Professional Documents
Culture Documents
A Parametrical Study of Disinfection With Hydrodynamic Cavitation
A Parametrical Study of Disinfection With Hydrodynamic Cavitation
com
Abstract
The physical and chemical conditions generated by cavitation bubbles can be used to destroy microorganisms and disinfect wastewater. The eect of dierent cavitation chamber designs and diverse operational parameters on the inactivation rate of Escherichia coli have
been studied and used to understand the mechanisms involved in cell disruption.
2007 Elsevier B.V. All rights reserved.
Keywords: Escherichia coli; Hydrodynamic cavitation; Ultrasonic cavitation; Disinfection; Parametrical; Venturi; Orice plates
1. Introduction
Disinfection constitutes an essential step in water treatment for public water supplies. After Pasteur and Koch
formulated the germ theory of disease, in 1881 Koch himself discovered the bactericidal properties of chlorination.
It was the beginning of the disinfection technologies.
The use of alternative technologies for disinfection
intends to overcome the weak points of the conventional
methods. Chemical biocides are usually eective and comparatively cheap, but can generate dangerous or inconvenient organic by-products (especially in chlorination). On
the other hand, physical technologies tend to be more
expensive, and UV-based techniques are inecient when
either turbidity or colorants are present due to a blocking
eect which inactivates or reduces the eciency of the
irradiation.
Cavitation acts as a biocide through chemical (generation of OH radicals [1]) and through physical mechanisms
(shock waves, pressure gradients, shear forces, etc. [2]). The
predominant mechanism depends on the cavitation process. Low frequencies tend to generate more violent collapses, producing strong shock waves and gas phase
reactions, but the low number of collapses per unit time
*
Corresponding author.
E-mail address: sarrojo@gmail.com (S. Arrojo).
1350-4177/$ - see front matter 2007 Elsevier B.V. All rights reserved.
doi:10.1016/j.ultsonch.2007.11.001
904
Flow-meter
Tank
Pump
Cavitation chamber
905
1.0
0.8
0.6
0.4
0.2
0
20
40
60
80
100
120
Time [min]
Fig. 2. Normalized E. coli concentration versus cavitation time for a
25 1 orice plate (triangles) and Venturi #3 (circles).
0.016
-1
906
0.014
0.012
0.010
0.008
0.006
0.004
0.002
0.000
OP1x5 OP6x2 OP25x1 Vent.1
Vent.2
Vent.3
Transducer 1
Transducer 2
Transducer 3
0.18
0.16
0.14
0.12
0.10
0.08
0.06
0.04
0.02
0.00
OP1x5
Vent.2
Vent.3
0.018
0.016
0.014
907
3
0.012
0.010
0.008
0.006
0.004
0.002
0.000
OP 25x1
Venturi 3
-1
10 CFU/mL
4
10 CFU/mL
5
10 CFU/mL
1.0
0.8
0.6
0.4
0.2
0.0
OP 25x1
Fig. 5. Rate of E. coli inactivation for the orice plate 25 1 and the
Venturi number 3, with a discharge pressure of 1 bar (diagonal stripes),
1.5 bar (grey) and 2 bar (horizontal stripes).
Venturi 3
4. Conclusions
Disinfection in cavitation is caused by both chemical
and physical cell disruption mechanisms. Whilst in UC
the chemical processes caused by OH radicals seem to play
a major role, theoretical predictions and experimental
observations have indicated that in HC, with comparatively slow pressure oscillations (low frequency), disinfection is mainly caused by mechanical disruption of
bacteria. Thus, the disinfection rates are maximized by
those congurations and operation parameters which promote large bubbles, extended pressure oscillations and a
larger number of cavitation events (i.e. those conditions
found in the Venturi tubes).
The results obtained in HC are competitive against
other physical methods but on the other hand, results are
signicantly worse than those obtained with chemical disinfectants. Nevertheless, there are some advantages, such
as avoiding the problems associated with the use and
manipulation of chemicals, and the independence of the
bacterial concentration and the eciency of the process.
Thus, although the study of disinfection processes in HC
can be interesting from a scientic point of view, the
authors consider that applied research should concentrate
on studying wastewater with very large bacterial concentrations or on the synergic eects of this technology with
chemical biocides.
Acknowledgements
This project has been funded by the Spanish government
and the CIEMAT. The authors would also like to thank
Miguel Angel Crespo Aguirre for his collaboration during
this work.
908
References
[1] P. Riesz, T. Kondo, Free Radical Biol. Med. 13 (1992) 247270.
[2] C.V. Ei, J. Overbeck, G. Haupt, M. Herrmann, S. Winckler, K.D.
Richter, G. Peters, H.U. Spiegel, J. Med. Microbiol. 49 (2000) 709
712.
[3] C. Petrier, A. Francony, Ultrason. Sonochem. 4 (1997) 295300.
[4] T.J. Mason, E. Joyce, S.S. Phull, J.P. Lorimer, Ultrason. Sonochem.
10 (2003) 319323.
[5] I. Hua, J.E. Thompson, Water Res. 24 (2000) 38883893.
[6] L. Jatzwauk, H. Schone, H. Pietsch, J. Hosp. Infect. 48 (2001) 580
583.
[7] S.S. Phull, A.P. Newman, J.P. Lorimer, B. Pollet, T.J. Mason,
Ultrason. Sonochem. 4 (1997) 157164.
[8] E. Dahl, Water Res. 10 (1976) 677684.
[9] K.K. Jyoti, A.B. Pandit, Biochem. Eng. J. 18 (2004) 919.
[10] R. Chand, D.H. Bremner, K.C. Namkung, P.J. Collier, P.R. Gogate,
Biochem. Eng. J. 35 (2007).
[11] T. Blume, U. Neis, Ultrason. Sonochem. 11 (2004) 333336.
[12] H. Duckhouse, T.J. Mason, S.S. Phull, J.P. Lorimer, Ultrason.
Sonochem. 11 (2004).
[13] E. Joyce, S.S. Phull, J.P. Lorimer, T.J. Mason, Ultrason. Sonochem.
10 (2003) 315318.
[14] S.S. Save, A.B. Pandit, J.B. Joshi, Food Bioprod. Process. 75 (1996)
4149.
[15] B. Balasundaram, A.B. Pandit, Biochem. Eng. J. 8 (2001) 251256.
[16] K.K. Jyoti, A.B. Pandit, Biochem. Eng. J. 7 (2001) 201212.
[17] S. Arrojo, C. Nern, Y. Benito, Ultrason. Sonochem. 14 (2006) 343
349.
[18] P.R. Gogate, I.Z. Shirgaonkar, M. Sivakumar, P. Senthilkumar, N.P.
Vichare, A. Pandit, AIChE J. 47 (2001) 25262538.
[19] T.E. Leighton, The Acoustic Bubble, Academic Press, San Diego,
1997.
[20] S. Arrojo, Y. Benito, Ultrason. Sonochem. 15 (2008) 203211.
[21] S. Arrojo, Y. Benito, in: Cav 2006, Wagenigen, Holland, 2006..
[22] S.D. Sharma, K. Mani, V.H. Arakeri, J. Sound Vib. 138 (1990) 255
283.
[23] K.K. Jyoti, A.B. Pandit, Ultrason. Sonochem. 10 (2003) 255264.
[24] K.K. Jyoti, A.B. Pandit, Biochem. Eng. J. 14 (2003) 917.
[25] P.R. Gogate, A.B. Pandit, AIChE J. 46 (2000) 16411649.
[26] A. Henglein, Ultrason. Sonochem. 2 (1994) 115120.
[27] P.R. Gogate, A.B. Pandit, Ultrason. Sonochem. 12 (2005) 2127.