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网格研究及其开发环境* 总被引:5,自引:0,他引:5
探讨了网格研究的基础理论、核心问题、具体研究内容和难点;仿真是研究网格资源管理和调度问题的重要方法,分析和评价了目前主要仿真工具的特点及应用;GT3已经成为网格项目开发的主流工具,给出了建立GT3 Core网格服务开发平台的方法;介绍了基于CGSP(China Grid Support Platform)的网格开发环境.以期有助于网格的创新研究和应用开发. 相似文献
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A new model, which combines in-bed and freeboard sulfation, significantly improves the ability to predict sulfur capture by limestone sorbents in fluidized-bed coal combustors. In this model, the in-bed hydrodynamics are described in terms of a bubble phase and an emulsion phase while the freeboard region has only a diluted emulsion phase. The solids, which are in the emulsion phases, are considered to be completely back-mixed; the gaseous bubble phase travels in plug-flow but exchanges with the emulsion phase. The sulfation reaction occurs principally in the emulsion phase and the reaction rate is a direct function of the sulfur dioxide concentration, the extent of the calcium oxide conversion (as measured by a thermogravimetric analyzer), and the amount of limestone present in the bed and in the freeboard. The amount present, or holdup, in the free-board is calculated from empirical correlations for elutriation and from particle-time trajectories as predicted from equations of motion.The model indicates that a significant amount of sulfur capture can occur in the freeboard region, especially with high superficial gas velocities and small particle sizes, both of which lead to increased freeboard holdup. For an overall sulfur retention of 90%, approximately 9% of the sulfur is predicted to be captured within the freeboard above a combustor bed 1.8 m by 1.8 m by 1.2 m high of 1200 μm diameter limestone particles that are fluidized at 2.4 m/s. The model also predicts that the sulfur captured by the entrained particles is negligible. These predictions compare favorably with the actual sulfur retentions experienced in similar sized pilot-scale combustors. 相似文献
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In Situ Bioorthogonal Metabolic Labeling for Fluorescence Imaging of Virus Infection In Vivo 下载免费PDF全文
Hong Pan Wen‐jun Li Xiang‐jie Yao Ya‐yun Wu Lan‐lan Liu Hua‐mei He Ren‐li Zhang Yi‐fan Ma Lin‐tao Cai 《Small (Weinheim an der Bergstrasse, Germany)》2017,13(17)
Optical fluorescence imaging is an important strategy to explore the mechanism of virus–host interaction. However, current fluorescent tag labeling strategies often dampen viral infectivity. The present study explores an in situ fluorescent labeling strategy in order to preserve viral infectivity and precisely monitor viral infection in vivo. In contrast to pre‐labeling strategy, mice are first intranasally infected with azide‐modified H5N1 pseudotype virus (N3‐H5N1p), followed by injection of dibenzocyclooctyl (DBCO)‐functionalized fluorescence 6 h later. The results show that DBCO dye directly conjugated to N3‐H5N1p in lung tissues through in vivo bioorthogonal chemistry with high specificity and efficacy. More remarkably, in situ labeling rather than conventional prelabeling strategy effectively preserves viral infectivity and immunogenicity both in vitro and in vivo. Hence, in situ bioorthogonal viral labeling is a promising and reliable strategy for imaging and tracking viral infection in vivo. 相似文献
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