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Yoichi NARUSE
1984 Volume 70 Issue 6 Pages
473-485
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Tetsuo KATO, Katsusi KUSAKA
1984 Volume 70 Issue 6 Pages
486-491
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Nobuo TAKISHIMA
1984 Volume 70 Issue 6 Pages
492-497
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Takashi NISHIYAMA
1984 Volume 70 Issue 6 Pages
498-503
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Noboru SAKAMOTO, Hiroshi FUKUYO, Yoshihito IWATA, Tsuneo MIYASHITA
1984 Volume 70 Issue 6 Pages
504-511
Published: April 01, 1984
Released on J-STAGE: February 15, 2010
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In order to produce sinter with high reducibility, a relation between sinter structure and its reducibility has been quantitatively investigated. Typical sinter structures and single mineral phases were synthesized using chemical reagents. An one-interface unreacted core model was applied to obtain the reduction rate parameters on these structures and the phases.
(1) The reducibility of the diffusion bonded type sinter was higher than that of the melting one, because of its high diffusivity of reducing gas through the reduced layer.
(2) As a result of the reduction tests on the single mineral phase, it was proved that the reducibility of the fine type hematite and calciumferrite were higher than that of the prismatic type calciumferrite in slag melt, because of the same reason as described above.
(3) By knowing the reducibility of the single mineral phase and each ratio of the phase in the sinter structure, the reducibility of their complex structures can be nearly estimated.
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Noboru SAKAMOTO, Hiroshi FUKUYO, Yoshihito IWATA, Tsuneo MIYASHITA
1984 Volume 70 Issue 6 Pages
512-519
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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A study on degradation of sinter structure during low temperature reduction has been made by considering strain formation in mineral phases and propagation of crack in the structure.
The results obtained are summarized as follows:
(1) The degradation is observed in any sinter structure, however the cracks propagated through melting bonded sinter structures are comparatively longer than that through diffusion bonded ones.
(2) X-ray diffraction patterns indicate that the spacing of lattice planes of alumina containing skeletal hematite are shrinked compared to that of fine type hematite. One of the causes of the degradation is considered to be due to the shrinkage.
(3) X-ray line broadening analysis revealed that the value of nonuiform strain in magnetite phase obtained from 550°C reduction was higher than that from 900°C reduction. The higher nonuniform strain is considered to cause the degradation during only low temperature reduction.
(4) By a statistical analysis of the crack propagations through various mineral phases, prismatic type calciumferrite and glassy slag were estimated to be unsuitable for sinter structure.
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Eiki KASAI, Ienbin SHU, Saburo KOBAYASHI, Yasuo OMORI
1984 Volume 70 Issue 6 Pages
520-526
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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A new sintering process was proposed which may cope with the increase in the ratio of fine iron ores. The basic concept associated with the new process using double layered mini-pellets (named duplex mini-pellets) was presented. The sintering experiments were conducted by using duplex mini-pellets and the quality of the produced sinter was evaluated by the various physical tests.
(1) Excellent permeability was observed for the sintering bed using the duplex mini-pellets compared with that for the current sinter practice.The bed-permeation resistance was reduced because size and structure of the pellets remained unchanged in the course of sintering before the fusion.
(2) By selecting the low melting region in CaO-Fe
2O
3 phase diagram as the chemical composition of the shell layer fines (CaO 20 wt%, Fe
2O
3 80 wt%), the sintering of the duplex mini-pellets was achieved at low temperature around 1230°C.
(3) The sinter produced by the method mentioned above had the texture of primary hematite and binary calciumferrite without secondary hematite.
(4) The sinter having such texture had excellent metallurgical properties, that is to say, low RDI, high JIS RI and good softening and melt-down properties.
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Rokuro KUWANO, Ynichi ONO
1984 Volume 70 Issue 6 Pages
527-532
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Effects of H
2S on the softening-melting properties of pellets during reduction under load have been experimentally studied with seven different brands of industrial pellets and an Fe
2O
3 pellet as samples. The results show that the presence of H2S in reducing gas has detrimental effects on the high temperature properties of the pellets. For example, the addition of only 0.1% of H
2S to 35%CO-65% N
2 gas mixture increased extremely the shrinking velocity of the pellets due to softening, although it hardly affected the reduction rate. Formation of easy-melting eutectic liquid from FeS and FeO has been found to be the main cause of the above-mentioned effects.
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Hideaki SUITO, Ryo INOUE
1984 Volume 70 Issue 6 Pages
533-540
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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The previous results on manganese distribution between liquid iron and Fe
tO-containing slags have been summarized. The apparent equilibrium constant
K'
Mn=
NMnO/([%Mn]·
NFetO) in the Fe
tO-MnO slags can be expressed as log
K'
Mn=7572/
T-3.559
The variations of
K'
Mn with slag compositions in the Fe
tO-MnO-MO
X(MO
X=PO
2.5, SiO
2, AlO
1.5, MgO, CaO) ternary melts as well as in MgO-saturated CaO-Fe
tO-SiO
2-MnO slags have been discussed on the basis of the regular solution model and the RICHARDSON's ideal silicate mixing.
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Kusuhiro MUKAI, Jyouki YOSHITOMI, Tsutomu HARADA, Kouichi HURUMI, Shoi ...
1984 Volume 70 Issue 6 Pages
541-548
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Local corrosion of clay bonded SiC specimen at the liquid iron alloy-slag interface has been investigated at 1550°C in order to elucidate the mechanism of local attack of blast furnace trough material at the slag-metal interface. Results obtained are as follows:
Local corrosion arises in the narrow zone just below the two liquid interface, regardless of partial pressure of oxygen of gas phase and also impurities contained in pig iron and slag. The extent of the corrosion depends on carbon concentration of the metal. The corrosion zone has a thin slag film between the specimen and the metal phase. It is estimated that the slag film plays important roles in the occurrence of the local corrosion because of its vigorous movements which accelerate the mass transfer and the abrasion of the specimen.
This movements are caused by the Marangoni effect and CO bubbles evolved as a product of SiO
2 reduction in the film by carbon in the metal. SiC granules on the surface of the specimen are oxidized by iron oxide in the film into carbon granules, which may facilitate the abrasion of the specimen by the turbulence of the film in the case of the metal not saturated with carbon. When the metal is saturated with carbon, the carbon granules remain in the film and may supress the local corrosion.
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Yoshiyuki UESHIMA, Hisashi YAMANA, Toyoko SUGIYAMA, Eiji ICHISE
1984 Volume 70 Issue 6 Pages
549-556
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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High temperature thermodynamic properties of Fe-W alloys were studied by the use of Knudsen cell mass spectrometer. As this alloy system has only single volatile component, the internal standard method was utilized to obtain activities in alloys. By taking advantage of high melting point of Fe-W alloys, Fe was used as the standard material. In applying this technique, the effect of the height of sample surface in the cell on the ion intensity was taken into consideration. Samples were melted and solidified preliminarily in a Knudsen cell before each run and then iron foil was placed on the sample surface so that the change in the height of sample surface in the cell on melting during the measurement was minimized.
Activities and free energy and enthalpy of mixing were derived at 1873 and 1773 K. The following were obtained
γ°
W(S)=7.6(±1.1), ε
WW=-2.2(±0.8), at 1873K
Values for the activities of Fe-Mo alloys were revised on the basis of the present knowledge about the influence of the height of sample surface on the ion intensity. The following values were obtained.
γ°
Mo(S)=2.2(±0.17), ε
MoMo=-0.14(±0.18) at 1823K
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Minoru UMEMOTO, Hideyuki OHTSUKA, Imao TAMURA
1984 Volume 70 Issue 6 Pages
557-564
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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The deformation of austenite below its recrystallization temperarure markedly accelerates the subsequent diffusional transformation. This acceleration is mostly caused by the increase in the nucleation rate. The increase in the nucleation rate per unit volume of specimen is attributed (1) to the increase in the austenite grain area by the elongation of grains, (2) to the increase in the nucleation rate per se per unit area of grain surface, and (3) to the formation of additional nucleation sites such as annealing twin boundaries, deformation bands, etc. Considering these effects, a kinetic equation for the deformed sepcimens was derived and from this equation, a method to estimate quantitatively the individual effect of the above three factors on the increase in the transformation rate was developed by defining the acceleration multiplying factors. Furthermore, the effects of the amout of rolling reduction and austenite grain size on the individual effect of the three factors on the acceleration of transformation were discussed based on the derived kinetic equation. Finally, as an application of the developed method, the acceleration multiplying factors for the pearlite transformation in the hot-rolled SKD 6 steel were calculated as functions of rolling reduction and austenite grain size.
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Takashi MATSUO, Tetsuya KISANUKI, Ryohei TANAKA, Shyuichi KOMATSU
1984 Volume 70 Issue 6 Pages
565-572
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Microstructural changes and degradation of high temperature tensile properties due to creep damage have been studied on 1Cr-1Mo-1/4V steel specimens obtained by interrupting the creep test up to 9 000 h at 600°C.
The loss of strength in the 1Cr-1 Mo-1/4V steel after long term creep exposure is due to three mechanisms: (I) the strength loss accompanying the change in the carbide morphology that usually occurs during tempering, (2) the strength loss resulted from local recovery of ferrite matrix in the vicinity of prior austenite grain boundary carbide particles, and (3) the strength loss due to formation of voids and cracks.
It is considered that the progress of creep damage during primary creep stage is attributed mainly to the first mechanism, and that of tertiary creep to the second one which is most important. On the other hand, no crack and the limited numbers of voids were observed at the grain boundary, then it is assumed that the third one is not essentially responsible for creep damage of Cr-Mo-V steel studied.
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Norio SHINYA, Junro KYONO, Shin YOKOI
1984 Volume 70 Issue 6 Pages
573-579
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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Creep cavity populations and resultant density changes have been measured on interrupted creep specimens with aim of assessing the bulid up of creep damage in Cr-Mo-V steel that eventually leads to fracture.
Metallographic observations have shown two types of creep cavities associated with either grain boundary carbides or with non-metallic inclusions. The number of creep cavities associated with grain boundary carbides increases linearly with increasing creep strain and growth of the cavities along grain boundaries leads to grain boundary cracks, whereas nucleation and growth of the creep cavities associated with non-metallic inclusions are limited by the number and size of the inclusions. The data of density change is expressed reasonably by the empirical equation
-Δ
D/
D=2.5×10
3εtσ
3.0exp(-234000/
RT)
where Δ
D/
D is the density change, εis the creep strain (%),
t is the time (h), σis the stress (kgf/mm
2),
R is the gas constant (8.314 J·mol
-1·K
-1), and
T is the absolute temperature (K). This equation can be used to estimate the residual life of Cr-Mo-V steel components working under creep conditions.
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Hisakichi SUNADA, Hisashi IZUMI, Imao TAMURA
1984 Volume 70 Issue 6 Pages
580-587
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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The sliding wear performance of high carbon-chromium steels has been investigated. The specimens were prepared by hot forging and isothermal rolling in order that the sizes of grains and size, shape and distributed carbide particles were varied. The wear tests were carried out by changing contact load, hardness of specimen and contact ring without lubricant. The wear resistance was determined by weight loss after 100 h sliding.
The results obtained were as follows:
1) The wear loss of quenched and tempered structure increased with increasing the contact load, decreasing the hardness of specimen and decreasing the ring hardness.
2) For as-worked structure, forged or pearlite structure had more improved wear resistance than rolled or ferritic structure. While wear resistance of rolled structure was better than that of forged one in the case of quenched-and-tempered structure.
3) As-forged structure which consisted of pearlite showed as much waer resistance as quenched structure.
4) Wear surface was flat in the case of hard specimen against hard ring, whereas combination of soft-soft tended to become rough. The thickness of wear damaged layer was almost constant in spite of hardness or structure.
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Hiroshi HIRAMATSU, Michio NAKATA, Hidehiko SUMITOMO, Hirofumi YOSHIMUR ...
1984 Volume 70 Issue 6 Pages
588-595
Published: April 01, 1984
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A study has been made of the influence of C, N and Ni contents and temper rolling on intergranular corrosion and mechanical properties of a 17Cr-7Ni steel, in order to develop a high strength stainless steel with high corrosion resistance. The results obtained are as follows:
(1) Intergranular corrosion sensitivity increases with increasing C content or temper rolling reduction. (2) 0.2% proof stress of annealed materials increases with increasing (C+2N) content. Tensile stress decreases with increasing stability of austenite phase, and increases with increasing C or N content in the case of the same austenite stability. Elongation increases with increasing austenite stability.
(3) The influence of C, N and Ni contents on the tensile properties of 25% temper rolled materials is similar to that on annealed materials and 0.2% proof stress increases with (2C+N) content. (4) The strengths of austenite and martensite phase increase with increasing C or N content. The effect of C content is smaller in austenite phase and is larger in martensite phase compared with the effect of N content. (5) Tensile stress and elongation of steel with 0.2% proof stress of 780 MPa increase with increasing C and N contents and decreasing Ni content. The optimum composition of 0.02C-17Cr-6.7Ni-0.12N has been determined by the consideration of corrosion resistance and high strength.
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Tetsujiro TAKEDA, Ken KANAYA, Kazunari YAMATO, Kiyotsugu EIRO, Zensaku ...
1984 Volume 70 Issue 6 Pages
596-602
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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There are many recently constructed power-transmission steel towers that are larger in size than ordinary ones. Higher strength steel is considered necessary for the large size tower to reduce its weight. Besides usual mechanical properties, the steel must have the resistance to zinc coating-induced cracking (ZIC) due to liquid metal embrittlement (LME).
1) Testing methods are developed to evaluate the ZIC susceptibility quantitatively. 2) Index for the ZIG susceptibility (
S400LM) is expressed as a function of chemical composition of steel. If the value of
S400LM is larger than 42%, the ZIC would not occur. 3) New 60 kg/mm
2 steels are developed as plate, UO pipe and ERW pipe for the use of a power-transmission tower. The steels show the excellent resistance properties to the ZIC and mechanical properties including buckling properties of pipes.
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Nobuyuki TSUTSUI, Yoshihiro TANAKA, Kazuyuki KOIKE
1984 Volume 70 Issue 6 Pages
603-607
Published: April 01, 1984
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[in Japanese], [in Japanese], [in Japanese], [in Japanese], [in Japane ...
1984 Volume 70 Issue 6 Pages
615-617
Published: April 01, 1984
Released on J-STAGE: June 30, 2009
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