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A Dynamic Adjustment Method of Service Function Chain Resource Configuration
( Xiaoyang Han ),( Xiangru Meng ),( Zhenhua Yu ),( Dong Zhai ) 한국인터넷정보학회 2021 KSII Transactions on Internet and Information Syst Vol.15 No.8
In the network function virtualization environment, dynamic changes in network traffic will lead to the dynamic changes of service function chain resource demand, which entails timely dynamic adjustment of service function chain resource configuration. At present, most researches solve this problem through virtual network function migration and link rerouting, and there exist some problems such as long service interruption time, excessive network operation cost and high penalty. This paper proposes a dynamic adjustment method of service function chain resource configuration for the dynamic changes of network traffic. First, a dynamic adjustment request of service function chain is generated according to the prediction of network traffic. Second, a dynamic adjustment strategy of service function chain resource configuration is determined according to substrate network resources. Finally, the resource configuration of a service function chain is pre-adjusted according to the dynamic adjustment strategy. Virtual network functions combination and virtual machine reusing are fully considered in this process. The experimental results show that this method can reduce the influence of service function chain resource configuration dynamic adjustment on quality of service, reduce network operation cost and improve the revenue of service providers.
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Xiaoyang Hou,Lilan Huang,Han Zhang,Qingping Xin,Hong Li,Hui Ye,Yuzhong Zhang 한국공업화학회 2023 Journal of Industrial and Engineering Chemistry Vol.123 No.-
Accumulation of endogenous and exogenous toxins in patients with chronic kidney disease increases thekidney burden. The newly developed plasma separation adsorption membranes provide a new model forthe removal of middle molecular toxins. In this study, the adsorption resin LX-1000H is physically pulverizedand blended into polyethersulfone matrixes to prepare adsorption resin/polyethersulfone (AR/PES) membranes by nonsolvent-induced phase separation for plasma separation and middle moleculartoxins absorption. The results show that the static adsorption capacity of AR/PES membrane for lysozyme(a typical mimic of middle molecular toxins) is up to 108.90 mg/g, which is 4 times that of AR. The maximumdynamic adsorption capacity reaches 102.80 mg/g, which is 93.4% of static adsorption. The adsorptionprocess is more consistent with the Langmuir model and the quasi-first-order kinetic model. Thepermeability of bovine serum albumin in simulated blood surpasses 90% and the cattle blood separatedby AR/PES membrane is colorless and transparent. The AR/PES membrane surface presents electronegativeat pH 7.4 and the water wettability is enhanced with the doping amount. No hemolysis and negligibleleakage indicated favorable hemocompatibility. This paper is devoted to providing a strategy forplasma separation and adsorption membranes.
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Dawei Tian,Binyuan Liu,Li Zhang,Xiaoyang Wang,Wei Zhang,Lina Han,Dae Won Park 한국공업화학회 2012 Journal of Industrial and Engineering Chemistry Vol.18 No.4
Four novel bifunctional aluminum–salen complexes (2a, 2b, 2c, and 2d) containing both Lewis acidic metal center and Lewis base quaternary phosphonium salt sites within one molecule and an aluminum–salen complex with a neutral tert-butyl group (2f) for comparison were synthesized and characterized by UV–vis, IR, 1H, 13C, 27Al NMR spectroscopy and Elemental analysis (EA). Their catalytic efficiencies as single-component catalysts toward the coupling reaction of carbon dioxide and propylene oxide were evaluated. These complexes exhibit catalytic activity in the order 2d > 2a > 2b > 2c 2f. 27Al NMR spectra reveal the existence of five- and six-coordinated metal centers in the aluminum–salen complexes bearing a quaternary phosphonium salt group, whereas only five-coordinate aluminum species were found in the aluminum–salen complex with a neutral tert-butyl group. This indicates the importance of the six-coordinate aluminum center in enhancing the catalytic activity as well as an intramolecular cooperative effect in bifunctional aluminum–salen complexes 2a–d. The effects of reaction variables on the catalytic performance were investigated in detail. These new catalysts are highly stable to moisture and air and robust to impurities in the coupling reaction.
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