scholarly journals Oxidation Mechanism of Al-Sn Bearing Alloys

Materials ◽  
2021 ◽  
Vol 14 (17) ◽  
pp. 4845
Author(s):  
Qiaoqin Guo ◽  
Jihui Chen ◽  
Jianping Li ◽  
Yongchun Guo ◽  
Zhong Yang ◽  
...  
Keyword(s):  
Oxidation Rate ◽  
Oxidation Mechanism ◽  
Oxidation Products ◽  
Oxidation Temperature ◽  
Alloy Surface ◽  
X Ray Diffraction ◽  
And Performance ◽  
Approach Zero ◽  
Bearing Alloy ◽  
Oxidation Weight Gain

Oxidation of Al-Sn bearing alloy occurs during production, processing and use, which reduces both alloy performance and performance of coatings applied to the alloy surface. Therefore, the oxidation mechanism of Al-Sn bearing alloy is studied at 25, 180, 300, and 500 °C. The oxidation morphologies of the alloy were observed by scanning electron microscopy (SEM), and the oxidation products were determined by X-ray diffraction (XRD). The oxidation weight gain curves were obtained by thermogravimetric analysis. The experimental results show that: Al-Sn bearing alloy is oxidized quickly to form Al2O3. As the oxidation temperature increases, Sn phase start to precipitate along the grain boundary and form networked spheroids of Sn on the alloy surface. The amount of precipitation increases with further increase of the oxidation temperature. Cracks and holes are left in the alloy. The oxide layer is mainly composed of Sn, SnO2, and Al2O3. At 25 °C, oxidation rate of Al-Sn alloy approach zero. At 180, 300, and 500 °C, the oxidation rate increases quickly conforming to a power function, and eventually remains stable at about 3 × 10−6 mg·mm−2·s−1.

scholarly journals Effect of Y on the Oxidation Behavior of a Directionally Solidified Ni-based Single Crystal Superalloy

2020 ◽  
Author(s):  
Zihan Zhao ◽  
Kai Guan ◽  
Renjie Cui ◽  
Jianchao Qin ◽  
Zhaohui Huang
Keyword(s):  
Weight Gain ◽  
Single Crystal ◽  
Oxide Scale ◽  
Oxidation Rate ◽  
Oxidation Behavior ◽  
Isothermal Oxidation ◽  
Oxidation Products ◽  
Single Crystal Superalloy ◽  
Directionally Solidified ◽  
Oxidation Weight Gain

Abstract The effect of Y addition on the oxidation behavior of a Ni-based directionally solidified single crystal superalloy was investigated. Isothermal oxidation test for the samples with different-level Y addition was conducted at 1100℃ in air. The Y content of the samples was demarcated by the actual pickup amount resulted from ICP-AES test. It was found that the addition of Y increased the oxide resistance by an adhesive double-layer oxide scale which was composed of Al2O3 and spinel Ni(Cr,Al)2O4. With 70ppm Y addition, the oxidation weight gain was decreased from 12.6g/m2 for the alloy without Y addition to 5.3g/m2, and the oxidation rate was significantly decreased. Besides, the internal nitride also disappeared after Y doping because of the increasing oxidation scale adherence and the decreasing of oxidation products. In this study, 660ppm Y addition alloy showed the best oxidation resistance.

High Temperature Oxidation Behaviour of Tial8Nb Alloy

2013 ◽  
Vol 58 (2) ◽  
pp. 477-480 ◽  
Author(s):  
K. Przybylski ◽  
J. Prazuch ◽  
T. Brylewski ◽  
E. Durda
Keyword(s):  
Oxidation Mechanism ◽  
Isothermal Oxidation ◽  
Metallic Substrate ◽  
Oxidation Products ◽  
X Ray Diffraction ◽  
Temperature Oxidation ◽  
X Ray ◽  
Cycle 24 ◽  
Oxidation In Air ◽  
Kinetics Of

The goal of this work is to determine the effect of niobium on the kinetics and mechanism of Ti-Al oxidation in air. In order to compare the oxidation kinetics of Ti-Al and Ti-Al with the addition of niobium, isothermal oxidation was performed on Ti-48Al and Ti-46Al-8Nb (in at.%) alloys at 1073 K in synthetic air. Cyclic oxidation of Ti-46Al and Ti-46Al-8Nb alloys was carried out in laboratory air for 42 cycles (1 cycle, 24 hrs). The morphology, as well as chemical and phase composition of the oxidation products were investigated using X-ray Diffraction (XRD) and Scanning Electron Microscopy combined with Energy Dispersive Spectroscopy (SEM-EDS). From these investigations it can be concluded that niobium addition increases the corrosion resistance of TiAl and, furthermore, improves the adherence between the metallic substrate and the oxide scale. The oxidation mechanism of Ti-46Al-8Nb was studied via secondary neutral mass spectroscopy (SNMS) after two-stage isothermal oxidation (24 hrs in 16O2 followed by 24 hrs in 18O2) at 1073 K. From this analysis it can be assumed that the oxidation mechanism of Ti-46Al-8Nb alloy consists of simultaneous outward titanium and aluminum diffusion and inward oxygen transport.

The High Temperature Oxidation Resistance and Anti-Oxidation Mechanism of Plasma-Sprayed NiCrAlY Coatings on Stainless Stell

2013 ◽  
Vol 652-654 ◽  
pp. 1814-1817
Author(s):  
Yan Ping Qu ◽  
Ji Shuang Qu ◽  
Jia Tao Liu ◽  
Yan Feng Wang
Keyword(s):  
Oxidation Reaction ◽  
Oxidation Mechanism ◽  
Oxidation Products ◽  
X Ray Diffraction ◽  
Al2o3 Film ◽  
Temperature Oxidation ◽  
Three Stages ◽  
Α Al2o3 ◽  
Plasma Sprayed ◽  
Superficial Coating

The coating was made of base coating (NiCrAlY) and superficial coating (ZrO2 + Y2O3) by plasma spray. The microstructure and phase structure of the coating were investigated by using the scanning electron microscope and the X-ray diffraction. The oxidation process can be divided into three stages: The main oxidation products is θ-Al2O3 but not continuous α-Al2O3 film in oxidation prophase; Continuous α-Al2O3 film generated quickly with the transition of θ-Al2O3 to α-Al2O3 in the oxidation reaction. The oxidation reaction becomes complicated when the content of Al decrease and Ni is also oxidized to NiO. Oxidation kinetics curves of 1200°C is basically accord with parabolic law.

scholarly journals Novel Preparation of Noncovalent Modified GO Using RAFT Polymerization to Reinforce the Performance of Waterborne Epoxy Coatings

Coatings ◽  
2019 ◽  
Vol 9 (6) ◽  
pp. 348 ◽  
Author(s):  
Baolei Liu ◽  
Mingqian Wang ◽  
Ying Liang ◽  
Zhicheng Zhang ◽  
Guohong Ren ◽  
...  
Keyword(s):  
Raft Polymerization ◽  
Salt Spray ◽  
Thermo Gravimetric Analysis ◽  
Analytical Techniques ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
Block Polymer ◽  
Reversible Addition ◽  
Waterborne Epoxy ◽  
And Performance

This work launches the first-ever report on the fabrication of waterborne epoxy-graphene oxide (GO) coatings (WEGC) using a block polymer as a dispersant of GO, wherein the block polymer was synthesized via reversible addition-fragmentation chain transfer (RAFT) polymerization of acrylic acid and oligo(ethylene glycol) methyl ether methacrylate A number of analytical techniques, such as Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), thermo gravimetric analysis (TGA), and salt spray tests, were utilized to explore the morphology and performance of the WEGC. It was confirmed that POEGMA950-b-PAA attached to the GO nanosheets, increasing the integral space of the sheets. Modified GO (MGO) layers were well-dispersed in the epoxy matrix through the formation of a GO-dispersant-epoxy ternary molecular structure. Furthermore, the presence of MGO substantially influenced the thermal properties, mechanical properties, and anticorrosion performance of the WEGC. TGA, salt spray tests, and pull-off testsshowed that 0.5 wt.% MGO content achieved the greatest improvement in the evaluated properties.

Effect of Modified NanoSiO2 Agents on the Morphologies and Performances of UHMWPE Microporous Membrane via Thermally Induced Phase Separation

2016 ◽  
Vol 848 ◽  
pp. 726-732 ◽  
Author(s):  
Rong Liu ◽  
Yan Wang ◽  
Jing Zhu ◽  
Zu Ming Hu ◽  
Jun Rong Yu
Keyword(s):  
Phase Separation ◽  
Water Flux ◽  
Microporous Membranes ◽  
Thermally Induced Phase Separation ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Thermally Induced ◽  
And Performance ◽  
Surface Modified ◽  
Ultra High Molecular Weight

The effects of Modified NanoSiO2 Agents on the morphology and performance of ultra-high-molecular weight polyethylene (UHMWPE) microporous membranes via thermally induced phase separation were investigated in this work. The NanoSiO2 was surface modified by silane coupling agent KH570 (KH570-NanoSiO2). Differential scanning calorimetry (DSC) and X-Ray Diffraction (XRD) were performed to obtain crystallization of UHMWPE/white oil/ KH570-NanoSiO2 doped system. The morphology and performance of the prepared UHMWPE microporous membranes were characterized with scanning electron microscopy (SEM) and microfiltration experiments. The results showed that the morphology of UHMWPE membrane could be disturbed by KH570-NanoSiO2. Porosity and the rejection of Bovine serum albumin (BSA) of the blend membrane increased with increasing concentration of Modified NanoSiO2, while the water flux slightly decreased.

The Effect of Ge Segregation on Oxidation of Si

1987 ◽  
Vol 105 ◽  
Author(s):  
E. C. Frey ◽  
N. R. Parikh ◽  
M. L. Swanson ◽  
M. Z. Numan ◽  
W. K. Chu
Keyword(s):  
High Pressure ◽  
Low Temperature ◽  
Epitaxial Layer ◽  
Atmospheric Pressure ◽  
Oxidation Rate ◽  
Oxidation Temperature ◽  
Pressure Oxidation ◽  
Enhanced Oxidation ◽  
High Pressure Oxidation

AbstractWe have studied oxidation of various Si samples including: Ge implanted Si, CVD and MBE grown Si(0.4–4% Ge) alloys, and MBE grown Si-Si(Ge) superlattices. The samples were oxidized in pyrogenic steam (800–1000°C, atmospheric pressure) and at low temperature and high pressure (740°C, 205 atm of dry O2). The oxidized samples were analyzed with RBS/channeling and ellipsometry.An enhanced oxidation rate was seen for all Ge doped samples, compared with rates for pure Si. The magnitude of the enhancement increased with decreasing oxidation temperature. For steam oxidations the Ge was segregated from the oxide and formed an epitaxial layer at the Si-SiO2 interface; the quality of the epitaxy was highest for the highest oxidation temperatures. For high pressure oxidation the Ge was trapped in the oxide and the greatest enhancement in oxidation rate (>100%) was observed.

Study on the Preparation and Performance of Carboxymethyl Chitosan Calcium and Carboxymethyl Chitosan Zinc Composite Materials

2016 ◽  
Vol 852 ◽  
pp. 1319-1324 ◽  
Author(s):  
Jing Li ◽  
Chang Ping Wei ◽  
Feng Ming Wang ◽  
Li Dan Dong ◽  
Shuang Sun ◽  
...  
Keyword(s):  
Chloride Solution ◽  
Water Solubility ◽  
Chloroacetic Acid ◽  
Sem Analysis ◽  
Carboxymethyl Chitosan ◽  
X Ray Diffraction ◽  
Test Study ◽  
Alkaline Conditions ◽  
And Performance ◽  
Better Than

In this paper,under alkaline conditions,with chloroacetic acid to modify chitosan,obtained carboxymethyl chitosan. At pH<7 conditions,the obtained carboxymethy chitosan respectively were reacted with calcium chloride solution,zinc chloride solution,after fully reacted,obtained carboxymethyl chitosan calcium and carboxymethyl chitosan zinc .Through infrared spectrum,X-ray diffraction and scanning electron microscopy (sem) analysis means,the structure of the products were characterized.Through the cutting of mice tail hemostasia test ,study the performance of the product.The results showed that the water solubility of carboxymethyl chitosan is better than that of chitosan and with excellent performance,and the performance of carboxymethyl chitosan calcium and carboxymethyl chitosan zinc was better than that of carboxymethyl chitosan.

scholarly journals In situ observation of phase changes of a silica-supported cobalt catalyst for the Fischer–Tropsch process by the development of a synchrotron-compatible in situ/operando powder X-ray diffraction cell

2018 ◽  
Vol 25 (6) ◽  
pp. 1673-1682 ◽  
Author(s):  
Adam S. Hoffman ◽  
Joseph A. Singh ◽  
Stacey F. Bent ◽  
Simon R. Bare
Keyword(s):  
High Pressure ◽  
Elevated Pressure ◽  
Phase Changes ◽  
In Situ Observation ◽  
X Ray Diffraction ◽  
Fischer Tropsch ◽  
X Ray ◽  
And Performance ◽  
Co Nanoparticles

In situ characterization of catalysts gives direct insight into the working state of the material. Here, the design and performance characteristics of a universal in situ synchrotron-compatible X-ray diffraction cell capable of operation at high temperature and high pressure, 1373 K, and 35 bar, respectively, are reported. Its performance is demonstrated by characterizing a cobalt-based catalyst used in a prototypical high-pressure catalytic reaction, the Fischer–Tropsch synthesis, using X-ray diffraction. Cobalt nanoparticles supported on silica were studied in situ during Fischer–Tropsch catalysis using syngas, H2 and CO, at 723 K and 20 bar. Post reaction, the Co nanoparticles were carburized at elevated pressure, demonstrating an increased rate of carburization compared with atmospheric studies.

scholarly journals Formation and sink of glyoxal and methylglyoxal in a polluted subtropical environment: observation-based photochemical analysis and impact evaluation

2020 ◽  
Vol 20 (19) ◽  
pp. 11451-11467
Author(s):  
Zhenhao Ling ◽  
Qianqian Xie ◽  
Min Shao ◽  
Zhe Wang ◽  
Tao Wang ◽  
...  
Keyword(s):  
Southern China ◽  
Oxidation Mechanism ◽  
Receptor Site ◽  
Oxidation Products ◽  
Chemical Mechanism ◽  
Major Pathway ◽  
Mixing Ratios ◽  
Heterogeneous Processes ◽  
The Pearl River ◽  
Improved Model

Abstract. The dicarbonyls glyoxal (Gly) and methylglyoxal (Mgly) have been recognized as important precursors of secondary organic aerosols (SOAs) through the atmospheric heterogeneous process. In this study, field measurement was conducted at a receptor site in the Pearl River Delta (PRD) region in southern China, and an observation-based photochemical box model was subsequently applied to investigate the production and evolution of Gly and Mgly as well as their contributions to SOA formation. The model was coupled with a detailed gas-phase oxidation mechanism of volatile organic compounds (VOCs) (i.e., Master Chemical Mechanism, MCM, v3.2), heterogeneous processes of Gly and Mgly (i.e., reversible partitioning in aqueous phase, irreversible volume reactions and irreversible surface uptake processes), and the gas–particle partitioning of oxidation products. The results suggested that without considering the heterogeneous processes of Gly and Mgly on aerosol surfaces, the model would overpredict the mixing ratios of Gly and Mgly by factors of 3.3 and 3.5 compared to the observed levels. The agreement between observation and simulation improved significantly when the irreversible uptake and the reversible partitioning were incorporated into the model, which in total both contributed ∼ 62 % to the destruction of Gly and Mgly during daytime. Further analysis of the photochemical budget of Gly and Mgly showed that the oxidation of aromatics by the OH radical was the major pathway producing Gly and Mgly, followed by degradation of alkynes and alkenes. Furthermore, based on the improved model mechanism, the contributions of VOC oxidation to SOA formed from gas–particle partitioning (SOAgp) and from heterogeneous processes of Gly and Mgly (SOAhet) were also quantified. It was found that o-xylene was the most significant contributor to SOAgp formation (∼ 29 %), while m,p-xylene and toluene made dominant contributions to SOAhet formation. Overall, the heterogeneous processes of Gly and Mgly can explain ∼ 21 % of SOA mass in the PRD region. The results of this study demonstrated the important roles of heterogeneous processes of Gly and Mgly in SOA formation and highlighted the need for a better understanding of the evolution of intermediate oxidation products.

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