一个切换混沌系统的设计与实现

利用反控制法构造了1个新的混沌系统,分析新系统的平衡点及在平衡点的特征值,分形维数,Lyapunov指数等性质,设计1个由2个混沌系统组成的可切换的实际电路并进行实验,通过1个开关选择器,电路可以实现2个子系统的功能,观察到2个子系统在各个相平面的混沌吸引子.     

Synthesis of Calix[4]arene‐grafted Magnetite Nanoparticles and Evaluation of Their Arsenate as Well as Dichromate Removal Efficiency

In this study, 5,17‐bis‐[(4‐benzylpiperidine)methyl]‐25,26,27,28‐tetrahydroxy‐calix[4]arene ( 3 ) has been prepared by the treatment of calix[4]arene with a secondary amine (4‐benzylpiperidine) and formaldehyde by means of Mannich reaction. The prepared Mannich base ( 3 ) has been grafted onto [3‐(2,3‐epoxypropoxy)‐propyl]‐trimethoxysilane‐modified Fe₃O₄ magnetite nanoparticles (EPPTMS‐MN) in order to obtain 5,17‐bis‐[(4‐benzylpiperidine)methyl]‐25,26,27,28‐tetrahydroxy calix[4]arene‐grafted EPPTMS‐MN (BP‐calix[4]arene‐grafted Fe₃O₄). All new compounds were characterized by a combination of FTIR and ¹H‐NMR analyses. The morphology of the magnetic nanoparticles was examined by transmission electron microscopy. Moreover, the studies regarding the removal of arsenate and dichromate ions from the aqueous solutions were also carried out by using 5,17‐bis‐[(4‐benzylpiperidine)methyl]‐25,26,27,28‐tetrahydroxy‐calix[4]arene in liquid–liquid extraction and BP‐calix[4]arene‐grafted Fe₃O₄ ( 4 ) in solid–liquid extraction experiments. The extraction results indicated that 3 is protonated at proton‐switchable binding sites in acidic conditions. Hence, facilitating binding of arsenate and dichromate is resulted from both electrostatic interactions and hydrogen bonding. To understand the selectivity of 3 , the retention of dichromate anions in the presence of Cl⁻, NO, and SO anions at pH 1.5 was also examined.     

一个自动切换混沌系统的设计与FPGA实现

为产生复杂的混沌吸引子,在现有混沌系统的基础上,利用混沌反控制法构造了1个新的混沌系统,它与原系统组成一个开关混沌系统。通过开关选择器,开关混沌系统能够在2个子系统之间自动切换。利用EDA技术在FPGA平台上实现了这个开关混沌系统,实验结果与仿真结果一致。     

Removal of Selected Micropollutants from Synthetic Wastewater by Electrooxidation Using Oxidized Titanium and Graphite Electrodes

Micropollutants cover a variety of compounds that mainly originate from the pharmaceutical and agricultural sectors. Even at trace concentrations, the discharge of micropollutants into water bodies pose a serious threat to the environment and human health. Their removal from wastewaters at treatment plants before their discharge into the environment has become one of the leading topics of research. Physical, chemical, and biological treatment methods have been listed in the literature for efficient removal of a variety of pollutants. In this study, seven micropollutants, namely 4‐tert‐octylphenol, atrazine, 2,4,6‐trichlorophenol, fluoxetine, estrone, penconazole, and di‐n‐octyl phthalate, are spiked into municipal simulated synthetic wastewater and treated by a laboratory‐scale electrooxidation (EO) system using oxidized titanium and graphite electrode as anode and cathode, respectively. Sensitive determination of the selected micropollutants by gas chromatography–mass spectrometry (GC‐MS) before and after treatment is performed after their pre‐concentration using an eco‐friendly switchable solvent liquid‐phase microextraction method (SSLPME). The pH value, applied current, and reaction period are optimized to enhance the removal efficiency of micropollutants. Results show that the highest removal efficiency of all micropollutants is obtained at pH 3, 20 min reaction period, and 3 A applied current. The operational costs are also investigated in this study.