Alcohol Determination in Distilled Alcoholic Beverages by Liquid Phase Fourier Transform Mid-Infrared and Near-Infrared Spectrophotometries

2016 ◽  
Vol 10 (1) ◽  
pp. 172-179 ◽  
Author(s):  
Ayalew Debebe ◽  
Abel Anberbir ◽  
Mesfin Redi-Abshiro ◽  
Bhagwan Singh Chandravanshi ◽  
Araya Asfaw ◽  
...  
NIR news ◽  
2018 ◽  
Vol 29 (3) ◽  
pp. 6-11 ◽  
Author(s):  
Michael K-H Pfister ◽  
Bettina Horn ◽  
Janet Riedl ◽  
Susanne Esslinger ◽  
Carsten Fauhl-Hassek

Fourier transform infrared spectroscopy becomes increasingly important for detecting adulterations in food due to a minimal sample preparation and a fast nondestructive measurement. Sunflower oil is a popular food ingredient, which might be contaminated or even adulterated by compounds with health concerns such as mineral oil. In this context a feasibility study was performed to compare the suitability of near- and mid-infrared spectroscopy for detecting mineral oil in sunflower oil. For this purpose, sunflower oils spiked with mineral oil in the concentration range of 0.001–1.0% w/w were analyzed by Fourier transform near- and mid-infrared spectroscopy, respectively, and spectra data were preprocessed prior to partial least squares regression. Hereby, the data preparation was optimized for each technique to account for model performance influences. The model performance was fairly similar for both approaches with a slightly better precision and thus limit of detection (near infrared 0.12% w/w, mid infrared 0.16% w/w) for the near-infrared-based model compared to the mid-infrared model. Consequently, both techniques are considered suitable for the determination of mineral oil in sunflower oil in the context of food authentication.


2000 ◽  
Vol 78 (4) ◽  
pp. 317-325 ◽  
Author(s):  
M Mengel ◽  
B P Winnewisser ◽  
M Winnewisser

We report the results of our observations of liquid parahydrogen in the mid-infrared and of liquid parahydrogen and orthodeuterium in their first and second overtone regions using a Bruker IFS 120 HR Fourier transform spectrometer. We have determined intensity parameters for individual absorption features where possible and indicate analogies between the spectrum of the liquid and the corresponding spectrum of the solid phase of the hydrogens. PACS Nos.: 33.20Ea, 33.70Fd, 67.90+z


1994 ◽  
Author(s):  
M. A. Czarnecki ◽  
Yong L. Liu ◽  
Yukihiro Ozaki ◽  
Masao Suzuki ◽  
Masahiro Iwahashi

ACS Omega ◽  
2021 ◽  
Author(s):  
Atchara Sankom ◽  
Warapa Mahakarnchanakul ◽  
Ronnarit Rittiron ◽  
Tanaboon Sajjaanantakul ◽  
Thammasak Thongket

2021 ◽  
Vol 29 (3) ◽  
pp. 4035
Author(s):  
Chiara Lindner ◽  
Jachin Kunz ◽  
Simon J. Herr ◽  
Sebastian Wolf ◽  
Jens Kießling ◽  
...  

1993 ◽  
Vol 47 (12) ◽  
pp. 2162-2168 ◽  
Author(s):  
Mirosław Antoni Czarnecki ◽  
Yongliang Liu ◽  
Yukihiro Ozaki ◽  
Masao Suzuki ◽  
Makio Iwahashi

Fourier transform near-infrared (FT-NIR) technique has been employed to determine the degree of dissociation and the thermodynamic parameters of octanoic acid in the liquid phase. FT-NIR absorption spectra of the acid over a temperature range of 15 to 92°C were recorded. From the spectra, intensities of the first overtone of the OH stretching mode due to the monomer form of the acid were extracted and were used to calculate the degree of dissociation and the thermodynamic parameters for the process of dissociation of dimeric octanoic acid into monomer species. In the 7400–6700 cm−1 region there appear many bands that are heavily overlapped; the attempts to apply curve-fitting and deconvolution algorithms to separate individual bands have failed. Here, a simple and reliable method of calculation of the intensities of the first overtone of the OH stretching mode due to the monomer is proposed. Also, an excellent procedure of determining the molar absorption coefficients (integrated and at peak position) through a series of measurements in CCl4 solution at very low concentrations is presented. The bands due to CH vibrations were eliminated in two ways; one way involved taking the concentration as a reference, and the other used the band area of the second overtone of the CH stretching modes as a reference. In the operation the spectrum of neat octanoic acid at 15.1°C was employed. The coefficients obtained by both methods are compared and discussed. The present studies indicate that both band areas and peak heights give results which are found to be in very good agreement.


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