Effect of Copper and Annealing Dew Point on Oxidation Behavior of C-Si-Mn Steels

2018 ◽  
Vol 913 ◽  
pp. 286-293
Author(s):  
Guang Rui Jiang ◽  
Hai Quan Wang ◽  
Li Bin Liu
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidation Behavior ◽  
Optical Emission ◽  
Sem Analysis ◽  
Dew Point ◽  
Emission Spectrometry ◽  
X Ray ◽  
External Oxidation ◽  
Effect Of Copper ◽  
Mn Steel

The effect of copper on oxidation behavior of a C-Si-Mn steel was investigated. The samples were heated to 820°C and held for 75s under four different dew points with 5vol% hydrogen. The results of glow discharge optical emission spectrometry (GDOES), X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM) analysis techniques revealed the differences in oxidation. It is proposed that the steel containing 0.3 wt.% copper has less external oxidation of silicon and manganese compared to the steel containing no copper for all different dew points. As researched in this paper the external oxidation of C-Si-Mn steels would be suppressed by adding copper.

scholarly journals Combined Pulsed RF GD-OES and HAXPES for Quantified Depth Profiling through Coatings

Coatings ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 702
Author(s):  
Muriel Bouttemy ◽  
Solène Béchu ◽  
Ben F. Spencer ◽  
Pia Dally ◽  
Patrick Chapon ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Depth Profiling ◽  
Chemical Characterization ◽  
Optical Emission ◽  
Emission Spectrometry ◽  
Chemical Information ◽  
Sampling Depth ◽  
Energy Excitation ◽  
X Ray ◽  
Pulsed Rf

Chemical characterization at buried interfaces is a real challenge, as the physico-chemical processes operating at the interface govern the properties of many systems and devices. We have developed a methodology based on the combined use of pulsed RF GD-OES (pulsed Radio Frequency Glow Discharge Optical Emission Spectrometry) and XPS (X-ray Photoelectron Spectroscopy) to facilitate the access to deeply buried locations (taking advantage of the high profiling rate of the GD-OES) and perform an accurate chemical diagnosis using XPS directly inside the GD crater. The reliability of the chemical information is, however, influenced by a perturbed layer present at the surface of the crater, hindering traditional XPS examination due to a relatively short sampling depth. Sampling below the perturbed layer may, however, can be achieved using a higher energy excitation source with an increased sampling depth, and is enabled here by a new laboratory-based HAXPES (Hard X-ray PhotoElectron Spectroscopy) (Ga-Kα, 9.25 keV). This new approach combining HAXPES with pulsed RF GD-OES requires benchmarking and is here demonstrated and evaluated on InP. The perturbed depth is estimated and the consistency of the chemical information measured is demonstrated, offering a new route for advanced chemical depth profiling through coatings and heterostructures.

scholarly journals Layered Double Hydroxide Clusters as Precursors of Novel Multifunctional Layers: A Bottom-Up Approach

Coatings ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 328 ◽  
Author(s):  
Cristina S. Neves ◽  
Alexandre C. Bastos ◽  
Andrei N. Salak ◽  
Maksim Starykevich ◽  
Daisy Rocha ◽  
...  
Keyword(s):  
Layered Double Hydroxide ◽  
Photoelectron Spectroscopy ◽  
Structural Changes ◽  
Optical Emission ◽  
Localized Corrosion ◽  
Emission Spectrometry ◽  
Water Contact ◽  
X Ray ◽  
Xrd Diffraction ◽  
Double Hydroxide

The specific microstructure of aluminum alloys is herein explored to grow spatially-resolved layered double hydroxide (SR-LDH) clusters on their surface. Upon chemical modification of LDHs via intercalation, adsorption and grafting with different functional molecules, novel surface-engineered surfaces were obtained. Crystal structure and phase composition were analyzed by X-ray diffraction (XRD) and surface morphology was observed by scanning electron microscopy (SEM). X-ray photoelectron spectroscopy (XPS) and glow discharge optical emission spectrometry (GDOES) were used to correlate structural changes upon ion-exchange and interfacial modifications with chemical composition and surface profiles of the SR-LDH films, respectively. The protection conferred by these films against localized corrosion was investigated at microscale using the scanning vibrating electrode technique (SVET). LDH-NO3 phase was obtained by direct growth onto AA2024 surface, as evidenced by (003) and (006) XRD diffraction reflections. After anion exchange of nitrate with 2-mercaptobenzothiazole (MBT) there was a decrease in the SR-LDH thickness inferred from GDOES profiles. The subsequent surface functionalization with HTMS was confirmed by the presence of Si signal in XPS and GDOES analyses, leading to an increase in the water contact angle (c.a 144° ± 3°). SVET measurements of the SR-LDH films revealed exceptional corrosion resistance, whereas the bioluminescent bacteria assay proved the anti-microbial character of the obtained films. Overall the results obtained show an effective corrosion protection of the SR-LDHs when compared to the bare substrate and the potential of these films for biofouling applications as new Cr-free pre-treatments.

Selective Oxidation Behavior of Medium Manganese Steel in Hot-Dip Galvanizing Process

2019 ◽  
Vol 960 ◽  
pp. 51-57
Author(s):  
Tong Yang ◽  
Yan Lin He ◽  
Hua Wang ◽  
Lin Li ◽  
Li Wang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidation Behavior ◽  
Surface Defect ◽  
Energy Dispersive Spectrometer ◽  
Dew Point ◽  
Manganese Steel ◽  
X Ray ◽  
Medium Manganese Steel ◽  
Surface Oxides ◽  
Scanning Electron

Surface oxides of medium manganese steel treated under different hot-dip galvanizing processes were analyzed by X-ray photoelectron spectroscopy, scanning electron microscope microscopy and energy dispersive spectrometer techniques. Combined with thermodynamic calculation, the effects of dew point and alloying elements on the formation of oxides were investigated. It was shown that many oxides such as Cr2O3 and Al2O3, which deteriorate galvanizing performance largely, were formed at lower dew point, and that the formation of Cr and Al oxides could be effectively inhibited at higher dew point. It was also shown that the formation of MnO could be controlled by regulating the rate of Al/Mn in the composition of experimental steel, thus reducing the surface defect.

scholarly journals The Effect of Mg and Zn Dopants on Pt/Al2O3 for the Dehydrogenation of Perhydrodibenzyltoluene

Catalysts ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 490
Author(s):  
Rudaviro Garidzirai ◽  
Phillimon Modisha ◽  
Innocent Shuro ◽  
Jacobus Visagie ◽  
Pieter van Helden ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Inductively Coupled Plasma ◽  
Flow Reactor ◽  
Plug Flow ◽  
Optical Emission ◽  
Catalytic Performance ◽  
Emission Spectrometry ◽  
Hydrogen Yield ◽  
X Ray ◽  
Temperature Programmed

The effects of Mg and Zn dopants on the catalytic performance of Pt/Al2O3 catalyst were investigated for dehydrogenation of perhydrodibenzyltoluene (H18-DBT) as a liquid organic hydrogen carrier. Al2O3 supports were modified with Mg and Zn to produce Mg-Al2O3 and Zn-Al2O3 with a target loading of 3.8 wt.% for dopants. The modified supports were impregnated with chloroplatinic acid solution to produce the catalysts Pt/Al2O3, Pt/Mg-Al2O3 and Pt/Zn-Al2O3 of 0.5 wt.% Pt loading. Thereafter, the catalysts were characterised using inductively coupled plasma- optical emission spectrometry, scanning electron microscopy-energy dispersive X-ray spectroscopy, hydrogen temperature-programmed reduction, carbon-monoxide pulse chemisorption, ammonia temperature-programmed desorption, X-ray diffraction and transmission electron microscopy. The dehydrogenation experiments were performed using a horizontal plug flow reactor system and the catalyst time-on-stream was 22 h. Pt/Mg-Al2O3 showed the highest average hydrogen flowrate of 29 nL/h, while an average of 27 nL/h was obtained for both Pt/Al2O3 and Pt/Zn-Al2O3. This has resulted in a hydrogen yield of 80% for Pt/Mg-Al2O3, 71% for Pt/Zn-Al2O3 and 73% for Pt/Al2O3. In addition, the conversion of H18-DBT ranges from 99% to 92%, Pt 97–90% and 96–90% for Pt/Mg-Al2O3, Pt/Zn-Al2O3 and Pt/Al2O3, respectively. Following the latter catalyst order, the selectivity to dibenzyltoluene (H0-DBT) ranges from 78% to 57%, 75–51% and 71–45%. Therefore, Pt/Mg-Al2O3 showed improved catalytic performance towards dehydrogenation of H18-DBT.

Deposition of Cobalt Doped Zinc Oxide Thin Film Nano-Composites Via Pulsed Electron Beam Ablation

MRS Advances ◽  
2016 ◽  
Vol 1 (6) ◽  
pp. 433-439 ◽  
Author(s):  
Asghar Ali ◽  
Patrick Morrow ◽  
Redhouane Henda ◽  
Ragnar Fagerberg
Keyword(s):  
Zinc Oxide ◽  
Electron Beam ◽  
Binding Energy ◽  
Photoelectron Spectroscopy ◽  
Xrd Analysis ◽  
Sem Analysis ◽  
Oxide Thin Film ◽  
X Ray ◽  
Pulsed Electron Beam ◽  
Deposited Films

AbstractThis study reports on the preparation of cobalt doped zinc oxide (Co:ZnO) films via pulsed electron beam ablation (PEBA) from a single target containing 20 w% Co on sapphire (0001) and silicon (100) substrates. The films have been deposited at various temperatures (350оC, 400оC, 450оC) and pulse frequencies (2 Hz, 4 Hz), under a background argon (Ar) pressure of about 3 mtorr, and an accelerating voltage of 14 kV. The surface morphology has been examined by atomic force microscopy (AFM) and scanning electron microscopy (SEM). According to SEM analysis, the films consist of nano-globules whose size is in the range of 80-178 nm. Energy dispersive x-ray spectroscopy (EDX) reveals that deposition is congruent and the prepared films contain ∼20±5 w% cobalt. It has been found that the nano-globules in the deposited films are cobalt-rich zones containing ∼70 w% Co. From x-ray photoelectron spectroscopy (XPS) analysis, Co 2p3/2 peaks indicate that the deposited films contain CoO (binding energy = 780.5 eV) as well as metallic Co (binding energy = 778.1-778.5 eV). X-ray diffraction (XRD) analysis supports the presence of metallic Co hcp phase (2ϴ = 44.47° and 47.43°) in the films.

High Temperature Oxidation Behavior of SUS310S Austenitic Stainless Steel

2014 ◽  
Vol 941-944 ◽  
pp. 212-215
Author(s):  
Tao Zheng ◽  
Jing Tao Han
Keyword(s):  
Photoelectron Spectroscopy ◽  
Oxidation Behavior ◽  
Layer Structure ◽  
Energy Dispersive Spectrometer ◽  
Austenitic Stainless Steels ◽  
Temperature Oxidation ◽  
X Ray ◽  
High Temperature Oxidation Behavior ◽  
High Oxidation Resistance ◽  
Ray Diffusion

The oxidation behavior of SUS310S austenitic stainless steels was studied in isothermal conditions at different temperatures between 800oC and 1100oC for 96h in air. The oxidation kinetics was analyzed, the surface and cross-section of the oxide scale grown by oxidation were characterized by using scanning electron microscopy (SEM), energy dispersive spectrometer (EDS), X-ray diffusion (XRD) and X-ray photoelectron spectroscopy (XPS). The SUS310S steel has high oxidation resistance at 800oC and with the increase of the temperature, the parabolic rate constants is constantly increasing. Examination of the morphology and composition of oxide layers reveals a double-layer structure, The inner layer is mainly chromium oxide (Cr2O3) and is covered by an uneven thinness outer layer of manganese-chromium or iron-chromium spinel oxide.

scholarly journals The effect of cobalt on morphology, structure, and ORR activity of electrospun carbon fibre mats in aqueous alkaline environments

2021 ◽  
Vol 12 ◽  
pp. 1173-1186
Author(s):  
Markus Gehring ◽  
Tobias Kutsch ◽  
Osmane Camara ◽  
Alexandre Merlen ◽  
Hermann Tempel ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Inductively Coupled Plasma ◽  
Elevated Temperatures ◽  
Current Collector ◽  
Alkaline Media ◽  
Emission Spectrometry ◽  
Free Standing ◽  
X Ray ◽  
Turbostratic Carbon ◽  
Current Densities

An innovative approach for the design of air electrodes for metal–air batteries are free-standing scaffolds made of electrospun polyacrylonitrile fibres. In this study, cobalt-decorated fibres are prepared, and the influence of carbonisation temperature on the resulting particle decoration, as well as on fibre structure and morphology is discussed. Scanning electron microscopy, Raman spectroscopy, X-ray diffraction, X-ray photoelectron spectroscopy, elemental analysis, and inductively coupled plasma optical emission spectrometry are used for characterisation. The modified fibre system is compared to a benchmark system without cobalt additives. Cobalt is known to catalyse the formation of graphite in carbonaceous materials at elevated temperatures. As a result of cobalt migration in the material the resulting overall morphology is that of turbostratic carbon. Nitrogen removal and nitrogen-type distribution are enhanced by the cobalt additives. At lower carbonisation temperatures cobalt is distributed over the surface of the fibres, whereas at high carbonisation temperatures it forms particles with diameters up to 300 nm. Free-standing, current-collector-free electrodes assembled from carbonised cobalt-decorated fibre mats display promising performance for the oxygen reduction reaction in aqueous alkaline media. High current densities at an overpotential of 100 mV and low overpotentials at current densities of 333 μA·cm−2 were found for all electrodes made from cobalt-decorated fibre mats carbonised at temperatures between 800 and 1000 °C.

scholarly journals Photocatalytic activity of graphene oxide–TiO 2 thin films sensitized by natural dyes extracted from Bactris guineensis

2019 ◽  
Vol 6 (3) ◽  
pp. 181824 ◽  
Author(s):  
William Vallejo ◽  
Angie Rueda ◽  
Carlos Díaz-Uribe ◽  
Carlos Grande ◽  
Patricia Quintana
Keyword(s):  
Thin Films ◽  
Raman Spectroscopy ◽  
Graphene Oxide ◽  
Photocatalytic Degradation ◽  
Photoelectron Spectroscopy ◽  
Chemical Characterization ◽  
Sem Analysis ◽  
Visible Range ◽  
X Ray ◽  
Natural Sensitizer

This study synthesized and characterized composites of graphene oxide and TiO 2 (GO–TiO 2 ). GO–TiO 2 thin films were deposited using the doctor blade technique. Subsequently, the thin films were sensitized with a natural dye extracted from a Colombian source ( Bactris guineensis ). Thermogravimetric analysis, X-ray diffraction, Raman spectroscopy, scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS) and diffuse reflectance measurements were used for physico-chemical characterization. All the samples were polycrystalline in nature, and the diffraction signals corresponded to the TiO 2 anatase crystalline phase. Raman spectroscopy and Fourier transform infrared spectroscopy (FTIR) verified the synthesis of composite thin films, and the SEM analysis confirmed the TiO 2 films morphological modification after the process of GO incorporation and sensitization. XPS results suggested a possibility of appearance of titanium (III) through the formation of oxygen vacancies (O v ). Furthermore, the optical results indicated that the presence of the natural sensitizer and GO improved the optical properties of TiO 2 in the visible range. Finally, the photocatalytic degradation of methylene blue was studied under visible irradiation in aqueous solution, and pseudo-first-order model was used to obtain kinetic information about photocatalytic degradation. These results indicated that the presence of GO has an important synergistic effect in conjunction with the natural sensitizer, reaching a photocatalytic yield of 33%.

scholarly journals Oil-based mud waste reclamation and utilisation in low-density polyethylene composites

2020 ◽  
Vol 38 (12) ◽  
pp. 1331-1344
Author(s):  
Shohel Siddique ◽  
Kyari Yates ◽  
Kerr Matthews ◽  
Laszlo J Csetenyi ◽  
James Njuguna
Keyword(s):  
Inductively Coupled Plasma ◽  
Oil And Gas ◽  
Microscopic Analysis ◽  
Optical Emission ◽  
Fluorescence Analysis ◽  
Xrd Analysis ◽  
Low Density Polyethylene ◽  
Emission Spectrometry ◽  
Low Density ◽  
X Ray

Oil-based mud (OBM) waste from the oil and gas exploration industry can be valorised to tailor-made reclaimed clay-reinforced low-density polyethylene (LDPE) nanocomposites. This study aims to fill the information gap in the literature and to provide opportunities to explore the effective recovery and recycling techniques of the resources present in the OBM waste stream. Elemental analysis using inductively coupled plasma–optical emission spectrometry (ICP-OES) and X-ray fluorescence analysis, chemical structural analysis by Fourier transform infrared (FTIR) spectroscopy, and morphological analysis of LDPE/organo-modified montmorillonite (LDPE/MMT) and LDPE/OBM slurry nanocomposites by scanning electron microscopy (SEM) have been conducted. Further analysis including calorimetry, thermogravimetry, spectroscopy, microscopy, energy dispersive X-ray analysis and X-ray diffraction (XRD) was carried out to evaluate the thermo-chemical characteristics of OBM waste and OBM clay-reinforced LDPE nanocomposites, confirming the presence of different clay minerals including inorganic salts in OBM slurry powder. The microscopic analysis revealed that the distance between polymer matrix and OBM slurry filler is less than that of MMT, which suggests better interfacial adhesion of OBM slurry compared with the adhesion between MMT and LDPE matrix. This was also confirmed by XRD analysis, which showed the superior delamination structure OBM slurry compared with the structure of MMT. There is a trend noticeable for both of these fillers that the nanocomposites with higher percentage filler contents (7.5 and 10.0 wt% in this case) were indicated to act as a thermal conductive material. The heat capacity values of nanocomposites decreased about 33% in LDPE with 7.5 wt% MMT and about 17% in LDPE with 10.0 wt% OBM slurry. It was also noted, for both nanocomposites, that the residue remaining after 1000°C increases with the incremental wt% of fillers in the nanocomposites. There is a big difference in residue amount (in %) left after thermogravimetric analysis in the two nanocomposites, indicating that OBM slurry may have significant influence in decomposing LDPE matrix; this might be an interesting area to explore in the future. The results provide insight and opportunity to manufacture waste-derived renewable nanocomposites with enhanced structural and thermal properties.

scholarly journals Plasma electrolytic oxidation of metals

2013 ◽  
Vol 78 (5) ◽  
pp. 713-716 ◽  
Author(s):  
Stevan Stojadinovic
Keyword(s):  
Photoelectron Spectroscopy ◽  
Plasma Electrolytic Oxidation ◽  
Dielectric Breakdown ◽  
Optical Emission ◽  
Active Surface ◽  
Spatial Density ◽  
Oxide Coatings ◽  
X Ray ◽  
Electrolytic Oxidation ◽  
Plasma Electrolytic

In this lecture results of the investigation of plasma electrolytic oxidation (PEO) process on some metals (aluminum, titanium, tantalum, magnesium, and zirconium) were presented. Whole process involves anodizing metals above the dielectric breakdown voltage where numerous micro-discharges are generated continuously over the coating surface. For the characterization of PEO process optical emission spectroscopy and real-time imaging were used. These investigations enabled the determination of electron temperature, electron number density, spatial density of micro-discharges, the active surface covered by micro-discharges, and dimensional distribution of micro-discharges at various stages of PEO process. Special attention was focused on the results of the study of the morphology, chemical, and phase composition of oxide layers obtained by PEO process on aluminum, tantalum, and titanium in electrolytes containing tungsten. Physicochemical methodes: atomic force microscopy (AFM), scanning electron microscopy (SEM-EDS), x-ray diffraction (XRD), x-ray photoelectron spectroscopy (XPS), and Raman spectroscopy served as tools for examining obtained oxide coatings. Also, the application of the obtained oxide coatings, especially the application of TiO2/WO3 coatings in photocatalysis, were discussed.

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