氧化铝纤维含量对Al2O3f＋Cf／ZL109混杂复合材料耐磨性能的影响

利用挤压铸造法制备了Al2O3f Cf/ZL09短纤维混杂金属基复合材料,并探讨了炭纤维体积分数为4％时,Al2O3纤维含量变化对该复合材料耐磨性能的影响。结果表明：随着Al2O3体积分数增加,复合材料的摩擦系数逐渐增大,复合材料从轻微磨损到急剧磨损的临界转变载荷大幅度提高,并随Al2O3含量的增加而逐渐增大;在临界载荷以下,影响复合材料磨损率的Al2O3含量临界值为12％,当Al2O3含量低于临界值时复合材料磨损表面无明显剥落,而当Al2O3含量超过临界值后,复合材料磨损表面存在大量的剥落坑,磨损率增大。     

Study on the microstructure and wear resistance of the composite coatings fabricated on Ti-6Al-4V under different processing conditions

Composite coatings mainly containing titanium carbides and borides were produced by laser surface alloying of Ti-6Al-4V with graphite and boron mixed powders. The test results show that the coatings have higher hardness (1600-1700 HV_0.1) and are more resistant to wear than the as-received sample. Laser scanning speed and the content of alloying elements (weight ratio of graphite to boron) have an effect on both the microstructure and the wear resistance of the coatings. TEM results show that strip titanium carbides and borides grow alternately and thus restrain the formation of coarse needle-like TiB and dendritic TiC crystals produced by laser alloying of titanium alloys with boron and graphite separately.     

Process prediction of Ni–SiC coatings based on RBF-BP model

The preparation of Ni–SiC coatings using magnetic field-assisted jet electrodeposition under various plating settings is described in this study. A RBF-BP composite neural network with 4 × 4 × 4 × 7 × 10 × 1 was used to predict the corrosion resistance of Ni–SiC coatings prepared by employing different plating parameters. The results show that the fitting degree between the expected value and the actual value of the RBF-BP composite neural network is 0.97497. Moreover, the hybrid neural network can accurately predict the corrosion resistance of Ni–SiC coatings prepared under different process parameters. The corrosion weight loss of the coating is the lowest at the current density of 4 A/dm², a jet rate of 3 m/s, a SiC particle concentration of 8 g/L, and at a magnetic field intensity of 0.8 T, demonstrating its corrosion resistance under these conditions. According to the coating characterization analysis, the coating's grain size was significantly refined, and the surface was smoother with a high amount of uniformly sized SiC nanoparticles.     

Evaluation of the corrosion resistance of electroless Ni-P and Ni-P composite coatings by electrochemical impedance spectroscopy

Electroless Ni-P composite coatings have gained a good deal of popularity and acceptance in recent years as they provide considerable improvement of desirable qualities such as hardness, wear, abrasion resistance, etc. The disagreement among researchers on the corrosion behaviour of these coatings warrants a thorough investigation. Among the various techniques available for the determination of corrosion resistance, electrochemical impedance spectroscopy (EIS) is considered to be superior as it provides not only an assessment of the corrosion resistance of different deposits but also enables the mechanistic pathway by which the deposits become corroded to be determined. The present investigation focuses on the evaluation of the corrosion resistance of electroless Ni-P and Ni-P-Si₃N₄, Ni-P-CeO₂ and Ni-P-TiO₂ composite coatings produced using an acidic hypophosphite-reduced electroless nickel bath, using EIS. The study makes evident that the same fundamental reaction is occurring on all the coatings of the present study but over a different effective area in each case. The charge transfer resistance of electroless Ni-P and Ni-P composite deposits are in the range 32,253–90,700 Ω cm², whereas the capacitances of these coatings are in the range 11–17 μF/cm². The improved corrosion resistance obtained for electroless Ni-P and Ni-P composite coatings is due to the enrichment of phosphorus on the electrode surface, which enables the preferential hydrolysis of phosphorus over that of nickel. The better corrosion resistance obtained for electroless Ni-P composite coatings can be ascribed to the decrease in the effective metallic area prone to corrosion. Among the three electroless Ni-P composite coatings, the corrosion resistance is in the following order: Ni-P-CeO₂=Ni-P-Si₃N₄>Ni-P-TiO₂. Electronic Publication     

Exoemission near phase transitions of epitaxial films of manganites with colossal magnetic resistance

Intense exoemission near phase transitions of epitaxial films of the La_0.16Sr_0.84MnO₃ and La_0.35Pr_0.35Sr_0.3MnO₃, manganites, which exhibit the colossal magnetic resistance (CMR), is detected in a wide temperature range from 278 to 623 K including the Curie temperature. The role of the absorbed and lattice oxygen in the exoemission and CMR phenomena is discussed. The aftereffect of the magnetic field directed along the film plane on the intensity of photostimulated exoemission is discussed.     

Measurement of microchannel fluidic resistance with a standard voltage meter

A simplified method for measuring the fluidic resistance (R_fluidic) of microfluidic channels is presented, in which the electrical resistance (R_elec) of a channel filled with a conductivity standard solution can be measured and directly correlated to R_fluidic using a simple equation. Although a slight correction factor could be applied in this system to improve accuracy, results showed that a standard voltage meter could be used without calibration to determine R_fluidic to within 12% error. Results accurate to within 2% were obtained when a geometric correction factor was applied using these particular channels. When compared to standard flow rate measurements, such as meniscus tracking in outlet tubing, this approach provided a more straightforward alternative and resulted in lower measurement error. The method was validated using 9 different fluidic resistance values (from ∼40 to 600 kPa s mm⁻³) and over 30 separately fabricated microfluidic devices. Furthermore, since the method is analogous to resistance measurements with a voltage meter in electrical circuits, dynamic R_fluidic measurements were possible in more complex microfluidic designs. Microchannel R_elec was shown to dynamically mimic pressure waveforms applied to a membrane in a variable microfluidic resistor. The variable resistor was then used to dynamically control aqueous-in-oil droplet sizes and spacing, providing a unique and convenient control system for droplet-generating devices. This conductivity-based method for fluidic resistance measurement is thus a useful tool for static or real-time characterization of microfluidic systems.     

Resistance of supersulfated cement to strong sulfate solutions

One of the principal uses of supersulfated cement has been for structures exposed to sea water and sulfate bearing ground waters. The resistance to such environments has been related to the absence of calcium hydroxide and the combination of much of the free alumina into ettringite during hydration. This paper reports the resistance of SSC to sulfate solutions in which ettringite has been decomposed. Prism samples were subjected to initial water storage at 25°C for both 28 days and 6 months. Samples were also cured for 6 months at 95°C and at both 11% and 100% R.H. The control samples of 28 days were compared with the 6 months samples of a more mature undecomposed SSC paste. After curing the prisms were measured and all the samples were immersed in three sulfate solutions (0.7M Na₂SO₄ , 0.7M MgSO₄ and saturated CaSO₄), and water at the same time. Measurements of linear expansion over 6 months were carried out. Core and surface material following immersion was examined by DTG and XRD. The study indicated that SSC is resistant to sodium and calcium sulfate solutions. Strong magnesium sulfate solutions decomposed the samples under all conditions. A possible mechanism for this attack is suggested. This revised version was published online in July 2006 with corrections to the Cover Date.