Solid oxide membrane-assisted controllable electrolytic fabrication of Ti5Si3/TiC composites in molten salt

Kai Zheng, Jierui Li, Cuilian Shi, Haitao Luo, H. Gong
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引用次数: 0

Abstract

The titanium silicide Ti5Si3 possesses many desirable properties, such as a high melting point, excellent high-temperature oxidation resistance, low density, and relatively high hardness, and it is considered a promising structural intermetallic compound. However, like most ceramic materials, originating from low symmetry (D88) in its crystal structure, Ti5Si3 has poor fracture toughness and limited flexibility at room temperature, and at high temperatures, its creep resistance also drops sharply, which hinders its application. To overcome these shortcomings, it is suggested that TiC is a practical addition to Ti5Si3 to overcome the brittleness. Compared with monolithic Ti5Si3, Ti5Si3/TiC composites have a higher fracture toughness. Ti5Si3/TiC composites can be prepared by many ways, which commonly require high energy cost, complex processes and provide low efficiency. Therefore, the search for environmentally friendly strategies for the production of Ti5Si3/TiC is still ongoing. This article proves that we can successfully prepare Ti5Si3/TiC composites from CaTiO3/SiO2/C precursor by using SOM technology and explores the reaction mechanism of electrochemical process. In the process of electroreduction of CaTiO3/SiO2/C particles into Ti5Si3/TiC composites, we mainly used SOM technology at 1273 K and 4.0 V in molten CaCl2 and under an argon atmosphere. The results show that the Ti5Si3/TiC composites can also be successfully electrosynthesized from CaTiO3/SiO2/C precursors by using SOM-based anode systems at 1273 K and 4.0 V in molten CaCl2. The Ti5Si3/TiC composites can been successfully electrosynthesized from CaTiO3/SiO2/C precursors by using SOM-based anode systems at 1273 K and 4.0 V in molten CaCl2. This work demonstrates that Ti5Si3/TiC composites have been successfully electrosynthesized from CaTiO3/SiO2/C precursors using SOM-based anode systems at 1273 K and 4.0 V in molten CaCl2. The Ti5Si3/TiC has a smooth surface and micro/nano-porous structure. The formation routes for Ti5Si3 and TiC are independent. In summary, the SOM-assisted controllable electroreduction process has the potential to provide a novel one-step route from CaTiO3/SiO2/C precursors to Ti5Si3/TiC composites in molten salts. In summary, this paper demonstrates that Ti5Si3/TiC composites have been successfully electrosynthesized from CaTiO3/SiO2/C precursors by using SOM-based anode systems at 1273 K and 4.0 V in molten CaCl2.the main intermediate stages in the electrolysis process include Ti2O3, Ca2SiO4, and SiC. The above steps of CaTiO3, SiO2, C → Ti2O3, Ca2SiO4, SiC → Ti5Si3/TiC make up the electroreduction process.Compared with the initial powders before electrolysis, the obtained Ti5Si3/TiC composite has a smooth surface and possesses a nodular microstructure.
固体氧化膜辅助熔盐中可控电解制备Ti5Si3/TiC复合材料
硅化钛Ti5Si3具有高熔点、优异的高温抗氧化性、低密度和较高的硬度等优点,是一种很有前途的结构金属间化合物。然而,与大多数陶瓷材料一样,由于其晶体结构对称性低(D88), Ti5Si3在室温下断裂韧性差,柔韧性有限,在高温下,其抗蠕变性能也急剧下降,阻碍了其应用。为了克服这些缺点,建议将TiC添加到Ti5Si3中以克服脆性。与单片Ti5Si3相比,Ti5Si3/TiC复合材料具有更高的断裂韧性。制备Ti5Si3/TiC复合材料的方法很多,但通常能耗高、工艺复杂、效率低。因此,寻找生产Ti5Si3/TiC的环保策略仍在进行中。本文证明了采用SOM技术可以成功地从CaTiO3/SiO2/C前驱体制备Ti5Si3/TiC复合材料,并对电化学过程的反应机理进行了探讨。在将CaTiO3/SiO2/C颗粒电还原成Ti5Si3/TiC复合材料的过程中,我们主要采用了SOM技术,温度为1273 K,温度为4.0 V,在熔融的CaCl2中,氩气气氛下进行。结果表明,以CaTiO3/SiO2/C为前驱体,在熔体CaCl2中,在1273 K和4.0 V的温度下,采用基于somm的阳极体系,可以成功地电合成Ti5Si3/TiC复合材料。以CaTiO3/SiO2/C为前驱体,在1273 K和4.0 V的温度下,以somm为阳极体系,在熔融CaCl2中成功地电合成了Ti5Si3/TiC复合材料。本研究表明,在熔融CaCl2中,在1273 K和4.0 V的温度下,以CaTiO3/SiO2/C前驱体为原料,采用基于somm的阳极体系,成功地电合成了Ti5Si3/TiC复合材料。Ti5Si3/TiC具有光滑的表面和微/纳米多孔结构。Ti5Si3和TiC的形成路径是独立的。综上所述,soms辅助可控电还原工艺有可能为熔融盐中CaTiO3/SiO2/C前驱体到Ti5Si3/TiC复合材料提供一种新的一步路线。综上所述,本文证明了以CaTiO3/SiO2/C前驱体为原料,在熔融CaCl2中,在1273 K和4.0 V的温度下,采用somm阳极体系成功地电合成了Ti5Si3/TiC复合材料。电解过程中的主要中间阶段有Ti2O3、Ca2SiO4和SiC。上述步骤由CaTiO3、SiO2、C→Ti2O3、Ca2SiO4、SiC→Ti5Si3/TiC组成电还原过程。与电解前的初始粉末相比,得到的Ti5Si3/TiC复合材料表面光滑,具有球状组织。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Current Materials Science
Current Materials Science Materials Science-Materials Science (all)
CiteScore
0.80
自引率
0.00%
发文量
38
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