Because of characteristics of large density, high viscosity and poor mobility, the processing and transportation of residual oil are difficult and challenging, viscosity reduction of residual oil is of great significance. In this paper, the effects of different placement forms of ultrasonic transducers on the sound pressure distribution of ultrasonic inside a cubic container have been simulated, the characteristics of oil bath heating and ultrasonic viscosity reduction were compared, viscosity reduction rule of residual oil was experimentally analyzed by utilizing Response Surface Method under conditions of changing ultrasonic exposure time, power and action mode, the mechanism of viscosity reduction was studied by applying Fourier transform infrared spectrometer, the viscosity retentivity experiment was carried out at last. Experiments were conducted using two kinds of residual oil, and results show that ultrasonic effect on the viscosity reduction of residual oil is significant, the higher viscosity of residual oil, the better effect of ultrasonic, ultrasonic power and exposure time are the significant factors affecting the viscosity reduction rate of residual oil. The maximum viscosity reduction rate is obtained under condition of ultrasonic power is 900W, exposure time is 14min and action mode of exposure time is 2s and interrupting time is 2s, viscosity reduction rate reaching up to 63.95%. The infrared spectroscopy results show that light component in residual oil increased. The viscosity retentivity experiment results show that the viscosity reduction effect remains very well. This paper can provide data reference for the application of ultrasonic in the field of viscosity reduction for residual oil.
Porcine epidemic diarrhea virus (PEDV), an enteropathogenic coronavirus, has catastrophic impacts on the global pig industry. Owing to the lack of effective vaccines and specific therapeutic options for PEDV, it is pertinent to develop new and available antivirals. This study identified, for the first time, a salinomycin that actively inhibited PEDV replication in Vero cells in a dose-dependent manner. Furthermore, salinomycin significantly inhibited PEDV infection by suppressing the entry and post-entry of PEDV in Vero cells. It did not directly interact with or inactivate PEDV particles, but it significantly ameliorated the activation of Erk1/2, JNK and p38MAPK signaling pathways that are associated with PEDV infection. This implied that salinomycin inhibits PEDV replication by altering MAPK pathway activation. Notably, the PEDV induced increase in reactive oxidative species (ROS) was not decreased, indicating that salinomycin suppresses PEDV replication through a pathway that is an independent pathway of viral-induced ROS. Therefore, salinomycin is a potential drug that can be used for treating PEDV infection.
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