scholarly journals In-site Preparation and Characterization Catalytic- Composite Used for Plastic Waste Degradation to Fuel.

2021 ◽  
Author(s):  
Ameen Abdelrahman ◽  
Asmaa S. Hamouda ◽  
A.H. Zaki
Keyword(s):  
Fixed Bed ◽  
Plastic Waste ◽  
High Density ◽  
Fixed Bed Reactor ◽  
Composite Catalyst ◽  
X Ray Diffraction ◽  
Spectroscopic Analyses ◽  
Transmission Electron ◽  
Waste Degradation ◽  
Gasification Reaction

Abstract In order to get renewable energy from plastic waste, it should find a pathway or create a new composite that is thermally stable, non-toxic, environmentally inexpensive, and highly efficient. Thus, in our research, we work with composite materials that provide a hetero catalyst designed to crack Polyethylene high Density ( PEHD) , which is composed of Metals (Mn, Ag) in Nano scales , and Graphene impregnated inside the PEG matrix. In order to evaluate fabricated composite catalyst, to be applicable on conversion plastic polyethylene high density to gases yields and solid char carbon using pyrolysis and gasification reaction . the process were carried out inside the fixed bed reactor. Various characteristics have been conducted for final products (gases and black char), further spectroscopic analyses like Ultraviolet–visible spectroscopy (UV) , Cyclic voltammetry (CV) , Transmission Electron Microscopy (TEM), X-Ray Diffraction (XRD ), and Thermogravimetric analysis (TGA) were investigated for the new composite.

scholarly journals Catalytic Dry Reforming and Cracking of Ethylene for Carbon Nanofilaments and Hydrogen Production Using a Catalyst Derived from a Mining Residue

Catalysts ◽  
2019 ◽  
Vol 9 (12) ◽  
pp. 1069 ◽  
Author(s):  
Abir Azara ◽  
El-Hadi Benyoussef ◽  
Faroudja Mohellebi ◽  
Mostafa Chamoumi ◽  
François Gitzhofer ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Fixed Bed ◽  
Dry Reforming ◽  
Fixed Bed Reactor ◽  
Molar Ratio ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Spent Catalysts ◽  
Temperature Programmed

In this study, iron-rich mining residue (UGSO) was used as a support to prepare a new Ni-based catalyst via a solid-state reaction protocol. Ni-UGSO with different Ni weight percentages wt.% (5, 10, and 13) were tested for C2H4 dry reforming (DR) and catalytic cracking (CC) after activation with H2. The reactions were conducted in a differential fixed-bed reactor at 550–750 °C and standard atmospheric pressure, using 0.5 g of catalyst. Pure gases were fed at a molar ratio of C2H4/CO2 = 3 for the DR reaction and C2H4/Ar = 3 for the CC reaction. The flow rate is defined by a GHSV = 4800 mLSTP/h.gcat. The catalyst performance is evaluated by calculating the C2H4 conversion as well as carbon and H2 yields. All fresh, activated, and spent catalysts, as well as deposited carbon, were characterized by Brunauer–Emmett–Teller (BET), X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectrometry (EDX), transmission electron microscopy (TEM), temperature programmed reduction (TPR), and thermogravimetric analysis (TGA). The results so far show that the highest carbon and H2 yields are obtained with Ni-UGSO 13% at 750 °C for the CC reaction and at 650 °C for the DR reaction. The deposited carbon was found to be filamentous and of various sizes (i.e., diameters and lengths). The analyses of the results show that iron is responsible for the growth of carbon nanofilaments (CNF) and nickel is responsible for the split of C–C bonds. In terms of conversion and yield efficiencies, the performance of the catalytic formulations tested is proven at least equivalent to other Ni-based catalyst performances described by the literature.

scholarly journals Effect of CO2 partial pressure on dry reforming of ethanol for hydrogen production

2018 ◽  
Vol 1 (1) ◽  
pp. 6-10
Author(s):  
Fahim Fayaz ◽  
Ahmad Ziad Sulaiman ◽  
Sharanjit Singh ◽  
Sweeta Akbari
Keyword(s):  
Partial Pressure ◽  
Fixed Bed ◽  
Dry Reforming ◽  
Fixed Bed Reactor ◽  
Bet Surface Area ◽  
Impregnation Method ◽  
X Ray Diffraction ◽  
Co2 Partial Pressure ◽  
Temperature Programmed ◽  
Al2o3 Catalyst

The effect of CO2 partial pressure on ethanol dry reforming was evaluated over 5%Ce-10%Co/Al2O3 catalyst at = PCO2 = 20-50 kPa, PC2H5OH = 20 kPa, reaction temperature of 973 K under atmospheric pressure. The catalyst was prepared by using impregnation method and tested in a fixed-bed reactor. X-ray diffraction measurements studied the formation of Co3O4, spinel CoAl2O4 and CeO2, phases on surface of 5%Ce-10%Co/Al2O3 catalyst. CeO2, CoO and Co3O4 oxides were obtained during temperature–programmed calcination. Ce-promoted 10%Co/Al2O3 catalyst possessed high BET surface area of 137.35 m2 g-1. C2H5OH and CO2 conversions was improved with increasing CO2 partial pressure from 20-50 kPa whilst the optimal selectivity of H2 and CO was achieved at 50 kPa.

Modified Cuo/ZnO/Al2O3 Catalysts for Methanol Synthesis from Co and CO2 Co-Hydrogenation

2013 ◽  
Vol 690-693 ◽  
pp. 1529-1534
Author(s):  
Wen Gui Gao ◽  
Hua Wang ◽  
Wen Yan Liu ◽  
Feng Jie Zhang
Keyword(s):  
Methanol Synthesis ◽  
Active Sites ◽  
Co Hydrogenation ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Total Carbon ◽  
X Ray Diffraction ◽  
Wet Impregnation ◽  
Temperature Programmed ◽  
Co Precipitation

A series of CuO-ZnO-Al2O3catalysts modified by different promoter were prepared by co-precipitation or incipient wet impregnation and characterized by X-ray diffraction (XRD), N2physisorption, hydrogen temperature-programmed reduction (H2-TPR) and carbon dioxide temperature-programmed desorption (CO2-TPD). The modified catalysts were tested for methanol synthesis from CO/CO2co-hydrogenation in a fixed bed reactor with feed containing CO, CO2and H2(CO:CO2:H2=1.0:1.08:6.24, volume radio). It is revealed that the catalysts modified by Zr, Mg, Ca has higher activity of methanol synthesis by CO and CO2co-hydrogenation. Especially, the addition of Zr enhances the conversion of total carbon and the selectivity of methanol, which is due to the improved surface area, much more active sites, and the synergistically interaction between CuO and ZnO caused by the addition of Zr promoter.

In Situ Synthesis of Cu-SAPO-34/Cordierite with Ultrasonic Treatment and its Property of NOx Removal

2013 ◽  
Vol 743-744 ◽  
pp. 449-454 ◽  
Author(s):  
Zhi Juan Gao ◽  
Wei Ren Bao ◽  
Li Ping Chang ◽  
Jian Cheng Wang
Keyword(s):  
Ultrasonic Treatment ◽  
Good Condition ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
X Ray Diffraction ◽  
Monolithic Catalyst ◽  
X Ray ◽  
Nox Conversion ◽  
Aging Property

A Cu-SAPO-34/cordierite monolithic catalyst was prepared by in-situ hydrothermal method. The effects of ultrasonic treatment were mainly investigated during the preparing process. The removal of NOX was evaluated using a fixed-bed reactor. X-ray diffraction, scanning electron microscopy were used to characterize the samples showing that the crystallinity of Cu-SAPO-34 molecular sieve have increased after ultrasonic treatment. The Cu-SAPO-34/cordierite prepared by ultrasonic treatment showed higher de-NOx activity and stronger anti-aging property. NOx conversion could reach more than 80% between 440 and 560°C over the fresh Cu-SAPO-34/cordierite catalyst with ultrasonic treatment (600 W, 2 h) and the highest conversion was 86%, however, the highest conversion was only 76% over the Cu-SAPO-34/cordierite catalyst without ultrasonic treatment. After aging (treated for 15 h at 720 °C in the presence of 200 ppm SO2 and 10% vapor), NOx conversion reached more than 45% between 400 and 520 °C over the catalyst with ultrasonic treatment and the highest conversion was 57%, however, the highest conversion was only 43% over the catalyst without ultrasonic treatment. The XRD and SEM results indicated that the structure and morphology of Cu-SAPO-34/cordierite monolithic catalyst kept in good condition after aging.

scholarly journals High Active Co/Mg1-xCex3+O Catalyst: Effects of Metal-Support Promoter Interactions on CO2 Reforming of CH4 Reaction

2021 ◽  
Vol 16 (1) ◽  
pp. 97-110
Author(s):  
Faris A. Jassim Al-Doghachi ◽  
Diyar M. A. Murad ◽  
Huda S. Al-Niaeem ◽  
Salam H. H. Al-Jaberi ◽  
Surahim Mohamad ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Fixed Bed ◽  
Fixed Bed Reactor ◽  
Dry Reforming Of Methane ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Co2 Reforming Of Ch4 ◽  
Temperature Programmed

Co/Mg1−XCe3+XO (x = 0, 0.03, 0.07, 0.15; 1 wt% cobalt each) catalysts for the dry reforming of methane (DRM) reaction were prepared using the co-precipitation method with K2CO3 as precipitant. Characterization of the catalysts was achieved by X-ray diffraction (XRD), X-ray fluorescence spectroscopy (XRF), X-ray photoelectron spectroscopy (XPS), temperature programmed reduction (H2-TPR), Brunauer–Emmett–Teller (BET), transmission electron microscopy (TEM), and thermal gravimetric analysis (TGA). The role of several reactant and catalyst concentrations, and reaction temperatures (700–900 °C) on the catalytic performance of the DRM reaction was measured in a tubular fixed-bed reactor under atmospheric pressure at various CH4/CO2 concentration ratios (1:1 to 2:1). Using X-ray diffraction, a surface area of 19.2 m2.g−1 was exhibited by the Co/Mg0.85Ce3+0.15O catalyst and MgO phase (average crystallite size of 61.4 nm) was detected on the surface of the catalyst. H2 temperature programmed reaction revealed a reduction of CoO particles to metallic Co0 phase. The catalytic stability of the Co/Mg0.85Ce3+0.15O catalyst was achieved for 200 h on-stream at 900 °C for the 1:1 CH4:CO2 ratio with an H2/CO ratio of 1.0 and a CH4, CO2 conversions of 75% and 86%, respectively. In the present study, the conversion of CH4 was improved (75%–84%) when conducting the experiment at a lower flow of oxygen (1.25%). Finally, the deposition of carbon on the spent catalysts was analyzed using TEM and Temperature programmed oxidation-mass spectroscopy (TPO-MS) following 200 h under an oxygen stream. Better anti-coking activity of the reduced catalyst was observed by both, TEM, and TPO-MS analysis. Copyright © 2021 by Authors, Published by BCREC Group. This is an open access article under the CC BY-SA   License (https://creativecommons.org/licenses/by-sa/4.0). 

High-density stacking faults in a supersaturated nitrided layer on austenitic stainless steel

2016 ◽  
Vol 49 (6) ◽  
pp. 1967-1971 ◽  
Author(s):  
Ke Tong ◽  
Fei Ye ◽  
Honglong Che ◽  
Ming Kai Lei ◽  
Shu Miao ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Stainless Steel ◽  
Austenitic Stainless Steel ◽  
Nitrided Layer ◽  
Stacking Faults ◽  
High Density ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron

The nitrogen-supersaturated phase produced by low-temperature plasma-assisted nitriding of austenitic stainless steel usually contains a high density of stacking faults. However, the stacking fault density observed in previous studies was considerably lower than that determined by fitting the X-ray diffraction pattern. In this work, it has been confirmed by high-resolution transmission electron microscopy that the strip-shaped regions of about 3–25 nm in width observed at relatively low magnification essentially consist of a series of stacking faults on every second {111} atomic plane. A microstructure model of the clustered stacking faults embedded in a face-centred cubic structure was built for these regions. The simulated X-ray diffraction and transmission electron microscopy results based on this model are consistent with the observations.

Effect of the Reduction Temperature on Nickel Phosphide Catalyst Structure and Catalytic Activity for Hydrodesulfurization

2014 ◽  
Vol 1025-1026 ◽  
pp. 782-786 ◽  
Author(s):  
Hua Song ◽  
Fu Yong Zhang ◽  
Zai Shun Jin ◽  
Huai Yuan Wang ◽  
Yan Ji Zhu ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Fixed Bed ◽  
Space Velocity ◽  
Fixed Bed Reactor ◽  
Reduction Temperature ◽  
Catalyst Structure ◽  
X Ray ◽  
Weight Hourly Space Velocity ◽  
Transmission Electron ◽  
Nickel Phosphate

Ni2P/TiO2-Al2O3catalysts were prepared by impregnation of nickel phosphate precursors followed by reduction in hydrogen. The catalysts were characterized by X-ray diffraction (XRD), N2-adsorption specific surface area measurements (BET), transmission electron microscope (TEM), X-ray photoelectron spectroscopy (XPS) and thermogravimetry differential thermal analysis (TG-DTA). The effects of reduction temperature on catalyst structure and HDS activity were studied using a lab-scale continuous flow fixed-bed reactor.. The results indicated that the catalyst prepared with reduction temperature of 973 K exhibited the best performance. At a reaction temperature of 606 K, a pressure of 3.0 MPa, a hydrogen/oil ratio of 500 (V/V), and a weight hourly space velocity (WHSV) of 2.0 h-1, the conversion of DBT HDS was 96.0%.

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