宽光谱棱镜型太阳光谱仪设计

为实现大气层外太阳光谱辐照度(SSI)变化的长期例行监测,设计了一种星载宽光谱太阳光谱仪结构。全系统仅使用单片折反式曲面棱镜实现太阳光谱250～2500 nm的分光,并通过棱镜转动实现谱平面上多探测器的同步扫描探测;同时基于Huygens子波点扩展函数（PSF）仿真了光谱仪的光谱响应函数（SRF）和光谱分辨率。分光棱镜在±2.5°扫描转角内的全谱段子午像差小于8μm;光谱分辨率在紫外谱段(250～400 nm)为0.7～3.5 nm,可见/近红外谱段(400～1000 nm)为3.5～35.0 nm,短波红外谱段(1000～2500 nm)内为28.5～41.2 nm。整个系统结构简单紧凑,性能稳定可靠,分光和像差校正能力满足大气层外太阳光谱辐照度长期监测需求。     

空间高层大气遥感远紫外成像光谱仪的光学系统

空间高层大气遥感远紫外成像光谱仪主要用于观测高层大气中的远紫外辐射和实现对其内部中尺度现象成像的功能。目前我国该类的相关仪器研究基础还比较薄弱,针对这种情况,在光学系统设计的角度上给出了一种适用于130～180nm波段探测的光学系统方案。该成像光谱仪光学系统以离轴抛物镜为物镜,串联Wadsworth结构为成像光谱系统;这种串联Wadsworth成像光谱系统采用离轴抛物镜做准直镜,分光器件为平面光栅和球面光栅串联,实现二次色散,同时球面光栅起到聚焦成像作用;在像差理论的基础上,对该结构的光程函数和各像差进行了分析,获得了改进结构的宽波段完善成像条件。针对低轨空间探测应用要求设计了相关改进型Wadsworth结构成像光谱仪光学系统,设计结果证明系统像差得到了充分校正,在奈奎斯特频率(20lp/mm)下全视场全波段调制传递函数值在0.6以上。该优化结构同时具备高空间分辨率和高光谱分辨率,性能优越。     

Evaluation of the Mn Lα and Lβ Spectra of Mn Metal and of Various Mn-Oxides

The Mn Lα and Lβ spectra of Mn, MnO, Mn₃O₄, Mn₂O₃, and MnO₂ have been measured. Each Mn La spectrum has been deconvoluted into two bands, Lα_A and Lα_B, and the integrated Lα_A/Lα_B intensity ratio was found to be inversely proportional to the Mn-0 inter-atomic distance, but proportional to the oxidation number. This finding tends to indicate the likelihood of crossover transition from oxygen to manganese. The intensity ratio Lβ/Lα_B of the pure metal was found to coincide closely with the statistically predicted value of 0.5. Furthermore, for Mn-metal, as well as for the oxides, the shift of the Lα_A band from the Lα_B band was found to agree with the change in the Lβ/Lα peak intensity ratio as a function of oxidation number.     

A green train scheduling model and fuzzy multi-objective optimization algorithm

Train scheduling model is traditionally formulated to minimize the energy consumption for reducing the operation cost. As the European Union formulates the first carbon emission trading scheme in the world, it is necessary to extend the operation cost to include the expenses for buying/selling the carbon emission allowances. In this paper, we propose a multi-objective train scheduling model by minimizing the energy and carbon emission cost as well as the total passenger-time, and named it as green train scheduling model. For obtaining a non-dominated timetable which has equal satisfactory degree on both objectives, we apply a fuzzy multi-objective optimization algorithm to solve the model. Finally, we perform two numerical examples to illustrate the efficiency of the proposed model and solution methodology.     

Fission and ternary cluster decay of hyper-deformed 56Ni

Coincidences between two heavy fragments have been measured from the fission of ⁵⁶Ni compound nuclei formed in the ³²S + ²⁴Mg reaction at E _lab( ^32S ) = 165.4 MeV. A unique experimental set-up consisting of two large-area position-sensitive (x, y) gas detector telescopes has been used allowing the complete determination of the observed fragments and their momentum vectors. In addition to binary fission events with subsequent particle evaporation, narrow out-of-plane correlations are observed for two fragments emitted in purely binary events and in events with a missing charge consisting of 2α - and 3α -particles (¹²C). These events are interpreted as ternary cluster decay from ⁵⁶Ni nuclei at high angular momenta through hyper-deformed shapes.     

Spectral Investigations of Solvatochromism and Preferential Solvation on 1,4-Dihydroxy-2,3-Dimethyl-9,10-Anthraquinone

Solvatochromic and preferential solvation of 1,4-dihydroxy-2,3-dimethyl-9,10-anthraquinone (DHDMAQ) have been investigated using optical absorption and fluorescence emission techniques. Optical absorption spectra of DHDMAQ in different solvents show the intra molecular charge transfer band in the region 400–550nm. The observed blue shift with solvent polarity indicates the delocalisation of the excited state, owing to reduction in quasiaromaticity of the chelate rings formed by intra molecular hydrogen bonds, due to electrostatic or hydrogen bonding interaction. This is also confirmed by the observed low oscillator strength and the transition dipole moment. The observed quantum yield of DHDMAQ in different solvents is due to the inter molecular hydrogen bond in the excited state in addition to the intra molecular hydrogen bond. It also reveals from the low oscillator strength, which indicates that the radiative decay is low. Excited state dipole moment of DHDMAQ is calculated by solvatochromic data and it shows a lower value than ground state dipole moment. The preferential solvation parameter shows that in dimethyl formamide (DMF) + ethanol mixture, the DHDMAQ is preferentially solvated by ethanol in DMF rich region and by DMF in ethanol rich region. In the case of DMF + dichloromethane mixture DHDMAQ is preferentially solvated by DMF.     

Simultaneous Determination of Naproxen and Diflunisal using Synchronous Luminescence Spectrometry

Binary mixtures of naproxen and diflunisal can be resolved by using zero-crossing first derivative emission spectrofluorimetry, first derivative constant wavelength synchronous luminescence spectrometry and first derivative constant energy synchronous luminescence spectrometry. These methods do not require any previous separation steps. The lowest quantitation limits for both drugs were obtained with first derivative constant wavelength synchronous luminescence spectrometry (0.002 and 0.015 μg ml⁻¹ for naproxen and diflunisal, respectively). The measurements were performed in 40% methanolic aqueous medium at pH 8.0 provided by adding 0.02 M phosphate buffer solution. The proposed methods were successfully applied to the simultaneous determination of naproxen and diflunisal in pharmaceuticals and human serum samples with high precision and accuracy. Linearity, accuracy, precision, limits of detection, limits of quantitation, and other aspects of analytical validation are included in the text.     

PSⅡ颗粒复合物低温荧光光谱特性

为了获得低温下PSⅡ颗粒复合物色素分子间的能量传递信息,运用荧光激发谱及荧光发射谱对273 K温度时不同波长光激发下菠菜的PSⅡ颗粒复合物的荧光光谱特性进行了研究,分析得出荧光强度的大小与激发光的波长有关,在实验所采用的激发波长中,436 nm的光激发产生的荧光强度最大,520 nm的最小.在能量传递过程中Chl a分子的荧光效率最高,Chl b分子次之.结合吸收谱分析还发现在PSⅡ颗粒复合物中至少存在四种具特征吸收的Chl分子： Chl a661660, Chl a/b672669,670,Chl a682680,Chl a690687.对436 nm光激发所得到的荧光发射谱进一步经高斯解析后得到五个光谱组分：661 nm,672 nm,682 nm,690 nm,730 nm,所占的比例分别为4.75%,9.89%,43.18%,22.08%,20.10%.     

An application of the dust grain charging model to determination of secondary electron spectra

Dust grains – objects of different shapes with a size distribution from micro to nanometers – are generally considered as a part of many space as well as laboratory plasmas. Among various dust charging processes, electron-induced secondary emission plays an important role in plasmas containing a noteworthy portion of high-energy electrons. Since a part of secondary electrons has not the energy high enough to overcome the surface potential barrier, the resulting grain charge is determined not only by the secondary emission yield (related to the grain material and size) but also by the secondary electron spectrum. We have developed a model of secondary electron emission from small dust grains. In the present contribution, we discuss the profile of a secondary emission yield that can be received from the model and the measured equilibrium grain charge, both as functions of an incident electron beam energy. A comparison of these quantities leads to an estimation of secondary electron spectra. We have found that: (1) the energy spectrum of secondary electrons does not change with the energy of primary electrons and (2) the energy spectrum depends on the target material being harder for gold and silver than for glass grains.