Effects of nonpolar solutes on the thermodynamic response functions of aqueous mixtures.

نویسندگان

  • Swaroop Chatterjee
  • Henry S Ashbaugh
  • Pablo G Debenedetti
چکیده

We investigate the effect of adding nonpolar solutes at atmospheric pressure on water's temperature of maximum density, isothermal compressibility, and isobaric heat capacity, using a statistical mechanical model of water solutions [H. S. Ashbaugh, T. M. Truskett, and P. G. Debenedetti, J. Chem. Phys. 116, 2907 (2002)]. We find that the temperature of maximum density increases with solute hydrophobicity, as characterized by its size, and decreases with its van der Waals attractive parameter a, in agreement with experiment. We predict similar trends for the addition of solutes on the isothermal compressibility and isobaric heat capacity: solute hydrophobicity causes an upward shift in water's anomalies, whereas dispersive interactions as measured by the solute's van der Waals attractive parameter shift the anomalies to lower temperatures. The locus along which the competing contributions of solute size sigma and interaction strength a to the shift in water's response functions balance each other obeys the scaling relationship sigma6 approximately a.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

A simple molecular thermodynamic theory of hydrophobic hydration

A recently developed microscopic model for associating fluids that accurately captures the thermodynamics of liquid water @Truskett et al., J. Chem. Phys. 111, 2647 ~1999!# is extended to aqueous solutions with nonpolar species. The underlying association model incorporates the highly directional and open nature of water’s hydrogen-bond network, and, as a result, captures a number of the distin...

متن کامل

Activity of water in aqueous systems; a frequently neglected property.

In this critical review, the significance of the term 'activity' is examined in the context of the properties of aqueous solutions. The dependence of the activity of water(l) at ambient pressure and 298.15 K on solute molality is examined for aqueous solutions containing neutral solutes, mixtures of neutral solutes and salts. Addition of a solute to water(l) always lowers its thermodynamic acti...

متن کامل

Estimating partition coefficients for fuel-water systems: developing linear solvation energy relationships using linear solvent strength theory to handle mixtures.

In many environmental transport problems, organic solutes partition between immiscible phases that consist of liquid mixtures. To estimate the corresponding partition coefficients, we evaluated the efficacy of combining linear solvation energy relationships (LSERs) developed for pure 1:1 systems via application of linear solvent strength theory. In this way, existing LSERs could be extended to ...

متن کامل

Structure and Thermodynamic Properties of Aqueous Solutions of Small Molecules and Proteins

Ab4'uci.t — The structures and reactivities of proteins are markedly influenced by water. In conformational energy calculations, the hydration of proteins is treated by a hydration-shell model. Originally, the shell model was parameterized with exoerimental data, but more recently empirical potentials were introduced to obtain these parameters by Monte Carlo and molecular dynamics techniques. T...

متن کامل

Origins of protein denatured state compactness and hydrophobic clustering in aqueous urea: inferences from nonpolar potentials of mean force.

Free energies of pairwise hydrophobic association are simulated in aqueous solutions of urea at concentrations ranging from 0-8 M. Consistent with the expectation that hydrophobic interactions are weakened by urea, the association of relatively large nonpolar solutes is destabilized by urea. However, the association of two small methane-sized nonpolar solutes in water has the opposite tendency ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • The Journal of chemical physics

دوره 123 16  شماره 

صفحات  -

تاریخ انتشار 2005