Your browser does not support JavaScript!
Water site headerMasthead Island, Great Barrier Reef Print-me keygo to Water Visitor Book contributions
Go to my page Water Structure and Science
Non-ionising radiation

Water and Microwaves

Liquid water absorbs microwave radiation so strongly that they can be used to cook with.


link Dielectric constant and polarization
link Complex dielectric permittivity
link Dielectric spectroscopy

V Dielectric loss
V Effect of salt
V Electromagnetic penetration


The microwave oven is part of modern life, but how do the microwaves interact with water in food to efficiently heat the food? The water dipole a attempts to continuously reorient in electromagnetic radiation's oscillating electric field (see external applet). Dependent on the frequency the dipole may move in time to the field, lag behind it or remain apparently unaffected. When the dipole lags behind the field then interactions between the dipole and the field leads to an energy loss by heating, the extent of which is dependent on the phase difference of these fields; heating being maximal twice each cycle [455]. d The ease of the movement depends on the viscosity and the mobility of the electron clouds. In water these, in turn, depend on the strength and extent of the hydrogen bonded network. In free liquid water this movement occurs at GHz frequencies (microwaves) whereas in more restricted 'bound' water it occurs at MHz frequencies (short radiowaves) and in ice at kHz frequencies (long radiowaves). The re-orientation process may be modeled using a 'wait-and-switch' process where the water molecule has to wait for a period of time until favorable orientation of neighboring molecules occurs and then the hydrogen bonds switch to the new molecule [343]. Microwave heating has been modeled using the TIP4P-FQ potential [570] and is due to the interaction of these moving dipoles. Although molecular vibrations of biomolecules may have microwave frequencies, it is not thought that such resonant coupling is significant due to their low energy compared with thermal energy and the strongly dampening aqueous environment [1331].


The applied field potential (E, volts) of electromagnetic radiation is given by;


E = Emax.cos(ωt)


where Emax is the amplitude of the potential, ω is the angular frequency in radians.second-1 and t is the time (seconds). If the polarization lags behind the field by the phase (δ, radians) then the polarization (P, coulombs) varies as


lagging cosine wave of the resultant polarisation; figure from Rainald Koch

P = Pmax.cos(ωt - δ)


where Pmax is the maximum value of the polarization.

Hence the current (I, amperes) varies as


I = (dP/dt) = -ωPmax.sin(ωt - δ)


The power (P, watts) given out as heat is the average value of (current ˣ potential). This is zero if there is no lag (that is, if δ = 0), otherwise 


P = 0.5 PmaxEmaxω.sin(δ)

[Back to Top to top of page]   

Dielectric loss

It is convenient to express the relative permittivity (dielectric constant) in terms of a complex number (εr*, complex dielectric permittivity) defined as:

εr* = εr´ - iLf 


Where εr´ is the ability of the material to be polarized by the external electric field, Lf (the loss factor, sometimes given as ε") quantifies the efficiency with which the electromagnetic energy is converted to heat and i = i. This equation may be visualized by considering the total current as the vector sum of the charging current and the loss current; the angle δ as the phase difference (lag) between the electric field and the resultant (orientation) polarization of the material (see similar treatment in rheology).

tan(delta) = loss current/charging current


tan(δ) = loss current/charging current = Lfr´

(see derivation)


The terms (εr*, εr´, Lf ) are all affected by the frequency of radiation; the relative permittivity (εr´, dielectric constant) at low frequencies (εS, static region c) and at high ( visible) frequencies the (ε, optical permittivity) are the limiting values. The relative permittivity changes with the wavelength (and hence frequency):


relative permittivity = optical permittivity + ((static permittivity - optical permittivity)/(1 + (critical frequency/frequency)squared)))


where εS is the relative permittivity at low frequencies (static region), and λS is the critical wavelength (maximum dielectric loss).

relative permittivity = optical permittivity + ((static permittivity - optical permittivity)/(1 +  angular frequency squared x relaxation time squared))                 (see more on complex dielectric permittivity)

where τ is the relaxation time (a measure of the time required for water to rotate (relaxation time = 4 x pi x viscosity x radius cubed/(Boltzman constant x temperature)where  r is the molecular radius, k is the Boltzmann constant and η is the viscosity), also considered as the delay for the particles to respond to the field change, or for reversion after disorientation. The maximum loss occurs when ω = 1/τ b. For water at 25 °C, τ is 8.27 ps (for hexagonal ice at 0 °C, τ ~20 µs) and r is half the (diffraction-determined) inter-oxygen distance (1.4 Å).


Shows the dimensionless dielectric and dielectric loss reducing with temperature at the microwave oven frequency 2.45 GHz

Figure 1. Dielectric permittivity and dielectric loss of water between 0 °C and 100 °C, the arrows showing the effect of increasing temperature (data is indicative only but based on [64, 135]; exact data is plotted below) or increasing water activity. The wavelength range 0.01 - 100 cm is equivalent to 3 THz - 0.3 GHz respectively. As the temperature increases, the strength and extent of the hydrogen bonding both decrease. This (1) lowers both the static and optical dielectric permittivities, (2) lessens the difficulty for the movement dipole and so allows the water molecule to oscillate at higher frequencies, and (3) reduces the drag to the rotation of the water molecules, so reducing the friction and hence the dielectric loss. Note that ε (that is, the dielectric permittivity at short wavelengths) does not change significantly with temperature. Most of the dielectric loss is within the microwave range of electromagnetic radiation (~1 - ~300 GHz, with wavenumber 0.033 cm-1 - 10 cm-1, and wavelength 0.3 m - 1.0 mm respectively). The frequency for maximum dielectric loss lies higher than the 2.45 GHz (wavenumber 0.0817 cm-1, wavelength 12.24 cm) produced by most microwave ovens. This is so that the radiation is not totally adsorbed by the first layer of water it encounters and may penetrate further into the foodstuff, heating it more evenly; unabsorbed radiation passing through is mostly reflected back, due to the design of the microwave oven, and absorbed on later passes.

Dielectric behavior of water and ice [2171]




Water and ice Ih show similar dielectric behavior at the melting point but separated by about 106 Hz, see left [2171]. d

Cole-Cole plot for water



The above data can also be plotted using a Cole-Cole plot, as opposite, of the dielectric permittivity versus the dielectric loss. The red circular arcs show the effects of temperature varied by 20 °C amounts from O °C to 100 °C, whereas the blue lines shows the variation with temperature at fixed wavelengths (1.3 - 201 GHz). Also shown for comparison is the plot (dashed line) for pure bulk ice [1230] (note the much lower frequencies). to top of page

Shows dielectric and dielectric loss changing with temperature ; includes the microwave oven frequency 2.45 GHz


Note that the shifts in the dielectric properties with temperature gives rise to maxima in the temperature behavior at constant frequency.


Plotted opposite are equations derived for pure water over the range for -20 °C ~ +40 °C [683], extrapolated (dashed lines) to indicate trends. The equations that generate these curves involve 15 optimized parameters. Further data has been published [1185].


The temperature effect on the dielectric relaxation time is shown on another page.

The dielectric loss factor (Lf) increases to a maximum at the critical frequency.


Loss factor= (static permittivity - optical permittivity) x (critical frequency/frequency))/(1 + (critical frequency/frequency)squared)                 Loss factor = (static permittivity - optical permittivity) x angular frequency x relaxation time /(1 +  angular frequency squared x relaxation time squared


Pressure has a considerable effect on the dielectric behavior of water. The effect of increased pressure on the dielectric and dielectric loss is to shift the curves to lower frequencies, such that the peak in the dielectric loss shifts to about 4 kHz at about -20 °C and 200 MPa [2072].

[Back to Top to top of page]   

Effect of salt

Dissolved salt depresses the relative permittivity (dielectric constant) dependent on its concentration (C ) and the average hydration number of the individual ions (HN)

relative permittivity = optical permittivity + ((static permittivity - (2 x ion hydration number x concentration) - optical permittivity)/(1 +  angular frequency squared x relaxation time squared))


Shows dielectric reducing but dielectric loss increasing with temperature at the microwave oven frequency, 2.45 GHz
Figure 2. Dielectric and dielectric loss of a dilute salt solution between 0 °C and 100 °C (dashed lines; the solid lines shows the pure water curves as Figure 1 above), the arrows showing the effect of increasing temperature. Data is indicative only; exact data is plotted below. The salt decreases the natural structuring of the water so reducing the static dielectric permittivity, in a similar manner to increased temperature. At the lower frequencies the ions are able to respond and move with the changing potential so producing frictional heat and increasing the loss factor (Lf). Thus whereas water becomes a poorer microwave absorber with rising temperature, a lossy salty food such as salt meat becomes a better microwave absorber with rising temperature. The rate that the temperature of such lossy salty food rises on microwaving increases as it is proportional to this increasing loss factor and inversely proportional to the density times specific heat (which change less with temperature); that is, the hotter it gets, the quicker it gets hotter. to top of page


Shows dielectric and dielectric loss changing with temperature  for a 1% w/w  salt solution



Plotted opposite are equations derived at 10 parts per thousand w/w (ppt) salinity for the range for -20 °C ~ +40 °C [683], extrapolated (dashed lines) to indicate trends. Further recent data is available [1074].

Dielectric and dielectric loss changing with temperature and salinity at the microwave oven frequency 2.45 GHz



Plotted opposite are equations derived at 2.45 GHz (typical microwave oven frequency) for different parts per thousand w/w (ppt) salinity for the range for -20 °C ~ +40 °C [683], extrapolated (dashed lines) to indicate trends. The equations that generate these curves involve 46 optimized parameters.

The dielectric loss is increased by a factor that depends on the conductivity (Λ, S cm2 mol-1; S = siemens = mho), concentration and frequency. It increases with rise in temperature and decreasing frequency.


Loss factor = ((static permittivity - (2 x ion hydration number x concentration) - optical permittivity) x (angular frequency x relaxation time)/(1 +  angular frequency squared x relaxation time squared)) + conductivity x concentration/(1000 x angular frequency x vacuum permittivity)


Ensuring that all units are SI, the 1000 factor in the denominator goes. This 1000 is a conversion between SI and cm, mol, L units. This emphasizes that careful consideration must be given to the units used in the microwave literature.

Bound water and ice have critical frequencies (λS) at about 10 MHz (τ about 0.1 μs) with raised static dielectric permittivities (εS). At the much higher frequency of microwave ovens such water has a low dielectric permittivity (for example, ice-1h, ε = 3.1; compare ice-1h, εS = 97.5 [94];  εS water (0 °C) = 87.9), and is almost transparent, absorbing little energy. This is particularly noticed on thawing where the thawed material may get very hot whilst unthawed material stays frozen. Therefore for balanced heating the thermal effects must be evenly distributed, that is, there should not be pockets of salty water within a poorly conducting matrix. [Back to Top to top of page]

Electromagnetic penetration

The electromagnetic penetration is infinite in a perfectly transparent substance and zero in reflective material (for example, metals). At the microwave oven frequency (2.45 GHz, λ = 12.24 cm), most energy is absorbed by water. The attenuation (α) is given by:


Attenuation = (2 x pi/wavelength) x square root of half (relative permittivity x  (square root of (1 + tan delta squared) - 1))



if tanδ is « 1

(square root of (1 + tan delta squared) - 1) approximately equals  tan delta squared


This equation may be approximated where the attenuation is (approximately) directly proportional to the loss factor and inversely proportional to the wavelength times the square root of the relative dielectric constant:


Attenuation = pi x loss factor/(wavelength x square root of (relative permittivity)) = (pi x tan delta x square root of (relative permittivity ))/frequency


For a plane wave, incident microwaves decrease to 1/e (0.36788; that is, 63% absorbed) in a penetration distance Dp given approximately by:


Penetration distance = 1/(2 x attenuation) = wavelength/(2 x pi x tan delta x square root of (relative permittivity ))]
Penetration distance in cm = 1.947 x square root of relative permittivity/loss factor


and so at 2.45 GHz:



Thus, using water at 25 °C, εr´ = 78. Lf =12, tanδ = 0.15, λ = 12.24 cm and Dp = 1.4 cm but the effect is much greater in supercooled water (that may be present in frozen food) where at -17.78 °C (that is, 0 °F), εr´ = 74.4. Lf =40.1, tanδ = 0.54 and Dp = 0.43 cm [1074].


The amount of power (P, in watts m-3) that is absorbed is given by:


P = 2πfε0LfE2


where ε0 = 8.854x10-12 F m-1, f is the frequency (Hz, = ω/2π) and E is the potential gradient (V m-1). [Back to Top to top of page]



a Hydroxyl groups in sugars and polysaccharides behave similarly, creating a high shear environment. Fats exhibit a lesser effect but their lower specific heat gives rise to rapid heating. [Back]


b Note the relaxation time is the reciprocal of the frequency in radians per second whereas the electromagnetic frequency is commonly reported in cycles per second (Hz). [Back]


c The change of static permittivity with temperature (-35 °C < t < 100 °C) may be approximated by the equation εS(t)=A.e-bt where A= 87.85306 and b=0.00456992 [588]. [Back]


d Due to the observed similarity of the dielectric spectra of water and ice (as they show the similar graphics, only shifted along the frequency axis by six decades), the dielectric spectra has been explained using the assumption of a random walk diffusion of protons without considering the H2O dipole orientations. This is shown to be sufficient to describe both the experimental dielectric spectra of water and ice, as well as their transformation at the freezing-melting point of 0 °C [2171]. [Back]



Home | Site Index | Theory and definitions | Complex dielectric permittivity | Microwaves and health | Water molecule  | Water spectra | Notes | LSBU | Top


This page was established in 2001 and last updated by Martin Chaplin on 1 February, 2017

Creative Commons License
This work is licensed under a Creative Commons Attribution
-Noncommercial-No Derivative Works 2.0 UK: England & Wales License