2006
DOI: 10.1007/s10953-006-9059-4
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Refractive Indices, Densities and Excess Molar Volumes of Monoalcohols + Water

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Cited by 188 publications
(149 citation statements)
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“…The red shifts of the peak position were observed with the increasing the ethanol concentration because the average of refractive index (na) of inverse opal are increasing and cause a red shift reflectance peak position. The trend curve in Figure 8c is consistent with the refractive index of ethanol-water mixture [29]. At higher ethanol concentration (>80%), the red shift reaches a plateau, which defines the detection limit of the TiO2 inverse opal film sensor.…”
Section: Ethanol Concentration Examined By Ps Opal and Tio 2 Inverse supporting
confidence: 72%
“…The red shifts of the peak position were observed with the increasing the ethanol concentration because the average of refractive index (na) of inverse opal are increasing and cause a red shift reflectance peak position. The trend curve in Figure 8c is consistent with the refractive index of ethanol-water mixture [29]. At higher ethanol concentration (>80%), the red shift reaches a plateau, which defines the detection limit of the TiO2 inverse opal film sensor.…”
Section: Ethanol Concentration Examined By Ps Opal and Tio 2 Inverse supporting
confidence: 72%
“…The most widely used is a mixing rule, when RI at a certain composition is calculated as a linear combination of the refractive indexes for the pure components [34], [35]. Our measurements for aqueous solutions did not confirm this tendency.…”
Section: Methodology Of Results Processingcontrasting
confidence: 59%
“…The e E and v E parameters represent the excess properties, which serve to correct for deviations associated with the methanol+ water mixture relative to ideal behaviour and numerical values are available in the literature (Herrá ez and Belda, 2006;Smith et al, 1998). Indeed, when mixing water with alcohols, a reorganization of the overall solution structure occurs with the formation of clusters wherein water accommodates the hydrophilic/hydrophobic organic components via H-bonding/physical interactions (Jouyban et al, 2004;Sengwa and Abhilasha, 2006;Sudo et al, 2002).…”
Section: Solvent Effects In the Hdh Of Halophenolsmentioning
confidence: 99%