1 s2.0 S1011134408001784 Main PDF
1 s2.0 S1011134408001784 Main PDF
1 s2.0 S1011134408001784 Main PDF
Comisin Nacional de Energa Atmica CNEA, Av. Gral. Paz 1499, cp BNK1650 San Martn, Buenos Aires, Argentina
Department of Physiology and Medical Physics, Royal College of Surgeons in Ireland, Dublin 2, Ireland
c
Plataforma Solar de Almera CIEMAT, P.O. Box 22, 04200 Tabernas, Almera, Spain
d
Escuela de Posgrado, Universidad Nacional de San Martn, Peatonal Belgrano 3563, B1650ANQ San Martn, Argentina
b
a r t i c l e
i n f o
Article history:
Received 18 February 2008
Received in revised form 1 July 2008
Accepted 25 August 2008
Available online 6 September 2008
Keywords:
Compound parabolic collector
Solar disinfection
Escherichia coli
Natural well-water
a b s t r a c t
Inactivation kinetics are reported for suspensions of Escherichia coli in well-water using compound parabolic collector (CPC) mirrors to enhance the efciency of solar disinfection (SODIS) for batch reactors
under real, solar radiation (cloudy and cloudless) conditions. On clear days, the system with CPC reectors achieved complete inactivation (more than 5-log unit reduction in bacterial population to below the
detection limit of 4 CFU/mL) one hour sooner than the system tted with no CPC. On cloudy days, only
systems tted with CPCs achieved complete inactivation. Degradation of the mirrors under eld conditions was also evaluated. The reectivity of CPC systems that had been in use outdoors for at least 3 years
deteriorated in a non-homogeneous fashion. Reectivity values for these older systems were found to
vary between 27% and 72% compared to uniform values of 87% for new CPC systems. The use of CPC
has been proven to be a good technological enhancement to inactivate bacteria under real conditions
in clear and cloudy days. A comparison between enhancing optics and thermal effect is also discussed.
2008 Elsevier B.V. All rights reserved.
1. Introduction
Many communities in developing countries cannot afford a conventional means of water treatment. As a result a large number of
the population who live in these areas do not have access to safe
water. This can lead to widespread occurrence of waterborne diseases most frequently in the form of diarrhoea. Infectious diarrhoea is also the leading cause of illness and death in children
less than 5 years of age. An economical and simple way to inactivate waterborne pathogens is required.
Water disinfection using the solar disinfection (SODIS) process
relies on the synergistic effect of sunlight and temperature upon
bacteria [13]. A great part of the research in understanding the
mechanism of this process has been done using transparent plastic
bottles exposed to sunlight under different operating conditions.
Results have shown that 6 h of solar exposure is sufcient to inactivate most bacterial pathogens in contaminated water when using
bottles of up to 2 L in volume [4,5].
The modern resurgence in SODIS was started by Acra et al. [6]
who reported that enteric bacteria were inactivated after exposure
to 6 h of sunlight. Subsequently other organisms have been tested,
156
Length = 1.50 m
Diameter = 0.05m
Closed end
Sampling valve
Optic axis
C = 90
CPC mirror
Fig. 1. (a) Glass tube conguration. (b) Design of CPC for the glass tube
experiments. (c) Experimental tube tted in CPC mirror inclined 37 with respect
to horizontal facing south.
arising from the transmittance, a comparison experiment was performed. The plastic bottle used for this experiment was a 2 L-bottle
with hexagonal cross sectional shape, 9 cm equivalent diameter
and 30 cm height. Both the bottle and the tube were exposed to
sunlight under the same atmospheric, radiometric and meteorological conditions in duplicated experiments.
2.2. CPC mirrors
We dene: aperture area = A; absorber area = Aabs; Sun zenith
angle on the concentrator = h; acceptance angle of the CPC = hc;
concentration factor = C = A/Aabs. The fundamental problem of radiation concentration is how can radiation which is incident on A and
uniformly distributed over a range of angles (h 6 hc) be concentrated onto the smaller absorber area Aabs without the need for
repositioning the system as the value of h varies [19]. For a cylindrically shaped SODIS reactor the concentrating system is twodimensional. In this case, the second law of thermodynamics states
157
Re-growth counts of bacteria were determined for all experiments, by leaving the last two samples at room temperature for
24 and 48 h. After 24 and 48 h the plate count method as described
above was used to determine bacterial counts on both LB agar
plates and Endo agar (SigmaAldrich, USA) plates. Endo agar is a
selective media, specic for the detection of coliforms and enteric
organisms in sources such as drinking water. Endo agar was also
used as a way to suppress and prevent growth of any non-coliforms or non-enteric organisms that might have grown during
the 24 and 48 h period and might interfere with accurate counts
of E. coli K-12. All samples of the experiments reaching the detection limit were evaluated in this way at the end of the experiment
and bacterial re-growth after stopping illumination was not observed within 24 and 48 h.
2.5. Water
Natural well-water was used in all experiments. The water was
extracted from a well located in the PSA area with a depth of approx. 200 m. The content of natural microorganisms is of around
100200 CFU/ml. The procedure to determine the background contamination was the same as that described in previous section. The
concentration of naturally occurring organisms was determined by
the plate enumeration technique using LB agar and was found to be
100-200 CFU/ml. These organisms were identied as non-coliforms
and non-enteric in nature due to their presentation as either irregular, colourless colonies on Endo agar or the complete lack of
growth also on Endo agar.
These studies were carried out using natural well-water so that
the microbiological and chemical environment within which the
SODIS inactivation occurred was as realistic as possible. Consequently, distilled water and other highly contaminated wastewaters (like municipal WW) were discarded as models of this study.
For similar reasons, the well-water was not autoclaved before each
experiment in order to preserve the chemical integrity of the original water matrix. A single batch of 100 L of well-water was withdrawn at once so that the same stock of water was used for all
the experiments, so that possible variations in the natural wellwater composition did not occur. Consequently all experimental
results could be compared. Table 1 shows general physical water
parameters averaged during the period of the experimental series.
3. Results
2.4. Bacteria
3.1. CPC inuence on clear sunny days
E. coli was used as a model target microorganism since it is
widely used as an indicator of faecal contamination in water.
E. coli K-12, ATCC 23631 was propagated in Luria Broth nutrient
medium (Millers LB Broth, Sigma-Aldrich, USA) and incubated at
37 C with constant agitation on a rotary shaker at 100 rpm for
24 h. The stationary phase of bacterial growth yielded a concentration of 109 CFU/mL. For all experiments, the range of initial concentrations (C0) of E. coli was from 106107 CFU/mL. Previous studies
by the authors (unpublished) have shown that this 1-log-unit variation in starting population had no inuence on the observed inactivation kinetics. E. coli suspensions were centrifuged at 800g for
10 min and re-suspended in PBS and inoculated in the 2.5-L tube to
reach the required cell density. Samples were serially diluted in
PBS and plated. Every sample was diluted at 1/10 relationship up
to three dilutions (D0, D1, D2, and D3) and consequently plated
on Luria agar (SigmaAldrich, USA). The detection limit for this
method of quantication is 4 CFU/mL. Inoculated samples were
incubated at 37 C for 24 h before counting. As a control, half of
the volume of the rst sample (7 mL) was kept in the dark at
37 C during the whole experiment and re-plated at the same time
as the last sample of the experiment.
Table 1
Average physical and chemical properties of the well-water used in the experiments
Natural well-water at PSA
Cl
NO
3
SO
4
F
Br
PO3
4
pH
Turbidity
355 mg/L
22 mg/L
329 mg/L
1 mg/L
2 mg/L
0.5 mg/L
7.3
12 NTU
Na+
NH4+
K+
Mg2+
Ca2+
HCO
3
Conductivity
Bacteria
370 mg/L
6 mg/L
11 mg/L
64 mg/L
122 mg/L
500 mg/L
2300 lS/cm
100 CFU/mL
158
Controls
10
Dark
50
10
40
10
UV Irradiance
30
10
10
Tube
Tube+CPC
20
Bottle
10
DL
10
UV Irradiance (W/m2)
10
60
10
11:00
12:00
13:00
14:00
15:00
Controls
10
60
10
50
No CPC
10
UV Irradiance
40
10
30
3
10
20
10
Old CPC
1
10
New CPC
DL
10
UV Irradiance (W/m2)
10
11:00
12:00
13:00
14:00
15:00
The plots show from 10:30 to 15:30 (x-axis) because the experiments were conducted during that period although points are only
plotted up until the time when the bacterial concentration decreased below the detection limit (DL).
Tube inactivation reaches the detection limit one hour before
the bottle. This can be attributed to the fact that the borosilicate
glass tube has a 45% UV-B transmittance (compared to 0% for
PET) and a 5% advantage over PET in the UV-A. Variations in UVA transmittance of both materials for the specic widths used
in the experiments yielded an average difference of just 5.3% (data
not shown). Larger differences in transmittance can be seen beyond UVA but since very little UVB and no UVC are present in terrestrial natural sunlight the effect of the different diameter of the
glass tube and the bottle [7] can be considered negligible.
Both glass tubes, with and without CPC, reached the detection
limit (4 CFU/mL). It can be seen that the system with the CPC
reached the detection limit one hour before the system with no
CPC. In terms of UVA-ux, the system with CPC reached detection
limit after receiving 150 kJ/m2 (Table 2) from the sun calculated
as the integral of the solar UVA irradiance (W m2) on the time of
exposure until DL was reached (s) , while that with no CPC needed
210 kJ/m2. This represents 40% more energy required to achieve
the same result on clear days with the non-CPC system. Hence
the system with CPC is more efcient in terms of energy usage.
159
29
29
29
29
24
24
24
May
May
May
May
May
May
May
2007
2007
2007
2007
2007
2007
2007
Solar
system
Solar
conditions
Averageb
solar UVA
irradiance (W m2)
Ci
Glass tube
Bottle/No CPC
Tube/No CPC
Tube/(new) CPC
Tube/No CPC
Tube/old CPC
Tube/new CPC
Dark
Sunny
Sunny
Sunny
Cloudy
Cloudy
Cloudy
35 5
35 5
35 5
28 8
28 8
28 8
(CFU mL1)
Cf
(CFU mL1)
Exposure to reach
DL (h)/UVA-uxe
(kJ/m2)
Minimummaximum
temperature (C)
Figure
21.327.5
21.329.5
21.530.4
21.033.0
20.728.7
20.331.2
20.233.0
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
Fig.
3/340 60
2/210 30
1.5/150 20
2/200 50
1.5/140 40
2a
2
2a
2a
2b
2b
2b
All the experiments were performed in duplicate in twin systems under the same climate conditions from 10:30 to 15:30 local time.
The average for the 5 h duration of the experiment.
c
Ci: initial bacterial concentration (CFU mL1)
d
Cf: nal bacterial concentration (CFU mL1). DL: when zero CFU was detected, concentration was the detection limit (DL: 4 CFU/mL). Each value of bacterial concentration
is the average measurement and errors are standard deviation from triplicate measurements taken in duplicated experiments.
e
Accumulated UVA-ux calculated as the integral of the solar UVA irradiance (W m2) on the time of exposure until DL was reached.
3.4. Modeling with Gearaerd and Van Impe inactivation model tting
tool
-1
above a temperature of 45 C for E. coli, S. typhimurium and S. exneri, while V. cholerae was already susceptible above 40 C. The
temperatures experienced in this work are relatively lower compared to those values.
Log10 N(CFU ml )
Sunny conditions
Geeraerd shoulder model
7
6
5
4
Bottle
Tube
Tube+CPC
DL
Table 3
Fitting results of the experimental data using the Gearaerd and Van Impe inactivation
model tting tool (GinaFiT)
Solar system
Fitting model
Sunny conditions
Bottle
Geeraerd shoulder
Glass tube
Geeraerd shoulder
Glass
Geeraerd shoulder
tube + new
CPC
Cloudy conditions
Glass tube
Geeraerd shoulder
and tail
Glass tube + old Geeraerd shoulder
CPC
Glass
Geeraerd shoulder
tube + new
CPC
Parameters
Shoulder
length;
kmax (min1)
TDL (min)
FDL
(kJ/m2)
48 6; 0.11 0.01
26 3; 0.15 0.01
16 8; 0.20 0.02
41 3; 0.14 0.01
log(Nres) = 3.60 0.03
26 5; 0.15 0.01
120.0 0.5 200 50
18 9; 0.16 0.04
TDL and FDL values (time and ux received required to reach DL) from real sunlight
exposure of the different solar systems studied.
0
-1
Log10 N(CFU ml )
60
120
180
Cloudy conditions
Geeraerd shoulder model
Geeraerd shoulder + tail model
6
5
No CPC
4
3
2
1
Tube+new CPC
Tube+old CPC
DL
0
0
60
120
180
240
300
Time (min)
Fig. 3. Inactivation curves of E. coli K12 during real sunlight exposure on clear days
(top) in a glass tube with CPC (-.-), without CPC (-d-), PET bottle (-N-), and on
cloudy days (bottom) in a glass tube with new CPC (-.-), old CPC (-N-), without CPC
(-d-). Lines represent theoretical ts using the Gearaerd and Van Impe inactivation
model tting tool (GinaFiT) [21].
the experiments carried out in the glass tube using the new CPC
yields the fastest inactivation rate (kmax) compared with the other
systems evaluated. All kinetics results obey the Geeraerd shoulder
model as expected for the SODIS process [1], except for the case of
the tube without CPC mirror under cloudy conditions which obeys
to the Geeraerd shoulder and tail model (Fig. 3).
4. Discussion
In previous SODIS experiments it was established that the minimum temperature at which a synergy effect can be observed is
around 4550 C for E. coli K12 [7]. Since in our experiments the
temperature never exceeded 33 C, synergy and thermal effects
were ignored so that the bacterial inactivation observed can only
be attributed to the effect of solar radiation.
There are a number of pioneering studies that have tried to enhance disinfection using some kind of solar thermal system. Martin
Dominguez et al. painted sections of the bottles with black paint so
that the water could reach a higher temperature [14]. Rijal et al.
circulated water over a black surface in an enclosed casing which
was transparent to UV-A light [13]. Saitoh et al. made a system that
enhanced temperature by using a solar collector attached to a double glass envelope container [22]. All of these studies have
160
OH HCO3 ! CO
3 H2 O
OH CO2
3 ! CO3 OH
5. Conclusions
The use of CPCs to enhance SODIS has been tested with natural
well-water and natural sunlight conditions. On clear days, a faster inactivation rate is obtained in the system with CPC compared to that without reectors. On cloudy days inactivation
to below the detection limit is only achieved using systems tted with CPCs. This technological enhancement can be used to
design future larger scale systems to treat high volumes of water
for several households.
The degradation of the mirrors under eld conditions should not
be underestimated and has to be considered if systems are
exposed outdoors for extended periods of time. After 3 years
of exposure, non-homogeneous degradation of mirrors was
observed through the reectivity measurements. New CPC
reectivity was around 82% while values between 27% and
72%were recorded for older CPCs. The faster inactivation rate
on clear sunny days was not signicant for systems with old
CPCs compared to systems with no reectors. However, on
cloudy days both new and older CPCs produced inactivations
to below the detection limit, a feat which is un-matched by systems without CPCs. This means that even with degradation, a
CPC provides a major advantage.
The CPC has been proven as a SODIS enhancement technology,
allowing more radiation to reach the absorbing volume leading
to a reduction in the SODIS exposure time and allowing the
treatment of higher volumes of water on the same day.
6. Abbreviations
CPC: compound parabolic collector; SODIS: solar disinfection.
Acknowledgements
The authors thank to Miss Aranxta Fernandez for making reectivity measurements of mirrors and for her helpful suggestions.
This work was nanced by the SODISWATER project (EU Contract:
INCO-CT-2006-031650) and Doctoral Fellowship from ANPCyT and
Grant MAE-AECI 2006-2007 (Spain) for C. Nanvtoft.
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