Influence of sampling on three-dimensional surface shape measurement

In order to accurately measure an object’s three-dimensional surface shape,the influence of sampling on it was studied.First,on the basis of deriving spectra expressions through the Fourier transform,the generation of CCD pixels was analyzed,and its expression was given.Then,based on the discrete expression of deformation fringes obtained after sampling,its Fourier spectrum expression was derived,resulting in an infinitely repeated"spectra island"in the frequency domain.Finally,on the basis of using a low-pass filter to remove high-order harmonic components and retaining only one fundamental frequency component,the inverse Fourier transform was used to reconstruct the signal strength.A method of reducing the sampling interval,i.e.,reducing the number of sampling points per fringe,was proposed to increase the ratio between the sampling frequency and the fundamental frequency of the grating.This was done to reconstruct the object’s surface shape more accurately under the condition of m>4.The basic principle was verified through simulation and experiment.In the simulation,the sampling intervals were 8 pixels,4 pixels,2 pixels,and 1 pixel,the maximum absolute error values obtained in the last three situations were 88.80%,38.38%,and 31.50%in the first situation,respectively,and the corresponding average absolute error values are 71.84%,43.27%,and 32.26%.It is demonstrated that the smaller the sampling interval,the better the recovery effect.Taking the same four sampling intervals in the experiment as in the simulation can also lead to the same conclusions.The simulated and experimental results show that reducing the sampling interval can improve the accuracy of object surface shape measurement and achieve better reconstruction results.

Research of Three-Dimensional Fluorescence Spectra of RE^(3+)(RE=Eu,Tb) and Na_2WO_4 Co-doped Silica Luminescence Materials

In the preparation of this precursor tetraethlortho silicate (TEOS), sodium tungstate, ethyl alcohol, HCl and RECl3(RE=Eu,Tb) were mixed and then heated at 800 ℃ for 2 h, leading to a luminescent compound. The structure of the materials was characterized by TG-DTA and IR analysis, and the results indicate that the materials were in SiO2 network structure. Three-dimensional fluorescence spectra was used to characterize the luminescent properties of the materials. The luminescence property of doped and un-doped Eu3+or Tb3+ and Na2WO4 in silica materials were prepared and measured. The results show that good energy transfer from WO2-4 to Eu3+ ion, sensitized the luminescence intensity of Eu3+ remarkably. Tb3+ ion incorporated silica materials expressed the inverse energy transition from Tb3+ to WO2-4, however, we got the materials with homogeneous green blue fluorescent light. Finally, the energy transfer of WO2-4 and Eu3+, WO2-4 and Tb3+ were explained by energy levels diagram.

Three-dimensional fluorescence spectral characterization of soil dissolved organic matters in the fluctuating water-level zone of Kai County,Three Gorges Reservoir

Three-dimensional fluorescence spectroscopy was used to investigate the fluorescent properties of soil dissolved organic matter(DOM)in the water-levelfluctuation zone(WLFZ)of Kai County,Three Gorges Reservoir(TGR).Most of the soil DOM analyzed in this study was found to contain four fluorescence peaks.Peaks A and C represent humic-like fluorescence,whereas peaks B and D represent tryptophan-like fluorescence.Peaks E and F,which represent tyrosine-like fluorescence,only appeared in certain soils.Soil humus was the main source of DOM in soil,and higher concentration of soil DOM was found in the exposed soil than submerged soil.Compared to the peaks A and B,the fluorescence intensities of peaks C and D were strongly influenced by the fluctuating water level.Analysis of fluorescence intensities of different peaks in soil DOM showed that WLFZ soil was not contaminated significantly.Soil DOM contained at least two types of humic-like fluorescence groups and two types of protein-like fluorescence groups.The proportion of the content of peak A in soil organic matter was quite stable.The soil DOM in exposed soil had relatively high humification and aromaticity,and periodic submerging and exposure of soil had an impact on the humification of soil DOM.

荧光光谱法研究钙试剂羧酸钠与牛血清白蛋白结合反应特征

不同温度下,研究了钙试剂羧酸钠与牛血清白蛋白作用的荧光猝灭光谱、同步荧光光谱、三维荧光光谱和紫外可见吸收光谱特征;分别用SternVolmer方程和LineweaverBurk双倒数方程等处理实验数据,得到了26℃时反应的结合常数为7.664×104mol/L,结合位点数为1.522,结合反应的标准焓变、标准熵变和标准吉布斯自由能变分别为-58.36kJ/mol,-101.7J/K和-27.958kJ/mol;分析所得光谱,证实了在实验浓度和温度范围内,CCS与BSA反应可形成具有一定结构的复合物,获得了CCS对BSA构型的影响等重要信息。

三种偶氮化合物的荧光光谱研究

The fluorenscence spectra of the three azo compounds have been tested.Geometric configurations of three azo compounds have been optimized by semiempirical method of quantum chemistry.Their fluorenscence spectra have also been calculated by RHF/CIS.The results of calculation are essentially consistent with experimental values.

Event patterns extracted from top quark-related spectra in proton-proton collisions at 8 TeV

We analyze the transverse momentum （PT） and rapidity （y） spectra of top quark pairs, hadronic top quarks, and top quarks produced in proton-proton （pp） collisions at center-of-mass energy √s=8 TeV. For PT spectra, we use the superposition of the inverse power-law suggested by the QCD （quantum chromodynamics） calculus and the Erlang distribution resulting from a multisource thermal model. For y spectra, we use the two-component Gaussian function resulting from the revised Landau hydrodynamic model. The modelling results are in agreement with the experimental data measured at the detector level, in the fiducial phase-space, and in the full phase-space by the ATLAS Collaboration at the Large Hadron Collider （LHC）. Based on the parameter values extracted from PT and y spectra, the event patterns in three-dimensional velocity （βx-βy-βz）, momentum （px-py-pz）, and rapidity （y1-y2-y） spaces are obtained, and the probability distributions of these components are also obtained. Keywords： top quark-related spectra, event pattern, three-dimensional space

Event patterns from negative pion spectra in proton-proton and nucleus-nucleus collisions at SPS

Rapidity-dependent transverse momentum spectra of negatively charged pions measured at different rapidities in proton-proton collisions at the Super Proton Synchrotron （SPS） at various energies within its Beam Energy Scan （BES） program are investigated by using one- and two-component standard distributions where the chemical potential and spin property of particles are implemented. The rapidity spectra are described by a double- Gaussian distribution. At the stage of kinetic freeze-out, the event patterns are structured by the scatter plots in the three-dimensional subspaces of velocity, momentum and rapidity. The results of the studies of the rapidityindependent transverse mass spectra measured at mid-rapidity in proton-proton collisions are compared with those based on the similar transverse mass spectra measured in the most central beryllium-beryllium, argon-scandium and lead-lead collisions from the SPS at its BES energies.

Crystal structures and thermal decomposition mechanism of four lanthanide complexes with halogen-benzoic acid and 1,10-phenanthroline

This paper describes syntheses and structure determination of four lanthanide complexes [Nd(2-Cl-4-FBA) 3 phen] 2 (1, 2-Cl-4-FBA = 2-chloro-4-fluorobenzoate, phen = 1,10-phenanthroline), [Ln(2,5-DClBA) 3 phen] 2 (Ln = Sm(2) and Tb(3), 2,5-DClBA = 2,5-dichlorobenzoate) and [Sm(2-Cl-4,5-DFBA) 3 (phen)(H 2 O)] 2 (4, (2-Cl-4,5-DFBA = 2-chloro-4,5-difluorobenzo- ate). The complexes were characterized by elemental analysis, infrared and ultraviolet spectra, and X-ray single-crystal diffraction. In the molecular structures of 1 4, two Ln 3+ ions are linked by four carboxyl groups, with two of them in a bridging bidentate mode and the other two in a bridging-chelating tridentate mode, forming four binuclear molecules. In addition, each Ln 3+ ion is also chelated to one phen molecule and one carboxyl group in the complexes, except each Sm 3+ ion in 4 which is bonded to one carboxyl group by unidentate mode and one H 2 O molecule. There are two different coordination polyhedrons for each Nd 3+ ion in the two similar molecular structures of 1 and they are a distorted monocapped square antiprismatic and a distorted tricapped triangular prism conformation, respectively. The coordination polyhedron for each Ln 3+ ion in 2 4 is a nine-coordinated distorted mono-capped square antiprismatic conformation. The complex 3 exhibits green luminescence under the radiation of UV light. The thermal decomposition behaviors of the complexes have been discussed by simultaneous TG/DSC-FTIR technique. The 3D surface graphs for the FTIR spectra of the evolved gases were recorded and the gaseous products were identified by the typical IR spectra obtained at different temperatures from the 3D surface graphs. Meanwhile, we discussed the nonisothermal kinetics of 1 4 by the integral isoconversional non-linear (NL-INT) method.