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A Novel Zero-Voltage-Switching Push-Pull Forward Converter with a Parallel Resonant Network
Chunwei Cai,Chunyu Shi,Yuxing Guo,Zi Yang,Fangang Meng 전력전자학회 2017 JOURNAL OF POWER ELECTRONICS Vol.17 No.1
A novel zero-voltage-switching (ZVS) push-pull forward converter with a parallel resonant network is presented in this paper. The novel topology can provide a releasing loop for the energy storage in a leakage inductor for the duration of the power switching by the resonant capacitors paralleled with the primary windings of the transformer. Then the transformer leakage inductor is utilized to be resonant with the parallel capacitor, and the ZVS operation is achieved. This converter exhibits many advantages such as lower duty-cycle losses, limited peak voltage across the rectifier diodes and a higher efficiency. Furthermore, the operating principles and key problems of the converter design are analyzed in detail, and the ZVS conditions are derived. A 500W experimental converter prototype has been built to verify the effectiveness of the proposed converter, and its maximum efficiency reaches 94.8%.
A Novel Zero-Voltage-Switching Push-Pull Forward Converter with a Parallel Resonant Network
Cai, Chunwei,Shi, Chunyu,Guo, Yuxing,Yang, Zi,Meng, Fangang The Korean Institute of Power Electronics 2017 JOURNAL OF POWER ELECTRONICS Vol.17 No.1
A novel zero-voltage-switching (ZVS) push-pull forward converter with a parallel resonant network is presented in this paper. The novel topology can provide a releasing loop for the energy storage in a leakage inductor for the duration of the power switching by the resonant capacitors paralleled with the primary windings of the transformer. Then the transformer leakage inductor is utilized to be resonant with the parallel capacitor, and the ZVS operation is achieved. This converter exhibits many advantages such as lower duty-cycle losses, limited peak voltage across the rectifier diodes and a higher efficiency. Furthermore, the operating principles and key problems of the converter design are analyzed in detail, and the ZVS conditions are derived. A 500W experimental converter prototype has been built to verify the effectiveness of the proposed converter, and its maximum efficiency reaches 94.8%.
Inactivation of Vibrio parahaemolyticus by Aqueous Ozone
( Lifang Feng ),( Kuo Zhang ),( Mengsha Gao ),( Chunwei Shi ),( Caiyun Ge ),( Daofeng Qu ),( Junli Zhu ),( Yugang Shi ),( Jianzhong Han ) 한국미생물생명공학회(구 한국산업미생물학회) 2018 Journal of microbiology and biotechnology Vol.28 No.8
Vibrio parahaemolyticus contamination causes serious foodborne illness and has become a global health problem. As a disinfectant, aqueous ozone can effectively kill a number of bacteria, viruses, parasites, and other microorganisms. In this study, three factors, namely, the aqueous ozone concentration, the exposure time, and the bacterial density, were analyzed by response surface methodology, and the aqueous ozone concentration was the most influential factor in the sterilization ratio. Under low aqueous ozone concentrations (less than 0.125 mg/l), the bacterial cell membranes remained intact, and the ozone was detoxified by intracellular antioxidant enzymes (e.g., superoxide dismutase and catalase). Under high aqueous ozone concentrations (more than 1 mg/l), cell membranes were damaged by the degree of peripheral electronegativity at the cell surface and the concentration of lactate dehydrogenase released into the extracellular space, and the ultrastructures of the cells were confirmed by transmission electron microscopy. Aqueous ozone penetrated the cells through leaking membranes, inactivated the enzymes, inhibited almost all the genes, and degraded the genetic materials of gDNA and total RNA, which eventually led to cell death.
Yu-Ying Liu,Wentao Yang,Shaohua Shi,Ya-Jie Li,Liang Zhao,Chunwei Shi,Fangyu Zhou,Yanlong Jiang,Jingtao Hu,Wei Gu,Gui-Lian Yang,Chun-feng Wang 대한수의학회 2017 Journal of Veterinary Science Vol.18 No.2
Goose parvovirus (GPV) continues to be a threat to goose farms and has significant economic effects on the production of geese. Current commercially available vaccines only rarely prevent GPV infection. In our study, Lactobacillus (L.) plantarum NC8 was selected as a vector to express the VP2 gene of GPV, and recombinant L. plantarum pSIP409-VP2/NC8 was successfully constructed. The molecular weight of the expressed recombinant protein was approximately 70 kDa. Mice were immunized with a 2 × 109 colony-forming unit/200 mL dose of the recombinant L. plantarum strain, and the ratios and numbers of CD11c+, CD3+CD4+, CD3+CD8+, and interferon gamma- and tumor necrosis factor alpha-expressing spleen lymphocytes in the pSIP409-VP2/NC8 group were higher than those in the control groups. In addition, we assessed the capacity of L. plantarum SIP409-VP2/NC8 to induce secretory IgA production. We conclude that administered pSIP409-VP2/NC8 leads to relatively extensive cellular responses. This study provides information on GPV infection and offers a clear framework of options available for GPV control strategies.
( Jing Liu ),( Guilian Yang ),( Xing Gao ),( Zan Zhang ),( Yang Liu ),( Xin Yang ),( Chunwei Shi ),( Qiong Liu ),( Yanlong Jiang ),( Chunfeng Wang ) 한국미생물 · 생명공학회 2019 Journal of microbiology and biotechnology Vol.29 No.1
The lactic acid bacteria species Lactobacillus plantarum (L. plantarum) has been used extensively for vaccine delivery. Considering to the critical role of dendritic cells in stimulating host immune response, in this study, we constructed a novel CD11c-targeting L. plantarum strain with surface-displayed variable fragments of anti-CD11c, single-chain antibody (scFv-CD11c). The newly designed L. plantarum strain, named 409-aCD11c, could adhere and invade more efficiently to bone marrow-derived DCs (BMDCs) in vitro due to the specific interaction between scFv-CD11c and CD11c located on the surface of BMDCs. After incubation with BMDCs, the 409-aCD11c strain harboring a eukaryotic vector pValac-GFP could lead to more efficient expression of GFP compared with wild-type strains shown by flow cytometry analysis, indicating the enhanced translocation of pValac-GFP from L. plantarum to BMDCs. Similar results were also observed in an in vivo study, which showed that oral administration resulted in efficient expression of GFP in both Peyer’s patches (PP) and mesenteric lymph nodes (MLNs) within 7 days after the last administration. In addition, the CD11c-targeting strain significantly promoted the differentiation and maturation of DCs, the differentiation of IL-4+ and IL-17A+ T helper (Th) cells in MLNs, as well as production of B220+ IgA+ B cells in the PP. In conclusion, this study developed a novel DC-targeting L. plantarum strain which could increase the ability to deliver eukaryotic expression plasmid to host cells, indicating a promising approach for vaccine study.