2017
DOI: 10.1016/j.molstruc.2016.10.055
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Molecular interaction forces in acetone + ethanol binary liquid solutions: FTIR and theoretical studies

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Cited by 41 publications
(10 citation statements)
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“…Thus, the chalcogenide waveguide sensor was able to differentiate ethanol and acetone vapor by their distinct mid-IR C–H absorption. This result agreed with previous Fourier transform infrared spectroscopy measurements showing that the C–H absorption band from acetone was narrower in the mid-IR regime compared to ethanol. , …”
Section: Resultssupporting
confidence: 93%
See 1 more Smart Citation
“…Thus, the chalcogenide waveguide sensor was able to differentiate ethanol and acetone vapor by their distinct mid-IR C–H absorption. This result agreed with previous Fourier transform infrared spectroscopy measurements showing that the C–H absorption band from acetone was narrower in the mid-IR regime compared to ethanol. , …”
Section: Resultssupporting
confidence: 93%
“…This result agreed with previous Fourier transform infrared spectroscopy measurements showing that the C−H absorption band from acetone was narrower in the mid-IR regime compared to ethanol. 37,38 To characterize the real-time sensing performance, the analyte was prepared by mixing the diluting gas N 2 (99.999%) with the ethanol vapor at different gas flow rates. Meanwhile, the laser wavelength was adjusted to the ethanol C−H absorption band at 3.46 μm to continuously trace the ethanol concentration.…”
Section: ■ Results and Discussionmentioning
confidence: 99%
“…7 More importantly, NH stretching gas-to-matrix shifts are rationalised and incrementally reproduced by stepwise nitrogen complexation in neon and argon matrices as well as supersonic expansions. All spectra as well as harmonic density functional theory predictions show a weak, but distinct downshift of the NH stretching vibration upon hydrogen bond formation, clearly correcting a proposed unusual upshift based on anharmonic calculations and nitrogen matrix spectra 23 which has received considerable attention 22,[28][29][30] despite being challenged by more reliable calculations. 19…”
Section: Introductionsupporting
confidence: 65%
“…They include hydrogen bonding between ethanol or acetone molecules, hydrogen bonding between ethanol and acetone molecules and dipole-dipole interactions between acetone molecules. From the association of ethanol molecules, dimers, and cyclic multimers (especially trimers and tetramers) can be formed [49]. At concentrations below 55 mol%, acetone tends to self-associate rather than form hydrogen bonds with ethanol, while self-association of ethanol molecules is more favorable at ethanol concentrations below 50 mol% [47].…”
Section: Solvent Effects On Lycopene Extractionmentioning
confidence: 99%