从实际工程应用角度出发,我们构建了非匀速运动介质(物体)系统中的动生麦克斯韦方程组(Maxwell’s equations for a mechano-driven media system),拟解决在非惯性系中低速变速运动介质以及介质形状和边界随时间/空间变化时电磁场的动...从实际工程应用角度出发,我们构建了非匀速运动介质(物体)系统中的动生麦克斯韦方程组(Maxwell’s equations for a mechano-driven media system),拟解决在非惯性系中低速变速运动介质以及介质形状和边界随时间/空间变化时电磁场的动力学演化规律.本文概括总结了动生麦克斯韦方程组理论的核心内容,包括方程组的构建背景、物理图像、基本特点、与经典方程组之间的区别和联系、求解方法、潜在应用范围等.深入探讨了动生麦克斯韦方程组和经典麦克斯韦方程组之间的四个主要区别,并提出近场电动力学与远场电动力学的基本概念.最后,对动生麦克斯韦方程组在科学和技术方面的潜在影响进行分析和展望.展开更多
The effects of 4-(2-hydroxyphenyl)-2-(morpholin-4-yl)-1,3-thiazole(Pr02), 1-(3,5-dibromo-2-hydroxyphenyl)-1-oxoethan-2-yl-N,N-diethyldithiocarbamate(Pr04) and 1-(5-bromo-2-hydroxy-3-methylphenyl)-1-oxoethan-2-yl-Oethy...The effects of 4-(2-hydroxyphenyl)-2-(morpholin-4-yl)-1,3-thiazole(Pr02), 1-(3,5-dibromo-2-hydroxyphenyl)-1-oxoethan-2-yl-N,N-diethyldithiocarbamate(Pr04) and 1-(5-bromo-2-hydroxy-3-methylphenyl)-1-oxoethan-2-yl-Oethyl xanthate(Pr06) on the aqueous oxidation of chalcopyrite(CuFeS2) in air-equilibrated solution at a temperature of 25 ℃ and a pH of 2.5 were studied. The effects were investigated by using potentiodynamic polarization, electrochemical impedance spectroscopy(EIS), scanning electron microscopy coupled with energy dispersive X-ray(SEM/EDX) analysis, aqueous batch experiments, Fourier transform infrared(FTIR) spectroscopy, Raman scattering and quantum chemical calculations. It is found that the anodic current densities decrease in the order of EtOH > Pr02 > Pr04 > Pr06. These results, along with those of the EIS measurements, show that Pr02, Pr04 and Pr06 are effective anodic inhibitors of chalcopyrite aqueous oxidation. Both Raman scattering and FTIR spectroscopy indicate that the elemental sulfur, polysulfide and ferric oxyhydroxides that form on the surface of the mineral are not responsible when it comes to the aqueous oxidation inhibition of chalcopyrite. Quantum chemical calculations show that the adsorption of the tested compounds on the chalcopyrite surface is energetically favorable and so, it can explain the inhibiting effects that were observed.展开更多
The time evolution of protons and 3He fragments from Au＋Au/Pb＋Pb reactions at 0.25, 2, and 20 GeV/nucleon is investigated with the potential version of the Ultrarelativistic Quantum Molecular Dynamics （UrQMD） mode...The time evolution of protons and 3He fragments from Au＋Au/Pb＋Pb reactions at 0.25, 2, and 20 GeV/nucleon is investigated with the potential version of the Ultrarelativistic Quantum Molecular Dynamics （UrQMD） model combined with the traditional coalescence afterburner. In the coalescence process, the relative distance R0 and relative momentum P0 are surveyed in the range of 3-4 fm and 0.25-0.35 GeV/c, respectively. For both clusters, a strong reversed correlation between R0 and Po is seen and it is time-dependent as well. For protons, the accepted （R0, P0） bands lie in the time interval 30-60 fm/c, while for 3He, a longer time evolution （at about 60-90 fm/c） is needed. Otherwise, much smaller R0 and P0 values should be chosen. If we further look at the rapidity distributions from both central and semi-central collisions, it is found that the accepted [tout, （R0, P0）] assemble can provide consistent results for proton yield and collective flows especially at mid-rapdities, while for 3He, the consistency is destroyed at both middle and projectile-target rapidities.展开更多
文摘从实际工程应用角度出发,我们构建了非匀速运动介质(物体)系统中的动生麦克斯韦方程组(Maxwell’s equations for a mechano-driven media system),拟解决在非惯性系中低速变速运动介质以及介质形状和边界随时间/空间变化时电磁场的动力学演化规律.本文概括总结了动生麦克斯韦方程组理论的核心内容,包括方程组的构建背景、物理图像、基本特点、与经典方程组之间的区别和联系、求解方法、潜在应用范围等.深入探讨了动生麦克斯韦方程组和经典麦克斯韦方程组之间的四个主要区别,并提出近场电动力学与远场电动力学的基本概念.最后,对动生麦克斯韦方程组在科学和技术方面的潜在影响进行分析和展望.
基金partly supported by a grant of the Romanian National Authority for Scientific Research,CNDI-UEFISCDI,project number 51/2012。
文摘The effects of 4-(2-hydroxyphenyl)-2-(morpholin-4-yl)-1,3-thiazole(Pr02), 1-(3,5-dibromo-2-hydroxyphenyl)-1-oxoethan-2-yl-N,N-diethyldithiocarbamate(Pr04) and 1-(5-bromo-2-hydroxy-3-methylphenyl)-1-oxoethan-2-yl-Oethyl xanthate(Pr06) on the aqueous oxidation of chalcopyrite(CuFeS2) in air-equilibrated solution at a temperature of 25 ℃ and a pH of 2.5 were studied. The effects were investigated by using potentiodynamic polarization, electrochemical impedance spectroscopy(EIS), scanning electron microscopy coupled with energy dispersive X-ray(SEM/EDX) analysis, aqueous batch experiments, Fourier transform infrared(FTIR) spectroscopy, Raman scattering and quantum chemical calculations. It is found that the anodic current densities decrease in the order of EtOH > Pr02 > Pr04 > Pr06. These results, along with those of the EIS measurements, show that Pr02, Pr04 and Pr06 are effective anodic inhibitors of chalcopyrite aqueous oxidation. Both Raman scattering and FTIR spectroscopy indicate that the elemental sulfur, polysulfide and ferric oxyhydroxides that form on the surface of the mineral are not responsible when it comes to the aqueous oxidation inhibition of chalcopyrite. Quantum chemical calculations show that the adsorption of the tested compounds on the chalcopyrite surface is energetically favorable and so, it can explain the inhibiting effects that were observed.
基金supported by the National Natural Science Foundation of China(Grant Nos.11375062,11547312,11275068,11505056 and11505057)SRF for ROCS,SEM and the Doctoral Scientific Research Foundation(Grant No.11447109)
文摘The time evolution of protons and 3He fragments from Au＋Au/Pb＋Pb reactions at 0.25, 2, and 20 GeV/nucleon is investigated with the potential version of the Ultrarelativistic Quantum Molecular Dynamics （UrQMD） model combined with the traditional coalescence afterburner. In the coalescence process, the relative distance R0 and relative momentum P0 are surveyed in the range of 3-4 fm and 0.25-0.35 GeV/c, respectively. For both clusters, a strong reversed correlation between R0 and Po is seen and it is time-dependent as well. For protons, the accepted （R0, P0） bands lie in the time interval 30-60 fm/c, while for 3He, a longer time evolution （at about 60-90 fm/c） is needed. Otherwise, much smaller R0 and P0 values should be chosen. If we further look at the rapidity distributions from both central and semi-central collisions, it is found that the accepted [tout, （R0, P0）] assemble can provide consistent results for proton yield and collective flows especially at mid-rapdities, while for 3He, the consistency is destroyed at both middle and projectile-target rapidities.
