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MEMBRANE BIOREACTOR ON
DOMESTIC WASTEWATER
ABSTRACT
The membrane bioreactor, with an increase of biomass concentration in the aeration tank,
permdt work with low F/M ratio and a reduction in s ludge production. The membrane bioreactor
potentialities have been tested on a laboratory pilo t for domestic wastewater treatment.
Various operating conditions (HRT, SRT) were applied to investigate organic and nitrogen
removal as well as sludge production.
Two modeling approaches were tested (maintenance phenomena, single sludge simulation process)
with unsuccessful1 predictions. Futher investigations are needed to better understand
biological kinetics and phenomena in membrane bioreactor and to obtain higher flux on membrane
processes.
KEYWORDS
wastewater treatment; activated sludge; membrane separation; s ludge production; maintenance.
INTRODUCTION
Conventional biological processes for wastewater treatment use biomass recycling to increase
the microorganism concentration in the aeration tank, and therefore the degradation rate of
organic and nitrogen compounds. Membrane separation techniques have been applied for biomass
recycling in biotechnology (Strathman, 198 5) and in wastewater treatment. Application of
membrane separation to anaerobic digestion was investigated to trea t dairy effluents (000 > 30
g. 1-1 ) (Li et al., 198 5) and domestic wastewater (Grethlein, 1978) . Combination of biological
treatment activated sludge with u ltrafiltration was first
reported by Smith et al.
(1969). The combined process is free from the limitation imposed by the settling tank used-rn
conventional activated sludge process.
Higher biomass concentrations may be used
without
bulking phenomenon problems and no effect of varied
loadings on treatment efficiency. In
Japan, this process was developed for domestic wastewater (Audic et al., 1986), and "in situ"
reclamation in large buildings (Kanayama et al., 1987 ; Arika et aI.:-I977). This process--Is
not cost effective and its application is-lImIted. The high power-consumption is due to the
recirculation pump . Yamamoto et al. (1989) have tested the direct solid-liquid separation
using hollow fiber membrane, out aoalance between surface area and cost, and energy input
has to be made. To predict membrane flux, Fane et al. (1980) developed a computer model of a
combined ultrafiltration and activated s ludge --wastewater treatment system. Regarding the
membrane aspect, the major resistance to flux is provided by the suspended solids. Goma et al.
(1986) and Bouillot et al. (1989) have investigated the biological reactors in a membrane
reactor treating syntnetICdomestic wastewater, incorporating the maintenance "concept". This
paper describes investigations on the effect of SRT and HRT on mbrane bioreactor
potentialities. Sludge production and steady state suspended solids concentration have been
studied. Two biological models for wastewater treatment were tested to evaluate the
performance of membrane._ bioreactor.
159 1
1592
Domesti
c
wastewater
effluent
DDS {tratlonl
I
Treated
Excess permeate
Retentate
1ii
r--
I]
LJ
Fig. 1.
a 4. 5 1
frll
t!:!J
/Reactor J
gH
J Heat exchanger L
Pump
Experimental Set-up
was
to
The feed supply was regulated by a level regulation in the reactor. The ultrafiltration
module, (De Danske SUkker-fabriker) was a plate and frame module, with four plates in a serial
design, equipped with polysulphone (GR 51PP) and cellulose membrane (ETNA) during run 1 and 2
respectively. Membrane cut-off was around 50 000 d, linear velocity along the membrane was
1. 5 m S-1 and transmembrane pressure was in a range of 1 to 2 bars. The ultrafiltration module
had a surface area of 0.42 m'. The additional loop shown in Figure 1 was used to test the
effect of inverse flow in the ultrafiltration module to prevent membrane clogging during run
1. During all the experiments, excess permeate was returned to the biological reactor.
The laboratory pilot plant had
8 1 total volume. Hydraulic and sludge retention times were
calculated from this total volume. Experimental conditions, for the different run, are
summarized on Table 1.
TABLE 1
HRT
SRT
Run r
o - rliOth
II Fi
roo a
Run 2
o - 28th
28 - 128th
128 - 17 5th
1 7 5 - 190th
8
4
2
2
100
100
50
100
h
h
h
h
d
d
d
d
Analytical methods
SUspended solids were obtained by membrane filtration (Millipore AP 20) or centrifugation and
drying 24 h at llOe. The organic fraction of the suspended solids (MLVSS) were determined
after drying at 5 50C. Kjeldahl nitrogen and chemical oxygen demand (COD) were measured
according to French Standard Methods AFNOR T 90-1 10 and T 90-103. The total organic carbon was
measured in an infrared analyser Tocamaster 9 1 5-B (Beckman).
1593
After dilution, nitrogen compounds (NH4 , N0 2 ,N03 ) were determined according to the
measurements, drazotation method using colorimetric
Method T 90-013. For NO - NO
and optical density meas ftremen i to 520 nm was made on an autoanalyser (Technicon).
Standard
reaction
Proteins were measured with the Lowry technique (LOWry et al., 1951) and polysaccharides with
the anthrone method (Dubois et al., 19 56). Microorganisms activity was evaluated by
measurement of oxygen consumption mth a respirometer (YSI Model S3 oxygen monitor) and
dehydrogenase activity with INT method (Trevors et al., 1982).
RESULTS AND DISCUSSION
The pilot plant has
run with two operating conditions ; run 1 with a. hydraulic retention
time of 8 h and a sludge retention time of 100 days and run 2 with different values of these
two parameters.
Run 1 with 8 h HRT and 100 days SRT.
The bioreactor was naturally seeded with the microorganisms present in the raw water.
Suspended solid concentrations from the raw water varied from 0. 5 g/l to 0.3 5 gil. Biomass
concentration in the bioreactor and theoretical accumulation of the suspended solids coming
from raw water (see S biomass steady states concentration
) were plotted in Figure 2. After
25 days, the biomass concentration reached a pseudo steady state. Figure 3 shows the TOC
removal efficiency of the bioreactor. The bioreactor efficiency was maximum from the
beginning.In spite of the variations of TOC or COD 9ncentrations in the raw water, the TOC
permeate concentration remained stable at 15 mg 1
This carbon corresponds to organic
compounds with a low molecular weight (inferior to the membrane cut-off), non-degradable by
the microorganisms contained in the bioreactor.
Total nitrification was observed in the operating conditions (SRT, HRT) applied to the
bior,ctor. In the raw water, the nitrogen compounds concentration varied little(NTK - 100
mg.l ). Figure 4 shows the variations of the permeate nitrogen compounds. Nitrification began
after 14 days. The nitrogen organic compounds such as proteins are degraded. The N-NTK
permeate concentration indicated that
part of the effluent TOC
originated from these non
biodegradable compounds. Table 2 summarize the results obtained during run 1.
LE 2
Performance
Suspended solids mg 1
-1
-1
200 - 400
Treated water
--- --------------
2 50 - 550
<
30
35 - 80
<
20
Proteins
10 - 12
<
N -
60 -1 50
<
10
<
0. 5
TOC soluble mg 1
-1
NTK
N - NH
Biomass concentration
40 - 80
8 - 10 g 1
-1
-3
-=1
Volumetric load
0.06-0.10 kg COD kg
SS d
-1
-1
SS d
0. 14 kg O2 kg
O2 consumption (respirometry)
d
-1
-1
1594
'"
:;
E
:J
u
u
'"
'"
50
200
;g
150
CI> Cl
'0 c
CI>
a.
100
"' ...
'O.!.:
'"
:J
fJ)
50
2'"
;;:
;;:
'"
....
20 -------
-- Suspended solids
....... Suspended solids accumulated
16
0,
'"
12
"0
'"
'0
CI>
'0
C
CI>
a.
'"
. .
..
:J
en
(lo
a:
. . ' .
.
.. .... .
..
. ..
.. .
40
..
, ... .
.
...
..... .
.
...
..
...
. ..
...
'
120
80
160
200
Time (days)
Fig. 2.
200 r------
160
0,
E
120
()
o
I-
0____-4________________
o
40
80
120
160
200
Time (days)
Fig. 3.
140 -------,
0,
E
C'l
o
z
<"II
o
z
..,.
J:
Z
20
. ..
. .i
.
f /_
A
. . ____
A
. __
.. _
o
.
o
80
160
200
40
120
Time (days)
Fig. 4.
1595
During the second part of the experiment the HRT varied from 8 h to 2 h and the SRT from 100
to 50 days, in order to study the steady state biomass concentrations at the different
operating conditions. Some problems on pilot operation have caused a loss of biomass (day
97 ). Figure 5 shows the variations of the biomass concentration in the bioreactor and the
accumulation of the suspended solids from raw water ; all the events on pilot operation are
reported in Figure 5.
E!
HRT
SRT
40
300
'C
..
Oi
:;
E
:::J
...
...
240
...
.
en
180
:!:!
'0
II)
01
1/1
:!:!
'0
II)
'C
..
8
100
2
50
100
1ojhours
days
100
- Suspended solids
...... Suspended solids accumulated
32
24
II)
'C
..
120
'C
C
16
..
'C
c
60
a.
1/1
:::J
II)
..
a.
1/1
:::J
II)
8
0
40
80
120
160
200
Time (days)
Fig. 5.
The biomass concentration increased slowly in the bioreactor (before day 30 ). During this
period a decrease of the membrane permeability was observed (see Figure 10). The influent and
effluent TOe concentrations are plotted in Figure 6.
160
...
.
en
u
._
120
80
I-
40
40
80
120
, 160
200
Time (days)
Fig. 6.
The TOe average concJiltration in the raw water was lower than in previous experiments (TOe
average
0.034 g.l ). Changes in operating conditions (SRT or HRT) had no effect on the
water quality produced (carboneous removal only). Some differences were observed on the
soluble part of the liquor circulating in the bioreactor. TOe, protein and polysaccharide
Figure 7.
(total sugars) concentrations are shown in
=
1596
Time
Fig. 7.
(days)
..
CI
III
"0
c:
o
0.
o
u
c:
G>
CI
140 r------,
...... NH4
120
N02
- -- N03
100
80
60
..:\;
.
40
Z
Time
Fig. 8.
(days)
VL COD
VL NH
Measurements of dehydrogenase
plotted on Figure 9.
COD
NH4
activity ( INT
5.04
kg COD
m
-3
-3
0.96
kg
0. 13
kg COD kg
0.026 kg N kg
activity)
N m
and O2
-1
-1
-1
-1
-1
-1
specific
consumption
are
1597
>;-
en
(/)
&. 12
E
ci
2i='
'?:
>
'"
'"'"
c
CI)
01
0
-0
>.t:
CI)
0
, 01
(/)
--
0.5
.2
0.2 ;
'"
..
'0
[}j
CI)
(;
. .
'
: l::
.
fl
.0.
,:.
; .'
!=:
./ .
0.1
...
i i
:l
consumption
.
activity
!\ ' f
.
::
L .f:..; :: :
.... : :. . ;':.:= .. :;.:
:f ....
-. .
'.'''' : .i!_.:: :! '!
.
::: :l:.."
E 0.4
N
0
E 0.3
02
INT
01
<>
CI)
.
(/)
.. i
.....
..
O-------------L------________L-____
80
40
120
Time (days)
160
200
Fig. 9.
These two activities are a good indicator of the active fraction of the biomass. During the
"growth" phase of this biomass, values for these parameters were higher than during steady
state. At the beginning, the biomass active fraction w as high.As the biomass aged, the specific
activities decreased, which can be explained by the decrease of the ratio of active/inactive
fraction of the biomass. The active fraction became only a small fraction of suspended solids
in the bioreactor.
Biomass steady state concentrations
Figures 2 and 5 report the biomass concentration in the reactor and the theorical accumulation
of suspended solids from the raw water
the calculation is the daily accumulation of
suspended solids.
SSac
TOe
run
The kinetics parameters were those proposed by the IAWPRC task group. Feed characteristics used
for the simulation are an average of the raw water characteristics during
2. The predicted
effluent COD of 0.002 g 1 '1 is slightly lower than experimental value 0.030 g 1 -1), whereas
the predicted
effluent concentration was very close to the experimental value.
NTK
The major disagreement between modeling and experimental approach is on biomass concentration
(suspended solids). Whereas the modeling approach predicted MLVSS concentration of 16 and 6 5
g 1 -1, for a n HR T o f 8 and 2 h respectively, the S S experimental values were around 1 0
36
g 1 -I (MLVSS
7 5 % of suspended solids concentration). This difference can be explained by
the large SRT (100 days) and the low HRT used in the experiment. Indeed the IAWPRC model,
which was valid
with results from typical activated sludge plant, does not incorporate
maintenance phenomena, important for processes w i
a low F/M ratio.
and
th
The maintenance concept was introduced by Pirt (196 5). It expressed the energy consumption
necessary for the endogeneous respiration of the microorganisms. The observed yield (Yobs) and
the specific growth rate (p) are related by the following equation
l/Y
obs
where
ms
is the
maintenance coefficient
l/Y
lim
and Y
lim
m /p
s
in batch
experiments.
1598
TABLE 3
COMPOUNDS
mg 1-1
CHARACTERISTICS
8 h
2 h
100 d
100 d
FEED
------
Heterotrophic organisms
1. 743
6.982
0. 0
Autotrophic organisms
0.189
0. 761
0.0
Particulate products
8. 81 5
3 5.273
0.0
Inert particulate
9 COD 1-1
5.2 50
21.000
0.03 5
Organics Particulate
0.146
0. 58 5
0.226
Soluble organics
9 COD . l - l
0.002
0.002
0.193
Soluble ammonia N
0.0003
0.0003
0.059
Soluble nitrate/
nitrite N 9 N 1-1
0.068
0.068
0.001
Soluble organics N
0.0004
0.0004
0.006 5
Biodeg. particulate
organics N 9 N 1-1
0.045
0. 045
0.009 5
4.0
4.0
16.145
64.6
9 COD 1-1
9 COD 1-1
9 COD 1-1
9 COD 1-1
9 N 1-1
9 N 1 -1
OXygen
mg O2 1-1
MLV5S
9 COD 1-1
9. 0
+ 1Ils
Ylim
with Dh - l/HRT and Dp
l/SRT. Using synthetic
domestic wastewater and the strain
Pseudomonas fluorescens, a maintenance oefficient and a growth yield were determined :
- 0.56 g.Ss.g.- COD
Ills - 0.035 h-i arid Y
lim
These
When the SRT is very high, therefore Dp is very low, equation 1 can be simplified:
Dh (COD inf - COD effl)
(2)
X - -------
ms
as a function
TABLE 4
Steady State
1599
Analysis
TOe
SS
SS
Raw water
Reactor
g 1-1
g 1 -1
-- - ----- -- -- ---- ----- --- ---37- 50th
Bh
100d
35.6 (14.9)
0. 25 (0.09)
10.07 (0.77)
5B- 72th
1
40.2 (9.4)
0. 33 (0.12)
10. 3 (0.79)
101- 115th
40.4 (21.7)
0.7B (0.03)
B.34 (0.75)
120-134th
39. 4 (11.6)
0.79 (0.05)
12. B6 (1.42)
---6-20th
Bh
100d 20
(7.67)
0. 20 (0.11)
2.0B (0.24)
4h
2B -42th
20.74 (4.67)
0.2B (0.07)
4.95 (2.03)
73-94th
2
5 5. 15 (B.33)
0.29 (0. 13)
27.43 (1.43)
160-l7Sth
2h
SOd SLOB (17.3)
O.lB (0.07)
25.BB (2.20)
100d
17B-1BBth
100. 32 (29. 54) 0.23 (0.06)
36.3 (3. 5 1)
Run
Period
HRT
SRT
Removal
mg 1-1
'!his approach was applied by using the experimental results summarized in Table 4, but a
maintenance coefficient cannot be estimated due to the important dispersion of values. This
result can be explained by the high concentration of suspended solids in raw water, which is
not considered separately in
Equation 1. The incorporation of the maintenance concept
into the IAWPRC model should solve this limitation.
Membrane flux
Membrane with different organic composition were used in these experiments.
Regardless of
rating conditions (suspended solids concentration) comparison seems difficult. Figure 10
the permeability variation of each membrane.
90 r-------
PS (Run 1)
ETNA (Run 2)
:c
..
CII
E
Cii
Co
CII
C
..
.c
E
CII
::!!
45
30
15
1\
:i
INV
ll
..'.,:,- .1.1..
... ":'"
".
OL-----------------
200
160
120
BO
40
o
Time (days)
INV - change of recirculation flow direction
Fig. 10. Membrane permeability (RunS 1 and 2)
The GR 5 1 PP membranes have a lower initial permeability than E'lNA membranes. During run 1
changes:.in recirculation flow direction have a slight effect on the membrane permeability. With
a higher biomass concentration, ETNA membranes seem to give a higher flux after 1 50 days.
COOCLUSICN
With a SRT of 100 days and a HRT of 2 hours, a good effluent quality is obtained.
low
1600
ACKNCl4LEDGEMENT
Acknowledgement to G.M. Faup, Head Ingenior of the Central Laboratory and J. Mamen for helpful
discussion, to M. Le Digabel and M. Hurtrez for typing and illustrations of this paper. Thanks
to C.P. Leslie Grady for providing the SSSP program (Simulation of Single Sludge Process).
This work was funded by EUREKA project with the collaboration of Lyonnaise des !aux and DDS
Company.
REFERENCES
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Audic, J.M., Fugita, Y. and Faup, G.M. (1986). Le couplage boues activees - membrane : une
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R.
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Cooper.
plenum Press, London-N.York.
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Tomoyasu, T. and
Katayama,
S.
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(1985). Membranes and membrane processes in biotechnology. Trends
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