Bedeutung der GC-Detektoreigenschaften

Ohne Zusammenfassung

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基于HSV的乳腺癌细胞识别方法

乳腺癌是女性致死率最高的疾病之一,严重威胁女性的身体健康。目前,病理医生判断病症等级,仍通过观察病理切片中的增殖细胞个数,具有很大的主观性。本文提出了一种将RGB彩色空间和HSV彩色空间模型结合的方法,采用各分量的色度特征,通过量化分析建立色度特征方程,实现从病理图像中检测识别乳腺癌增殖细胞。经20组乳腺癌病理切片图像验证,准确性达到了94.2%,优于单色彩空间模型方法约4%,本文提出方法能够更精确识别乳腺癌细胞,为乳腺癌细胞识别提供了一种新方法。     

基于无人机的空地信道特性测量系统

随着各种飞行器和通信一体化的发展,对空地信道特性的研究变得愈发重要且迫切。针对空地通信场景,本文研制了一套由无人机发射单元和地面接收单元组成的无人机空地信道测量系统。该系统选取具有平坦功率谱特性和大动态范围的ZC序列作为测量序列,利用硬件实现实时提取信道冲激响应(Channel Impulse Response, CIR),并通过采样偏差恢复、系统响应校正等方式,提高信道测量系统的准确性。实测验证结果表明,本文研制的信道测量系统与信道模拟器模拟结果和射线跟踪(Ray Tracing, RT)仿真结果基本一致。最后,开展了校园场景空地实测活动,分析了该场景路径损耗(Path Loss, PL)、莱斯K因子、均方根时延扩展(Root Mean Square-Delay Spread, RMS-DS)等信道特性。     

太赫兹带阻滤波器工艺研究

以中心工作频率130 GHz、衰减深度为-40 dB的太赫兹带阻滤波器为制备对象,介绍了其在制备过程中蒸镀、光刻、显影及湿法刻蚀等工艺步骤中的一些技术细节。制备得到的太赫兹滤波器加工误差<±3 μm,考察了加工误差对滤波器传输性能的影响,该加工误差在可接受范围。为进一步验证工艺的可靠性,使用空间测量装置获得了滤波器样品传输性能,测试结果与设计值吻合度较好。最后,探讨了本工艺推广至更高频率器件的适用性及需要改进之处。文中介绍的硅基太赫兹器件加工工艺适用于电子器件与光子器件的融合发展。     

基于5G-R系统的高铁站台场景信道特性

为推进智能铁路总体建设,实现高速铁路智能化,高铁信息基础设施将应用第五代移动通信技术(5G)建设铁路5G专用移动通信系统,2.1 GHz有望成为铁路5G专用移动通信系统的承载频段。高铁站台作为客货乘降与调度中转的功能核心,其在2.1 GHz下的电波传播特性亟待研究。本文以厦门北站高铁站台为研究场景,利用射线跟踪(RT)技术仿真2.1 GHz频段下的电波传播,基于仿真结果分析此场景无线信道特性,包括均方根时延扩展(RMS DS)、到达/离开方位角扩展、到达/离开俯仰角扩展(ASA/ASD, ESA/ESD)、交叉极化比(XPR)和以上参数的互相关。根据以上结果,对高铁站台场景中铁路5G专用移动通信系统的设计和评估提出相关建议。     

亚稳态能量转移发射光谱法测定镉的研究

本文提出了一种测定镉的亚稳态能量转移发射光谱法。利用低功率交流介电法获得活化氮。采用电热蒸发微量进样装置进样,在波长为326.1nm处,测得镉的检出限为0.2 ng/mL。     

Classifying Structural Characteristics to Enhance Computation of Enthalpy of Formation of Halohydrocarbons

Density functional theory (DFT) calculations are made and least squares calibration performed for various halohydrocabons, which were 27 straight‐chain alkyl halides, 20 branch‐chain alkyl halides and 19 aromatic halides, to determine their enthalpies of formation (ΔH_f). The mean absolute error (M. |A.E.|) in ΔH_f across 66 molecular computations was only 7.8 kJ/mol (1.9 kcal/mol). Grouping the molecules by their structural characteristics improved M. |A.E.| of ΔH_f by 0.2–2.2 kJ/mol over that obtained using corresponding modified data for the same 66 unclassified molecules.     

An Investigation on the Effect of Arsenic Poisoning on Humans,Agriculture, and Fisheries

The purpose of this investigation is to try and understand the degree of arsenic poisoning in the waste water from agricultural chemical factories which release effluents into the waterways in their vicinity. The method of determination is to use the water samples, soil, fish, clams, shell-fish, etc. found in the areas along the canals and aqueducts and those which lie upstream, midstream, and downstream and also the hair samples of people living in the contiguous areas, to check for the levels of arsenic in them by emission spectroscopy. From the analysis during a one year investigation, we find that the level of As in the water creatures of Chungkang Stream and Lu-Er-Men Stream is much higher than in the other water areas of Taiwan such as along beaches and the other rivers; the levels in the hair of the people who live nearby these water courses have a certain degree of correspondence with their eating habits and the quantity of food eaten; however, even those people who eat relatively little have almost 3% As, beyond the 2 mg/kg limit allowed for human beings. We are fully aware of the high level of food contamination on Taiwan, and this fact has been taken into consideration. The effect of As contamination in the soil on agricultural produce does not seem to have any apparent relationship. By the way, the influence of the monthly average rainfall on As contamination in the soil is not obvious.     

Thermodynamic characteristics of solvation of individual ions in ethanol at −50 to 55°C

Experimentally determined are the enthalpies of solution of 12 electrolytes (LiBr, LiI, NaBr, NaI, NaBPh₄, Et₄NCl, Et₄NBr, Pr₄Br, Bu₄NBr, Am₄NBr, Ph₄PCl, Ph₄PBr) in ethanol at –50 to 55°C. _sH^o values obtained on the basis of four different extrapolation equations are analyzed. The effect of temperature changes on the thermodynamic parameters of solvation indindividual ions are calculated using thermodynamic data for the salt crystals (lattice) with the assumption that _solvC _p ^o (Ph₄P⁺)=_solvC _p ^o (Ph₄P^-).