Vision system for three-dimensional position measurement based on stereo disparity

A stereo disparity-based range finding technique was developed for measuring three-dimensional coordinates of object points. It used an image-matching algorithm which functionally consisted of scene reduction, epipolar line selection, and features matching. Experiments implementing this technique were performed on an industrial vision system. An error analysis indicated that image resolution was the major source of measurement inaccuracy.     

Fission-track dating of Macusanite glasses with plateau and size correction methods

Two Macusanite pebbles (MB1 and MB2) were dated with the fission-track method. Six irradiations were carried out in different nuclear reactors: Pavia (Italy), IPEN-CNEN (Brazil) and IPEN-Lima (Peru). Measurements of the thorium and uranium induced-fission per target nucleus using natural thorium thin films and natural U-doped glasses calibrated against natural uranium thin films, together with a λ_F of 8.46×10⁻¹⁷ a⁻¹ were used to determine the ages. The apparent ages were corrected using the plateau and size correction methods. Track measurements were performed by different analysts, using different counting criteria. In addition, tracks were measured on samples which had been submitted to thermal treatment as well as on samples which had not been heated. Thermal treatments were carried out to erase the fossil tracks before neutron irradiation. No significant differences have been found in individual results, using the two Macusanite pebbles and the different nuclear reactors, age correction techniques, analysts, track-counting criteria, and thermal treatments before neutron irradiation. The great majority of the results (14/17) is compatible with the Ar–Ar ages of 5.12±0.11 and 5.10±0.11 Ma, Macusanite MB1 and MB2, respectively. However, the fission-track ages are systematically less (8%) than the Ar–Ar ages of the two Macusanite samples studied.     

电视摄象机测量误差探讨

本文简述了用电视摄象机进行工业尺寸测量的微分法与拟合法的基本原理,同时详细的讨论了各自所能达到的精度极限。本文用实验验证了理论计算的结果,最后对二维工件测量时,如何根据工件的不同形状与位置以及光学系统的特点,提出了在测量时工件的放置应该注意的问题以及对工件拐角处如何进行处理的方法。     

怀柔EAS阵列的Monte Carlo研究

用GENAS程序包为怀柔阵列产生了36万Monte Carlo模拟EAS事例,用它们研究了怀柔阵列的性能,确定了最佳的事例判造条件,对实验数据进行了正确性检验,得到了怀柔EAS Size(即簇射在观测面的总荷电粒子数)与初级宇宙线能量之间的转换关系.这项研究表明,怀柔阵列的EAS心位和方向测定精度分别好于3m和2.5°;EASSize测定误差典型值约8%;近垂直簇射的Size(N)与初能(E)的关系为E≈10^10.64N^0.84.     

基于超声波测量技术的颗粒尺寸分布模型的研究

提出了一种利用单颗粒背向散射信号来进行粒径分布估算的超声波测量技术,系统阐述了其 理论基础及基本工作原理。被测颗粒的散射信号幅度与它在探测区中的位置、颗粒尺寸和形状有关。 通过理论分析,建立了一个可用于描述散射信号幅度概率分布与颗粒系尺寸分布之间关系的数学模 型,对该模型的反演计算便可得到颗粒系的尺寸分布信息。为了避免求解过程中的病态系数矩阵问 题,将模型求解转化成了易于解决的最优化问题。仿真实例结果验证了该技术的可行性。     

Sizes of water-soluble luminescent quantum dots measured by fluorescence correlation spectroscopy

In this paper, fluorescence correlation spectroscopy (FCS) was applied to measure the size of water-soluble quantum dots (QDs). The measurements were performed on a home-built FCS system based on the Stokes-Einstein equation. The obtained results showed that for bare CdTe QDs the sizes from FCS were larger than the ones from transmission electron microscopy (TEM). The brightness of QDs was also evaluated using FCS technique. It was found that the stability of the surface chemistry of QDs would be significantly improved by capping it with hard-core shell. Our data demonstrated that FCS is a simple, fast, and effective method for characterizing the fluorescent quantum dots, and is especially suitable for determining the fluorescent nanoparticles less than 10 nm in water solution.     

Size exclusion chromatography with dual-beam refractive index gradient detection of polystyrene samples

Non-aqueous size exclusion chromatography (SEC) of polystyrenes (as model analytes) is examined using the microscale molar mass sensor (μ-MMS) for detection. The μ-MMS is combined with SEC to demonstrate this simultaneously universal and molar mass selective detection method for polymer characterization. The μ-MMS is based on measuring the refractive index gradient (RIG) at two positions (upstream and downstream) within a T-shaped microfluidic channel. The RIG is produced from a sample stream (eluting analytes in the mobile phase) merging with a mobile phase stream (mobile phase only). The magnitude of the RIG is measured as a probe beam deflection angle and is related to analyte diffusion coefficient, the time allowed for analyte diffusion from the sample stream toward the mobile phase stream, and the bulk phase analyte refractive index difference relative to the mobile phase. Thus, two deflection angles are measured simultaneously, the upstream angle and the downstream angle. An angle ratio is calculated by dividing the downstream angle by the upstream angle. The μ-MMS was found to extend the useful molar mass calibration range of the SEC system (nominally limited by the total exclusion and total permeation regions from ∼100,000 g/mol to ∼800 g/mol), to a range of 3,114,000-162 g/mol. The injected concentration LOD (based on 3 s statistics) was 2 ppm for the upstream detection position. The point-by-point time-dependent ratio, termed a ‘ratiogram’, is demonstrated for resolved and overlapped peaks. Within detector band broadening produces some anomalies in the ratiogram shapes, but with highly overlapped distributions of peaks this problem is diminished. Ratiogram plots are converted to molar mass as a function of time, demonstrating the utility of SEC/μ-MMS to examine a complex polymer mixture.     

The role of variable surface charge and surface complexation in the adsorption of humic acid on magnetite

The ionic strength dependence of humic acid (HA) adsorption on magnetite (Fe₃O₄) was investigated at pH 5, 8 and 9, where variable charged magnetite is positive, neutral and negative, respectively. The adsorption studies revealed that HA has high affinity to magnetite surface especially at lower pH, where interacting partners have opposite charges. However, in spite of electrostatic repulsion at pH 9 notable amounts of humate are adsorbed. Increasing ionic strength enhances HA adsorption at each pH due to charge screening. The dominant interaction is probably a ligand-exchange reaction, nevertheless the Coulombic contribution to the organic matter accumulation on oxide surface is also significant under acidic condition. The results from size exclusion chromatography demonstrate that the smaller size HA fractions enriched with functional groups are adsorbed preferentially on the surface of magnetite at pH 8 in dilute NaCl solution.     

Study of archaeological ceramics by total-reflection X-ray fluorescence spectrometry: Semi-quantitative approach

Total-reflection X-ray fluorescence spectrometry has been compared with Instrumental Neutron Activation Analysis in order to test its potential application to the study of archaeological ceramics in the archaeometric field. Two direct solid non-chemical sample preparation procedures have been checked: solid sedimentation and solid chemical homogenization. For sedimentation procedure, total-reflection X-ray fluorescence allows the analysis of the elemental composition with respect to the size fraction but not the average evaluation of the composition. For solid chemical homogenization procedure, total-reflection X-ray fluorescence provides precise (from 0.8% to 27% of coefficient of variation) and accurate results (from 91% to 110% of recovery) for 15 elements (Cr, Hf, Ni, Rb, Al, Ba, Ca, K, Mn, Ti, V, Cu, Ga, Y and Fe) with an easy sample preparation process of the solid clay and without previous chemical treatment. The influence of the particle sizes has been checked by total-reflection X-ray fluorescence sample angle scans and anomalous behaviors have been found for three additional detected elements: As, Sr and Zn, which can be attributed to interference effects of the mineral grain sizes of their associated chemical phases in the total-reflection X-ray fluorescence interference region. The solid chemical homogenization procedure produces data useful for archaeological interpretation, which is briefly illustrated by a case-study. Finally, the decantation procedure data can be also useful for size chemical speciation and, consequently, for alternative environmental total-reflection X-ray fluorescence applications.