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Träfflista för sökning "L773:1073 5623 OR L773:1543 1940 srt2:(2000-2004)"

Sökning: L773:1073 5623 OR L773:1543 1940 > (2000-2004)

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1.
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2.
  • Divakar, M., et al. (författare)
  • Thermodynamics of surfaces and adsorption in the Fe-C-S-O system
  • 2000
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940 .- 1073-5615 .- 1543-1916. ; 31:2, s. 267-276
  • Tidskriftsartikel (refereegranskat)abstract
    • Surface tension experiments have been conducted on Fe-C-S-O alloys using the sessile drop technique at 1823, 1873, and 1923 K in a purified argon atmosphere. The experimental data indicate lowering of surface tension values for alloys with low carbon and oxygen contents relative to the corresponding ternary Fe-S-O system of comparable compositions. The data exhibit an increasing trend of the surface tension values as a function of carbon and oxygen contents and temperature of the melt, Modified Butler's equations have been used in conjunction with the consistent thermodynamic relations for a dilute quaternary system to calculate the surface tensions and adsorption functions of the system, The calculated values are in excellent agreement with those of the experimental data for compositions having lower oxygen at 1823 K, however, the values for the alloys containing higher oxygen contents depart from those of the experimental data. The calculated surface tension values agree within 150 mN/m with those of the experimental data at 1873 K. The agreement, in general, has been favorable despite the constraints involved in the calculations as discussed in the text.
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3.
  • Seetharaman, Seshadri, et al. (författare)
  • Estimation of viscosities of ternary silicate melts using the excess Gibbs energy of mixing
  • 2000
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940 .- 1073-5615 .- 1543-1916. ; 31:1, s. 105-109
  • Tidskriftsartikel (refereegranskat)abstract
    • A correlation to predict the viscosities of ternary Silicates using the Gibbs energies of mixing of the silicate melts has been developed. This correlation has been employed to predict the viscosities of liquid slags in the systems FeO-MnO-SiO2, FeO-MgO-SiO2, CaO-FeO-SiO2, CaO-MnO-SiO2, and CaO-MgO-SiO2. The good agreement between the calculated viscosities and the experimental data in the ternary silicate systems has indicated that this approach can be successfully employed to predict the viscosities of ternary silicate melts.
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4.
  • Bratberg, Johan, et al. (författare)
  • An experimental and theoretical analysis of the phase equilibria in the Fe-Cr-V-C system
  • 2004
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940. ; 35A:12, s. 3649-3663
  • Tidskriftsartikel (refereegranskat)abstract
    • New experimental phase equilibria information about the Fe-Cr-V-C system are presented and used to modify the thermodynamic description of the system. The main interest was focused on the composition of the MC and M7C3 carbides and the necessary adjustment of the Cr and V distribution between carbides and matrix. A new set of thermodynamic parameter values describing the Gibbs energy of different phases was obtained. A number of calculated sections of the Cr-C, Cr-V-C, Fe-Cr-C, and the Fe-Cr-V-C systems are presented and compared against both new and old experimental information. Calculations on commercial alloys to verify the improvements in multicomponent systems are also presented. The present calculation using the Thermo-Calc software shows much better agreement with the new experimental results than previous assessments.
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5.
  • Cao, Haiping, et al. (författare)
  • Effect of microstructure on mechanical properties of as-cast Mg-Al alloys
  • 2004
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940. ; 35:1, s. 309-319
  • Tidskriftsartikel (refereegranskat)abstract
    • The mechanical properties of Mg-Al alloys are mainly determined by the microstructure, i.e., the amount and morphology of the phases, but also by the presence of defects arising from the melt handling and casting process. In order to obtain information about the isolated effect of the microstructure, it is, therefore, necessary to minimize the amounts of defects. In this study, this has been achieved by remelting and solidifying the alloys in a gradient furnace. The drawing rate was varied from 0.3 to 6 mm/s, which yielded a wide variety of microstructures. Three samples were produced for each parameter set, in order to have a statistical basis for the evaluation. The results showed that homogeneous and reproducible samples could be produced, and that the tensile properties obtained showed a very small scatter. The effects of microstructural parameters such as grain size, secondary dendrite arm spacing (SDAS), eutectic fraction, and eutectic morphology on the yield strength, ultimate tensile strength (UTS), fracture elongation, and hardness has been investigated.
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6.
  • Das, D. K., et al. (författare)
  • Effect of prealuminizing diffusion treatment on microstructural evolution of high-activity pt-aluminide coatings
  • 2000
  • Ingår i: Metallurgical and Materials Transactions. A. - 1073-5623 .- 1543-1940. ; 31:8, s. 2037-2047
  • Tidskriftsartikel (refereegranskat)abstract
    • The effect of prealuminizing (or prior) diffusion treatment on the evolution of Pt-aluminide coatings on the Ni-based superalloy CM-247 has been studied by using a single-step, high-activity aluminizing process. Coatings generated without any prior diffusion treatment, as well as those formed by adopting two extreme prior-diffusion schedules (at 850 °C for 0.5 hours and at 1034 °C for 5 hours), were investigated by analyzing the coating structures at various stages of aluminizing. When the dilution of the Pt layer, caused by its interdiffusion with the substrate during the prior diffusion treatment, is only marginal (as in the case of no prior diffusion and diffusion at 850 °C for 0.5 hours), the equilibrium Pt-aluminide coating structure evolves through the formation of two transient layers during the initial stages of aluminizing. In contrast, for diffusion at 1034 °C for 5 hours, which results in extensive dilution of the Pt layer, the two-phase equilibrium structure (PtAl2 in a matrix of NiAl) in the outer layer of the coating is found to develop during very early stages of aluminizing and remains unchanged, even over extended periods of aluminizing. Further, in the case of prior diffusion at 1034 °C for 5 hours, Pt is found to remain distributed to a greater extent over the entire thickness of the coating than in the cases of limited prior diffusion treatment. The present findings underline the significance of the nature of the prior-diffusion schedule on the microstructural evolution of Pt-aluminide coatings. It has also been found that a prealuminizing diffusion treatment is particularly important for Pt-aluminide coatings from the point of view of coating adhesion to the substrate.
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7.
  • Dhindaw, B. K., et al. (författare)
  • Characterization of the peritectic reaction in medium-alloy steel through microsegregation and heat-of-transformation studies
  • 2004
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940. ; 35A:9, s. 2869-2879
  • Tidskriftsartikel (refereegranskat)abstract
    • In the present work, the phenomenon of the peritectic reaction was characterized in a medium-ailoy steel. Several directional solidification and thermal-analysis experiments were done to investigate the reaction process. Directional solidification experiments carried out did not tend to show any direct evidence of a peritectic reaction. Microsegregation studies on the directionally solidified samples and those solidified under isothermal conditions bring out some interesting features. It has been documented that if the segregation ratio for Ni is higher than that for Cr, there is a correlation that the peritectic reaction had occurred in that region. On the other hand, a higher Cr segregation ratio as compared to Ni showed the possibility that the liquid had directly transformed to gamma-austenite without undergoing a peritectic reaction. Measurement of energies of transformations and the analysis of their values in different segments of the cooling-curve differential thermal analysis (DTA) experiments have helped in understanding the peritectic reaction. It is revealed that the transformation is more like diffusionless transformation, where gamma-austenite directly precipitates from delta-ferrite. Indeed, this proposition is also supported by the segregation patterns for Cr and Ni obtained in the solidified samples of this steel during directional solidification and DTA experiments and also by calculations to show the presence of enough lattice defects or vacancies to aid the aforementioned transformation.
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8.
  • Du, H., et al. (författare)
  • Microstructural and compositional evolution of compound layers during gaseous nitrocarburizing
  • 2000
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940. ; 31:1, s. 195-211
  • Tidskriftsartikel (refereegranskat)abstract
    • Compound layers developed at 848 K during gaseous nitrocarburizing of iron and iron-carbon specimens were investigated for several combinations of N and C activities imposed at the specimen surface by gas mixtures of NH3, N-2, CO2, and CO. The microstructural evolution of the compound layer was studied by light microscopy and by X-raydiffraction analysis. Composition-depth profiles were determined by electron probe (X-ray) microanalysis. Layer growth kinetics was investigated by layer thickness measurements. The influence Of the N and C activities on the microstructural and compositional evolution and the growth kinetics of the compound layers formed is discussed for the iron substrate. The results indicate that the microstructure is governed by a fast C and a slow N absorption at the surface in an early stage of gaseous nitrocarburizing. The influence of carbon in the substrate on the microstructural and compositional evolutions and on the growth kinetics was evaluated from comparing the results obtained for: a: normalized Fe-0.8C alloy with those for iron under identical nitrocarburizing conditions.
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9.
  • Hillert, Mats (författare)
  • Nature of massive transformation
  • 2004
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940. ; 35A:1, s. 351-352
  • Tidskriftsartikel (refereegranskat)abstract
    • A description of massive transformation is presented. Massive transformation is defined as a kind of composition-invariant nucleation-and-growth formation of a solid phase from another solid phase. The nature of massive transformation is often described as diffusional. The concentration of nucleation to grain boundaries in the parent phase is a significant feature of massive transformation.
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10.
  • Hillert, Mats, et al. (författare)
  • Role of carbon and alloying elements in the formation of bainitic ferrite
  • 2004
  • Ingår i: Metallurgical and Materials Transactions. A. - : Springer Science and Business Media LLC. - 1073-5623 .- 1543-1940. ; 35A:12, s. 3693-3700
  • Tidskriftsartikel (refereegranskat)abstract
    • One approach to the prediction of the carbon content of austenite, remaining after the precipitation of bainitic ferrite, is based on the assumption that bainitic ferrite during growth inherits the carbon content of the parent austenite. An alternative approach is based on the assumption that bainitic ferrite grows with a low carbon content and there is no major difference between Widmanstatten ferrite and bainitic ferrite. The two approaches are now compared using information from alloyed steels with considerable amounts of Si, where the formation of cementite is retarded. The former approach does not account for the effect of Mn and fails severely at low alloy contents. The latter approach seems more promising but is not without difficulties. In particular, in order to explain the effects of Cr and Mo, it seems necessary to introduce a kinetic effect, presumably caused by solute drag.
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