Characteristic wavelength selection of volatile organic compounds infrared spectra based on improved interval partial least squares

As important components of air pollutant,volatile organic compounds(VOCs)can cause great harm to environment and human body.The concentration change of VOCs should be focused on in real-time environment monitoring system.In order to solve the problem of wavelength redundancy in full spectrum partial least squares(PLS)modeling for VOCs concentration analysis,a new method based on improved interval PLS(iPLS)integrated with Monte-Carlo sampling,called iPLS-MC method,was proposed to select optimal characteristic wavelengths of VOCs spectra.This method uses iPLS modeling to preselect the characteristic wavebands of the spectra and generates random wavelength combinations from the selected wavebands by Monte-Carlo sampling.The wavelength combination with the best prediction result in regression model is selected as the characteristic wavelengths of the spectrum.Different wavelength selection methods were built,respectively,on Fourier transform infrared(FTIR)spectra of ethylene and ethanol gas at different concentrations obtained in the laboratory.When the interval number of iPLS model is set to 30 and the Monte-Carlo sampling runs 1000 times,the characteristic wavelengths selected by iPLS-MC method can reduce from 8916 to 10,which occupies only 0.22%of the full spectrum wavelengths.While the RMSECV and correlation coefficient(Rc)for ethylene are 0.2977 and 0.9999 ppm,and those for ethanol gas are 0.2977 ppm and 0.9999.The experimental results show that the iPLS-MC method can select the optimal characteristic wavelengths of VOCs FTIR spectra stably and effectively,and the prediction performance of the regression model can be significantly improved and simplified by using characteristic wavelengths.

Infrared Spectra of La_(0.65)Ba_xMnO_(3-δ) Oxides

The infrared spectra of La_(0.65)Ba_xMnO_(3-|?￡(c) (x = 0.35, 0.33 and 0.30) were investigated experimentally. The result shows that the sample La_(0.65)Ba_xMnO_(3-|?￡(c) has the largest Curie temperature and the smallest resistivity and wave number of the stretching vibration mode of MnO_6 octaheUron at 300 K among the investigated samples. However, the absorption strength for the stretching vibration mode of Mn0_6 octahedron in La_(0.65)Ba_xMnO_(3-|?￡(c) is stronger for parainagnetic phase than that for ferromagnelic phase, which may be connected with the reducing of the dynamic in- coherent Jahn-Teller distortion below Curie temperature. In addition, the large shift of wave number for the stretching mode at the temperatures from 293 to 423 K has been observed in La_(0.65)Ba_xMnO_(3-|?￡(c), which may be due to the in- crease of the Mn-O bond length with temperature increasing.

Syntheses and Infrared Spectra of Rare Earth Complexes with Diethyl Phosphate

The title complexes Ln(DEP),(Ln=La,Sm,Eu,Ho and Yb)were synthesized by reaction of triethyl phosphate with trivalent rare earth chlorides.The mechanism of thermo-decomposition of the complexes has been studied.According to their IR spectra,the residues of the thermo-decomposition of the complexes were identified as Ln(PO_3)_3.Their IR spectra were measured and principal IR bands were assigned.The experimental results of the IR spectra of the complexes show that the title complexes have the same coordination form and mo- lecular configuration as rare earth,e.g.Sm,complex with dimethyl phosphate(Sm(DMP)_3).Each of the rare earth ion links three rare earth ions nearby through double“O-P-O”bridges to form a special network of rings-linking-rings,each of which consists of twenty-four atoms.The Ln-O bond is principally ionic.

Identification of Complex Ions of Nb(V)in FLINAK-O^(2-)System by Infrared Spectra

The FT-IR spectra for K_2NbF_7-FLINAK-O^(2-) solution were measured and compared with the spectra of crystalline K_2NbF_7 and K_2NbOF_6.The results show that the niobium fluoro-complex and/or oxyfluoro-complex ions are presented in these solutions.NbF_7^(2-) complex ion is the predominant species in Nb(V)-FLINAK solution(not considering oxide impurity).The influence of O^(2-) on the oxyfluoro-complex ions shows that NbOF_6^(3-) as a stable monooxyfluoro-complex anion presented in FLINAK-O^(2-) systems and the number of NbOF_6^(3-) species are increased with increasing of O^(2-) when molar ratio of O^(2-)/Nb(V) is less than 1.

Alcohols＇ Classification by Infrared Spectra Segment Based on Support Vector Machines

This paper studies various classifiers to identify primary, secondary or tertiary alcohols by using segmental spectra and their combinations to support vector machines （SVMs）. The results showed that the O-H in-plane bending absorption contributed most to identification their substitute. This conclusion disagrees with related known research results.

Application of Embedded Zerotree Wavelet to the Compression of Infrared Spectra

In this paper the embedded zerotree wavelet (EZW) method and Huffman coding are proposed to compress infrared (IR) spectra. We found that this technique is much better than others in terms of efficiently coding wavelet coefficients because the zerotree quantization is an effective way of exploiting the self-similarities of wavelet coefficients at various resolutions.

Ab Initio Calculation of Structure and Raman and Infrared Spectra of Trifluoromethylthiosulphenyl Chloride

The molecular model of Trifluoromethylthiosulphenyl Chloride,CF_(3)SSCl,was presented.Ab initio method was used to calculate the structure and Raman and Infrared spectra.The results show that CF_(3)SSCl possess stereoscopic structure of C_(1)symmetry with a torsional angle of 94.2°.The potential energy distribution and isotope replacement methods were applied to determine the vibrational assignment.The vibrational frequencies and corresponding modes of the molecule were obtained.The calculated vibrational frequencies are in good agreement with experiments.

Isotopic Shifts of the infrared Spectra of Cholic Acid and Sodium Cholate

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The Splittings of p_± States in Infrared Spectra of Thermal Donors in Silicon

p -type CZ silicon crystals annealed at 450℃ have been investigated by low temperature infrared spectroscopy with high resolusion. It has been shown that the 2p± and 3p± bands of neutral thermal donors TD~° are all split into two bands, which have not been reported before. In addition, the concentrations ofindi- vidual TD_i and total TD have been derived from the heights of 2po bands, and the boron concentrations de- rived from that of 320 cm^(-1) band. The room temperature resistivities of samples have been evaluated and the comparison with practically measured resistivities have been made.

Study on Membrane Microstructures and Characteristics of Infrared Spectra and Nitrogen Release of Solid-Liquid Reaction Coated Urea

The membrane microstructures and the mechanism of two coated ureas formed through solid- liquid reaction were observed by scanning electron microscope and infrared spectra, the relation of the structural characteristics with the nitrogen release feature was also discussed by combining with nitrogen dissolution in water. The results showed that the membranes were made of solid particles tightly connected to each other and were piled up layer by layer through liquid glue. Porosity and aperture of membrane were determined by compactness of piled layers and the particles in a single layer and also related to the characteristics of coating materials. Research of the infrared spectra of membrane, made of a solid powder and a liquid glue, proved that O-H on the solid surface was bonded with the double bond of the liquid glue, thus forming membrane and keeping it stable. It was found that the two coated ureas showed obvious differences in nitrogen releasing due to their membrane structures, the porosity and aperture of membrane were the critical factors for nitrogen releasing.

Substructure Prediction from Infrared Spectra by Using Support Vector Machines

The potential of support vector machines （SVMs） for the substructure elucidation of infrared spectra have been investigated. The trained SVMs can identify the 16 substructures with high accuracy.

Raman and infrared spectra of complex low energy tetrahedral carbon allotropes from first-principles calculations

Up to now,at least 806 carbon allotropes have been proposed theoretically.Three interesting carbon allotropes(named Pbam-32,P6/mmm,and I43d)were recently uncovered based on a random sampling strategy combined with space group and graph theory.The calculation results show that they are superhard and remarkably stable compared with previously proposed metastable phases.This indicates that they are likely to be synthesized in experiment.We use the factor group analysis method to analyze theirΓ-point vibrational modes.Owing to their large number of atoms in primitive unit cells(32 atoms in Pbam-32,36 atoms in P6/mmm,and 94 atoms in I43d),they have many Raman-and infrared-active modes.There are 48 Raman-active modes and 37 infrared-active modes in Pbam-32,24 Raman-active modes and 14 infrared-active modes in P6/mmm,and 34 Raman-active modes and 35 Raman-and infrared-active modes in I43d.Their calculated Raman spectra can be divided into middle frequency range from 600 cm-1 to 1150 cm-1 and high frequency range above 1150 cm-1.Their largest infrared intensities are 0.82,0.77,and 0.70(D/Å)2/amu for Pbam,P6/mmm,and I43d,respectively.Our calculated results provide an insight into the lattice vibrational spectra of these sp3 carbon allotropes and suggest that the middle frequency Raman shift and infrared spectrum may play a key role in identifying newly proposed carbon allotropes.

Solvent effects on infrared spectra of 2—Methyl—4,5—dimethoxy—3—oxo—2H—Pyridizine：Part 2.Binary Solvent SYstems

This research on the solvent effects of 2 methyl 4,5 dimethoxy 3 oxo 2H pyridizine (MDOP) in binary solvent systems on the infrared spectra for MDOP in n hexane/CHCl 3 mixture solvents showed that there were three forms of carbonyl stretching vibration band [ υ (C=O)] of MPOP as the mole fraction of CHCl 3 in the binary solvents changes. In pure n hexane solvent, the υ (C=O) of MDOP appeared at a relatively high wavenumber. With CHCl 3 added, the υ (C=O) shifted to lower wavenumbers. Two new bands were observed over a certain range of mixture solvent compositions. The origin of the bands was discussed in the terms of two kinds of hydrogen bond together with their individual dependence on mixture composition. Comparisons were drawn for the solvent sensitivities of υ (C=O) for propanone.

Infrared Low-Resolution Spectra of HAEBE Stars

IRAS low-resolution spectra are presented for 36 HAEBE stars. It is found that silicate dust in amorphous or glassy form is common material in the circumstellar disks or/and shells of HAEBE stars. It is also found that the PAH feature is often appeared as well.

Ab initio potential energy surface and anharmonic vibration spectrum of NF_(3)^(+)

Potential energy surfaces(PESs), vibrational frequencies, and infrared spectra are calculated for NF_(3)^(+) using ab initio calculations, based on UCCSD(T)/cc-p VTZ combined with vibrational configuration interaction(VCI). Based on an iterative algorithm, the surfaces(SURF) program adds automatic points to the lattice representation of the potential function, the one-dimensional and two-dimensional PESs are calculated after reaching a convergence threshold, finally the smooth image of the potential energy surface is fitted. The PESs accurately account for the interaction between the different modes, with the mode q_(6) symmetrical stretching vibrations having the greatest effect on the potential energy change of the whole system throughout the potential energy surface shift. The anharmonic frequencies are obtained when the VCI matrix is diagonalized. Fundamental frequencies, overtones, and combination bands of NF_(3)^(+) are calculated, which generate the degenerate phenomenon between their frequencies. Finally, the calculated anharmonic frequency is used to plot the infrared spectra.Modal antisymmetric stretching ν_(5) and symmetric stretching ν_(6) exhibit a phenomenon of large-intensity borrowing. This study can provide data to support the characterization in the laboratory.

A New Expert System for Structural Interpretation of IR Spectra

A new expert system has been developed which can be used to aid chemists in structural interpretation of infrared spectra. The system consists of five essential portions: knowledge-base , inference engine, database, knowledge-acquisition module and explanatory interface. The system is implemented in Turbo PROLOG artificial intelligence language. Compared with other spectral interpretation systems this system is of the following advantages, i. e. the system has a friendly user interface, two kinds of methods for managing toowledge-base, several useful explanatory facilities such as why and how should explanation be made, etc. ; in addition, it can be run on the IBM PC/XT and its compatible microcomputers. Another important feature of the system is that it can simulate the reasoning procedure by which experienced chemists may interpret spectra as well as deduce complete molecular structures. So the system can also be used as a helpful learning tool for training chemistry students in IR spectrum interpretation and organic structure elucidation.

FOURIER TRANSFORM INFRARED STUDIES OF POLY (ETHYLENE TEREPHTHALATE) FILM IN THE GLASS TRANSITION REGION

Three specimens from a solution-cast poly (ethylene terephthalate) (PET) film, one being liquid-N_2 quenched from 92℃(Q), one being slowly cooled from 92℃(SC) and one being quenched and sub-T_g annealed at 67℃(AN), have been studied by specimen difference spectra Q-SC and AN-Q and temperature difference spectra T-70 and T_2-T_1 for every 2℃ steps on heating to 90℃ at 2℃ /min. SC and AN showed more gauche conformers than Q. That means that the PET chain has more trans conformers at higher temperatures and some of these are frozen during quenching through T_g. A band at 1340 cm^(-1) has been found to be complex containing overlapping bands reflecting trans in crystalline regions and trans in amorphous regions. The temperature difference spectra on heating through T_g showed that the spectral changes in Q are gradual while a rather abrupt change occurs in AN at 80—82℃ for the bands at 1340, 1042 and 1020 cm^(-1). No new conformational structure or new vibrational mode is involved. A kind of locking mechanism is suggested which hinders the molecular vibrational changes in AN below T_g until a sudden release occurs at T_g. These locking sites can be nothing else than sites of tighter local packing of chain segments. Consequently it is believed that inter-chain van der Waals attraction energy plays a dominating role in the volume relaxation and sub-T_g annealing of quenched amorphous polymers.

Spectral distortion of dual-comb spectrometry due to repetition rate fluctuation

Dual-comb spectrometry suffers the fluctuations of parameters in combs. We demonstrate that the repetition rate is more important than any other parameter, since the fluctuation of the repetition rate leads to a change of difference in the repetition rate between both combs, consequently causing the conversion factor variation and spectral frequency misalignment. The measured frequency noise power spectral density of the repetition rate exhibits an integrated residual frequency modulation of 1.4 Hz from 1 Hz to 100 kHz in our system. This value corresponds to the absorption peak fluctuation within a root mean square value of 0.19 cm-1 that is verified by both simulation and experimental result. Further, we can also simulate spectrum degradation as the fluctuation varies. After modifying misaligned sPectra and averaging, the measured result agrees well with the simulated spectrum based on the GEISA database.

Density functional study on chirospectra of hydrogen-bonded systems X^-(H_2O)_3(X=F,Cl,Br,I)

This paper calculates the molecular structures, infrared, Raman, circular dichroism spectra and optical rotatory powers of some hydrogen-bonded supramolecular systems as a cyclic water trimer, （H2O）3 and its pyramidal halide complexes, X- （H2O）3 （X= F, Cl, Br, I） with the gradient-corrected density functional theory method at the B3LYP/6- 311＋＋G（2d,2p） and B3LYP/Aug-cc-pVTZ levels. It finds that the complexation of halide anions with the water trimer can efficiently modulate the chirally optical behaviors. The calculated vibrational circular dichroism spectrum illuminates that the vibrational rotational strength of S（＋） （H2O）3 mostly originates from the O-H rocking modes, whereas chirality of S（-）-X-（H2O）3 （X = F, Cl, Br, I） has its important origin in the O-H stretching modes. The calculated optical rotatory power demonstrates that S（＋） （H2O）3 and S（＋）-F-（H2O）3 are positively chiral, whereas S（-）-X-（H2O）3 （X=Cl, Br, I） are negatively chiral. With the polarizable continuum model, calculated bulk solvent effect in the solvents water and carbontetrachloride and argon shows that the positive chirality of S（＋）-（H2O）3 is enhanced and the negative chirality of S（-）-X-（H2O）3 （X=Cl, Br, I） and the positive chirality of S（＋）-F-（H2O）3 are reduced with an augmentation of the solvent dielectric constant.

INFRARED SPECTROSCOPIC CHARACTERIZATION OF CONFORMATIONAL DEFECTS OF POLYBENZAMIDE

Theoretical results of normal coordinate analysis of polybenzamide performed with two conformational isomerized models, the cis trans and the all-trans conformation, have been adopted to examine a number of infrared spectra of films of the polymer treated in a subsequent annealing process and a cooling process. It shows, in this investigation, that two sets of infrared spectral profiles around 1400 cm^(-1) and 900 cm^(-1) behave quite attractively. Their spectral behaviours have been correlated to the conformational defect variation in samples, and reasonably predicted by the normal coordinate calculation.