RESUMO
The effect of CuO/B2O3 additions on the sintering behaviors, microstructures, and microwave dielectric properties of 0.95LaAlO3-0.05CaTiO3 ceramics is investigated. It is found that the sintering temperatures are lowered efficiently from 1600 °C to 1350 °C, as 1 wt % CuO, 1 wt % B2O3, and 0.5 wt % CuO +0.5 wt % B2O3 are used as the sintering aids due to the appearance of the liquid phase sintering. The microwave dielectric properties of 0.95LaAlO3-0.05CaTiO3 ceramics with the sintering aid additions are strongly related to the densification and the microstructure of the sintered ceramics. At the sintering temperature of 1300 °C, the 0.95LaAlO3-0.05CaTiO3 ceramic with 0.5 wt % CuO + 0.5 wt % B2O3 addition shows the best dielectric properties, including a dielectric constant (εr) of 21, approximate quality factor (Q × f) of 22,500 GHz, and a temperature coefficient of the resonant frequency (τf) of -3 ppm/°C.
RESUMO
Dissipative particle dynamics (DPD), a mesoscopic simulation approach, is used to investigate the effect of volume fraction of polyethylene (PE) and poly(l-lactide) (PLLA) on the structural property of the immiscible PE/PLLA/carbon nanotube in a system. In this work, the interaction parameter in DPD simulation, related to the Flory-Huggins interaction parameter χ, is estimated by the calculation of mixing energy for each pair of components in molecular dynamics simulation. Volume fraction and mixing methods clearly affect the equilibrated structure. Even if the volume fraction is different, micro-structures are similar when the equilibrated structures are different. Unlike the blend system, where no relationship exists between the micro-structure and the equilibrated structure, in the di-block copolymer system, the micro-structure and equilibrated structure have specific relationships.
RESUMO
Molecular dynamics simulation (MD) has been used to investigate the structure property of water/PMMA interface under compression and compression release. A virtual repulsive wall was employed to generate a normal compression strain on the simulation model, leading a compressive system. In order to understand the difference of interfacial phenomenon between the system under strain and under release, the hydrogen bond and density distributions of water and PMMA along the normal direction are calculated. The results show that the hydrogen bond distribution profile of compressive system is different from that of the release system at the same strain. It demonstrates that the characteristic structure of water/PMMA interface under a compression-release cycle is not reversible.
