The Location of Tantalum Atoms in Ni3Al

1988 ◽  
Vol 133 ◽  
Author(s):  
Hui Lin ◽  
David P. Pope

ABSTRACTAn X-ray powder diffraction method was used to determine the location of tantalum atoms in Ni3Al. A series of Ni3 (Al,Ta) alloys were produced with tantalum content ranging from 0.1 to 3.0 at%. Fine powders with average particle sizes less than 80 pm were made from melt-spun ribbons by a grinding process. The values of the superlattice peak intensities normalized to the intensity of the (200) fundamental peak agreed with the calculated values assuming that tantalum atoms substitute on aluminum sites, not on nickel sites. Thus it is concluded from our experiments that tantalum atoms substitute for aluminum in Ni3Al, except for Ta contents around 0.2 at% where the data can not be interpreted in terms of a simple substitution scheme.

1990 ◽  
Vol 5 (4) ◽  
pp. 763-768 ◽  
Author(s):  
Hui Lin ◽  
David P. Pope

An x-ray powder diffraction method was used to determine the location of tantalum atoms in Ni3Al. A series of Ni3(Al, Ta) alloys were produced with tantalum contents ranging from 0.1 to 3.0 at.%. Fine powders with average particle sizes less than 80 μm were made from melt-spun ribbons by a grinding process. The values of the intensity of the (100) superlattice peak normalized to that of the (200) fundamental peak as a function of tantalum content agreed with the calculated values, assuming that tantalum atoms substitute on aluminum sites, not on nickel sites, and also assuming small amounts of anti-site defects exist in the ordered fee structure of Ni3(Al, Ta) alloys. It is concluded from our experiments that tantalum atoms substitute for aluminum in Ni3Al. The long-range order parameters thus calculated of the Ni3(Al, Ta) alloys are generally above 0.84 and below 0.95, except for Ni75Al24.8Ta0.2, at which composition the long-range order parameter is close to unity.


1994 ◽  
Vol 364 ◽  
Author(s):  
L. Lutterotti ◽  
S. K. Pradhan ◽  
S. Gialanella ◽  
A. R. Yavari

AbstractFollowing a previous study in which we presented some microstructural aspects of meltspun ribbons having a composition close to Zr-25 at.% Al, we discuss now the crystallography of the phases observed in similar samples. We performed X-Ray diffraction analyses of ribbons and refined the observed crystallographic structures. We could identify a number of stable and metastable structures, according to the actual composition of the ribbons. We also estimated the percentage of each one of these phases. We did the same for some ribbons annealed at 750°C for several times. In this way we could follow the kinetics leading from the initial as-spun condition to the final one, featuring the L12 ordered Zr3Al, as the major phase, and other intermetallic phases of the Zr-Al phase diagram.


2005 ◽  
Vol 20 (3) ◽  
pp. 563-566 ◽  
Author(s):  
Tetsuji Saito ◽  
Hiroyuku Takeishi ◽  
Noboru Nakayama

We report a new compression shearing method for the production of bulk amorphous materials. In this study, amorphous Nd–Fe–B melt-spun ribbons were successfully consolidated into bulk form at room temperature by the compression shearing method. X-ray diffraction and transmission electron microscopy studies revealed that the amorphous structure was well maintained in the bulk materials. The resultant bulk materials exhibited the same magnetic properties as the original amorphous Nd–Fe–B materials.


2015 ◽  
Vol 723 ◽  
pp. 544-547
Author(s):  
Xiang Wei Cheng ◽  
Da Jin Xiong ◽  
Chao Huo

Using intermittent bubbling carbonation method to prepare nanoCaCO3, the effect of crystal orientation agents on the morphology of nanoCaCO3 was studied. The nanoCaCO3 was characterized by means of field emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD), Laser particle analyzer. The results showed that the different shapes nanoCaCO3 was synthesized by adding different crystal orientation agents to control the shape of the product. The as-prepared CaCO3 were pure calcite crystal and the average particle sizes were within the range of 25.7 to 60.9 nm.


2012 ◽  
Vol 05 ◽  
pp. 841-846
Author(s):  
AMIR KEYVANARA ◽  
REZA GHOLAMIPOUR ◽  
SHAMSEDIN MIRDAMADI ◽  
FARZAD SHAHRI ◽  
HOSSEIN SEPEHRI AMIN

Melt spun ribbons of Co 64 Fe 4 Ni 2 B 19 Si 8 Cr 3 alloy have been prepared and the nanocrystallization process was carried out by the heat treatment of the as spun ribbons above the crystallization temperature. Structural studies of the samples have been performed by transmission electron microscopy and X-ray diffraction. Magnetic properties of the samples and magnetoimpedance measurements were investigated and it was revealed that magnetic properties and magnetoimpedance of the samples deteriorate by the formation of nanocrystalline phases.


2009 ◽  
Vol 24 (6) ◽  
pp. 2042-2050 ◽  
Author(s):  
Du Yuan ◽  
Guang Shun Yi ◽  
Gan Moog Chow

Bulk NaYF4:Yb,Er particles (∼1.4 μm particle size) were synthesized using a hydrothermal method. As-synthesized particles were subsequently ball milled to three average particle sizes, namely, ∼260 nm, 160 nm, and 100 nm. The x-ray diffraction pattern showed an hcp phase for as-synthesized and ball-milled particles with a predominant (100) peak. Room temperature emission spectra showed no size dependent peak shifts or peak broadening. The intensities of both green and red emissions decreased with increasing milling time. Segregation of Er ions was detected on the surfaces of milled particle that reduced the sensitizer-activator transition probability, resulting in decreased emission intensities. The green-to-red emission ratio was correlated to the surface enrichment of Er, which affected the cross-relaxation of luminescence dynamics.


2017 ◽  
Vol 58 (7) ◽  
pp. 981-985 ◽  
Author(s):  
P. Kozikowski ◽  
M. Ohnuma ◽  
M. Ohta ◽  
Y. Terakado ◽  
Y. Yoshizawa ◽  
...  

2011 ◽  
Vol 194-196 ◽  
pp. 660-664 ◽  
Author(s):  
Hua Lin ◽  
Bo Wan Tao ◽  
Qing Li ◽  
Yan Rong Li

V2O3 and VN nanocrystals have been conveniently synthesized from thermal ammonolysis of the precursor VOC2O4•H2O in a resistance tubular furnace at 500°С and 780°С for 30 min, respectively. The products were characterized by X-ray diffractometer (XRD)、X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) techniques. The average particle sizes of V2O3 and VN are both in the ranges of 20~35 nm. The evolution from precursor to hexagonal V2O3 and then to cubic VN was explored. The crucial factors,such as the reaction temperature and time,have also been discussed.


2019 ◽  
Vol 60 (10) ◽  
pp. 116-123
Author(s):  
Aygul A. Mammadova ◽  
◽  
Sevinj N. Osmanova ◽  
Sabira A. Agayeva ◽  
Aydar A. Mejidov ◽  
...  

The hydrothermal reduction of cobalt, manganese and lithium nitrates with ethylene glycol was studied in the temperature range 100-270 оС in order to obtain nanostructured spinels. The phase composition, particle sizes of the reaction products, and their morphology studied by using IR spectroscopy, X-ray diffractometry, and scanning electron microscopy. We found that the nature of the reaction product of manganese and cobalt nitrates with ethylene glycol (EG) depends on the reaction temperature, the ratio of metal nitrate: ethylene glycol and reaction time. In excess of the reducing agent at temperatures up to 140 оС, observed the formation of metal oxalates. The main product of hydrothermal reduction of manganese nitrate with ethylene glycol at temperatures of 150 оC and 180 оC is manganese oxide Mn3O4 (Hausmanite). At 200 оС obtained the mixture of manganese oxide (Mn3O4) and carbonate (MnCO3). In accordance with the data of X-ray phase analysis at 220 оС and 240 оС, the only reaction product in both cases is manganese carbonate. It was obtained two types of structures on electron-microscopic images of the non-calcined sample at 200 оC: needle-shaped and spherical clusters. It can be assumed that these structures belong to the phases Mn3O4 (Hausmanite) and manganese carbonate MnCO3, respectively. When reduced cobalt nitrate with ethylene glycol in the temperature range 120-220 оC, gives a main amorphous phase, and on X-ray diffraction patterns are observed weak reflections corresponding to cobalt oxide Co3O4. It was shown that upon calcination (at 750 оС) of the samples during the reduction of the mixture of cobalt and manganese nitrates, was obtained the spinel phase of the composition (Co,Mn)(Co,Mn)2O4. In a similar way were obtained Li2CoMn3O8 and LiCoO2 phases (with average particle sizes of 42 nm and 30 nm), which can be used as cathodes in lithium batteries.


Metals ◽  
2021 ◽  
Vol 11 (6) ◽  
pp. 903
Author(s):  
Wojciech Maziarz ◽  
Paweł Czaja ◽  
Robert Chulist ◽  
Anna Wójcik ◽  
Łukasz Żrodowski ◽  
...  

Selective Laser Melting was successfully used as a fabrication method to produce Ni-Mn-Ga and Ni-Mn-Ga-Fe ferromagnetic shape memory alloys. The starting material in a powder form with an average particle size of about 17.6 µm was produced by milling of as melt-spun ribbons. The microstructure, phase composition, and martensitic transformation behavior of both powder precursors and laser melted alloys were investigated by several methods, including high energy X-ray diffraction, electron microscopy, and vibrating sample magnetometry. The as laser melted materials are chemically homogenous and show a typical layered microstructure. Both alloy compositions have a duplex structure consisting either of austenite and 10M martensite (Ni-Mn-Ga) or a mixture of 14M and NM martensitic phases (Ni-Mn-Ga-Fe), contrary to the as milled powder precursors showing fcc structure in both cases. The forward martensitic transformation takes place at 336 and 325 K for Ni-Mn-Ga and Ni-Mn-Ga-Fe, respectively, while the magnetic response is much stronger for Ni-Mn-Ga than for the quaternary alloy. The results show that Selective Laser Melting allows for producing of good quality, homogenous materials. However, their microstructural features and consequently shape memory behavior should be tailored by additional heat treatment.


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