Intensity-Value Corrections for Integrating Sphere Measurements of Solid Samples Measured behind Glass

2014 ◽  
Vol 68 (11) ◽  
pp. 1224-1234 ◽  
Author(s):  
Timothy J. Johnson ◽  
Bruce E. Bernacki ◽  
Rebecca L. Redding ◽  
Yin-Fong Su ◽  
Carolyn S. Brauer ◽  
...  

Accurate and calibrated directional-hemispherical reflectance spectra of solids are important for both in situ and remote sensing. Many solids are in the form of powders or granules and to measure their diffuse reflectance spectra in the laboratory, it is often necessary to place the samples behind a transparent medium such as glass for the ultraviolet (UV), visible, or near-infrared spectral regions. Using both experimental methods and a simple optical model, we demonstrate that glass (fused quartz in our case) leads to artifacts in the reflectance values. We report our observations that the measured reflectance values, for both hemispherical and diffuse reflectance, are distorted by the additional reflections arising at the air–quartz and sample–quartz interfaces. The values are dependent on the sample reflectance and are offset in intensity in the hemispherical case, leading to measured values up to ∼6% too high for a 2% reflectance surface, ∼3.8% too high for 10% reflecting surfaces, approximately correct for 40–60% diffuse-reflecting surfaces, and ∼1.5% too low for 99% reflecting Spectralon® surfaces. For the case of diffuse-only reflectance, the measured values are uniformly too low due to the polished glass, with differences of nearly 6% for a 99% reflecting matte surface. The deviations arise from the added reflections from the quartz surfaces, as verified by both theory and experiment, and depend on sphere design. Empirical correction factors were implemented into post-processing software to redress the artifact for hemispherical and diffuse reflectance data across the 300–2300 nm range.

2017 ◽  
Vol 10 (6) ◽  
pp. 2077-2091 ◽  
Author(s):  
Sabina Assan ◽  
Alexia Baudic ◽  
Ali Guemri ◽  
Philippe Ciais ◽  
Valerie Gros ◽  
...  

Abstract. Due to increased demand for an understanding of CH4 emissions from industrial sites, the subject of cross sensitivities caused by absorption from multiple gases on δ13CH4 and C2H6 measured in the near-infrared spectral domain using CRDS has become increasingly important. Extensive laboratory tests are presented here, which characterize these cross sensitivities and propose corrections for the biases they induce. We found methane isotopic measurements to be subject to interference from elevated C2H6 concentrations resulting in heavier δ13CH4 by +23.5 ‰ per ppm C2H6 ∕ ppm CH4. Measured C2H6 is subject to absorption interference from a number of other trace gases, predominantly H2O (with an average linear sensitivity of 0.9 ppm C2H6 per  % H2O in ambient conditions). Yet, this sensitivity was found to be discontinuous with a strong hysteresis effect and we suggest removing H2O from gas samples prior to analysis. The C2H6 calibration factor was calculated using a GC and measured as 0.5 (confirmed up to 5 ppm C2H6). Field tests at a natural gas compressor station demonstrated that the presence of C2H6 in gas emissions at an average level of 0.3 ppm shifted the isotopic signature by 2.5 ‰, whilst after calibration we find that the average C2H6 : CH4 ratio shifts by +0.06. These results indicate that, when using such a CRDS instrument in conditions of elevated C2H6 for CH4 source determination, it is imperative to account for the biases discussed within this study.


2020 ◽  
Vol 12 (19) ◽  
pp. 3211
Author(s):  
Xiaobin Qi ◽  
Zongcheng Ling ◽  
Jiang Zhang ◽  
Jian Chen ◽  
Haijun Cao ◽  
...  

Until 29 May 2020, the Visible and Near-Infrared Imaging Spectrometer (VNIS) onboard the Yutu-2 Rover of the Chang’e-4 (CE-4) has acquired 96 high-resolution surface in-situ imaging spectra. These spectra were acquired under different illumination conditions, thus photometric normalization should be conducted to correct the introduced albedo differences before deriving the quantitative mineralogy for accurate geologic interpretations. In this study, a Lommel–Seeliger (LS) model and Hapke radiative transfer (Hapke) model were used and empirical phase functions of the LS model were derived. The values of these derived phase functions exhibit declining trends with the increase in phase angles and the opposition effect and phase reddening effect were observed. Then, we discovered from in-situ and laboratory measurements that the shadows caused by surface roughness have significant impacts on reflectance spectra and proper corrections were introduced. The validations of different phase functions showed that the maximum discrepancy at 1500 nm of spectra corrected by the LS model was less (~3.7%) than that by the Hapke model (~7.4%). This is the first time that empirical phase functions have been derived for a wavelength from 450 to 2395 nm using in-situ visible and near-infrared spectral datasets. Generally, photometrically normalized spectra exhibit smaller spectral slopes, lower FeO contents and larger optical maturity parameter (OMAT) than spectra without correction. In addition, the band centers of the 1 and 2 μm absorption features of spectra after photometric normalization exhibit a more concentrated distribution, indicating the compositional homogeneity of soils at the CE-4 landing site.


1995 ◽  
Vol 3 (3) ◽  
pp. 143-153 ◽  
Author(s):  
James B. Reeves

The spectral region from 10,000 to 8000 cm−1 (1000 to 1250 nm) is often used for high moisture samples and fibre optic systems. The first objective of this work was to determine the effects of water on the spectra of various types of materials in this spectral region. The second objective was to determine the origin/nature of spectral effects/artifacts seen in the spectral region from 14,000 to 11,500 cm−1 (714 to 870 nm) when water was added to gums and proteins (increases in peak intensities and shifts in position due to the presence of water). Spectra were obtained by diffuse reflectance and transmission using a Fourier transform spectrometer. The results showed that the effects seen in the mid-infrared and near infrared from 8000 to 4000 cm−1 (1250 to 2500 nm) were also common in this part of the near infrared (i.e. peak shifts, loss of spectral features etc). Thus, the spectra of crystalline glucose and sucrose, while distinctively different as crystalline solids, were very similar when in solution and changes in the spectra of materials, such as acetone, pyridine and ethanol, were very similar in nature to those previously found in the near infrared from 8000 to 4000 cm−1 (1250 to 2500 nm). Finally, detailed examination of spectra in the region from 10,000 to 8000 or 6000 cm−1 (1000 to 1250 or 1667 nm) did not show any spectral effects similar to those seen in gums and proteins in the 14,000 to 11,500 cm−1 (714 to 870 nm) region. Thus, the nature of these effects is still unknown.


1983 ◽  
Vol 37 (1) ◽  
pp. 32-38 ◽  
Author(s):  
W. Richter

Spectral measurements of the directional hemispherical reflectance of samples exhibiting variant reflection behavior were performed in the near and mid infrared spectral region using the integrating sphere method. The main components of the experimental setup were a sphere with a diffuse gold coating and a commercial Fourier transform spectrometer for the spectral analysis of the radiation incident on and reflected by the sample which is located in the center of the sphere. The capability of the device to measure absolute reflectances was tested with polished slices of high purity silicon and germanium, the reflectances of which can be calculated from the refractive indices. Agreement between the measured and calculated values was found to be within 0.01. Diffuse reflectance standards are not yet available in the infrared. The uncertainty of absolute reflectance measurements is estimated to be ±0.02. Several examples of chemical and technical applications are presented. A relatively low spectral resolution, 16 cm−1, was used to keep the measurement times short, within the range of a few minutes, thereby minimizing signal drifts. Higher resolution, sometimes necessary for special purposes in chemical analysis, can be attained by longer measurement times. No extensive sample preparation and adjustment is necessary besides the choice of the desired angle of incidence.


2002 ◽  
Vol 56 (8) ◽  
pp. 1094-1097 ◽  
Author(s):  
N. Ghosh ◽  
A. Datta ◽  
P. K. Gupta

Light scattering properties of ghee (a form of clarified butter) and vanaspati (partially hydrogenated vegetable oil) have been investigated in order to explore the use of optical techniques for detection of adulteration of vanaspati in ghee. Significant differences in the diffuse reflectance spectra of ghee and vanaspati were observed. The estimates for the reduced scattering coefficient (μs′) and the absorption coefficient (μa) for ghee and vanaspati were also obtained from integrating sphere measurements. These suggest that the differences in the diffuse reflectance spectra of ghee and vanaspati are primarily due to the differences in their absorption characteristics in the spectral range of 400 to 550 nm. Further, the results obtained show that the ratio of diffuse reflectance at 460 nm to that at 410 nm could be used to detect adulteration of vanaspati in ghee.


2021 ◽  
Vol 136 (2) ◽  
Author(s):  
Dario Barni ◽  
Luisa Raimondo ◽  
Anna Galli ◽  
Rossella Yivlialin ◽  
Simone Caglio ◽  
...  

AbstractAcrylic colors are mixtures of several components that can be identified as pigments, binders, and fillers, so that, when analyzed, the characteristic response of the different components may not be recognizable. This limits the accuracy of spectroscopic techniques, nonetheless particularly useful as they are noninvasive and can be applied in situ on real artworks. Here, a method is proposed to chemically separate and identify the different components of acrylic colors, in order to be able to study their spectroscopic response separately, in particular by ultraviolet–visible–near-infrared diffuse reflectance. The results clearly show that the chemical and analytical method developed here is fully reliable, with the advantage of clearly separating the response of the different components without any change of their chromatic/chemical properties. As a case study, the new method is applied here to original acrylic colors used by the Italian artist Ico Parisi, in view of building a spectra database.


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