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介绍了KR法铁水脱硫工艺的发展、脱硫的原理、该工艺的优、缺点及影响脱硫效果的因素,对喷吹和KR脱硫工艺进行了比较,为铁水脱硫装置的选择提供借鉴. 相似文献
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The densities of molten nickel mattes Cu2S-Ni3S2 and FeS-Ni3S2 were measured in the temperature interval 970° to 1321°C over the complete composition range. Several density values were
also obtained for the ternary matte Cu2S-FeS-Ni3S2 in the same temperature range. The densities of the binary mattes Cu2S-Ni3S2, FeS-Ni3S2 and ternary matte Cu2S-FeS-Ni3S2 were measured as 4.94 to 5.83 g per cu cm, 3.55 to 6.23 g per cu cm, and 2.65 to 4.92 g per cu cm, respectively. Molar volumes
and excess molar volumes of the binary mattes were evaluated. 相似文献
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The deoxidation equilibria of aluminum-magnesium and aluminum-manganese in liquid nickel equilibrated with Al2O3-saturated MgAl2O4 and MnAl2O4, respectively, were investigated in the temperature range of 1773 to 1873 K. At 1773 K, the oxygen levels could be reduced
to 5.8 to 6.6 ppm with 2.5 to 10 ppm magnesium and 0.05 to 0.9 mass pct aluminum in the Ni-Mg-Al-O system, and to less than
20 ppm with more than 1.5 mass pct manganese and 30 ppm aluminum in the Ni-Mn-Al-O system. With the experimental results mainly
obtained in the present work, the interaction parameters, e
Mg
Al
, e
Mn
Al
, e
O
Mg
, e
O
Mn
, and e
O
Al
, and the equilibrium constants, log
, log
, log K
Mg(Ni), log K
Mn(Ni), and log K
Al(Ni), were estimated using a multiple regression analysis. 相似文献
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A. F. Lisovskii 《Powder Metallurgy and Metal Ceramics》1980,19(11):759-761
Conclusions A study was made of some aspects of molten nickel penetration into titanium carbide hard metals. It is shown that, when such a liquid phase migrates through a semiinfinite rod, the variation of the concentration of the binder metal along the length of the rod may be described by a hyperbolic function. The dependence of the thickness of the layer of increased nickel content on time of contact between the specimen and the melt was determined. It is demonstrated that, by employing the method of infiltration of a hard metal with a liquid metal, it is possible to produce parts possessing varying physicomechanical properties.Translated from Poroshkovaya Metallurgiya, No. 11(215), pp. 25–38, November, 1980. 相似文献
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The thermodynamic properties of dilute solutions of sulfur in pure liquid nickel were investigated at 1500, 1550, and 1575°C
for sulfur concentrations up to 0.7 wt pct. Based on the infinitely dilute, wt pct standard state, the equilibrium data obtained
for the reaction: H2(g) + S = H2S(g) were fitted by the equations: logK = − 1489/T − 1.772, and ΔG° = 6812 + 8.11T, cal/mole. For the solution ofS
2(g) in pure Ni according to the reaction: 1/2S
2(g) = S (in Ni), the standard free energy of solution is found to be: ΔG° = - 28,342 + 3.62T, cal/mole. For the very dilute
solutions of sulfur normally encountered in nickel-base melting, the activity coefficient of sulfur in pure Ni at 1575°C is
given by: log fS= -0.035 (pct S). The effects of alloying elements normally used in nickel-base alloys on the activity coefficient of sulfur
in molten nickel were investigated. The activity coefficient of sulfur is increased by all of the alloying elements studied,
as evidenced by the interaction parameters: eS
fe = +0.005, eS
Cr = +0.030, eS
Mo = +0.053, eS
Ti = +0.160, and eS
A1 = +0.133. Measured values of the activity coefficient of sulfur in the quaternary system Ni-S-Cr-Fe agreed reasonably well
with those predicted from binary and ternary data.
This work constitutes a portion of the work performed by W. F. VENAL for the Ph.D. degree from the University of Illinois
at Chicago Circle.
Formerly Professor of Metallurgical Engineering at UICC. 相似文献
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J. J. Byerley G. L. Rempel N. Takebe 《Metallurgical and Materials Transactions B》1972,3(8):2133-2138
The kinetics and mechanism of the reduction of M3S2 by hydrogen have been investigated between 1133° and 1300°C. When high flow rates of hydrogen and argon or helium bubbling through the melt are maintained the rate-determining step is a chemical process which can be expressed by a rate law of the form $$\begin{gathered} r_{H_2 S} = k_{expt} (N_S - \alpha )^2 p_{H_2 }^{1/2} \hfill \\ p_{H_2 } \geqslant 0.88atm \hfill \\ \end{gathered} $$ where kexpt = 85.1 atm-1/2 min-1, α = 0.17 at 1250°C. The experimental activation energy for this process is 20.1 ±3.0 kcal per mole. These results are discussed in terms of possible catalysis by nickel. 相似文献
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Tsuyoshi Nishi Hiroyuki Shibata Yoshio Waseda Hiromichi Ohta 《Metallurgical and Materials Transactions A》2003,34(12):2801-2807
New attempts were made for the measurement of thermal diffusivity of molten iron, cobalt, and nickel at temperatures close
to 1900 K by a laser flash method. A simple but useful sample cell system was developed to keep the molten metal shape uniform
for a given thickness. It is also necessary to consider the effect of not only the radiative heat loss but also the conductive
heat loss at the interface between the molten metal sample and the sample cell material under the present experimental conditions.
The conductive heat loss was found, through computational simulation, to be negligibly small for the present laser flash measurements.
Thermal conductivity values of molten iron, cobalt, and nickel were calculated by combining the present thermal diffusivity
data with specific heat and density, and the resulting values are given in the following equations (unit: W m−1 K−1)
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《Canadian Metallurgical Quarterly》2013,52(4):205-210
AbstractSynthetic ferrites and sulphides of nick-el and cobalt were sulphated in the presence of molten sodium pyrosulphate and sodium bisulphate. The ferrites may be sulphated readily; hence it is unlikely that they would retain unreacted nickel or cobalt during the sulphation of the corresponding oxides.In the presence of either sodium pyrosulphate or sodium bisulphate, nickel and cobalt sulphides may be sulphated directly, but at higher temperatures the oxide forms as an intermediate compound. Résumé Des ferrites et des sulfures synthétiques de nickel et de cobalt ont été sulfatés en présence de pyrosulfate et de bisulfate de sodium fondus. Les ferrites peuvent être facilement sulfatés, dès lors il parait improbable qu'ils accaparent du nickel ou du cobalt durant la sulfatation des oxydes correspondants.En présence, soit de pyrosulfate de sodium soit de bisulfate, les sulfures de nickel et de cobalt peuvent être sulfatés directement, mais à températures élevées, il y a formation d'oxyde en tant que composé intermédiaire. 相似文献
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