L.
Berthod
ab,
G.
Roberts
a,
A.
Sharpe‡
a,
D. C.
Whitley
b,
R.
Greenwood
c and
G. A.
Mills
*b
aAstraZeneca Brixham Environmental Laboratory, Freshwater Quarry, Brixham, Devon TQ5 8BA, UK
bSchool of Pharmacy and Biomedical Sciences, University of Portsmouth, St Michael's Building, White Swan Road, Portsmouth, Hampshire PO1 2DT, UK. E-mail: graham.mills@port.ac.uk
cSchool of Biological Sciences, University of Portsmouth, King Henry Building, King Henry I Street, Portsmouth, Hampshire PO1 2DY, UK
First published on 26th October 2015
Assessment of the fate of pharmaceutical residues in the environment involves the measurement or prediction of their sewage sludge partition coefficient (Kd). Sewage sludge can be classified into four types: primary, activated, secondary and digested, each one with different physical and chemical properties. Published studies have measured Kd for pharmaceuticals in a variety of sludge types. This paper discusses the variability of reported Kd values of pharmaceuticals in different types of sewage sludge, using a dataset generated from the literature. Using a meta-analysis approach, it was shown that the measured Kd values depend on the type of sludge used in the test. Recommendations are given for the type of sludge to be used when studying the partitioning behaviour of pharmaceuticals in waste water treatment plants. Activated sludge is preferred due to its more homogenous nature and the ease of collection of consistent samples at a plant. Weak statistical relationships were found between Kd values for activated and secondary sludge, and for activated and digested sludge. Pooling of Kd values for these sludge types is not recommended for preliminary fate and risk assessments. In contrast, statistical analyses found stronger similarities between Kd values reported for the same pharmaceutical in primary and activated sludges. This allows the pooling of experimental values for these two sludge types to obtain a larger dataset for modelling purposes.
Water impactActive pharmaceutical ingredients (API) in waste water treatment plants partition between aqueous and sludge phases. Understanding this behaviour is important for regulatory purposes. A partition coefficient (Kd) describes how chemicals distribute between these phases and can be measured experimentally using specific tests. A number of Kd values have been published for APIs in a range of sludge types. This paper undertakes a meta-analysis of these Kd values to investigate how the partitioning is affected by the different sludge types and if there are correlations between the datasets. This information is useful to make initial predictions of the fate of an API during treatment processes and may reduce the need to undertake time-consuming OECD tests in preliminary environmental risk assessments. |
Kd = [API]sludge/[API]aqueous | (1) |
Values of Kd can be measured experimentally or estimated by mathematical models. Usually, experimental measurements use specific guidelines, e.g. Organisation for Economic Co-operation and Development (OECD) 106,19 OECD 121 (ref. 20) or the US Environmental Protection Agency's Office of Prevention, Pesticides and Toxic Substances (OPPTS) guideline 835.1110.21 The OPPTS 835.1110 guideline is currently the only one applicable to the measurement of partitioning behaviour in sewage sludge. In this guideline, a series of experiments are performed using different aqueous concentrations of sludge and the linear section of the slope of the resultant isotherm is used to calculate Kd. The guideline recommends the use of activated sewage sludge, even though this matrix may not exhibit all of the different types of partitioning mechanism that can potentially occur in a WWTP.
Within a WWTP different types of sewage sludge are present, each with varying physico-chemical properties (Table 1). Typically, four types of sludge (primary, activated, secondary and anaerobically digested) can be found within a plant (Fig. 1). All of these have been used in reported laboratory-based sorption experiments to measure Kd (Table 2). The matrix used has been shown to have an effect on the experimental values obtained. For example, comparisons have been made between primary and secondary,6,16 activated and primary8,13,17 and activated and digested.11 Activated sludge was found to be comparable to primary sludge.13,17 Primary sludge behaved differently to secondary sludge. This was attributed to differences in pH6 and surface properties of the material.16 The relationship between activated sludge and digested sludge was less clear.11
Sludge type | Primary | Activated | Secondary | Digested |
---|---|---|---|---|
a Tchobanoglous et al. 2002 (ref. 22). b Wick et al. 2011 (ref. 27). c Wick et al. 2009 (ref. 14). d Carballa et al. 2007 (ref. 28). e Ternes et al. 2004 (ref. 6). f Radjenović et al. 2009 (ref. 13). g TSS: total suspended solids. h TOC: total organic carbon. i VSS: volatile suspended solids. j COD: chemical oxygen demand. k P/TSS: phosphorus per TSS. l Fe(III)/TSS: iron(III) per TSS. m N/TSS: nitrogen per TSS. | ||||
pH | 5.0–8.0a | 6.8b | 6.8c | 7.7–8.6a |
TSSg | 50–125d g L−1 | 10–35d g L−1 | 9c g L−1 | 27–42a g L−1 |
TOCh | 35%e | 29b–49% | 25c–34e% | 25% |
VSSi | 25–70d g L−1 (50–80%a) | 10–30d g L−1 (87f–100%) | 60%e | 12–20d g L−1 (44–48%) |
CODj | 45–120d g L−1 | 10–50d g L−1 | — | 15–32d g L−1 |
COD/TSS | 90–96%, 146%e | 100–143% | 110%e | 56–76% |
P/TSSk | 0.8a–3.0%e | 2.8–11.0%a | 3.0%e | 1.5–4.0%a |
Fe(III)/TSSl | <1.0%e | — | 4.0%e | 3.0–8.0%a |
N/TSSm | 1.5–4.0%a | 2.4–5.0%a | 5.8%e | 1.6–3.0%a |
Compound | K d activated | K d primary | K d secondary | K d digested |
---|---|---|---|---|
a Stevens-Garmon et al. 2011 (ref. 17). b Radjenović et al. 2009 (ref. 13). c Hörsing et al. 2011 (ref. 16). d Lajeunesse et al. 2012 (ref. 18). e Barron et al. 2009 (ref. 12). f Wick et al. 2009 (ref. 14). g Urase and Kikuta 2005 (ref. 9). h Suárez et al. 2008 (ref. 11). i Joss et al. 2005 (ref. 8). j Ternes et al. 2004 (ref. 6). k Andersen et al. 2005 (ref. 29). l Carballa et al. 2008 (ref. 10). m Stuer-Lauridsen et al. 2000 (ref. 5). n Göbel et al. 2005 (ref. 7). | ||||
Acetaminophen | 595.0 (134.3)a,b | 18.0 (89.8)a,b | — | — |
Alfuzosin | — | 1800.0c | 1200.0c | — |
Amitriptyline | 4555.0a | 4897.0 (23.0)a,c | 5020.0 (120.6)c,d | 1049.0e |
Androstenedione | 156.0a | 174.0a | — | — |
Androsterone | 579.0a | 534.0a | — | — |
Atenolol | 44.0 (40.4)a,b,f | 200.3 (112.9)a,b,c | 2800.0c | 11.0e |
Atorvastatin | 198.0a | 216.0a | — | — |
Atracurium | — | 350.0c | 1600.0c | — |
Azelastine | — | 6400.0c | 470.0c | — |
Biperiden | — | 820.0c | 750.0c | — |
Bisoprolol | 40.0f | — | 110.0c | — |
Bupropion | — | 85.0c | 140.0c | — |
Caffeine | 30.0a | 30.0a | — | 14.0e |
Carbamazapine | 53.8 (97.0)a,b,f,g,h | 102.3 (154.9)a,b,h,i | 120.6 (140.0)d,i,j | 39.5 (9.7)e,h,j |
Chlorprothixene | — | 38000.0c | 20000.0c | — |
Citalopram | — | 540.0c | 2105.0 (127.3)c,d | 282.0e |
Clofibric Acid | 25.5g | — | 4.8j | 5.0e |
Clomipramine | — | 17000.0c | 6700.0c | — |
Clotrimazol | — | 32000.0c | 34000.0c | 8128.0e |
Clozapine | 1642.0a | 1730.0a | — | — |
Cyclophosphamide | — | 55.0j | 2.4j | — |
Cyproheptadine | — | 11000.0c | 3600.0c | — |
Desloratadine | — | 3700.0c | 2900.0c | — |
Diazapam | 91.8 (109.7)a,f,h | 125.0 (115.0)a,h,j | 21.0i | — |
Diclofenac | 55.3 (104.2)b,g,h | 384.7 (43.3)b,h,i,j | 16.0i,j | 77.5 (50.2)e,h |
Dicycloverine | — | 1400.0c | 1700.0c | — |
Dilantin | 81.0a | 45.0a | — | — |
Donepezil | — | 3600.0c | 970.0c | — |
Duloxetine | — | 13000.0c | 2900.0c | — |
Erythromycin | 116.0 (51.2)b,h | 309.0b | — | 190.0e |
Estradiol (E2) | 787.8 (64.1)a,g,h,k | 560.0a | — | 375.5 (69.7)l,h |
Estriol | 63.0a | 58.0a | — | — |
Estrone (E1) | 424.2 (42.8)a,g,h,k | 636.0a | — | 352.1 (62.7)l,h |
Ethinylestradiol (EE2) | 763.0 (69.2)a,g,h,k | 515.3 (84.3)a,h,j | 349.0j | 414.1 (100.4)l |
Ezetimibe | — | 2300.0c | 3000.0c | — |
Fexofenadine | — | 2700.0c | 360.0c | — |
Fluoxetine | — | 10000.0c | 7400 (26.8)c,d | — |
Flutamide | — | 1500.0c | 750.0c | — |
Gemfibrozil | 54.8 (75.3)a,b,g | 34.0 (45.8)a,b | — | — |
Glibenclamide | 239.0b | 1941.0 (120.9)b,c | 1300.0c | — |
Glimepiride | — | 2100.0c | 960.0c | — |
Haloperidol | — | 10000.0c | 2900.0c | — |
Hydrochlorothiazide | 20.2b | 25.8b | — | — |
Hydroxyzine | 819.0a | 989.0 (30.2)a,c | 720.0c | — |
Ibuprofen | 32.4 (127.3)g,h,m | 14.8 (50.3)b,h,i | 183.6 (136.0)c,i,j | 31.4 (28.8)h,j |
Ifosfamide | — | 22.0j | 1.4j | — |
Indomethacin | 39.0g | — | — | 214.0e |
Iopromide | 10.0h | 10.0i | 11.0j | 10.0 (43.4)h,j |
Irbesartan | — | 700.0c | 940.0c | — |
Ketoconazole | — | 9700.0c | 8500.0c | — |
Ketoprofen | 22.5 (40.9)b,g | 226.0b | — | — |
Loperamide | — | 14000.0c | 5500.0c | — |
Loratidine | 3321.0b | 2336.0b | — | — |
Maprotiline | — | 6700.0c | 4500.0c | — |
Mefenamic acid | 434.0b | 294.0b | — | — |
Meprobamate | 30.0a | 42.0a | — | — |
Metoprolol | 65.0f | — | — | 18.0e |
Mianserin | — | 3000.0c | 910.0c | — |
Naproxen | 24.0g | 217.0i | 217.0i | 29.0e,h |
Nefazodone | — | 14000.0c | 8300.0c | — |
Nortriptyline | — | — | 6200.0k | 600.0e |
Omeprazole | 107.0a | 130.0a | — | — |
Oxazepam | 13.0f | 790.0c | 1100.0c | — |
Paroxetine | — | 14000.0c | 11650.0 (40.7)c,d | — |
Phenylphenol | 347.0a | 652.0a | — | — |
Pizotifen | — | 4700.0c | 3100.0c | — |
Primidone | 18.5 (87.9)a,f | 45.0a | — | — |
Progesterone | — | 750.0c | 1100.0c | — |
Propanolol | 354.5 (10.2)b,f | 641.0b | — | 331.0e |
Repaglinide | — | 170.0c | 210.0c | — |
Risperidone | 861.0a | 1432.0c | 650.0c | — |
Roxithromycin | 282.0h | 400.0i | 170.0i | 49.0 (70.8)h,l |
Sertraline | — | 35000.0c | 24000.0 (41.2)c,d | 1883.0e |
Sotalol | 18.0f | — | 360.0c | — |
Sulfamethoxazole | 205.0 (54.4)b,h,n | 161.6 (129.9)b,c | 370.0c | 24.7 (103)e,h,l |
Testosterone | 157.0a | 178.0a | — | — |
Tramadol | 447.0f | 110.0c | 190.0c | — |
Trimethoprim | 195.0 (28.6)a,b,h,n | 356.0 (26.1)a,b,c | 420.0c | 68.0e |
Verapamil | 1501.0a | 1722.0 (6.4)a,c | 400.0c | — |
The location of the sampling point for the sludge within the WWTP is important but there is often inconsistency in different studies. For example, primary sludge can be sampled before the first clarifier6,17 or after it (Fig. 1).13 In one study primary sludge was sampled from a primary clarifier that had no secondary sludge recirculation.16 Comparison of sludge samples obtained from two different types of digesters, mesophilic and thermophilic, showed that sorption was not influenced by the operational conditions of the digester as long as the pH remained between 5.4 and 6.9.10 A study of the effect of sludge retention time on sorption, comparing the sorption behaviour of APIs with secondary sludge of different ages, found that sorption was lower with short retention times (2–3 days), than with longer retention times (10 days).16
Sewage sludge is a complex matrix. The physico-chemical properties of the sludge vary from plant to plant as well as between different locations within a WWTP. This contributes to the variability of the Kd values reported in the literature for APIs and related compounds. These inconsistencies could lead to incorrect environmental risk assessments (ERA) being made for some APIs. For example, Kd values are frequently measured using activated sludge as the solid phase. However, if assessing the potential of leaching of an API to soil when waste material is subsequently applied to land, it may be more appropriate to use digested sludge as the solid matrix in laboratory measurements.
This paper undertakes a meta-analysis of the Kd values of APIs published in the literature. It aims to identify the possible effects that the type of sewage sludge used in sorption experiments may have on the measured Kd values, and to investigate possible associations between the sorption behaviour of these matrices. This information may be useful in guiding the disposal of sewage sludge, aiding preliminary ERA and generating larger datasets for use in developing predictive mathematical models that describe the partitioning behaviour of APIs.
The key physico-chemical properties (pH, total suspended solids (TSS), total organic carbon (TOC), volatile suspended solids (VSS) and chemical oxygen demand (COD)) of the four sludge types, where available, are detailed in Table 1.
K d activated | K d primary | K d secondary | K d digested | ||
---|---|---|---|---|---|
K d activated | Correlation coefficient | 1 | |||
p-value | |||||
n | 45 | ||||
K d primary | Correlation coefficient | 0.72 | 1 | ||
p-value | <0.001 | ||||
n | 40 | 73 | |||
K d secondary | Correlation coefficient | 0.48 | 0.85 | 1 | |
p-value | 0.027 | <0.001 | |||
n | 21 | 51 | 55 | ||
K d digested | Correlation coefficient | 0.82 | 0.88 | 0.80 | 1 |
p-value | <0.001 | <0.001 | <0.001 | ||
n | 19 | 19 | 16 | 23 |
Paired differences | |||||||
---|---|---|---|---|---|---|---|
n | Mean | Standard deviation | 95% confidence interval of the difference | t | p | ||
Lower | Upper | ||||||
t = Student's t-statistic. p = p-value associated with the t-test. | |||||||
lnKd activated–lnKd primary | 40 | −0.33 | 1.16 | −0.70 | 0.04 | −1.79 | 0.082 |
lnKd activated–lnKd secondary | 21 | −0.57 | 1.78 | −1.38 | 0.24 | −1.47 | 0.157 |
lnKd activated–lnKd digested | 19 | 0.58 | 0.93 | 0.13 | 1.03 | 2.73 | 0.014 |
lnKd primary–lnKd secondary | 51 | 0.42 | 1.16 | 0.09 | 0.75 | 2.58 | 0.013 |
lnKd primary–lnKd digested | 19 | 1.18 | 0.99 | 0.70 | 1.65 | 5.19 | <0.001 |
lnKd secondary–lnKd digested | 16 | 1.52 | 1.57 | 0.69 | 2.36 | 3.88 | 0.001 |
The orthogonal regression of lnKd activated against lnKd primary gave a regression coefficient of 0.96, an intercept of 0.54 and a RMSE (the root mean square of the orthogonal distance from the data points to the regression line) of 0.81 (Fig. 2). These results showed that activated and primary sludge have similar sorption properties for a diverse set of APIs (n = 40). These findings are consistent with the observation that primary and activated sludge have similar physico-chemical properties; both have a relatively neutral pH, high TOC and comparable COD (Table 1).
Within a WWTP there are several distinct stages where partitioning takes place. The first of these occurs in the primary clarifier.22 Hence primary sludge is the result of all the partitioning processes occurring prior to and including the primary clarifier (Fig. 1). As shown above, partitioning in activated sludge was similar to that in primary sludge. This means that partitioning in the WWTP would be similar in all compartments of the WWTP up to and including the activation tank.
It should be noted that, although the average reported Kd values for activated and primary sludge were found to be similar, a higher variability in Kd values was observed for some APIs with primary sludge than for activated sludge. For example, in primary sludge, Kd values ranging from 194 to 501 were reported for the anti-inflamatory diclofenac, from 20 to 314 for the anti-convulsant carbamazepine, from 46 to 460 for the cardiovascular drug atenolol, from 32 to 320 for the antibiotic sulfamethoxazole and from 251 to 427 for the antibiotic trimethoprim. This may have been due to differences in the location of the sampling point. In most cases primary sludge was collected after the first clarifier, while in a few instances material was collected by sedimentation/filtration of influent wastewater. By comparison, in activated sludge the variability in Kd values was lower, ranging from 16 to 128 for diclofenac, 17 to 135 for carbamazepine, 30 to 64 for atenolol, 77 to 282 for sulfamethoxazole and 119 to 253 for trimethoprim (Table 2). This was attributed to the activated sludge being a more homogeneous material due to the aeration process used in the activation tank. These differences aside, analysis of the available data suggests that using either activated or primary sludge would lead to similar measured values of Kd.
The regression analysis of these two sludge types for the available dataset (n = 21) gave a RMSE of 1.22 (Fig. 3).
In a WWTP, secondary sludge is formed mainly from activated sludge which has been allowed to settle, and their physico-chemical properties, with the exception of TSS, are broadly similar (Table 1). This would suggest that the sorption properties of these two sludges would be similar, but this was not supported by our analysis of the data reported in the literature. It is difficult to explain these statistical results. Sorption of pharmaceuticals to sewage sludge is a complex process. Unlike some other environmental media, such as soils, the partitioning mechanisms involved are not well understood. The bulk properties commonly used to characterise sewage sludge may not be adequate to describe fully these interactions and the inclusion of other properties of the matrix such as cation-exchange capacity may be required.
These observed differences between the sorptive properties of activated and digested sludge may be influenced by their physico-chemical properties and the availability of oxygen. Generally, digested sludge is more basic than activated sludge (Table 1). The pH of the sludge affects the sorption of ionic compounds and will be more influential for APIs with pKa values in the range 6–9. There were differences in other physico-chemical properties, such as TOC, TSS and VSS, between these sludge types but their effect on sorption is more difficult to predict. Sorption may also have been affected by local variations of the bacterial population in the digester.
The orthogonal regression of the lnKd values for primary and secondary sludge (n = 51) gave a RMSE of 0.81, a regression coefficient of 1.06 and intercept −0.81 (Fig. 5). This indicated that the sorption properties of APIs between primary and secondary sludge were correlated, with APIs sorbed more strongly to primary sludge than to secondary sludge (Fig. 5).
Some differences in the physico-chemical properties of primary and secondary sludge are apparent (Table 1). Most notably, TSS is markedly lower for secondary sludge compared with primary sludge. A smaller difference between TOC values suggests that the higher TSS value in primary sludge is mainly due to inorganic material.
The correlation coefficients of the lnKd values for primary and secondary sludge with digested sludge were 0.88 and 0.80, respectively (both with p-values <0.001) (Table 3). The paired sample t-tests show that these sludge pairs behave differently, with p-values below the threshold and confidence intervals not containing the origin (Table 4). The orthogonal regressions of the lnKd values between primary and digested sludge (n = 19), and between secondary and digested sludge (n = 16) gave RMSE values of 0.65 and 1.00, respectively. Their corresponding regression coefficients were 0.86 and 0.76.
The statistical analysis of the different sludge pairs is summarized in Table 5. This includes suggested criteria for the pooling of Kd values based on the three statistical tests.
Correlation matrix | Paired t-test | Orthogonal regression | ||||||
---|---|---|---|---|---|---|---|---|
Pearson coefficient | p-value | p-value | Confidence interval | Regression coefficient | Intercept | RMSE | Pooled | |
Pooling criteria | Close to 1 | <0.05 | >0.0083 | To include 0 | Close to 1 | Close to 0 | Close to 0 | |
Sludge pairs | ||||||||
lnKd activated–lnKd primary | 0.72 | <0.001 | 0.082 | Yes | 0.96 | 0.54 | 0.81 | Yes |
lnKd activated–lnKd secondary | 0.48 | 0.027 | 0.157 | Yes | 1.08 | 0.20 | 1.22 | No |
lnKd activated–lnKd digested | 0.82 | <0.001 | 0.014 | No | 0.99 | −0.54 | 0.64 | No |
lnKd primary–lnKd secondary | 0.85 | <0.001 | 0.013 | No | 1.06 | −0.81 | 0.81 | No |
lnKd primary–lnKd digested | 0.88 | <0.001 | <0.001 | No | 0.86 | −0.33 | 0.65 | No |
lnKd secondary–lnKd digested | 0.80 | <0.001 | 0.001 | No | 0.76 | −0.02 | 1.00 | No |
APIs can also undergo biodegradation within a WWTP. Different plant designs will influence the extent of these aerobic and anaerobic processes. The treatment of urban effluents can be further complicated by the presence of both APIs and their metabolites. Often, metabolites can be biodegraded (e.g. conjugation products) during various treatments to yield the parent compound, which may then undergo sorption to a sludge in later compartments of the plant.
This is in contrast to soils, where the matrices are more clearly defined, for example as clays, loams, sands and silts, which are available commercially as standard materials for testing the sorption behaviour of compounds. Activated sewage sludge is recommended for use in regulatory sorption tests (EPA, 1998). The data (Kd) from such tests may be used to model the distribution of a chemical in a WWTP and these results can be used to assesses the potential for release of APIs from the WWTP in aqueous effluent. However, it is important to understand the partitioning of chemicals with other sludge types. For example, if digested sludge is disposed of to land, there is a subsequent potential for desorption of the API from the sludge and the leaching of APIs into ground and surface waters.
APIs form a diverse set of chemicals, but tend to occupy specific regions in physico-chemical property space, for example satisfying the Lipinski rules.24 Unlike many pollutants, the majority of APIs exhibit ionic behaviour which must be considered when their environmental fate is assessed. The sorption behaviour of APIs reported in the literature covers a large range of Kd values (up to ~40000), but these are not distributed uniformly, with large regions containing few values. To strengthen the statistical analysis of the reported Kd values with all the different sewage types, further measurements are needed to obtain a more comprehensive dataset with more even coverage of the range of the observed partitioning behaviour of these compounds. In particular, there is a paucity of data for digested sludge.
An extensive body of work has been undertaken on the fate of regulated (priority) pollutants in sewage sludge and soils. This has been necessary as frequently sludge has been applied to land as a means of disposal.25 Emerging pollutants of recent concern such as APIs have received much less attention, although this situation is changing rapidly.26 As awareness of the presence of these chemicals in the environment increases, there is an urgent need to understand fully their fate. The analysis carried out in this study brings together the available sorption data for APIs and may be beneficial to those responsible for performing environmental risk assessment for these types of substances.
Comparisons of the sorption behaviour of other sludge pairs did not show such strong similarities. Therefore, it is not recommended that the experimental Kd values for these matrices are combined directly. The orthogonal regressions between the different sludge pairs did not provide evidence for different sorption behaviour, with the 95% confidence intervals for the slope and intercept containing 1 and 0, respectively, in each case. However, the RMSE values for the activated–secondary and secondary–digested pairs were above one ln unit. The paired t-tests showed that the primary–digested and secondary–digested pairs could not be pooled and the correlation coefficient for the activated–secondary pair was very low, showing these sludge types behaved differently in terms of their sorption properties.
This analysis shows that there are statistical grounds for pooling the Kd values for APIs in activated and primary sludge. The evidence for pooling the other sludge types is weaker and is therefore not recommended for the purposes of preliminary ERA. In order to obtain a full understanding of the sorption behaviour of APIs within a WWTP additional experimental measurements are needed to ascertain Kd values for secondary and digested sludge.
Footnotes |
† Electronic supplementary information (ESI) available. See DOI: 10.1039/c5ew00171d |
‡ Current address: AstraZeneca UK Ltd., Alderley Park, Macclesfield, SK10 8TG, UK. |
This journal is © The Royal Society of Chemistry 2016 |