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Clustering mechanism of ethanol-water mixtures investigated with photothermal microfluidic cantilever deflection spectroscopy.


ABSTRACT: The infrared-active (IR) vibrational mode of ethanol (EtOH) associated with the asymmetrical stretching of the C-C-O bond in pico-liter volumes of EtOH-water binary mixtures is calorimetrically measured using photothermal microfluidic cantilever deflection spectroscopy (PMCDS). IR absorption by the confined liquid results in wavelength dependent cantilever deflections, thus providing a complementary response to IR absorption revealing a complex dipole moment dependence on mixture concentration. Solvent-induced blue shifts of the C-C-O asymmetric vibrational stretch for both anti and gauche conformers of EtOH were precisely monitored for EtOH concentrations ranging from 20-100%?w/w. Variations in IR absorption peak maxima show an inverse dependence on induced EtOH dipole moment (?) and is attributed to the complex clustering mechanism of EtOH-water mixtures.

SUBMITTER: Ghoraishi MS 

PROVIDER: S-EPMC4820714 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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Clustering mechanism of ethanol-water mixtures investigated with photothermal microfluidic cantilever deflection spectroscopy.

Ghoraishi M S MS   Hawk J E JE   Phani Arindam A   Khan M F MF   Thundat T T  

Scientific reports 20160405


The infrared-active (IR) vibrational mode of ethanol (EtOH) associated with the asymmetrical stretching of the C-C-O bond in pico-liter volumes of EtOH-water binary mixtures is calorimetrically measured using photothermal microfluidic cantilever deflection spectroscopy (PMCDS). IR absorption by the confined liquid results in wavelength dependent cantilever deflections, thus providing a complementary response to IR absorption revealing a complex dipole moment dependence on mixture concentration.  ...[more]

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