Synthetic calibration and quantitative analysis of gas-phase FT-IR spectra

被引:312
作者
Griffith, DWT
机构
[1] Department of Chemistry, University of Wollongong, Wollongong, NSW 2522, Northfields Avenue
关键词
FT-IR spectroscopy; calibration; trace gas analysis; quantitative analysis; solar FT-IR spectroscopy; open path FT-IR spectroscopy; classic least-squares; CLS;
D O I
10.1366/0003702963906627
中图分类号
TH7 [仪器、仪表];
学科分类号
0804 ; 080401 ; 081102 ;
摘要
A method for the quantitative analysis of gas-phase infrared spectra is described in which calibration spectra are calculated from a database of absorption line parameters rather than measured in a real spectrometer. The synthetic calibration spectra are computed with the use of the program MALT (Multiple Atmospheric Layer Transmission), including environmental (pressure, temperature, pathlength, etc.) and instrumental (resolution, line shape, wavenumber shift) effects in the calculation, so that the calculated spectra closely approximate real measured spectra. The synthetic calibration spectra are then used in quantitative analysis as if they were real spectra. In conventional laboratory studies, the method circumvents the need for time-consuming collection of large sets of laboratory calibration spectra often required when many absorbing gases must be analyzed. It is particularly useful in long open-path and solar FT-IR spectroscopy when no sample cell is available for recording calibration spectra. Examples are presented from conventional laboratory spectra in a closed-cell, open-path FT-IR spectra used to determine trace gas fluxes in an open field, and solar absorption spectroscopy using ground-based FT-IR spectrometers.
引用
收藏
页码:59 / 70
页数:12
相关论文
共 31 条
[1]   ERRORS IN ABSORBANCE MEASUREMENTS IN INFRARED FOURIER-TRANSFORM SPECTROMETRY BECAUSE OF LIMITED INSTRUMENT RESOLUTION [J].
ANDERSON, RJ ;
GRIFFITHS, PR .
ANALYTICAL CHEMISTRY, 1975, 47 (14) :2339-2347
[2]  
[Anonymous], IPCC CLIMATE CHANGE
[3]  
BRAULT JW, 1985, HIGH RESOLUTION ASTR, P1
[4]   MOLECULAR LINE PARAMETERS FOR THE ATMOSPHERIC TRACE MOLECULE SPECTROSCOPY EXPERIMENT [J].
BROWN, LR ;
FARMER, CB ;
RINSLAND, CP ;
TOTH, RA .
APPLIED OPTICS, 1987, 26 (23) :5154-5182
[5]   VIBRATION-ROTATIONAL AND ROTATIONAL INTENSITIES FOR CO ISOTOPES [J].
CHACKERIAN, C ;
TIPPING, RH .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1983, 99 (02) :431-449
[6]   RAPID COMPUTATION OF VOIGT PROFILE [J].
DRAYSON, SR .
JOURNAL OF QUANTITATIVE SPECTROSCOPY & RADIATIVE TRANSFER, 1976, 16 (07) :611-614
[7]   APPLICATION OF A FOURIER-TRANSFORM IR SYSTEM FOR MEASUREMENTS OF N2O FLUXES USING MICROMETEOROLOGICAL METHODS, AN ULTRALARGE CHAMBER SYSTEM, AND CONVENTIONAL FIELD CHAMBERS [J].
GALLE, B ;
KLEMEDTSSON, L ;
GRIFFITH, DWT .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D8) :16575-16583
[8]  
GALLERY WO, 1983, AFGLTR830065 AIR FOR
[9]   OPTICAL REMOTE MEASUREMENT OF TOXIC GASES [J].
GRANT, WB ;
KAGANN, RH ;
MCCLENNY, WA .
JOURNAL OF THE AIR & WASTE MANAGEMENT ASSOCIATION, 1992, 42 (01) :18-30
[10]  
GRIFFITHS P, 1986, FOURIER TRANSFORM IN