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61.
Surface rolling was employed to fabricate a densified layer on a powder metallurgy (PM) Fe–2Cu–0.6C piece. A densified surface layer with a depth of 335?μm and a surface hardness of 330?HV0.1 was obtained, in which the lamellar spacing of pearlite and grain size of ferrite were refined. Friction and wear behaviours of the surface densified material were studied. Results indicated that friction coefficient of the rolled material decreased as the load increased, which was lower than that of the un-rolled material. Wear volumes were lower than that of the un-rolled material, which increased as the load increased. Wear loss was caused by flake spalling and grooves, and the wear mechanism mainly was abrasive wear. The surface densified layer with higher hardness and lower porosity can hinder the cracks initiation and propagation on the surface and under the surface, which enhance the wear resistance of the PM material. 相似文献
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Amphiphilic TiO2 nanotube arrays (TiO2 NTs) were fabricated through electrochemical oxidation of Ti in solution containing H3PO4 and NaF. Scanning electron microscopic analysis shows that the as-prepared TiO2 NTs have an average pore diameter of 100 nm and a wall thickness of 15 nm. The electrochemical oxidation of Ti can be divided into four stages. In the first stage, when the potential is very low, oxygen formation and Ti dissolution are the major reactions. The second stage corresponds to a slightly higher potential, but less than 2.5 V. In this stage, the formation of TiO2 film occurs. When the potential is increased to the even higher range from 2.5 V to 6 V, the TiO2 film dissolves and nanoporous surface structure is generated. This is the third stage. Further increase of the potential enters stage four. The high potentials cause the self-organization of the nanostructure and allow the formation of well-aligned TiO2 NTs. We also found that the change in surface condition of Ti by annealing heat treatment affects the film dissolution kinetics. As compared with TiO2 thin film, the TiO2 NTs show higher photocatalytic activity on decomposing Rhodamine B. The surface of the TiO2 NTs can be wetted by both water and oil. Such an amphiphilic property comes from the capillary effect of the nanochannel structure of the TiO2 NTs. Because of the amphiphilic property and the photocatalytic activity, we conclude that the TiO2 NTs have the capability of self-cleaning. 相似文献
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A novel and efficient method to produce water dispersible superparamagnetic Fe3O4 nanoparticles is described. Nanoparticles prepared by non‐hydrolytic organic phase methods are subsequently functionalized with (3‐glycidyloxypropyl)trimethoxysilane, a linker that prevents aggregation and is available for subsequent coupling reactions with a wide range of polymers and biomolecules. Ring opening coupling reactions were used to coat the epoxy‐functionalized magnetite nanoparticles with aminated polymers (polyetheramines) or small molecules (arginine). The resulting nanoparticles, with hydrodynamic size of 13 nm, are found to be very stable over extended periods in water or PBS due to the presence of a dense stabilizer layer covalently anchored to the surface. Exceptionally high spin‐lattice relaxivity, r1, values of 17 s?1 mM?1, and low r2/r1 ratios of 3.3–3.8 were exhibited in the clinical MRI frequency range, irrespective of the molecule selected for nanoparticle stabilization. As a result the dispersions are excellent candidates for incorporation into multi‐functional assemblies or for use as positive contrast agent for MRI. 相似文献
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基于暗电流模型,通过变温I-V分析长波器件(截止波长为9~10μm)的暗电流机理和主导机制.实验对比了不同衬底、不同成结方式、不同掺杂异质结构与暗电流成分的相关性.结果表明,对于B+离子注入的平面结汞空位n~+-on-p结构,替代衬底上的碲镉汞(HgCdTe)器件零偏阻抗(R0)在80 K以上与碲锌镉(CdZnTe)基碲镉汞器件结阻抗性能相当.但替代衬底上的HgCdTe因结区内较高的位错,使得从80 K开始缺陷辅助隧穿电流(I_(tat))超过产生复合电流(I_(g-r)),成为暗电流的主要成分.与平面n~+-on-p器件相比,采用原位掺杂组分异质结结构(DLHJ)的p~+-on-n台面器件,因吸收层为n型,少子迁移率较低,能够有效抑制器件的扩散电流.80 K下截止波长9.6μm,中心距30μm,替代衬底上的p~+-on-n台面器件品质参数(R0A)为38Ω·cm2,零偏阻抗较n-on-p结构的CdZnTe基碲镉汞器件高约15倍.但替代衬底上的p+-on-n台面器件仍受体内缺陷影响,在60 K以下较高的Itat成为暗电流主导成分,其R0A相比CdZnTe基n~+-on-p的HgCdTe差了一个数量级. 相似文献
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