非均匀部分相干光束在自由空间中的传输

本文介绍了非均匀部分相干光束的概念, 并用数值模拟的方法详细研究了其在自由空间传输后的变化. 研究结果表明, 经过自由空间传输后非均匀部分相干光束会发生不同于传统相干模型光束的显著变化. 这种变化和光束传输距离、光源空间相干度分布、光源光强分布密切相关. 经过传输后, 源平面自相干附近点的空间相干度发生突变, 在短距离传输过程中源平面高相干区域的空间相干度会降低, 接收面各点的空间相干曲线不再相同, 随着传输距离增加, 非均匀空间相干度会逐渐趋于均匀.     

电离辐射环境下的部分耗尽绝缘体上硅n型金属氧化物半导体场效应晶体管可靠性研究

随着半导体技术的进步, 集成小尺寸绝缘体上硅器件的芯片开始应用到航空航天领域, 使得器件在使用中面临了深空辐射环境与自身常规可靠性的双重挑战. 进行小尺寸器件电离辐射环境下的可靠性试验有助于对器件综合可靠性进行评估. 参照国标GB2689.1-81恒定应力寿命试验与加速寿命试验方法总则进行电应力选取, 对部分耗尽绝缘体上硅n型金属氧化物半导体场效应晶体管进行了电离辐射环境下的常规可靠性研究. 通过试验对比, 定性地分析了氧化物陷阱电荷和界面态对器件敏感参数的影响, 得出了氧化物陷阱电荷和界面态随着时间参数的变化, 在不同阶段对器件参数的影响. 结果表明, 总剂量效应与电应力的共同作用将加剧器件敏感参数的退化, 二者的共同作用远大于单一影响因子.     

Approximative compactness and continuity of the set-valued metric generalized inverse in Banach spaces

In this paper, continuity of the set-valued metric generalized inverse T^∂$T^{\partial }$ in approximatively compact Banach spaces is investigated by means of the methods of geometry of Banach spaces. Necessary and sufficient conditions for upper semicontinuity (continuity) for the set-valued metric generalized inverses T^∂$T^{\partial }$ are given. Moreover, authors also prove that if X is a nearly dentable space and H is a hyperplane of X, then H   is approximatively compact iff _PH(x)$P_H(x)$ is compact for any x∈X$x\in X$.     

基于TDC-GP2的时间间隔测量系统设计

精确的时间间隔测量在时间同步系统有着至关重要的作用,为了满足大量程和高精度的需求,介绍了一种直接计数法和时间-数字装换法相结合的时间间隔测量系统;设计中采用两片TDC-GP2时间-数字转换芯片,结合FPGA和上位机,可以实现精度为1 ns时差测量;经过大量的实际测量,系统的分辨率为70 ps,精度为1 ns,最大可以测量1 s的时间间隔;该设计的系统具有可靠性高、功耗低、精度高、使用灵活等优点。     

Identification of Metabolites of Epimedin A in Rats Using UPLC/Q–TOF–MS

Herba Epimedii (Epimedium) is a kind of tonic herb, widely used in China. Epimedin A is a major component of Herba Epimedii with bioactivities. Analysis of the metabolic profile in vivo plays a pivotal role in understanding how traditional Chinese medicine works. And the metabolites of epimedin A might influence the effects of Herba Epimedii. Moreover, the metabolic routes of epimedin A provide an important basis for safety evaluation. Until now, little has been known about the metabolism of epimedin A. The current study was designed to characterize the metabolic pathways of epimedin A in vivo. The metabolites in rat plasma, bile, feces, and urine were identified by UPLC/Q–TOF–MS analysis. A total of 27 metabolites from epimedin A were detected or tentatively identified. The major metabolic processes were hydrolysis, hydrogenation, hydroxylation, dehydrogenation, demethylation, and conjugation with glucuronic acid and different sugars. The present study revealed the metabolic pathways of epimedin A in rat for the first time, and epimedin A could undergo extensive phase I and phase II metabolism in rat. These findings would provide an important basis for the further study and clinical application of epimedin A. In addition, the results of this work have shown the feasibility of the UPLC/Q–TOF–MS approach for rapid and reliable characterization of metabolites.     

Synthesis and Electronic/ionic Transport Properties of MoO2/rGO Anode for Lithium Ion Batteries

MoO₂/rGO (reduced graphite oxide) composites have been synthesized by hydrothermal method followed by anneal and characterized by X‐ray diffraction (XRD) and scanning electron microscope (SEM). Galvanostatic charge/discharge testing and electrochemical impedance spectroscopy (EIS) techniques are employed to evaluate the kinetic behaviors of the MoO₂/rGO during lithiation/delithiation. The obtained MoO₂‐based materials have monoclinic crystal structure, and worm like shape with average dimensions of 100‐200 nm width and 500 nm‐1 μm length. There are two steps of lithium ion intercalation/de‐intercalation for the MoO₂/rGO anode at the potential ranging from 1.0 to 3.5 V, locating at E_Li/Li⁺ = 1.60/1.75 V, 1.25/1.40 V, and the first discharge and charge capacities are, respectively, 221.0 and 185.4 mAh g^?1. The resistances of R_SEI and R_CT for the MoO₂/rGO anode are 2‐4 Ω and below 5 Ω. Moreover, the lithium diffusion coefficient calculated from the EIS measurement is about 3.6×10^?9 cm² s^?1.     

Cyclodextrin-Modified Gold Nanoparticle Capillary Electrochromatography with Online Sample Stacking for Simultaneous and Sensitive Determination of Aminobenzoic Acid Isomers

A newly-developed method of complete separation and sensitive determination of o-, m-, and p-aminobenzoic acid isomers was achieved by combining open-tubular columns for capillary electrochromatography (OT-CEC) and online sample stacking. In this study, spherical gold nanoparticles were modified by a covalent attachment of mono-6-thio-β-cyclodextrin, and OT-CEC was formed by immobilizing cyclodextrin-modified gold nanoparticles (CD-AuNP) on prederivatized 3-mercaptopropyl-trimethoxysilane fused-silica capillaries. Based on the theory of moving chemical reaction boundary, effects of several important factors such as the pH and concentration of running buffer and the conditions of stacking analytes were optimized. The optimized separations were carried out in 58 mmol/L HAc buffer at pH 3.0 using a capillary coated with CD-AuNP, while the optimized concentration was carried out in 50 mmol/L disodium hydrogen phosphate (pH 9.5). The linear ranges for m-, p-, and o-aminobenzoic acid were from 5.0 × 10⁻⁴–0.1, 5.0 × 10⁻⁴–0.1 and 1.0 × 10⁻⁴–0.1 mmol/L, respectively. And the detection limits (S/N = 3) were as low as 8.22 × 10⁻⁵, 8.21 × 10⁻⁵, and 3.76 × 10⁻⁵ mmol/L for m-, p-, and o-aminobenzoic acid, respectively. The run-to-run, day-to-day, and column-to-column reproducibilities of migration time were satisfactory with relative standard deviation values of less than 4.5 % in all cases. This method was successfully used in determining procaine hydrochloride injection sample with recoveries in the range of 96.1–106.6 % and relative standard deviations less than 5.0 %.

     

Cyclodextrin-Modified Gold Nanoparticle Capillary Electrochromatography with Online Sample Stacking for Simultaneous and Sensitive Determination of Aminobenzoic Acid Isomers

A newly-developed method of complete separation and sensitive determination of o-, m-, and p-aminobenzoic acid isomers was achieved by combining open-tubular columns for capillary electrochromatography (OT-CEC) and online sample stacking. In this study, spherical gold nanoparticles were modified by a covalent attachment of mono-6-thio-β-cyclodextrin, and OT-CEC was formed by immobilizing cyclodextrin-modified gold nanoparticles (CD-AuNP) on prederivatized 3-mercaptopropyl-trimethoxysilane fused-silica capillaries. Based on the theory of moving chemical reaction boundary, effects of several important factors such as the pH and concentration of running buffer and the conditions of stacking analytes were optimized. The optimized separations were carried out in 58 mmol/L HAc buffer at pH 3.0 using a capillary coated with CD-AuNP, while the optimized concentration was carried out in 50 mmol/L disodium hydrogen phosphate (pH 9.5). The linear ranges for m-, p-, and o-aminobenzoic acid were from 5.0 × 10^?4–0.1, 5.0 × 10^?4–0.1 and 1.0 × 10^?4–0.1 mmol/L, respectively. And the detection limits (S/N = 3) were as low as 8.22 × 10^?5, 8.21 × 10^?5, and 3.76 × 10^?5 mmol/L for m-, p-, and o-aminobenzoic acid, respectively. The run-to-run, day-to-day, and column-to-column reproducibilities of migration time were satisfactory with relative standard deviation values of less than 4.5 % in all cases. This method was successfully used in determining procaine hydrochloride injection sample with recoveries in the range of 96.1–106.6 % and relative standard deviations less than 5.0 %.     

Synthesis and Biological Activities of 3‐Substituted Analogues of Tenuazonic Acid

A series of tenuazonic acid analogues in which the acetyl group was replaced with electron‐withdrawing substituents have been synthesized with the aim of obtaining molecules with various bioactivities. Substituents such as cyano, sulfonyl, and amido were introduced at the 3‐position of the pyrrolidine‐2,4‐dione nucleus of tenuazonic acid. 3‐Cyano and sulfonyl pyrrolidine‐2,4‐dione compounds ( 2 and 6 ) were prepared via a Dieckmann cyclization as key step. 3‐Amido pyrrolidine‐2,4‐dione compounds ( 9 ) were prepared by a microwave‐assisted amidation reaction from corresponding 3‐carboxylate derivative. The target compounds were evaluated; their herbicidal, fungicidal, and insecticidal activities, and the preliminary bioassay data showed that some 3‐cyanopyrrolidine‐2,4‐diones 2 gave good insecticidal activity, whereas some 3‐amido compounds 9 exhibited moderate to strong fungicidal activity against Pythium dissimile at 20 mg/L.     

Crystal structure and fluorescent properties of a 2D cadmium coordination polymer

A new 2D cadmium(II) coordination polymer {[Cd(MBD)(L)]·(H₂O)₂} _n (1) (H₂MBD = 5-methoxycarbonyl-benzene-1,3-dicarboxylic acid, L = 1,3-bis(benzimidazol-l-yl)-2-propanol) is synthesized, in which the starting linker (benzene-1,3,5-tricarboxylic acid) undergoes selective monoesterification during the synthesis. In the structure of complex 1, each cadmium center is octahedrally coordinated by four O atoms from three carboxylate groups and two N of distinct L ligands. A detailed structural analysis reveales that compound 1 exhibits a unique 2D binodal (3,5)-connected (4².6⁷.8)(4².6) topology structure. Furthermore, the 2D layer is extended into a 3D network through π-π stacking interactions. The solid-state fluorescence properties of 1 are investigated at room temperature.