Dielectric Properties of Water at Microwave Frequencies

DOI : 10.17577/IJERTCONV3IS03027

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Dielectric Properties of Water at Microwave Frequencies

Ravika Vijay1, Ritu Jain2 and K. S. Sharma2

1Department of Physics, Poornima Group of Institution, Jaipur 302022 2 Department of Physics, The IIS University, Jaipur 302020

Abstract The complex permittivity of water was measured, .

in terms of the dielectric constant (') and dielectric loss factor ('') over the frequency range from 1 GHz to 50 GHz and

  1. MATERIAL AND METHOD

    temperatures ranging from 300C to 600C. The PNA network analyzer model E8364C and open ended coaxial probe 85070E

    were used for the analysis. '-f and ''-f curves plotted at different temperatures. ' decreases with increasing frequency at all temperatures. In frequency range 9-10 GHz, dispersion region is found. '' increase with increasing frequency, a peak value is obtained at frequency about 19.5 GHz (relaxation frequency) and then show decreasing trend with increasing frequency at lower temperature (300C). As the temperature

    increases, reduces the drag to the rotation of the water molecules, so reducing the friction and hence the dielectric loss. As the temperature increases, the relaxation time decreases, and the loss factor peak shift to higher frequencies. In this frequency range re-orientation process of water molecules is observed.

    Keywords dielectric constant, dielectric loss factor, relaxation frequency, temperature, water.

    1. INTRODUCTION

      The dielectric behaviour of pure water has been the subject of study in numerous laboratories over the past fifty years. As a result there is a good understanding of how the complex permittivity * = – j " varies with frequency from DC up to a few tens of GHz and it is generally agreed that the dielectric dispersion in this range can be represented either by the Debye equation or by some function involving a small distribution, of relaxation times [1]. The interactions of electromagnetic fields with materials are described through the fundamental electrical property i.e., relative permittivity of the material.

      Distilled water as needed for the present research was obtained from the Chemistry lab CEERI, Pilani. The dielectric constant (') and loss factor ('') of the water were measured in the frequency range 1 GHz to 50 GHz by using a PNA network analyzer, model Agilent E8364C. The test probe consists of an open ended coaxial probe system (Agilent, 85070E). The system software calculates the dielectric properties of the sample from the changes in the phase and amplitude of the microwave signal delivered by the probe of open-ended coaxial line due to reflection at the interface with the sample to be analyzed. The calibration of the Network analyzer was done by using three different loads, viz., (i) air,

      (ii) a short circuit with the metal contacts, and (iii) distilled water at room temperature. After calibration, the analyzer and the probe system were tested by taking measurements on a standard liquid (methanol, in the present case) of known dielectric properties. The measured values of dielectric constant (') and loss factor ('') for methanol at frequencies 1 to 50 GHz at room temperature (250C) are displayed in Fig. 1, along with standard dielectric data (up to 5 GHz) reported by Gregory and Clarke [5] and the values reported by Mishra et al. [6] up to 20 GHz. The values of dielectric parameters for methanol above 20 GHz are not available in literature for a meaningful comparison.

      80

      '

      The relative permittivity (*) is also a complex quantity with real and imaginary components given by Risman [2].

      * = – j " [1]

      where, is the real component of * (called as dielectric constant) and = imaginary component of * (called as dielectric loss factor), and j appearing in equation 1.2 is a imaginary unit (= -1). The real component of the permittivity (i.e., dielectric constant – ) represents the effective capacitance of a substance and serves as a measure of the ability of the substance to store electrical energy. The

      70 '

      60

      Permittivity

      Permittivity

      50

      40

      30

      20 ''

      10

      0

      ''

      imaginary component, (i.e., the dielectric loss factor – ) is related to various mechanisms of energy absorption, responsible for energy dissipation in the material and is always positive and usually much smaller in magnitude than dielectric constant. The substance is lossless if dielectric loss factor = 0 [3-4].

      0 10 20 30 40 50

      Fig. 1. Variation of dielectric Constant (') and loss factor ('') of water with frequency at room temperature (250C)

      35

      ' measured values

      ' Misra et al. up to 20 GHz

      ' NPL Data up to 5 GHz

      '' measured values

      '' Misra et al. up to 20 GHz

      '' NPL Data up to 5 GHz

      ' measured values

      ' Misra et al. up to 20 GHz

      ' NPL Data up to 5 GHz

      '' measured values

      '' Misra et al. up to 20 GHz

      '' NPL Data up to 5 GHz

      30

      '

      '

      25

      Permittivity

      Permittivity

      20

      15

      10

      ''

      ''

      5

      0

      0 10 20 30 40 50

      Frequency (f) (GHz)

      oscillations of dipoles are faster and since at high temperatures molecular agitations also increase. At high temperatures, increased molecular agitations and rapid oscillations under the influence of high frequency EM radiation result in fluctuations in ' values, giving rise to zig- zag behavior, i.e., ups and downs in '-f curves at high temperatures in the high frequency region (35 50 GHz).

      30 C

      40 C

      50 C

      60 C

      30 C

      40 C

      50 C

      60 C

      80

      70

      Dielectric Constant (')

      Dielectric Constant (')

      60

      50

      Fig. 2. Variation of dielectric constant (') and loss factor ('') of methanol with frequency at room temperature (250C)

      Dielectric polarization under the influence of external electric field and lagging of the polarization vector behind the high frequency electric field by virtue of the inertia of the molecules, are the phenomenon responsible for the frequency dependence of dielectric properties [7]. The temperature dependence of the dielectric properties of materials is a complex phenomenon. It may increase or decrease with the temperature depending on the nature of material.

  2. RESULT AND DISCUSSIONS

    In its pure form, water is a classic example of a polar dielectric. The water molecules behave as dipoles with dipole moment 6.2 x 10-30 Coulomb-meter. In Figs. 3 and 4, variation of dielectric constant (') and loss factor ('') respectively of water with frequency is shown for temperatures (30°C to 60°C) over the frequency range 1 GHz to 50 GHz. From Fig. 3, it is observed that as the frequency is increased from 1 GHz to 50 GHz, ' decreases with frequency at all temperatures, the rate of decrease with frequency being faster at low temperatures and slow at higher temperatures. It is also observed that the '-f curves for at 300 and 400C, intersect each other at frequency 8.5 GHz, while

    40

    30

    20

    10

    0 10 20 30 40 50

    Fig. 3. Frequency dependence of the dielectric constant (') of water at indicated temperatures

    This is because in liquid water the molecular stretching and molecular librations shif the frequency of molecular vibrations to higher side, on raising the temperature (as hydrogen bonding weakens at higher temperatures, the covalent O-H bonds strengthen causing them to vibrate at higher frequencies) [8].

    40

    35

    Dielectric loss factor ('')

    Dielectric loss factor ('')

    30

    the curves at 500 and 600C, intersect each other at frequency 25

    14.5 GHz. Thus, the '-f curves for different temperatures intersect each other somewhere in the frequency region (8.5 GHz f 14.5 GHz). These curves show dielectric dispersion to this intersection frequency region. Below this frequency region (f < 8.5 GHz) ' decreases with increasing temperature whereas above this frequency region (f > 14.5 GHz) ' increases with increasing temperature. This behavior of variation of ' with frequency at different temperatures may be attributed to the effect of temperature on the

    dispersion of EM waves in water. Further, it can be noticed from Fig. 4.3 that at low temperature (300C), a smooth curve of '- f is obtained, but at higher temperatures (40- 600C) and at higher frequencies (35- 50 GHz) overlapping of many absorption peaks are observed. When temperature is increased, both the strength and extent of the hydrogen bonding decrease. These results in lowering of dielectric constant at low frequencies but at high frequencies

    20

    30 C

    15 40 C

    50 C

    10 60 C

    5

    0

    0 10 20 30 40 50

    Fig. 4. Frequency dependence of the dielectric loss factor ('') of water at indicated temperatures

    From Fig. 4, it is observed that at low temperature (300C)

    dielectric loss factor ('') of water increases with increasing frequency, acquires a maximum value at a frequency of about

    19.5 GHz (relaxation frequency) and then slowly decreases with increasing frequency. A smooth ''-f curve is obtained at this temperature (300C). An increase in temperature, reduces

    the drag associated with the rotation of the water molecules, so reducing the friction and hence the dielectric loss. As such, in the low frequency region the value of '' at a particular frequency decreases as the temperature is increased as observed from Fig. 4. As the temperature increases, the relaxation time decreases (i.e., relaxation frequency increases) and hence the loss factor maxima shifts to higher frequencies, as evidenced by Fig. 4, from which it is apparent that the maxima in ''-f curves shifts from 19.5 GHz to about

    38.0 GHz as the temperature is increased from 300C to 600C. In the higher frequency range (30 50 GHz) where the operating frequency is greater than the relaxation frequency, re-orientation process of water molecules is becomes active. The re-orientation process may be modeled by using a wait-

    and-switch process where the water molecules have to wait for a period of time until favorable orientation of neighboring molecules occurs and then the hydrogen bonds switch to the new molecule [9]. At these frequencies (30 to 50 GHz) and at higher temperatures (40 to 600C), multiple relaxation losses are observed.

  3. CONCLUSION

The dielectric properties of fresh juice of water can be efficiently and accurately measured by E8364C PNA network analyzer and 85070E coaxial probe in the frequency range 1 GHz to 50 GHz. The present values of ' and '' are found to be in good agreement with the values reported by other researcher. These measurements may be useful in dielectric heating applications and for quality sensing application as well for developing new techniques.

ACKNOWLEDGMENT

The authors are grateful to the Vice Chancellor, The IIS University for providing necessary facilities for this work. They are also grateful to Emeritus Scientist Dr. S. N. Joshi, and Gyrotron Laboratory, CEERI, Pilani, India for useful discussions and permitting use of the Network Analyzer for this work. Ravika Vijay also, thanks Director, Poornima Foundation, Jaipur for permitting her to take up this research work.

REFERENCES

  1. E. H. Grant, S. Sznowski, and R. J. Sheppard, Biological Effects of Nonionizing Radiation, Chapter 2, Vol. 157, pp. 4756 ACS Symposium Series, 1981.

  2. P.O. Risman, Terminology and notation of microwave power and electromagnetic energy, Microw Power Electromagn Energy, Vol. 26, pp. 243250, 1991.

  3. R. E. Mudgett, Electrical properties of foods, In: Engineering Properties of Foods (Edited by M. A. Rao and S. S. H. Rizvi), pp. 329 390, Marcel Dekker, New York. 1986.

  4. E. Nyfors, and P. Vainikainen, Industrial microwave sensors, Chapter

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  5. A. P. Gregory, and R. N. Clarke Tables of the complex permittivity of dielectric reference liquids at frequencies up to 5 GHz, NPL Report (CETM 33) (2012).

  6. D. Misra, M. Chabbra, R. Epstein Benjamin, M. Mirotznik, and R. Foster Kenneth, Noninvasive Electrical Characterization of Materials at Microwave Frequencies Using an Open- Ended Coaxial Line: Test of an Improved Calibration Technique, IEEE Trans on Microwave Theory and Techniques, Vol. 38, pp. 8-14. 1990.

  7. M. S. Venkatesh, and G. S. V. Raghavan, An overview of microwave processing and dielectric properties of agri-food materials, Biosystem Eng. Vol. 88, pp. 118, 2004.

  8. M. Praprotnik, D. Janezic, and J. Mavri, Temperature dependence of water vibrational spectrum: a molecular dynamics simulation study, J. Phys. Chem. A. Vol. 108, pp. 11056-11062, 2004.

  9. U. Kaatze, R. Behrends and R. Pottel, Hydrogen network fluctuations and dielectric spectrometry of liquids, J. Non-Cryst. Solids, Vol. 305, pp. 19-28, 2002.

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