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  • 1
    ISSN: 1520-5002
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0167-2738
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 32 (1997), S. 4559-4573 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The chemical reactivity of boron carbide (B4C) with metallic aluminium (Al) was studied at temperatures ranging from 900 to 1273 K (627–1000°C). Al–B4C powder mixtures were cold pressed, heated for 1–450 h under 105 Pa of purified argon and characterized by X-ray diffraction (XRD) optical metallography (OM), scanning electron microscopy (SEM) and electron probe microanalysis (EPMA). Whatever the temperature in the investigated range, B4C has been observed to react with solid or liquid Al. As long as the temperature is lower than 933 K (660°C), i.e. as long as Al is in the solid state, interaction proceeds very slowly, giving rise to the formation of ternary carbide (Al3BC) and to diboride (AlB2). At temperatures higher or equal to 933 K, Al is in the liquid state and the reaction rate increases sharply. Up to 1141±4 K (868±4°C), the reaction products are Al3BC and AlB2: at temperatures higher than 1141 K, Al3 BC is still formed while Al3B48C2 (β-AlB12) replaces AlB2. In the three cases, interaction proceeds via the same mechanism including, successively, an incubation period, saturation of aluminium in B and C, nucleation and growth by dissolution–precipitation of Al3BC and a C-poor boride and, finally, the passivation of B4C by Al3BC. These results are discussed in terms of solid–liquid phase equilibria in the Al–B–C ternary system, with reference to the binary invariant transformation: α-AlB12+L⇔AlB2, which has been found to occur at 1165±5 K (892±5°C).
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of applied electrochemistry 15 (1985), S. 421-429 
    ISSN: 1572-8838
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Electrical Engineering, Measurement and Control Technology
    Notes: Abstract A new manufacturing process of negative composite grids for lead acid accumulators is described and discussed. In this process long grid preforms are woven with both conductive carbon fibres and nonconductive glass or polypropylene fibres. Then, lead is selectively deposited on to the conductive carbon fibres by continuous electroplating and, after rinsing and drying, the composite grids are stamped out of the impregnated preforms. In these grids, the carbon fibres, embedded with lead, form the connector and the grid-bars. The non-conductive glass or polypropylene fibres provide the necessary cohesion of the woven preform before electroplating, and retension of the active material pasted into the grids. These negative composite grids are about four times lighter than the classical lead-alloy grids of similar size. They exhibit the excellent corrosion resistance and hydrogen overpotential of pure lead. Negative plates made from these grids have been subjected to CEI-type charge-discharge cycles (12 h cycles, 75% discharge depth): they have undergone more than 250 cycles without deterioration.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 19 (2000), S. 2039-2041 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 17 (1998), S. 757-760 
    ISSN: 1573-4811
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract This work was undertaken in order to provide more detailed information on the chemical and mechanical behaviour of carbon fibres during the elaboration of graphite-magnesium composite materials. For this purpose, PAN-based T300, pitch-based P55 and P100 carbon fibres were isothermally heat treated, at temperatures ranging from 450 to 700 °C, under a saturated vapour pressure of magnesium. The composition, microstructure and tensile strength of the resulting samples were characterized by chemical and electron probe microanalysis, Raman spectrometry, X-ray diffraction and mechanical test of single filaments. From the results obtained, it has been concluded that highly graphitized fibres such as pitch-based P55 or P100 are not affected by long-time annealing in the presence of magnesium vapour, whereas impure and disorded fibres such as PAN-based T300 undergo some chemical and microstructural modifications decreasing their mechanical properties.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of materials science 25 (1990), S. 1842-1850 
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract An experimental investigation was carried out on the Al-C-Si ternary system under atmospheric pressure and at temperatures up to 1900 K. From the results obtained, a thermodynamic model based on stable and metastable phase equilibria in the Al-C-Si ternary system was set up in order to provide a general description of the chemical interaction between aluminium and SiC. According to this model, aluminium and SiC are in thermodynamic equilibrium at every temperature lower than 923 K. At 923±3 K, i.e. at 10 K below the melting point of pure aluminium, a quasiperitectic invariant transformation occurs in the Al-C-Si system. In this transformation, solid aluminium reacts with SiC to give Al4C3 and a ternary (Al-C-Si) liquid phase. The carbon content of this liquid phase is very low; its silicon content is 1.5±0.4 at%. From 923 to about 1620 K, aluminium partially reacts with an excess of SiC, leading to a metastable monovariant equilibrium involving SiC, Al4C3 and an aluminium-rich (Al-C-Si) ternary liquid phase, L. The carbon content of this liquid phase, L, remains very low whereas its silicon content increases with temperature from 1.5±0.4 at% at 923 K to 16.5±1 at% at 1620 K. In the temperature range 1670 to 1900 K, two other three-phased monovariant equilibria can be reached by reacting aluminium and SiC. These equilibria involve on the one hand SiC, Al4SiC4 and a liquid phase, L′, and on the other hand, Al4SiC4, Al4C3 and a liquid phase, L″. The former is a stable equilibrium, the latter is a metastable one. At temperatures higher than about 2200 K, the latter metastable equilibrium is replaced by two monovariant stable phase equilibria including the ternary carbide Al8SiC7.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1573-4803
    Source: Springer Online Journal Archives 1860-2000
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract Previous investigations of phase equilibria in the ternary system Al-C-Si have shown that silicon carbide is attacked by pure aluminium at temperatures higher or equal to 923±3 K and up to about 1600 K, according to the chemical reaction: 4Al+3SiC ↔ Al4C3+3Si In the present work, a study has been carried out to obtain more detailed information on the mechanism and kinetics of this reaction. For that purpose, 6H silicon carbide platelets with broad Si (0 0 0 1) and C (0 0 0 ¯1) faces were isothermally heated at 1000 K in a large excess of liquid aluminium. Characterization of the resulting samples by Auger electron spectroscopy (AES) and scanning electron microscopy (SEM) revealed that the reaction proceeds in both faces via a dissolution-precipitation mechanism. However, the polarity of the substrate surface strikingly influences the rate at which silicon carbide decomposes: dissolution starts much more rapidly on the Si face than on the C face, but, while a barrier layer of aluminium carbide is formed on the Si face protecting it against further attack, the major part of the C face remains directly exposed to liquid aluminium and thus may continue to dissolve at a low but constant rate up to complete decomposition of the α-SiC crystal.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Interface science 1 (1994), S. 213-221 
    ISSN: 1573-2746
    Keywords: Composite materials ; magnesium ; silicon carbide ; reaction ; wettability ; transmission electron microscopy (TEM)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Abstract An amorphous SiO2 layer, 100–150 nm thick, has been produced on the surface of α-SiC particles by controlled oxidation in air. The as-treated particles were immersed for 1.5h at 1,000 K in a large excess of liquid magnesium, which resulted in the formation by pressureless infiltration of a composite region with a particle volume fraction about 50%. Conventional transmission electron microscopy (CTEM) and high-resolution TEM (HRTEM) were used to characterize and localize the different species present in the transition zone between the Mg matrix and the α-SiC particles. The results are discussed in terms of the physico-chemical processes occurring during formation of the composite region or during cooling of the Mg ingot. A reaction mechanism based on local equilibria and liquid phase diffusion is proposed. Four steps are involved in this mechanism: (i) rapid conversion of SiO2 into MgO and Si; (ii) formation of a true Mg/SiC interface; (iii) partial decomposition of SiC into carbon and silicon; and (iiii) precipitation of β-SiC and Mg2Si on cooling.
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