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基于粒子群的虚像相位阵列光谱仪光谱反演算法

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虚像相位阵列光谱仪是一种兼具宽谱、高分辨率优点的新型正交色散型光谱仪.使用虚像相位阵列光谱仪在6900~6990 cm-1波段对二氧化碳(CO2)开展了宽光谱测量,发展了一种基于粒子群的吸收光谱反演优化算法.首先基于HITRAN数据库建立CO2分子吸收模拟谱线,然后在对实测谱线进行三次多项式波长标定的基础上,通过粒子群优化模拟吸收峰的峰值位置参数,实现模拟谱线与实测谱线位置上的最佳吻合,从而提高吸收光谱的参数反演精度.结合超连续光源和Chemin型光学多通池检测了不同体积分数的CO2吸收光谱.实验结果表明未优化峰值位置时CO2体积分数反演结果与理论值相差约33%,优化峰值位置后,体积分数反演结果与理论值的偏差仅为1.8%,证明该粒子群优化算法可用于虚像相位阵列光谱仪的分子体积分数的反演优化.
Spectral Inversion Algorithm of Virtual Image Phase Array Spectrometer Based on Particle Swarm Optimization
Objective Carbon dioxide(CO2)is a principal byproduct of hydrocarbon fuel combustion.Real-time detection of CO2 can evaluate combustion temperature and efficiency,playing a crucial role in combustion diagnosis.Compared with the probe method and other contact techniques,laser absorption spectroscopy offers rapid,precise and non-intrusive measurement of CO2 in combustion environments.This method has attracted increasing attention and research,becoming a mainstream technology for combustion diagnosis.Among various approaches,combining a broadband laser source with broadband absorption spectrum measurement allows capturing more sample absorption characteristics,especially when sample absorption is weak or subject to interference from other absorbents,providing the advantage of multi-wavelength absorption spectrum detection.The virtual image phase array(VIPA)spectrometer,characterized by its wide spectral range and high resolution,represents a novel type of orthogonal dispersion spectrometer.However,when directly applying the VIPA spectrometer to gas parameter inversion,the measured spectral frequency axis exhibits deviations from theoretical values due to the nonlinear dispersion of the VIPA element and discrete sampling by the array detector,leading to reduced accuracy in gas inversion.This paper presents a spectral inversion accuracy optimization algorithm based on particle swarm optimization(PSO)aimed at enhancing the precision of CO2 detection using the VIPA spectrometer for wide-spectrum CO2 detection.Methods The CO2 measurement system,centered around the VIPA spectrometer,primarily consists of two components:the CO2 concentration detection part and the gas preparation part.Light emitted by a supercontinuum light source,after filtration through a 1.42-1.45 μm filter,combined with a fiber collimator,enters a Chernin-type optical absorption multi-pass cell with an optical path length of 4 m.An optical fiber coupler directs the light exiting the multi-pass cell into a single-mode fiber,which is then connected to the VIPA spectrometer's fiber interface.Initially,the Voigt absorption line model for the CO2 molecule is established by the HITRAN database.The peak position of the absorption model and the experimental peak's pixel position are fitted using a cubic polynomial to achieve preliminary calibration of the frequency axis.Subsequently,the PSO algorithm corrects the peak position of the simulated spectrum line to ensure optimal agreement between the simulated and measured spectra.Finally,the gas volume fraction is determined through the least square method.During peak position correction of PSO algorithm,the spectrum is divided into several sub-intervals using the trough of the spectrum line as the cut-off point.Adjacent sub-intervals with peak spacing less than 1 cm-1 are grouped into a single fitting interval,and each interval's peak is corrected individually.Results and Discussions The cubic polynomial fitting spectrum extraction algorithm yields a frequency axis with a position deviation ranging from 0-0.1 cm-1 compared to the theoretical positions[Fig.4(c)].Residual analysis indicates that frequency axis calibration deviations are the primary source of these discrepancies.Given the disparity between the measured spectrum's frequency axis and the theoretical spectrum,the PSO algorithm is used to adjust peak positions(Fig.5).As iterations increase,peak position distribution stabilizes,with the algorithm generally converging by the 30th iteration.The reliability of the PSO peak correction algorithm for gas volume fraction retrieval is examined by measuring CO2 concentrations of 30%,40%,50%and 60%within the range of 6900 to 6990 cm-1.Without PSO correction,the average deviation of inversion is 33.27%(Fig.8),and the maximum relative error reaches 35.43%.The average deviation of inversion after PSO correction is 1.81%,and the maximum relative error is 2.58%.The accuracy of the inversion is significantly improved after PSO correction of the peak value.Conclusions To address the issue of substantial parameter inversion errors due to insufficient spectrometer frequency axis calibration accuracy,an optimization algorithm of absorption spectrum inversion accuracy based on PSO is introduced in our study.By employing the PSO algorithm to adjust the simulated peak positions of the measured spectrum line of pure gas,an optimal match between simulated and measured spectral lines is achieved.Using corrected peak positions,simulated absorption lines serve as a basis for solving the volume fraction as an independent variable through least squares fitting to experimental lines.Pre-and post-peak correction fitting outcomes for pure CO2 measurement and simulation spectra demonstrate that the PSO-based peak correction algorithm effectively enhances peak location accuracy and reduces fitting residuals.According to CO2 measurement data spinning 30%-60%volume fractions,the average deviation in corrected volume fraction inversion stands at 1.81%,with an average root mean square error of 1.01×10-5,indicating the method's efficacy in improving the inversion accuracy of volume fraction and verifying the algorithm's applicability to VIPA spectral parameter inversion.This algorithm also offers reference value for gas parameter inversion optimization in other spectrometers.

virtual image phase array spectrometerparticle swarm optimizationhigh resolutioncarbon dioxide detection

吕丙选、赵卫雄、周昊、崔卫华、方波、杨娜娜、张为俊

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中国科学技术大学,安徽 合肥 230036

中国科学院合肥物质科学研究院安徽光学精密机械研究所,安徽 合肥 230031

虚像相位阵列光谱仪 粒子群优化 高分辨率 二氧化碳探测

2024

光学学报
中国光学学会 中国科学院上海光学精密机械研究所

光学学报

CSTPCD北大核心
影响因子:1.931
ISSN:0253-2239
年,卷(期):2024.44(24)