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It can’t satisfy the requirement of correction for response non-uniformity at systematic levelif only if the array detector for spatial heterodyne spectrometer is corrected. Traditional methods, such as irradiation with uniform source and column-flat-fielding, are not suitable for spatial heterodyne spectrometer. The article expounds convection arm-blocking method for spatial heterodyne spectrometer briefly at first. This method leads to kinds of mismatches including pixel and sub-pixel level shift and rotation in a single arm data after gluing gratings. The effect of registration accuracy of flatfielding coefficients has been analyzed for the experimental breadboard. The result shows that the registration accuracy of flatfielding coefficients needs to be better than 0.1 pixel for the breadboard. The shift at pixel level is calculated by solving the rotational degree by using logarithm-polar coordinate and phase correlation method for the requirement of registration. The shift at sub-pixel level is estimated with DFT based on matrix multiplication. The flow path of flatfielding method at systematic level is concluded. The integral condition of interferometer after actual gluing is modulated by adjusting the positions of gratings slightly. The flatfielding flow path is applied to the data acquired from the modulated interferometer after gluing. Then, the result is compared with the spectrum after the correction with totally matched signal arm data. The final result shows that the spectral deviation is 0.6% between the two spectra compared with the spectral deviation of 4.1% without correction. The accuracy of recovered spectrum after correction has been improved markedly. This can be the foundation for the follow data processing.

Spatial heterodyne Raman spectroscopy (SHRS) is a new type of Raman spectroscopic detection technique with characteristics of high optical throughout, high spectral resolution, and no moving parts. SHRS is very suitable for the planetary exploration missions, which can be used to the analysis of minerals and find the biomarkers maybe exist on the surface of planetary. The authors have applied the technique to the standoff Raman spectroscopic detection, analyzed the main characteristics, including spectral resolution, bandpass and signal to noise (SNR), of standoff SHRS and proved it through experiments. The basic theory of standoff SHRS has been described briefly while a breadboard has been designed, built and calibrated. On the basis, the Raman spectra of some inorganic solids, organic liquids and some natural minerals have been achieved at a distance of 10 m, the SNR of the breadboard has been estimated. Due to the poor adjustment and the defects of the optical elements, the breadboard is far away from an ideal system. But the results show that the SNR is better than 5 for most of the main Raman peaks of the samples, which can meet the basic requirement of clear positive detection of typical Raman peaks and the feasibility of standoff SHRS has been proved. SHRS can overcome the main defects of dispersive grating Raman spectrometers and Fourier transform Raman spectrometers and it has a great application prospect on the detection and analysis of the planetary surface. The work of the authors can prove the potentiality of SHRS on standoff detection and can provide reference for the engineering realization of standoff SHRS.

The interaction between 20(S)-protopanaxatriol (PPT) and bovine serum albumin ( BSA) was studied with fluorescence quenching technique and ultra-violet absorption spectroscopy. The results indicated that PPT led to the intrinsic fluorescence quenching of BSA through a static quenching process .The binding constants of PPT with BSA obtained with fluorescence quenching method were calculated as 0.926 3×10(3) (298 K), 0.618 2×10(3) (308 K), 0.414 4×10(3) L·mol(-1)(318 K), respectively; while the number binding sites n were close to unity. The results showed that the driving force of the interaction between PPT and BSA was hydrogen bond and Van der Waals force. The result of synchronous fluorescence spectra showed that binding of PPT with BSA could induce conformational changes in BSA, that the part of tryptophan became more closely. According to Föster fluorescence resonance energy transfer theory, the binding distance r and energy-transfer efficiency E were respectively 26.2 nm and 0.32.

The Visible absorption and Raman spectra of β-carotene were measured in dimethyl sulfoxide in temperature ranging from 81 to 25 ℃ and in carbon disulfide in pressure range from 0.04 to 0.60 GPa, respectively. The results indicated that the visible absorption and Raman spectra are both red-shifted, Raman scattering cross section increase with the temperature decreasing. And with the pressure increasing, the visible absorption spectra are red-shifted, but the frequency shift towards higher frequencies in the Raman spectra, the Raman scattering cross section decrease unexpectedly. The latter can’t be explained by the model of “effective conjugation length” and “coherent weakly damped electron-lattice vibrations”. In this paper, we combined electron-vibration coupling rule with theoretical calculations and found that the electron-phonon coupling constant had a certain changing trend with the temperature and pressure variation, which Indicate that the interaction between π-electron and CC bond vibration was essential for this experiment result. Thus, the turning effect of energy gap of the π on CC vibration mode is responsible for such phenomenon.

By using doppler asymmetric spatial heterodyne spectroscopy and doppler effect, the wind speed can be achieved through detecting the interferogram of airglow in the upper atmosphere. This paper mainly analyses the data processing method of the interferogram and then derive the interferometer phase in order to get the wind speed. Comparing with the traditional spatial heterodyne spectroscopy, not only the noise and error of the system should be taken into consideration, but the window function that used to isolate the spectrum has a great influence during the data processing. Then the effect of window type and window width on phase difference of interferogram and the wind error curve are simulated through software. On basis of this the wind error curve under the noise of system and flat field factor are simulated by choosing appropriate window function. The window function simulation indicates that although the joining of window leads to a distortion of the interferogam and phase, the wind speed error can be less than 0.5% with Hanning window in the appropriate optical path difference. The noise of the system simulation indicates that the wind speed error increases with the noise, so it is necessary to control the system noise and preprocess the sampling data. The research on data processing method has great theoretical significance and practical value for designing the system parameter and improving the precision of spatial heterodyne wind detection.

Restrictive relationship exists between spectral resolution, spectral range and number of pixels of traditional Spatial Heterodyne Spectroscopy (SHS). The main difference between Asymmetric Spatial Heterodyne Spectroscopy (ASHS) and SHS accelerates the space of one grating from the beamsplitter. It greatly increases spectral resolution while system parameters remain unchanged. First of all, this paper elaborates the fundamentals of the ASHS, the derived formulas of the system parameters and theoretical relationship between grating offset and the spectral resolution increases. As an important parameter of the ASHS, offset is restricted by the pixel number of short double side interferogram and the spectral resolution requirements. According to the experimental breadboard parameters of laboratory, the selection principle and the results of the offset are presented. In the case of the same device parameters, two types of theoretical performance parameters are calculated. The simulation is carried out. The results show that two of them have the same spectral range, but the ASHS has a higher spectral resolution. The relationship between resolution and offset increased consistent with theoretical calculation. Finally the ASHS breadboard is calibrated with the monochromatic light scanning method. The derived spectral range and resolution are in good agreement with the theoretical value.

The detection of hyper-spectral atmosphere CO2 needs remote sensor to be characterized and calibrated precisely while spectral calibration is the most basic work. The high uncertainty of wavelength calibration coefficient is a big problem as to the traditional laboratory calibration methods. In order to solve this problem, the research of error correction of spectral calibration based on gas absorption principle is carried out. The method is in accordance with the using conditions of instrument and it improves the practicability of the calibration coefficient. First, theoretical spectrum and error components are simulated by using radiative transfer. Then, the experiment of atmosphere CO2 absorption spectrum measurement is performed based on the atmosphere environmental simulation calibration house. Last, spectral error is corrected and optimized with LM algorithm. The result of spectral calibration of error correction shows that the mean value of spectral error deviation decreases from 0.03 cm-1 before correction to 0.008 cm-1 after correction, and systematic and mutable errors are removed. The spectral calibration precision on the ground is improved significantly, which lays the foundation for the subsequent greenhouse gas retrieval.

All-trans-β-carotene has important functions of light collection and light protection, and it is also an important electrooptical material. The Raman spectra of polyenes are a result of the modulation effect of the π electron energy gap on the vibration of CC bonds, which associate with the external field. So it has higher theoretical significance and practical value to study the molecular structure and properties change under the external field. Ultraviolet-visible absorption spectra and resonant Raman spectra of all-trans-β-carotene in cyclohexanol were measured from 341 to 275 K. The liquid-solid phase transition of the sample appears at 295 K. The characteristic energy describes the conformational change of all-trans-β-carotene molecule. After the solution phase transition, the characteristic energy ε of all-trans-β-carotene molecule becomes bigger. And when temperature decreasing, the rate of change of the Huang-Rhys, the wavelength of UV absorption peak, electron-phonon Parameter, RSCSs of the CC bond increase. the Huang-Rhys in solid phase is an order of magnitude higher then liquid phase. The characteristic energy of liquid is 0.206 7 eV. The characteristic energy of liquid is 0.559 6 eV. The increasing of the characteristic energy ε makes the rate of increasing of the effectively conjugated length becomes bigger. The decreasing of the π electric energy gap quickens. The function of moderation from electron energy gap to all-trans-β-carotene molecule enhances. Electron-phonon Parameter increases. RSCSs of the CC bond substantially increases.

Beta-carotene is an important kind of polyene biomolecules, which has significant applications on researching optoelectronic and functional materials. In-situ high pressure Raman spectra of beta-carotene are measured in CS2 solution and water respectively at pressure range from 0-0.60 GPa. Then we compared both of them the Raman shift and CC bond of the full width at half maximum (FWHM) of the Raman spectra. It is therefore concluded that both of the samples' Raman shift moved to the high wave number and the full width at half maximum increased depending of the pressure. The experiment phenomena were interpreted by the theory of "coherent weakly damped electronic-lattice vibration model" and "effective conjugation length model". The mechanism is that the beta-carotene is compressed and has the lower structure order, shorte the effective conjugation length, decreased Raman active, weaker the coherent weakly damping CC bond vibration in high pressure. Because of the CC bond length become short, so the Raman spectra are found to blueshift. The CC bond of the full width at half maximum (FWHM) of the Raman spectra increased is attributed to the increase of difference in C--C and C==C bond lengths. Moreover, due to dissolving in non-polar CS2 solvent, the beta-carotene encounters the interaction of the surrounding solvent molecules. So the dispersion force interaction between solute and solvent is more sensitive to pressure. Then it makes that the slop of Raman shift and the full width at half maximum in the CS2 solution are faster than dissolved in water with increasing pressure. This paper provides an application value for research on molecular structure change under the external field and the presence form of polyenes biomolecules in the solvent.

The spectral response of spatial heterodyne spectroscopy (SHS) is determined by the spectrum property of narrow-band filter. As discussed in previous studies, the symmetric heterodyned interferogram of high frequency waves modulated by SHS and lack of sample lead to spectral confusion, which is associated with the true and ghost spectra. Because of the deviation from theoretical index of narrow-band filter in the process of coating, the boarded spectral response and middle wave shift are presented, and conditions in the theoretical Littrow wavelength made the effective wavelength range of SHS reduced. According to the measured curve of filter, a new wavenumber of zero spatial frequency can be reset by tunable laser, and it is easy for SHS to improve the spectral aliasing distortion. The results show that it is utilized to the maximum extent of the effective bandwidth by adjusting the grating angle of rotation to change the Littrow wavelength of the basic frequency, and the spectral region increased to 14.9 nm from original 12.9 nm.

Fermi resonance is a phenomenon of molecular vibrational coupling and energy transfer occurred between different groups of a single molecule or neighboring molecules. Many properties of Fermi resonance under different external fields, the investigation method of Raman spectroscopy as well as the application of Fermi resonance, etc need to be developed and extended further. In this article the research results and development about Fermi resonance obtained by Raman spectral technique were introduced systematically according to our work and the results by other researchers. Especially, the results of the behaviors of intramolecular and intermolecular Fermi resonance of some molecules under some external fields such as molecular field, pressure field and temperature field, etc were investigated and demonstrated in detail according to the Raman spectra obtained by high pressure DAC technique, temperature variation technique as well as the methods we planed originally in our group such as solution concentration variation method and LCOF resonance Raman spectroscopic technique, and some novel properties of Fermi resonance were found firstly. Concretely, (1) Under molecular field. a. The Raman spectra of C5H5 N in CH3 OH and H2O indicates that solvent effect can influence Fermi resonance distinctly; b. The phenomena of the asymmetric movement of the Fermi resonance doublets as well as the fundamental involved is tuned by the Fermi resonance which had not been found by other methods were found firstly by our variation solution concentration method; c. The Fermi resonance properties can be influenced distinctly by the molecular group reorganization induced by the hydrogen bond and anti-hydrogen bond in solution; d. Fermi resonance can occurred between C7 H8 and m-C8H10, and the Fermi resonance properties behave quite differently with the solution concentration; (2) Under pressure field. a. The spectral lines shift towards high wavenumber with increasing pressure, and frequency difference Δ varies with pressure, which induced the change of W; b. The W of νi + ν4 ν3 of CCl4 in C6H6 decreased more quickly in solution than in pure liquid with increasing pressure and the Fermi resonance disappeared ahead of that in pure liquid, which indicates that the phenomenon of Fermi resonance induced by pressure effect can reveal the mechanism of some solvent effects. (3) Under temperature field. a. The Fermi resonance properties of different molecules behave quite differently with temperature. For an instance, the one of CO2 can be influenced distinctly by temperature, while the one of CS2 behaves no change with temperature. This article offers systematic theoretical and experimental support to the investigation of identification and assignment of molecular spectral line, the confirmation of molecular conformation and conformers, the effect of hydrogen bond on molecular structure and properties, etc.

To study the thermal effort on optical properties of spatial heterodyne spectroscopy (SHS), the relation between the change in temperature and the degradation of optical properties was analyzed, including collimator lens, imaging lens and interferometer unit. The theoretical model was verified and corrected by simulation and thermal-optical test, which was established to describe the relation between spectral-line shift and groove density change of gratings. The results show that spectrum measurements are not affected by small temperature changes in the instrument since the primary effects. are a slight defocus of the focal plane array in collimating lens and re-imaging lens under the temperature from 15 to 25 °C. Spectral-line shift obtained by the thermal optical analysis is well coincident with the ones calculated by thermal optical experiment because of the temperature chan- ges of interferometer unit. The Littrow wavelength accuracy is better than 2.3 nm unless the temperature change is less than 2.5 °C under the interferometer unit by use of the material BK7.

The present paper summarizes the characteristics of resonance Raman spectra of the linear polymer molecule, and its relations with the molecular structure, including: electronic spectra(ultraviolet-visible absorption spectrum), Raman spectra characteristics and its relations with external field; Modulation relation between the electron energy gap and CC atom vibration; Several experimental results were obtained: The UV-visible absorption spectra are red-shifted with decreasing temperature, increasing solvent density and reducing solution concentration, and because the linear polymer molecule has high structured order, decreasing pi electron energy gap; extended pi electronic delocalization, large effective conjugation length, large intensity of the Raman activity, Ramrnan spectrum are red-shifted, with large scattering cross section. "Am plitude modes" are the ideal theory models to study the linear polymer molecule.

The present paper cited that R Tubino and other people introduced a kind of electron-phonon coupling constants with dimension, which can establish the relation with the Huang-Rhys factor and calculate the electron-phonon coupling constants of every C-C bond vibration mode. There are many reports about the visible absorption and Raman spectra of all-trans-beta-carotene with pressure. But the study about the Raman scattering cross section and the Huang-Rhys factor with pressure have not been reported now. Visible absorption and Raman spectra of all-trans-beta-carotene were measured in carbon disulfide in the pressure range from 0. 04 to 0. 60 GPa. The results indicated that the visible absorption spectra of beta-carotene in nonpolar solvent carbon disulfide are red-shifted with pressure increasing, but the frequency shifts towards higher frequencies in the Raman spectra, the Raman scattering cross section decreases, Huang-Rhys factor increases, and the electron-phonon coupling constants of CC bond vibration modes increase. The mechanism is that all-trans-beta-carotene caused by compression and a decrease in the structurally ordered properties of the molecules leads to narrow energy gap of the pi, shortens effective conjugation length, hinders delocalization of pi-electron, decreases the Raman scattering cross section, and increases the Huang-Rhys factor and the electron-phonon coupling constants.

In the present paper, DMSO/H2O mixture with the ratio of volume 1:1 was measured in the cooling process by Raman spectroscopy, and the Raman assignments was made to the DMSO molecular and water molecular. The results showed that the behavior between intra-molecular hydrogen bonds and inter-molecular hydrogen bonds of DMSO and water leads to the change in the Raman spectra of the S==O stretching vibration of DMSO and the O--H stretching vibration of water. Further analysis showed that the hydrogen bond between DMSO and water was enhanced in the course of temperature decreasing process (27 to -30 degrees C), and the intramolecular hydrogen bonds between water and water replaced the intermolecular hydrogen bonds of DMSO and water in the course of temperature decreasing process (-30 to -60 degrees C). The research provides experimental basis for hydrogen bonding theory in aqueous solution.

In the present paper, studies on in-situ Raman spectra at high pressure up to 12.85 Gpa were performed on beta-carotene using a diamond anvil cell (DAC), and the effects of pressure on the characteristic peaks and pi-electron delocalization of beta-carotene were discussed. The results showed that Raman frequencies of the main characteristic peaks of beta-carotene shifted to high wavenumber with the increase in pressure. The relation between pressure and the three main characteristic peaks of beta-carotene was given as follows: nu1, (C==C) = 4. 74P + 1511.4, w (C-C) = 2.55P + 157.6 and nu3 (CH3) = 2.25P + 1011.3. Under the pressure of 5.38 GPa, Raman spectrum of nu1 + nu2 sum frequency of beta-carotene was subjected to cleavage. Fuethermore, the degree of relectron decolization was reduced with the increase in pressure, leading to C==C double bond more compressible than C-C bond on the main chain of beta-carotene.

A visible absorption and Raman spectra of all-trans-beta-beta-carotene was measured in cyclohexanol solution in the temperature range from 68 degrees C to 26 degrees C. The results indicated that the visible absorption spectra are red-shifted, Raman scattering cross section increases, Huang-Ryes factor and electron-phonon coupling constants of CC bond vibration modes decreases with the temperature decreasing. The changes are interpreted using the theory of "coherent weakly damped electronic-lattice vibration model" and "effective conjugation length model". The red shift of the absorption spectra and intensity of the Raman active are attributed to the thermal conformational change-induced increase in the effective conjugation length in all-trans-beta-carotene chains. All-trans-beta-carotene has strong coherent weakly damped CC bonds vibrational properties, which lead to large Raman scattering cross section in the solvent of low temperature. The electron-phonon coupling constants with dimension are used, which can easily establish relation with the Huang-Rhys factor and calculate the electron-phonon coupling constants of CC bond vibration modes. Effective conjugation length, the pi-electron delocalization range and the Raman scattering cross section are described by the electron-phonon coupling constants.

Stimulated Raman scattering was studied in water and heavy water using pulse laser at the wavelength of 532nm, not only obtaining the stimulated Raman of O-H and O-D stretching vibration, but also obtaining the stimulated Raman lattice vibration. When the laser energy was 130 mJ, the low frequency Stokes and anti-Stokes 313 cm(-1) line of water could be observed; When the laser energy was 160 mJ, the low frequnecy Stokes and anti-Stokes 280 cm(-1) line of heavy water could be observed. The results were explained by physics mechanism of laser induced plasma.

Raman spectra of ice VII phase were obtained at room temperature when the pressure was from 2.5 to 23 GPa. The experimental results indicate that the oxygen atoms distance do-o of ice decreased with pressure increasing,which results in that hydrogen bond is shortened, O--H bond is lengthened,force constant is reduced, and Raman spectra are red shifted. The orientation order of proton (hydrogen atom) is first increased and then decreased with varying the pressure, which leads to the Raman intensity increasing and then decreasing, and Raman linewidth is decreased and then increased, and the linewidth is the least when the pressure is 13 GPa.

In the summer 2008, Enteromorpha Prolifra broke out in Yellow Sea and East Sea on a large scale for the first time, and became a marine disaster. The authors constructed a stereoscopic monitoring system which monitored the disaster continuously, dynamically and in real time. The present paper introduced the construction of the stereoscopic monitoring system; through analyzing the spectral characteristics of Enteromorpha Prolifra and ocean water which were acquired in a field experiment, confirmed Enteromorpha Prolifra retrieval models based on multi-platform multi-sensor and multi-spectral remote sensing data, contrasted the different scale monitoring results, and analyzed the evolvement rules with time-series analysis. This system was applied to the Enteromorpha Prolifra emergency monitoring in the 29th Olympic sailing area. It was proved feasible and valuable for the Olympic safeguard.

The values of Raman scattering coefficients of some molecules in which Fermi resonance occurs vary with solution concentration variation. We measured the Raman spectra of some solvents such as CCl4, CS2, C6H6, etc by changing the concentration of the solutions ranging from 10% to 100% in volume. As a result, the authors obtained the general law of Fermi resonance. We found some weak Fermi resonance phenomena as well that the two bands of Raman spectrum shift asymmetrically and that the fundamental of overtone is tuned by Fermi resonance and moves towards the same direction with the overtone simultaneously, which is same as the results Bier K. D. obtained by means of high-pressure technique. By means of this method, the authors demonstrated the conclusion that only the fundamental in combinations which has the same symmetry as the fundamental involved in Fermi resonance directly can its intensity variation influence the Fermi resonance. In this article, the authors present a new method to study Fermi resonance. This method is valuable in the identification and the assignment of spectral lines of solutions, the determination of molecular configuration of enzyme, the discrimination of isomer, as well as the influences on the molecular structures and properties caused by hydrogen bond.

The Raman spectra of binary solution (CCl4 and C6 H6) and pure liquid were measured up to pressures of 11 GPa. The results show that pressure effect on binary solution is different from that on pure liquid: When mixing two liquids, owing to the changes in the density of the solution, intermolecular distance decreases and interaction energy increases, the frequency shift (blue shift) of spectral bands increases, and the frequency shift of binary liquid is faster than pure liquid frequency shift. Phase transitions (spectral bands splitting) change earlier and natural frequency difference delta0 increases with increasing pressure, while the Fermi resonance bands nu1 + nu6 and nu8 of benzene and nu1 + nu4 and nu3 of CCl4 disappear as the pressure decreases gradually, the spectral bands with different compressibility have different speed, whereas CCl4 has smaller density, longer bond, smaller force constant and larger compressibility and is easy to compress, C6H6 has larger density, smaller bond, larger force constant, smaller compressibility and is hard to compress. The frequency shift of CCl4 is faster than benzene. In this paper we provide good reference on Raman bands assignment and certification under high pressure, and also provide methods and ideas for study of the different environment of high pressure effect, intermolecular interaction and solvent effect.

The Raman scattering coefficients of the fundamental v1 (992 cm(-1)) of C6 H6 and the fundamental v1 (656 cm(-1) ) of CS2 changed dramatically with relative concentration of the binary solution of CS2 and C6 H6. The Raman spectra of the binary solution with different relative concentrations were measured. The results show that both the v1 fundamentals intensities changed dramatically with the relative concentration of the solution and the fundamental v1 of C6 H6 has little effect on the Fermi resonance v1 +v6-v8. On the contrary, the change in the v1 fundamental intensity of the CS2 changed which has more effect not only on the Fermi resonance v1 - 2v2 but also on the v2 fundamental. In this report, the experimental results were analyzed based on the J. F. Bertran theory and group theory.

Raman spectra of liquid carbon disulfide (CS) and carbon tetrachloride (CCl4) were measured. And the spectral intensity was analyzed using the J. F. Bertran theory and the group theory. The rule about Fermi resonance was obtained from the Raman spectra of carbon disulfide (CS) and carbon tetrachloride (CCL4): (1) The energy can transfer between a fundamental and an overtone frequency about Fermi resonance; the two spectra have the same intensity. The spectral intensity of the two spectra was equal (R=1) about Fermi resonance, when the difference between fundamental of Fermi resonance and overtone of Fermi resonance was very small. (2) The intensity of overtone is stronger than that of fundamental's. (3) The spectrum of Fermi resonance was observed, but the fundamental frequency was not. This article has very good reference value for the assignments in the molecular structure and the research of contents.

The binary systems of 1,1,3,3-tetramethylurea (TMU) with water, TMU with methanol, TMU with ethanol and N,N-dimethylformamide(DMF) with water were measured by Raman method. With the analysis of the frequency changes of stretching vibration of carboxyl with concentration the authors found that the frequency shift underwent two processes: first, the frequency of stretching vibration of carboxyl down shifts with the increase in hydrogen-bond acceptor concentration; secondly, when the concentration of binary system surpasses a critical value, the wave number remains almost constant, and only the rela tive intensity changes. Through this critical volume ratio, the authors found that the large self-associated water molecule was in volved in the TMU aqueous binary system; while the small self-associated molecule or dimer formation was present in other binary systems.

Lycopene and beta-carotene are two important nutritional components in tomato. The main Raman spectrum group of lycopene and beta-carotene abundant in tomato is identical and difficult to be distinguished through fundamental frequency. With excitation wavelength of 514.5 nm, the excited light was just present in the half width range of the main absorption bands of Lycopene and beta-carotene, so the resonance Raman effect can occur. Based on resonance Raman spectra, by on-body measuring the second harmonic of stretching vibration of carbon-carbon conjugated double bond in lycopene and beta-carotene, the content of lycopene and beta-carotene can be obtained according to the integrated intensity of each component calculated by software. And this provides a method for on-body determining the content of the components with the homologous group.

Raman spectrum is an important and effective method for the study of biological molecules in water. Measuring the Raman spectra for biological molecules in water, however, is very difficult because of the small Raman scattering cross section and the high electronic excitation energy of water molecules. In the present paper, the authors applied both technologies of liquid-core optical fiber and the resonance Raman spectra, then the intensity of Raman spectra was enhanced to a great extent. In this experiment, we chose the laser wavelength 514.5 of Ar+ ion laser as excitation laser, because we could obtain the maximal intensity of resonance Raman spectra at this wavelength. The experiment results show that, for the trace inspecting study of beta-carotene biological molecules in water, the concentration in the range of 10(-7)-10(-9) mol x L(-1) can be detected by quartz liquid-core optical fiber and the concentration in the range of 10(-9)-10(-10) mol x L(-1) by Teflon liquid-core optical fiber. The detecting utmost will be further reduced if improving the quality of optical fiber.

Ten meter single mode silica fiber was used to study the temperature characteristics of stimulated Raman scattering (SRS), and additional peaks (double-humped structure) were observed at both sides of pump light and first-order Stokes light in the experiment. The peak intensity increased first, and then decreased as the temperature increased from 80 K to 295 K. The first-order Stokes double-humped wave peaks disappeared when the temperature was 295 K. The double-humped peaks phenomenon was caused by simulated four photon mixing (SFPM), according to stimulated four-photon mixing theoretical calculation. At the same time, the phenomenon that the frequency shift of first-order Stokes spectrum line in SRS increased from 706.9 to 712.9 cm(-1) and its half width increased from 1.75 to 2.18 nm was theoretically explained, and the theoretical results are well consistent with experiments.

Raman spectra of 1,1,3,3-tetramethylurea in 20 solvents were obtained to investigate the solute-solvent interactions and to correlate solvent properties such as the Kirkwood-Bauer-Magat (KBM)equation, the solvent acceptor number (AN)and the linear solvation energy relationships (LSER), respectively, with the Raman shifts of carbonyl group. There is little linear relation between dielectric constants and the Raman shift. These solvents were divided into two sections by the acceptor number. The two sections exhibit a good correlation with AN, respectively. These frequencies show a better correlation with LSER than the solvent AN. How the solvents interacts with the C==O can be obtained from the regression coefficients.

The distribution of energy levels of the ground state and the low-lying excited states of hydrogenic impurities in InAs quantum ring was investigated by applying the effective mass approximation and the perturbation method. In 2D polar coordinates, the exact solution to the Schrödinger equation was used to calculate the perturbation integral in a parabolic confinement potential. The numerical results show that the energy levels of electron are sensitively dependent on the radius of the quantum ring and a minimum exists on account of the parabolic confinement potential. With decreasing the radius, the energy spacing between energy levels increases. The degenerate energy levels of the first excited state for hydrogenic impurities are not relieved, and when the degenerate energy levels are split and the energy spacing will increase with the increase in the radius. The energy spacing between energy levels of electron is also sensitively dependent on the angular frequency and will increase with the increases in it. The degenerate energy levels of the first excited state are not relieved. The degenerate energy levels of the second excited state are relieved partially. The change in angular frequency will have a profound effect upon the calculation of the energy levels of the ground state and the low-lying excited states of hydrogenic impurities in InAs quantum ring. The conclusions of this paper will provide important guidance to investigating the optical transitions and spectral structures in quantum ring.

Fermi resonance is one of the general and important phenomena in vibration spectra. The method of solvent variation is one of the main methods to study Fermi resonance. In the present paper, FTIR spectroscopy was used to study the Fermi resonance of p-benzoquinone in thirteen solvents. The results show that there are some function relationships between the dielectric constant of solvent and the intensity ratio of Fermi resonance. And the empirical formula was obtained by curve fitting. The equation of Kirkwood-Bauer-Magat was applied to the study of Fermi resonance. And the authors obtained the relation between the intensity ratio R and the dielectric constant epsilon. This result is in accordance with the empirical formula. In order to confirm our result, the infrared data of R. A. Nyquist and J. K. Seehra were analyzed. These results are in accord with that of p-benzoquinone.

The objective of this study was to develop a method for the determination of isorhamnetin in Hippophae rhamnoides Linn from West Sichuan plateau using near infrared diffuse reflectance spectroscopy. Applying the method of mixing with SiO2, the near infrared spectra (NIS) with the range of 12 000-4 000 cm(-1) were recorded for the Hippophae rhamnoides Linn containing isorhamnetin with the content of 0.1%-0.8%. Calibration models were established using the PLS (partial least squares). Different spectra pretreatments methods were compared. The study showed that spectral information can be extracted thoroughly by constant offset elimination (COE) pretreatments method with the correlation coefficient (r2) of 0.739 8, SEC of 0.107 (standard deviation of the calibration sets) and SEP of 0.073 (standard deviation of the prediction sets). The results indicate that near infrared diffuse reflectance spectroscopy is more rapid and convenient than conventional methods.

Raman spectra of acetone's carbonyl stretching in 16 solvents were measured, and were also calculated by self-consistent reaction field (SCRF) method in Gaussian03. The frequency shift in experiment was analyzed by donor-acceptor model, Kirkwood model and SCRF model respectively. Among them, the donor-acceptor model can explain the shift very well. The SCRF method can do it also, while not as well as the donor-acceptor model, but is better than Kirkwood model. Correlating the mechanisms of the 3 methods, it was found that the donor-acceptor model is powerful in explaining the vibrational spectra of molecular bond, which is nucleophilic reagent. The SCRF model considers not only the influence of dielectric constant epsilon, but also the influence of the bulk and the structure of molecule etc. Although the model is complex and difficult to calculate, but it takes many factors into account, so the calculated results accord with experiment better than the Kirkwood model. The main parameter of the Kirkwood model is epsilon, so it is very simple and easy to calculate, nonetheless the trend of frequency shift can still be reflected, indicating that the dielectric constant epsilon is a main character affecting the frequency shift.

Fermi resonance is a very common phenomenon in molecule vibration spectra, especially in polyatomic molecule with complex structure. Fermi resonance appears when a fundamental vibration frequency lies closely to an overtone or combination frequencies. One can observe two peaks coming from Fermi resonance and the energy transfer also occurs between the two peaks. Fermi resonance phenomenon appears in both infrared spectrum and Raman spectrum. The Raman spectrum of CCl4 was measured. The frequency separation between the two peaks in a Fermi resonance doublet was observed and the integrated intensities were calculated with the software of Origin Pro 7.5. Fermi resonance interaction was caused by the CCl4 C-Cl f-symmetrical stretching fundamental nu3 coupling. The combination frequency (nu1 + nu4) of C-Cl a1-symmetrical stretching nu1 and band C-Cl2 f-symmetrical bending nu4 was calculated. Based on Bertran's theory, Fermi coupling coefficient W was calculated and the theoretical value nu3(0) of nu3 was estimated. The present article provided good reference for better understanding of the relationship between molecular vibration frequency and molecular structure.

The present article studied the fermentation liquid's absorption spectra, bacteria growth period and elastase' production in elastase fermentation, and compared and analyzed the their relation. The results show that the changes in the absorption spectra were closely related with bacteria growth and elastase' production. The UV spectroscopic technique is helpful for detecting the change of the organic nitrogen base and enzyme. The study offers a new method to detect fermentation process and is basic for detecting fermentation process on line by UV spectroscopic technique.

Cartilage of youth and elder was measured by Fourier transform infrared (FTIR). Area integrations were done on the major composition of organic and inorganic substance's infrared bands processed using OMNIC 5. 2. Calculation of the ratio of the integrated areas under the organic and inorganic substance's peaks allowed the comparisons of the ratio brtween organic and inorganic substance's contents. As indicated from the results, the ratio of organic to inorganic substance in youth is 5-7 times larger than that in elder, but there was a big difference in the content of lipids between youth and elder. Calculating the ratio of the integrated areas under lipids peaks (1 747 cm(-1)) to that under inorganic phosphates peaks, the authors can see that the content of lipids in the bone of elder is significantly higher than that of youth. The authors admitted that with the increment of age, less organic substance (collagen) (but more lipids) and more inorganic substance (phosphate, carbonate etc) is a symbol of the degeneration of cartilage. Therefore, makes the cartilage more brittle, less elastic and less wearable. This can result in the disease of bone and injuring the bone easily.

In order to meet the needs of highly dense and overall farmland information gathering, wireless data communicating, and real-time processing in the precision agriculture, this system integrated GPS, GIS and RS based on the technology of computer and wireless data transmission. On the one hand, the system makes DGPS and Hyper-spectrograph integrated through the AT891v52 MCU, providing the accurate space position and realizing the integration of spectrum data acquisition and orientation. On the other hand, the system realizes the communication between the data gathering control system and the microcomputer by using the nRF905 system. Meanwhile the system has realized the visualized analysis and management of the spectrum data by integrating Visual Basic and Map-Objects into GIS, displaying real-time trace of moving point and some related attributes of the moving point in map layers, and calculating crop derivative spectra and crop vegetation index NDVI etc. Thus, sufficient information was provided for expert system and decision support system of precision agriculture.

The visible absorption spectra of p-benzoquinone (PBQ) in CS2 were measured, and a weak absorption band around 507 nm attributed to n-pi* singlet-triplet transition was denonstrated. Using the resonance Raman effect excited in liquid-core optical fiber which can enhance Raman intensity by 6-9 orders of magnitude, the authors obtained the 514.5 nm excited resonance Raman (RR) spectra of PBQ at 1439 cn(-1) in the concentration range from 10(-3) to 10(-6) mol x L(-1). The new characteristic RR band is attributed to the symmetric C==O stretch (v(C==O)) of n-pi* singlet-triplet transition of PBQ. The resonance Raman shift is blue-shifted with decreasing concentration. The results of this paper are helpful for understanding the relationship between the electric structure and the photophysical properties of PBQ, and for obtaining more abundant structural information of molecules.

In order to meet the precision agriculture needs that highly dense and overall farmland information is gathered, this system uses Visual Basic and Map-Objects to carry on integration of GPS, GIS and RS. On the one hand, the system can provide the space seat attribute of high precision for the spectral data gathered by way of integration GPS, and realizes integration in spectrum data gathering, orientation and storage. On the other hand, by way of integrated GIS, the system has realized the function of visualizing analysis and management of the spectrum data, displaying real-time trace of moving point, providing some related attribute of the moving point in map layers, and calculating crop derivative spectra and crop vegetation index NDVI etc. The sufficient information is put forward for expert system and decision support system of precision agriculture.