and X-ray fluorescence (XRF). The results showed that surface areas for metal-M/aluminum carbonate sorbents were only about 11~12 m2/g and the metal ratio loaded was more than 80%. Lab-scale tests mercury removal efficiency in the temperature range of 200–300 oC indicated that there was an improvement in the performance of mercury removal by increasing reaction temperature. Cu–Al, Fe–Al and Mn–Al all three sorbents reached their absorption equivalent of 256.6, 253.3 and 247.0 μg/g under 300 oC operating temperature and 19736 h-1 gas hourly space velocity. Additionally, the presence of transition metals can significantly improve the efficiency of mercury removal of the absorption materials.

scholarly journals Hydrothermal synthesis of monocopper sulfide for hydrogen peroxide-assisted photodegradation of paraquat

2020 ◽  
Vol 26 (1) ◽  
Author(s):  
Rattabal Khunphonoi ◽  
Kitirote Wantala ◽  
Nurak Grisdanurak
Keyword(s):  
Photoelectron Spectroscopy ◽  
Reaction Rate ◽  
Ageing Time ◽  
Reaction Rate Constant ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Energy Band Gap ◽  
X Ray ◽  
Synthesis Parameters ◽  
Transmission Electron

Copper sulfide was prepared by a hydrothermal method at 130°C. The copper to sulfur molar ratio (6-10) and ageing time (24-72 h) were their synthesis parameters. The obtained materials were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), transmission electron microscope (TEM), UV-DR spectroscopy and X-ray photoelectron spectroscopy (XPS). In order to obtain monocopper sulfide, CuS, named as covellite, the molar recipe ratio of sulfur to copper should be less than 8 in any hydrothermal ageing time. The morphology showed spherical-like structure with energy band gap of 1.88-2.04 eV. CuS was tested for its photocatalytic degradation of paraquat under visible light irradiation. It exhibited excellent activities in the presence of H<sub>2</sub>O<sub>2</sub>. The kinetic of paraquat degradation was also investigated using Langmuir-Hinshelwood-Hougen-Watson (LHHW) model. The reaction rate constant was three times higher than TiO<sub>2</sub> under the same studied conditions.

Preparation, Characterization of Phosphorus Doped Titania Photocatalysts with High Photocatalystic Properties

2010 ◽  
Vol 113-116 ◽  
pp. 2154-2157 ◽  
Author(s):  
Si Yao Guo ◽  
Jin Bing Sun ◽  
Feng Lu Wang ◽  
Lin Yang ◽  
Feng Zhang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Titania Nanoparticles ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
Step Method ◽  
X Ray ◽  
One Step ◽  
Titania Photocatalyst ◽  
Calcination Method ◽  
Doped Titania

Phosphor-doped titania nanoparticles were synthesized by a one step method, which were prepared by conventional calcination method. These samples have much higher photocatalytic activity for methylene blue degradation. The resulting materials were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), etc. Moreover, we use high P/TiO2 molar ratio to get the most suitable proportion for the synthesis of P-doped titania photocatalyst.

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