Evolution of Toughening Mechanisms in PH13-8Mo Stainless Steel during Aging Treatment.

PH13-8Mo stainless steel has been widely used in aerospace, petroleum and marine construction, obtaining continuous investigation attention in recent years. Based on the response of a hierarchical martensite matrix and possible reversed austenite, a systematic investigation of the evolution of the toughening mechanisms in PH13-8Mo stainless steel as a function of aging temperature was carried out. It showed there was a desirable combination of high yield strength (~1.3 GPa) and V-notched impact toughness (~220 J) after aging between 540 and 550 °C. With the increase of aging temperature, the martensite matrix was recovered in terms of the refined sub-grains and higher ratio of high-angle grain boundaries (HAGBs). It should be noted there was a reversion of martensite to form austenite films subjected to aging above 540 °C; meanwhile, the NiAl precipitates maintained a well-coherent orientation with the matrix. Based on the post mortem analysis, there were three stages of the changing main toughening mechanisms: Stage I: low-temperature aging at around 510 °C, where the HAGBs contributed to the toughness by retarding the advance of cracks; Stage II: intermediate-temperature aging at around 540 °C, where the recovered laths embedded by soft austenite facilitated the improvement of toughness by synergistically increasing the advance path and blunting the crack tips; and Stage III: without the coarsening of NiAl precipitates around 560 °C, more inter-lath reversed austenite led to the optimum toughness, relying on "soft barrier" and transformation-induced plasticity (TRIP) effects.

Yeast-template synthesized Fe-doped cerium oxide hollow microspheres for visible photodegradation of acid orange 7.

Fe-doped cerium oxide (CeO2) hollow microspheres were successfully synthesized by a simple co-precipitation route using yeast asa bio-template and nitrate as the oxide precursor. The products were characterized by scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, N2 adsorption-desorption isotherms and UV-Vis diffuse reflectance spectroscopy. It was found that the products had a well-defined ellipsoidal morphology and the size of the hollow microspheres was about 1.5-2.5µm. The formation mechanism of Fe-doped CeO2 hollow microspheres was proposed and discussed as well. The photocatalytic test results showed that the Fe-doped CeO2 hollow microspheres exhibited a higher photocatalytic activity in the degradation of acid orange 7 (AO7) aqueous solutions containing H2O2 under visible irradiation compared with CeO2 hollow microspheres and Fe-doped CeO2 nanoparticles, which was attributed to their more oxygen vacancies, higher specific surface area and lower band gap. The degradation rate of the Fe-doped CeO2 hollow microspheres was found to be 93% after 80min and the degradation reaction followed pseudo-first-order kinetics.

Two-step hydrothermally synthesized carbon nanodots/WO3 photocatalysts with enhanced photocatalytic performance.

In this study, carbon nanodots (C-dots)/WO3 photocatalysts were prepared via a two-step hydrothermal method. The morphologies and optical properties of the as-prepared materials were investigated. Compared with the prepared WO3 and C-dots, the C-dots/WO3 possessed stronger photocatalytic capability and excellent recyclability for photocatalytic elimination of Rhodamine B. For example, the achieved first order reaction rate constant of 0.01942 min-1 for C-dots/WO3 was ∼7.7 times higher than that of the prepared WO3. The enhanced photocatalytic activity of C-dots/WO3 was attributed to the enhanced light harvesting ability and efficient spatial separation of photo-excited electron-hole pairs resulting from the synergistic effect of WO3 and C-dots. The high photocatalytic activity of C-dots/WO3 remained unchanged even after 3 cycles of use. Meanwhile, a possible mechanism of C-dots/WO3 for the enhanced photocatalytic activity was proposed.