2004
DOI: 10.1023/b:jory.0000041506.39568.81
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On Internal Pressure, Its Temperature Dependence, and the Structure of Liquid-Phase Systems

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Cited by 29 publications
(35 citation statements)
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“…The dependence of ∆P i /∆T on W for the microemulsions (Fig. 3) resembles the most exotic dependences of coefficient ∆P i /∆T on the composition of binary aqueous solutions [12]: first, there are two virtually linear parts with different slopes; second, there is a break on the concentration dependence of the ∆P i /∆T coefficient; and third, the sign of the ∆P i /∆T coefficient changes, i.e., there is the concentration inversion of the temperature coefficient of internal pressure.…”
Section: Resultsmentioning
confidence: 60%
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“…The dependence of ∆P i /∆T on W for the microemulsions (Fig. 3) resembles the most exotic dependences of coefficient ∆P i /∆T on the composition of binary aqueous solutions [12]: first, there are two virtually linear parts with different slopes; second, there is a break on the concentration dependence of the ∆P i /∆T coefficient; and third, the sign of the ∆P i /∆T coefficient changes, i.e., there is the concentration inversion of the temperature coefficient of internal pressure.…”
Section: Resultsmentioning
confidence: 60%
“…The internal pressure of homogeneous liquid-phase systems with a constant number of particles can be found from dilatometric measurements [12]: P i = P -T α / β T , where α is the thermal expansion coefficient and β í is the isothermal compressibility of the system. At the atmospheric pressure ( ê = ê atm ), ratio [ P /( α T / β T )] < 1 × 10 -3 ; therefore, 1 1 The exception is water near 4 ° C [11].…”
Section: Theoretical Approach To the Calculation Of Internal Pressurementioning
confidence: 99%
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