Analysis of Near-Infrared Spectra of Complicated Biological Fluids by Two-Dimensional Correlation Spectroscopy: Protein and Fat Concentration-Dependent Spectral Changes of Milk

1999 ◽  
Vol 53 (12) ◽  
pp. 1582-1594 ◽  
Author(s):  
Bogusława Czarnik-Matusewicz ◽  
Koichi Murayama ◽  
Roumianna Tsenkova ◽  
Yukihiro Ozaki
2020 ◽  
Vol 28 (3) ◽  
pp. 148-152 ◽  
Author(s):  
Ishita Joshi ◽  
Vi Khanh Truong ◽  
J Chapman ◽  
D Cozzolino

The variations in temperature during the analysis of alcoholic beverages are of importance to develop protocols based on near infrared spectroscopy. The objective of this study was to evaluate the effect of increasing temperature on the near infrared spectra of whisky samples using two-dimensional correlation spectroscopy. Whisky samples from different commercial labels were analyzed at four different temperatures (25°C, 35°C, 45°C, and 55°C) using a UV–VIS–NIR instrument. Asynchronous and synchronous two-dimensional correlation spectroscopy was used to reveal the effect of temperature on the near infrared spectra of the samples. The results of this study indicated that temperatures between 40°C and 55°C alter absorption at specific wavelengths in the near infrared region of the whisky samples analyzed. The combination of near infrared spectroscopy with two-dimensional correlation spectroscopy has the potential to dramatically improve the efficiency of analytical laboratories, considering the range of data that can be collected.


2007 ◽  
Vol 15 (5) ◽  
pp. 307-315 ◽  
Author(s):  
James B. Reeves ◽  
Gregory W. McCarty ◽  
David W. Rutherford ◽  
Robert L. Wershaw

The objective of this research was to investigate the effect of charring on near infrared spectra of materials likely to be present in forest fires in order to determine the feasibility of determining charred carbon in soils. Four materials (cellulose, lignin, pine bark and pine wood) and char from these materials created by charring for various durations (1 to 168 h) and at various temperatures (200 to 450°C) were studied. Near infrared spectra and measures of acidity (total acids, carboxylic acids, lactones and phenols as determined by titration) were available for 56 different samples (Not all samples charred at all temperatures/durations). Results showed spectral changes that varied with the material, temperature and duration of charring. Examination of spectra and correlation plots indicated that changes in the constituents of the materials in question, such as loss of OH groups in carbohydrates, rather than direct determination of typical products produced by charring, such as carboxylic acids, lactones and phenols, were the basis for the spectral changes. Finally, while the spectral changes resulting from charring appeared to be relatively unique to each material, PLS calibrations for total acids, carboxylic acids, lactones and phenols were successfully created (with R2 of 0.991, 0.943, 0.931 and 0.944, respectively) indicating that there is a sufficient commonality in the changes to develop calibrations without the need for unique calibrations for each specific set of charring conditions (i.e. material, temperature and time of heating).


1995 ◽  
Vol 49 (3) ◽  
pp. 295-303 ◽  
Author(s):  
James B. Reeves

The objectives of this work were to examine similarities and differences in the near-infrared and mid-infrared spectral regions when one is working with high-moisture materials and to study spectral changes in these regions as a method to identify the relationship of spectral information in the near-IR to fundamental absorptions in the mid-IR. Near- and mid-infrared spectra were taken with a Digilab FTS-65 Fourier transform spectrometer. Liquids were examined by transmission and solids by reflectance. Results with solutions showed that less spectral distortion arises when one is subtracting water from mid- rather than from near-infrared spectra. It was also easier to produce high-quality spectra in the mid-infrared by using attenuated total reflectance than by using transmission in the near-infrared. While mid-infrared spectra showed changes (induced by water, pH, physical state, and ionic strength) similar to those found in the near-infrared, there appeared to be more information available in the mid-infrared, even in the presence of water.


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