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Apurv Dash Jürgen Malzbender Robert Vaßen Olivier Guillon Jesus Gonzalez-Julian 《Journal of the American Ceramic Society》2020,103(12):7072-7081
The compressive creep of silicon carbide fiber reinforced Ti3SiC2 MAX phase with both fine and coarse microstructure was investigated in the temperature range of 1000-1300°C. Comparison of only steady-state creep was done to understand the response of fabricated composite materials toward creep deformation. It was demonstrated that the fibers are more effective in reducing the creep rates for the coarse microstructure by an increase in activation energy compared to the variant with a finer microstructure, being partly a result of the enhanced creep rates for the microstructure with larger grain size. Grain boundary sliding along with fiber fracture appears to be the main creep mechanism for most of the tested temperature range. However, there are indications for a changed creep mechanism for the fine microstructure for the lowest testing temperature. Local pores are formed to accommodate differences in strain related to creeping matrix and predominantly elastically deformed fibers during creep. Microstructural analysis was done on the material before and after creep to understand the deformation mechanics. 相似文献
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Soroush Etebarian Hossein Sarpoolaky Hamid Reza Rezaie Mohammad Velashjerdi 《International Journal of Applied Ceramic Technology》2023,20(4):2166-2174
Titanium silicon carbide (Ti3SiC2) MAX phase powder was synthesized from elemental reactants using the molten salt synthesis (MSS) method. Optimum experimental parameters were also investigated to determine the purity and synthesis pathway of the Ti3SiC2 MAX phase. The results showed that Ti3SiC2 was not synthesized using carbon black as the carbon source in the starting materials because of the high quantity of TiC formed along with the TiSi2 silicide phase. However, Ti3SiC2 was successfully synthesized in a relatively high purity (93%) at 1200°C for 2 h using graphite as the source of carbon because of the formation of TiC and Ti5Si3 intermediate phases. The Ti5Si3 silicide phase was found to play a crucial role in the formation of the Ti3SiC2 MAX phase using the MSS method. Moreover, applying a pressure of 150 MPa to the prepared samples and using the eutectic mixture of NaCl–KCl (molar ratio: 1:1) instead of NaCl also resulted in the higher formation of the Ti3SiC2 MAX phase. The formation mechanism of Ti3SiC2 was determined to be the reaction among Ti5Si3, TiC, and residual carbon through the template-growth and dissolution–precipitation mechanisms that occurred at different stages of the synthesis process. 相似文献
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层状结构的Ti3SiC2属六方晶体结构,结合了金属和陶瓷的许多优异性能,如良好的导热和导电性能,优良的可加工性,耐氧化、耐化学腐蚀,优异的抗热震性,良好的自润滑性等,具有广阔的应用前景.本文介绍了Ti3SiC2的结构和性能,对其制备方法及应用进行了阐述. 相似文献
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Ti3SiC2及其复合材料的研究现状及发展趋势 总被引:4,自引:0,他引:4
介绍了Ti3SiC2陶瓷材料的微观结构与性能,认为该材料良好的综合性能有望解决陶瓷材料的脆性问题.并概述了Ti3SiC2及Ti3SiC2基复合材料各种制备方法的特点和研究状况、应用前景和发展趋势. 相似文献
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Microstructure and Mechanical Properties of (TiB2 + SiC) Reinforced Ti3SiC2 Composites Synthesized by In Situ Hot Pressing 下载免费PDF全文
Fully dense (TiB2 + SiC) reinforced Ti3SiC2 composites with 15 vol% TiB2 and 0–15 vol% SiC were designed and synthesized by in situ reaction hot pressing. The increase in SiC content promoted densification and significantly inhibited the growth of Ti3SiC2 grains. The in situ incorporated TiB2 and SiC reinforcements showed columnar and equiaxed grains, respectively, providing a strengthening–toughening effect by the synergistic action of particulate reinforcement, grain's pulling out, “self‐reinforcement,” crack deflection, and grain refining. A maximum bending strength of 881 MPa and a fracture toughness of 9.24 MPam1/2 were obtained at 10 vol% SiC. The Vickers hardness of the composites increased monotonously from 9.6 to 12.5 GPa. 相似文献
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YIN Hongfeng FAN Qiang REN Yun ZHANG Junzhan 《中国耐火材料》2008,17(1):10-13
Ti3SiC2/SiC composites were fabricated by reactive hot pressing method. Effects of hot pressing temperature, the content and particle size of SiC on phase composition, densification, mechanical properties and behavior of stress-strain of the composites were investigated. The results showed that : ( 1 ) Hot-pressing temperature influenced the phase composition of Ti3SiC2/SiC composites. The flexural strength and fracture toughness of composites increased with hot pressing temperature. (2) It became more difficult for the composites to densify when the content of SiC in composites increased. It need be sintered at higher temperature to get denser composite. The flexural strength and fracture toughness of composites increased when the content of SiC added in composites increased. However, when the content of SiC reached 50 wt%, the flexural strength and fracture toughness of composites decreased due to high content of pore in composites. (3) When the content of SiC was same, Ti3SiC2/SiC composites were denser while the particle size of SiC added in composites is 12. 8 μm compared with the composites that the particle size of SiC added is 3 μm. The flexural strength and fracture toughness of composites increased with the increase of particle size of SiC added in composites. (4) Ti3SiC2/SiC composites were non-brittle fracture at room temperature. 相似文献
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采用Ti3SiC2粉体和金刚石粉体为原料,通过微波烧结制备Ti3SiC2结合剂金刚石复合材料,研究金刚石的含量和粒度对该复合材料的物相组成与显微形貌的影响.结果表明,通过高温微波烧结Ti3SiC2结合剂金刚石复合材料,金刚石表面会形成不同的涂层,从而与基体结合剂结合良好.金刚石的粒度和含量对复合材料中基体组成和金刚石的表面涂层状态有显著影响.烧结过程中,金刚石会不同程度的影响Ti3SiC2的分解.Ti3SiC2分解后生成Si与TiC.当金刚石含量相同(10%)、粒度较粗(30/40)时,金刚石表面会形成钛硅相与SiC涂层组织;基体的主相为Ti3SiC2、钛硅相与SiC.当金刚石粒度较细(W20)时,金刚石表面的C元素充分地与Si反应生成SiC涂层,基体主相变成TiC和Ti3SiC2.当金刚石粒度适中(120/140目与170/200目)时,基体的主相为Ti3SiC2.选取金刚石粒度为170/200目、金刚石含量较低时(5%与10%),基体的组成为Ti3SiC2与少量的SiC.金刚石含量较高时(20%与30%),基体的组成为Ti3SiC2与少量的TiC和SiC.各试样中金刚石表面都会形成钛硅相与SiC涂层组织. 相似文献
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Pavel Istomin Elena Istomina Aleksandr Nadutkin Vladislav Grass Mikhail Kaplan 《International Journal of Applied Ceramic Technology》2019,16(2):746-752
Dense Ti3SiC2-SiC, Ti4SiC3-SiC, and Ti3SiC2-Ti4SiC3-SiC ceramic composites were fabricated through carbosilicothermic reduction of TiO2 under vacuum, followed by hot pressing of the as-synthesized products under 25 MPa at 1600°C. In the reduction step, SiC either alone or in combination with elemental Si was used as a reductant. A one-third excess of SiC was added in the reaction mixtures in order to ensure the presence of approximately 30 vol.% SiC in the products of synthesis. During the hot pressing step, the samples that contained Ti3SiC2 showed better densification compared to those containing Ti4SiC3. The obtained composites exhibited the strength properties typical of coarse-grained MAX-phase ceramics. The flexural strength values of 424 and 321 MPa were achieved in Ti3SiC2-SiC, and Ti3SiC2-Ti4SiC3-SiC composites, respectively. The fracture toughness values were 5.7 MPa·m1/2. 相似文献
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Chenlong Wu Rui Zhang Fuyan Liu Biao Chen 《International Journal of Applied Ceramic Technology》2023,20(3):1846-1854
The electrochemical corrosion behaviors of Ti3SiC2/Cu composite and polycrystalline Ti3SiC2 in a 3.5% NaCl medium were investigated by dynamic potential polarization, potentiostat polarization, and electrochemical impedance spectroscopy. The polycrystalline Ti3SiC2 was tested on the identical condition as a control. The characterizations of XRD, X-ray photoelectron spectroscopy, scanning electron microscope, and energy-dispersive spectrometer were used to study the relevant passivation behavior and corrosive mechanism. The self-corrosion current density of Ti3SiC2/Cu (6.46 × 10−6 A/cm2) was slightly higher than that of Ti3SiC2 (1.64 × 10−7 A/cm2). Under open circuit potential, the corrosion resistance of Ti3SiC2/Cu was better than that of Ti3SiC2. Ti3SiC2/Cu exhibited a typical passivation feature with a narrow passivation interval and a breakdown phenomenon. The better corrosion resistance of Ti3SiC2 was due to the more stable Si layer of the former. In comparison, for Ti3SiC2/Cu composites, Cu reacted with the reactive Si layers in Ti3SiC2 to form Cu–Si compounds and TiC, destroying the weak interaction between Si layers and Ti–C layers. In the other hand, the as-formed Cu–Si compounds and TiC dissolved during the corrosion of Ti3SiC2/Cu in the 3.5% NaCl medium, causing to the destruction of the passivation film on its surface. 相似文献
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在Ar气氛中,以TiH_2/Si/2Ti C复合粉体为原料,利用无压烧结技术在1500°C下保温3 h成功制备出高纯Ti_3SiC_2,并利用氢氟酸对Ti_3SiC_2粉体进行刻蚀,研究其耐腐蚀性。XRD检测结果表明,在常压下Ti_3SiC_2样品经氢氟酸腐蚀前后的物相没有发生变化,且不随反应时间和温度的变化而发生变化。但是,扫描电镜图片显示样品中存在一些二维片层和腐蚀孔洞,这表明HF与Ti_3SiC_2发生了部分刻蚀反应。由于Ti_3SiC_2与酸的反应活性依赖于Si与酸的反应活性,而Si与HF在常压下反应较慢,因此Ti_3SiC_2与HF反应较困难。然而,Ti_3SiC_2与HF在180°C水热条件下则能完全反应,晶体结构遭到破坏,这表明Ti_3SiC_2在常温常压下对HF具有良好的耐腐蚀性,而在水热条件下Ti_3SiC_2易受HF的腐蚀。 相似文献
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为了进一步了解Ti3SiC2/nSiC复合材料优良的综合性能,特别是其高温力学性能,本文以热等静压原位合成技术制备的Ti3SiC2/4SiC复相陶瓷为试验材料,对其高温拉伸和高温弯曲行为进行研究。结果表明:Ti3SiC2/4SiC复相陶瓷的高温抗拉强度比室温抗拉强度高;Ti3SiC2/4SiC复相陶瓷的高温抗弯强度在900℃出现一极大值,1000℃后具有好的高温塑性。 相似文献
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Apurv Dash Jürgen Malzbender Khushbu Dash Marcin Rasinski Robert Vaßen Olivier Guillon Jesus Gonzalez-Julian 《Journal of the American Ceramic Society》2020,103(10):5952-5965
The compressive creep of a SiC whisker (SiCw) reinforced Ti3SiC2 MAX phase-based ceramic matrix composites (CMCs) was studied in the temperature range 1100-1300°C in air for a stress range 20-120 MPa. Ti3SiC2 containing 0, 10, and 20 vol% of SiCw was sintered by spark plasma sintering (SPS) for subsequent creep tests. The creep rate of Ti3SiC2 decreased by around two orders of magnitude with every additional 10 vol% of SiCw. The main creep mechanisms of monolithic Ti3SiC2 and the 10% CMCs appeared to be the same, whereas for the 20% material, a different mechanism is indicated by changes in stress exponents. The creep rates of 20% composites tend to converge to that of 10% at higher stress. Viscoplastic and viscoelastic creep is believed to be the deformation mechanism for the CMCs, whereas monolithic Ti3SiC2 might have undergone only dislocation-based deformation. The rate controlling creep is believed to be dislocation based for all the materials which is also supported by similar activation energies in the range 650-700 kJ/mol. 相似文献
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