Estimation of the Octane Number of Automobile Gasoline by Fourier Transform Infrared Absorption Spectrometry

1992 ◽  
Vol 46 (6) ◽  
pp. 966-971 ◽  
Author(s):  
M. Ichikawa ◽  
N. Nonaka ◽  
I. Takada ◽  
S. Ishimori

A method to estimate the octane number of automobile gasoline by Fourier transform infrared absorption spectrometry has been studied. Thirty-six kinds of regular gasoline and 38 of unleaded premium gasoline, collected from the market from winter to summer, were used as samples, and the absorptions of the C-H stretching vibration in the 3150-2800 cm−1 range of their IR spectra were used to plot each sample in a two-dimensional space, followed by an attempt to graphically classify the two broad types. On the other hand, the IR spectra of other samples with known octane numbers (88.0 to 100.8 in octane number) and, on that basis, samples with known octane numbers, were mapped into the space in which the regular gasolines and the premium gasolines were classified to determine their dispersion in this space. A further attempt was made to formulate a linear regression equation for use in octane number estimation. As a result, it was found that regular and premium gasolines could be definitely distinguished from each other according to the C-H stretching vibration in the 3150-2800 cm−1 near-infrared range, and that the octane number could be visually estimated. The formulation of a satisfactory regression equation was also made possible. These results are reported.

1981 ◽  
Vol 35 (5) ◽  
pp. 461-465 ◽  
Author(s):  
Theophile Theophanides

Fourier transform infrared (FT-IR) spectra of deoxyribonucleic acid (DNA) and its reaction products with the anticancer drug cis-Pt(NH3)2Cl2, cis-diamminodichloroplatinum (abbreviated cisplatin) in water and heavy water solutions or gels have been obtained and studied. The mid-IR spectra show considerable changes in the carbonyl (C=0) region and weaker, but significant perturbations in the sugar-phosphate absorption region (PO2−, OPC and COP). The carbonyl bands at 1710 and 1686 cm−1 of the control DNA in H2O and D2O, respectively, disappear and shift to lower frequencies in the spectra of cisplatin + DNA with a r = Pt/P = 0.2. Furthermore, the sugar-phosphate band at 1054 cm−1 of the C—O stretching vibration of the ribose-phosphate bond is reduced in intensity and slightly shifted to higher frequencies, indicating a reorientation of the phosphate group. In addition, the P—O stretching vibration frequency at 970 cm−1 is reduced in intensity on interaction with the drug. These changes depend to some extent on the water content in the control DNA and in the cisplatin + DNA complex. The water molecules in DNA in the presence of cisplatin reorganize themselves. The attack of the platinum drug at the N7 site of the guanine molecule in DNA exerts an effect on the DNA structure through a modification of the water average configuration and its stabilizing effect on the secondary structure.


2018 ◽  
Vol 762 ◽  
pp. 48-53
Author(s):  
Liene Pluduma ◽  
Karlis Agris Gross ◽  
Christian Rey ◽  
Arnolds Ubelis ◽  
Astrida Berzina

The amount and alignment of hydroxyl ions influence the bioactivity of hydroxyapatite. Hydroxyl ions in hydroxyapatite are the most mobile and upon heating are the first to leave the lattice to form oxyhydroxyapatite. This work describes a method for producing hydroxyapatite with different amounts of hydroxyl ions, and reports on the changes in Fourier transform infrared absorption at increasing level of dehydroxylation. Detailed analysis of spectra in the 500 – 700 cm-1 range showed a peak shift for the hydroxyl ion absorption line at 632 cm-1 to 637 cm-1 and an increase in the wavenumber for the phosphate line at 575 cm-1.


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