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## Water SA

*On-line version* ISSN 1816-7950

### Water SA vol.35 n.5 Pretoria Oct. 2009

**Evaluation of modifications to a physicochemical method for determination of readily biodegradable COD**

**A Escalas-Cañellas ^{I,II,*}, MA Ortiz-Balderas^{II}; MG Barajas-López^{I,II}**

^{I}Centro de Investigación y Estudios de Posgrado, Facultad de Ingeniería, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 8, Edificio P, Zona Universitaria, C.P. 78290, San Luis Potosí, SLP, Mexico

^{II}Programa Multidisciplinario de Posgrado en Ciencias Ambientales, Universidad Autónoma de San Luis Potosí, Av. Dr. Manuel Nava 201, 2do piso, Zona Universitaria, C.P. 78210, San Luis Potosí, SLP, Mexico

**ABSTRACT**

In the Mamais-Jenkins-Pitt method for determination of readily biodegradable COD (S_{S}), 2 alternatives were proposed for the intermediate determination of soluble inert COD (S_{I}). When a full-scale treatment plant exists, influent S_{I} = effluent truly soluble COD. When there is no full-scale plant, then the truly soluble COD of the effluent of a 24 h fill-and-draw batch reactor treating the wastewater is taken as influent S_{I}.

In this study, both S_{I} methods were statistically compared on 24 wastewater samples from 2 municipal wastewater treatment plants (WWTPs). While average S_{I} obtained for the 2 methods was the same, individual samples usually had very different S_{I} values. In fact, virtually no correlation was found between the 2 methods. Also, the S_{S} values obtained using both S_{I} alternatives were statistically compared. A good correlation was observed, in spite of the poor S_{I} correlation – low, dispersed S_{I} values did not seriously affect the correlation between both S_{S} determinations. A method was proposed for determination of the limit of detection and the limit of quantification (LOQ) for both S_{S} methods. The LOQ resulted in 28.6 mg/l and 32.6 mg/l, respectively, for the full-scale and the laboratory-scale alternatives.

Some assumptions of the original laboratory-scale (LS) method could potentially be sources of error in S_{I} determination. Two modifications to the laboratory-scale method were implemented in order to avoid these potential problems: Washing biomass with tap water, and correcting S_{I} in the fill-and-draw reactor by the S_{I} of the original biomass suspension.

These method modifications were tested on wastewater samples from the mentioned WWTPs. The fundamentals and results of both modifications are discussed in this paper, as well as the imprecision associated with estimating influent S_{I} from effluent CODsol in all studied methods, and its impact on S_{S} determination.

**Keywords:** readily biodegradable COD, physicochemical, wastewater

**Nomenclature**

ASCE | American Society of Civil Engineers |

ASM1 | Activated Sludge Model No. 1 |

ASM2d | Activated Sludge Model No. 2d |

ASM3 | Activated Sludge Model No. 3 |

BNR | biological nutrient removal |

BOD | biochemical oxygen demand |

BTE | batch-test effluent |

COD | chemical oxygen demand |

CODsol | soluble COD (Mamais-Jenkins-Pitt method) |

DO | dissolved oxygen |

DOC | dissolved organic carbon |

EFF | full-scale plant effluent |

EPA US | Environmental Protection Agency |

F/M | food to micro-organisms ratio |

FS | full scale |

HRT | hydraulic retention time |

IWA | International Water Association |

LOD | limit of detection |

LOQ | limit of quantification |

LS | laboratory scale |

LSC | laboratory-scale method correcting effluent S_{I} by biomass S_{I} |

LS | laboratory-scale method correcting effluent S |

LSTW | laboratory-scale method using tap water for biomass washing |

LS | laboratory-scale method using tap water for biomass washing |

MCRT | mean cell retention time |

PPT ' | Parque Tangamanga 1-B' WWTP |

R | determination coefficient |

RSD | relative standard deviation |

S | fermentation products |

SBR | sequencing batch reactor |

S | fermentable matter |

S | soluble inert organic matter |

SLP | State of San Luis Potosí, Mexico |

S | readily biodegradable organic substrate |

TSS | total suspended solids |

TTV | 'Tanque Tenorio-Villa de Reyes' WWTP |

V | volume of initial mixed liquor in a batch test |

VSS | volatile suspended solids |

V | volume of wastewater in a batch test |

WEF | Water Environment Federation (USA) |

WW | wastewater |

WWTP | wastewater treatment plant |

X | particulate inert organic matter |

X | slowly biodegradable substrate |

**Introduction**

Increased usage of BNR has promoted COD fractionation as a tool for wastewater evaluation and process design and control (Spérandio and Paul, 2000). IWA models for BNR use several COD fractions as state variables, so COD fractions must be evaluated for model initialisation, calibration and validation. Both ASM1 and ASM3 models consider 4 wastewater COD components, namely: readily biodegradable organic substrate (S_{S}), soluble inert organic matter (S_{I}), slowly biodegradable substrate (X_{S}) and particulate inert organic matter (X_{I}) (Henze et al., 2000). Other wastewater COD fractions are biomass-related: biomass components, biomass decay particles and internal storage products. Though biomass can account for 10 to 20% of total organic matter in wastewater, not considering it in raw wastewater would not affect the modelling considerably (Henze, 1992). In this case, biomass would be included in the slowly hydrolysable organic fraction, according to the same author. In ASM2d, S_{S} is split into fermentable matter (S_{F}) and fermentation products (S_{A}). However, S_{S} is useful for ASM2d, since S_{F} can be obtained as the difference between S_{S} and S_{A}. So, readily biodegradable COD is a basic and useful COD fraction, and several respirometric and physicochemical methods have been developed for S_{S} determination.

In IWA models, S_{S} and X_{S} fractions are set in terms of their aerobic biodegradation rates, which can be determined by respirometry. Thus, several respirometric methods have been proposed or modified for estimation of readily biodegradable COD (Ekama et al., 1986; Spanjers and Vanrolleghem, 1995; Wentzel et al., 1999; Spérandio and Paul, 2000). At the same time S_{S} is considered soluble, while X_{S} is colloidal or particulate, which allows for physicochemical determination of S_{S}. When compared to respirometric methods, physicochemical methods require simpler and cheaper apparatus, since they are usually based on filtration techniques. However, equivalence between both methods has been a subject of discussion. Filtration through 0.45 µm filters does not ensure the complete removal of colloidal matter, which is slowly biodegradable (Melcer, 2004). The 0.45 µm filtrate can include about 50% of X_{S}, while the rest is S_{S} and S_{I} (Henze, 1992). The colloidal fraction has been successfully removed by either ultrafiltration (Dold et al, 1986) or flocculation and filtration (Mamais et al., 1993; Hu et al., 2002).

The method by Mamais et al. (1993) provides a simple physicochemical technique for determination of truly soluble COD (herein referred to as CODsol) and readily biodegradable COD. In this method wastewater CODsol is determined as the COD of the filtrate obtained after sample flocculation, and filtration through a 0.45 µm filter. Then, wastewater S_{I} is determined as the CODsol of the effluent of an aerobic biological plant treating the studied wastewater. More precisely, 2 alternatives were given by Mamais et al. (1993) for S_{I}:

- To determine S
_{I}as the effluent CODsol of a full-scale plant treating the wastewater (if a full-scale plant exists) - In the absence of a full-scale plant, to determine CODsol as the effluent CODsol of a laboratory-scale fill-and-draw plant treating the wastewater of interest, and having a mean cell retention time (MCRT) of greater than 3 d and an HRT of 24 h.

Some assumptions of the Mamais et al. (1993) method could be potential sources of error in S_{I} determination and, consequently, on S_{S}, as discussed next.

In the full-scale (FS) alternative, it is assumed that effluent S_{S} is null. According to a plant survey cited in WEF-ASCE (1998), 42 activated sludge treatment plants had an annual mean effluent BOD of 15.5 mg/l (EPA, 1981) with a wide range of plant averages, namely 11 mg/l to 39 mg/l. TSS averaged 18.5 mg/l, with a wide range too. Assuming effluent BOD and TSS being roughly equal, and assuming effluent SS having a BOD of approximately 50% of their weight (WEF-ASCE, 1998), soluble BOD would reasonably average 7.5 mg/l with a range of 5.5 to 19.5 mg/l in secondary effluents of activated sludge plants. In ASM1 and ASM3, soluble BOD, being soluble and biodegradable, can only be included in the S_{S} fraction of COD. Though the 5.5 mg/l to 19.5 mg/l range is rather low, it can account for a considerable fraction of effluent soluble COD in municipal wastewaters, thus affecting S_{I} determination by the FS alternative and, consequently, S_{S} determination in the low S_{S} range. The LS test conditions (24 h HRT, longer than FS activated sludge plants) could perhaps achieve lower effluent S_{S}.

In this study, CODsol, S_{I} and S_{S} were determined by both the FS and LS alternatives of the Mamais et al. (1993) method, on wastewater samples of 2 municipal, activated sludge WWTPs, and the results of both alternatives were compared for S_{I} and S_{S}, in order to determine whether these methods were equivalent and, particularly, whether S_{I} was lower, and S_{S} higher, by the LS alternative.

Since influent S_{I} can be assumed variable, effluent S_{I} must be variable too, even considering equalisation effects throughout the plant. In a previous research, Escalas et al. (2003) studied dissolved organic carbon (DOC) evolution throughout a municipal, continuous-flow activated sludge plant. Though primary clarifiers provoked a clear peak reduction, and secondary treatment yielded a smooth effluent DOC curve, the effluent DOC range was still 13 mg/l to 34 mg/l over a period of one week. This is a considerable variability for soluble organic matter, which includes the inert soluble fraction. The S_{I} subtracted from the CODsol in the method has an intrinsic variability that has not yet been evaluated and this issue is addressed in this paper.

In the LS alternative, a wastewater with a given S_{I} is mixed with a biomass (mixed liquor) that has a different S_{I}, since mixed liquor S_{I} depends on the variable S_{I} fed to the reactor in the previous batches. This could affect S_{I} and S_{S} determination.

In the present study, the issue of S_{I} variability was addressed by analysing effluent CODsol variability in the effluent of the 2 WWTPs studied. In order to suppress or minimise the effect of mixed-liquor S_{I} on LS effluent S_{I}, two LS method modifications were essayed:

- To wash biomass with tap water before the LS test, in order to remove CODsol from biomass, thus suppressing the biomass interference on S
_{I}determination (LS_{TW}alternative) - To determine biomass S
_{I}, and correct effluent S_{I}for this value (LS_{C}alternative).

**Experimental**

**General experimental design**

Twenty-four wastewater samples and their corresponding full-scale secondary effluents were taken at 2 municipal wastewater treatment plants in the city of San Luis Potosí (SLP), central–north highlands of Mexico: Parque Tangamanga 1-B plant (PPT) and Tanque Tenorio-Villa de Reyes plant (TTV). In a first campaign, 16 wastewater samples were taken, corresponding to low and high influent concentration at the plants. A 2^{2} factorial design (Montgomery and Runger, 2003) with 4 replicates was applied (4x2^{2}), with plant (TTV/PPT) and influent concentration (low/high) as design variables. Eight additional wastewater samples were taken at the PPT plant, 4 corresponding to high concentration and 4 to low concentration time bands, for a total of 24 samples between the 2 plants. A previous 24 h sampling (12 samples per plant) was performed in order to determine the time bands of low- and high-influent COD concentration. An overview of the general methodology is shown in Fig. 1.

TSS, volatile suspended solids (VSS), COD and CODsol were determined on the samples, and the following alternatives were applied for S_{I} and S_{S} determination:

**FS alternative**: wastewater S_{I} was determined as the CODsol of the secondary treatment effluent of the full-scale plant, in accordance with one of the Mamais et al. (1993) alternatives (Eq. (1) and (2)).

where:

(S

_{I})_{FS}is the un-biodegradable soluble COD according to the FS alternative

(CODsol)_{EFF}is the truly soluble COD at the FS plant effluent, determined by the Mamais et al. (1993) method

(S_{S})_{FS}is the readily biodegradable COD according to the FS alternative

(CODsol)_{WW}is the truly soluble COD of wastewater

**LS alternative**: wastewater S_{I} was determined as the effluent CODsol of a laboratory-scale 24 h fill-and-draw reactor, as in the other Mamais et al. (1993) alternative. Equations (3) and (4):

where:

(S

_{I})_{LS}is the wastewater un-biodegradable soluble COD according to the LS alternative (DQOsol)_{ BTE}is the truly soluble COD of the batch test effluent

**LS _{TW} alternative**: As in the LS alternative, wastewater S

_{I}was determined from the effluent CODsol of a laboratory-scale 24 h fill-and-draw reactor. However, the biomass was first washed with tap water in order to remove the CODsol present in the mixed liquor, before mixing with wastewater for the batch test. This process results in a dilution of wastewater S

_{I}, so a correction must be applied to S

_{I}(Eq. (5)) before S

_{S}calculation (Eq. (6)).

where:

(S

_{I})_{LSTW}is the un-biodegradable soluble COD of wastewater according to this method alternative

V_{ML}and V_{WW}are respectively the volumes of initial mixed liquor and wastewater used for the batch test

S_{S})_{LSTW}is the readily biodegradable COD according to this method alternative

**LS _{C} alternative**: As in the LS and LS

_{TW}alternative, wastewater S

_{I}was determined from the effluent CODsol of a laboratory-scale 24-h fill-and-draw reactor (Eq. (7)), but the S

_{I}of the initial mixed liquor was determined before addition of wastewater to the reactor (Eq. (8)), and a correction was applied to wastewater S

_{I}determination. An S

_{I}balance applied to the batch test can be written (Eq. (9)), which allows calculating the corrected wastewater S

_{I}(Eq. (10)). The usual calculation is applied for S

_{S}(Eq. (11)):

where:

(S

_{I})_{BTE}is the un-biodegradable soluble COD of the batch test effluent

(S_{I})_{ML}is determined as the CODsol of the batch reactor mixed liquor before addition of wastewater

(S_{I})_{LSC}is the un-biodegradable soluble COD of wastewater according to this procedure

FS and LS alternatives of the Mamais et al. (1993) method were compared in order to check for equivalence between both methods of S_{I} determination. The resulting S_{S} was also compared between both methods. Also, the LS_{TW} and LS_{C} alternatives were compared to the FS alternative, which was taken as reference.

**Sampling and storage**

Wastewater samples were taken at the 2 municipal wastewater treatment plants mentioned above (PPT and TTV). PPT is an 8 640 m^{3}/d SBR plant with 2 alternating reactors, and TTV is a 60 500 m^{3}/d continuous-flow activated sludge plant with enhanced primary treatment. Both flow rates are operational. At the PPT plant, grab influent samples were taken at the SBR feed-pipe discharge. At the TTV plant, characterisation was applied to grab samples of the secondary treatment influent, in order to avoid interference from the physicochemical primary treatment on the method essayed. Effluent grab samples were taken at the SBR discharge (PTT) or at the secondary settling effluent (TTV). Sampling after disinfection (PPT) or after full tertiary treatment (TTV) was avoided, in order to prevent chemical oxidation of effluent CODsol to interfere with the measured S_{I}. Raw wastewater and mixed liquor samples were analysed and used in the batch tests upon arrival at the laboratory, while effluents and filtrates were stored at 4ºC for less than 12 h before analysis.

**Standard analyses, CODsol, S _{I} and S_{S}**

TSS, VSS, COD, pH and dissolved oxygen (DO) were determined according to *Standard Methods* (1998). COD was determined by the closed reflux, 5520 D spectrophotometric method (*Standard Methods*, 1998), using a DR/4000 spectrophotometer (Hach, Loveland, CO, USA). CODsol was determined by the Mamais et al. (1993) method of zinc sulphate flocculation, settling, and supernatant filtration through 0.45 µm filters (Whatman, cellulose nitrate membrane, Ø47 mm, 0.45 µm pore filters). S_{I} was determined as detailed above (Eq. (1), (3) and (6)), depending on the method alternative. S_{S} was always computed as the difference between CODsol and S_{I}. Duplicate analyses were run for all samples. In the case of CODsol and S_{I}, duplicate flocculation and filtration procedures were also run. Triplicate COD analyses were run on each sample replicate in the low-range COD method, duplicate analysis for the high-range method.

The high- and low-range variants of the *Standard Methods* (1998) spectrophotometric COD method were validated by analysing the potassium hydrogen phthalate calibration curves for linearity, limit of detection (LOD), limit of quantification (LOQ), repeatability and recovery. Linearity was evaluated through the determination coefficient (R^{2}) (Miller and Miller, 2002). LOD was computed from the y-intercept absorbance in the calibration-line plus three times the standard deviation (3*s*) of the blank (from 10 blanks) (Miller and Miller, 2005). For the LOQ, a 5*s* criterion was applied (Eurachem, 1998). Repeatability was checked through the per cent relative standard deviation (RSD) of COD when computed from 3 calibration lines obtained on the same day (Eurachem, 1998).

**Previous COD regime characterisation**

Sample diversity was achieved by sampling 2 different plants at different times of the day, so they could present different concentration and COD composition. It was necessary to know the COD evolution of wastewater at the sampling points (COD regime) beforehand. So, samples were taken every 2 h at the sampling points of both plants, in a daylong sampling operation starting at 20:00. Plant influent (PPT), secondary treatment influent (TTV) and secondary effluent samples (both plants) were analysed for COD and CODsol. S_{I} and S_{S} were calculated in accordance with the FS alternative of the physicochemical method (Eq. (1) and (2)).

**Main sampling design**

Table 1 displays the main sample design, a 2^{2} factorial with four replicates (4x2^{2}), based on the variables 'plant' (TTV/PPT) and 'COD concentration' (low/high). The replicates were set in four 2^{2} blocks. Randomisation was applied inside each block, as a usual measure to ensure independent sampling. Due to higher COD and CODsol variability observed at that PPT, 8 additional samples were taken later at this plant for better characterisation, 4 samples corresponding to low concentration, and 4 to low concentration.

**Laboratory-scale, 24-h batch tests**

For the LS alternatives, mixed liquor from the biological reactors of each WWTP were mixed with wastewater and the mixture was kept aerated for 24 h. Mixed liquor samples were taken at the exit of the biological reactors (TTV) or at the end of the aerated 'react' phase of the SBR cycle (PPT). These biomasses were already acclimated to the wastewaters used in the batch tests, so they were directly used. Mixed liquor (0.5 ℓ) and appropriate wastewater volumes were mixed in order to maintain an F/M of 0.075 g COD/(g VSS.d). Duplicate batch tests were carried out for each sample and experimental condition, in 600 to 2000 ml beakers, aerated through ceramic diffusers. Dissolved oxygen was kept at above 2 mg/l throughout the tests.

**Biomass washing**

In the tests with previous tap water biomass washing, 0.5 l of mixed liquor from the full-scale plant were settled for 20 min in a 500 ml graduated cylinder. Thereafter the supernatant was decanted and tap water was added to complete the volume to 0.5 l. This process was repeated 2 more times to complete 3 settle-decant-refill operations, which allowed the removal of 99% of the original liquid phase.

**Evaluation of method alternatives**

The analytical precision of a given method alternative was evaluated through the standard deviation from a pair of sample replicates. First, sample standard deviations were calculated for each pair of replicates. Then, the squares of the maximum and the minimum sample standard deviations were compared in an F-test at 5% significance (Montgomery and Runger, 2003). If they resulted equal, all samples were assumed to have the same analytical variance which was then computed from individual sample standard deviations through the pooled estimator (*s _{P}^{2}*) (Eq. (12)):

This is a generalisation of the 2-sample pooled estimator in Montgomery and Runger (2003), where *s _{i}* is the analytical standard deviation of sample

*i*,

*n*is the number of replicates for sample

_{i}*i*, N is the number of samples (24 for all methods, except for LS

_{TW}, 16),

*s*is the pooled analytical standard deviation of the method.

_{P}If maximum and minimum individual variances were not equal in the above-mentioned F-test, it was concluded that there was not a common *s* for all samples, and the individual standard deviations lying outside the centred 95% percentile were discarded. Then a pooled *s* was calculated for the N_{h} samples sharing a common variance in the upper *s* range within the centred 95% percentile of standard deviations. These upper ranges included 75% to 100% of all samples. Finally, the analytical precision of a sample result (mean of two replicates) was calculated as *S _{p}*/.

This analytical precision was applied to all (CODsol)_{WW} and (CODsol)_{EFF} determinations. However, when directly estimating influent S_{I} from (CODsol)_{EFF} in grab samples, precision is not only affected by analytical issues, but by the fuzzy relationship between (CODsol)_{EFF} and influent S_{I}, as discussed next. The following assumptions were applied to all influent S_{I} values when directly estimated from (CODsol)_{EFF}, as in Eq. (1), (3) and (7):

- Population means of influent and effluent S
_{I}are equal, as derived from ASM1 and Mamais et al. (1993) method assumptions - However, it is not possible to precisely associate the CODsol of a given effluent grab sample to a particular influent sample, due to total or partial mixing and time-delays throughout the plant. Consequently, (CODsol)
_{EFF}of a grab sample, i.e. influent S_{I}'s estimate, should be considered a random variable having the same mean as influent S_{I}, and a variance which can be estimated as the square standard deviation of all (CODsol)_{EFF}values. Consequently, S_{I}precision for grab effluent samples from a WWTP was estimated from the standard deviation of all effluent samples (herein called 'overall standard deviation').

Method comparison was carried out through 3 different approaches:

- Means of all samples by 2 methods were compared through t-tests at 5% significance, with previous investigation of equal/different variances using F-tests for variance comparison at 5% significance
- Means of 2 methods were also compared through paired t-tests (Montgomery and Runger, 2003)
- Regressions of method modifications against a reference method were performed. Equality of methods would be ideally proved through zero y-intercept, unit slope and unit R
^{2}(Miller and Miller, 2005).

The FS alternative was taken as reference method for comparisons.

**Variance estimation for linear combinations of variables**

When estimated from a simple set of data, variance was estimated as the square standard deviation. When estimating the variance of a linear combination of variables (Eq. (13)), it was computed from the square standard deviations of the individual variables and their sample covariance, through a general equation assuming correlation (Montgomery and Runger, 2003) (Eq. (14)). This was the case in Eqs. (2), (4), (5), (6), (10) and (11), where S_{I} and S_{S} are linear combinations.

where

x,yandzare variables (e.g., CODsol, S_{I}and S_{S}),

aandbare the coefficients of the linear combination,

s,_{x}sand_{y}sare the respective standard deviations, and_{z}

cov(xy)is the sample covariance ofxandy.

Non-correlation was not assumed, so *cov(xy)* was always computed when using Eq. (14). When effluent S_{I} was involved in these calculations, the overall S_{I} standard deviation was used, while the analytical standard deviation was used for (CODsol)_{WW}.

**Limit of detection and limit of quantification for S _{S}**

The limit of detection is generally defined as the concentration which gives an instrument signal (y) significantly different from the blank signal. Typically, the sample signal should be greater than the mean blank signal plus three times the blank signal standard deviation, i.e., LOD = y_{B}+3*s*_{B} (Miller and Miller, 2002). Considering CODsol as the method 'signal', then effluent CODsol (i.e., S_{I}) can be considered a blank for the method, since it nominally corresponds to zero S_{S}, and its 'signal' is subtracted to the influent sample signal ((CODsol)_{WW}) (see Eq. (2) and (4)). So, for an S_{S} value to be detectable, wastewater CODsol should be significantly higher than effluent CODsol. Accordingly, the CODsol corresponding to the limit of detection was computed as the mean S_{I} plus 3 times the standard deviation of S_{I} (Eq. (15):

where:

(CODsol)

_{LOD}is the 'signal' corresponding to the limit of detection for S_{S }is the average S_{I}ands(S_{I}) is the overall standard deviation of S_{I}

The limit of detection for S_{S} was obtained from (CODsol)_{LOD} by substituting this value into the regression equations of CODsol vs. S_{S} (Fig. 6), and then isolating S_{S}.

The limit of quantification was considered under a 5*s* criterion. The 'signal' corresponding to the LOQ was computed (Eq. (16)), and then the LOQ for S_{S} was computed by substituting (CODsol)_{LOQ} into the regression equations in Fig. 6, and then isolating S_{S}.

**Results and discussion**

**COD method validation**

Table 2 displays the results of COD method validation. Linearity was excellent (0.9995 to 0.9996). LOD and LOQ for the low-range method were respectively 3.0 and 4.9 mg/l, below all COD or CODsol values obtained in this study, and well below most of them. LOD and LOQ for the high range method were nominally 4.6 and 7.7 mg/l, though the high range was 80-500 mg/l.

**Previous COD regime characterisation**

Figure 2 shows the evolution of COD (a) and CODsol (b) in influent samples from TTV and PPT. Both WWTPs presented typical COD daily oscillations, with a sharper COD profile at PTT, which does not have primary treatment and its peak-reduction effect mentioned above. The CODsol curve was also sharper for PPT, while the TTV curve was rather flat, making it difficult to define a high/low CODsol concentration regime. For this reason, time bands of high and low COD concentration were determined, and used to set up the experimental design for the main sampling.

The high concentration intervals were 16:00 to 04:00 (TTV) and 12:00 to 02:00 (PPT), while low-concentration intervals were, respectively, 06:00 to 14:00 and 04:00 to 10:00. Table 3 displays time bands and their COD and CODsol averages. The overall COD and CODsol ranges for all samples in both WWTPs were, respectively, 127 to 577 and 38 to 78 mg/l. The different wastewater origin and concentration ranges ensured considerable wastewater variability for the samples involved in the main sampling, as it was intended.

**Results from the main sampling**

Table 4 displays raw results from the main sampling at TTV and PPT plants, while Table 5 presents S_{I} and S_{S} obtained by the four method alternatives presented above (FS, LS, LS_{TW} and LS_{C}). These results are discussed below.

**Influent CODsol**

The influent CODsol had an overall average (both WWTPs) of 123 mg/l, with a range of 36 to 215 mg/l, much wider than in the main sampling. The analytical standard deviation of CODsol ranged 0 to 11.0 mg/l for the set of 24 samples (centred 95% percentile), with a pooled analytical standard deviation of 3.9 mg/l (3.2% RSD), 2.8 mg/l for the mean of 2 samples.

**Precision of S _{I} determination by the FS and LS alternatives**

The analytical standard deviation of the pairs of replicates of (S_{I})_{FS} ranged 0.1 to 2.9 mg/l (centred 95% percentile), with a pooled standard deviation of 1.2 mg/l to 0.9 mg/l for the mean of 2 samples – which is excellent. However, the overall standard deviation of S_{I} by the FS method was computed for each WWTP, resulting in 6.7 mg/l at TTV plant (50% RSD), and 5.0 mg/l at PPT plant (29% RSD). These *s* values were found statistically equal in an F-test, and a pooled overall standard deviation of 5.7 mg/l was used for (S_{I})_{FS}. These results indicate that a high relative imprecision (36% RSD) was found associated to S_{I} determination as CODsol of the FS plant effluent.

Similar results were obtained for the LS alternative. The analytical precision – standard deviation of (S_{I})_{LS} in individual samples – ranged 0.3 to 4.0 mg/l, with a pooled standard deviation of 1.6 mg/l to 1.1 mg/l for the mean's standard deviation. The overall standard deviation of estimating S_{I} by the LS method was 6.7 mg/l (46% RSD) and 6.6 mg/l (38% RSD) for, respectively, TTV and PPT. Again, a high relative imprecision was associated to (S_{I})_{LS} determination as the CODsol of the LS plant effluent. The pooled overall standard deviation for both plants was 6.6 mg/l (40% RSD).

As conclusion, the effluent CODsol of a single grab sample can be determined with a considerable precision (*s *= 1.2 mg/l). However, when attributing effluent CODsol to an (S_{I})_{EFF} representing influent S_{I}, the overall variability of effluent CODsol applies, which is much greater, ranging 5.0-6.7 mg/l (29 to 50% RSD) for the two plants and methods herein analysed.

**Comparing FS and LS alternatives for S _{I} determination**

It would be reasonable that a 24 h HRT laboratory-scale reactor could yield lower effluent CODsol than the FS method, since the hypothesis of zero effluent S_{S} seems more feasible for a 24 h HRT reactor. However, the overall means for the 2 series of 24 results (15.8 and 16.4 mg/l) were compared in a simple t-test for equal variances (verified through an F-test), resulting in statistically equal means. Also, a paired t-test was applied to the two series of S_{I} values, resulting again in equality between the means. It can be conclude that the average (S_{I})_{FS} and (S_{I})_{LS} obtained from 24 samples were statistically equal for the set of samples obtained from the two WWTPs.

Finally, a correlation study between LS and FS alternatives was carried out for S_{I} by running a linear regression of (S_{I})_{LS} *vs.* (S_{I})_{FS}. Figure 3 displays the correlation results. The determination coefficient was R^{2}=0.0598, pointing to very low correlation between both methods. The y-intercept was quite imprecise and different from zero (11.9 mg/l± 8.4 mg/l), while the slope had large imprecision and was statistically null (0.284 ± 0.498). These results do not meet the conditions for equivalence between two analytical methods (Miller and Miller, 2005). Figure 3 shows great dispersion between (S_{I})_{LS} and (S_{I})_{FS}. The difference between both S_{I} estimates distributes almost randomly over a wide range (-10.3 to +12.5 mg/l, 95% centred percentile) for a mean difference of 0.7 mg/l. In conclusion, while the S_{I} averages of a number of samples by both methods were very close and statistically equal, a very poor correlation between (S_{I})_{FS} and (S_{I})_{LS} confirms that these methods proved to be non equivalent for individual sample determination. Regarding the hypothesis of (S_{I})_{LS} being lower than (S_{I})_{FS}, it was rejected in the t-tests.

**S _{S} by FS and LS alternatives**

Table 5 displays the results from S_{S} determination by these 2 method alternatives. Similar means (107 and 106 mg/l), ranges (29.6 to 197 and 25.1 to 203 mg/l) and overall standard deviations (50.6 and 50.9 mg/l) were obtained for, respectively, the FS and LS alternatives. Equivalence between both methods is discussed further in this section. First, LOD, LOQ and variance issues of these methods are addressed.

The limits of detection were computed for (S_{S})_{FS} and (S_{S})_{LS}. The LOD signal values ((CODsol)_{LOD}) were respectively 33.0 and 36.4 mg/l. In order to calculate the corresponding LOD for S_{S}, plots and regressions of CODsol *vs.* S_{S} were performed (Fig. 6). The linearity was quite good (R^{2} of 0.987 and 0.983), so LOD(S_{S}) a was computed from the regression equations in Fig. 6, resulting in 17.2 and 19.2 mg/l, respectively, for (S_{S})_{FS} and (S_{S})_{LS}. LOQ were analogously obtained and were 28.6 and 32.6 mg/l, respectively, for (S_{S})_{FS} and (S_{S})_{LS}. No sample fell below the limit of quantification for (S_{S})_{FS}, while 2 samples (8.3%) did fall below that of (S_{S})_{LS}. However, lower S_{S} can be common in WWTP influents values. In fact, 15% of samples in Mamais et al. (1993) fell below this LOQ for (S_{S})_{FS}, as well as 8% in Orhon et al. (1997), 17% in Spérandio and Paul (2000) and 57% in Ginestet et al (2002).

Standard deviation of (S_{S})_{FS} replicates – computed through Eq. (14) – ranged between 5.7 and 17.0 mg/l. A pooled *s* existed for all (S_{S})_{FS} (7.5 mg/l, 5.3 mg/l for the mean of 2 replicates). Since S_{S} variance was computed through Eq. (14) the contributions of CODsol and S_{I} variances were analysed, using *s*^{2} as variance estimates. (S_{I})_{FS} accounted for 78% of (S_{S})_{FS} variance, while CODsol variance represented 21% only. The rest was due to covariance. So, most of (S_{S})_{FS} uncertainty was attributable to (S_{I})_{FS} uncertainty. The latter derives from effluent CODsol variability and its fuzzy relationship with influent S_{I}, as pointed above. Similar results were obtained for the LS alternative. Standard deviation of (S_{S})_{LS} replicates – computed through Eq. (14) – ranged 6.6-15.5 mg/l. A pooled *s* could be computed (8.1 mg/l, 5.7 mg/l for the mean of two replicates). Since the (S_{S})_{LS} range was 25.1 to 203 mg/l, RSD ranged, respectively, 22.9-2.8%.

Equivalence between FS and LS alternatives for S_{S} is discussed next, based on the same tests applied to S_{I} methods. An overall t-test for S_{S} mean comparison (for variances found equal) was resulted in statistically equal averages at 5% significance; a paired t-test yielded the same result. So, the two means of 24 samples were statistically equal at 5% significance.

A correlation study between FS and LS alternatives for S_{S} was carried out by running a linear regression of (S_{S})_{LS} *vs.* (S_{S})_{FS} (Fig. 4). A quite good linearity was obtained (R^{2}=0.977), with statistically unit slope (0.995 ± 0.067) and statistically zero y-intercept (-0.01 ± 7.9 mg/l). These results indicate that FS and LS alternatives are equivalent. However, the standard error of estimate was 7.8 mg/l, showing some dispersion between both methods, particularly affecting the lower S_{S} results. This can be mostly attributed to uncertainties in S_{I} determination by both methods, as pointed above.

In conclusion, the main source of uncertainty for S_{S} in FS and LS alternatives was the lack of precision in S_{I} determination, which seriously affected S_{S} determination in the low range. Also, S_{I} imprecision greatly determined LOD and LOQ. In a regression analysis, FS and LS methods for S_{S} proved to be equivalent though some dispersion between both methods was found, attributable to S_{I} imprecision. Regarding the hypothesis of (S_{I})_{LS} being lower than (S_{I})_{FS}, it was rejected, since they were found statistically equal.

**S _{I} and S_{S} by the LS_{TW} alternative**

The results of this section are shown in Tables 4 and 5. (DQOsol)_{BTE} in LS_{TW} alternative was somewhat lower than in the LS alternative. However, when the dilution correction was applied (Eq. (5)), higher (S_{I})_{LSTW} values were obtained. The (S_{I})_{LSTW} mean was 32.4 mg/l, vs. 15.8 mg/l the mean of the FS alternative. This difference was statistically significant (t-test at 5% significance). It has been shown that a common batch test (LS) estimated the same mean S_{I} as the FS alternative. Obtaining systematically higher S_{I} values in this modified LS test (LS_{TW}) should be caused by the particular conditions of this method.

It was hypothesised that submitting biomass to tap water, with usually lower salinity and organic matter concentrations than mixed liquor or wastewater, could provoke some COD solubilisation either by desorption, osmotic processes or, even, biomass lysis. An experiment was used to confirm and eventually quantify solubilisation in the LS_{TW} batch tests. A fixed amount of tap water washed biomass from PPT was mixed with three different volumes of the same influent sample from PPT. The volumes were calculated to keep three food to microorganism (F/M) ratios of 0.025, 0.05 and 0.1 g COD/(g VSS.d), corresponding to 25%, 50% and 100% of the full-scale plant F/M. The mixtures were aerated for 24 h in new LSTW tests, and replicates were run for each F/M ratio. The whole design was repeated on another day. Under no-solubilisation conditions, the final amount of CODsol (mg) in the batch test reactor should be proportional to the volume of wastewater added to the mixture, since CODsol had been removed from biomass by tap water washing. So, a plot of mg CODsol vs. wastewater volume should yield a line with positive slope, good linearity and zero y-intercept.

Figure 5 shows the plots of mg CODsol vs. added wastewater volume at the end of the LS_{TW} batch tests. The lines presented quite good linearity (R^{2} of 0.930 and 0.981) and positive slope (0.037 and 0.068 mg CODsol/ml). The y-intercepts of the lines in Fig. 5 were statistically non-zero, as verified in t-tests at 5% significance (95% confidence intervals: 12.1 ± 3.2 and 3.8 ± 2.1 mg CODsol). These y-intercepts represent the extrapolation of residual CODsol if no wastewater volume had been added to the reactor. It means this CODsol was not supplied by wastewater, and could only be supplied by the biomass. Though these amounts can seem low or moderate, they are assigned to wastewater volumes between 60 and 350 ml, introducing an average concentration perturbation of +62 mg CODsol/l (ranging from +16 to +138 mg/l). The lower the wastewater volume, the higher the perturbation in CODsol concentration. The amounts of CODsol released per unit biomass were, respectively, 7.5 and 3.2 mg CODsol/g VSS. As a result of COD solubilisation, (S_{S})_{LSTW} average and range in the main sampling were significantly lower than those of (S_{S})_{LS}, in accordance with the higher S_{I} obtained by the LSTW method.

In conclusion, the LS_{TW} alternative led to COD solubilisation during the batch LS test, resulting in abnormally high S_{I} values and lower S_{S} estimates. Consequently, this alternative was discarded for S_{I} and S_{S} determination. Washing with a solution having a more controlled salinity and osmotic pressure could be explored as an alternative.

**S _{I} and S_{S} by the LS_{C} alternative**

Table 5 displays the results for these variables, while Table 4 shows other variables required for calculations, namely means and standard deviations of CODsol, (CODsol)_{BTE} and (CODsol)_{ML}. The mean (S_{I})_{LSC} was 12.9 mg/l, *vs.* 15.8 mg/l for the FS alternative. This difference was not significant in a t-test for different variances at 5% significance, neither in an analogous paired t test. However, (S_{I})_{LSC} *vs.* (S_{I})_{FS} presented very poor correlation (R^{2}=0.0027) and a large standard error of estimate (38.8 mg/l), indicating that while the S_{I} means of two sets of 24 samples were equal, individual samples presented large differences between the 2 method alternatives, which should not be considered equivalent.

In addition, 7 samples (29%) presented negative (S_{I})_{LSC} values, which makes no sense. This can be attributed to a sharp variance amplification through (S_{I})_{LSC} calculation, see Eq. (10), a linear combination of (S_{I})_{BTE} and (S_{I})_{ML.} For the samples studied, the *a ^{2}* and

*b*coefficients in Eq. (14) averaged 16.7 and 9.9, thus introducing a strong variance amplification in (S

^{2}_{I})

_{LSC}calculation. While the independent variables in Eq. (10) ((S

_{I})

_{BTE}and (S

_{I})

_{ML}) had sample variances of 44.1 and 72.2 mg

^{2}/l

^{2}, the sample variance estimated through Eq. (14) for (S

_{I})

_{LSC}was 1.465 mg

^{2}/l

^{2}, resulting in a standard deviation of 38.3 mg/l. This value is in accordance with that obtained from the 24 (S

_{I})

_{LSC}values (38.0 mg/l). Since the mean difference between 1

^{st}and 2

^{nd}terms in the right side of Eq. (10) was just 12.9 mg/l, the probability of (S

_{I})

_{LSC}being negative was 37%, assuming a normal distribution with µ=12.9 mg/l and σ=38.3 mg/l. Actually, 29% of samples presented negative (S

_{I})

_{LSC}, as pointed out above.

(S_{S})_{LSC} estimation resulted in high imprecision, with a pooled standard deviation of 38.6 mg/l (27.1 mg/l for the mean of 2 values) which would be unacceptable for at least the lower half of the (S_{S})_{LSC} range, assuming a maximum acceptable RSD of 20%. Most of (S_{S})_{LSC} variance (97%) was contributed by (S_{I})_{LSC}. In conclusion, the LS_{C} alternative did not allow a reliable S_{I} estimation, mostly due to a sharp increase in S_{I} variance, introduced via (S_{I})_{LSC} calculation through Eq. (10). This resulted in excessively dispersed (S_{S})_{LSC} values. Consequently, the proposed LS_{C} alternative was discarded.

**Importance of S _{I} precision**

It has been found that most of the methods' shortcomings derive from the lack of precision in S_{I} determination by either the FS or the LS methods. Improving precision for S_{I} would allow reliable physicochemical measurement of S_{S} below the limits found in this study. This would require an improved calculation of influent S_{I} from effluent CODsol, either by the FS or the LS alternative, taking into account influent and effluent CODsol regimes, as well as mixing conditions inside the WWTP.

**Conclusions**

A high relative imprecision is associated with determination of un-biodegradable soluble COD by the full-scale and the laboratory-scale variants of the Mamais et al. (1993) method. This is due to the variability of effluent CODsol both in full-scale and laboratory-scale plants, and to the fact that it is not possible to associate a grab effluent sample with a given influent sample, due to complete or partial mixing in the WWTP. FS and LS S_{I} had relatively high standard deviations, and ranges somewhat greater than the mean S_{I} values. When comparing the full-scale and the laboratory-scale variants, (S_{I})_{FS} and (S_{I})_{LS} averages were statistically equal at 5% significance. However, the differences between (S_{I})_{FS} and (S_{I})_{LS} in individual samples were very wide. In addition, a very poor correlation between (S_{I})_{LS} and (S_{I})_{FS} was found, indicating that these methods were not equivalent for the samples in this study.

The LOQ for (S_{S})_{FS} and (S_{S})_{LS} were respectively 28.6 mg/l and 32.6 mg/ℓ. Most samples (92%) were above these limits, because their S_{S} were rather high. However, significant fractions of samples fell below this LOQ in some literature studies. Determination of S_{S} by the FS and LS methods had standard deviations of, respectively 5.3 mg/l and 5.7 mg/l, mostly associated with S_{I} determination uncertainty. This affected the precision of S_{S} determination by both methods at low S_{S} values.

On the other hand, good correlation was found between FS and LS alternatives (R^{2}=0.978, zero y-intercept and unit slope), which means equality of the methods. However, a standard error of estimate of 7.6 g/l indicates a moderate dispersion between methods, relatively more important at low S_{S}. The hypothesis of (S_{I})_{LS} being lower than (S_{I})_{FS} was rejected, since they were found statistically equal.

Washing biomass with tap water before the laboratory-scale test (LS_{TW} alternative) resulted in significant COD solubilisation from biomass, which tended to overestimate S_{I} and underestimate S_{S}, especially at low F/M ratios. The solubilisation was quantified as a function of F/M, but the mechanism was not determined. Consequently, this method was discarded as a modification for suppressing influent mixed liquor S_{I} interference. Washing with a solution having a more controlled salinity and osmotic pressure could be explored as an alternative.

The LS_{C} alternative did not result in a statistically different average for S_{I} when compared with the original LS method. However, a regression analysis could not conclude equality between both methods. In addition, Eq. (10) used to calculate (S_{I})_{LSC} introduced a sharp increase in S_{I} variance, resulting in much larger dispersion of results, including some negative, nonsense S_{I} values. Under the conditions of this research, the probability of a sample to have a negative estimated (S_{I})_{LSC} was 37%. This method was discarded as an alternative for improving S_{I} and S_{S} determination. However, increasing precision of S_{I} determination in mixed liquor and batch test effluent could allow a re-evaluation of this method alternative.

Most of the methods' shortcomings derive from the lack of and precision in S_{I} determination by either the FS or the LS methods. Improving precision for S_{I} could allow more reliable physicochemical measurement of S_{I} below the limit found in this study. It is possible that the assumption of S_{I} conservation, implicit in the ASM1 model and in the Mamais et al. (1993) method, could be a source of uncontrolled error. However, S_{I} generation in the biological reactors is difficult to quantify and would complicate this simple physicochemical method.

**Acknowledgements **

The authors thank the Comisión Estatal del Agua in San Luis Potosí for authorisations, Grupo Proaqua SA de CV and Degrémont de México SA de CV for plant information and sampling support. Ma. de los Angeles Ortiz Balderas received scholarships from CONACYT (No. 198456) and Santander-Universia. This research was funded through CONACYT Project No. C07-ACIPC-01-08.88, UASLP Projects C06-FAI-03-18.21, C07-FAI-11-33.69; *Programa Integral de Fortalecimiento de la UASLP* (PIFI 1.0 to 3.4) – *Plan de Desarrollo del Cuerpo Académico Tecnología Ambiental* 2006 – 2008 (P/CA-116 2006-24-36 and P/CA 116-2007-24-42).

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*Received 10 February 2009; accepted in revised form 14 July 2009.*

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