scholarly journals Synthesis of NiO Nanotubes via a Dynamic Thermal Oxidation Process

Materials ◽  
2019 ◽  
Vol 12 (5) ◽  
pp. 805 ◽  
Author(s):  
Wenfeng Xiang ◽  
Zibin Dong ◽  
Yi Luo ◽  
Jiali Zhao ◽  
Jia-ou Wang ◽  
...  
Keyword(s):  
Thermal Oxidation ◽  
Photoelectron Spectroscopy ◽  
Oxidation Process ◽  
X Ray Diffraction ◽  
Critical Transition Temperature ◽  
X Ray ◽  
Annealing Temperatures ◽  
Thermal Oxidation Process ◽  
Shell Nanowires ◽  
Scanning Electron

Nickel oxide (NiO) nanotubes were synthesized via a thermal oxidation process from Ni nanowires. The effects of oxidation temperature on the morphology, microstructures, and composition of nanowires were investigated using scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy. The results show that the Ni nanowires convert initially to Ni/NiO core-shell nanowires with increasing annealing temperatures, and then to the nanotubes at the critical transition temperature of about 425 °C. Our findings provide useful information for the preparation of NiO nanotubes to meet the required applications.

SURFACE MORPHOLOGY AND X-RAY DIFFRACTION ANALYSIS FOR SILICON NANOCRYSTAL-BASED HETEROSTRUCTURES

2013 ◽  
Vol 20 (05) ◽  
pp. 1350046 ◽  
Author(s):  
EVAN T. SALIM
Keyword(s):  
Surface Morphology ◽  
Thermal Oxidation ◽  
Oxidation Process ◽  
Oxidation Temperature ◽  
Silicon Nanocrystal ◽  
X Ray Diffraction ◽  
X Ray ◽  
Rapid Thermal Oxidation ◽  
O Phase ◽  
Thermal Oxidation Process

In this work, we studied the effect of rapid thermal oxidation process on the structural and surface morphology of silicon nanocrystal-based heterostructures. PLD technique was employed in combination with rapid thermal oxidation process to form multilayers heterostructures. Results show the dependence of the surface roughness and structure on the oxidation temperature. Best surface morphology was achieved at 723 K oxidation temperature, at which, the X-ray diffraction result ensured the formation of the Cu 2 O phase at (111) and (002) diffraction plain with uniform porous surface.

EFFECT OF PRE-ANNEALING TEMPERATURE ON THE GROWTH OF ALIGNED α-Fe2O3 NANOWIRES VIA A TWO-STEP THERMAL OXIDATION

2016 ◽  
Vol 23 (04) ◽  
pp. 1650027
Author(s):  
NORHANA MOHAMED RASHID ◽  
NAOKI KISHI ◽  
TETSUO SOGA
Keyword(s):  
Thermal Oxidation ◽  
Annealing Temperature ◽  
Oxidation Process ◽  
High Density ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dry Air ◽  
Small Grains ◽  
Xrd Patterns ◽  
Thermal Oxidation Process

Pre-annealing as part of a two-step thermal oxidation process has a significant effect on the growth of hematite ([Formula: see text]-Fe2O3) nanowires on Fe foil. High-density aligned nanowires were obtained on iron foils pre-annealed at 300[Formula: see text]C under a dry air flow for 30[Formula: see text]min. The X-ray diffraction (XRD) patterns indicate that the nanowires are transformed from the small [Formula: see text]-Fe2O3 grains and uniquely grow in the (110) direction. The formation of a high-density of small grains by pre-annealing improved the alignment and density of the [Formula: see text]-Fe2O3 nanowires.

ROOM TEMPERATURE PHOTOLUMINESCENCE OF POLYCRYSTALLINE SIC PREPARED FROM CARBON-SATURATED SI MELT

2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Room Temperature ◽  
Uv Light ◽  
X Ray Diffraction ◽  
X Ray ◽  
Room Temperature Photoluminescence ◽  
Composition And Structure ◽  
Light Excitation ◽  
Scanning Electron

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.

Synthesis and characterization of homogeneous lead-substituted tin oxide with the (110) face of rutile structure

2000 ◽  
Vol 15 (10) ◽  
pp. 2076-2079
Author(s):  
Chika Nozaki ◽  
Takashi Yamada ◽  
Kenji Tabata ◽  
Eiji Suzuki
Keyword(s):  
Electron Microscopy ◽  
Tin Oxide ◽  
Photoelectron Spectroscopy ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
Rutile Structure ◽  
X Ray ◽  
Transmission Electron ◽  
Scanning Electron

Synthesis of a rutile-type lead-substituted tin oxide with (110) face was investigated. The characterization was performed by x-ray diffraction, scanning electron microscopy, transmission electron microscopy, energy dispersive x-ray spectroscopy, infrared spectroscopy, x-ray photoelectron spectroscopy, and Brunauer–Emmett–Teller surface area measurements. The homogeneous rutile-type lead-substituted tin oxide was obtained until 4.1 mol% of tin was substituted with lead. The surface of obtained oxide had a homogeneously lead-substituted (110) face.

scholarly journals Reduced Graphene Oxide–Epoxy Grafted Poly(Styrene-Co-Acrylate) Composites for Corrosion Protection of Mild Steel

Coatings ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. 666
Author(s):  
Xinchuan Fan ◽  
Yue Hu ◽  
Yijun Zhang ◽  
Jiachen Lu ◽  
Xiaofeng Chen ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Corrosion Properties ◽  
X Ray ◽  
Transmission Electron ◽  
Reduced Graphene ◽  
Scanning Electron

Reduced graphene oxide–epoxy grafted poly(styrene-co-acrylate) composites (GESA) were prepared by anchoring different amount of epoxy modified poly(styrene-co-acrylate) (EPSA) onto reduced graphene oxide (rGO) sheets through π–π electrostatic attraction. The GESA composites were characterized by Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The anti-corrosion properties of rGO/EPSA composites were evaluated by electro-chemical impedance spectroscopy (EIS) in hydroxyl-polyacrylate coating, and the results revealed that the corrosion rate was decreased from 3.509 × 10−1 to 1.394 × 10−6 mm/a.

Effect of Cu Content on the Tribological Performance of Cr-N Coatings at High Temperatures (840°C)

2009 ◽  
Author(s):  
Kyriaki Polychronopoulou ◽  
Claus Rebholz ◽  
Nicholaos G. Demas ◽  
Andreas A. Polycarpou ◽  
P. N. Gibson
Keyword(s):  
Vapor Deposition ◽  
Photoelectron Spectroscopy ◽  
Physical Vapor Deposition ◽  
Tribological Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Cu Content ◽  
Glancing Angle ◽  
Scanning Electron ◽  
Ball On Disc

Cr-N and Cu-Cr-N coatings with Cu content between 3–65 at.%, Cu/Cr ratios in the 0.04–4.5 range and 21–27 at.% N, synthesized by twin e-beam Physical Vapor Deposition (EBPVD) at 450°C, were investigated. Using X-ray photoelectron spectroscopy (XPS), glancing angle X-ray diffraction (GAXRD) and scanning electron microscopy (SEM), in combination with nanoindentation mechanical property measurements and laboratory controlled ball-on-disc sliding experiments, it is shown that Cu-Cr-N coatings with low Cu content (3 at.%) possess sufficient wear resistance for high temperature demanding tribological applications.

scholarly journals Preparation of Cerium Dioxide Layers on Titanium by Electrodeposition with Organic Solution

2017 ◽  
Vol 2017 ◽  
pp. 1-9
Author(s):  
Vaijayanti Namdeo Nande ◽  
Diana Kostyukova ◽  
Jeonghee Choi ◽  
Yong Hee Chung
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Cerium Dioxide ◽  
Average Crystallite Size ◽  
X Ray Diffraction ◽  
Organic Solution ◽  
X Ray ◽  
Titanium Foils ◽  
Scanning Electron

Layers of cerium dioxide nanoparticles were prepared on titanium by electrodeposition with organic solution. Three concentrations of cerium ions were used at 31.6 V. The organic solution was isobutanol and titanium foils were used as anodes and cathodes. Currents were monitored during the electrodeposition. Deposition times ranged from 0.5 to 8 h. Deposited Deposited layers were calcined at 700 K for 30 min. The morphology and composition of the deposited layers were examined by scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). As-prepared and calcined deposition layers were assayed to be cerium dioxide. The average crystallite size increased from 4 to 7 nm through calcination at 700 K. Sizes of calcined cerium oxide agglomerates were ranging from 73 to 146 nm for 30 min deposition and 209 to 262 nm for 8 h deposition. The electrodeposition efficiencies of 0.5 h deposition at three concentrations were measured to be highest.

Photoelectrocatalytic Degradation of HCB by N-Doped TiO2 Nanotube Arrays

2013 ◽  
Vol 652-654 ◽  
pp. 1580-1584
Author(s):  
Yu Jiang Guan ◽  
Zi Bo Wang ◽  
Shu Li Bai ◽  
Qin Xue
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ph Value ◽  
Nanotube Arrays ◽  
Simulated Sunlight ◽  
X Ray Diffraction ◽  
X Ray ◽  
Photoelectrocatalytic Degradation ◽  
Doping Behavior ◽  
Doped Titanium Dioxide ◽  
Scanning Electron

N-doped Titanium dioxide (TiO2) nanotube arrays were characterized by scanning electron microscope (SEM)，X-ray Diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) to analyse its surface morphology, crystal types and the doping behavior of nitrogen. The material was used as electrode for photoelectrocatalytic degradation of hexachlorobenzen under irradiation of simulated sunlight. The effects of photocatalysis, electrocatalysis, photoelectrocatalysis, the concentration of Na2SO4 and pH value on degradation of HCB were investigated.

Preparation and Characterization of N Doped TiO2/ Sepiolite Composite Materials

2011 ◽  
Vol 284-286 ◽  
pp. 597-600
Author(s):  
Dai Mei Chen ◽  
Hai Peng Ji ◽  
Jian Xin Wang ◽  
Jian Chen ◽  
Xin Long Luan ◽  
...  
Keyword(s):  
Composite Materials ◽  
Photoelectron Spectroscopy ◽  
Sol Gel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nitrogen Doped ◽  
Nitrogen Contents ◽  
Scanning Electron ◽  
Oxygen Atoms

Nitrogen doped TiO2/sepiolite composite materials (N-TiO2/sep) with different nitrogen contents were prepared by a sol-gel method and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), respectively. XRD and SEM results showed that anatase-TiO2nanoparticles were distributed homogenously on the surface of sepiolite. XPS revealed that N atoms could incorporate into the lattice of anatase TiO2substituting the oxygen atoms sites of oxygen atoms.

Behavior of UO2 in the RBMK-1000 Spent Fuel under Oxidizing Conditions

2004 ◽  
Vol 824 ◽  
Author(s):  
A. B. Kolyadin ◽  
V. Ya. Mishin ◽  
K. Ya. Mishin ◽  
A. S. Aloy ◽  
T. I. Koltsova
Keyword(s):  
Thermal Oxidation ◽  
Spent Nuclear Fuel ◽  
Oxidation Process ◽  
Spent Fuel ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dry Storage ◽  
Different Temperatures ◽  
Xrd Techniques

AbstractThe oxidation of UO2–type spent nuclear fuel (SNF) in gaseousmedia was studied at different temperatures and oxygen contents using gravimetric and powder X-ray diffraction (XRD) techniques. The aim of the study was to determine the mechanism(s) of thermal-oxidation alteration of SNF during long-term dry storage. The samples used in the experiments were chips of RBMK-1000 fuel rods.Oxidation of UO2with a mean burn-up of 10.7 and 19.73 MW d/kg in humid air was observed at a temperature as low as 150°C. At 200°C nearly all of the UO2was transformed into U3O8 between 3500-4000 hours. In a humid nitrogen environment containing of 0.05-1.3 vol. % oxygen at 300°C, the UO2 completely transformed to U3O8 between 2500-3000 hours. Oxidation of UO2in samples with small amounts of jacket damage (e.g., <0.04 MM2)ll progresses more slowly and after â3000 hours the oxygen-to-uranium ratio was 2.56.Stabilization of the oxidation process was not observed in the fuel samples upto an O/U ratio of 2.4, which may be attributed to the smallburn-up of the fuel under investigation.

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