高能激光能量计溯源问题研究北大核心

由于高能激光能量计标定过程中没有标准的能量测量装置和标准的激光源,无法采用常规方法对其进行标校。提出了一种利用现有小能量计从低到高逐级多次传递不确定度的方法,以及一种利用能量等效原理对激光能量计进行标校的方法。不确定度传递法方法简单,但环节较多导致不确定度较大。等效标定法包括电标法和光标法,电标法对设计要求较高,但求解过程相对简单。光标法工程实现难度要低得多,但必须事先对灯组余热及热损失进行测算。等效法的三个条件与误差大小关系紧密,在结构设计中必须严格考虑,它是提高测量准确性的根本,其次要尽量减少不确定度传递的中间环节,最后需要对误差项进行科学分析和测定,在此基础上对这些项进行相应的修正和补偿。     

挠性陀螺捷联系统场地快速标定

本文给出了捷联式惯性导航系统一种简单实用的场地标定方法。在系统中，对挠性陀螺仪采用特殊安装，把组合件旋转１８０°，用两位置数据测出陀螺的标度系数、常值漂移、加速度计零位和系统真方位。在标定过程中不需要对惯性组合件做水平调整。     

Nanometer Calibration Particles: What is Available and What is Needed?

Information on available polystyrene calibration spheres is presented regarding the particle diameter, uncertainty in the size, and the width of the size distribution for particles in a size range between 20 and 100nm. The use of differential mobility analysis for measuring the single primary calibration standard in this size range, 100nm NIST Standard Reference Material®1963, is described along with the key factors in the uncertainty assessment. The issues of differences between international standards and traceability to the NIST Standard are presented. The lack of suitable polystyrene spheres in the 20–40nm size range will be discussed in terms of measurement uncertainty and width of the size distributions. Results on characterizing a new class of molecular particles known as dendrimers will be described and the possibilities of using these as size calibration standards for the size range from 3 to 15nm will be discussed.     

一种近红外探测器的光谱响应率测量

对近红外辐射功率光谱绝对响应率的定标技术进行了研究。设计了一种制冷扩展波长型的InGaAs探测器，为了使其能够作为功率传递的标准探测器工作在（1.2～2.5）μm波长范围，对探测器的光谱响应率进行了测量。首先在1260nm波长下进行绝对功率传递的标定试验，然后用基于红外单色仪的光谱比较系统（SCF）测量了探测器的相对光谱响应率。结合2个步骤的数据，最终可以得到探测器的绝对光谱响应率。     

北京谱仪Ⅲ飞行时间计数器系统刻度中的关联分析

利用电子对事例对北京谱仪Ⅲ飞行时间的测量误差, 以及不同测量之间的关联因子随击中位置的变化进行了仔细的研究. 加权的飞行时间由不同的测量值及其相关的误差矩阵计算而得. 蒙特卡罗研究表明. 为北京谱仪Ⅲ开发的关联分析算法 可以正确地处理包含公有误差项的多个实验测量结果的合并, 并且能够为粒子鉴别提供可靠的飞行时间信息.     

摄像机标定技术在活塞视觉检测与分选中的应用研究

在机器人视觉检测及自动化分捡中,准确地校正摄像机镜头畸变对获取物体精确图像及确定物体准确位置具有重要意义。采用了带有径向畸变的小孔摄像机模型及基于线段斜率的标定方法。在标定过程中,应用线性算法求解出了镜头的径向畸变系数。实验表明,采用的标定方法简捷有效,其标定结果能够满足研究需要。     

Homography of central points for optical distortion compensation

The paper presents a novel radial lens distortion modelling method for vision systems. It is based on single images of chessboard planar pattern, in which calibration points (corners of chessboard squares) are localised. The points, which are situated near the image centre, where the distortion is negligible, are used to determine undistorted grid of calibration points by the estimation of homographic matrix. The differences in the localisation of undistorted and distorted points are used to find parameters of radial model by the linear least square method. Having the distortion model, the dense compensation is performed with support of bilinear interpolation and a sparse compensation by Newton iterative scheme providing subpixel accuracy.     

低能量阈高纯锗探测器用于暗物质探测实验研究

一个位于韩国江原道襄阳郡地下实验室的暗物质WIMP探测实验中, 采用了低能量阈高纯锗探测器, 带有碘化铯晶体反符合探测器作为主动屏蔽体. 整个系统设置和能量标定已经完成, 并且已经积累了约155d的本底数据. 还应用外置伽玛源和中子源进行了实验, 以判断本底的来源. 介绍了数据的分析和初步结果, 并给出了实验诱人的前景.     

Every Continuous Operator Has an Invariant Measure

We prove the existence of an invariant measure for a large class of random processes with discrete time without assuming their linearity. Our main examples are “processes with variable length”, in which components may appear and disappear in the course of functioning. One of these examples displays non-uniqueness of invariant measure in a 1-D process.     

Multivariate standard addition method solved by net analyte signal calculation and rank annihilation factor analysis

This article describes the use of the net analyte signal (NAS) concept and rank annihilation factor analysis (RAFA) for building two different multivariate standard addition models called “SANAS” and “SARAF.” In the former, by the definition of a new subspace, the NAS vector of the analyte of interest in an unknown sample as well as the NAS vectors of samples spiked with various amounts of the standard solutions are calculated and then their Euclidean norms are plotted against the concentration of added standard. In this way, a simple linear standard addition graph similar to that in univariate calibration is obtained, from which the concentration of the analyte in the unknown sample and the analytical figures of merit are readily calculated. In the SARAF method, the concentration of the analyte in the unknown sample is varied iteratively until the contribution of the analyte in the response data matrix is completely annihilated. The proposed methods were evaluated by analyzing simulated absorbance data as well as by the analysis of two indicators in synthetic matrices as experimental data. The resultant predicted concentrations of unknown samples showed that the SANAS and SARAF methods both produced accurate results with relative errors of prediction lower than 5% in most cases.