锁相检测式二维小角度测量装置

介绍了一种新型的二维小角度检测装置。由于该装置采用了光电自准直结构,以高灵敏度的四象限硅光电探测器作为检测元件,采用交流调制,锁相放大的方法对信号进行了处理,所以有效地消除了直流漂移的影响,提高了稳定性和测试精度。分析了光斑的形状和大小对测试结果的影响,研制了专门的标定装置。首先由高精度的光电自准直仪标定测量角度与输出信号的关系,并将相关数据存入单片机,然后由软件拟合出关系曲线。测量时,既可自动显示角度的大小,同时也可以与计算机相连。该测试系统结构小巧,具有较高的测量精度。     

Synthesis of multi-walled carbon nanotubes using CoMnMgO catalysts through catalytic chemical vapor deposition

The Co Mg O and Co Mn Mg O catalysts are prepared by a co-precipitation method and used as the catalysts for the synthesis of carbon nanotubes（CNTs） through the catalytic chemical vapor deposition（CCVD）. The effects of Mn addition on the carbon yield and structure are investigated. The catalysts are characterized by temperature programmed reduction（TPR） and X-ray diffraction（XRD） techniques, and the synthesized carbon materials are characterized by transmission electron microscopy（TEM） and thermo gravimetric analysis（TG）. TEM measurement indicates that the catalyst Co Mg O enclosed completely in the produced graphite layer results in the deactivation of the catalyst. TG results suggest that the Co Mn Mg O catalyst has a higher selectivity for CNTs than Co Mg O. Meanwhile, different diameters of CNTs are synthesized by Co Mn Mg O catalysts with various amounts of Co content, and the results show that the addition of Mn avoids forming the enclosed catalyst, prevents the formation of amorphous carbon, subsequently promotes the growth of CNTs, and the catalyst with decreased Co content is favorable for the synthesis of CNTs with a narrow diameter distribution.The Co Mn Mg O catalyst with 40% Co content has superior catalytic activity for the growth of carbon nanotubes.     

化学链燃烧中Fe氧化过程产物层生长特性

利用TGA、SEM研究了化学链燃烧中Fe氧化反应过程产物层的生长机理,以及产物层形貌对化学反应动力学的影响。考虑了不同的反应条件,包括氧化时间、反应温度、O_2浓度的影响。实验结果表明,氧化产物呈三维岛状生长,反应初期产物岛较小但密度较大,随着反应的进行,产物岛不断长大,但密度先减小后增加;温度及O_2浓度对产物层生长均有影响。产物岛的成核与生长改变了产物层的表观形貌,减小了表观反应速率。     

In-situ EXAFS study on the thermal decomposition of TiH_2

Thermal decomposition behaviors of TiH_2 powder under a flowing helium atmosphere and in a low vacuum condition have been studied using an in situ EXAFS technique.By an EXAFS analysis containing the multiple scattering paths including H atoms,the changes of the hydrogen stoichiometric ratio and the phase transformation sequence are obtained.The results demonstrate that the initial decomposition temperature is dependent on experimental conditions,which occurs,respectively,at about 300 and 400℃ in a low vacuum condition and under a flowing helium atmosphere.During the decomposition process of TiH_2 in a low vacuum condition,the sample experiences a phase change process:δ(TiH_2)→δ(TiH_x)→δ(TiH_1)+β(TiH_x)→δ(TiH_x)+β(TiH_x)+α(Ti)→β(TiH_x)+α(Ti)→α(Ti)+β(Ti).This study offers a way to detect the structural information of hydrogen.A detailed discussion about the decomposition process of TiH_2 is given in this paper.     

厚二氧化硅光波导薄膜制备及其特性分析

以硅烷和氧化二氮作为反应气体，采用等离子体增强化学气相沉积(PECVD)技术，不使用掺杂，在单晶硅衬底上制备了用于平面光波导的二氧化硅薄膜。研究了薄膜折射率和淀积速率与工艺参量之间的关系，通过棱镜耦合仪、傅里叶变换红外光谱、原子力显微镜等测试手段，分析了薄膜的结构和光学特性。结果表明，实验能快速生长厚二氧化硅薄膜，薄膜表面平整，颗粒度均匀，同时薄膜具有折射率精确可控和红外透射性能好的特点，非常适合制作光波导器件。     

Light induced microstructure transformation in a-Si：H films

A series of a-Si:H films are deposited by hot wire assisted microwave electron cyclotron resonant chemical vapour deposition (HW-MWECR-CVD), subsequently exposed under simulated illumination for three hours. This paper studies the microstructure change during illumination by Fourier Transformation Infrared (FTIR) spectra. There are two typical transformation tendencies of microstructure after illumination. It proposes a model of light induced structural change based on the experimental results. It is found that all samples follow the same mechanism during illumination, and intrinsic structure of samples affect the total H content.     

色谱—原子光谱应用于环境中痕量金属有机物的分析

不同形态的元素其生物效应差别很大，决定它们在环境中的行为和归宿。金属有机化合物分析属金属形态分析。这类化合物的分离多用色谱法。但色谱所用的检测器如电子捕获检测器、火焰离子化检测器和紫外可见光度计对金属的选择性较差，而原子光谱由于对金属有较好的选择性，用作色谱的检测器可以避免在测定过程中的许多干扰。本报告简要介绍色谱和原子光谱的各种联用方法及其在环境分析中的应用。     

A Method for Quantitative Analysis of Chemical Mixtures with THz Time Domain Spectroscopy

A method for analysing chemical mixtures quantitatively with terahertz time domain spectroscopy is proposed. The experimental results demonstrate the feasibility of this technique. Transmission coefficient of THz wave at the sample surface is taken into account to improve the analytic precision, lsomer mixtures are chosen as the experimental samples. Compared to similar techniques, the analytic precision could be improved evidently in this method.