1968
DOI: 10.1021/je60036a034
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Binary freezing point behavior of some normal octadecenoic acids

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Cited by 3 publications
(12 citation statements)
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“…Oleic acid has two polymorphic solid phases, with transformation temperatures at 16.5 °C (a stable form) and 13.5 °C (a metastable form). 35 However, due to the supercooling effect, the observed crystallization point for oleic acid droplets can be lower than either of the thermodynamic transformation temperatures. Oleic acid droplets, which were placed on the Ge crystal within the ATR cell, were cooled progressively while the IR spectra were monitored as a function of temperature.…”
Section: Experimental Methodsmentioning
confidence: 99%
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“…Oleic acid has two polymorphic solid phases, with transformation temperatures at 16.5 °C (a stable form) and 13.5 °C (a metastable form). 35 However, due to the supercooling effect, the observed crystallization point for oleic acid droplets can be lower than either of the thermodynamic transformation temperatures. Oleic acid droplets, which were placed on the Ge crystal within the ATR cell, were cooled progressively while the IR spectra were monitored as a function of temperature.…”
Section: Experimental Methodsmentioning
confidence: 99%
“…35 Mod et al reported on a lower transformation temperature (13.5 °C) as the solid oleic acid sample is warmed. 35 Before reaching an apparent equilibrium at 13.5 °C, oleic acid has been observed to resolidify due to the formation of a higher-melting-point crystalline modification of oleic acid during the warming process. 35 In our case, the melting point is observed at ∼12 °C (Figure 5B), indicating that this solid oleic acid was in the metastable form.…”
Section: Effects Of the Thermodynamic Phase On The Oxidation Of Oleic...mentioning
confidence: 99%
“…When the long spacings of these compounds are plotted vs. number of carbons, the three longer compounds fall squarely on a straight line (the C13 compound is slightly off the line) represented by eq 4. The calculated angle L = 2.40 + 6.60 (4) of tilt of these long-chain methyl ketones is therefore sin"1 2.40/2.54 = 70°53'.…”
Section: Resultsmentioning
confidence: 94%
“…Unless otherwise indicated, the compounds were prepared and purified by the procedures previously described for the amine salts (1), the acid-free amides (2), the N-substltuted amides (3), the octadecenoic acids (4), and the various amlnopyridlne salts (5,6). The A form of palmltamide was obtained by recrystalllzatlon of the B form from a dilute methanol solution.…”
Section: Methodsmentioning
confidence: 99%
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