Eigenvalue Spectrum of a Dirac Particle in Static and Spherical Complex Potential

It has been observed that a quantum theory need not be Hermitian to have a real spectrum. We study the non-Hermitian relativistic quantum theories for many complex potentials, and obtain the real relativistic energy eigenvalues and corresponding eigenfunctions of a Dirac-charged particle in complex statically and spherically symmetric potentials. Complex Dirac–Eckart, complex Dirac–Rosen–Morse II, complex Dirac–Scarf and complex Dirac–Poschl–Teller potential are investigated.     

Relaxation of Paramagnetic Centers during Modulation of a Stationary Magnetic Field

It has been found that the phase shift _min in the synchronous detection block that ensures the minimum amplitude of the EPR lines of ruby, diphenylpicrylhydrazyl, and MnSO₄·5H₂O, depends on the amplitude of the modulationH _m of a stationary magnetic field. The dependence of _min on H _m is explained by the inertial nature of the recovery of the stationary states of paramagnetic centers on a change in the magnetic field strength.     

Calculation of Normal Vibrations of Chlorin by the Method of Density Functionals

Using the DFT/B3LYP method with a 6-31G(d) basis set, the structure, normal vibration frequencies, and the absolute band intensities in the IR spectra of the chlorin molecule and its four symmetric isotopomers have been calculated. Scaling of the force field by the Pulay method in independent and natural coordinates has been carried out. A method for obtaining effective force fields without using experimental data on the fundamental vibration frequencies is proposed. By comparing the vibration modes and constructing special matrices, complete assignment of the fundamental frequencies of porphin and chlorin has been carried out. It has been shown that the majority of porphin macroring vibrations upon pyrrolenine ring hydrogenation are frequency-characteristic and only 12 vibrations change considerably. A frequency correlation with regard for the mode transition between chlorin and all its isotopomers under consideration has been established. Comparative analysis of the force fields of porphin and chlorin in dependent natural coordinates has revealed the unique nonlocal character of the change in force constants of the macroring upon hydrogenation of one pyrrolenine ring. Modeling of the IR spectra of chlorin and its isotopomers has been performed. Assignment and interpretation of the normal vibrations of the molecules under consideration have been carried out.     

利用傅里叶变换红外光谱法鉴定小麦品种

利用傅里叶变换红外(FTIR)光谱法分析了8个不同小麦品种根部的红外光谱图,对红外光谱图的吸收峰进行了归属分析,通过对各谱图的比对发现,在相同波数范围内,不同的小麦品种其红外谱图的形状、波数及吸收峰的多少有所不同。结果表明不同小麦品种的红外光谱图有明显的差异,其一在2800～2980cm-1波数范围内,此区反映的主要是甲基、亚甲基的伸缩振动,化合物分子链的长短、分子量的大小在此区有显现;其二差别较大的区域在1510～1730cm-1范围内,它反映的主要是酰胺的氮原子及α碳原子取代基的性质,可能是源于基因的差异,此区域内谱图差异较大。因此FTIR光谱法可用于不同小麦品种的鉴别。     

细胞培养基的吸收光谱研究

使用日本岛津UV 310 1分光光度计分别测量培养了宫颈癌细胞 (Hela)和鼻咽癌细胞 (CNE)的RP MI 16 4 0培养基和DMEM高糖培养基的紫外吸收光谱 ,分析了培养基中蛋白质的紫外吸收特性。RPMI16 4 0培养基的 2 2 7nm吸收峰在培养细胞生长过程中位移至 2 2 2或 2 18nm ,2 78nm的吸收峰位移至 2 80nm ;而DMEM高糖培养基 2 2 4nm吸收峰在培养细胞生长过程中位移至 2 2 1nm附近 ,2 78nm吸收峰基本没有位移。这些位移说明培养基中芳香族氨基酸中各种氨基酸如色氨酸和酪氨酸的含量有变化。也就是说 ,癌细胞在生长过程中对色氨酸和酪氨酸的消耗不是按等量比的。实验也说明Hela和CNE在生长过程中 ,对RPMI 16 4 0培养基和DMEM高糖培养基中氨基酸的消耗是不同的。实验结果为癌细胞生长过程中所需培养基中氨基酸的含量提供了依据     

Regression-based model of skin diffuse reflectance for skin color analysis

A simple regression-based model of skin diffuse reflectance is developed based on reflectance samples calculated by Monte Carlo simulation of light transport in a two-layered skin model. This reflectance model includes the values of spectral reflectance in the visible spectra for Japanese women. The modified Lambert Beer law holds in the proposed model with a modified mean free path length in non-linear density space. The averaged RMS and maximum errors of the proposed model were 1.1 and 3.1%, respectively, in the above range.     

Complex-number asymmetry parameters of the optical Fano effect in ring resonators

We studied the sharp asymmetric Fano line shape in fiber ring resonator systems and provided an explicit expression for asymmetry parameters using the physical parameters of the system. The fiber ring system was controllable and reconfigurable, allowing us to produce a variety of Fano line shapes in different configurations. Experimentally observed asymmetric spectral structures were fully reproduced using the complex-number asymmetry parameters, validating the approximations used to reduce the analytical expression for the line shape to the phenomenological Fano formula. The results may be useful in the design of on-chip application systems.     

Spectral target-detecting system using sine-wave modulation

Target detection is one of the key technology of precision chemical application.Previously the digital coding modulation technique was commonly used to emit and receive the optical signal in the target detection systems previously in China.It was difficult to adjust the output power,and the anti-interference ability was weak in these systems.In order to resolve these problems,the target detection method based on analog sine-wave modulation was studied.The spectral detecting system was set up in the aspects ...     

Point defects and orientation-dependent transport of matter and charge in iron-containing olivines

The variation of the oxygen content, x_O, of synthetic fayalite (Fe₂SiO₄) single crystals was investigated thermogravimetrically at 1130 °C as a function of the oxygen activity, a_O2 (= P_O2/P_O2° ≈ f_O2/f_O2° with P_O2° ≈ f_O2° = 1 bar ≈ 1 atm). It was found that x_O varies less in fayalite single crystals than in polycrystalline Fe₂SiO₄ studied earlier. The majority defects are most likely cation vacancies, (V_Me²⁺)″, ferric ions on M-sites, (Fe³⁺_Me²⁺), and ferric ions on Si-sites, (Fe³⁺_Si⁴⁺)′. Furthermore, the diffusion of iron in synthetic olivine single crystals ((Fe_xMg_1 − x)₂SiO₄) was studied at 1130 °C as a function of orientation, oxygen activity, and cationic composition. The observed oxygen activity dependencies suggest that cations move via different types of cation vacancies, most likely isolated vacancies, (V_Fe²⁺)″, and possibly neutral associates, {2(Fe³⁺_Me²⁺) ⋅ (V_Me²⁺)^′ ? ′}^x, the latter being minority defects. In addition, the electrical conductivity, σ, of fayalite single crystals was investigated as a function of orientation and oxygen activity within the stability field of fayalite at 1130 °C. The observed oxygen activity dependencies are compatible with (V_Me²⁺)^′ ? ′, (Fe³⁺_Me²⁺), and (Fe³⁺_Si⁴⁺)′ being the majority point defects at high a_O2 and with h^⋅ and e′ as the majority defects at low a_O2. The electrical conduction in fayalite is governed by contributions of electrons and holes. This extended point defect model for fayalite is also compatible with data for the variation of the oxygen content and for the iron tracer diffusion.