Article body

Nomenclature

SI:

soluble inert substrate concentration (mgO2•L‑1)

Ss:

readily biodegradable soluble substrate concentration (mgO2•L‑1)

XI:

inert-particulate substrate concentration (mgO2•L‑1)

Xs:

particulate slowly biodegradable substrate concentration (mgO2•L‑1)

SND:

soluble biodegradable organic nitrogen concentration (mgN•L‑1)

SNH:

ammonium concentration (mgN•L‑1)

SNO:

nitrate and nitrite nitrogen concentration (mgN•L‑1)

So:

dissolved oxygen concentration (mgO2•L‑1)

XB,A:

active autotrophic biomass concentration (mgO2•L‑1)

XB,H:

active heterotrophic biomass concentration (mgO2•L‑1)

XND:

particulate biodegradable organic nitrogen concentration (mgN•L‑1)

Xp:

particulate product from biomass decay concentration (mgO2•L‑1)

SALK:

alkalinity

TSS:

total suspended solids (mg•L‑1)

VSS:

volatile suspended solids (mg•L‑1)

MSS :

mineral suspended solids (mg•L‑1)

Index i:

values of ASM1 variables at t0 in the sludge

Index 0:

values of ASM1 variables in the incoming wastewater

1. Introduction

Activated sludge processes are widespread for the biological treatment of domestic and industrial wastewater. Continuous systems are recommended when large amounts of water have to be treated. On the contrary, Sequencing Batch Reactors (SBRs) have been proposed for small communities and industries discharging very specific wastewaters (KARGI et al., 2005; KIM et al., 2004) because they have a higher degree of flexibility than continuous systems. According to the incoming pollutant concentration and to the specifications of the discharged water, the operating mode of Sequencing Batch Reactor (SBR) is based on a series of aerated and non-aerated reaction phases of variable duration (KARGI et UYGUR, 2003).

Many technical possibilities are available for SBR management and optimization but they are expensive and time- consuming to test experimentally. Models which are dedicated to describe the system performances in a SBR are available in the literature (ARTAN et al., 2006; BOAVENTURA et al., 2001; CARVALHO et al., 2004; COELHO et al., 2000; HVALA et al., 2001; MOUSSA et al., 2005; WU et al., 2001). Therefore, modelling and simulation offer interesting alternatives (ARTAN et al., 2006; HVALA et al., 2001).The models used are mostly the ASM1 or ASM2d or an adaptation of the ASM. Models are used to validate experimental data and more rarely to design SBR systems except in the data provided by ARTAN et al. (2006) who describe the use of the ASM model to optimize the filling in batch reactors for nitrogen removal, but without lab or pilot scale validation.

Many strategies are proposed for the setting-up of wastewater treatment plants, but their evaluation and comparison are difficult. This is partly due to the variability of the influent, to the complexity of the physical and biochemical phenomena and to the large range of time constants (from a few minutes to several days), inherent to the activated sludge process. One of the difficulties for the application of modelling to a specific site lies in the wastewater fractionation corresponding to the local wastewater. The quality and the validity of the simulations depend on the quality of the initial variables. Efforts to identify ASM state variables in SBR systems are rarely reported, most authors preferring to use literature data (COELHO et al., 2000) or online calibration of ASM parameters (ANDREOTTOLA et al., 1997; DOSTA et al., 2007).

Different methods of identifying or calibrating ASM1 state variables and parameters can be found in the literature. Most of them are collected by SIN et al. (2005) and a complete review of ASM variables and parameters identification is reported by PERTERSEN (2000). Many of them are based on respirometric methods (BROUWER et al., 1998; CHECCHI et MARSILI-LIBELLI, 2005]) defined as the measurement and interpretation of the oxygen uptake rate of activated sludge (EKAMA et al., 1986; SPANJERS et al., 1999). Interpretation of respirometric data can be achieved, for example, by fitting a model to the measured data (COEN et al., 1998; SPANJERS et VANROLLEGHEM, 1995). SS, parts of XS, SNH, parts of SND and XND can be determined through respirometric techniques; nevertheless, it is not possible to identify all ASM1 variables such as SI and XI. The respirometric techniques cannot be easily applied. It is necessary to conduct a thorough analysis of the respirograms, and to manage properly the nutrients to biomass ratio (SPERANDIO, 2007). Physico-chemical methods can also be used to identify some ASM1 variables and especially SS (MAMAIS et al., 1993; NAIDOO et al., 1998). The main failure of these methods is the lack of distinction between non-biodegradable and biodegradable matter. That is why it is necessary to combine these methods with biodegradation tests. STRICKER (2000) described biodegradation tests which led to more complete identification.

This work presents the coupling of a mathematical model and wastewater fractionation to define an optimal sequence of a SBR, with the aim of treating carbon and nitrogen from domestic wastewater (Figure 1). In this paper, two kinds of wastewater fractionation were compared: the fractionation given by the Benchmark (BSM1) and a specific one for Limoges (France) wastewater that remained to be established more accurately. Modelling and fractionation were used to compare two kinds of setting up of a SBR: 12-hour cycles and 24-hour cycles. The interest of a specific identification for the choice of the cycle duration between 12-hour and 24‑hour cycles is demonstrated during dry and rainy weathers. The cycle defined using the low cost strategy was tested in lab-scale and pilot- scale reactors.

Figure 1

Methodology used for the optimization of wastewater treatment (C and N removal) in a SBR.

Méthodologie utilisée pour l’optimisation du traitement d’une eau usée (élimination de C et N) dans un SBR.

Methodology used for the optimization of wastewater treatment (C and N removal) in a SBR.

-> See the list of figures

2. Materials and Methods

2.1 Models description

Modelling the biodegradation phases. The Activated Sludge Model N°. 1 (ASM1) (HENZE et al., 1987) was chosen to simulate the biological process. Thirteen state variables described the fate of biodegradable and non-biodegradable, soluble and insoluble, carbon and nitrogen-based pollution as well as bacteria (heterotrophs and autotrophs): the biological processes are described by 19 kinetic and stoechiometric parameters. The values of the kinetic and stoechiometric parameters were the default values proposed by HENZE et al. (1987) at 20°C.

Except for oxygen, the general mass balance during non-settling phases was:

where Z was a state variable, V the working volume, r the reaction rate, t the time and qin and qout the feed and discharge rate respectively. During feeding:

During the discharge and wastage phases, which were assumed to be non-reactive:

and

Dissolved oxygen during aerated phases was controlled by a discrete PI controller by manipulation of the oxygen transfer coefficient.

For dissolved oxygen (SO):

where S*O was the dissolved oxygen concentration at saturation and KLa the oxygen transfer coefficient.

During aerobic phases of the simulations, the oxygen concentration S0 was maintained at 2 mg O2•L‑1 and was equal to 8 mg O2•L‑1. The oxygen transfer coefficient (KLa) was constant during aerobic phases and equal to 16 h‑1 and was reduced to 0 during anoxic and anaerobic phases.

Modelling the settling phase: The double-exponential settling velocity model proposed by TAKACS et al. (1991) was selected to describe the behaviour of the sludge during the settling phase, which was not supposed to be reacting. The number of layers has been set to m and their thickness is adjusted for each cycle, with respect to the actual working volume. The first layer was at the bottom of the tank, where wastage was taking place. The partial discharge of a layer was taken into account to calculate the amount of sludge remaining in the reactor. Wastage and discharge were not supposed to disturb the layers.

Initialisation of the mathematical program: sludge and wastewater characteristics: The kinetic and settling parameters used to simulate the SBR behaviour were those given in the COST BSM1 (COPP, 2002; HENZE et al., 1987).

2.1.1 Sludges ASM1 variables

The values of ASM1 variables in the sludge at t0 were the same whatever the kind of fractionation used for the incoming wastewater (Benchmark values or specific identification for the incoming wastewater (Limoges WWTP)). The values of sludge ASM1 state variables at t0 in the SBR (XIi , XB,Hi, XB,Ai, XPi) have been fixed according to theoretical calculation (equations 7 to 10) based on the knowledge of TSS and VSS concentrations of the sludge (expressed in mg O2•L‑1). The variable Xp was calculated according to the concept of endogenous respiration.

f’p is a factor representing the part of biomass lost in the endogenous respiration concept. Its value was taken as equal to 0.208. The TSS was considered equal to 5 g•L‑1 that is to say 6499, 4 mg O2•L‑1. The COD values for VSS and MSS were respectively equal to 5000 and 1499.4 mg O2•L‑1. The values for the different state variables expressed inmg O2•L‑1 are respectively: SIi = 60, SSi = 0, XIi = 2142, XSi = 0, XB,Hi = 4750, XB,Ai = 250, XPi = 1040, SOi = 0, SNOi = 10, SNHi = 0, SNDi = 1, XNDi = 5, Salki = 7.

2.1.2 Wastewater ASM1 variables

For predictive simulations, two kinds of influent fractionation were considered to feed the SBR. The influent composition was considered to remain unchanged during the complete simulation period.

  • An influent of constant composition determined by the average of the values given by the benchmark program (BSM1) (dry and rainy weathers) (see Table 1).

  • An influent of constant composition determined after an influent fractionation (see 2.2) for the wastewater used (dry and rainy weathers) (see Table 1).

For the pilot scale validation, the ASM1 state variables were calculated according to real values of wastewater composition.

  • Simulation conditions: the SBR results discussed thereafter have been obtained using a FORTRAN code and the set of differential equations was integrated using a 4th-order Runge-Kutta algorithm and a constant integration step size (0.002 hr). A stabilization time of 100 days was used. This time was tested in an open loop (no control of dissolved oxygen) and the oxygen transfer coefficient set to its maximal value.

Table 1

Values of ASM1 state variables: Benchmark (BSM1) values, and results of the incoming wastewater identification.

Valeurs des variables d’état du modèle ASM1 : Valeurs issues de la base de données (Benchmark, BSM1), valeurs issues de l’identification spécifique pour l’eau d’entrée.

ASM1 State variables

SI 0

SS0

XI0

XS0

XB,H0

SNH0

SND 0

XND 0

Unit

mgO2•L‑1

mgN•L‑1

 

Benchmark fractionation

Dry weather

30

65.2

45.6

192,7

26.5

30.1

6.5

9.95

Rainy weather

27.8

60.5

42

178

24.5

27.9

6

9.2

 

Incoming wastewater specific fractionation

Dry weather

34

131

51

352

26.5

16

17

19

Rainy weather

26

219

114

294

24.5

14

15

11

-> See the list of tables

2.2 Experimental methods

Reactor characteristics: The working volume of the lab scale reactor used for the simulations was 2 L. The incoming wastewater volume was equal to 0.9 L per cycle. The length of the phases, the control of dissolved oxygen concentration (2 mg/L) and the feeding and discharge of the reactor were controlled and monitored through the Bioexpert© software. Feeding and discharge of the reactor were achieved using peristaltic pumps. The agitation rate was regulated at 80 rpm.

The working volume of the pilot scale SBR was 1320 litres. It was stirred at 40 rpm during the aerobic phase and at 30 rpm during the anoxic phase. The volume of incoming wastewater represented 50% of the working volume of the reactor. The reactor was monitored and controlled through the TSX Premium© (Télémécanique) software.

Fractionation of the incoming wastewater: The incoming wastewater was a mixture of domestic (85% v/v) and industrial wastewater (15% v/v).

The ASM1 state variables for the incoming wastewater have been identified by different methods: a) coagulation-floculation followed by 0.45 µm pore size membrane filtration and b) biodegradation tests in closed reactors.

The fractionations were achieved under dry and rainy conditions.

  1. The soluble fraction of COD (Ss0) was also identified by physico-chemical methods described by (MAMAIS et al., 1993; NAIDOO et al., 1998).The first step consisted in the elimination of suspended solids by using a coagulant flocculant. The supernatant was then filtered at 0.45 µm. Ss0 corresponds to the COD measured in the filtrate. Two coagulant flocculants were evaluated FeCl3 (1 g•L‑1) and ZnSO4 (3 g•L‑1).

  2. The state variables of ASM1 (SI0, SS0, XS0, XI0, SNI0, SND0, XNI0, XND0) were measured by a method inspired by STRICKER (2000): two reactors were filled with wastewater: the first one (working volume of 4 L) was filled with untreated wastewater (collected after pre-treatment in the WWTP of Limoges) and the second was filled with 4 L of filtered wastewater (1.2 µm). According to STRICKER (2000) recommendations, the reactors were inoculated with activated sludge (1/1000 v/v). The biodegradation tests lasted 30 days and were conducted twice for rainy weather and three times during the dry weather period of time, in order to have an accurate identification. Soluble and insoluble COD and nitrogen species were monitored every day.

Performance criteria, removal efficiency, analytical methods: The exit concentration of soluble carbon and nitrogen was compared to French standards. The removal efficiency (RE) was calculated according to equation 11:

Input value corresponded to the values reported in table 1 and output values were given by the simulator after ten SBR cycles.

French standards methods were used to determine pollution parameters: chemical oxygen demand (COD) (NFT 90‑101), total Kjeldhal nitrogen (TKN) (ISO 5663-1984(F)), total suspended solids (TSS, VSS, MSS) (NFT 90-105-1), nitrate, nitrite and orthophosphate ions (NF EN 10304-2). Ammonium ions concentrations were measured by ionic chromatography (Dionex DX 100).

3. Results and Discussions

According to the bibliographic study, two kinds of overall lengths were chosen for the treatment of urban wastewater in a SBR: 12 hours and 24 hours. The sequence and duration of the different phases are reported in table 2.

Table 2

Basic phases sequencing for the 12 and 24 hour cycles.

Séquences de base pour les cycles de 12 heures et de 24 heures.

Phase nb

24 h cycles

length (%)

12 h cycles

length (%)

Feeding

Aeration

Mixing

Discharge/Wastage

1

4.2

8.3

Yes

No

Yes

No

2

2.1

4.2

No

No

Yes

No

3

33.3

37.5

No

Yes

Yes

No

4

48.9

27.1

No

No

Yes

No

5

1

2.1

No

Yes

Yes

No

6

4.2

8.3

No

No

No

No

7

4.2

8.3

No

No

No

Yes

8

2.1

4.2

No

No

No

No

-> See the list of tables

3.1 Use of ASM 1 for the prediction of the phases and cycle lengths of a SBR.

Modelling carbon and nitrogen removal during 12‑hour and 24‑hour cycles (Benchmark fractionation): In a first part the effectiveness of BSM1 fractionation for SBR sizing was assessed. The characterisation of the incoming wastewater was determined according to the fractionation given by the Benchmark (BSM1) (see in table 1). The results, in terms of removal efficiencies and composition of the treated wastewater, respectively for 12‑hour and 24‑hour cycles of a SBR are given in table 3.

Table 3

Removal efficiencies and outgoing concentrations of the 12-hr and 24-hr simulated cycles with the benchmark distribution (BSM1), compared to the incoming wastewater specific identification of ASM1 state variables during dry and rainy weathers.

Efficacités d’abattement et concentrations de sortie des cycles simulés de 12 heures et 24 heures avec la distribution de la base de données (Benchmark, BSM1), comparée à l’identification spécifique sur l’eau d’entrée des variables d’état du modèle ASM1 par temps sec et par temps de pluie.

 

Origin of ASM1 state variables fractionation

24-h cycles

12-h cycles

French standard

Dry weather

Rainy weather

Dry weather

Rainy weather

 

Average outgoing CODsoluble (mgO2.L‑1)

BSM1

35 ± 5.6

33.3 ± 6

32.4 ± 4

30.4 ± 4.4

125

This study

35 ±  5.5

32.9 ± 6

36.2 ± 3.5

28.7 ± 4.6

COD Removal Efficiency

(%)

BSM1

90

90

91

91

70‑90

This Study

94

95

94

96

Average outgoing Nsoluble

(mgN.L‑1)

BSM1

5.7 ± 0,5

5.5 ± 0,5

15.3 ± 0,5

12.7 ± 0,5

10‑15

This study

5.7 ± 0.5

4.2 ± 0.2

10.6 ± 0.5

4.8 ± 0.5

TN Removal Efficiency (%)

BSM1

88

87

67

71

70‑80

This study

90

92

80

89

-> See the list of tables

Table 3 shows that it was possible with the 24-hour cycles to reach both the French standard and low level of exit concentration, especially for nitrogen (5.5 and 5.7 mg N•.L‑1) - whatever the climatic conditions. On the contrary, the exit concentrations of the 12-hour SBR cycles reached the upper limit of the French standards especially for total nitrogen (15.3 and 12.7 mg N•.L‑1). In a first approach, this result may lead to the rejection of 12‑hour cycles because of a possible lack of reliability of 12-hour SBR cycles.

The distribution of ASM1 state variables given by the benchmark (BSM1) can be a useful tool at first, but it might prove to be incomplete if one considers the high variability of wastewater, according to the kind of effluent it contains (presence of industrial wastewater, separated or combined sewer system). It is then necessary to achieve a specific identification of ASM1 state variables for local wastewater later used in a lab scale or pilot scale reactor.

Specific fractionation of the influent: The incoming wastewater was a combination of industrial and domestic wastewater. The wastewater characterization might differ significantly from standard municipal wastewater used in the Benchmark (BSM1), but was a good example of the interest of using modelling and fractionation.

The results obtained for the variables in relation with carbon and nitrogen species are reported in tables 5 and 6. It is assumed in this study that SI0 and XI0 were not produced during aerobic batch tests from biomass decay, as the sludge inoculum was very low.

Table 4

Identification of SS0 expressed as a percentage of the total COD of the incoming wastewater.

Identification de Ss0 exprimé en pourcentage de la DCO totale de l’eau d’entrée.

Climatic conditions

SS0 (%)

Biodegration tests in closed reactors

SS0 (%)

Coagulation floculation + 0.45 µm filtration

FeCl3

SS0 (%)

Coagulation floculation + 0.45 µm filtration

ZnSO4

Rainy

27.46

16

16

Dry

17

13

20

Dry

25

18

19

-> See the list of tables

Table 5

Comparison between the average values of ASM1 carbon variables (percentage of the total COD) of the incoming wastewater and the most frequent values of the bibliography for urban wastewater.

Comparaison entre les valeurs moyennes des variables carbonées d’ASM1 (pourcentage de la DCO totale) de l’eau d’entrée et des valeurs les plus fréquentes de la bibliographie pour des eaux usées urbaines.

Reference

Climatic conditions

SI0 (%)

XI0 (%)

SS0 (%)

XS0 (%)

XB,H0 (%)

This study

Dry

6

9

23

62

/

This study

Rainy

4

17.5

33.5

45

/

STRICKER (2000)

Dry

4

15

31

50

/

STRICKER (2000)

Rainy

6

11

28

55

/

Most frequent values

 

6‑13

8‑13

7‑30

40‑60

15‑20

Extreme values

 

3‑20

4‑26

1‑54

15‑80

3‑20

HENZE et al. (1987)

 

8‑11

11‑20

4‑32

43‑49

/

Benchmark (BSM1)

 

8.3

12.7

18.1

53.5

7.3

-> See the list of tables

Table 6

Comparison between the average values of ASM1 nitrogen variables (percentage of the total Nitrogen) of the incoming wastewater and the most frequent values of the bibliography for urban wastewater.

Comparaison entre les valeurs moyennes des variables azotées d’ASM1 (pourcentage de l’azote total) de l’eau d’entrée et des valeurs les plus fréquentes de la bibliographie pour des eaux usées urbaines.

Reference

Climatic conditions

SNH0 (%)

SND0 (%)

XND0 (%)

SNI0 (%)

XNI0 (%)

This study

Dry

27.7

29

32.7

7.9

2.7

This study

Rainy

26

28.75

21.25

16.75

7.25

HENZE et al. (1987)

Default values

 

29 to 40

50 to 59

10 to 12

neglected

HENZE (1992)

 

 

 

 

 

4

HENZE et al. (1993)

 

 

45

55

neglected

neglected

STRICKER (2000)

Dry

 

33

45

10

12

STRICKER (2000)

Rainy

 

/

/

5

6

Benchmark (BSM1)

 

64.7

14

21.3

/

/

-> See the list of tables

An accurate identification of SS0 is of interest, as the availability of readily biodegradable carbon substances is important for the successful achievement of denitrification. The results showed that the method of biodegradation tests in closed reactors led to an overestimation of the Ss0 fraction, compared to physico-chemical methods (see in Table 4). The estimation of SS0 includes a part of colloidal matter. It is in agreement with LEVINE et al. (1985), who concluded that it was necessary to use a 1.0 µm pore-size membrane to separate correctly the true soluble and particulate forms. Nevertheless, 0.45 µm pore-size membranes are widely used.

The specific identification of carbon ASM1 state variables during rainy or dry weather presented good correlations with other results found in literature (Table 5). The largest part of COD is biodegradable (soluble or particulate). Especially during dry periods, the largest part of biodegradable COD is particulate.

The results of nitrogen ASM1 variables (Table 6) showed that the distribution for the incoming wastewater differs partly from literature data. The proportion of inert species was not negligible, hence the interest of a specific identification.

For carbonaceous species, it was possible to conclude to a good agreement with the literature values, but it was not the case for nitrogen variables, the distribution of which appearing to be really specific when compared to the references. These results might be due to the presence of industrial effluent in the wastewater.

It appeared from these experimental data that:

  • The reliability of Ss determination depended on the applied pore-size of the membrane, which confirms the work of LEVINE et al. (1985);

  • Parts of the soluble and settleable fraction might belong to Xs (SOLLFRANK et GUJER, 1991);

  • It was not possible to identify the variable XB,H. In her important work on calibration, identifiability and optimal experimental design of activated sludge models, PETERSEN (2000) reported that this variable was not negligible. SPERANDIO (1998) evaluated this fraction at 10% of the global COD, and HENZE (1992) at 15-20%.

Modelling carbon and nitrogen removal during 12‑hours and 24‑hour cycles with a specific influent fractionation: The modelling of the 12‑hour and 24‑hour cycles, using the specific distribution of ASM1 state variables of incoming wastewater, is presented at figure 2. The average values of COD and TN were measured during rainy and dry weathers over three months, in the Wastewater Treatment Plant of Limoges (see Table 7).

Figure 2

Evolution of the soluble Nitrogen concentrations during the simulations over ten days for the 24-h and the 12-h cycles (dry and rainy weathers). The continuous lines represent the exit concentration evolutions of soluble nitrogen at the end of the cycle, just before the discharge; the broken line represents the French standards required for the exit water.

Évolution de la concentration en azote soluble au cours des simulations sur dix jours pour les cycles de 24 heures et de 12 heures (temps sec et temps de pluie). Les lignes continues représentent la concentration de sortie de l’azote soluble à la fin du cycle, juste avant la vidange, les traits pointillés correspondent à la norme française exigée en sortie.

(a)

24h dry weather

24h dry weather

(b)

24h rainy weather

24h rainy weather

(c)

12h dry weather

12h dry weather

(d)

12h rainy weather

12h rainy weather

-> See the list of figures

Table 7

Average values of total COD, TN, ammonium ion, and organic nitrogen concentrations in the incoming wastewater during dry or rainy weather. The results are given for several months of measurement.

Valeurs moyennes des concentrations en DCO, azote total, ions ammonium, azote organique dans l’eau d’entrée par temps sec et par temps de pluie. Les résultats sont donnés après plusieurs mois de mesures.

 

Global COD

(mgO2•L‑1)

TN

(mgN•L‑1)

NH4+

(mgN•L‑1)

Norganic

(mgN•L‑1)

Rainy weather

653 ± 326

52 ± 18,6

13.1 ± 4.2

38.8 ± 16.3

Dry weather

568 ± 237

58 ± 20

15.6 ± 5.2

41 ± 18.8

-> See the list of tables

The exit concentrations taken into account for the carbon forms are Ss and SI (soluble forms of COD) and the ones for nitrogen are SNH, SND (soluble forms of nitrogen) as we assumed that particular species concentration were negligible in the effluent.

The results of the simulations for 12‑hour and 24‑hour cycles with incoming wastewater specific identification of ASM1 state variables are collected in table 3. The exit concentrations and removal efficiency of nitrogen and carbon of the simulations show that it was now possible to treat the incoming wastewater with 12‑hour cycles in a SBR (Figure 2). It was, especially during dry weather, possible to reach exit concentrations of the treated wastewater below the French standards (Figure 2).

3.2 Lab scale and pilot scale validation of cycles determined thanks to modelling

In order to test the validity of the above strategy (fractionation and modelling), 12‑hour cycles have been carried out at lab scale and then at pilot scale for several months. The incoming organic loading rate had an average value of 0.05 kg BOD5•kg TSS•cycle‑1. The sludge retention time was equal to ten days. The results are presented in table 8.

Table 8

Removal efficiencies of 12-hour cycles, lab scale and pilot scale.

Taux d’abattement obtenus pour les cycles de 12 heures à l’échelle du laboratoire et à l’échelle pilote.

 

Average outgoing concentration of the treated wastewater(mg•L‑1)

Average Removal Efficiency (%)

COD

BOD5

TN

COD

BOD5

TN

Lab scale

54 ± 37

5 ± 3

11 ± 6

92 ± 6

99 ± 1

85 ± 8

Pilot scale

26 ± 8

5 ± 5

11 ± 5

94 ± 3

97 ± 5

82 ± 7

French standard

125

25

10‑15

75

70‑90

70‑80

-> See the list of tables

The different tests completed for the 12-hour cycles defined above, both at a lab scale or pilot scale, led to satisfactory results, in terms of carbon (> 90%) and nitrogen (> 80%) removal. The model validation was then controlled during one cycle for carbon and nitrogen removal. The results are presented for the pilot scale validation (Figures 3 and 4).

Figure 3

Correlation between model and experiment for COD during a pilot scale cycle.

Corrélation entre le modèle et l’expérience pour la DCO au cours d’un cycle de fonctionnement.

Correlation between model and experiment for COD during a pilot scale cycle.

-> See the list of figures

Figure 4

Correlation between model and experiment for N-NH4+ during a pilot scale cycle.

Corrélation entre le modèle et l’expérience pour l’azote ammoniacal au cours d’un cycle de fonctionnement.

Correlation between model and experiment for N-NH4+ during a pilot scale cycle.

-> See the list of figures

The specific identification of ASM1 state variables for the incoming wastewater during rainy or dry weather makes it possible to describe the experimental data with sufficient accuracy:

  • Soluble carbon removal was very well described by ASM1, as well as the nitrification process, the increase of the soluble COD between 10 h and 11 h was linked to the withdrawal of the reactor (increase of the relative concentration);

  • It was considered in this study that the effluent was only made of soluble forms of carbon. Possible underestimation of soluble carbon and especially SI by ASM1 could be possible as it was a part of biomass decay (PETERSEN, 2000). This phenomenon was observed for the lab scale simulation but not for the pilot scale. Some authors mentioned that for long solid and hydraulic retention times, ASM1 did not give a good description of carbon consumption (SPERANDIO, 2006).

  • The modelling of nitrogen removal with ASM1 has been largely discussed in the literature. Some authors mentioned difficulties for ASM1 to correctly describe the nitrification and denitrification processes, especially when the nitrogen content of the influent was important. On the other hand, COELHO et al. (2000), SMETS et al. (2003) showed that it was possible, in the context of domestic wastewater, to describe correctly N removal through a simplification of ASM1. BOAVENTURA et al. (2001) stated that for better accuracy of simplified ASM1 model, it was necessary to use robust mathematical filters.

  • In this study, ASM1 was used without any simplification. An overestimation of ammonium concentration could be observed, probably due to the fact that biological reactions have not been considered during the modelling of the settling phase. KELLER et YUAN (2002) proposed to remedy this problem by using a combination of a hydraulic and a biological (ASM2d) model during the settling phase; in particular when the influent was fed in the bottom of the reactor during this phase.

4. Conclusion

There are many possibilities for the set up of an SBR; testing the different scenarios in the labscale is both costly and time-consuming. The ASM1 makes it possible to test different scenarios during rainy and dry weather, with different distributions for ASM1 state variables.

In a very reduced time (three months) and very reduced cost compared to the cost of labscale tests needed to test so many scenarios (2 global length*2 kind of weather = 4) we demonstrated that it was possible to define an accurate optimal SBR sequence for the treatment of carbon and nitrogen, with any kind of urban wastewater.

To initialize the mathematical model, it was possible to use predefined state variables (BSM1) or to achieve a specific fractionation for the wastewater of interest.

It was necessary to have an accurate description of ASM1 state variables especially when the model was supposed to describe the treatment of industrial or combined domestic and industrial wastewater (COEN et al., 1997). The incoming wastewater entered in this field was a mixture of domestic and industrial effluent. This conclusion is important, for the transposition of this methodology to an industrial effluent.

The specific fractionation results showed that it was possible to treat the incoming wastewater correctly, with 12‑hour cycles whereas the BSM1 distribution led to 24-hour cycles. This conclusion is of major interest, as it leads to doubling the effectiveness of the reactor in terms of the amount of treated nitrogen (CASELLAS, 2002).

The SBR cycle, defined thanks to the above strategy, was tested in a lab scale and pilot scale strategy. The experimental validation led to very good results, in terms of carbon and nitrogen removal: more than 90% of COD removal and more than 80% of total nitrogen removal. Moreover, specific fractionation for the incoming wastewater led to good adequacy between the experimental data and model prediction, even though better model adequacy could have been reached by completing the measurement of ASM kinetics and stoechiometric parameters.

ASM1 state variable identifications led to a more accurate definition of SBR phase lengths and species concentration evolution during one cycle. This methodology can be easily used for sizing a SBR treating urban wastewater.