Structure and tribological properties of Si/a-C:H(Ag)multilayer film in stimulated body fluid

Si/a-C:H(Ag)multilayer films with different modulation periods are prepared to test their potential applications in human body.The composition,microstructure,mechanical and tribological properties in the simulated body fluid are investigated.The results show the concentration of Ag first decreases and then increases with the modulation period decreasing from 984 nm to 250 nm.Whereas the C content has an opposite variation trend.Notably,the concentration of Ag plays a more important role than the modulation period in the properties of the multilayer film.The a-C:H sublayer of the film with an appropriate Ag concentration(8.97 at.%)(modulation period of 512 nm)maintains the highest sp3/sp2 ratio,surface roughness and hardness,and excellent tribological property in the stimulated body fluid.An appropriate number of Ag atoms and size of Ag atom allow the Ag atoms to easily enter into the contact interface for load bearing and lubricating.This work proves that the Ag nanoparticles in the a-C:H sublayer plays a more important role in the tribological properties of the composite-multilayer film in stimulated body fluid condition.

Investigation of radionuclide～(63)Ni(Ⅱ) sequestration mechanisms on mordenite by batch and EXAFS spectroscopy study

The sorption behavior and microscopic sequestration mechanisms of radionuclide 63Ni（II） on mordenite as a function of aging time, ionic srength, initial 63Ni（II） concentrations, solid content and coexistent electrolyte ions were investigated by the combination of batch and EXAFS techniques. Macroscopic experiment results show that the sorption of 63Ni（II） is dependent on ionic strength at pH〈7, and independent of ionic strength at pH〉7. The sorption percentage of 63Ni（II） on mordenite increases with increasing solid content, while the sorption capacity decreases as solid content increases. The presence of different electrolyte ions can enhance or inhibit the sorption of Ni（II） on mordenite in various degrees. EXAFS analysis results of the sam- ples under three different ionic strengths suggest that the retained 63Ni（II） in these samples exists in an octahedral environment with six water ligands. In the initial period of rapid uptake, the sorption of 63Ni（II） is dominated by the formation of innersphere surface complexes. As aging time increases, 63Ni（II） sequestration behavior tends to be mainly controlled by the formation of Ni phyllosilicate coprecipitates and/or Ni（OH）2（s） precipitates. Results for the second shell fit of the sample prepared at an initial 63Ni（II） concentration of 100 mg/L indicate the possible formation of Ni polynuclear surface complexes. Both the macroscopic sorption data and the molecular level evidence of 63Ni（II） surface speciation at the mordenite/water interfaces should be factored into better predictions of the mobility and bioavailability of 63Ni（II） in environment mediums.