近红外光谱定性分析中的特征波长筛选研究

提出了一种以样品光谱类间相关系数之和最小为准则进行光谱波长逐步筛选的方法(stepwise selection basing on minimum sum of correlation coefficients, SMCC),以类间距离与类内距离和的比值最大化(符合分析者主观预期目标)作为定性分析中特征波长筛选效果的评价依据,并使用红塔集团提供的2012年17种不同类型工业分级烟叶作为试验样品,以验证筛选方法的有效性。研究表明,采用CO1分级烟叶光谱作为参照类别,筛选出10个特征波长点：采用特征波长计算得到的类内欧氏距离的平均值为采用全部波长计算得到的平均值的1.69倍,采用特征波长计算得到的类间欧氏距离的平均值为采用全部波长计算得到的平均值的3.70倍,采用特征波长计算得到的类间欧氏距离与类内欧氏距离和的比值的平均值为采用全部波长计算得到的平均值的2.21倍。特征波长的类间与类内欧氏距离和的比值增大,说明筛选出来的特征波长能更加有效的表达不同类间的远近关系以及同一类内的离散度,SMCC算法是一种有效的、可应用于近红外光谱定性分析中的特征波长筛选方法。     

All electron ab initio investigations of the electronic states of the FeC molecule

The low-lying electronic states of the molecule FeC have been investigated by performing all electron ab initio multi-configuration self-consistent-field (CASSCF) and multi reference configuration interaction (MRCI) calculations. The relativistic corrections for the one-electron Darwin contact term and the relativistic mass-velocity correction have been determined in perturbation calculations. The electronic structure of the FeC molecule is interpreted as antiferromagnetic couplings of the localized angular momenta of the ions and resulting in a triple bond in the valence bond sense. The electronic ground state is confirmed as being . The spectroscopic constants for the ground state and eleven excited states have been derived from the results of the MRCI calculations. The spectroscopic constants for the ground state have been determined as and ,and for the low-lying state as and . The values for the ground state agree well with the available experimental data. The FeC molecule is polar with charge transfer from Fe to C. The dipole moment has been determined as in the ground state and as 1.51 D in the state. From the results of the MRCI calculations the dissociation energy, , is determined as 2.79 eV, and D₀ as 2.74 eV. Received: 2 October 1998 / Received in final form: 30 March 1999     

Ultrasound fields in attenuating media

For medical ultrasonic imaging and for nondestructive testing, the attenuation of pressure waves and the resulting shift in wave velocity are important features in commonly used transmission media such as biological tissue. An algorithm for the numerical evaluation of pressure field distributions generated by ultrasonic transducers is presented. The attenuation and dispersion of the sound transmission medium are taken into consideration. The sound fields are computed numerically for continuous wave as well as pulse excitation. The transducer has plane or gently curved geometry and is embedded in a plane rigid baffle. The numerically determined pressure fields are presented as 3D plots, as gray-scale images for a fixed time stamp (like a snapshot), or as isobars regarding the maximum values over time for each local point in the area under investigation. The algorithm described here can be utilized as a tool for design of ultrasound transducers, especially array antennas.     

Preparation and Spectral Characterization of Fluorescence Probes Based on 4-N,N-Dimethylamino Benzoic Acid and Sterically Hindered Amines

The adducts of simple chromophore 4-N,N-dimethylamino benzoic acid with 2,2,6,6-tetrametyl-4-hydroxy- or 4-amino-piperidine were examined as fluorescence probes (spin double sensors) to monitor radical processes. The links in the adducts were either an ester or amide group, and the sterically hindered amines were in the form of -NH, -NO? and -NOR. The spectral properties of the three related derivatives (esters or amides) were quite similar. The maxima of the absorption spectra were in the range of 295-315?nm, and the maximum of fluorescence was located in the range of 330-360?nm, depending on the polarity of the solvent. In polar solvents, a red-shifted fluorescence band at 460-475?nm was observed. The fluorescence of these derivatives was rather weak as compared to anthracene under the same conditions. The Stokes shift was large, as high as 6,000?cm(-1), indicating the formation of a twisted intra-molecular charge transfer (TICT) state. No large differences in Stokes shifts were observed in polymer matrices of poly(methyl methacrylate), polystyrene and poly(vinyl chloride). The extent of intramolecular quenching was expressed as Φ(NX)/Φ(NO) (X?=?H, NOR) and was in the range of 1-3 in solution and as high as 8 in polymer matrices. The low efficiency of intramolecular quenching limits the application of these new adducts as fluorescence probes for the monitoring of radical processes in solution but favors their application in polymer matrices.     

Volatile Phthalocyanines: Vapor Pressure and Thermodynamics

The current review summarizes the data of saturated vapor pressure and thermodynamic parameters of the sublimation process of different phthalocyanines as reported in the literature as well as in our work. The volatility of phthalocyanines is analyzed from the standpoint of their molecular and crystal structure. The differences in the saturated vapor pressure value of the investigated phthalocyanines may reach some orders of magnitude and are determined by the Van der Waals and electrostatic interaction of the peripheral atoms of adjacent molecules, as well as to a specific interaction, the type and number of which depend on the type of molecules packing in the crystal.     

Hypergeometric solution of the Stark-ladder effect in crystals

The motion of electrons in a crystal subjected to a linear electric field is studied by means of the molecular orbital method. The field perturbation of the resonance integrals, as well as the Coulomb ones, results in the Schroedinger equation being expressed as a hypergeometric difference equation, whose solution gives rise to the well-known Stark-ladder picture of the tilted energy band. It is found that the part played by the resonance integral perturbation is just as important as that of the Coulomb integral perturbation and, therefore, cannot be neglected as in earlier investigations.     

Nanoparticle decoration with surfactants: Molecular interactions,assembly, and applications

Nanostructures of diverse chemical nature are used as biomarkers, therapeutics, catalysts, and structural reinforcements. The decoration with surfactants has a long history and is essential to introduce specific functions. The definition of surfactants in this review is very broad, following its lexical meaning “surface active agents”, and therefore includes traditional alkyl modifiers, biological ligands, polymers, and other surface active molecules. The review systematically covers covalent and non-covalent interactions of such surfactants with various types of nanomaterials, including metals, oxides, layered materials, and polymers as well as their applications. The major themes are (i) molecular recognition and noncovalent assembly mechanisms of surfactants on the nanoparticle and nanocrystal surfaces, (ii) covalent grafting techniques and multi-step surface modification, (iii) dispersion properties and surface reactions, (iv) the use of surfactants to influence crystal growth, as well as (v) the incorporation of biorecognition and other material-targeting functionality. For the diverse materials classes, similarities and differences in surfactant assembly, function, as well as materials performance in specific applications are described in a comparative way. Major factors that lead to differentiation are the surface energy, surface chemistry and pH sensitivity, as well as the degree of surface regularity and defects in the nanoparticle cores and in the surfactant shell. The review covers a broad range of surface modifications and applications in biological recognition and therapeutics, sensors, nanomaterials for catalysis, energy conversion and storage, the dispersion properties of nanoparticles in structural composites and cement, as well as purification systems and classical detergents. Design principles for surfactants to optimize the performance of specific nanostructures are discussed. The review concludes with challenges and opportunities.     

The use of positive muons in metal physics

The present status of work in metal physics by the new method of “muon spin rotation” is reviewed. This spectroscopy is based on the spin interactions of positive or negative muons and resembles NMR as far as the interpretation of interactions in metals is concerned. The positive muon behaves in several respects as a light isotope of hydrogen in metals. Local properties like site symmetry, local magnetic field, dynamic effects from surrounding spins as well as effects from the diffusion of the particle itself can be measured with high sensitivity.A brief review of the technical aspects is given. The problems of diffusion of light positive particles in metals are discussed, with regard to specific mechanisms at low temperatures, trapping of muons by impurities, etc. The local electronic structure around this kind of impurity in normal metals as well as ferromagnets has been subject to a large nnumber of studies. Other applications include the interaction of muons with other kinds of defects, the study of metal hydrides and measurements on the dynamics of spin glasses.     

A systematic approach to the Hartree-Fock problem in the thermodynamic limit

A systematic procedure is proposed in order to look for non-plane-wave solutions to the Hartree-Fock equations in the thermodynamic limit. The corresponding Hartree-Fock states are seen to arise as the self-consistent eigenvectors of a special matrix, as in Roothaan's method. The attractive delta problem is tackled as an example. The corresponding solution fulfills the monotonicity requirement for the energy as a function of the density, which no other known solution to the problem verifies, and coincides, in the zero-density limit, with the lower bound of Lieb and de Llano.     

Exact results for the one dimensional asymmetric exclusion model

The asymmetric exclusion model describes a system of particles hopping in a preferred direction with hard core repulsion. These particles can be thought of as charged particles in a field, as steps of an interface, as cars in a queue. Several exact results concerning the steady state of this system have been obtained recently. The solution consists of representing the weights of the configurations in the steady state as products of non-commuting matrices.     

On the momentum correlations in the fragmentation of <Superscript>197</Superscript>Au + <Superscript>197</Superscript>Au reactions

We aim to present the formation of fragments using static as well as momentum-dependent interactions and larger nucleonic cross-sections. We shall also examine, in detail, the role of momentum correlations in these situations which are close to the fire-ball as well as to the spectator matter decay. The role of momentum correlations will be studied by imposing an additional cut in the momentum space. A clear need of a momentum cut is demonstrated in both fire-ball as well as spectator matter physics. The momentum-dependent interactions and larger cross-sections play a drastic role in peripheral reactions, whereas the role of momentum cut remains the same in these situations.     

Characterization of Synthetic-Coal Char Particles using fractal dimension analysis

The development and change of surface ruggedness in chars was studied at conditions typical in a pulverized coal furnace. The fractal dimension, a measure of surface ruggedness, of chars was measured using physisorption techniques. By adjusting the temperature encountered (1173 to 1773 K) and residence time (0.1 to 1.5 s) of the synthetic coal (sized to 46–106 μm diameter), chars at different stages of combustion were prepared in a laminar flow (drop-tube) furnace. The particles were quickly cooled and quenched in an inert atmosphere. The samples were examined using a scanning electron microprobe, and their fractal dimensions were determined using gas physisorption. The adsorption data were used to test if the char surface was fractal on a molecular scale, to determine the fractal dimension, and to quantify changes in the fractal dimension during combustion. The fractal dimension of the unburned synthetic coal was approximately 2. The fractal dimension increased as high as 2.85 as the carbon matrix burned away and exposed mineral moieties. However, as combustion continued the carbon burned completely away leaving a mineral fly ash particle with a fractal dimension as low as 2.47.     

Decreasing electrical resistivity of silver along the melting boundary up to 5 GPa

The electrical resistivity of Ag was experimentally measured at high pressures up to 5?GPa and at temperatures up to ～300?K above melting. The resistivity decreased as a function of pressure and increased as a function of temperature as expected and is in very good agreement with 1 atm data. Observed melting temperatures at high pressures also agree well with previous experimental and theoretical studies. The main finding of this study is that resistivity of Ag decreases along the pressure- and temperature-dependent melting boundary, in conflict with prediction of resistivity invariance. This result is discussed in terms of the dominant contribution of the increasing energy separation between the Fermi level and 4d-band as a function of pressure. Calculated from the resistivity using the Wiedemann–Franz law, the electronic thermal conductivity increased as a function of pressure and decreased as a function of temperature as expected. The decrease in the high pressure thermal conductivity in the liquid phase as a function of temperature contrasts with the behavior of the 1 atm data.     

Fluorescence Properties of Selected Benzo[c]phenanthridines

The fluorescence properties of selected benzo[c]phenanthridines (BPs) were examined. The effect of structure, pH and solvent on the fluorescence properties has been investigated. It was found out that the presence of charged iminium nitrogen significantly decreased the fluorescence of the compounds. The fluorescence (intensity as well as emission spectra shape) of the investigated compounds was significantly dependent on pH as well as used solvent. The utilization in epigenetic modification mechanisms studies as demethylase probe and as possible pH indicator was suggested.     

Jerk系统耦合的分岔和混沌行为

通过分析耦合的Jerk系统的平衡点及其稳定性,给出了参数空间中不同的分岔集,进而将参数空间划分为对应于各种动力学行为的不同区域.探讨了耦合系统随不同参数变化的动力学演化过程,重点分析了系统耦合强度变化对其动力学行为的影响.揭示了多种运动模式共存及倍周期分岔等各种非线性现象的产生机理.     

New structural picture of the Ge2Sb2Te5 phase-change alloy

Using electron microscopy and diffraction techniques, as well as first-principles calculations, we demonstrate that as much as 35% of the total Ge atoms in the cubic phase of Ge2Sb2Te5 locate in tetrahedral environments. The Ge-vacancy interactions play a crucial stabilizing role, leading to Ge-vacancy pairs and the sharing of vacancies that clusters tetrahedral Ge into domains. The Ge2Sb2Te5 structure with coexisting octahedral and tetrahedral Ge produces optical and structural properties in good agreement with experimental data and explains the property contrast as well as the rapid transformation in this phase-change alloy.     

Characterization of carbonate rocks through X-ray microfluorescence and X-ray computed microtomography

Carbonate rocks play an important role in petroleum geology by acting as reservoir rocks, generators, and even hydrocarbon sealants, accounting for about half of the oil and gas reserves known in the world. The study of these carbonate rocks have become very important in the hydrocarbon exploration scene in Brazil because of they consist in analogous for reservoir rocks of the presalt interval. Thus, the objective of this research was to use X-ray microfluorescence (micro-XRF) and X-ray microtomography analysis, as complementary techniques, in order to characterize samples of carbonate rocks in respect to their structures, textures, mineralogy, and pores. The microtomographic analyses allowed the identification of the horizontal structures as parallel lamination, horizontal, and vertical fractures filled by calcite and biotic constituents (gastropods bioclasts). Different composition of minerals were also identified, as calcite, quartz, feldspars, iron sulfides, and oxides. The porosity (ranges <1 to17%), and the high-density elements could also be quantified, as well as their distribution in each sample. The micro-XRF analysis present a direct relationship with the distribution of minerals that compound carbonate rocks, highlighting some structures, as well as helping to identify trace and minor elements in the carbonates (Mn, Sr, and Mg).     

On operating deflection shapes of the violin body including in-plane motions

Earlier investigations have assumed only "out-of-plane" vibrations of the plates of the violin. The violin body can, however, be described as a thin-walled, double-arched shell structure and as such it may very well elongate in one direction as it contracts in another. Therefore, at least two orthogonal vibration components have to be included to describe the vibrations. The operating deflection shapes (ODSs) of a good, professionally made and carefully selected violin were therefore measured in several directions by TV holography to determine both "in-plane" and out-of-plane vibration components of the ODSs. The observations were limited to the frequency range 400-600 Hz, as this interval includes two most-prominent resonance peaks of bridge mobility and sound radiation as well as a third poorly radiating resonance. These three peaks clearly showed orthogonal vibration components in the ODSs. The vibration behavior of the violin body, sectioned in the bridge plane, was interpreted as the vibrations of an "elliptical tube" with nodal diameters. The number of nodal diameters increases from two to three in the selected frequency range. The TV holography measurements were supported by electrodynamical point measurements of bridge mobility, of air volume resonances, and by reciprocity, of radiation properties. Furthermore, a fourth mode, the air mode, A1, is involved indirectly in the sound radiation via influence on the body vibrations.     

Interfacial density of states in magnetic tunnel junctions

Large zero-bias resistance anomalies as well as a collapse of magnetoresistance were observed in Co/Al2O3/Co magnetic tunnel junctions with thin Cr interfacial layers. The tunnel magnetoresistance decays exponentially with nominal Cr interlayer thickness with a length scale of approximately 1 A more than twice as fast as for Cu interlayers. The strong suppression of magnetoresistance, as well as the zero-bias anomalies, can be understood by considering a strong spin-dependent modification of the density of states at Co/Cr interfaces. The role of the interfacial density of states is shown by the use of specially engineered structures. Similar effects are predicted and observed in junctions with Ru interfacial layers.