A brief review and analysis of two historical models of the electron, the charged spinning sphere and Goudsmit and Uhlenbeck’s concept, is presented. It is shown that the enormous potential of classical electrodynami...A brief review and analysis of two historical models of the electron, the charged spinning sphere and Goudsmit and Uhlenbeck’s concept, is presented. It is shown that the enormous potential of classical electrodynamics has been underutilized in particle physics. Such observation leads to discovery of a principal component in the electron inner structure—the charged c-ring. The intrinsic (fundamental) electron model based on the charged c-ring successfully explains the ontology of the charge fractionation in quantum chromodynamics and the formation of Cooper pairs in superconductivity. The c-ring properties are explained on the basis of the General Compton Conditions as defined. Properties of the charged c-ring include the explanation of the boundary conditions, electro-magnetostatic field configuration, self-mass, spin, magnetic moment, and the gyromagnetic ratio. The self-mass of the intrinsic electron is 100% electro-magnetostatic and it is shown how to compute its value. The classical-quantum divide no longer exists. Relation between the intrinsic electron and the electron is fundamentally defined. The electron is the composite fermion consisting of the intrinsic electron and the neutrino. The ontology of the anomaly in the electron magnetic moment is demonstrated—it is due to the addition of the neutrino magnetic moment to the overall electron magnetic moment. The intrinsic electron replaces the W? boson in particle physics, resulting in a fundamental implication for the Standard Model.展开更多
Under ideally polarizable conditions, TiO2 film electrode/solution electrolyte interface exhibited frequency dispersion, The effects of external factors such as the concentration of KNO3, various electrolytes and appl...Under ideally polarizable conditions, TiO2 film electrode/solution electrolyte interface exhibited frequency dispersion, The effects of external factors such as the concentration of KNO3, various electrolytes and applied potentials near the flat band potential on the CPE behavior of TiO2 film electrode were studied in electrolyte solution by using A.C. impedance spectra. It was found that concentration of KNO3 had a significant effect on the CPE exponent n only when the concentration is smaller than 0.1 mol· L－ 1. In this concentration range, the CPE exponent n went up with increase of KNO3 concentration, once the concentration was larger than this value, however, the CPE exponent n approached to a constant, irrelevant of the concentration. Near the flat band potential, the influence of applied potential on the exponent n depended on the selected frequency range. When the frequency was in lower range, that is smaller than 0.1 Hz, this influence was obvious,on the other hand, it bore no relation to applied potential in higher frequency. Types of electrolytes only affected the CPE constant Q, having nothing to do with the CPE exponent n.展开更多
本文测定了三个3(或4)-取代苯甲亚氨酸乙酯(1)和八个N-氰甲基-3(或4)-取代苯甲亚氨酸乙酯(2)的^(13)C-NMR谱。归属了1 和2和各碳化学位移。求得了的取代基化学位移(substituent Chemical Shift,SCS)。碳-13化学位移与单取代苯的取代基...本文测定了三个3(或4)-取代苯甲亚氨酸乙酯(1)和八个N-氰甲基-3(或4)-取代苯甲亚氨酸乙酯(2)的^(13)C-NMR谱。归属了1 和2和各碳化学位移。求得了的取代基化学位移(substituent Chemical Shift,SCS)。碳-13化学位移与单取代苯的取代基化学位移(SCS)的相关分析表明:4-取代苯甲亚氨酸酯1 b～g和2b～e中,除C_(2,6)外,其他各芳碳的化学位移值与加和规则基本相符;3-取代苯甲亚氨酸酯1h～j和2f～h中,除C_1外,其他各芳碳的化学位移值与加和规则基本相符。另外,本文还进行了碳-13化学位移与σ_(I)/σ_(R)~O和F/M的双参数相关分析。展开更多
文摘A brief review and analysis of two historical models of the electron, the charged spinning sphere and Goudsmit and Uhlenbeck’s concept, is presented. It is shown that the enormous potential of classical electrodynamics has been underutilized in particle physics. Such observation leads to discovery of a principal component in the electron inner structure—the charged c-ring. The intrinsic (fundamental) electron model based on the charged c-ring successfully explains the ontology of the charge fractionation in quantum chromodynamics and the formation of Cooper pairs in superconductivity. The c-ring properties are explained on the basis of the General Compton Conditions as defined. Properties of the charged c-ring include the explanation of the boundary conditions, electro-magnetostatic field configuration, self-mass, spin, magnetic moment, and the gyromagnetic ratio. The self-mass of the intrinsic electron is 100% electro-magnetostatic and it is shown how to compute its value. The classical-quantum divide no longer exists. Relation between the intrinsic electron and the electron is fundamentally defined. The electron is the composite fermion consisting of the intrinsic electron and the neutrino. The ontology of the anomaly in the electron magnetic moment is demonstrated—it is due to the addition of the neutrino magnetic moment to the overall electron magnetic moment. The intrinsic electron replaces the W? boson in particle physics, resulting in a fundamental implication for the Standard Model.
文摘Under ideally polarizable conditions, TiO2 film electrode/solution electrolyte interface exhibited frequency dispersion, The effects of external factors such as the concentration of KNO3, various electrolytes and applied potentials near the flat band potential on the CPE behavior of TiO2 film electrode were studied in electrolyte solution by using A.C. impedance spectra. It was found that concentration of KNO3 had a significant effect on the CPE exponent n only when the concentration is smaller than 0.1 mol· L－ 1. In this concentration range, the CPE exponent n went up with increase of KNO3 concentration, once the concentration was larger than this value, however, the CPE exponent n approached to a constant, irrelevant of the concentration. Near the flat band potential, the influence of applied potential on the exponent n depended on the selected frequency range. When the frequency was in lower range, that is smaller than 0.1 Hz, this influence was obvious,on the other hand, it bore no relation to applied potential in higher frequency. Types of electrolytes only affected the CPE constant Q, having nothing to do with the CPE exponent n.
文摘本文测定了三个3(或4)-取代苯甲亚氨酸乙酯(1)和八个N-氰甲基-3(或4)-取代苯甲亚氨酸乙酯(2)的^(13)C-NMR谱。归属了1 和2和各碳化学位移。求得了的取代基化学位移(substituent Chemical Shift,SCS)。碳-13化学位移与单取代苯的取代基化学位移(SCS)的相关分析表明:4-取代苯甲亚氨酸酯1 b～g和2b～e中,除C_(2,6)外,其他各芳碳的化学位移值与加和规则基本相符;3-取代苯甲亚氨酸酯1h～j和2f～h中,除C_1外,其他各芳碳的化学位移值与加和规则基本相符。另外,本文还进行了碳-13化学位移与σ_(I)/σ_(R)~O和F/M的双参数相关分析。
