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Takashi Sakamoto
1991 Volume 38 Issue 7 Pages
839-843
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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It is known that an addition of small amount of Ni powder in Mo powder compact is effective to increase the sintered density.
This paper describes the sintering characteristics of Mo-(0-3.0)%Ni powder compacts with the addition of B, NiB, MoB or C, when sintered at 1200 or 1300°C for 3.6 ks in vacuum.
The results are as follows:
(1) B and C powders are both effective on densification.
(2) The densification is considered to be due to the liquid phases formed during sintering, this being examined by DTA and SEM.
(3) The process of densification is verified by TMA.
(4) NiB and MoB powders are also effective, but the bending strength is lower than that of the B addition.
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Hidenori Kuroki, Koji Komatsu, Tokuhiko Mishida
1991 Volume 38 Issue 7 Pages
844-848
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Powders coarser than and similar to those for most metal injection molding processes were compared
to each other. The 13μm and 7μm water-atomized SUS316L powders were pressed so as to form compacts 10 mm in diameter and about 7 mm in height with a low density of about 4.85 Mg/m
3 which is rather close to that of the injection molded samples. They were sintered at 1373-1673K for 60 min in hydrogen.
The 7μm powder densified with the disappearance of small pores and the transitional growth of large pores as the sintering temperature rose, though the 13μm powder changed the pores into rounded shapes at low temperatures, and quickly reduced the total porosity at temperatures above 1573K. At 1623K or above, the difference between the pore structures of these powders almost disappeared. Any differences in tensile strength and elongation of these powder samples prepared actually by metal injection molding, also disappeared at 1623K.
The shrinkage of unidirectionally pressed compacts by sintering and that by cold isostatic pressing showed a similar anisotropy, giving a larger shrinkage in the lateral direction in both cases.
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Hiroshi Horiguchi, Toshiro Terakawa, Hideaki Baba, Katuhisa Takane
1991 Volume 38 Issue 7 Pages
849-853
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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As the raw material of MIM (Metal Injection Molding), carbonyl and atomized iron powders have been utilized.
In stead of those expensive powders, pulverized iron powder was developed and the possibility of application for MIM was checked. The results are as follows:
(1) By a globular treatment, the fluidity of the powder is improved in injection molding process.
(2) As concerns sintered compacts, the relative density is over 95%, and the tensile strength and elongation obtained are satisfactory.
(3) When a debinded compact contains much oxygen, a low temperature reduction is effective for increasing sintered density.
(4) Furthermore, the reduction is effective for carbon control of sintered compact, and a high carbon compact can be manufactured easily.
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Hidehito Fujiuchi, Koji Hayashi
1991 Volume 38 Issue 7 Pages
854-857
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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The effect of test temperature on the hardness (H
V) of fine-graind sintered compacts with the average crystal grain size of 0.10-0.35 μm, which were prepared from ultrafine powders of 0.02 μm, was investigated for Fe, Co, Ni, Fe-Co, Fe-Ni, Co-Ni and Fe-Co-Ni systems. The test temperature dependence of Hv for the Fe sintered com-pact was compared with those of medium or coarse-grained sintered compacts of 0.82-3.5 μm.
The results obtained were as follows: (1) The order of H
v observed at room temperature among the alloy systems did not change in general at the higher test temperatures. (2) The H
v of Fe fine-grained compacts decreased sharply at about 500 K, which was much lower than that (about 800 K) for coase-grained compacts of 3.5 μm. This was attributed to the fact that creep deformation easily occurs even at such low temperatures for fine-grained compacts.
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Masatomo Kamada, Shinya Ozaki, Youichi Tokunaga
1991 Volume 38 Issue 7 Pages
858-863
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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Phosphorus and 0.1 wt% carbon were added to SUS304L powder compacts in order to strengthen the P/M austenitic stainless steels. Effects of phosphorus content on the sintering and age hardening behavior were in-vestigated, in association with the tensile properties of the compacts. The results are summarized as follows:
Phosphorus can dissolve in austenitic matrix up to about 0.45 wt% at 1523 K. In the compacts containing over 0.45 wt% of phosphorus, a liquid phase is formed through eutectic reactions and remains during the sintering. This results in the densification of compacts and the pore rounding.
Tensile strength of as-sintered compacts increases with an increase in phosphorus content to reach the peak of 470 MPa at 0.6 wt% P, because of the solid solution hardening and the promotion of sintering. Phosphorus addition over 0.6 wt% produces a large amount of eutectic microstructure which affects negatively to the improvement of strength.
Tensile strength of 0.6 wt% P compact increases to 590 MPa by the aging at 1023 K for 30 ks. The relation between porosity (ε) and strength ratio of porous compacts to full density compact (σ/σ
0) is expressed by (σ/σ
0) =(1-ε)/(1+6ε) for the 0.6 wt% P compacts aged in optimum conditions.
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Takeshi Kaneko
1991 Volume 38 Issue 7 Pages
864-871
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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This report describes the results of investigations on the improvement of characteristics of tungsten heavy alloys which were produced with addition of suitable amount of Co (with Ni/Fe ratio of about 2.0) to basic composition of W-Ni-Fe, and an optimum amount of Co addition obtained. The mechanical properties at room temperature of the (91.8-93.4 wt% W) alloys increased with increasing Co content and attained a maximum with Co content of about 1.5 wt%, while the 95.4 wt% W alloys attained a maximum with Co content of about 0.5 wt%.
In the alloys with (addition of) suitable amount of Co, smaller dihedral angle between W-W grain and better "Wettability" were obtained, and it was made clear that those effect resulted in homogeneity of alloys, and the improved mechanical properties.
The SEM photographs of the fracture surfaces show that Co content alloys strengthen mainly the interface between W-binder phase boundaries and W-W grain boundaries.
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Won-Seung Cho, Koji Hayashi
1991 Volume 38 Issue 7 Pages
872-878
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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The effects of contents of Y
2O
3 sintering aid (4-14 mol%) and SiC whisker (SiC(w): as-received one (5-30 vol%) and sieved one (20 vol% only)) on the transverse-rupture strength and fracture toughness of SiC(w)/Si
3N
4-Y
2O
3-6 mol%Al
2O
3 composite ceramics were investigated, paying attention to the changes in the grain boundary phase, the size of acicular Si
3N
4 grains and the fracture source.
Results obtained were as follows: (1)Both the strength and toughness of the composites with 20 vol% as-received-and sieved-SiC(w) became a maximum at 8 mol%Y
2O
3, in the same way as the monolith. This was con-sidered mainly due to the largest acicular Si
3N
4 grain size and partly to the appearance of grain boundary phase of 5Y
2O
3⋅Si
3N
4⋅Al
2O
3 at such a Y
2O
3 content. (2)With increasing SiC(w) content, the strength decreased in spite of the increase in the toughness, which was attributed to the increase in the size of microstructural defects as a fracture source. (3)In spite of higher strength level of the specimens than those in the other reports, the fracture sources were large Si
3N
4 aggregate of 10-50 pm in the monolith, SiC(w) aggregate of 60-190 μm in the composite with as-received SiC(w) and SiC(w) aggregate of 18-80 μm in the composite with sieved SiC(w).
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Tamotsu Ueyama, Takashi Yamamoto
1991 Volume 38 Issue 7 Pages
879-886
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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The effects of the W metallizing condition and silver brazing condition on the bonding reliability of the nail head lead pins of the multilayer ceramic substrates manufactured by co-firing was examined. High bonding strength by the silver brazing to the W metallized layer was obtained when the W metallizing layer was 23 μm thick or thicker and the quantity of the silver solder used was 0.24-0.38 mg/mm
2 and the silver brazing temperature was 820-840°C. The bonding strength by the silver brazing was decreased after the brazed parts were heat-treated at 900°C. The cause of the degradation of the bonding strength was that the silver solder permeates into the W metallized layer and destroys the network of the W in that layer.
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Hideaki Yagi, Takehiko Saiki
1991 Volume 38 Issue 7 Pages
887-892
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Humidity sensors using various NASICON materials were experimentally produced by a thick film printing method. Among the NASICON materials, a humidity sensor using Na
4Zr
2Si
3O
12 material showed comparatively lower resistance in low humidity. The relation between a logarithm of its resistance and relative humidity was almost linear and showed nonhysteresis (2M-10kΩ in a range of 20-90%RH). Also, the humidity sensor using Na
4Zr
2Si
2O
12 in comparison with one using a usual NASICON was improved on the stability of a long term and durability in various environment tests.
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Shigetaka Wada
1991 Volume 38 Issue 7 Pages
893-894
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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The effect of the fracture toughness of impact particles on the erosive wear of ceramics was examined. Six kinds of Al
2O
3 abrasive particles, which were almost the same in size, figure and hardness, but different only in fracture toughness, were used as impact particles. Sintered Si
3N
4, Al
2O
3 (HA9O) and glass were used as target materials. Irrespective of the target materials, the erosive wear rate was qualitatively proportional to the fracture toughness of the impact particles.
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[in Japanese]
1991 Volume 38 Issue 7 Pages
896
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Akihisa Inoue, Tsuyoshi Yamamoto, Tsuyoshi Masumoto
1991 Volume 38 Issue 7 Pages
897-902
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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The influence of applied pressure on the structural relaxation, glass transition, crystallization and consolidation for an amorphous phase was examined by using a typical glassy Pd
48Ni
32P
20 alloy in a spherical powder or a ribbon form. The Pd-Ni-P alloy was chosen because of the existence of a wide supercooled liquid region in the temperature range below crystallization temperature (Tx). The relaxation and crystallization are significantly suppressed by the application of compressive load, presumably because of the increase in viscosity and the decrease in diffusivity. As a result, the pressing at a high temperature of 0.97Tx is required to produce an amorphous bulk with high relative density. Furthermore, an intermediate annealing between pressings was found to be effective for the reduction of the enhanced viscosity. The multi-stage pressing treatment consisting of pressing and annealing enabled to produce a highly dense amorphous bulk even at a relatively low temperature near Tg.
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Eugene Ivanov, Boris Bokhonov, Irina Konstanchuk
1991 Volume 38 Issue 7 Pages
903-905
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Mechanical alloying (MA) was used to obtain quasicrystalline; phases Mg
3Zn
5-xAlx (x=2-4) and i-Mg
32Cu
8Al
4 starting from the elementary metal powders.Mechanical disordering(MD) of cubic Frank-Kasper (F-K) phases such as Mg
32(Zn, A1)
49 lead to formation of relative quasicrystalline structures as well.The X-ray diffraction patterns of i-phases are identical to those obtained by rapid quenching. SAD patterns of both MA and MD samples demonstrated 2, 3, 6, and 5-fold symmetry pictures.There are ten sets of Bragg spots with angles between them 36°. The values of the interplanar distances in i-Mg
32(Zn, Al)49 are d
1=0.141nm, d
2=0.228nm, d
3=0.369nm, d
4=0.597nm, d
n=d
n-1t, where t=(1+5
1/2)/2.The cubic phases Mg
32(Zn, Al)
49 and Mg32(Cu, Al)49 are F-K structures with local 5-fold symmetry units.The icosa-hedral structure can be described in terms of cubic F-K phase containing discli-nations.The MD of F-K phases lead to progressive broadering of X-ray peaks due to the structural, defects arising in cubic lattice and the icosahedral phases were formed apparently due to the formation of disclination network during MD.
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Nobuo Asahi, Masaaki Oyama
1991 Volume 38 Issue 7 Pages
906-909
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Ag
30Dy
70 alloy was mechanically alloyed from pure crystalline Ag and Dy powders by high energy ball milling (Fritsch "Pulverisette 7") with the speed settings 7 or 3 in an argon atmosphere. The alloying process was investigated by X-ray diffraction, optical microscopy and differential scanning calorimetry.
In the first milling stages, the Ag and Dy powders have a well-aligned layered microstructure. This microstructure is typical for mechanical alloyed specimens during the early stages of milling and gets finer with increasing milling time. At this stage intermetallic compound AgDy has obtained. After 200 h of milling, the X-ray diffraction peaks of AgDy and Dy powders have hardly changed in intensity and the broad peak characteristic of an amorphous Ag
30Dy
70 powder was not produced by mechanical alloying from crystalline elemental powders.
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Junji Kuyama, Keiichi N Ishihara, Paul Hideo Shingu
1991 Volume 38 Issue 7 Pages
910-913
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Mechanical alloying (MA) of Fe-Mo binary system was performed by the low energy ball mill method. Elemental Fe and Mo powders were ball-milled up to 1000h. We characterized the reaction products by X-ray diffraction analysis, high resolution electron microscopy (HREM), and EDX analysis. From the X-ray diffraction patterns of MA powders, it was found that an amorphous phase was obtained in the composition of 30-50at%Mo and single bcc phase was obtained in the composition of 10-20at%Mo and 60-90at%Mo. The amorphization started from an early stage of MA and the amorphous region extended as MA continued. HREM investigation of Fe-30at%Mo and Fe-50at%Mo revealed that fine grains whose particle sizes are several nano-meters exist in the amorphous matrix. By the quantitative analysis by EDX, these grains were found to be Mo rich in composition.
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Young Ho Paark, Katsuhisa Yamauchi, Hitoshi Hashimoto, Ryuzo Watanabe
1991 Volume 38 Issue 7 Pages
914-919
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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Ti/Al powder mixture(Ti:Al=1:1) was mechanically alloyed by vibratory ball milling to analyze the action of milling ball size on the formation of an amorphous phase, by using X-ray diffraction analysis, electrical resistivity measurement, microhardness measurement, optical microscopy, SEM and TEM. As a result, the size of milling balls was found to play a decisive role in the amorphous phase formation. The electrical measurement made for the first time on the mechanically alloyed Ti/Al powder to monitor the phase transformation was found to catch successfully the formation of the amorphous phase and its crystallization during milling. TEM observation on the amorphous powder particles revealed that nano-sized crystalline intermetallic compounds were precipitated in the amorphous particles, which suggests that for the formation of the perfect amorphous phase it is of great importance to use milling balls smaller than 4.76mm.
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Osamu Kimura
1991 Volume 38 Issue 7 Pages
920-924
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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The ultrafine Mn-Zn ferrite (MnO)
0.37 (ZnO)
0.10(Fe
2O
3)
0.53 has been prepared by the amorphous citrate process. Extra pure manganese metal (99. 95%), zinc metal(>99. 99%) and iron metal (>99. 99%) are dissolved into 6N HNO
3 to prepare stoichiometric aqueous solution of manganese nitrate, zinc nitrate and ferric nitrate. Nitrate salts are avoided as starting materials, since they are strongly hygroscopic in nature. The nitrate solution is mixed with citric acid and ethylene glycol in a uniform solution. The water and nitric oxides are evaporated at around 90°C and ethylene glycol is dried at aruond 120°C to yield a solid precursor material. The precursor is fired to high temperature to form the desired compound. The decomposition mechanism is studied with thermogravimetric analysis, differential thermal analysis and X-ray diffraction. Also, magnetic properties and BET surface areas are measured for heat-treated powders.
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Osamu Kimura, Hiroshi Ochiai
1991 Volume 38 Issue 7 Pages
925-929
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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The high-Hc ultrafine hexaferrite SrO-n(Fe
2O
3)(n=5.4, 5.5, 5.8, 6.0)has been prepared by the amor-phous citrate process. An extra pure iron metal(>99.99%) and a pure strontium carbonate(99.7%) are dissolved into 6N HNO
3 to prepare stoichiometric aqeous solution of strontium nitrate and ferric nitrate. Nitrate salts are avoided as starting materials, since they are strongly hygrosc-opic in nature. The nitrate solution is mixed with citric acid and ethyleneglycol in a uniform solution. The water and nitric oxides are evaporated at around 90 °C and ethyleneglycol is dried at around 120 °C to yield a solid precursor material. The precursor is fired to high temperature to form the desired compound. The decomposition mechanism is studied with thermogravimetric analysis, differential thermal analysisand X-ray diffraction. Also, magnetic properties and BET surface areas are measured for heat-treated powders. Coercive force He reaches 6700 Oe at 10KG for the powder obtained by firing the precursor in air to 700 °C for lhr and nearly pure-phase strontium hexaferrite powders are formed at 1000 °C for lhr.
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Masahiro Oguchi, Yoshio Harakawa, Yoichi Shimizu, Akihisa Inoue, Tsuyo ...
1991 Volume 38 Issue 7 Pages
930-933
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Amorphous Co
70.3Fe
4.7Si
10B
15 powders were produced by a two-stage quenching technique consisting of high-pressure gas atomization followed by centrifugal spinning. The amorphous powders have a flaky morphology with a disk or an ellipsoidal shape. The thickness is as small as 1 to 3 μm and the dimension along the longitudinal direction is 25 to 300 μm leading to large aspect ratios of about 20 to 300. The composite consisting of the flaky amorphous powders embedded in phenol resin exhibits significantly anisotropic magnetic properties because of a well developed arrangement of the flaky powders along the direction perpendicular to the hot-pressing direction. Judging from the combined characteristics of the unique powder morphology and the magnetic properties inherent to the Co-based amorphous phase, the flaky amorphous powders are concluded to have a further enhanced engineering potentiality.
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M.Sherif El-Eskandarany, Hiroshi Suzuki, Kiyoshi Aoki, Kenji Suzuki
1991 Volume 38 Issue 7 Pages
934-939
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Previously published calorimetric study of amorphous Ta-50 at.%Al alloy powders is complemented by structure and morphological studies. The alloy powders were prepared by mechanical alloying (MA) from pure elemental powders of Ta and Al. The alloy powders have been characterized by optical microscopy, scanning electron microscopy and transmission electron microscopy. The results have shown the MA process takes place through three stages, that is to say, agglomeration, amorphization and homogenization stages.
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Toshiharu Fukunaga, Eiji Ishikawa, Uichiro Mizutani
1991 Volume 38 Issue 7 Pages
940-943
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Cr and Fe elemental powders at 7:3 atomic propotion were milled in a vibrational ball mill under N
2 gas atmosphere. The concentration of N atoms in the Cr
0.7Fe
0.3-N powders increased with increasing MA time and approached to about 15at%N after 320 hours of milling. The amorphization was observed by X-ray diffraction and DSC measurements.
RDF(r) shows that the 2nd nearest neighbor atoms in BCC crystal preferentially moved out of their positions during the amorphization process and the 1st nearest neighbor distance between metal atoms increases with increasing the milling time. The nearest coordination number around a metal atom within about 3.3 A decreases from 14 to 12.5 atoms while the amorphization proceeds. These results definitely tell us that the octahedral unit in a BCC structure is destroyed and is transformed into the tetrahedral unit during the amorphization process. An increase in the metal-metal distance of the 1st nearest neighbor with increasing nitrogen content can be interpreted by the penetration of a nitrogen atom into a polyhedron formed by metal atoms.
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Junji Saida, Akihisa Inoue, Tsuyoshi Masumoto
1991 Volume 38 Issue 7 Pages
944-947
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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Amorphous ultra-fine powders in (Fe, Co, Ni)-B systems were prepared by a chemical reduction method using KBH
4. The powders have a spherical morphology with diameters ranging from 20 to 50 nm. The boron concentration is in the range of 25 to 35 at.% and chemical composition of the metal elements can be controlled by changing the concentration of metal ions. Crystallization temperature (Tx) and heat of crystallization for an ultra-fine Fe
50Ni
22B
28 powder agree with those obtained for the amorphous alloy with the same composition prepared by melt spinning. The reaction process consists mainly of the process of preparing Me
2B and Me (Me=Fe, Co, Ni). Furthermore, the amorphous powders were found to be consolidated to a fully dense amorphous bulk by uniaxial pressing at temperatures below Tx. Their densities are almost equal to those of the corresponding arc-melted crystalline powders. Hardness values of the hot-pressed compacts are considerably lower than those of the melt-spun amorphous ribbons with the same composition.
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Yoshihito Kawamura, Akihisa Inoue, Tsuyoshi Masumoto
1991 Volume 38 Issue 7 Pages
948-952
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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High-strength Mg-Cu-Y amorphous alloys with significant supercooled liquid region have attracted attention as a structural light metal. The future application of the new alloys seems to be dependent on the development of a technique of consolidating the amorphous powders to an amorphous bulk. The effects of applied pressure, pressing temperature and flow strength of an alloy on the densification of amorphous powders by uniaxial warm pressing were examined for an amorphous Mg
65Cu
25Y
10 alloy with a wide supercooled liquid region of 67K.
The amorphous alloy with a distinct glass transition phenomenon is easily consolidated near Tg, especially above Tg, and the minimum consolidation pressure required to obtain an amorphous bulk with true density is about four times as high as the flow strength of the alloy at the consolidation temperature. As the pressing temperature approaches Tg the effect of applied pressure on the densification decreases. The amorphous Mg
65Cu
25Y
10 bulk with true density was obtained even at a small pressure of 0.2GPa, when the pressing temperature is 10K higher than Tg. The significant temperature dependence is attributed to the drastic decrease in the flow strength of the amorphous alloy by the glass transition.
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Katsumasa Ohtera, Takeshi Terabayashi, Hidenobu Nagahama, Akihisa Inou ...
1991 Volume 38 Issue 7 Pages
953-956
Published: September 25, 1991
Released on J-STAGE: December 04, 2009
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Aluminium-based amorphous powders of A185Ni5Y10 and A188.5Ni8Mm3.5 were produced by high-pressure gas atomization. Since the amorphous A185Ni5Y10 alloy exhibits the glass transition before crystallizaion, the extrusion of the A185Ni5Y10 amorphous powder was performed at temperatures below crystallization temperature(Tx). The resulting extruded bulk consists mainly of an amorphous phase and the compressive strength is as high as 1052MPa. On the other hand, the amorphous A188.5Ni8Mm3.5 powder without glass transition was extruded at temperatures above Tx and the highest tensile strength reached 94OMPa for the extruded bulk with a finely mixed structure of Al11(Ce, La)3 and Al3Ni embedded in an aluminium matrix.
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Minoru Umemoto, Tsuyoshi Itsukaichi, Isao Okane, Yasutoshi Mizuno, Ter ...
1991 Volume 38 Issue 7 Pages
957-962
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Mechanical alloying is applied to prepare Sm
2Fe
17N
x permanent magnet. Starting from elemental powders, the formation of hard magnetic phase of Sm
2Fe
17N
x by milling in a horizontal ball mill and a successive solid-state reaction was studied. The effect of starting composition of powder on product phase was first investigated. At as milled condition powder was found to consist of α-Fe and Sm-Fe alloy amorphous phases when Sm content is less than 19 at% and consist of α-Fe and SmFe
2 phase when Sm content is 26 at%. After heating and nitriding treatments pow-der was found to consist of α-Fe and Sm
2Fe
17N
x when Sm content is less than 15 at% and consist of α-Fe and SmN when the Sm content is 26 at%. When Sm content was 19 at%, nitrided MA powder consists of mostly Sm
2Fe
17N
x phase. The effect of milling time was studied for the powder of starting composition of Sm
19Fe
81. When powder was milled longer than 180ks, almost single phase of Sm
2Fe
17N
x was formed after nitriding. Coercivity was observed to increase linearly with logarithm of milling time from around 72ks and reached to 1200kA/m after 360ks of milling. This high value of coercivity was cosidered to be obtained by ultra fine grain size of Sm
2Fe
17N
x produced by ball milling and heat treatment.
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Shinya Shiga, Tsuyoshi Itsukaichi, Minoru Umemoto, Isao Okane
1991 Volume 38 Issue 7 Pages
963-966
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Elemental powders of Al and Ni with the composition of Al
25Ni
75 was mechanically alloyed in an Ar gas atmosphere for various periods using a horizontal ball mill. A single phase of Ni solid solution with Al super saturation was obtained by a long time milling. This Ni solid solution transformed into AINi
3 compound (Ll
2:ordered FCC) at around 700K with the enthalpy of 4.6kJ/mol. The hardness of hot-pressed compacts prepared from MA powders was higher than that of melted and solidified, irrespective of the MA time. The hot pressed compacts of MA powders showed compositional inhomogeneity when powders were milled shorter than 36ks and showed voids when powders were milled longer than 360ks. The suitable MA time for sintering was in the range between 72 and 180ks.
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Shinya Shiga, Tsuyoshi Itsukaichi, Minoru Umemoto, Isao Okane
1991 Volume 38 Issue 7 Pages
967-970
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Elemental Powders of Al and Ni with the composition of Al
50Ni
50 was mechanically alloyed in an Ar gas atmosphere for various periods using a horizontal ball mill. A single phase of AM compound (B2:ordered BCC) was synthesized by milling longer than 360ks. The powder particle size was substantially decreased to about 0.5 μm in diameter by MA associated with the formation of AlNi compound. The MA powders were hot-pressed under the condition of 150MPa at 973K for 1.8ks. The hot-pressed compacts showed compositional inhomogeneity when powders were milled shorter than 72ks. When MA time is longer than 180ks, the unsintered region appeared in the hot-pressed compact and the area increased with the increase in MA time. The powder milled for 1800ks did not sinter at all. The hardness of hot-pressed compacts showed maximum of 500Hv at MA time of 18ks and reduced gradually with MA time. The suitable MA time for sintering was considered to be around 100ks.
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Shinya Shiga, Tsuyoshi Itsukaichi, Minoru Umemoto, Isao Okane
1991 Volume 38 Issue 7 Pages
971-975
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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Elemental powders of Al and Ni with the composition of Al
75Ni
25 was mechanically alloyed in an Ar gas atmosphere for various periods using a horizontal ball mill. A single phase of disordered AlNi structure (BCC) was obtained by milling of 1800ks. This BCC structure transformed into Al
3Ni compound (DO
20) at around 600K. The hot-pressed compacts of MA powders showed compositional inhomogeneity and voids produced by isothermal solidification when powders were milled shorter than 72ks and showed well sintered structure when powders were milled longer than 180ks. The hardness of hot-pressed compacts prepared from MA powders milled between 36ks and 360ks reached at around 750Hv. The suitable MA time for sintering was considered to be between 180ks and 360ks.
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Shinya Shiga, Takayuki Norimatsu, Tsuyoshi Itsukaichi, Minoru Umemoto, ...
1991 Volume 38 Issue 7 Pages
976-980
Published: September 25, 1991
Released on J-STAGE: May 22, 2009
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The structural change in Al
75Ni
25 powder during MA and MG was studied using SEM, X-ray diffraction and DSC. MA was carried out for the mixture of elemental Al and Ni powders and MG was done for the powder of Al
3Ni intermetallic compound prepared by arc melting. In both MA and MG processes, the major end product was found to be disordered AlNi (BCC) which was identified by X-ray diffraction. DSC and x-ray diffraction analysis showed that the disordered AlNi phase transformes directly to Al
3Ni intermetallic compound by heating. It was noted that the transformation temperature of disordered AlNi structure to Al
3Ni compound in MG powder is higher than that of MA powder. The amount of exothermic heat associated with this transformation in MG powder (1.0kJ/mol) was found to be smaller than that of MA powder (2.5kJ/mol). This difference may arise from the fact that in the case of MG powder Al
3Ni compound still partially remains even after heating up to 973K.
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