基于国产仪器研究钨丝原子吸收光谱

用标准的150 W幻灯灯泡的钨丝作原子化加热材料,设计制作了一种新颖的、结构简单的钨丝电热原子化器,同时还设计了该原子化器的电源电路和信号的数据采集电路.该原子化器能的最高原子化温度可达3100 K左右;编写了硬件的控制软件和信号处理的应用软件.用该原子化器将实验室一台火焰原子吸收光谱仪改装成钨丝原子吸收光谱仪,并以铜元素标准溶液和PerkinElmer公司多元素标准溶液对仪器性能作了研究.仪器对铜的检出限为0.0133 μg/mL,线性范围为0.10～4.0 μg/mL;对1.0 μg/mL的铜标准溶液测试的相对标准偏差为RSD=4.1%(测试次数n=10),每次分析所需样品量20 μL.     

在分光计实验中的几何关系探究

从空间几何的角度来对分光计的构造、结构以及调节方法等方面来加以说明，以便从根本上掌握分光计设计的原理、调节的思路以及拓展的方法。     

SOA-based loop mirror for tunable pulse-width generation

We propose and experimentally demonstrate a system for the generation of pulses of tunable pulse-width as those required in high spectral efficiency optically routed networks. Pulse narrowing of 500 ps pulses by 90% is accomplished through a SOA based non-linear loop mirror. Optical switching through the SOA loop mirror is used to shape and carve these large pulses (e.g., 500 ps) generated by non-expensive low-frequency optoelectronic components to narrow pulses (e.g., 50 ps). We also calculate the minimum loop size and optimum repetition rate of the original pulse train for the generation of the shorter pulse-width pulse train.     

Improvements on the third generation of electron momentum spectrometer

The significant modifications to our recently constructed electron momentum spectrometer have been implemented. Compared with our previous report, the energy and the angle resolutions are significantly improved and reach △E = 0.45 eV, △θ = ±0.53° and △φ = ±0.84°, respectively. Moreover, the details of data reduction and the relation between azimuthal angle range and the sensitivity are discussed.     

Personal neutron dosimetry in the space station MIR and the Space Shuttle

A passive neutron dosemeter based on nuclear track detectors and TLD's was used in 1995 and 1997 on the MIR station and in Space Shuttle flights to MIR. As it is equipped with neutron converters and shieldings of different types the track detector system allows the neutron dose equivalent to be determined in rough energy intervals. The results of the measurements on the MIR station and in the Space Shuttle flights are presented and the influence of charged particles in the complex mixed radiation field in space is discussed. Improvements are possible by means of a new active neutron dosemeter which is under development at the PTB. First measurements with a prototype in the high-energy reference fields at CERN are presented and discussed.     

Field sweep broadline NMR spectroscopy

A novel NMR spectrometer is described that is uniquely versatile in its ability to accurately record broad lines by sweeping the superconducting magnetic field and to perform standard high resolution solid state NMR experiments. Broadline observation is illustrated by ²⁷Al spectra from static samples. Such an instrument opens up many nuclei for serious study by NMR in the solid state for the first time.     

Determination of line strengths for selected transitions in the v2 band relative to the v1 and v5 bands of H2CO

The spectral line strengths in the v₂ band of H₂CO (segments spanning 1720-) have been determined relative to two sets of spectral line groups in the v₁ and v₅ band, using tunable diode laser spectroscopy. Simultaneous detection using a dual-diode instrument with a absorption cell was employed to assure identical H₂CO column density for the two spectral regions. The results in the selected regions of this study are in good agreement with the line positions and the relative intensities specified in an unpublished complete line listing for the v₂ band prepared by Linda Brown (see full text for reference). Based upon measurements of individual groups of spectral lines in the P, Q and R branches, the absolute band strength has been determined to be .     

Modeling, measuring, and minimizing the instrument response function of a tunable diode laser spectrometer

The instrument response function (IRF) of a spectrometer limits the accuracy of measured spectroscopic parameters by broadening recorded spectral lines/features. We describe methods to model the effects of the IRF on spectral data, to minimize the IRF widths, and to measure the resulting width of the spectrometer IRF. We have modeled the IRF of our Tunable Diode Laser Spectrometer as a Voigt function. A real-time method of eliminating the effects of low-frequency spectrometer drift has been implemented and has resulted in a substantial reduction in the width of the IRF, its residual Gaussian component reduced from about to about . An accurate measurement of the IRF Gaussian width utilizes a computationally simple method making use of the spectral dependence of the RMS noise of each signal-averaged data point. Various noise sources affecting the spectrometer (preamp/detector noise, laser AM noise, and laser FM noise) are identified and separately quantified by use of the same method. The IRF Gaussian-width measurement can be automatically applied to each measured spectrum of an experimental data set. A related method is discussed which allows accurate determination of the spectral dependence of statistical noise appropriate for use in quantitative Chi-square fitting of absorption spectra. We explore simple, efficient numerical processes which can dramatically enhance the quality and usefulness of acquired spectral data, improving the ability to apply TDL spectroscopy to high-precision, quantitative measurements and the determination of detailed spectroscopic lineshape parameters. This paper provides a guide for interested readers to implement these developments in their own spectrometers.     

Determination of molecular parameters for 1,3-butadiene and propylene using infrared tunable diode laser absorption spectroscopy

A technique has been developed for the determination of molecular parameters, including infrared absorption line positions, strengths, and nitrogen-broadened half-widths for 1,3-butadiene (C(4)H(6)) and propylene (C(3)H(6)). The parameters for these two molecules are required for quantitation using Tunable Diode Laser Absorption Spectroscopy (TDLAS). These molecules have populations of highly overlapping infrared absorption lines in their room temperature spectra. The technique reported here provides a procedure for estimating the molecular parameters for these overlapping absorption lines from quantitative reference spectra taken with the TDLAS instrument at different pressures and concentrations. The system was developed for the quantitation of gaseous constituents in a single puff of cigarette smoke and this paper will describe the procedure and some of the factors that influence the accuracy of quantitation for 1,3-butadiene, including the approach taken to minimize the adverse effects of the absorption due to propylene in the same spectral region.