Field emission from nano-patterned amorphous carbon

Electron emission from nano-patterned amorphous carbon is realized in this paper. The patterned carbon consists of islands with size of tens of nanometers, and is formed by etching uniform carbon film in oxygen plasma using a bismuth island-like film as the mask. Uniform and stable electron emission is reproducibly obtained, and the emission efficiency is above 2% at an anode voltage of 3 kV. Small carbon particles between large islands are supposed to be necessary for stable electron emission.     

工艺应力模拟技术中的热相似律

分析了热处理及焊接的热过程，从热传导的基本方程及边界条件出发，结合不同工艺过程的特点，提出了用光弹法模拟整体淬火热应力，表面淬火热应力和焊接过程热应力及残余应力的热相似律。     

抗核辐射条件的应变计粘贴与防护技术

本文介绍了在重水反应堆中进行应变测量的若干技术成果，主要是较好地解决了用在核辐射条件下，有水流冲刷的环境中的应用变计的粘贴与防护技术。在具有核辐射的环境中测试，通常选用聚酰亚胺胶作粘结剂。但是这种胶需在高温条件下固化，如果被测构件较大，是无法实现的。经测试筛选出具有防水防辐射性能的常温固化胶，并介绍了可用航空导线替代具有抗辐射性能的铠装电缆在堆内进行测量问题。采用有关措施后，经标定，在核辐射前后应     

足底压力统计变化规律测试与侦破技术

利用现场足迹特征,分析罪犯的性别、年龄、身高、体态、行走姿势等个人形体特点,常称为给罪犯“画像”。这一技术在侦破案件中起了一定作用。（１）研究人在常态下行走时留在地面上的平面足迹反映出压力的分布和变化规律,分析压力与年龄的相关性,从中研究出分析年龄的科学方法,提高分析年龄的准确率。（２）研究平面足迹压力与人的性别、身高、体态、行走姿势的相关性找出各自的科学分析方法。（３）从分析理论上全面加以提高,     

Determination of 16 Mycotoxins in Maize by Ultrahigh-Performance Liquid Chromatography–Tandem Mass Spectrometry

An ultrahigh-performance liquid chromatography–tandem mass spectrometry method was developed and validated for the simultaneous determination of sterigmatocystin, verruculogen, enniatin A, fusarenon-X, fumonisins B1, B2, B3, aflatoxins B1, B2, G1, G2, ochratoxin A, deoxynivalenol, 3-acetyldeoxynivalenol, 5-acetyldeoxynivalenol, and zearalenone. The mycotoxins were extracted and cleaned up using a multitoxin column, separated on a C18 column, and then detected on a triple-quadrupole mass spectrometer. The limits of detection and quantification ranged within 0.2–2?µg/kg and 1–10?µg/kg, respectively. The recoveries ranged from 70.8 to 118.4%, with relative standard deviations below 15%. The method was used to analyze 80 samples obtained from Shandong Province in China. Fifty-eight samples were contaminated with 10 mycotoxins at concentrations ranging from 1.4 to 6566.1?µg/kg. Some samples exceeded the maximum limits in China and in European regulations for mycotoxins in unprocessed maize.     

可变孔径超高真空盒波纹管的应力实验研究

可变孔径超高真空盒系电子对撞机实施同步辐射装置扩建工程的关键部件。本文给出了不同孔径变化的８－环型波纹管在超高真空状态下电测应力实验结果。本实验选用了七个截面，布片较多，测出了不同截面的应力分布规律。同时，测出了装配应力对结构的影响。该测试结果为改进设计正式投入生产提供了可靠的科学依据。     

微波消解-电感耦合等离子体质谱(ICP-MS)法测定山东小麦中铬、镍、铜、砷、镉、铅、锌的含量

建立了微波消解-电感耦合等离子体质谱(ICP-MS)法测定山东小麦中7种重金属元素(Cr、Ni、Cu、As、Cd、Pb、Zn)的方法,并对山东地区千余份小麦进行分析。结果表明,通过使用适宜的内标和He碰撞模式,7种重金属元素的方法检出限在0.0007~0.09 mg/kg,相对标准偏差(RSD,n=6)在10%以内,标准曲线线性关系良好,相关系数均大于0.999,方法用于国家有证标准物质(GSB-3、GSB-4、GSB24)的测定,结果与标准值相符。方法灵敏度高,重现性好,定量准确,可用于大批量小麦样品的测定。     

Photocontrollable analyte-responsive fluorescent probes: a photocaged copper-responsive fluorescence turn-on probe

Analyte-responsive fluorescent probes are valuable chemical tools for dissecting complex living systems. However, the major shortcoming of fluorescent probes is that once they enter the cells, control over them is basically lost. It is critical to regulate fluorescent probes in a spatial and temporal manner, as functions of biomolecules are spatiotemporal. On the other hand, light can be manipulated in time and in the application site, so the photocaging technique allows researchers to control the biomolecules of interest in a temporal and spatial fashion. Herein, we propose for the first time the combination of the merits of sensing and photocaging technologies, which may afford the caging version of analyte-responsive fluorescent probes, referred to as photocontrollable analyte-responsive fluorescent probes (PCAFPs). These "smart" fluorescent probes apparently have the intrinsic advantage of spatiotemporal control when compared to traditional fluorescent probes, as the "sensing activity" of PCAFPs is photocontrollable. This should enable biologists to interrogate complex biological systems in a spatial and temporal manner with an innovative chemical tool. In this work, for proof of concept, we report the rational design, synthesis, photocontrollable sensing in solution and in living cells, and mechanistic studies of a molecular prototype of PCAFP for copper as the first paradigm of this new class of smart fluorescent probes. We believe that PCAFPs represent a substantial breakthrough in the sensing and photocaging fields, and that the general concept of PCAFPs should be broadly applicable for a wide variety of biologically relevant species.     

Development of FRET-based dual-excitation ratiometric fluorescent pH probes and their photocaged derivatives

Dual-excitation ratiometric fluorescent probes allow the measurement of fluorescence intensities at two excitation wavelengths, which should provide a built-in correction for environmental effects. However, most of the small-molecule dual-excitation ratiometric probes that have been reported thus far have shown rather limited separation between the excitation wavelengths (20-70 nm) and/or a very small molar absorption coefficient at one of the excitation wavelengths. These shortcomings can lead to cross-excitation and thus to errors in the measurement of fluorescence intensities and ratios. Herein, we report a FRET-based molecular strategy for the construction of small-molecule dual-excitation ratiometric probes in which the donor and acceptor excitation bands exhibit large separations between the excitation wavelengths and comparable excitation intensities, which is highly desirable for determining the fluorescence intensities and signal ratios with high accuracy. Based on this strategy, we created a coumarin-rhodamine FRET platform that was then employed to develop the first class of FRET-based dual-excitation ratiometric pH probes that have two well-resolved excitation bands (excitation separations>160 nm) and comparable excitation intensities. In addition, these pH probes may be considered as in a kind of "secured ratioing mode". As a further application of these pH probes, the dual-excitation ratiometric pH probes were transformed into the first examples of photocaged dual-excitation ratiometric pH probes to improve the spatiotemporal resolution. It is expected that the modular nature of our FRET-based molecular strategy should render it applicable to other small-molecule dual-dye energy-transfer systems based on diverse fluorescent dyes for the development of a wide range of dual-excitation ratiometric probes with outstanding spectral features, including large separations between the excitation wavelengths and comparable excitation intensities.