阳极氧化法制备Y型TiO2纳米管

在含有质量分数为0.5%的NH₄F和体积分数为5% 的H₂O的乙二醇混合溶液中,采用三步阳极氧化法制备了表面形貌高度有序的Y型TiO₂纳米管阵列。讨论了钛片预处理过程对优化TiO₂纳米管阵列表面形貌的影响以及采用升温法制备Y型TiO₂纳米管的内在机理,并在较宽的温度范围内(20~60 ℃)对钛片进行阳极氧化。实验结果表明当阳极氧化第三步的电解液温度设置在40 ℃以上时,Y型TiO₂纳米管阵列的顶端将出现环状纳米线、管壁破裂以及管长减小等现象,不利于保证Y型TiO₂纳米管阵列的整体质量。因此,30~40 ℃是选取阳极氧化第三步温度的理想范围。     

一种基于空间一致性降元的高光谱图像非监督分类

为了提高分类精度和边缘辨识性,该文引入图像空间一致性降元(pixels reduction with spatial coherence property, PRSCP)及线性回归分析,提出了一种基于空间一致性降元的非监督分类。该方法从像元光谱相似性出发,利用像元最小关联窗口合并相邻相似像元为像块完成降元。使用线性关系建模像块内像元的光谱向量,并利用F检验判断像块数据的线性显著性。利用一元线性回归(one dimensional linear regression, ODLR)估计出像块的基准向量,根据基准向量合并相似(同类)像块完成分类。利用AVIRIS数据评估了该方法性能,实验结果表明：与K-MEANS和ISODATA方法相比,该方法精度高、边缘辨识度好及鲁棒性强。     

0.4 THz回旋行波管的设计与模拟

利用三维粒子模拟仿真软件,对共焦波导结构的0.4 THz回旋行波管进行了注波互作用的模拟研究。以共焦波导的冷腔色散以及衍射损耗入手,最终选定HE06模作为互作用工作模式。为了对寄生振荡进行抑制,在互作用结构中引入了截断。在模拟过程中,通过调节束压、束流、工作磁场、电子束横纵速度比,得到了最优的工作参数。最终,在束压34 kV、磁场14.25、束流2 A、横纵速度比0.75的工作参数下,当输入信号为1 W时,得到了最高2.76 kW的功率输出,增益超过34 dB,3 dB带宽为8 GHz,效率达到4%。     

改进型Czerny-Turner成像光谱仪光学系统设计方法

像散是目前影响Czerny-Turner结构成像光谱仪空间分辨率最大的像差。首先引入柱面反射镜,利用光焦度衡量像散大小,推导出易于计算的像散校正公式,有效地校正了像散。给出准直镜到光栅距离的计算方法,有效校正了成像光谱仪边缘视场像差。给出了成像光谱仪像面倾角的计算方法,实现了宽波段的像差校正。最终利用上述方法设计了一套用于115～200nm的改进型Czerny-Turner成像光谱仪,焦距f′=48mm,F数为5.0,全视场、全波段调制传递函数(MTF)在0.7以上。全波段光谱分辨率为0.22nm,像面大小为8mm×7mm。设计方法适用于多种结构要求的成像光谱仪。     

定向红外对抗系统的激光源模拟研究

针对半实物仿真中定向红外对抗系统的有效模拟问题,在分析定向红外对抗激光源技术的基础上,依据实战应用,计算得到3 m~5 m波段定向红外对抗激光源的辐射能量为飞机红外辐射强度绝对值的8倍,结合波长4 m处简化的大气传输透过率随传输距离的变化,推导出实战应用中红外导引头上辐射照度随飞机导弹之间距离的变化规律。设计半实物仿真中定向红外对抗的模拟方案,依据逼真模拟的原则,计算得到模拟激光源能量随飞机导弹之间距离和飞机辐射强度的变化规律,据此将飞机导弹相互距离1 km时刻的红外干扰源辐射能量设置为波长4 m模拟激光源能量,其他距离的模拟能量通过衰减片来控制。为提高定向红外对抗模拟的通用性和智能性,设计了模拟激光源的闭环控制方案。     

Elucidating Molecule–Plasmon Interactions in Nanocavities with 2 nm Spatial Resolution and at the Single‐Molecule Level

The fundamental understanding of the subtle interactions between molecules and plasmons is of great significance for the development of plasmon‐enhanced spectroscopy (PES) techniques with ultrahigh sensitivity. However, this information has been elusive due to the complex mechanisms and difficulty in reliably constructing and precisely controlling interactions in well‐defined plasmonic systems. Herein, the interactions in plasmonic nanocavities of film‐coupled metallic nanocubes (NCs) are investigated. Through engineering the spacer layer, molecule–plasmon interactions were precisely controlled and resolved within 2 nm. Efficient energy exchange interactions between the NCs and the surface within the 1–2 nm range are demonstrated. Additionally, optical dressed molecular excited states with a huge Lamb shift of ≈7 meV at the single‐molecule (SM) level were observed. This work provides a basis for understanding the underlying molecule–plasmon interaction, paving the way for fully manipulating light–matter interactions at the nanoscale.     

Liquid crystalline behaviours of some 3-perfluoroalkylbenzoate esters

A series of 3-perfluoroalkylbenzoate esters are synthesised. They tend to exhibit enantiotropic SmA and SmC phases. The clearing points are decreased with increasing the alkoxy chain length and show odd-even effect. With increasing the fluorocarbon chain length, the melting and clearing points increase; however, the SmC phase is suppressed.     

Validated liquid chromatography–tandem mass spectrometry method for quantification of ticagrelor and its active metabolite in human plasma

A rapid, simple and sensitive LC–MS/MS method was established and validated for simultaneous quantification of ticagrelor and its active metabolite AR‐C124910XX in human plasma. After plasma samples were deproteinized with acetonitrile, the post‐treatment samples were chromatographed on a Dikma C₁₈ column interfaced with a triple quadrupole tandem mass spectrometer. Electrospray negative ionization mode and multiple reaction monitoring were adopted to assay ticagrelor and AR‐C124910XX. Acetonitrile and 5 mΜ ammonium acetate was used as the mobile phase with a gradient elution at a flow rate of 0.5 mL/min. The method was linear in the range of 0.781–800 ng/mL for both ticagrelor and AR‐C124910XX with a correlation coefficient ≥0.994. The intra‐ and inter‐day precisions were within 12.61% in terms of relative standard deviation and the accuracy was within ±7.88% in terms of relative error. The LC–MS/MS method was fully validated for its sensitivity, selectivity, stability, matrix effect and recovery. This convenient and specific LC–MS/MS method was successfully applied to the pharmacokinetic study of ticagrelor and AR‐C124910XX in healthy volunteers after an oral dose of 90 mg ticagrelor.     

Simultaneous quantification of levofloxacin,pefloxacin, ciprofloxacin and moxifloxacin in microvolumes of human plasma using high‐performance liquid chromatography with ultraviolet detection

Levofloxacin, pefloxacin, ciprofloxacin and moxifloxacin are four fluoroquinolones used in the treatment of serious bacterial infections. The antibacterial activity of fluoroquinolones is concentration dependent. Therefore, therapeutic drug monitoring in daily clinical practice is warranted to ensure the therapy's efficacy and prevent bacterial resistance. The purpose of the present study was to develop a method using high‐pressure liquid chromatography with an ultraviolet detector for simultaneous quantification of these four fluoroquinolones in human plasma. A 50 μL aliquot of plasma was precipitated by 200 μL of methanol using gatifloxacin as internal standard. The chromatographic separation was performed on a Kinetex XB‐C₁₈ column using a mobile phase composed of a mixture of orthophosphoric acid 0.4% (v/v), acetonitrile and methanol at a flow rate of 1.2 mL/min. Dual UV wavelength mode was used, with levofloxacin and moxifloxacin monitored at 293 nm, and pefloxacin and ciprofloxacin monitored at 280 nm. The calibration was linear over the ranges of 0.125–25 mg/L for levofloxacin, 0.1–20mg/L for moxifloxacin and 0.05‐10 mg/L for both pefloxacin and ciprofloxacin. Inter‐ and intra‐day trueness and precision were <13% for all the compounds under study. The proposed method was simple, reliable, cost‐effective and suitable for therapeutic drug monitoring or pharmacokinetics studies.