Deformation Behavior of Bulk Amorphous Zr-Base Alloys

1998 ◽  
Vol 554 ◽  
Author(s):  
A. Leonhard ◽  
M. Heilmaier ◽  
J. Eckert ◽  
L. Schultz
Keyword(s):  
Room Temperature ◽  
Small Volume ◽  
Volume Fraction ◽  
High Volume ◽  
X Ray Diffraction ◽  
Crystalline Phases ◽  
Ni Alloys ◽  
Young’S Moduli ◽  
Transmission Electron ◽  
Complex Parts

AbstractBulk Zr-Al-Cu-Ni alloys were produced by die casting into a copper mold under Aratmosphere. The microstructure of fully amorphous as well as partially crystalline samples was analyzed by X-ray diffraction (XRD), scanning (SEM) and transmission electron microscopy (TEM), and chemical analysis with special emphasis on the size and composition of the crystallites. The mechanical behavior of the different samples was investigated by constant compression rate tests. At room temperature the samples show inhomogeneous deformation and, independent of the chosen composition, relatively low Young's moduli of about 70 GPa, flow stresses around 2 GPa and elastic strains of up to 3 %. Fully amorphous samples show microplasticity of up to 2 % strain without significant work hardening while specimens with a fairly high volume fraction of crystalline phases are extremely brittle. In contrast, at high temperatures around the glass transition temperature T8 both amorphous and partially crystalline specimens exhibit at low strain rates homogeneous deformation with an initial stress overshoot followed by an extended region of plastic flow. As compared to room temperature, the peak stresses are much lower and are hardly influenced by the presence of small volume fractions of crystalline phases. The observed thermal stability against crystallization provides a promising possibility for easy shaping of complex parts at temperatures around Tg.

Synthesis of nanostructured metal (Fe, Al)-C60 composites

2010 ◽  
Vol 1276 ◽  
Author(s):  
I. I. Santana García ◽  
V. Garibay Febles ◽  
H. A. Calderon
Keyword(s):  
Raman Spectroscopy ◽  
Mechanical Milling ◽  
Volume Fraction ◽  
High Volume ◽  
X Ray Diffraction ◽  
Nanostructured Composite ◽  
Plasma Sintering ◽  
Transmission Electron ◽  
Show Evidence ◽  
Spark Plasma

AbstractComposites of M-2.5 mol. % Fullerene C60 composites (where M= Fe or Al) are prepared by mechanical milling and Spark Plasma Sintering (SPS). The SPS technique has been used to consolidate the resulting powders and preserve the massive nanostructure. Results of X-Ray Diffraction and Raman Spectroscopy show that larger milling balls (9.6 mm in diameter) produce transformation of the fullerene phase during mechanical milling. Alternatively smaller milling balls (4.9 mm in diameter) allow retention of the fullerene phase. SEM shows homogeneous powders with different particle sizes depending on milling times. Sintering produces nanostructured composite materials with different reinforcing phases including C60 fullerenes, diamonds and metal carbides. The presence of each phase depends characteristically on the energy input during milling. Transmission Electron Microscopy (TEM) and Raman Spectroscopy show evidence of the spatial distribution and nature of phases. Diamonds and carbides can be identified for the sintered Fe containing composites with a relatively high volume fraction.

Ultra-Thin Al2O3 Formation at Room Temperature

2010 ◽  
Vol 93-94 ◽  
pp. 113-116
Author(s):  
Puenisara Limnonthakul ◽  
Artorn Pokaipisit ◽  
Pichet Limsuwan
Keyword(s):  
Crystal Structure ◽  
Silicon Wafer ◽  
Room Temperature ◽  
Volume Fraction ◽  
Effective Medium Approximation ◽  
X Ray Diffraction ◽  
Dc Magnetron Sputtering ◽  
X Ray ◽  
Transmission Electron ◽  
Sputtering Power

Ultra-thin Al films were deposited with different deposition times on silicon wafer and copper grid by dc magnetron sputtering. The sputtering power of 200 watt and Ar flow rate of 20 sccm were used to prepare the films. The deposition times were 40, 120 and 240 second, respectively. The deposited Al films were, then, left in the air under the humidity of 60% for 20 days. The crystal structure of ultra-thin Al films deposited on silicon wafer and copper grid were investigated by glazing x-ray diffraction (GXRD) and transmission electron microscopy (TEM), respectively. The XRD results show that after the ultra thin Al films were exposed to the air, the Al was oxidized and the Al2O3 was formed at room temperature. In addition, Al deposited for 120 and 240 second can form polycrystalline of -Al2O3 with preferred orientations of (110) and (311) planes. The TEM images show that the particle size of -Al2O3 was about 8.5 nm for deposited time of 120 second. Moreover, the spectroscopic ellipsometry (SE) data and simulation model of Bruggemann effective medium approximation (BEMA) was used to determine the volume fraction of Al2O3.

scholarly journals Characterization of γ′ Precipitates in Cast Ni-Based Superalloy and Their Behaviour at High-Homologous Temperatures Studied by TEM and in Situ XRD

Materials ◽  
2020 ◽  
Vol 13 (10) ◽  
pp. 2397 ◽  
Author(s):  
Łukasz Rakoczy ◽  
Ondrej Milkovič ◽  
Bogdan Rutkowski ◽  
Rafał Cygan ◽  
Małgorzata Grudzień-Rakoczy ◽  
...  
Keyword(s):  
Volume Fraction ◽  
Matrix Material ◽  
High Volume ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
In Situ Xrd ◽  
Transmission Electron ◽  
The Matrix

In situ X-ray diffraction and transmission electron microscopy has been used to investigate René 108 Ni-based superalloy after short-term annealing at high-homologous temperatures. Current work is focused on characterisation of γ′ precipitates, their volume fraction, evolution of the lattice parameter of γ and γ′ phases and misfit parameter of γ′ in the matrix. Material in the initial condition is characterised by a high-volume fraction (over 63%) of γ′ precipitates. Irregular distribution of alloying elements was observed. Matrix channels were strongly enriched in Cr, Co, W and Mo, whereas precipitates contain large amount of Al, Ti, Ta and Hf. Exposure to high-homologous temperatures in the range 1100–1250 °C led to the dissolution of the precipitates, which influenced the change of lattice parameter of both γ and γ′ phases. The lattice parameter of the matrix continuously grew during holding at high temperatures, which had a dominant influence on the more negative misfit coefficient.

MICROSTRUCTURE OF FeCo–Cu NANOGRANULAR FILMS WITH GIANT MAGNETORESISTANCE

2007 ◽  
Vol 21 (20) ◽  
pp. 1297-1305
Author(s):  
CHANGZHENG WANG ◽  
PEIMING ZHANG ◽  
YIQING ZHANG ◽  
XIAOGUANG XIAO ◽  
YONGHUA RONG ◽  
...  
Keyword(s):  
Giant Magnetoresistance ◽  
Room Temperature ◽  
Volume Fraction ◽  
X Ray Diffraction ◽  
Coherent Interface ◽  
X Ray ◽  
Cu Films ◽  
Transmission Electron ◽  
The Relationship ◽  
Fcc Structure

A series of ( Fe 50 Co 50)x Cu 1-x granular films were prepared using a magnetron-controlled sputtering system. The microstructure and giant magnetoresistance of FeCo–Cu films deposited at room temperature and then annealed at various temperatures were investigated through X-ray diffraction, transmission electron microscope and conventional four-probes method under room temperature, respectively. The results revealed that FeCo–Cu films consisted of fine FeCo granules uniformly dispersed in the Cu matrix and formed fcc structure. Meanwhile the Cu (111) interplaner lattice spacing decreased with increasing magnetic volume fraction (x) due to the presence of the metal coherent interface strains and FeCo–Cu alloying. Upon varying the magnetic volume fraction (x), the giant magnetoresistance of as-deposited FeCo–Cu films reached a maximum of about 0.7% at the volume fraction of 31%, corresponding to the fact that the giant magnetoresistance has a non-monotonic relationship with the granule size. In addition, the relationship between the full width at half maximum (FWHM) or the sensitivity of the giant magnetoresistance and the volume fraction are discussed in detail.

Silica/GO hybrids reinforced NR: Better interface interaction and dynamic behavior

2019 ◽  
Vol 52 (7) ◽  
pp. 575-592
Author(s):  
Kaikai Liu ◽  
Yuanyuan Shang ◽  
Liu Yang ◽  
Aihua Du
Keyword(s):  
Mechanical Performance ◽  
Volume Fraction ◽  
High Volume ◽  
Interfacial Interaction ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Interface Interaction ◽  
Transmission Electron ◽  
Strong Interfacial Interaction ◽  
Filler Dispersion

With silica firstly modified by 3-aminopropyl-triethoxysilane (APES), graphene oxide (GO) was prepared by modified Hummer’s method. APES-silica/GO (AsGO) hybrids were fabricated through hydrogen bond to reduce the polarity of silica and GO and increase the compatibility between natural rubber (NR) and AsGO. Subsequently, AsGO was incorporated into NR latex. The interaction between GO and silica in AsGO was characterized by X-ray diffraction, Raman, and Zeta potential. It was confirmed by transmission electron microscopy that the silica was uniformly dispersed on the surface of the GO. The filler–rubber interfacial interaction was thoroughly investigated. The amount of constrained region was quantified through differential scanning calorimetry results, and it showed that the high volume fraction of constrained region is responsible for the strong interfacial interaction. Besides, the mechanical performance, dynamic property, and electrical and thermal conductivity of NR-AsG x were studied. The results showed that the overall performance of NR-AsG x has an optimum value when the GO loading is 1.5 phr, which is due to the good filler dispersion and strong interface interaction.

Photoluminescence Enhancement of CdS Nanocrystals Fabricated on Dithiocarbamate Functionalized PET Substrates

2012 ◽  
Vol 512-515 ◽  
pp. 1511-1515
Author(s):  
Chun Lin Zhao ◽  
Li Xing ◽  
Xiao Hong Liang ◽  
Jun Hui Xiang ◽  
Fu Shi Zhang ◽  
...  
Keyword(s):  
Room Temperature ◽  
Hexagonal Structure ◽  
Diffraction Measurement ◽  
X Ray Diffraction ◽  
Visible Absorption ◽  
X Ray ◽  
Cds Nanocrystals ◽  
Morphological Studies ◽  
Transmission Electron

Cadmium sulfide (CdS) nanocrystals (NCs) were self-assembled and in-situ immobilized on the dithiocarbamate (DTCs)-functionalized polyethylene glycol terephthalate (PET) substrates between the organic (carbon disulfide diffused in n-hexane) –aqueous (ethylenediamine and Cd2+ dissolved in water) interface at room temperature. Powder X-ray diffraction measurement revealed the hexagonal structure of CdS nanocrystals. Morphological studies performed by scanning electron microscopy (SEM) and high-resolution transmission electron microscope (HRTEM) showed the island-like structure of CdS nanocrystals on PET substrates, as well as energy-dispersive X-ray spectroscopy (EDS) confirmed the stoichiometries of CdS nanocrystals. The optical properties of DTCs modified CdS nanocrystals were thoroughly investigated by ultraviolet-visible absorption spectroscopy (UV-vis) and fluorescence spectroscopy. The as-prepared DTCs present intrinsic hydrophobicity and strong affinity for CdS nanocrystals.

scholarly journals Facile Organometallic Synthesis of Fe-Based Nanomaterials by Hot Injection Reaction

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1141
Author(s):  
Georgia Basina ◽  
Hafsa Khurshid ◽  
Nikolaos Tzitzios ◽  
George Hadjipanayis ◽  
Vasileios Tzitzios
Keyword(s):  
Room Temperature ◽  
Colloidal Particles ◽  
Iron Pentacarbonyl ◽  
Vibrating Sample Magnetometer ◽  
X Ray Diffraction ◽  
Organometallic Synthesis ◽  
X Ray ◽  
Transmission Electron ◽  
Hot Injection ◽  
The Stability

Fe-based colloids with a core/shell structure consisting of metallic iron and iron oxide were synthesized by a facile hot injection reaction of iron pentacarbonyl in a multi-surfactant mixture. The size of the colloidal particles was affected by the reaction temperature and the results demonstrated that their stability against complete oxidation related to their size. The crystal structure and the morphology were identified by powder X-ray diffraction and transmission electron microscopy, while the magnetic properties were studied at room temperature with a vibrating sample magnetometer. The injection temperature plays a very crucial role and higher temperatures enhance the stability and the resistance against oxidation. For the case of injection at 315 °C, the nanoparticles had around a 10 nm mean diameter and revealed 132 emu/g. Remarkably, a stable dispersion was created due to the colloids’ surface functionalization in a nonpolar solvent.

Structural, Morphological, Magnetic and Self-Heating Studies of One-Step Polyol Synthesized Manganese Ferrite (MnFe2O4) Nanoparticles

2019 ◽  
Vol 19 (01) ◽  
pp. 1950003
Author(s):  
P. R. Ghutepatil ◽  
S. H. Pawar
Keyword(s):  
Room Temperature ◽  
Synthesis Method ◽  
Average Crystallite Size ◽  
Superparamagnetic Nanoparticles ◽  
Polyol Synthesis ◽  
X Ray Diffraction ◽  
Self Heating ◽  
Transmission Electron ◽  
One Step ◽  
Mnfe2o4 Nanoparticles

In this paper, uniform and superparamagnetic nanoparticles have been prepared using one-step polyol synthesis method. Structural, morphological and magnetic properties of obtained MnFe2O4 nanoparticles have been investigated by using X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscope (FE-SEM), transmission electron microscopy (TEM), vibrating sample magnetometry (VSM) and thermogravimetric analysis (TGA) techniques. Structural investigation showed that the average crystallite size of obtained nanoparticles was about 10[Formula: see text]nm. Magnetic study revealed that the nanoparticles were superparamagnetic at room temperature with magnetization 67[Formula: see text]emu/g at room temperature. The self-heating characteristics of synthesized MnFe2O4 nanoparticles were studied by applying external AC magnetic field of 167.6 to 335.2[Formula: see text]Oe at a fixed frequency of 265[Formula: see text]kHz. The SAR values of MnFe2O4 nanoparticles were calculated for 2, 5, 10[Formula: see text]mg[Formula: see text]mL[Formula: see text] concentrations and it is observed that the threshold hyperthermia temperature is achieved for all concentrations.

Synthesis and Photoluminescence Properties of Novel SnO2 Zigzag Nanoribbons

2010 ◽  
Vol 97-101 ◽  
pp. 4213-4216
Author(s):  
Jian Xiong Liu ◽  
Zheng Yu Wu ◽  
Guo Wen Meng ◽  
Zhao Lin Zhan
Keyword(s):  
Electron Microscopy ◽  
Room Temperature ◽  
Vapour Deposition ◽  
Chemical Vapour ◽  
Photoluminescence Properties ◽  
X Ray Diffraction ◽  
X Ray ◽  
Selected Area Electron Diffraction ◽  
Transmission Electron ◽  
Ceramic Boat

Novel single-crystalline SnO2 zigzag nanoribbons have been successfully synthesized by chemical vapour deposition. Sn powder in a ceramic boat covered with Si plates was heated at 1100°C in a flowing argon atmosphere to get deposits on a Si wafers. The main part of deposits is SnO2 zigzag nanoribbons. They were characterized by means of X-ray diffraction (XRD), field-emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM) and selected-area electron diffraction (SAED). SEM observations reveal that the SnO2 zigzag nanoribbons are almost uniform, with lengths near to several hundred micrometers and have a good periodically tuned microstructure as the same zigzag angle and growth directions. Possible growth mechanism of these zigzag nanoribbons was discussed. A room temperature PL spectrum of the zigzag nanoribbons shows three peaks at 373nm, 421nm and 477nm.The novel zigzag microstructures will provide a new candidate for potential application.

Preparation and Properties of Nano-Crystalline Cellulose Electro-Rheological Fluid

2015 ◽  
Vol 815 ◽  
pp. 217-221
Author(s):  
Ling Li Xu ◽  
Xing Ling Shi ◽  
Qing Liang Wang
Keyword(s):  
Room Temperature ◽  
Silicone Oil ◽  
Strong Acid ◽  
Crystalline Cellulose ◽  
Methyl Silicone ◽  
Shearing Stress ◽  
X Ray Diffraction ◽  
X Ray ◽  
Nano Crystalline ◽  
Transmission Electron

nanocrystalline cellulose (NCC) was prepared from micro-crystalline cellulose (MCC) by strong acid hydrolysis. The characteristics of such particle were studied by transmission electron microscopy, X-ray diffraction and Fourier transform infrared spectroscopy. Electro-rheological fluids (ERF) were prepared by dispersing NCC and MCC in methyl-silicone oil, and their ER effects were measured. Experimental results indicated that NCC ERF exhibited a remarkable ER effect. The highest static shearing stress of NCC ERF (3.5 g/ml) was 5.1 kPa at the room temperature under a 4 .2 kV/mm electric field, increased about 5.5 times compared to MCC ERF, and sedimentation of NCC ERF was not observed even after 60 days.

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