Microstructure Evolution of a Fine Grain Al-50wt%Si Alloy Fabricated by High Energy Milling

2011 ◽  
Vol 479 ◽  
pp. 54-61 ◽  
Author(s):  
Fei Wang ◽  
Ya Ping Wang
Keyword(s):  
Grain Growth ◽  
Microstructure Evolution ◽  
Room Temperature ◽  
Milling Time ◽  
High Energy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Laser Method ◽  
X Ray ◽  
Fine Grain

Microstructure evolution of high energy milled Al-50wt%Si alloy during heat treatment at different temperature was studied. Scanning electron microscope (SEM) and X-ray diffraction (XRD) results show that the size of the alloy powders decreased with increasing milling time. The observable coarsening of Si particles was not seen below 730°C in the high energy milled alloy, whereas, for the alloy prepared by mixed Al and Si powders, the grain growth occurred at 660°C. The activation energy for the grain growth of Si particles in the high energy milled alloy was determined as about 244 kJ/mol by the differential scanning calorimetry (DSC) data analysis. The size of Si particles in the hot pressed Al-50wt%Si alloy prepared by high energy milled powders was 5-30 m at 700°C, which was significantly reduced compared to that of the original Si powders. Thermal diffusivity of the hot pressed Al-50wt%Si alloy was 55 mm2/s at room temperature which was obtained by laser method.

Microstructural Transformations of an Amorphous Fe90 Zr10 Alloy Induced by High-Energy Ball-Milling

2006 ◽  
Vol 510-511 ◽  
pp. 698-701
Author(s):  
Pyuck Pa Choi ◽  
Young Soon Kwon ◽  
Ji Soon Kim ◽  
Dae Hwan Kwon
Keyword(s):  
Ball Milling ◽  
Milling Time ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Melt Spun ◽  
Energy Ball ◽  
Induced Crystallization

Mechanically induced crystallization of an amorphous Fe90Zr10 alloy was studied by means of X-ray diffraction (XRD) and differential scanning calorimetry (DSC). Under high-energy ball-milling in an AGO-2 mill, melt-spun Fe90Zr10 ribbons undergo crystallization into BCC α- Fe(Zr). Zr atoms are found to be solved in the Fe(Zr) grains up to a maximum supersaturation of about 3.5 at.% Zr, where it can be presumed that the remaining Zr atoms are segregated in the grainboundaries. The decomposition degree of the amorphous phase increases with increasing milling time and intensity. It is proposed that the observed crystallization is deformation-induced and rather not attribute to local temperature rises during ball-collisions.

Study on Generation of Fine Grained Titanium Aluminide Through Ball Milling of Ti, Al and Ni-P Coated Graphite Powder

2009 ◽  
Vol 67 ◽  
pp. 45-51
Author(s):  
Rohit Kumar Gupta ◽  
Vijaya Agarwala ◽  
Sunayan Thakur ◽  
Ramesh Chandra Agarwala ◽  
Bhanu Pant
Keyword(s):  
Particle Size ◽  
Ball Milling ◽  
Titanium Aluminide ◽  
Milling Time ◽  
Stoichiometric Composition ◽  
High Energy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Final Particle ◽  
X Ray

High energy ball milling (HEBM) had been carried out to produce submicron size titanium aluminide intermetallics (TiAl) using elemental powders of Ti and Al alongwith Ni-P coated graphite. 1% graphite powders was added to stoichiometric composition of Ti48Al and ball milling was conducted for different milling time at varying rpm. The effect of milling time and rpm on particle size has been studied. The prepared samples have been characterized using X-ray diffraction, differential scanning calorimetry (DSC) and scaning elecron microscopy (SEM). Grain size as low as 500 nm could be achieved. Formation of Ti3Al, TiAl and carbon containing intermetallic compounds had been confirmed through X-ray diffraction. Milling time and rpm of mill is found to be important factors which control the final particle size.

Magnetic Properties and Hardness of Nanostructured WC-Co Cemented Carbide

2012 ◽  
Vol 727-728 ◽  
pp. 430-435
Author(s):  
J.B. Manuel ◽  
M.J. Diniz ◽  
Uílame Umbelino Gomes ◽  
Ariadne de Souza Silva ◽  
J.H. Araújo
Keyword(s):  
Magnetic Properties ◽  
Vickers Hardness ◽  
Milling Time ◽  
High Energy ◽  
Cemented Carbides ◽  
Time Increase ◽  
X Ray Diffraction ◽  
X Ray ◽  
Grain Sizes ◽  
Fine Grain

Nacrystalline WC-10wt.%Co powders were prepared by high energy milling and liquid phase sintered. The powders with different milling time were characterized by X-ray diffraction and SEM. After sintered the WC-10wt.%Co cemented carbides exhibits ultra fine grain sizes. Coercitive field and Vickers hardness measurements on the consolided samples detected a significant increase and decrease Vickers hardness with the milling time increase in sintered samples.

scholarly journals Mechanical Amorphization and Recrystallization of Mn-Co(Fe)-Ge(Si) Compositions

Metals ◽  
2019 ◽  
Vol 9 (5) ◽  
pp. 534 ◽  
Author(s):  
Antonio Vidal-Crespo ◽  
Jhon J. Ipus ◽  
Javier S. Blázquez ◽  
Alejandro Conde
Keyword(s):  
Room Temperature ◽  
Crystal Size ◽  
Milling Time ◽  
Phase Evolution ◽  
Intermetallic Phases ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Bcc Phase ◽  
Thermal Stability Of

Mechanical alloying using a planetary ball mill allowed us to obtain two homogeneous systems formed by units with nanometer size and MnCo0.8Fe0.2Ge1−xSix stoichiometry (x = 0 and 0.5). The phase evolution of the systems with the milling time was analyzed using X-ray diffraction. Thermal stability of the final products was studied using differential scanning calorimetry. Room temperature 57Fe Mössbauer spectroscopy was used to follow the changes in the Fe environments. A paramagnetic Co-based amorphous phase developed in both alloys as milling progressed. However, while the presence of Si stabilized the Mn-type phase, mechanical recrystallization was observed in a Si-free composition leading to the formation of a MnCo(Fe)Ge intermetallic (Pnma space group) with a crystal size of 7 ± 1 nm. Mössbauer results indicate that Fe atoms migrate from the initial bcc phase to the amorphous and intermetallic phases.

scholarly journals Size Effect on the Structural and Magnetic Properties of Nanosized PerovskiteLaFeO3Prepared by Different Methods

2012 ◽  
Vol 2012 ◽  
pp. 1-6 ◽  
Author(s):  
Nguyen Thi Thuy ◽  
Dang Le Minh
Keyword(s):  
Magnetic Properties ◽  
Electron Microscope ◽  
Room Temperature ◽  
High Energy ◽  
Ferromagnetic Behavior ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation

Nanosized LaFeO3material was prepared by 3 methods: high energy milling, citrate gel, and coprecipitation. The X-ray diffraction (XRD), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA) show that the orthorhombic LaFeO3phase was well formed at a low sintering temperature of 500°C in the citrate-gel and co-precipitation methods. Scanning electron microscope (SEM) and transmission electron microscope (TEM) observations indicate that the particle size of the LaFeO3powder varies from 10 nm to 50 nm depending on the preparation method. The magnetic properties through magnetization versus temperatureM(T)and magnetization verses magnetic fieldM(H)characteristics show that the nano-LaFeO3exhibits a weak ferromagnetic behavior in the room temperature, and theM(H)curves are well fitted by Langevin functions.

scholarly journals Structures of a Phosphoryl Derivative of 4-Allyl-2,4-dihydro-3H-1,2,4-triazole-3-thione: An Illustrative Example of Conformational Polymorphism

Crystals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 1126
Author(s):  
Ivan V. Fedyanin ◽  
Aida I. Samigullina ◽  
Ivan A. Krutov ◽  
Elena L. Gavrilova ◽  
Dmitry V. Zakharychev
Keyword(s):  
Room Temperature ◽  
Lattice Energy ◽  
Energy Difference ◽  
High Energy ◽  
Cohesion Energy ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Molecular Conformations ◽  
X Ray ◽  
Polymorphic Forms

Two polymorphic forms of a conformationally flexible molecule, 5-[(Diphenylphosphoryl)methyl]-4-(prop-2-en-1-yl)-2,4-dihydro-3H-1,2,4-triazole-3-thione, were obtained by crystallization and characterized by X-ray diffraction analysis and differential scanning calorimetry. The relative stability of polymorphic forms was estimated with DFT calculations of crystal structures and isolated molecules. It turns out, that in the first more dense polymorph with higher cohesion energy and crystal lattice energy, the molecule adopts an energetically unfavorable conformation, and forms dimers with lower H-bond strength, as compared to the second polymorph. On the other hand, in the second polymorph, the molecule adopts almost the lowest-energy conformation and forms infinite chains via strong H-bonds. The first form that seems to be more thermodynamically stable at room temperature transforms into the second form via two endothermic phase transitions; the apparent irreversibility of the transition is due to high energy difference between the molecular conformations in crystals.

Room Temperature Screw Form Rolling of AZ91D Magnesium Alloy through Processing by Extrusion-Torsion Simultaneous Working

2014 ◽  
Vol 783-786 ◽  
pp. 375-379
Author(s):  
Mitsuaki Furui ◽  
Shouyou Sakashita ◽  
Kazuya Shimojima ◽  
Tetsuo Aida ◽  
Kiyoshi Terayama ◽  
...  
Keyword(s):  
Magnesium Alloy ◽  
Room Temperature ◽  
Hardness Measurement ◽  
Rolling Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Az91d Magnesium Alloy ◽  
Microstructure Observation ◽  
Fine Grain ◽  
Simultaneous Processing

Extrusion-torsion simultaneous processing is a very attractive technique for fabricating a rod-shape material with fine grain and random texture. We have proposed a new screw form rolling process combined with preliminary extrusion-torsion simultaneous working. Microstructure evolution and mechanical property change of AZ91D magnesium alloy during extrusion-torsion simultaneous processing was examined through microstructure observation, X-ray diffraction analysis and micro-Vickers hardness measurement. By the addition of torsion, the crystal orientation of AZ91D magnesium alloy workpiece was drastically changed from basal crystalline orientation to the random orientation. Crystal grain occurred through the dynamic recrystallization and tended to coarsen with an increase of extrusion-torsion temperature. Grain refinement under 2 um was achieved at the lowest extrusion-torsion temperature of 523 K. M8 gauge AZ91D magnesium alloy screw was successfully formed at room temperature using the extrusion-twisted workpiece preliminary solution treating at 678 K for 345.6 ks. It was found that the extrusion-torsion temperature of 678 K must be selected to fabricate the good screw without any defects.

Study in performance and morphology of polyamide 12 produced by selective laser sintering technology

2018 ◽  
Vol 24 (5) ◽  
pp. 813-820 ◽  
Author(s):  
Junjie Wu ◽  
Xiang Xu ◽  
Zhihao Zhao ◽  
Minjie Wang ◽  
Jie Zhang
Keyword(s):  
Selective Laser Sintering ◽  
Polarized Light ◽  
Chain Scission ◽  
High Energy ◽  
Laser Sintering ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Content Type ◽  
X Ray ◽  
Polyamide 12

Purpose The purpose of this paper is to investigate the effect of selective laser sintering (SLS) method on morphology and performance of polyamide 12. Design/methodology/approach Crystallization behavior is critical to the properties of semi-crystalline polymers. The crystallization condition of SLS process is much different from others. The morphology of polyamide 12 produced by SLS technology was investigated using scanning electron microscopy, polarized light microscopy, differential scanning calorimetry, X-ray diffraction and wide-angle X-ray diffraction. Findings Too low fill laser power brought about bad fusion of powders, while too high energy input resulted in bad performance due to chain scission of macromolecules. There were three types of crystal in the raw powder material, denoted as overgrowth crystal, ring-banded spherulite and normal spherulite. Originality/value In this work, SLS samples with different sintering parameters, as well as compression molding sample for the purpose of comparison, were made to study the morphology and crystal structure of sintered PA12 in detail.

scholarly journals Viability of the microencapsulation of a casein hydrolysate in lipid microparticles of cupuacu butter and stearic acid

2013 ◽  
Vol 2 (1) ◽  
Author(s):  
Samantha Cristina Pinho ◽  
Janaina Costa Da Silva
Keyword(s):  
Stearic Acid ◽  
Room Temperature ◽  
Casein Hydrolysate ◽  
Polysorbate 80 ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
Initial Amount ◽  
X Ray ◽  
Lipid Mixtures ◽  
Lipid Microparticles

Solid lipid microparticles produced with a mixture of cupuacu butter and stearic acid were used to microencapsulate a commercial casein hydrolysate (Hyprol 8052). The composition of the lipid matrix used for the production of the lipid microparticles was chosen according to data on the wide angle X-ray diffraction (WAXD) and differential scanning calorimetry (DSC) of bulk lipid mixtures, which indicated that the presence of 10 % cupuacu butter was sufficient to significantly change the crystalline arrangement of pure stearic acid. Preliminary tests indicated that a minimum proportion of 4 % of surfactant (polysorbate 80) was necessary to produce empty spherical lipid particles with average diameters below 10 mm. The lipid microparticles were produced using 20 % cupuacu butter and 80 % stearic acid and then stabilized with 4 % of polysorbate 80, exhibiting an encapsulation efficiency of approximately 74 % of the casein hydrolysate. The melting temperature of the casein hydrolysate-loaded lipid microparticles was detected at 65.2 °C, demonstrating that the particles were solid at room temperature as expected and indicating that the incorporation of peptides had not affected their thermal behavior. After 25 days of storage, however, there was a release of approximately 30 % of the initial amount of encapsulated casein hydrolysate. This release was not thought to have been caused by the liberation of encapsulated casein hydrolysate. Instead, it was attributed to the possible desorption of the adsorbed peptides present on the surface of the lipid microparticles.

Influence of Gd Addition on the Structure and Capability of Ni-Mn-In Metamagnetic Shape Memory Alloys

2012 ◽  
Vol 535-537 ◽  
pp. 950-953
Author(s):  
Li Na Bai ◽  
Gui Xing Zheng ◽  
Zhi Jian Duan ◽  
Jian Jun Zhang
Keyword(s):  
Differential Scanning Calorimetry ◽  
Magnetic Properties ◽  
Magnetic Property ◽  
Transition Temperature ◽  
Martensitic Transformation ◽  
Room Temperature ◽  
Vibrating Sample Magnetometry ◽  
X Ray Diffraction ◽  
Scanning Calorimetry ◽  
X Ray

The influences of Gd concentration on martensitic transformation and magnetic properties of NiMnIn alloys were investigated by differential scanning calorimetry (DSC) , vibrating sample magnetometry (VSM), X-ray diffraction (XRD) and etc. It is Observed through the experiment: the addition of Gd enhances martensite transition temperature;X-ray diffraction analysis of experimental alloys is revealed that to the mixture is martensite and austenite at room temperature; content of Gd is not proportional to the improvement of magnetic property.

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