AbstractAluminum-based composites containing 0.06, 0.09, 0.12 fractions of insitu-synthesized TiC (Titanium carbide) particles have been prepared through in-melt reaction from Ai–SiC–Ti system following a simple and cost-effective stir-casting route. The TiC forms by the reaction of Ti with carbon which is released by SiC at temperatures greater than 1073 K. However, some amount of titanium aluminide (Al3Ti) is also formed. The formation of TiC has been confirmed through X-ray diffraction studies of the composite. The hardness and tensile strength have been found to increase with increasing amount of TiC. The friction and wear characteristics of the composites have been determined by carrying out dry sliding tests on pin-on-disc machine at different loads of 9.8 N, 19.6 N, 29.4 N, 39.2 N at a constant sliding speed of the 1 m/s speed. The wear rate i.e. volume loss per unit sliding distance has been found to increase linearly with increasing load following Archard’s law. However, both the wear rate and friction coefficient have been observed to decrease with increasing amount of TiC in the composite. This has been attributed to (i) a relatively higher hardness of composites containing relatively higher amount of TiC resulting in a relatively lower real area of contact and (ii) the formation of a well-compacted mechanically mixed layer of compacted wear debris on the worn surface which might have inhibited metal–metal contact and resulted in a lower wear rate as well as friction coefficient. 相似文献
In this study, the effect of TiC nanoparticles as a reinforcement on the mechanical and tribological properties of Aluminum-based self lubricating composite was investigated. The microstructure, relative density, hardness, and tribological properties of Al/graphite and Al/TiC/graphite composites were examined as a function of graphite content. The tribo-surfaces of the samples were analyzed using SEM and EDS elemental mapping. The results indicated that the addition of TiC nanoparticles not only decreased the wear rate and coefficient of friction of the composites, but also facilitated the formation of a stable graphite layer at longer sliding distances and high sliding velocities by forming a durable graphite/TiC composite on the tribo-surface. Therefore, the stability of graphite layer can be considered as a possible cause for decrease in wear rate of the Al/TiC/graphite composite. 相似文献
This article describes the interfacial regions in CVD grown TiC/κ-Al2O3 multilayers. A number of microanalytical techniques were used including HREM, EDX and EELS. Occasionally, the first 50 nm of the alumina layers deposited on the intermediate TiC layers grew as a cubic alumina, heavily faulted, containing small amounts of sulphur (S), maybe as a stabiliser. The presence of slightly rounded TiC (111) facets may act as preferred nucleation sites for the cubic Al2O3 phase, with a ‘cube on cube’ orientation relationship. In this way the nucleation of κ-Al2O3 is less favourable. After some tens of nanometres the cubic phase cannot be stabilised any longer and the layer continues to grow as κ-Al2O3. A number of observations point towards the reaction zone (RZ) being η- and/or γ-Al2O3. The diffraction work and the FFT analysis of the HREM images show that the RZ is an fcc phase with a=7.9 Å, which matches with η- and γ-Al2O3. The EELS Al fine structure indicate more tetrahedral Al ions than in κ-Al2O3, as in η- and γ-Al2O3. The RZ contains small amounts of S, as has been reported for γ-Al2O3. Due to the structural similarities between η- and γ-Al2O3 it was not possible to determine which of these cubic phases is present in the RZ. 相似文献
We have conducted a soft X-ray emission spectroscopy (SXES) and a photoemission electron microscopy (PEEM) study on the heat-treated Ti/4H–SiC system. This spectro-microscopy approach is an ideal surface and interface characterization techniques due to the non-destructive nature of SXES and the real-time surface imaging of PEEM.
The Si L2,3 and C K soft X-ray emission spectra, which reflect Si (s+d) states and C p states, respectively, revealed formations of Ti5Si3 and TiC in the reacted interfacial region of Ti (50 nm)/4H–SiC(0 0 0 1) sample.
The surface of the Ti films on 4H–SiC samples during heat-treatment up to 850 °C was investigated by PEEM. The variation in brightness in the image of the sample was attributed to the surface deoxidation in the early stage of the treatment and to the formation of reacted region at the later stage. The darkening of the surface could be attributed to the formation of TiC and/or excess C atoms that could have migrated to the surface. 相似文献