Microstructure of 430L Stainless Steel Powders during High-Energy Ball Milling

2007 ◽  
Vol 561-565 ◽  
pp. 1251-1254
Author(s):  
Hong Wei Ni ◽  
Hang He ◽  
G.Q. Li ◽  
Wei Ting Zhan ◽  
Da Qiang Cang ◽  
...  
Keyword(s):  
Particle Size ◽  
Grain Size ◽  
Stainless Steel ◽  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Initial Stage ◽  
Energy Ball ◽  
The Mean

Preparation of nanocrystalline 430L stainless steel powders by high-energy ball milling has been investigated. The samples were characterized by scanning electron microscope (SEM), X-ray Diffraction (XRD) and Matersizer. The SEM observation confirmed that the cold welding and fragmentation behaviors occurred during high-energy ball milling, which has important effect on the changes of the particle size. In the initial stage (0-10h), particle size increased and crystalline grain size decreased evidently. The mean particle size got to 330μm and the crystalline grain size got to 23nm for sample of 10h ball milling. In the later stage, the particle size decreased and the refinement of crystalline grain became difficult. The crystalline grain size of sample for 50h ball milling only got to 15nm.

High Energy Ball-Milling of Tin Titanate Zirconate for Use in Microwave Applications

2006 ◽  
Vol 45 ◽  
pp. 480-485 ◽  
Author(s):  
V.L. Arantes ◽  
Dulcina P.F. Souza
Keyword(s):  
Particle Size ◽  
Dielectric Properties ◽  
Ball Milling ◽  
High Energy ◽  
Liquid Phase Sintering ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Microwave Frequencies ◽  
Particle Size Analyzer ◽  
Energy Ball

Tin titanate zirconate (ZTS) is widely known for its good dielectric properties at high frequencies and has been widely employed as a dielectric resonator. ZTS does not sinter easily by solid state difusion and it is necessary to introduce sintering aids capable of increasing diffusion coefficients and/or leading to liquid phase sintering. Consequently, the dielectric properties in microwave frequencies can be reduced. This work focused on the utilization of high energy ball-milling as a method of reducing initial particle size and further improving sintering of ZTS.The powders obtained were characterized by X-ray diffraction as a function of milling time, as well as by a light scattering particle size analyzer.

scholarly journals Hydroxyapatite/iron oxide nanocomposite prepared by high energy ball milling

2019 ◽  
Vol 13 (2) ◽  
pp. 210-217
Author(s):  
Milica Vucinic-Vasic ◽  
Bratislav Antic ◽  
Marko Boskovic ◽  
Aleksandar Antic ◽  
Jovan Blanusa
Keyword(s):  
Particle Size ◽  
Iron Oxide ◽  
Particle Size Distribution ◽  
Size Distribution ◽  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
X Ray ◽  
Energy Ball

Nanocomposites (HAp/iron oxide), made of hydroxyapatite (HAp) and ferrimagnetic iron oxide, were synthesized by high-energy ball milling a mixture consisting of iron oxide nanoparticles and the starting materials used for the HAp synthesis: calcium hydrogen phosphate anhydrous (CaHPO4), and calcium hydroxide (Ca(OH)2). Two HAp/iron oxide samples with the magnetic phase content of 12 and 30 wt.% were prepared and their microstructure, morphology and magnetic properties were analysed by X-ray diffraction and transmission electron microscopy. Furthermore, the measurement of particle size distribution was performed by laser scattering, and temperature/field dependence on magnetization was determined. X-ray diffraction data confirmed the formation of two-phased samples (HAp and spinel iron oxide) without the presence of any other parasite phase. The shape of particles was nearly spherical in both samples, ranging from only a few to several tens of nanometres in diameter. These particles formed agglomerates with the most common value of the number-based particle size distribution of 380 and 310 nm for the sample with 12 and 30wt.% of iron oxide, respectively. Magnetization data showed that both HAp/iron oxide composites had superparamagnetic behaviour at room temperature.

scholarly journals Analysis of the influence of β-TCP particle size on deagglomeration processes

2020 ◽  
Vol 9 (4) ◽  
pp. e175943067
Author(s):  
João Augusto Martins Almeida ◽  
Bruna Horta Bastos Kuffner ◽  
Gilbert Silva ◽  
Patrícia Capellato ◽  
Daniela Sachs
Keyword(s):  
Particle Size ◽  
Ball Milling ◽  
High Energy ◽  
Milling Process ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
Powder Morphology ◽  
Heterogeneous Distribution ◽  
X Ray ◽  
Energy Ball

There are a class of material widely used in bone tissue repair. This material is calcium phosphate ceramics (CPCs)that can be used on two phases: α and β. However, β-TCP is more used in bone regeneration than α–TCP due to the biocompatible and bioactive properties.In the present work evaluate the influence of these two distinct processes to deagglomeration and the consequence in the particle size of the β-TCP obtained through solid-state reaction. Among all of the routes used in research and industry to reduce the particles size of different materials, the high energy ball milling is one of the most effective, due to the high rotation speed that this process achieves. The deagglomeration through agate mortar is considered a cheaper process when compared with the high energy ball milling. The characterization of both powders, deagglomerated in high energy ball milling and agate mortar, was realized through scanning electron microscopy, to analyze the powder morphology, and laser granulometry, to determine the size of the particles. Also, the forerunner powder was previously submitted to x-ray diffraction to confirm the formation of the β-TCP phase. The analysis through x-ray diffraction confirmed that the phase formed during the calcination process corresponded to the β-TCP. The results obtained after the deagglomeration processes indicated that the morphology was predominantly irregular for both powders. In relation to the granulometry, the deagglomeration performed through agate mortar showed to produce particles with smaller size (11,4µm e 0,9µm) and heterogeneous distribution, while the high energy ball milling process produced particles with larger size (11,4µm a 1,8µm) and higher homogeneity.

Effect of High-Energy Ball Milling on the Mg Alloy Powders under Alcohol Protection

2007 ◽  
Vol 534-536 ◽  
pp. 785-788
Author(s):  
Gang Li ◽  
Xing Xing Liu ◽  
Qi Guo ◽  
Jian Ren Tang ◽  
Biao Yan
Keyword(s):  
Ball Milling ◽  
Fine Particles ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Mg Alloy ◽  
Powder Size ◽  
X Ray Diffraction ◽  
Eds Analysis ◽  
Initial Stage ◽  
Energy Ball

Study about the feasibility and effect of high-energy ball milling on a specific Mg alloy under protection medium of alcohol was presented via comparing with conventional vacuum milling. More fine particles with wider powder size distribution but more irregular shape were shown from image analysis of the SEM pictures of the powder milled under alcohol. No obvious oxide was revealed from the X-ray diffraction of the two kinds of Mg alloy powders with limited milling time. And since slip induced in a preferential direction, the (002) texture was formed in the Mg alloy powders at the initial stage of alcohol milling. With deformation occurred randomly, the texture disappeared regularly. More O and Fe contaminants were introduced into the powders milled under alcohol according to the EDS analysis, for which the hot-pressed Mg alloy samples fabricated with that powders exhibited lower UTS.

Phase development during high-energy ball-milling of zinc oxide and iron – the impact of grain size on the source and the degree of contamination

2015 ◽  
Vol 44 (43) ◽  
pp. 18870-18881 ◽  
Author(s):  
G. Štefanić ◽  
S. Krehula ◽  
I. Štefanić
Keyword(s):  
Grain Size ◽  
Zinc Oxide ◽  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Degree Of Contamination ◽  
Phase Development ◽  
Energy Ball ◽  
The Impact

The impact of grain size on the source and the degree of contamination.

Mössbauer, X-ray diffraction and magnetization studies of Fe–Mn–Al–Nb alloys prepared by high energy ball milling

2006 ◽  
Vol 168 (1-3) ◽  
pp. 1057-1063 ◽  
Author(s):  
Ligia E. Zamora ◽  
G. A. Perez Alcazar ◽  
J. M. Greneche ◽  
S. Suriñach
Keyword(s):  
Ball Milling ◽  
High Energy ◽  
High Energy Ball Milling ◽  
X Ray Diffraction ◽  
X Ray ◽  
Energy Ball

Nanostructured Al Powder Obtained by High Energy Ball Milling at Ambient and Cryogenic Temperatures

2014 ◽  
Vol 802 ◽  
pp. 125-129
Author(s):  
Heronilton Mendes de Lira ◽  
Pilar Rey Rodriguez ◽  
Oscar Olimpio de Araújo Filho ◽  
Cezar Henrique Gonzalez ◽  
Severino Leopoldino Urtiga Filho
Keyword(s):  
Particle Size ◽  
Ball Milling ◽  
High Performance ◽  
Pure Aluminum ◽  
High Energy ◽  
High Energy Ball Milling ◽  
Nanocrystalline Powders ◽  
Protective Atmosphere ◽  
Energy Ball ◽  
Size And Morphology

High performance nanostructured light metals and alloys are very interesting for replacing conventional heavier materials in many industrial components. High Energy Ball Milling and Cryomilling are useful techniques to obtain nanocrystalline powders. In this work the effect of several milling conditions such as rotation speed, time, ball to powder ratio and temperature on the crystallite and particle size and morphology in pure aluminum are presented. X-Ray Diffraction, Laser Diffraction and Scanning Electron Microscopy are used. High energy ball milling at ambient and cryogenic temperature of Al powders rapidly leads to a nanometer size down to about 35 nm. High ball to powder ratio promotes both low crystallite and particle size. Small crystallite size like 18 nm and particle size as 4 μm were achieved in the most energetic conditions at ambient temperature. Isopropyl alcohol used as liquid media and protective atmosphere has a strong influence on the results depending on the milling temperature of Al.

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