The total molecular dipole moment for liquid water

نویسندگان

  • Anna V. Gubskaya
  • Peter G. Kusalik
چکیده

For the water molecule, the dipole is the first nonzero multipole moment; it represents the polarity of the molecule and has been widely used in describing solvation behavior. A rather wide range of theoretically determined values for the total molecular dipole moment of water in condensed phases has been reported in the literature. This paper describes a means by which the average total dipole moment for the water molecule in the liquid state can be linked to experimental refractive index data. Three components comprise the mean-field approach that is employed. A formal framework is developed that relates the temperature dependence of the effective molecular polarizability to the average local electric field experienced by a liquid water molecule over a chosen temperature range. A characterization of the distributions of local fields and field gradients is also necessary, and this has been determined from the computer simulations of liquid water samples at several different temperatures for two standard water potentials. The final component, the electric response properties of the water molecule ~including nonlinear contributions up to fourth order!, were determined from ab initio calculations for gasand liquid-phase molecules, and are reported elsewhere @A. V. Gubskaya and P. G. Kusalik, Mol. Phys. 99, 1107 ~2001!#. By combining these three components, the temperature dependence of the average local electric field, and consequently the average total dipole moment, are extracted from data for the refractive index of liquid water. An almost 10% variation in the dipole moment with temperature is observed over the range 273 to 373 K. The value obtained for the molecular dipole moment at 300 K, 2.9560.2 D, is in excellent agreement with a recently reported result extracted from x-ray scattering data, as well as with some recent theoretical predictions. © 2002 American Institute of Physics. @DOI: 10.1063/1.1501122#

برای دانلود رایگان 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

An Improved ISM Equation of State for Polar Fluids

We developed an equation of state (EOS) by Ihm, Song, and Mason (ISM) for polar fluids. The model consists of four parameters, namely, the second virial coefficient, an effective van der Waals co-volume, a scaling factor, and the reduced dipole moment. The second virial coefficient is calculated from a correlation that uses the heat of vaporization, and the liquid density at the normal boiling ...

متن کامل

A Molecular-Based Equation of State for Vapour-liquid Equilibrium of Pure Substances

A semi-empirical equation of state has been studied for modelling vapour-liquid data of pure substances. The specific molecular based equation of state is employed here as basis because of its mathematical simplicity. The semi-empirical extension has been accomplished to real fluids by correlating the density dependence of the attraction term to vapour liquid data of a reference fluid. The resu...

متن کامل

Dipole moment of water molecules in narrow pores

We use ab initio molecular dynamics simulation to calculate the dipole moment of water molecules in one-dimensional hydrogen bonded chains in narrow pores. The electronic charges are partitioned among the water molecules using maximally localized Wannier functions. For water molecules confined to the interior of a carbon nanotube we find an average dipole moment of about 2.7 D, almost 10 % lowe...

متن کامل

Electronic polarization of liquid water: converged Monte Carlo-quantum mechanics results for the multipole moments

Sequential Monte Carlo/Quantum Mechanical (S-MC/QM) calculations of the dipole moment of liquid water using extensive and different quantum chemical methods and statistically converged results give an induced dipole moment of 0:74 0:14 D. This corresponds to a dipole moment of liquid water of 2:60 0:14 D, in excellent agreement with the value derived from the dielectric constant and other previ...

متن کامل

Hydrogen bonding and induced dipole moments in water: predictions from the Gaussian charge polarizable model and Car-Parrinello molecular dynamics.

We compare a new classical water model, which features Gaussian charges and polarizability (GCPM) with ab initio Car-Parrinello molecular dynamics (CPMD) simulations. We compare the total dipole moment, the total dipole moment distribution, and degree of hydrogen bonding at ambient to supercritical conditions. We also compared the total dipole moment calculated from both the electron density (p...

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

عنوان ژورنال:

دوره   شماره 

صفحات  -

تاریخ انتشار 2002