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Influence of temperature, stress, and grain size on behavior of nano-polycrystalline niobium
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作者 晏玉平 张柳亭 +2 位作者 张丽攀 芦刚 涂志新 《Chinese Physics B》 SCIE EI CAS CSCD 2024年第7期467-474,共8页
Atomic simulations are executed to investigate the creep responses of nano-polycrystalline(NC) niobium established by using the Voronoi algorithm. The effects of varying temperature, applied stress, and grain size(GS)... Atomic simulations are executed to investigate the creep responses of nano-polycrystalline(NC) niobium established by using the Voronoi algorithm. The effects of varying temperature, applied stress, and grain size(GS) on creep properties and mechanisms are investigated. Notably, the occurrence of tertiary creep is exclusively observed under conditions where the applied stress exceeds 4.5 GPa and the temperature is higher than 1100 K. This phenomenon can be attributed to the significant acceleration of grain boundary and lattice diffusion, driven by the elevated temperature and stress levels. It is found that the strain rate increases with both temperature and stress increasing. However, an interesting trend is observed in which the strain rate decreases as the grain size increases. The stress and temperature are crucial parameters governing the creep behavior. As these factors intensify, the creep mechanism undergoes a sequential transformation: initially from lattice diffusion under low stress and temperature conditions to a mixed mode combining grain boundaries(GBs) and lattice diffusion at moderate stress and mid temperature levels, and ultimately leading to the failure of power-law controlled creep behavior, inclusive of grain boundary recrystallization under high stress and temperature conditions. This comprehensive analysis provides in more detail an understanding of the intricate creep behavior of nano-polycrystalline niobium and its dependence on various physical parameters. 展开更多
关键词 creep behavior molecular dynamics simulation activation energy stress exponent nano-polycrystalline niobium
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Preparation and Characterization of Y_3Sc_2Ga_3O_(12) Nano-Polycrystalline Powders by Co-Precipitation Method 被引量:1
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作者 苏静 张庆礼 +3 位作者 邵淑芳 谷长江 万松明 殷绍唐 《Journal of Rare Earths》 SCIE EI CAS CSCD 2007年第3期302-305,共4页
In order to grow high-quality gallium garnet crystals,polycrystalline materials were used as starting materials.YSGG precursor was synthesized by co-precipitation method using aqueous ammonia as a precipitator,and the... In order to grow high-quality gallium garnet crystals,polycrystalline materials were used as starting materials.YSGG precursor was synthesized by co-precipitation method using aqueous ammonia as a precipitator,and the precursor was then sintered at different temperatures.The results showed that the feasible pH range was 8.3~9.84 in the process of co-precipitation reaction.The YSGG precursor and the powders sintered at different temperatures were characterized by IR,XRD and TEM methods.It was found that the precursor transformed to pure YSGG polycrystalline phase at 800 ℃.YSGG nano-polycrystalline powders sintered at 800~1000 ℃ were well dispersed and the sizes of the YSGG grains were about 40~100 nm. 展开更多
关键词 co-precipitation method YSGG nano-polycrystalline powder rare earths
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Synthesis of indium tin oxide nano-polycrystalline powders by ultrasonic spray pyrolysis
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作者 Li-Hua Zhang Sheng-Hui Guo +3 位作者 Chao-Jin Zhou Jin-Hui Peng Shao-Hua Ju Jian-Bo Lan 《Rare Metals》 SCIE EI CAS CSCD 2022年第10期3579-3584,共6页
Indium tin oxide(ITO) nano-polycrystalline powders were prepared by ultrasonic spray pyrolysis(USP) method using a precursor solution of indium and tin chlorides in a simple one-step process without any post-heat trea... Indium tin oxide(ITO) nano-polycrystalline powders were prepared by ultrasonic spray pyrolysis(USP) method using a precursor solution of indium and tin chlorides in a simple one-step process without any post-heat treatment,additives and other complex operations.The morphology and crystal structure of ITO powders were studied by thermogravimetric and differential thermal analysis(TG-DTA),X-ray diffraction(XRD),energy-dispersive spectrometer(EDS),scanning electron microscopy(SEM),laser particle size analyzer(LPSA),transmission electron microscope(TEM),high-resolution transmission electron microscopy(HRTEM) and selected area electron diffraction(SAED),respectively.The results indicate that pure cubic ITO solid solution could be obtained at and above the pyrolysis temperature of 600℃.Through adjusting the size of atomized precursor droplets,the particles with regular spherical shape and smooth surface are also obtained.The spherical particles have a narrow size distribution with a dominant diameter size in the range of 0.52-1.28 μm,and the average value is 1.01 μm.The clear lattice fringes in HRTEM image confirm a polycrystalline structure of ITO particles with the growth direction along(222) direction. 展开更多
关键词 Indium tin oxide Ultrasonic spray pyrolysis nano-polycrystalline powder Chloride precursor
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Characterization of diamond MWCNTs composite fiber synthesized under high pressure and high temperature 被引量:1
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作者 Deng Fuming~(1,2) Lu Xuejun~(1,3) Liu Ruiping~1 Xu Guojun~3 Chen Quwu~1 Li Wenzhu~2 (1.Department of Materials Science and Engineering,China University of Mining and Technology,Beijing Campus,Beijing 100083,China) (2.Department of Physics,Zhejiang University,Hangzhou 310027,China) (3.Beijing Institute of Electro-machining,Beijing 100083,China) 《金刚石与磨料磨具工程》 CAS 北大核心 2008年第S1期62-67,共6页
A regrown composite fiber was synthesized during the sintering of diamond under high pressure 5.8 GPa and high temperature 1500℃for 1 min,using 3wt%MWCNTs as additive.SEM observation of the fiber after alkali and aci... A regrown composite fiber was synthesized during the sintering of diamond under high pressure 5.8 GPa and high temperature 1500℃for 1 min,using 3wt%MWCNTs as additive.SEM observation of the fiber after alkali and acid treatment revealed that the outer layer of the fiber is composed of nano-polycrystalline diamond.EDS,XPS,XRD and Raman spectrum analysis further identified that the fiber is composed of MWCNTs in the inner part and nano-polycrystalline diamond in the out layer.It is proposed that the untransformed MWCNTs may act as a template for the regrown outer layer of nano diamond fiber under high pressure and high temperature. 展开更多
关键词 Mullti-walled carbon nanotubes(MWCNTs) nano-polycrystalline DIAMOND fiber HIGH pressure/high temperature(HP-HT) Sintering
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Microstructure and properties of the sintered diamond reinforced by diamond-MWCNTs composite fibers
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作者 Deng Fuming~(1,2) Lu Xuejun~(1,3) Liu Ruiping~1 Xu Guojun~3 Chen Quwu~1 Li Wenzhu~2 (1.Department of Materials Science and Engineering,China University of Mining and Technology,Beijing Campus,Beijing,100083,China) (2.Department of Physics,Zhejiang University,Hangzhou,310027,China) (3.Beijing Institute of Electro-machining,Beijing,100083,China) 《金刚石与磨料磨具工程》 CAS 北大核心 2008年第S1期56-61,共6页
A new type of sintered diamond reinforced by diamond MWCNTs composite fibers which were randomly orientated and even distributed in the diamond matrix was synthesized by using 3wt%mullti-walled carbon nanotubes(MWCNT... A new type of sintered diamond reinforced by diamond MWCNTs composite fibers which were randomly orientated and even distributed in the diamond matrix was synthesized by using 3wt%mullti-walled carbon nanotubes(MWCNTs) as starting additive under high pressure of 5.8 GPa at temperature of 1500℃for 1 min.A special polycrystalline diamond structure of direct bonding of both diamond to diamond and diamond to diamond-MWCNTs composite fiber was observed.The testing results show that it possesses not only high hardness(49~52 GPa) and Young’s modulus(878 GPa) but also high bending strength(1320~1540 GPa) and fracture toughness(9.0~9.2 MPa·m<sup>1/2</sup>) as it was theoretically predicted.The high performances of the composite were contributed by the fiber strengthening effect and the special structure which can offer more extensive diamond to diamond bonding. 展开更多
关键词 mullti-walled carbon nanotubes(MWCNTs) nano-polycrystalline DIAMOND fiber HIGH pressure HIGH temperature(HP-HT) properties
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