Assessment of ODS Ferritic Alloy for Advanced Nuclear Energy System

Author(s):  
Zhangjian Zhou ◽  
Ming Li ◽  
Lu Liao ◽  
Pei He ◽  
Yingli Xu

Development of cladding materials which can work at high temperature is crucial to realize highly efficient and high-burnup operation of Generation IV nuclear energy systems. Oxide dispersion strengthened (ODS) steels are the most promising class of materials with a potential to be used at elevated temperature under severe corrosion and strong neutron exposure environment. ODS ferritic steels with Cr content of 12–18% were designed and fabricated through the mechanical alloying (MA) route. The characterization of ODS ferritic steels were conducted for evaluation their potential applications for advanced nuclear energy system. Mechanical properties were measured at room temperature and high temperature. High-temperature (700 °C–1000 °C) oxidation resistance were carried out using a muffle. Microstructures of the oxidation layer were observed and compared.

2020 ◽  
Vol 999 ◽  
pp. 72-80
Author(s):  
Zhang Jian Zhou ◽  
Ling Zhi Chen ◽  
Yuan Gao ◽  
Qi Wang

The development of materials for core components which can serve in high temperature corrosive environments for a long service time is crucial to realize high efficiency and high-burnup operation of advanced nuclear reactors. Alumina forming austenitic (AFA) alloy is a kind of promising materials with improved corrosion resistance as well as strength at elevated temperature. The progress on the composition design and characterization of AFA alloys are reviewed in this work for evaluation their potential applications in advanced nuclear reactors. AFA alloys without the addition of carbon have been fabricated. Microstructures were observed by SEM and TEM. Mechanical properties were measured at room temperature and high temperature.


2012 ◽  
Vol 18 (S2) ◽  
pp. 1658-1659
Author(s):  
D.T. Hoelzer ◽  
K.A. Unocic ◽  
D.W. Coffey ◽  
Z. Feng

Extended abstract of a paper presented at Microscopy and Microanalysis 2012 in Phoenix, Arizona, USA, July 29 – August 2, 2012.


2006 ◽  
Vol 15-17 ◽  
pp. 696-701 ◽  
Author(s):  
Jung Ho Ahn ◽  
Sang Hyun Lee ◽  
Jin Sung Jang

Oxide-dispersion strengthened (ODS) ferritic stainless steels have been considered as promising high-temperature materials such as interconnects for oxide-fuel cells and nuclear materials for Liquid Metal Fast Reactors or Super-Critical-Water-Cooled Reactors. In the present work, we have prepared Fe-14Cr-2Al-1Si-0.3Ta-1Y2O3 ferritic stainless steels which were dispersion-strengthened by nano-sized Y2O3 via mechanical alloying of elemental powder mixtures and subsequent hot consolidation. A comparison was made with MA 957 and DY-01 alloys. The mechanically alloying behaviour and consolidated mechanical properties of the Fe-14Cr-2Al-1Si- 0.3Ta-1Y2O3 ferritic steels were strongly influenced by processing parameters, especially milling atmosphere. The stability of yttrium oxides and oxidation resistance at high temperatures were examined. The preliminary result shows that the mechanically alloyed Fe-14Cr-2Al-1Si-0.3Ta- 1Y2O3 ferritic stainless steel exhibits interesting properties to be exploited as high temperature materials.


2021 ◽  
Author(s):  
◽  
Sujay Prabakar

<p>This thesis is concerned with the synthesis and characterization of nanostructured materials in the solution, in particular silicon and germanium nanocrystals, their applica-tion as fluorescent whitening agents and titanium disulphide nanostructures. The aim of this research with regards to the synthesis of silicon and germanium nanocrystals was to obtain size control and provide functionality using simple room temperature solution techniques. In the case of the nanostructures of titanium disulphide, the focus was to synthesize in the colloid using simple one-pot bench top techniques. The above were realized with chemical techniques in the solution using organic solvents and surfactants to control their size. The morphology, chemical composition and crystal structure of the synthesized nanomaterials were characterized using techniques such as High Resolution Transmission Electron Microscopy (HRTEM), Selected Area Electron Diffraction (SAED), Scanning Electron Microscopy (SEM), Energy Dispersive X-Ray Spectrosco-py (EDX) and Optical Spectroscopies. Whilst chapter one is a brief introduction of the thesis, chapter two talks in detail about the various characterization techniques used in this research.  Chapter three of the thesis focuses on the synthesis of alkyl- and amine-functionalized silicon nanocrystals using a microemlusion technique. The effect of reducing agents, surfactants and precursors on particle size was studied. The surfactant C12E5 was found to be very effective in producing silicon nanocrystals that were freestanding and pure. Whilst the hydride reducing agents lithium aluminium hydride and lithium tri-ethyl borohydride were found to be effective in synthesizing nanocrystals of narrow size distribution, it was found that using silicon tetrachloride yielded smaller particles compared to silicon tetrabromide.  The fourth chapter in the theses is concerned with the synthesis and characterization of germanium nanocrystals by both microemulsion and high temperature techniques. Using lithium aluminium hydride; a strong reducing agent, very small nanocrystals were obtained, whilst weaker reductants such as sodium borohydride produced larger nano-crystals. Another effective method to control the particle size of germanium nanocrystals was found to be by varying the concentration of precursor. The germanium nanocrystals which were amine capped were found to luminesce in the blue and were used to image HePG2 cells. Toxicity studies on these nanocrystals proved their relative non-toxicity. The high temperature experiments, though not as flexible as the room temperature syntheses were found to facilitate a certain degree of size control.  Chapter five of the theses deal with the application of silicon and germanium nanocrys-tals as fluorescent whitening agents in wool fabrics. Both nanocrystals, when applied to the fabric were found to emit matching blue fluorescence that was demonstrated to be more suited to improving the brightness properties of fabric than the commercial fluo-rescing whitening agent Uvitex. In particular Silicon-amine and Silicon-hexene functionalized nanocrystal (low concentration) treated fabrics were found to have improved color stability against both UVA and UVB radiation. The treated fabrics were in addition found to maintain a stable color than untreated fabric. Silicon-amine treated fabrics were found to have a stable color even after 48h exposures to UVA radiation. It should be noted that this is the first evidence of the application of group IV semiconductor nanocrystals as fluorescing whitening agents.  The sixth chapter of this thesis deals with the one-pot synthesis of titanium disulphide nanostructures using both coordinating and non-coordinating solvents and their subse-quent characterization. By varying the injection temperature of the titanium source into the 1-Octadecene sulphur solution, two different morphologies were synthesized. Two different pathways were suggested for the formation of the flower-like and flake-like morphologies; an instant nucleation to form titanium disulphide flakes whilst spherical nuclei to form flower-like nanostructures. The flower-like nanostructures were found to have higher BET surface area compared to the flake-like nanostructures and previously reported surface areas for analogous TiS₂ nanostructures. Whilst using oleylamine as solvent, the low temperature injection yielded hollow spheres of TiS₂ and the high temperature injection, fullerene-like nanoparticles of TiS₂. The property of oleylamine to selectively bind to the nanostructure surface in conjunction with the effect of injection temperature was understood to be behind the growth of these nanostructures. The synthesis of flower-like and flake-like morphologies by solution phase techniques were the first evidence of this kind for titanium disulphide and provides a new and exciting material for a variety of applications.  A final chapter on conclusions and recommendations for future work is then presented.</p>


2001 ◽  
Vol 7 (S2) ◽  
pp. 550-551
Author(s):  
E.A. Kenik ◽  
D. Hoelzer ◽  
P.J. Maziasz ◽  
M.K. Miller

The high temperature application of iron-based ferritic alloys is limited by their rapid decrease of yield strength at temperatures approaching 1000°C. It has been shown that mechanical-alloying (MA) to produce oxide dispersion-strengthened (ODS) ferritic alloys improves their high temperature mechanical properties. Prior characterization of such materials has shown that in certain as-processed alloys the original yttria oxide particles are replaced by nanoscale (2-5 nm diameter) clusters containing Ti, Y and O. As a result of the high density of these fine clusters, dislocation pinning produced a ∼10-fold increase in dislocation density relative to similar ODS materials not exhibiting the nanoscale clustering. The improved creep resistance of the clustered material was attributed both to the higher dislocation density, additional dislocation pinning and resistance to recovery during creep. The current work examines clustering in a related alloy, as well as the effects of high temperature creep on the stability of such clusters.


Author(s):  
J. A. Sutliff ◽  
B. P. Bewlay

In-situ composite Nb-Si alloys have been studied by several investigators as potential high temperature structural materials. The two major processing routes used to fabricate these composites are directional solidification and extrusion of arc-cast solidified ingots. In both cases a stable microstructure of primary Nb dendrites in a eutectoid of Nb and Nb5Si3 phases is developed after heat treatment. The Nb5Si3 phase is stable at room temperature and forms as a decomposition product of the high temperature Nb3Si phase. The anisotropic microstructures developed by both directional solidification and extrusion require evaluation of the texture to fully interpret the fracture and other orientation dependent mechanical behavior of these composites.In this paper we report on the microstructural characterization of a directionally solidified (DS) and heat treated Nb-16 at.%Si alloy. The microtexture of each of the phases (Nb, Nb5Si3) was determined using the Electron BackScattering Pattern (EBSP) technique for electron diffraction in the scanning electron microscope. A system employing automatic diffraction pattern recognition, crystallographic analysis, and sample or beam scanning was used to acquire the microtexture data.


2010 ◽  
Vol 638-642 ◽  
pp. 3833-3838 ◽  
Author(s):  
Chun Liang Chen ◽  
G.J. Tatlock ◽  
Andy R. Jones

Oxide Dispersion Strengthened (ODS) Fe-based alloys often contain 0.5wt% of fine, uniformly dispersed, yttrium oxide particles in a Fe-Cr-Al matrix. They are ideal candidates for high temperature applications such as high temperature heat exchangers or nuclear power plants due to their good combination of creep and oxidation resistance. Numerous studies of annealing phenomena have shown that nucleation and growth of recrystallized grains, as well as the recrystallization texture, strongly depend on the deformed state of a previously cold worked alloy. In the present work, we examined the effect of strain heterogeneity on the development of recrystallized grain structures using bend samples. A bend test introduces a stress gradient and both compressive and tensile deformation. After a further heat treatment at 1380°C for 1 hour in air, the recrystallization behavior was characterized on both the tension and compression sides of the samples at varied levels of strain. Electron backscattering diffraction (EBSD) was used to analyze recrystallization behavior and texture. The results demonstrated that: recrystallized grains only formed in areas of sample subject to plastic compression; maximum grain size increased with increasing severity of bending deformation; there was heterogeneity in the recrystallized grain size, which varied with distance from the bending neutral axis. This indicates that the strain heterogeneity conducive to recrystallization was introduced by the non-uniform plastic strains in the compression region. However, the regions of tensile bending in all samples remained unrecrystallized and strong shear banding was evident.


2011 ◽  
Vol 66 (2) ◽  
pp. 107-114 ◽  
Author(s):  
Stephanie C. Neumair ◽  
Johanna S. Knyrim ◽  
Oliver Oeckler ◽  
Reinhard Kaindl ◽  
Hubert Huppertz

The cubic iron hydroxy boracite Fe3B7O13OH・1.5H2O was synthesized from Fe2O3 and B2O3 under high-pressure/high-temperature conditions of 3 GPa and 960 °C in a modified Walker-type multianvil apparatus. The crystal structure was determined at room temperature by X-ray diffraction on single crystals. It crystallizes in the cubic space group F4̄3c (Z = 8) with the parameters a = 1222.4(2) pm, V = 1.826(4) nm3, R1 = 0.0362, and wR2 = 0.0726 (all data). The B-O network is similar to that of other cubic boracites.


Author(s):  
S. D. Walck ◽  
J. S. Zabinski ◽  
N.T. McDevitt ◽  
J. E. Bultman

ZnO-WS2 is a potential high temperature solid film lubricant for aerospace applications that exhibits adaptive lubricant behavior. An adaptive lubricant undergoes phase and/or chemical changes in response to thermal, environmental, and tribological conditions; with the resulting phase or wear debris also being lubricious. Pulsed laser deposited (PLD) ZnO-WS2 thin films deposited at room temperature (RT) and wear-tested at room temperature have been shown to have coefficients of friction of 0.04 or less which are comparable to WS2 films, but have much longer wear lives. In the as-deposited state, PLD ZnO-WS2 films are amorphous, but when wear-tested, the phases WS2, WO3, and ZnWO4 are produced. Of these, WS2 is a lubricant phase at low temperatures (⪯ ~450°C) while ZnWO4 is a lubricant phase above about 600°C. The purpose of this work was to characterize the microstructural and chemical changes that occur when the RT-PLD ZnO-WS2 films are heated in air.The RT-PLD ZnO-WS2 films were deposited in a system having a base pressure of 9×l0-7 Pa with a typical pressure during deposition of 6×10-5 Pa.


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