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1.
Zhe-Feng Zhang Zheng Ming Sun Hitoshi Hashimoto Toshihiko Abe 《Journal of the American Ceramic Society》2003,86(3):431-436
Ti/Si/2TiC powders were prepared using a mixture method (M) and a mechanical alloying (MA) method to fabricate Ti3 SiC2 at 1200°–1400°C using a pulse discharge sintering (PDS) technique. The results showed that the Ti3 SiC2 samples with <5 wt% TiC could be rapidly synthesized from the M powders; however, the TiC content was always >18 wt% in the MA samples. Further sintering of the M powder showed that the purity of Ti3 SiC2 could be improved to >97 wt% at 1250°–1300°C, which is ∼200°–300°C lower than that of sintered Ti/Si/C and Ti/SiC/C powders using the hot isostatic pressing (HIPing) technique. The microstructure of Ti3 SiC2 also could be controlled using three types of powders, i.e., fine, coarse, or duplex-grained, within the sintering temperature range. In comparison with Ti/Si/C and Ti/SiC/C mixture powders, it has been suggested that high-purity Ti3 SiC2 could be rapidly synthesized by sintering the Ti/Si/TiC powder mixture at relatively lower temperature using the PDS technique. 相似文献
2.
Tamer El-Raghy Michel W. Barsoum Antonios Zavaliangos Surya R. Kalidindi 《Journal of the American Ceramic Society》1999,82(10):2855-2860
In this article, the second part of a two-part study, we report on the mechanical behavior of Ti3 SiC2 . In particular, we have evaluated the mechanical response of fine-grained (3–5 μm) Ti3 SiC2 in simple compression and flexure tests, and we have compared the results with those of coarse-grained (100–200 μm) Ti3 SiC2 . These tests have been conducted in the 25°–1300°C temperature range. At ambient temperature, the fine- and coarse-grained microstructures exhibit excellent damage-tolerant properties. In both cases, failure is brittle up to ∼1200°C. At 1300°C, both microstructures exhibit plastic deformation (>20%) in flexure and compression. The fine-grained material exhibits higher strength compared with the coarse-grained material at all temperatures. Although the coarse-grained material is not susceptible to thermal shock (up to 1400°C), the fine-grained material thermally shocks gradually between 750° and 1000°C. The results presented herein provide evidence for two important aspects of the mechanical behavior of Ti3 SiC2 : (i) inelastic deformation entails basal slip and damage formation in the form of voids, grain-boundary cracks, kinking, and delamination of individual grains, and (ii) the initiation of damage does not result in catastrophic failure, because Ti3 SiC2 can confine the spatial extent of the damage. 相似文献
3.
Da Chen Kiroshi Shirato Michel W. Barsoum Tamer El-Raghy Robert O. Ritchie 《Journal of the American Ceramic Society》2001,84(12):2914-2920
The cyclic fatigue and fracture toughness behavior of reactive hot-pressed Ti3 SiC2 ceramics was examined at temperatures from ambient to 1200°C with the objective of characterizing the high-temperature mechanisms controlling crack growth. Comparisons were made of two monolithic Ti3 SiC2 materials with fine- (3–10 μm) and coarse-grained (70–300 μm) microstructures. Results indicate that fracture toughness values, derived from rising resistance-curve behavior, were significantly higher in the coarser-grained microstructure at both low and high temperatures; comparative behavior was seen under cyclic fatigue loading. In each microstructure, Δ K th fatigue thresholds were found to be essentially unchanged between 25° and 1100°C; however, there was a sharp decrease in Δ K th at 1200°C (above the plastic-to-brittle transition temperature), where significant high-temperature deformation and damage are first apparent. The substantially higher cyclic-crack growth resistance of the coarse-grained Ti3 SiC2 microstructure was associated with extensive crack bridging behind the crack tip and a consequent tortuous crack path. The crack-tip shielding was found to result from both the bridging of entire grains and from deformation kinking and bridging of microlamellae within grains, the latter forming by delamination along the basal planes. 相似文献
4.
The effect of vacuum annealing on the thermal stability and phase transition of Ti3 SiC2 has been investigated by X-ray diffraction (XRD), neutron diffraction, synchrotron radiation diffraction, and secondary ion mass spectroscopy (SIMS). In the presence of vacuum or a controlled atmosphere of low oxygen partial pressure, Ti3 SiC2 undergoes a surface dissociation to form nonstoichiometric TiC and/or Ti5 Si3 C x that commences at ∼1200°C and becomes very pronounced at ≥1500°C. Composition depth profiling at the near surface of vacuum-annealed Ti3 SiC2 by XRD and SIMS revealed a distinct gradation in the phase distribution of TiC and Ti5 Si3 C x with depth. 相似文献
5.
P. Mogilevsky Tai-Il Mah T. A. Parthasarathy C. M. Cooke 《Journal of the American Ceramic Society》2006,89(2):633-637
Composites in the SiC–TiC–Ti3 SiC2 system were synthesized using reactive hot pressing at 1600°C. The results indicate that addition of Ti3 SiC2 to SiC leads to improved fracture toughness. In addition, high microhardness can be retained if TiC is added to the material. The best combination of properties obtained in this study is K I c =8.3 MPa·m1/2 and H v =17.6 GPa. The composition can be tailored in situ using the decomposition of Ti3 SiC2 . Ti3 SiC2 decomposed rapidly at temperatures above 1800°C, but the decomposition could be conducted in a controlled manner at 1750°C. This can be used for synthesis of fully dense composites with improved properties by first consolidating to full density a softer Ti3 SiC2 -rich initial composition, and then using controlled decomposition of Ti3 SiC2 to achieve the desired combination of microhardness and fracture toughness. 相似文献
6.
Erdong Wu Erich H. Kisi Daniel P. Riley Ronald I. Smith 《Journal of the American Ceramic Society》2002,85(12):3084-3086
The reactive sintering of 3Ti/SiC/C to form the layered ternary carbide Ti3 SiC2 was studied in situ by time-resolved neutron powder diffraction. A number of intermediate processes occur during the synthesis beginning with the α-β transition in Ti. Concurrent with the α-β transition, two intermediate phases, TiC x and Ti5 Si3 C x ( x ≤ 1), form. These phases account for almost the entire sample in the range 1500–1600°C beyond which they react with each other and a small amount of free C to form the product phase Ti3 SiC2 . 相似文献
7.
Sui Lin Shi Wei Pan Ming Hao Fang Zhen Yi Fang 《Journal of the American Ceramic Society》2006,89(2):743-745
Ti3 SiC2 /HAp composites with different Ti3 SiC2 volume fractions were fabricated by spark plasma sintering (SPS) at 1200°C. The effects of Ti3 SiC2 addition on the mechanical properties and microstructures of the composites were investigated. The bending strength and fracture toughness of the composites increased with increasing of Ti3 SiC2 content, whereas the Vickers hardness decreased. The bending strength and fracture toughness reached 252±10 MPa and 3.9±0.1 MPa·m1/2 , respectively, with the addition of 50 vol% Ti3 SiC2 . The increases in the mechanical properties were attributed to the matrix strengthening and interactions between cracks and the Ti3 SiC2 platelets. 相似文献
8.
José M. Córdoba María J. Sayagués María D. Alcalá Francisco J. Gotor 《Journal of the American Ceramic Society》2007,90(3):825-830
Titanium silicon carbide (Ti3 SiC2 ) and Ti3 SiC2 -based composite powders were synthesized by isothermal treatment in an inert atmosphere as a function of initial compositions (mixtures). A high content of TiC was obtained in the final product when the initial mixtures contained free carbon. The use of TiC as a reagent was unsuccessful in obtaining Ti3 SiC2 . High Ti3 SiC2 conversion was found for the initial mixtures containing SiC as the main source for silicon and carbon. An initial mixture with a large excess of silicon, 3Ti/1.5SiC/0.5C, was needed to obtain high-purity Ti3 SiC2 . A reaction mechanism, where Ti3 SiC2 nucleates on Ti5 Si3 C crystals and grows by long-range diffusion of Ti and C, is proposed. The reaction mechanism was proposed to be based on silicon loss during the formation of Ti3 SiC2 . 相似文献
9.
Erich H. Kisi Erdong Wu Jennifer S. Zobec Jennifer S. Forrester Daniel P. Riley 《Journal of the American Ceramic Society》2007,90(6):1912-1916
It is demonstrated that the M n +1 AX n phase Ti3 AlC2 may be readily synthesized by sintering a stoichiometric mixture of the lower order MAX phase Ti2 AlC mixed with a stoichiometric amount of TiC in the temperature range 1350°–1450 °C. High-quality Ti3 AlC2 was readily produced using sintering times in the range 2–5 h. In general, <2% of unwanted or remnant phases were found to be present and in some samples none could be detected at all. 相似文献
10.
Adrish Ganguly Michel W. Barsoum Roger D. Doherty 《Journal of the American Ceramic Society》2007,90(7):2200-2204
In this work, we report on the interdiffusion of Ge and Si in Ti3 SiC2 and Ti3 GeC2 , as well as that of Nb and Ti in Ti2 AlC and Nb2 AlC. The interdiffusion coefficient, D int , measured by analyzing the diffusion profiles of Si and Ge obtained when Ti3 SiC2 –Ti3 GeC2 diffusion couples are annealed in the 1473–1773 K temperature range at the Matano interface composition (≈Ti3 Ge0.5 Si0.5 C2 ), was found to be given by
Dint increased with increasing Ge composition. At the highest temperatures, diffusion was halted after a short time, apparently by the formation of a diffusion barrier of TiC. Similarly, the interdiffusion of Ti and Nb in Ti2 AlC–Nb2 AlC couples was measured in the 1723–1873 K temperature range. The D int for the Matano interface composition, viz. ≈(Ti0.5 ,Nb0.5 )2 AlC, was found to be given by
At 1773 K, the diffusivity of the transition metal atoms was ≈7 times smaller than those of the Si and Ge atoms, suggesting that the former are better bound in the structure than the latter. 相似文献
D
At 1773 K, the diffusivity of the transition metal atoms was ≈7 times smaller than those of the Si and Ge atoms, suggesting that the former are better bound in the structure than the latter. 相似文献
11.
Bouchaib Manoun Surendra K. Saxena Hanns-Peter Liermann Michel W. Barsoum 《Journal of the American Ceramic Society》2005,88(12):3489-3491
We measured the volume thermal expansion of Ti3 SiC2 from 25° to 1400°C using high-temperature X-ray diffraction using a resistive heated cell. A piece of molybdenum foil with a 250 μm hole contained the sample material (Ti3 SiC2 +Pt). Thermal expansion of the polycrystalline sample was measured under a constant argon flow to prevent oxidation of Ti3 SiC2 and the molybdenum heater. From the lattice parameters of platinum (internal standard), we calculated the temperature by using thermal expansion data published in the literature. The molar volume change of Ti3 SiC2 as a function of temperature in °C is given by: V M (cm3 /mol)=43.20 (2)+9.0 (5) × 10−4 T +1.8(4) × 10−7 T 2 . The temperature variation of the volumetric thermal expansion coefficient is given by: αv (°C−1 )=2.095 (1) × 10−5 +7.700 (1) × 10−9 T . Furthermore, the results indicate that the thermal expansion anisotropy of Ti3 SiC2 is quite mild in accordance with previous work. 相似文献
12.
pela Kunej Sreo D. kapin Danilo Suvorov 《Journal of the American Ceramic Society》2009,92(10):2373-2377
In this study we used solid-state synthesis to determine the phase relations in the pyrochlore-rich part of the Bi2 O3 −TiO2 −Nd2 O3 system at 1100°C. The samples were analyzed using X-ray powder diffraction and scanning electron microscopy with energy- and wavelength-dispersive spectroscopy. A single-phase pyrochlore ceramic was obtained with the addition of 4.5 mol% of Nd2 O3 . We determined the solubility limits for the three solid solutions: (i) the pyrochlore solid solution Bi(1.6–1.08 x ) Nd x Ti2 O(6.4+0.3 x ) , where 0.25< x <0.96; (ii) the solid solution Bi4− x Nd x Ti3 O12 , where 0< x <2.6; and (iii) the Nd2− x Bi x Ti2 O7 solid solution, where 0< x <0.35. The determined phase relations in the pyrochlore-rich part are presented in a partial phase diagram of the Bi2 O3 −TiO2 −Nd2 O3 system in air at 1100°C. 相似文献
13.
Formation of titanium silicon carbide (Ti3 SiC2 ) by mechanical alloying (MA) of Ti, Si, and C powders at room temperature was experimentally investigated. A large amount of granules less than 5 mm in size, consisting of Ti3 SiC2 , smaller TiC particles, and other silicides, have been obtained after ball milling for only 1.5 h. The effect of excess Si in the starting powders on the formation of Ti3 SiC2 was studied. The formation mechanism of Ti3 SiC2 was analyzed. It is believed that a mechanically induced self-propagating reaction is ignited during the MA process. A possible reaction mechanism was proposed to explain the formation of the final products. 相似文献
14.
Shuichi Kawano Junichi Takahashi Shiro Shimada 《Journal of the American Ceramic Society》2003,86(9):1609-1611
Nano-sized TiO2 powders were prepared by controlled hydrolysis of TiCl4 and Ti(O-i-C3 H7 )4 solutions and nitrided in flowing NH3 gas at 700°–1000°C to form TiN. Nano-sized TiN was densified by spark plasma sintering at 1300°–1600°C to produce TiN ceramics with a relative density of 98% at 1600°C. The microstructure of the etched ceramic surface was observed by SEM, which revealed the formation of uniformly sized 1–2 μm grains in the TiCl4 -derived product and 10–20 μm in the Ti(O-i-C3 H7 )4 -derived TiN. The electric resisitivity and Vickers micro-hardness of the TiN ceramics was also measured. 相似文献
15.
Y. C. Zhou D. T. Wan Y. W. Bao J. Y. Wang D. T. Wan 《International Journal of Applied Ceramic Technology》2006,3(1):47-54
Ti3 SiC2 has many salient properties including low density, high strength and modulus, damage tolerance at room temperature, good machinablity, and being resistant to thermal shock and oxidation below 1100°C. However, the low hardness and poor oxidation resistance above 1100°C limit the application of this material. The poor oxidation resistance at temperatures above 1100°C was because of the absence of protective layer in the scale and the presence of TiC impurity phase. TiC impurity could be eliminated by adding a small amount of Al to form Ti3 Si(Al)C2 solid solutions. Although the high-temperature oxidation resistance was significantly improved for the Ti3 Si(Al)C2 solid solutions, the strength at high temperatures was lost. One important way to enhance the high-temperature strength is to incorporate hard ceramic particles like SiC. In this article, we describe the in situ synthesis and simultaneous densification of Ti3 Si(Al)C2 /SiC composites using Ti, Si, Al, and graphite powders as the initial materials. The effect of SiC content on high-temperature mechanical properties and oxidation resistance were investigated. The mechanisms for the improved high-temperature properties are discussed. 相似文献
16.
Jing-Feng Li Toshiro Matsuki Ryuzo Watanabe 《Journal of the American Ceramic Society》2002,85(4):1004-1006
Mechanical alloying (MA) has been used to synthesize Ti3 SiC2 powder from the elemental Ti, Si, and C powders. The MA formation conditions of Ti3 SiC2 were strongly affected by the ball size for the conditions used. MA using large balls (20.6 mm in diameter) enhanced the formation of Ti3 SiC2 , probably via an MA-triggered combustion reaction, but the Ti3 SiC2 phase was not synthesized only by the MA process using small balls (12.7 mm in diameter). Fine powders containing 95.8 vol% Ti3 SiC2 can be obtained by annealing the mechanically alloyed powder at relatively low temperatures. 相似文献
17.
Porous Cr3 C2 grains (∼300 to 500 μm) with ∼10 wt% of Cr2 O3 were prepared by heating a mixture of MgCr2 O4 grains and graphite powder at 1450° to 1650°C for 2 h in an Al2 O3 crucible covered by an Al2 O3 lid with a hole in the center. The porous Cr3 C2 grains exhibited a three-dimensional network skeleton structure. The mean open pore diameter and the specific surface area of the porous grains formed at 1600°C for 2 h were ∼3.5 (μm and ∼6.7 m2 /g, respectively. The present work investigated the morphology and the formation conditions of the porous Cr3 C2 grains, and this paper will discuss the formation mechanism of those grains in terms of chemical thermodynamics. 相似文献
18.
S. Shimada T. Onuma H. Kiyono M. Desmaison 《Journal of the American Ceramic Society》2006,89(4):1218-1225
Isothermal oxidation of dense TiC ceramics, fabricated by hot-isostatic pressing at 1630°C and 195 MPa, was performed in Ar/O2 (dry oxidation), Ar/O2 /H2 O (wet oxidation), and Ar/H2 O (H2 O oxidation) at 900°–1200°C. The weight change measurements of the TiC specimen showed that the dry, wet, and H2 O oxidation at 850°–1000°C is represented by a one-dimensional parabolic rate equation, while the oxidation in the three atmospheres at 1100° and 1200°C proceeds linearly. Cross-sectional observation showed that the dry oxidation produces a lamellar TiO2 scale consisting of many thin layers, about 5 μm thick, containing many pores and large cracks, while H2 O-containing oxidation decreases pores in number and diminishes cracks in scales. Gas evolution of CO2 and H2 with weight change measurement was simultaneously followed by heating the TiC to 1400°C in the three atmospheres. Cracking in the TiO2 scale accompanied CO2 evolution, and the H2 O-containing oxidation produced a small amount of H2 . A piece of single crystal TiC was oxidized in 16 O2 /H2 18 O to reveal the contribution of O from H2 O to the oxidation of TiC by secondary ion mass spectrometry. 相似文献
19.
The conditions necessary for synthesizing Al4 SiC4 from mixtures of aluminum, silicon, and carbon and kaolin, aluminum, and carbon, as starting materials, were examined in the present study. The standard Gibbs energy of formation for the thermodynamic reaction SiC( s ) + Al4 C3 ( s ) = Al4 SiC4 ( s ) changed from positive to negative at 1106°C. SiC and Al4 C3 formed as intermediate products when the mixture of aluminum, silicon, and carbon was heated in argon gas, and Al4 SiC4 then formed by reaction of the SiC and Al4 C3 at >1200°C. Al4 C3 , SiO2 , Al2 O3 , SiC, and Al4 O4 C formed as intermediate products when the mixture of kaolin, aluminum, and carbon was heated under vacuum, and Al4 SiC4 formed from a reaction of those intermediate products at >1600°C. 相似文献
20.
Yong Du Julius C. Schuster Hans J. Seifert Fritz Aldinger 《Journal of the American Ceramic Society》2000,83(1):197-203
The 1100°C isothermal section and the isopleths at 5, 10, and 15 at.% C in the Ti–Si–C system were determined by DTA and XRD methods. Five invariant reactions (L (liquid) = Si + SiC + TiSi2 at 1330°C, L = TiSi + TiSi2 + Ti5 Si3 C x at 1485°C, L + Ti5 Si3 C x = Ti3 SiC2 + TiSi2 at 1485°C, L + Ti3 SiC2 = TiSi2 + SiC at 1473°C, and L + TiC = bcc-(Ti) + Ti5 Si3 C x at 1341°C) were observed. The transition temperature for L + TiC = Ti3 SiC2 + SiC was measured by the Pirani technique. Optimized thermodynamic parameters for the Ti–Si–C system were then obtained by means of the CALPHAD (calculation of phase diagrams) method applied to the present experimental results and reliable literature data. The calculations satisfactorily account for most of the experimental data. 相似文献