Characterization of Ni75Mo25 Alloy Prepared by Mechanical Alloying and Heat Treatment

2013 ◽  
Vol 203-204 ◽  
pp. 394-397
Author(s):  
Joanna Panek ◽  
Bożena Bierska-Piech ◽  
Jolanta Niedbała
Keyword(s):  
Heat Treatment ◽  
Mechanical Alloying ◽  
Weight Ratio ◽  
Milling Process ◽  
Particle Sizes ◽  
X Ray Diffraction ◽  
Powder Synthesis ◽  
X Ray ◽  
Microscopy Techniques

The process of Ni75Mo25powder synthesis via mechanical alloying (MA) was studied. Process was carried out from pure elements: Ni and Mo with a particle size under 150 μm. A ball-to-powder weight ratio and the rotational speed were 5:1 and 500 rpm, respectively. Oxidation was reduced by milling under an argon atmosphere. The milling process was performed during up to 60 hours. X-ray diffraction (XRD) and scanning electron microscopy techniques have been used to investigate resulting products. It was found that the particle sizes decrease with the increase in milling time. The resulting powder consists of metastable Ni(Mo) and Mo(Ni) solid solutions. Milled Ni75Mo25 powder was subjected to heat treatment at temperature of 773K, 973K and 1173K. As a result of annealing the formation of Ni4Mo and NiMo intermetallic phases was observed.

Mechanical Alloying of Fe-Nb-N with Different Ball to Powder Weight Ratio for the Formation of Fe-NbC Composite

2012 ◽  
Vol 620 ◽  
pp. 94-98 ◽  
Author(s):  
Siti Zalifah Md Rasib ◽  
Zuhailawati Hussain
Keyword(s):  
Mechanical Alloying ◽  
Weight Ratio ◽  
Milling Process ◽  
X Ray Diffraction ◽  
Electron Microscopic ◽  
X Ray ◽  
Microstructure Characteristics ◽  
Scanning Electron Microscopic ◽  
Small Crystallite

Milling process through mechanical alloying method was performed on a powder mixture of Fe-80.11 wt%, Nb-17.62 wt% and C-2.26 wt% to produce Fe-NbC composite by in situ reaction. Ball to powder weight ratio parameter was selected since formation of phase and microstructure characteristics of this composite were expected to depend on ball collision event during milling. The as-milled and sintered Fe-NbC was characterized by X-ray diffraction (XRD) and Scanning Electron Microscopic (SEM). We found that formation of Fe-NbC by in situ required mechanical alloying of the mixture using 10:1 of ball to powder weight ratio to achieve small crystallite size and more homogeneous of NbC phase.

scholarly journals Synthesis and characterization of apatite silicated powders with wet precipitation method

2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Analytical Techniques ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wet Precipitation ◽  
Scanning Electron

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.

Characterization of Electrospun Poly(Lactic Acid)/polyaniline Blend Nanofibers

2011 ◽  
Vol 332-334 ◽  
pp. 317-320 ◽  
Author(s):  
Hui Qin Zhang
Keyword(s):  
Lactic Acid ◽  
Composite Nanofibers ◽  
Weight Ratio ◽  
Electrospinning Process ◽  
Poly Lactic Acid ◽  
X Ray Diffraction ◽  
Sem Images ◽  
X Ray ◽  
Ft Ir

In this study, composite nanofibers of polyaniline doped with dodecylbenzene sulfonic acid (PANI-DBSA) and Poly(lactic acid) (PLA) were prepared via an electrospinning process. The surface morphology, thermal properties and crystal structure of PLA/PANI-DBSA nanofibers are characterized using Fourier transform infrared spectroscopy (FT-IR), wide-angle x-ray diffraction (WAXD) and scanning electron microscopy (SEM). SEM images showed that the morphology and diameter of the nanofibers were affected by the weight ratio of blend solution.

Effect of Milling Speed on the Synthesis of In-Situ Cu-25 Vol. % WC Nanocomposite by Mechanical Alloying

2012 ◽  
Vol 59 (2) ◽  
Author(s):  
Nurulhuda Bashirom ◽  
Nurzatil Ismah Mohd Arif
Keyword(s):  
Stainless Steel ◽  
Mechanical Alloying ◽  
Weight Ratio ◽  
High Energy ◽  
Milling Process ◽  
Nominal Composition ◽  
X Ray Diffraction ◽  
The Matrix ◽  
Steel Balls

This paper presents a study on the effect of milling speed on the synthesis of Cu-WC nanocomposites by mechanical alloying (MA). The Cu-WC nanocomposite with nominal composition of 25 vol.% of WC was produced in-situ via MA from elemental powders of copper (Cu), tungsten (W), and graphite (C). These powders were milled in the high-energy “Pulverisette 6” planetary ball mill according to composition Cu-34.90 wt% W-2.28 wt% C. The powders were milled in different milling speed; 400 rpm, 500 rpm, and 600 rpm. The milling process was conducted under argon atmosphere by using a stainless steel vial and 10 mm diameter of stainless steel balls, with ball-to-powder weight ratio (BPR) 10:1. The as-milled powders were characterized by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). XRD result showed the formation of W2C phase after milling for 400 rpm and as the speed increased, the peak was broadened. No WC phase was detected after milling. Increasing the milling speed resulted in smaller crystallite size of Cu and proven to be in nanosized. Based on SEM result, higher milling speed leads to the refinement of hard W particles in the Cu matrix. Up to the 600 rpm, the unreacted W particles still existed in the matrix showing 20 hours milling time was not sufficient to completely dissolve the W.

Characterization of aluminosilicate (mullite) precursors prepared by a mechanochemical process

1998 ◽  
Vol 13 (8) ◽  
pp. 2184-2189 ◽  
Author(s):  
J. Temuujin ◽  
K. Okada ◽  
K. J. D. MacKenzie
Keyword(s):  
Heat Treatment ◽  
Nmr Spectra ◽  
Spinel Phase ◽  
Mas Nmr ◽  
X Ray Diffraction ◽  
Hydrated Alumina ◽  
X Ray ◽  
New Si ◽  
Grinding Time

Aluminosilicate precursors were prepared by mechanochemical treatment of gibbsitesilica gel mixtures. The effect of grinding on their structure and thermal behavior has been examined by 27Al and 29Si MAS NMR, x-ray diffraction (XRD), differential thermal analysis-thermogravimetry (DTA-TG), and Fourier transform infrared (FTIR). After 8 h grinding, the hydrated alumina was completely changed to an amorphous phase which showed a new exothermic DTA peak at about 980 °C due to the formation of γ–Al2O3 or spinel phase. This behavior was related to changes in the Al and Si environments, as deduced from the MAS NMR spectra. With increased grinding time, some 4-coordinated Al appears, together with an Al resonance at about 30 ppm. Simultaneously, a new Si resonance appears at about −90 ppm, indicating a greater degree of homogeneity in the ground samples. Mullite crystallizes at 1200 °C from samples ground for 8–20 h, its XRD intensity increasing with increased milling times, in agreement with the NMR, DTA, and FTIR data. Changes in the Al and Si environments during heat treatment, as reflected by the NMR spectra, are also reported.

Neodymium Incorporation in Zirconolite-Based Glass-Ceramics

2000 ◽  
Vol 663 ◽  
Author(s):  
P. Loiseau ◽  
D. Caurant ◽  
N. Baffier ◽  
C. Fillet
Keyword(s):  
Heat Treatment ◽  
Glass Ceramics ◽  
Fission Products ◽  
Treatment Temperature ◽  
Spent Fuel ◽  
X Ray Diffraction ◽  
Parent Glass ◽  
X Ray ◽  
Spin Resonance

ABSTRACTThe investigations on enhanced reprocessing of nuclear spent fuel, and notably on separating the long-lived minor actinides, such as Am and Cm, from the other fission products have led to the development of highly durable specific matrices such as glass-ceramics for their immobilization. This study deals with the characterization of zirconolite (CaZrTi2O7) based glass-ceramics synthesized by devitrification of an aluminosilicate parent glass. Trivalent actinide ions were simulated by neodymium, which is a paramagnetic local probe. Glass-ceramics with Nd2O3 contents ranging from 0 to 10 weight % were prepared by heat treatment of a parent glass at two different growth temperatures: 1050° and 1200°C. X-ray diffraction (XRD), energy dispersive X-ray analysis (EDX) and electron spin resonance (ESR) measurements clearly indicate that Nd3+ ions are partly incorporated in zirconolite crystals formed in the bulk of the glass-ceramic samples. The amount of neodymium in the crystalline phase was estimated using ESR results and was found to decrease with increasing either heat treatment temperature or total Nd2O3 content.

Preparation and Characterization of Cellulose Nanowhiskers in N, N-Dimethylacetamide

2012 ◽  
Vol 528 ◽  
pp. 35-38 ◽  
Author(s):  
Ping Qu ◽  
Xuan Wang ◽  
Li Ping Zhang
Keyword(s):  
High Specific Surface Area ◽  
Degree Of Crystallinity ◽  
Gravimetric Analysis ◽  
Cellulose Nanowhiskers ◽  
X Ray Diffraction ◽  
Physical Treatment ◽  
X Ray ◽  
Microscopy Techniques ◽  
Amorphous Character

Reinforcement of polymer with plant whiskers is a way of improving mechanical properties. Cellulose nanowhiskers (CNW) were separated from commercially available wood pulpboard. Different microscopy techniques, thermal gravimetric analysis, X-ray diffraction were used to study the structure and properties of the microcrystalline cellulose (MCC) and CNW. Because of the high specific surface area of CNW, the increases in total amorphous character of the cellulose decrease the relative degree of crystallinity. After chemical and physical treatment, the CNW in the length of several μm and diameters ranging from 20 - 50 nm was obtained. Both the initial decomposing temperature and temperature of maximum decomposing rate of CNW is higher than MCC, but lower than wood pulpboard.

Processing of Nano Hydroxyapatite from Eggshell and Seashell

2010 ◽  
Vol 659 ◽  
pp. 159-164 ◽  
Author(s):  
Gréta Gergely ◽  
Ferenc Wéber ◽  
Mihály Tóth ◽  
Attila Lajos Tóth ◽  
Zsolt E. Horváth ◽  
...  
Keyword(s):  
Heat Treatment ◽  
Grain Size ◽  
Ball Milling ◽  
Milling Process ◽  
Effect Of Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Attrition Milling ◽  
Milling Method ◽  
Scanning Electron

Hydroxyapatite (HAp) was successfully produced from recycled eggshell, seashell and phosphoric acid by using two different type of milling method (attrition milling and ball milling). According to the analysis, the attrition milling resulted nanosize HAp even after milling, while the ball milling process provided HAp only after a 400oC, 2 h long heat treatment. The grain size in both cases were approximately preserved during the heat treatment. The effect of temperature on stoichiometry, morphology and crystallinity of HAp powders were investigated. The structures of the HAp were characterized by X-ray diffraction and Scanning Electron Microsopy.

Study of Nanocrystalline NiAl Alloys Prepared by Mechanical Alloying

2012 ◽  
Vol 329 ◽  
pp. 19-28 ◽  
Author(s):  
M. Gherib ◽  
A. Otmani ◽  
A. Djekoun ◽  
A. Bouasla ◽  
M. Poulain ◽  
...  
Keyword(s):  
Mechanical Alloying ◽  
Crystallite Size ◽  
Milling Time ◽  
Structural Features ◽  
Milling Process ◽  
X Ray Diffraction ◽  
X Ray ◽  
Size Refinement ◽  
20 Nm ◽  
Kinetics Of

Nanostructured Powders of Ni-20wt%Al and Ni-50wt%Al Were Prepared, by Mechanical Alloying under an Argon Atmosphere, from Elemental Ni and Al Powders Using a Planetary Ball Mill (type Fritsch P7) for Different Times (0.5-24h).). Microstructural and Structural Features of the Final Products Were Characterized by X-Ray Diffraction (XRD) and Scanning Electron Microscopy (SEM). the Results of the XRD Shows the Formation of the B2 (Ni Al) Phase after 2 Hours of Milling for both Systems. Also Detected Was the Ni3al Phase in Ni80al20after 4 Hours. Crystallite Size Refinement of the Final Product Occurred down to Nanometer Scales when the Milling Time Increased, and Attained 17 Nm in the Ni50al50System and 20 Nm in the other System, at 24 Hours. this Decrease in Crystallite Size Is Accompanied by an Increase in the Interval Level Strain. the Kinetics of Al Dissolution during the Milling Process of Ni50al50System Can Be Described by Two Regimes, Characterised by Different Values of Avrami Parameters which Are Calculated by Using the Johnson–Mehl–Avrami Formalism.

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