The electric dipole moment (μ) of a molecule is directed from the center of negative charge (-q) to the center of positive charge (+q) distance r away. The units are usually given in Debye (= 3.336 x 10-30 A s m).
μ = qr
In liquid water, molecules possess a distribution of dipole moments (range ~1.9 - 3.1 D) due to the variety of hydrogen bonded environments.
If two charges q1 and q2 are separated by distance r, the (Coulomb) potential energy is V (joule)
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where ε0 is the permittivity of a vacuum (= 8.854 x 10-12 C2 J-1 m-1; the ability of a material to store electrostatic energy).
In a medium it is lower
where ε is the medium's permittivity.
The dielectric constant (εr) of the medium (also known as the relative permittivity) is defined as
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and clearly approaches unity in the dilute gas state. In liquid
water, it is proportional to the mean-square fluctuation in the
total dipole moment. In liquid water, the dielectric
constant is high and there is a linear correlation between it
and the number of hydrogen bonds [239]. [Back to Top
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The polarization (P) of a substance is its electric dipole moment density (see also). The charge density vector (D) is the sum of the effect of the applied field and the polarization.
D = ε0E + P
But as
D = εE
P = (εr - 1)ε0E
The dielectric constant (εr) is related to the molar polarization of the medium (Pm) using the Debye equation

where ρ is the mass density (kg m-3), M is the molar mass (kg). At high dielectric constant, such as water, the left hand side of the above equation approximates to unity and the molar polarization (calculated from equation(1) below = 181.5x10-6 m3 at 25°C) should approximate to the molar volume (18.0685x10-6 m3 at 25°C) but it clearly does not in the case of water. The molar polarization of the medium (Pm) is defined as
where α is the polarizability of the molecules, which is the proportionality constant between the induced dipole moment μ* and the field strength E (μ* = αE), NA is the Avogadro number, Mk is the Boltzmann constant (=R/NA), T is the absolute temperature and μ is permanent dipole moment. Unfortunately, in line with many other anomalies of water, this equation is not a good predictor for the behavior of water, which shows a minimum molar polarization at about 15°C. The term in (εr + 2) comes from the relationship between the local field (E') and the applied field (E).
E' = (E/3)(εr + 2)
The polarizability (α) may be given as the polarizability volume (α´) where
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The second term in equation (1) is due to the contribution from the permanent dipole moment, which is negligible when the medium is non-polar or when the frequency of the applied field is sufficiently high that the molecules do not have time to change orientation. In this case the Clausius-Mossotti equation holds (but again not for water):
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The refractive index (ηr) in the visible and ultraviolet is the ratio of the speed of light in a vacuum (c) to that in the medium (c´); ηr = c/c´. It is also related to the relative permittivity (εr), the absorption coefficient (α) and wavelength (λ) [177].

This reduces to ε∞ = ηr2 where ε∞ is the relative permittivity at visible frequencies (4x1014 - 8x1014 Hz, ηr ~ 1.34) and εS = ηr2 where εS is the relative permittivity
at low frequencies (static region; < 109 Hz, ηr ~ 9). It also follows that, as the temperature is raised, εr tends towards ηr2 [423]. [Back to Top
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This page was last updated by Martin Chaplin on 25 June, 2008