Size-Dependent Phase Transformation during Gas Atomization Process of Cu⁻Sn Alloy Powders.

For binary element atomization, it is essential to investigate the phase transformation from liquid to solid as a functions of the droplet sizes, as well as the reaction competitiveness, during gas atomizing solidification of their nuclei. In the present work, a series of phase transformations of undercooled Cu (60.9 wt.%)/Sn droplets were analyzed when atomized by pressure gas. The results indicated that the microstructures of the obtained powders and their morphologies were highly relevant to the droplet size. According to the phase characteristics analyzed by the microstructural observations in combination with the transient nucleation theory, powders with sizes from 10 to 100 µm were divided into three categories, exhibiting lotus-leaf, island, and stripe morphologies. The competitive formation of Cu6Sn5 or Cu3Sn was also controlled by the droplet sizes, and a diameter of approximately 45 µm was identified as the threshold size. After heat treatment at 300 °C for 4 h, the powders consisted of a single η' Cu6Sn5 phase. The obtained Cu6Sn5 phase powders can be used in the field of high-temperature applications as intermetallic balls for integrated chip interconnects.

Exploration of Bcl-2 family and caspases-dependent apoptotic signaling pathway in Zearalenone-treated mouse endometrial stromal cells.

Zearalenone (ZEA) is a nonsteroidal estrogenic mycotoxin found in several food commodities worldwide. Although the toxicity of ZEA have been widely studied in a number of cell types, the mechanistic role of ZEA on apoptosis of endometrial stromal cells (ESCs) remains poorly understood. The objective of this study was to determine the effects of ZEA on apoptosis of mouse ESCs and explore the signaling pathway underlying the cytotoxicity of ZEA. The results showed that ZEA treatment caused obvious apoptosis in ESCs as determined by the flow cytometry and terminal deoxynucleotidyl transferase-mediated deoxyuridine triphosphate nick end labeling (TUNEL) assay. Immunoblotting and real-time quantitative polymerase chain reaction (RT-qPCR) revealed that ZEA treatment increased the ratio of Bax/Bcl-2. The enzymatic activity assays revealed that caspases-3 and caspase-9 were activated by ZEA treatment in a dose-dependent manner. In addition, flow cytometry show that the apoptotic percentages of cells pretreated with Z-VAD-FMK and Z-LEHD-FMK were markedly reduced compared to the ZEA-treated cells. Overall, the results suggested that ZEA induced obvious apoptosis in ESCs via a Bcl-2 family and caspases-dependent signaling pathway.