Electroacoustic phenomena

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Electroacoustic phenomena arise when ultrasound propagates through a fluid containing ions. The associated particle motion generates electric signals because ions have electric charge. This coupling between ultrasound and electric field is called electroacoustic phenomena. Fluid might be a simple Newtonian liquid, or complex heterogeneous dispersion, emulsion or even a porous body. There are several different electroacoustic effects depending on the nature of the fluid.

Ion Vibration Current[edit]

Historically, the IVI is the first known electroacoustic effect. It was predicted by Debye in 1933.[1] He pointed out that the difference in the effective mass or friction coefficient between anion and cation would result in different displacement amplitudes in a longitudinal wave. This difference creates an alternating electric potential between various points in sound wave. This effect was extensively used in 1950's and 1960s for characterizing ion solvation. These works are mostly associated with names of Zana and Yaeger, who published a review of their studies in 1982.[2]

Streaming Vibration Current[edit]

Streaming Vibration Current was experimentally observed in 1948 by Williams.[3] A theoretical model was developed some 30 years later by Dukhin and others.[4] This effect opens another possibility for characterizing the electric properties of the surfaces in porous bodies. A similar effect can be observed at a non-porous surface, when sound is bounced off at an oblique angle. The incident and reflected waves superimpose to cause oscillatory fluid motion in the plane of the interface, thereby generating an AC streaming current at the frequency of the sound waves.[5]

Double Layer Compression[edit]

The electrical double layer can be regarded as behaving like a parallel plate capacitor with a compressible dielectric filling. When sound waves induce a local pressure variation, the spacing of the plates varies at the frequency of the excitation, generating an AC displacement current normal to the interface. For practical reasons this is most readily observed at a conducting surface.[6] It is therefore possible to use an electrode immersed in a conducting electrolyte as a microphone, or indeed as a loudspeaker when the effect is applied in reverse.[7]

Colloid Vibration Potential / Current[edit]

Colloid vibration potential measures the AC potential difference generated between two identical relaxed electrodes, placed in the dispersion, if the latter is subjected to an ultrasonic field. When a sound wave travels through a colloidal suspension of particles whose density differs from that of the surrounding medium, inertial forces induced by the vibration of the suspension give rise to a motion of the charged particles relative to the liquid, causing an alternating electromotive force. The manifestations of this electromotive force may be measured, depending on the relation between the impedance of the suspension and that of the measuring instrument, either as colloid vibration potential or as colloid vibration current. [8]

Colloid Vibration Potential/Current was first reported by Hermans and then independently by Rutgers in 1938. It is widely used for characterizing the ζ-potential of various dispersions and emulsions. The effect, theory, experimental verification and multiple applications are discussed in the book by Dukhin and Goetz.[9]

ElectricSonic Amplitude[edit]

Electric Sonic Amplitude was experimentally discovered by Cannon with co-authors in early 1980s.[10] It is also widely used for characterizing ζ-potential in dispersions and emulsions. There is review of this effect theory, experimental verification and multiple applications published by Hunter.[11]

Theory of CVI and ESA[edit]

With regard to the theory of CVI and ESA, there was an important observation made by O'Brien,[12] who linked these measured parameters with dynamic electrophoretic mobility μd.

 \ CVI(ESA) = A\phi\mu_d\frac{\rho_p-\rho_m}{\rho_m}


A is calibration constant, depending on frequency, but not particles properties;
ρp is particle density,
ρm density of the fluid,
φ is volume fraction of dispersed phase,

Dynamic electrophoretic mobility is similar to electrophoretic mobility that appears in electrophoresis theory. They are identical at low frequencies and/or for sufficiently small particles.

There are several theories of the dynamic electrophoretic mobility. Their overview is given in the Ref.5. Two of them are the most important.

The first one corresponds to Smoluchowski limit. It yields following simple expression for CVI for sufficiently small particles with negligible CVI frequency dependence:

 \ CVI(ESA) = A\phi\frac{\varepsilon_0\varepsilon_m\zeta\Kappa_s}{\eta\Kappa_m}\frac{\rho_p-\rho_s}{\rho_s}


ε0 is vacuum dielectric permittivity,
εm is fluid dielectric permittivity,
ζ is electrokinetic potential
η is dynamic viscosity of the fluid,
Ks is conductivity of the system,
Km is conductivity of the fluid,
ρs is density of the system.

This remarkably simple equation has same wide range of applicability as Smoluchowski equation for electrophoresis. It is independent on shape of the particles, their concentration.

Validity of this equation is restricted with the following two requirements.

First of all it is valid only for thin Double Layer, when Debye length is much smaller than particles radius a:

 {\kappa}a >> 1

Secondly, it neglect contribution of the surface conductivity. This assumes small Dukhin number:

 Du << 1

Restriction of the thin Double Layer limits applicability of this Smoluchowski type theory only to aqueous systems with sufficiently large particles and not very low ionic strength. This theory does not work well for nano-colloids, including proteins and polymers at low ionic strength. It is not valid for low- or non-polar fluids.

There is another theory that is applicable for other extreme case of thick Double Layer, when

 {\kappa}a < 1

This theory takes into consideration overlap of Double Layer that inevitably occur for concentrated systems with thick Double Layer. This allows introduction of so-called "quasi-homogeneous" approach, when overlapped diffuse layers of particles cover complete inter particle space. Theory becomes much simplified in this extreme case, as shown by Shilov and oth.[13] Their derivation predict that surface charge density σ is better parameter than ζ-potential for characterizing electroscoustic phenomena in such systems. Expression for CVI simplified for small particles follows:

 \ CVI = A\frac{2{\sigma}a}{3\eta}\frac{\phi}{1-\phi}\frac{\rho_p-\rho_s}{\rho_s}


  1. ^ Debye.P."A method for the determination of the mass of electrolyte ions"J. Chem. Phys., 1,13-16,1933
  2. ^ Zana.R. and Yeager. E. "Ultrasonic Vibration Potentials" Mod.Aspects of Electrochemistry, 14, 3-60, 1982
  3. ^ Williams.M. " An Electrokinetic Transducer" The review of scientific instruments, 19, 10, 640-646, 1948
  4. ^ Dukhin, S.S., Mischuk, N.A., Kuz'menko, B.B and Il'in, B.I. "Flow current and potential in a high-frequency acoustic field" Colloid J., 45, 5, 875-881,1983
  5. ^ Glauser, A.R., Robertson P.A., Lowe, C.R., "An electrokinetic sensor for studying immersed surfaces, using focused ultrasound" Sensors Actuators B, 80, 1, 68-82, 2001
  6. ^ F.I. Kukoz, L.A. Kukoz, "The nature of audioelectro-chemical phenomena" Russ. J. Phys. Chem. 36 (1962) pp. 367-369
  7. ^ N. Tankovsky, "Capacitive ultrasound transducer, based on the electrical double layer in electrolytes" J. App. Phys. 87 (2000) pp. 538-542
  8. ^ DELGADO, A. V.; GONZÁLEZ-CABALLERO, F.; HUNTER, R.J.; KOOPAL, L.K.; LYKLEM, J. "MEASUREMENT AND INTERPRETATION OF ELECTROKINETIC PHENOMENA". Pure Appl. Chem. (University of Granada, Granada, Spain; University of Sydney, Sydney, Australia; Wageningen University, Wageningen, The Netherlands: INTERNATIONAL UNION OF PURE AND APPLIED CHEMISTRY, PHYSICAL AND BIOPHYSICAL CHEMISTRY DIVISIO) 77 (10): 1753–1805. doi:10.1351/pac200577101753. 
  9. ^ Dukhin, A.S.; Goetz, P.J. (2002). "Electroacoustic Theory". Ultrasound for Characterizing Colloids. Elsevier. p. 153. Retrieved 2007-10-03. 
  10. ^ Oja, T., Petersen, G., and Cannon, D. "Measurement of Electric-Kinetic Properties of a Solution", US Patent 4,497,208,1985
  11. ^ Hunter, R.J. "Review. Recent developments in the electroacoustic characterization of colloidal suspensions and emulsions", Colloids and Surfaces, 141, 37-65, 1998
  12. ^ O'Brien, R.W. "Electro-acoustic effects in a dilute suspension of spherical particles" J. Fluid Mech., 190, 71-86,1988
  13. ^ Shilov, V.N., Borkovskaya, Y.B. and Dukhin A.S. "Electroacoustic theory for concentrated colloids with overlapped DLs at arbitrary ka. Application to nanocolloids and nonaqueous colloids". JCIS, 277, 347-358 (2004)

Further reading[edit]

  • Dukhin, Andrei S.; Philip J. Goetz (2002). "Electroacoustic Theory". Ultrasound for Characterizing Colloids. Elsevier. p. 153. Retrieved 2007-10-03. 


Interface and Colloid Science