Hydrodesulfurization of thiophene on highly deactivated coal-liquid hydrotreatment catalyst: effect of deposited iron sulfide

1993 ◽  
Vol 32 (8) ◽  
pp. 1637-1644 ◽  
Author(s):  
A. P. Raje ◽  
D. B. Dadyburjor
Keyword(s):  
Iron Sulfide ◽  
Catalyst Effect ◽  
Hydrotreatment Catalyst

Point and planar defects in the iron sulfide compounds Fe1-xS

1984 ◽  
Vol 42 ◽  
pp. 434-435
Author(s):  
Thao A. Nguyen
Keyword(s):  
Low Temperatures ◽  
Direct Evidence ◽  
Iron Sulfide ◽  
Planar Defects ◽  
Selective Area ◽  
Vacancy Ordering ◽  
Different Types ◽  
Lattice Images ◽  
The Subject ◽  
Beam Lattice

It is well known that the large deviations from stoichiometry in iron sulfide compounds, Fe1-xS (0≤x≤0.125), are accommodated by iron vacancies which order and form superstructures at low temperatures. Although the ordering of the iron vacancies has been well established, the modes of vacancy ordering, hence superstructures, as a function of composition and temperature are still the subject of much controversy. This investigation gives direct evidence from many-beam lattice images of Fe1-xS that the 4C superstructure transforms into the 3C superstructure (Fig. 1) rather than the MC phase as previously suggested. Also observed are an intrinsic stacking fault in the sulfur sublattice and two different types of vacancy-ordering antiphase boundaries. Evidence from selective area optical diffractograms suggests that these planar defects complicate the diffraction pattern greatly.

Methane Combustion over Pd/Al2O3 Catalyst: Effect of Cal-cination Temperature

2011 ◽  
Vol 31 (11) ◽  
pp. 1363-1368
Author(s):  
Diannan GAO ◽  
Sheng WANG ◽  
Ying LIU ◽  
Chunxi ZHANG ◽  
Shudong WANG
Keyword(s):  
Methane Combustion ◽  
Catalyst Effect

scholarly journals A Hierarchically Ordered Mesoporous-Carbon-Supported Iron Sulfide Anode for High-Rate Na-Ion Storage

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4349
Author(s):  
Anupriya K. Haridas ◽  
Natarajan Angulakshmi ◽  
Arul Manuel Stephan ◽  
Younki Lee ◽  
Jou-Hyeon Ahn
Keyword(s):  
Mesoporous Carbon ◽  
Anode Materials ◽  
Iron Sulfide ◽  
Carbon Composite ◽  
Ordered Mesoporous Carbon ◽  
Cycle Life ◽  
High Rate ◽  
Volume Changes ◽  
Ordered Mesoporous ◽  
Ion Storage

Sodium-ion batteries (SIBs) are promising alternatives to lithium-based energy storage devices for large-scale applications, but conventional lithium-ion battery anode materials do not provide adequate reversible Na-ion storage. In contrast, conversion-based transition metal sulfides have high theoretical capacities and are suitable anode materials for SIBs. Iron sulfide (FeS) is environmentally benign and inexpensive but suffers from low conductivity and sluggish Na-ion diffusion kinetics. In addition, significant volume changes during the sodiation of FeS destroy the electrode structure and shorten the cycle life. Herein, we report the rational design of the FeS/carbon composite, specifically FeS encapsulated within a hierarchically ordered mesoporous carbon prepared via nanocasting using a SBA-15 template with stable cycle life. We evaluated the Na-ion storage properties and found that the parallel 2D mesoporous channels in the resultant FeS/carbon composite enhanced the conductivity, buffered the volume changes, and prevented unwanted side reactions. Further, high-rate Na-ion storage (363.4 mAh g−1 after 500 cycles at 2 A g−1, 132.5 mAh g−1 at 20 A g−1) was achieved, better than that of the bare FeS electrode, indicating the benefit of structural confinement for rapid ion transfer, and demonstrating the excellent electrochemical performance of this anode material at high rates.

scholarly journals The Catalytic Oxidation of Formaldehyde by FeOx-MnO2-CeO2 Catalyst: Effect of Iron Modification

Catalysts ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 555
Author(s):  
Yaxin Dong ◽  
Chenguang Su ◽  
Kai Liu ◽  
Haomeng Wang ◽  
Zheng Zheng ◽  
...  
Keyword(s):  
Low Temperatures ◽  
Oxygen Vacancies ◽  
Catalytic Performance ◽  
Active Oxygen ◽  
Molar Ratio ◽  
N2 Adsorption ◽  
Structure Activity ◽  
Iron Modification ◽  
Surface Active ◽  
Catalyst Effect

A series of FeOx-MnO2-CeO2 catalysts were synthesized by the surfactant-templated coprecipitation method and applied for HCHO removal. The influence of Fe/Mn/Ce molar ratio on the catalytic performance was investigated, and the FeOx-MnO2-CeO2 catalyst exhibited excellent catalytic activity, with complete HCHO conversion at low temperatures (40 °C) when the molar ratio of Fe/Mn/Ce was 2/5/5. The catalysts were characterized by N2 adsorption and desorption, XRD, H2-TPR, O2-TPD and XPS techniques to illustrate their structure–activity relationships. The result revealed that the introduction of FeOx into MnO2-CeO2 formed a strong interaction between FeOx-MnO2-CeO2, which facilitated the improved dispersion of MnO2-CeO2, subsequently increasing the surface area and aiding pore development. This promotion effect of Fe enhanced the reducibility and produced abundant surface-active oxygen. In addition, a great number of Oα is beneficial to the intermediate decomposition, whereas the existence of Ce3+ favors the formation of oxygen vacancies on the surface of the catalyst, all of which contributed to HCHO oxidation at low temperatures.

scholarly journals Electrochemical removal of pyrite scale using green formulations

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Musa Ahmed ◽  
Ibnelwaleed A. Hussein ◽  
Abdulmujeeb T. Onawole ◽  
Mohammed A. Saad ◽  
Mazen Khaled
Keyword(s):  
Hydrogen Sulfide ◽  
Current Density ◽  
Iron Sulfide ◽  
Chelating Agent ◽  
Electrical Current ◽  
Electrochemical Process ◽  
Chemical Dissolution ◽  
Hydrocarbon Production ◽  
Rotational Rate ◽  
Diethylenetriamine Pentaacetic Acid

AbstractPyrite scale formation is a critical problem in the hydrocarbon production industry; it affects the flow of hydrocarbon within the reservoir and the surface facilities. Treatments with inorganic acids, such as HCl, results in generation toxic hydrogen sulfide, high corrosion rates, and low dissolving power. In this work, the dissolution of pyrite scale is enhanced by the introduction of electrical current to aid the chemical dissolution. The electrolytes used in this study are chemical formulations mainly composed of diethylenetriamine-pentaacetic acid–potassium (DTPAK5) with potassium carbonate; diethylenetriamine pentaacetic acid sodium-based (DTPANa5), and l-glutamic acid-N, N-diacetic acid (GLDA). DTPA and GLDA have shown some ability to dissolve iron sulfide without generating hydrogen sulfide. The effect of these chemical formulations, disc rotational rate and current density on the electro-assisted dissolution of pyrite are investigated using Galvanostatic experiments at room temperature. The total iron dissolved of pyrite using the electrochemical process is more than 400 times higher than the chemical dissolution using the same chelating agent-based formulation and under the same conditions. The dissolution rate increased by 12-folds with the increase of current density from 5 to 50 mA/cm2. Acid and neutral formulations had better dissolution capacities than basic ones. In addition, doubling the rotational rate did not yield a significant increase in electro-assisted pyrite scale dissolution. XPS analysis confirmed the electrochemical dissolution is mainly due to oxidation of Fe2+ on pyrite surface lattice to Fe3+. The results obtained in this study suggest that electro-assisted dissolution is a promising technique for scale removal.

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