ORCID Profile
0000-0002-6482-5787
Current Organisation
University of Ulster
Does something not look right? The information on this page has been harvested from data sources that may not be up to date. We continue to work with information providers to improve coverage and quality. To report an issue, use the Feedback Form.
Publisher: Informa UK Limited
Date: 14-03-2014
DOI: 10.1080/09593330.2014.892539
Abstract: This study focuses on the performance of a submerged membrane photocatalytic reactor for the removal of 17beta-oestradiol (E2) in the presence of humic acid (HA). In addition to the impact of operating parameters, such as membrane pore size, ultraviolet (UV) intensity and hydraulic retention time (HRT), the influence of long-term operation was also assessed by advanced characterization of the fouling layer formed on the membrane. The tighter (0.04 microm) hollow fibre polyvinylydene fluoride (PVDF) membrane was found to exhibit not only higher HA removal than the (0.2 microm) module (85% and 75%, respectively), but also greater transmembrane pressure (TMP) values and higher irreversible fouling. Long-term operation conditions have been simulated by conducting an ageing catalyst process and demonstrated a decrease in performance obtained with time. The artificially aged TiO2 resulted in higher TMP values and lower HA removals (about 10-20% decrease) compared with the non-aged catalyst. For E2 removal in the presence of HA, the passive adsorption of the oestrogen onto the organic matter was found to be significant (40% of the E2 adsorbed after I h), demonstrating the importance of the nature of the water matrix for this type of treatment process. An increase in the UV light intensity was observed to favour the E2 elimination, leading to more than 90% removal when using 64 W combined with PVDF membrane and an HRT of 3 h.
Publisher: Elsevier BV
Date: 03-2015
DOI: 10.1016/J.ENVINT.2014.11.012
Abstract: A range of trace chemical contaminants have been reported to occur in swimming pools. Current disinfection practices and monitoring of swimming pool water quality are aimed at preventing the spread of microbial infections and diseases. However, disinfection by-products (DBPs) are formed when the disinfectants used react with organic and inorganic matter in the pool. Additional chemicals may be present in swimming pools originating from anthropogenic sources (bodily excretions, lotions, cosmetics, etc.) or from the source water used where trace chemicals may already be present. DBPs have been the most widely investigated trace chemical contaminants, including trihalomethanes (THMs), haloacetic acids (HAAs), halobenzoquinones (HBQs), haloacetonitriles (HANs), halonitromethanes (HNMs), N-nitrosamines, nitrite, nitrates and chloramines. The presence and concentrations of these chemical contaminants are dependent upon several factors including the types of pools, types of disinfectants used, disinfectant dosages, bather loads, temperature and pH of swimming pool waters. Chemical constituents of personal care products (PCPs) such as parabens and ultraviolet (UV) filters from sunscreens have also been reported. By-products from reactions of these chemicals with disinfectants and UV irradiation have been reported and some may be more toxic than their parent compounds. There is evidence to suggest that exposure to some of these chemicals may lead to health risks. This paper provides a detailed review of various chemical contaminants reported in swimming pools. The concentrations of chemicals present in swimming pools may also provide an alternative indicator to swimming pool water quality, providing insights to contamination sources. Alternative treatment methods such as activated carbon filtration and advanced oxidation processes may be beneficial in improving swimming pool water quality.
Publisher: Elsevier BV
Date: 2014
Publisher: Royal Society of Chemistry (RSC)
Date: 1995
DOI: 10.1039/AN9952002873
Publisher: Elsevier BV
Date: 03-2014
DOI: 10.1016/J.WATRES.2013.10.056
Abstract: We investigated water quality at an advanced water reclamation plant and three conventional wastewater treatment plants using an "ecotoxicity toolbox" consisting of three complementary analyses (chemical analysis, in vitro bioanalysis and in situ biological monitoring), with a focus on endocrine disruption. The in vitro bioassays were chosen to provide an appropriately wide coverage of biological effects relevant to managed aquifer recharge and environmental discharge of treated wastewater, and included bioassays for bacterial toxicity (Microtox), genotoxicity (umuC), photosynthesis inhibition (Max-I-PAM) and endocrine effects (E-SCREEN and AR-CALUX). Chemical analysis of hormones and pesticides using LCMSMS was performed in parallel to correlate standard analytical methods with the in vitro assessment. For two plants with surface water discharge into open drains, further field work was carried out to examine in situ effects using mosquitofish (Gambusia holbrooki) as a bioindicator species for possible endocrine effects. The results show considerable cytotoxicity, phytotoxicity, estrogenicity and androgenicity in raw sewage, all of which were significantly reduced by conventional wastewater treatment. No biological response was detected to RO water, suggesting that reverse osmosis is a significant barrier to biologically active compounds. Chemical analysis and in situ monitoring revealed trends consistent with the in vitro results: chemical analysis confirmed the removal trends observed by the bioanalytical tools, and in situ s ling did not reveal any evidence of endocrine disruption specifically due to discharge of treated wastewater (although other sources may be present). Biomarkers of exposure (in vitro) and effect (in vivo or in situ) are complementary and together provide information with a high level of ecological relevance. This study illustrates the utility of combining multiple lines of evidence in the assessment of water quality.
Publisher: Elsevier BV
Date: 08-2004
Publisher: Elsevier BV
Date: 03-2018
DOI: 10.1016/J.SCITOTENV.2017.10.148
Abstract: There are over 40,000 chemical compounds registered for use in Australia, and only a handful are monitored in the aquatic receiving environments. Their effects on fish species in Australia are largely unknown. Mosquitofish (Gambusia holbrooki) were s led from six river sites in Southeast Queensland identified as at risk from a range of pollutants. The sites selected were downstream of a wastewater treatment plant discharge, a landfill, two agricultural areas, and two sites in undeveloped reaches within or downstream of protected lands (national parks). Vitellogenin analysis, histopathology of liver, kidney and gonads, morphology of the gonopodium, and chemical body burden were measured to characterize fish health. Concentrations of trace organic contaminants (TrOCs) in water were analyzed by in vitro bioassays and chemical analysis. Estrogenic, anti-estrogenic, anti-androgenic, progestagenic and anti-progestagenic activities and TrOCs were detected in multiple water s les. Several active pharmaceutical ingredients (APIs), industrial compounds, pesticides and other endocrine active compounds were detected in fish carcasses at all sites, ranging from <4-4700ng/g wet weight, including the two undeveloped sites. While vitellogenin protein was slightly increased in fish from two of the six sites, the presence of micropollutants did not cause overt sexual endocrine disruption in mosquitofish (i.e., no abnormal gonads or gonopodia). A correlation between lipid accumulation in the liver with total body burden warrants further investigation to determine if exposure to low concentrations of TrOCs can affect fish health and increase stress on organs such as the liver and kidneys via other mechanisms, including disruption of non-sexual endocrine axes involved in lipid regulation and metabolism.
Publisher: Elsevier BV
Date: 11-2016
DOI: 10.1016/J.SCITOTENV.2016.06.085
Abstract: The occurrence of five organophosphate flame retardants (PFRs) consisting of tributyl phosphate (TNBP), tris(2-chloroethyl) phosphate (TCEP), tris(1-chloro-2-propyl) phosphate (TCIPP), tris(1.3-dichloro-2-propyl) phosphate (TDCIPP) and triphenyl phosphate (TPHP) in swimming pools were investigated. Fifteen chlorinated public swimming pools were s led, including indoor pools, outdoor pools and spa pools. The analyses were carried out using isotope dilution gas chromatography tandem mass spectrometry. All five PFRs were detected in swimming pool waters with concentrations ranging from 5-27ng/L (TNBP), 7-293ng/L (TCEP), 62-1180ng/L (TCIPP), 10-670ng/L (TDCIPP) and 8-132ng/L (TPHP). The concentrations of PFRs were generally higher in indoor swimming pools compared to outdoor swimming pools. In municipal water supplies, used to fill the swimming pools in three of the s ling locations, the five PFRs were all below the limit of quantifications, eliminating this as the source. Potential leaching of PFRs from commonly used swimming equipment, including newly purchased kickboards and swimsuits was investigated. These experiments revealed that PFRs leached from swimsuits, and may be a source of PFRs in swimming pools. A quantitative risk assessment revealed that the health risk to PFRs via swimming pools was generally low and below commonly applied health risk benchmarks.
Publisher: Elsevier BV
Date: 2015
Publisher: Springer Science and Business Media LLC
Date: 02-07-2014
DOI: 10.1007/S11356-014-3235-7
Abstract: Studies on endocrine disruption in Australia have mainly focused on wastewater effluents. Limited knowledge exists regarding the relative contribution of different potential sources of endocrine active compounds (EACs) to the aquatic environment (e.g., pesticide run-off, animal farming operations, urban stormwater, industrial inputs). In this study, 73 river sites across mainland Australia were s led quarterly for 1 year. Concentrations of 14 known EACs including natural and synthetic hormones and industrial compounds were quantified by chemical analysis. EACs were detected in 88 % of s les (250 of 285) with limits of quantification (LOQ) ranging from 0.05 to 20 ng/l. Bisphenol A (BPA LOQ = 20 ng/l) was the most frequently detected EAC (66 %) and its predicted no-effect concentration (PNEC) was exceeded 24 times. The most common hormone was estrone, detected in 28 % of s les (LOQ = 1 ng/l), and the PNEC was also exceeded 24 times. 17α-Ethinylestradiol (LOQ = 0.05 ng/l) was detected in 10 % of s les at concentrations ranging from 0.05 to 0.17 ng/l. It was detected in many s les with no wastewater influence, and the PNEC was exceeded 13 times. In parallel to the chemical analysis, endocrine activity was assessed using a battery of CALUX bioassays. Estrogenic activity was detected in 19 % (53 of 285) of s les (LOQ = 0.1 ng/l 17β-estradiol equivalent EEQ). Seven s les exhibited estrogenic activity (1-6.5 ng/l EEQ) greater than the PNEC for 17β-estradiol. Anti-progestagenic activity was detected in 16 % of s les (LOQ = 8 ng/l mifepristone equivalents MifEQ), but the causative compounds are unknown. With several compounds and endocrine activity exceeding PNEC values, there is potential risk to the Australian freshwater ecosystems.
Publisher: Elsevier BV
Date: 07-2007
DOI: 10.1016/J.JHAZMAT.2007.04.049
Abstract: 1,4-dioxane is a synthetic compound found in industrial effluent and subsequently contaminates water bodies due to its high solubility and high volatility. It is of concern due to its toxic and hazardous nature and has been listed as a class 2B carcinogen. This study involved optimisation of the photocatalytic and H(2)O(2)/UVC processes for 1,4-dioxane removal. Different photocatalysts and loadings were investigated for the degradation of low concentrations of 1,4-dioxane in water including a commercial P25, a synthesised magnetic photocatalyst and an immobilised sol-gel system. A commercial catalyst (Degussa P25) was the most efficient. A lifetime study of the sol-gel reactor showed that the coating was stable over the time period studied. The optimum H(2)O(2) concentration in the H(2)O(2)/UVC process was found to be 30ppm. The addition of H(2)O(2) to the photocatalytic process for 1,4-dioxane removal caused a decrease in rate for the commercial P25 photocatalyst and an increase in rate for the lab-made magnetic photocatalyst.
Publisher: Elsevier BV
Date: 04-2024
DOI: 10.1016/J.SCITOTENV.2015.12.083
Abstract: Trace organic chemical (TrOC) contaminants are of concern for finished water from water recycling schemes because of their potential adverse environmental and public health effects. Understanding the impacts of seasonal variations on fate and removal of TrOCs is important for proper operation, risk assessment and management of treatment systems for water recycling such as membrane bioreactors (MBRs). Accordingly, this study investigated the fate and removal of a wide range of TrOCs through a full-scale MBR plant during summer and winter seasons. TrOCs included 12 steroidal hormones, 3 xeno-estrogens, 2 pesticides and 23 pharmaceuticals and personal care products. Seasonal differences in the mechanisms responsible for removing some of the TrOCs were evident. In particular the contribution of biotransformation and biomass adsorption to the overall removal of estrone, bisphenol A, 17β-estradiol and triclosan were consistently different between the two seasons. Substantially higher percentage removal via biotransformation was observed during the summer s ling period, which compensated for a reduction in removal attributed to biomass adsorption. The opposite was observed during winter, where the contribution of biotransformation to the overall removal of these TrOCs had decreased, which was offset by an improvement in biomass adsorption. The exact mechanisms responsible for this shift are unknown, however are likely to be temperature related as warmer temperatures can lower sorption efficiency, yet enhance biotransformation of these TrOCs.
Publisher: IWA Publishing
Date: 03-2010
DOI: 10.2166/WST.2010.884
Abstract: The concentrations of some important endocrine disrupting chemicals and pharmaceuticals after various stages of wastewater treatment were investigated. The endocrine disrupting chemicals included natural and synthetic estrogenic and androgenic steroids. The pharmaceuticals included a series of sulfonamide antibiotics and trimethoprim. The removal efficiency of a membrane bioreactor (MBR) was investigated and compared with a conventional activated sludge (CAS) system. S les were analysed by liquid chromatography tandem mass spectrometry. Results showed that the MBR and CAS systems effectively removed steroidal estrogens and androgens, but only partially eliminated the target antibiotics from wastewater. The MBR was shown to be more effective than the CAS system which was possibly attributed to the high solid retention time and concentration of biosolids in the MBR. The results highlight the potential wider application of MBRs for the removal of trace chemical contaminants in wastewater and their potential for use as decentralised wastewater treatment systems.
Publisher: Elsevier BV
Date: 2005
Publisher: Elsevier BV
Date: 2016
Publisher: Elsevier BV
Date: 05-2002
Publisher: Elsevier BV
Date: 11-2002
Publisher: IWA Publishing
Date: 12-2008
DOI: 10.2166/WST.2008.573
Abstract: There are limited studies on the fate and levels of endocrine disrupting chemicals in sewage treatment plants in Australia. Research undertaken in Europe and North America has shown biologically significant levels of both oestrogenic and androgenic chemicals in sewage effluent. The aim of this work was to determine the oestrogenic and androgenic activities of raw and treated sewage from sewage treatment plants run by MidCoast Water, New South Wales, Australia. Oestrogenic and androgenic activities were measured using a yeast screen bioassay. Results showed that the raw effluent contained biologically significant levels of both oestrogenic (0.58–2.91 ng/l) and androgenic (216–480 ng/l) activities. Androgenic activity was significantly higher than oestrogenic activity, which was consistent with other Australian studies and was attributed to the higher levels of androgens in domestic waste from human excretion compared to oestrogens. Secondary treatment (using activated sludge) removed the majority of the oestrogenic and androgenic activity (up to 99%). Tertiary treatment by UV removed varying levels of oestrogenic (19–69%) and androgenic (5–55%) activities. A Membrane Bioreactor (MBR) at one of the STPs, which consists of an MBR followed by electrochlorination removed over 87% of the oestrogenic activity and over 98% of androgenic activity from raw sewage s les. However, levels which could be biologically significant still remained after secondary and tertiary treatment (& .1 ng/l oestrogenic activity and & ng/l androgenic activity).
Publisher: Elsevier BV
Date: 03-2013
DOI: 10.1016/J.ENVPOL.2012.11.018
Abstract: A liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed for the simultaneous analysis of 6 ectoparasiticides - 2 synthetic pyrethroids (deltamethrin, cypermethrin) and 4 macrocyclic lactones (abamectin, doramectin, ivermectin and eprinomectin) in biosolids. The method was used to investigate the occurrence of these ectoparasiticides in beef cattle feedlot wastes in Australia from 5 commercial feedlot operations which employ varying waste management practices. Deltamethrin and cypermethrin were not detected in any of the s les while abamectin, ivermectin, doramectin and eprinomectin were detected in some of the s les with concentrations ranging from 1 to 36 μg/kg dry weight (d.w.) freeze dried feedlot waste. Levels of macrocyclic lactones detected in the feedlot wastes varied and were dependent on s le type. The effect of seasonal variations and waste management practices were also investigated in this study.
Publisher: Elsevier BV
Date: 12-2007
Publisher: Elsevier BV
Date: 10-2010
DOI: 10.1016/J.JHAZMAT.2010.06.001
Abstract: 1,4-Dioxane, is a synthetic organic compound used widely throughout industry as a solvent. 1,4-Dioxane causes liver damage and kidney failure and has been shown to be carcinogenic to animals, and is a potential carcinogen to humans. Its recalcitrant nature means that conventional water treatment methods are ineffective in removing it from water. A class of technologies called advanced oxidation technologies has been shown to completely mineralise 1,4-dioxane. In this study the effects of pH on TiO(2) photocatalysis reactor systems were investigated. pH was found to significantly affect the efficiencies of these processes with neutral pH conditions the most effective.
Publisher: IWA Publishing
Date: 06-2012
DOI: 10.2166/WRD.2012.010
Abstract: Submerged membrane bioreactors (MBRs) have attracted a significant amount of interest for decentralised treatment systems due to their small footprint and ability to produce high quality effluent, which is favourable for water reuse applications. This study provides a comprehensive overview of the capacity of a full-scale decentralised MBR to eliminate 17 endocrine disrupting chemicals (EDCs) and five indigenous microbial indicators. The results show that the MBR consistently achieved high removal of EDCs (& .5%). Only 2 of the 17 EDCs were detected in the MBR permeate, namely two-phenylphenol and 4-tert-octylphenol. Measured log10 reduction values of vegetative bacterial indicators were in the range of 5–5.3 log10 units, and for clostridia, they were marginally lower at 4.6 log10 units. Removal of bacteriophage was in excess of 4.9 log10 units. This research shows that MBRs are a promising technology for decentralised water reuse applications.
Publisher: Elsevier BV
Date: 2000
Publisher: IWA Publishing
Date: 11-2012
DOI: 10.2166/WST.2012.374
Abstract: Emerging wastewater treatment processes such as membrane bioreactors (MBRs) have attracted a significant amount of interest internationally due to their ability to produce high quality effluent suitable for water recycling. It is therefore important that their efficiency in removing hazardous trace organic contaminants be assessed. Accordingly, this study investigated the removal of trace organic chemical contaminants through a full-scale, package MBR in New South Wales, Australia. This study was unique in the context of MBR research because it characterised the removal of 48 trace organic chemical contaminants, which included steroidal hormones, xenoestrogens, pesticides, caffeine, pharmaceuticals and personal care products (PPCPs). Results showed that the removal of most trace organic chemical contaminants through the MBR was high (above 90%). However, amitriptyline, carbamazepine, diazepam, diclofenac, fluoxetine, gemfibrozil, omeprazole, sulphamethoxazole and trimethoprim were only partially removed through the MBR with the removal efficiencies of 24–68%. These are potential indicators for assessing MBR performance as these chemicals are usually sensitive to changes in the treatment systems. The trace organic chemical contaminants detected in the MBR permeate were 1 to 6 orders of magnitude lower than guideline values reported in the Australian Guidelines for Water Recycling. The outcomes of this study enhanced our understanding of the levels and removal of trace organic contaminants by MBRs.
Publisher: Springer Science and Business Media LLC
Date: 26-12-2016
DOI: 10.1007/S11356-015-5967-4
Abstract: The aim of this research was to investigate the presence and daily variability of pharmaceuticals and personal care products (PPCPs) in public swimming pools. Various types of public swimming pool water were analysed, taken from freshwater indoor swimming pools, outdoor swimming pools, spa pools and seawater swimming pools. Swimming pool water s les were analysed for 30 PPCPs using solid phase extraction (SPE) followed by isotope dilution liquid chromatography tandem mass spectrometry (LC-MS/MS). All PPCPs were below quantification limits in seawater pools. However, caffeine was detected in 12 chlorinated swimming pools at concentrations up to 1540 ng/L and ibuprofen was observed in 7 chlorinated pools at concentrations up to 83 ng/L. Caffeine and ibuprofen concentrations were below quantification limits in all fill water s les, eliminating this as their source in swimming pools. High variations in caffeine concentrations monitored throughout the day roughly reflect bather loads in swimming pools. Future monitoring of these compounds may assist in evaluating what portion of organic matter measured in swimming pools may come from human excretions.
Publisher: Elsevier BV
Date: 03-2011
DOI: 10.1016/J.CHROMA.2011.01.068
Abstract: A rapid gas chromatography-tandem mass spectrometry (GC-MS/MS) analytical method was developed for the simultaneous analysis of 7 estrogenic hormones (17α-estradiol, 17β-estradiol, estrone, mestranol, 17α-ethynylestradiol, levonorgestrel, estriol) and 5 androgenic hormones (testosterone, androsterone, etiocholanolone, dihydrotestosterone, androstenedione) in aqueous matrices. This method is unique in its inclusion of all 12 of these estrogens and androgens and is of particular value due to its very short chromatographic run time of 15 min. The use of isotope dilution for all analytes ensures the accurate quantification, accounting for analytical variabilities that may be introduced during s le processing and instrumental analysis. Direct isotopically labelled analogues were used for 8 of the 12 hormones and satisfactory isotope standards were identified for the remaining 4 hormones. Method detection levels (MDLs) were determined to describe analyte concentrations sufficient to provide a signal with 99% certainty of detection. The established MDLs for most analytes were 1-5 ngL(-1) in a variety of aqueous matrices. However, slightly higher MDLs were observed for etiocholanolone, androstenedione, testosterone, levonorgestrel and dihydrotestosterone in some aqueous matrices. S le matrices were observed to have only a minor impact on MDLs and the method validation confirmed satisfactory method stability over intra-day and inter-day analyses of surface water and tertiary treated effluent s les.
Publisher: Elsevier BV
Date: 10-2005
Publisher: IWA Publishing
Date: 06-2007
DOI: 10.2166/WST.2007.421
Abstract: This research involves the removal of contaminants of concern in water supplies using advanced oxidation technologies, in particular titanium dioxide photocatalysis. Photocatalysis for the removal of 1,4-dioxane and the natural (17β-oestradiol, oestriol) and synthetic (17α-ethynyloestradiol) oestrogens in water was investigated using both UVA and solar radiation. The H2O2/UVC process, solar, UVC and UVA light alone were also investigated and the processes compared. It was found that TiO2 photocatalysis is an effective method for the degradation of the natural (17β-oestradiol and oestriol) and the synthetic (17α-ethynyloestradiol) oestrogens in water in immobilised Degussa P25 and sol-gel spiral reactors with both UVA and solar radiation as the light source. Photocatalysis using the commercial catalyst Degussa P25 as an immobilised reactor with a UVA l shows the best performance. Photocatalysis was shown to completely mineralise 1,4-dioxane to CO2 in Degussa P25 suspension and sol-gel reactors using both UVA and solar radiation. The commercial catalyst Degussa P25 in suspension with UVA radiation shows the best performance. Photocatalysis is much more efficient than H2O2/UVC, UVA, UVC and solar radiation alone for all contaminants investigated.
Publisher: Elsevier BV
Date: 04-2017
DOI: 10.1016/J.AQUATOX.2017.02.008
Abstract: In Australia, trace organic contaminants (TrOCs) and endocrine active compounds (EACs) have been detected in rivers impacted by sewage effluent, urban stormwater, agricultural and industrial inputs. It is unclear whether these chemicals are at concentrations that can elicit endocrine disruption in Australian fish species. In this study, native rainbowfish (Melanotaenia fluviatilis) and introduced invasive (but prevalent) mosquitofish (Gambusia holbrooki) were exposed to the in idual compounds atrazine, estrone, bisphenol A, propylparaben and pyrimethanil, and mixtures of compounds including hormones and personal care products, industrial compounds, and pesticides at environmentally relevant concentrations. Vitellogenin (Vtg) protein and liver Vtg mRNA induction were used to assess the estrogenic potential of these compounds. Vtg expression was significantly affected in both species exposed to estrone at concentrations that leave little margin for safety (p<0.001). Propylparaben caused a small but statistically significant 3× increase in Vtg protein levels (p=0.035) in rainbowfish but at a concentration 40× higher than that measured in the environment, therefore propylparaben poses a low risk of inducing endocrine disruption in fish. Mixtures of pesticides and a mixture of hormones, pharmaceuticals, industrial compounds and pesticides induced a small but statistically significant increase in plasma Vtg in rainbowfish, but did not affect mosquitofish Vtg protein or mRNA expression. These results suggest that estrogenic activity represents a low risk to fish in most Australian rivers monitored to-date except for some species of fish at the most polluted sites.
Publisher: Elsevier BV
Date: 10-2005
Publisher: Wiley
Date: 12-2009
DOI: 10.1897/08-531.1
Abstract: A membrane bioreactor (MBR) was assessed for the removal of estrogens, androgens, and a selection of pharmaceuticals and personal care products. The biomass and aqueous components of the MBR were investigated to determine whether removal was by biodegradation or by adsorption to the biomass. Removal was monitored using chemical analysis by gas chromatography/mass spectrometry (GC-MS) as well as biological analysis using estrogenic and androgenic yeast assays. Results showed that the MBR was effective in removing the compounds of concern from raw influent with removal rates between 78 and 99%. Removal efficiencies were comparable or better than those reported for conventional activated sludge systems, which was attributed to the relatively high sludge retention time of the MBR. The biomass component showed significant concentrations of salicylic acid, triclosan, and 4-tert-octylphenol. Estrogenic and androgenic activity was also measured in the biomass. Estrone was identified as the main compound responsible for the estrogenic activity. It was concluded that the main removal pathway was biodegradation, but sorption to biomass may also be important, particularly for triclosan and 4-tert-octylphenol.
Publisher: Elsevier BV
Date: 03-2014
DOI: 10.1016/J.BIORTECH.2013.12.123
Abstract: The removal of microbial indicators through a full-scale membrane bioreactor (MBR) was characterised. The overall log reduction of Escherichia coli and total coliforms were in the range of 5.0-5.9log10 units, while the reduction of clostridia was marginally less at 4.9log10 units. Removal of bacteriophage was in excess of 4.6log10 units. The impact of membrane cleaning on the elimination of microbial indicators was also assessed since this had been identified by pilot-scale studies as a potential hazardous event. Membrane cleaning temporarily reduced the log removal values of E. coli and total coliforms each by 1log10 unit, but did not affect the removal of bacteriophage or clostridia. Very little research has previously examined the consequences of hazardous events on the performance of full-scale MBRs, and thus the findings presented here will facilitate improvements for the risk assessment and management of MBRs used in water recycling schemes.
Publisher: IWA Publishing
Date: 02-2010
DOI: 10.2166/WST.2010.950
Abstract: The capacity for removing wastewater-borne endocrine disrupting chemicals (EDCs) was investigated for two wastewater treatment plants (WWTPs) incorporating waste stabilisation ponds (WSPs) as the principal treatment technology. S les were analysed for a number of steroidal oestrogens and androgens using liquid chromatography–tandem mass spectrometry (LC/MS/MS). Removal efficiency for steroid androgens was high for both WWTPs (93–100%) but WSP treatment was observed to be less effective for removing steroid oestrogens, particularly oestriol.
Publisher: Wiley
Date: 09-2014
Abstract: Trace organic contaminant (TrOC) studies in Australia have, to date, focused on wastewater effluents, leaving a knowledge gap of their occurrence and risk in freshwater environments. This study measured 42 TrOCs including industrial compounds, pesticides, and pharmaceuticals and personal care products by liquid chromatography tandem mass spectrometry at 73 river sites across Australia quarterly for 1 yr. Trace organic contaminants were found in 92% of s les, with a median of three compounds detected per s le (maximum 18). The five most commonly detected TrOCs were the pharmaceuticals salicylic acid (82%, maximum = 1530 ng/L), paracetamol (also known as acetaminophen 45%, maximum = 7150 ng/L), and carbamazepine (27%, maximum = 682 ng/L), caffeine (65%, maximum = 3770 ng/L), and the flame retardant (2-chloroethyl) phosphate (44%, maximum = 184 ng/L). Pesticides were detected in 28% of the s les. To determine the risk posed by the detected TrOCs to the aquatic environment, hazard quotients were calculated by iding the maximum concentration detected for each compound by the predicted no-effect concentrations. Three of the 42 compounds monitored (the pharmaceuticals carbamazepine and sulfamethoxazole and the herbicide simazine) had a hazard quotient >1, suggesting that they may be causing adverse effects at the most polluted sites. A further 10 compounds had hazard quotients >0.1, indicating a potential risk these included four pharmaceuticals, three personal care products, and three pesticides. Most compounds had hazard quotients significantly <0.1. The number of TrOCs measured in this study was limited and further investigations are required to fully assess the risk posed by complex mixtures of TrOCs on exposed biota.
Publisher: Elsevier BV
Date: 10-2015
DOI: 10.1016/J.TALANTA.2015.04.091
Abstract: The widespread use of organophosphate flame retardants (PFRs) in commercial products have led to their increased presence in the environment. In this study, a rapid and reliable analytical method was developed for the analysis of five PFRs in water using gas chromatography tandem mass spectrometry (GC-MS/MS) with electron ionisation (EI) and a run time of 13 min. The PFRs investigated were tributyl phosphate (TBP), tris(2-chloroethyl) phosphate (TCEP), tris(1-chloro-2-propyl) phosphate (TCPP), tris(1,3-dichloro-2-propyl) phosphate (TDCP) and triphenyl phosphate (TPP). Solid phase extraction (SPE) was undertaken to extract and concentrate target analytes from aqueous matrices. All water s les were extracted from a volume of 500 mL. Isotopically labelled compounds were used to account for analytical variability and for accurate quantification by isotope dilution. Method recoveries for all compounds were above 80% in all tested water s les. Method detection limits for all target analytes ranged from 0.3 to 24 ng/L in ultrapure water, tap water, seawater, surface water, secondary effluent and swimming pool water. Validation of this method confirmed satisfactory method stability with less than 1% coefficients of variation, verifying that this approach produced good reproducibility.
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
Location: United Kingdom of Great Britain and Northern Ireland
No related grants have been discovered for Dr Heather Coleman.