A comparison of removal performance of volatile organic and sulfurous compounds between odour abatement systems.

Three types of odour abatement systems in sewer networks in Australia were studied for 18 months to determine the removals of different compounds. Six volatile sulfurous compounds and seven volatile organic compounds (VOCs) were further investigated. All types of odour abatement systems exhibited good removal of hydrogen sulfide with the biotrickling filters (BTFs) showing the highest consistent removal. Biofilters outperformed BTFs and activated carbon (AC) filters in the removal of dimethyl mono-, di- and tri-sulfide species at the low inlet concentrations typically found. AC filters exhibited little VOC removal with no compound consistently identified as having a removal greater than 0%. Biofilters outperformed BTFs in VOC removal, yet both had high removal variability.

Survey of the effect of odour impact on communities.

In the context of environmental malodour, surveys are valuable as they allow for the relatively detailed analysis of multiple factors pertaining to odour perception and subsequent reaction. However, the causes for an individual to experience odour impact while a neighbour will not are still not understood. The goal of this current survey design was to consolidate varying research paths for surveys within the environmental odour research space. This survey investigated the area of effect for wastewater treatment plants by using stratified random sampling techniques that radiated from the industrial areas. Additionally, this survey provided a "non-alerted" response to environmental malodour that represents a step forward for ecological validity. We found a small number of items relating to odour annoyance and home ownership that can be used in order to predict odour impact for individual community members. However, we also did not find any relationship with odour impact and perceived control. This survey design and analysis reconciles the varied approaches towards community surveys administered in prior literature, as well as providing information to improve future community engagement policies.

Sulfur flows and biosolids processing: Using Material Flux Analysis (MFA) principles at wastewater treatment plants.

High flows of sulfur through wastewater treatment plants (WWTPs) may cause noxious gaseous emissions, corrosion of infrastructure, inhibit wastewater microbial communities, or contribute to acid rain if the biosolids or biogas is combusted. Yet, sulfur is an important agricultural nutrient and the direct application of biosolids to soils enables its beneficial re-use. Flows of sulfur throughout the biosolids processing of six WWTPs were investigated to identify how they were affected by biosolids processing configurations. The process of tracking sulfur flows through the sites also identified limitations in data availability and quality, highlighting future requirements for tracking substance flows. One site was investigated in more detail showing sulfur speciation throughout the plant and tracking sulfur flows in odour control systems in order to quantify outflows to air, land and ocean sinks. While the majority of sulfur from WWTPs is removed as sulfate in the secondary effluent, the sulfur content of biosolids is valuable as it can be directly returned to soils to combat the potential sulfur deficiencies. Biosolids processing configurations, which focus on maximising solids recovery, through high efficiency separation techniques in primary sedimentation tanks, thickeners and dewatering centrifuges retain more sulfur in the biosolids. However, variations in sulfur loads and concentrations entering the WWTPs affect sulfur recovery in the biosolids, suggesting industrial emitters, and chemical dosing of iron salts are responsible for differences in recovery between sites.

Odorous volatile organic compound (VOC) emissions from ageing anaerobically stabilised biosolids.

Opportunities for the beneficial re-use of biosolids are limited by nuisance odour emissions. Volatile organic compounds (VOCs) from anaerobically stabilised biosolids were measured to identify compounds that could contribute to the overall odour character of nuisance emissions. Flux hood sampling and chemical analysis were used to identify VOCs emitted from biosolids as they were stored in ambient conditions. Compounds emitted varied as the biosolid cakes were stored for a period of 50 days. VOCs detected in the biosolids are likely to occur from catchment sources as well as abiotic and biotic generation in the wastewater processing and the biosolids as they are stored. Odour activity values (OAVs) were used to compare odorants. Trimethylamine was the only VOC detected that exceeded the sulfur compounds in terms of OAVs. Other compounds such as limonene, ethyl methyl benzene and acetic acid were detected at concentrations exceeding their olfactory detection limits, however at lower OAVs than sulfur compounds.

Reduced sulfur compounds in the atmosphere of sewer networks in Australia: geographic (and seasonal) variations.

The management of odorous emissions from sewer networks has become an important issue for sewer system operators resulting in the need to better understand the composition of reduced sulfur compounds (RSCs). Gaseous RSCs including hydrogen sulfide (H2S), methanethiol (MeSH), dimethyl sulfide (DMS), carbon disulfide (CS2), dimethyl disulfide (DMDS) and dimethyl trisulfide (DMTS) were measured in the atmosphere of selected sewer networks in two major Australian cities (Sydney and Melbourne) during 2011-2012. The RSC concentrations in the sewer air were detected in a highly variable range. H2S and MeSH were found at the highest concentrations, followed by DMS (39.2-94.0 µg/m(3)), CS2 (18.3-19.6 µg/m(3)), DMDS (7.8-49.6 µg/m(3)) and DMTS (10.4-35.3 µg/m(3)). Temporal trends in the occurrence of targeted RSCs were observed and the highest sulfur concentration occurred either in summer or spring, which are typically regarded as the warmer seasons. Statistical significant difference in the magnitude of targeted RSCs was found between samples collected in Sydney and Melbourne.

Is H2S a suitable process indicator for odour abatement performance of sewer odours?

Odour abatement units are typically designed and maintained on H(2)S concentrations, but operational failures are reported in terms of overall odour removal, suggesting a wide range of malodorous compounds emitted from sewers that may not be efficiently removed by existing odour abatement processes. Towards providing greater insight into this issue, several activated carbon filters and biofilters treating odorous emissions from sewer systems in Sydney (Australia) were monitored by collecting and analysing gas samples before and after treatment. The monitoring studies were conducted by both olfactometric measurements and gas-chromatography-based chemical analysis. Single H(2)S assessment often failed to indicate the odour abatement performance for treatment systems in the abatement units studied, particularly when the incoming H(2)S concentrations were in the sub-ppm range (i.e. below H(2)S odour threshold). Chemical analysis indicated that some non-H(2)S odorous compounds were not removed efficiently during odour treatment. Additionally, when odour eliminations were correlated with the removal of individual compounds (Pearson's correlations) it was observed that the correlation (with a coefficient of 0.79) was best when the overall removal of all the measured odorous compounds that exceeded their odour threshold values was used for the analysis. These findings may help to further advance the design and operation of odour abatement processes to address the treatment of sewer odour emissions.

Odorous emissions of synthetic turf and its relationship with local communities.

Synthetic turf has been a mainstay of field sports and local communities for decades, and in that time, has faced both community and government pressure to ensure its safety and fitness for purpose. Considerable research and regulations have been applied to synthetic turf with regards to its safety, construction, potential toxicity, sports impact, as well as environmental considerations. However, very little attention has been paid to reports of odorous impacts from synthetic turf fields. This is problematic as odours are both a source of most complaints by communities towards other industries, as well as the fact that synthetic turf has a unique placement within communities themselves. It is wholly possible that the concerns surrounding synthetic turf are being modulated by the odours that the fields themselves produce through previously identified psychological mechanisms. As a result, ensuring good standards for synthetic turf with regards to odorous emissions should be benchmarked for community acceptability. This review investigates prior research into synthetic turf with regards to identified volatile organic compounds emitted, as well as proposing the means by which community stakeholders engage with synthetic turf, as well as how they should be consulted. From here, this review provides trajectories for future research within this space, and how regulatory bodies should address potential issues. This research space is currently in its infancy and therefore information relating to synthetic turf odour factors must be carefully considered.

Review of scientific research on air quality and environmental health risk and impact for PICTS.

Air quality (AQ) significantly impacts human health, influenced by both natural phenomena and human activities. In 2021, heightened awareness of AQ's health impacts prompted the revision of the World Health Organization (WHO) guidelines, advocating for stricter pollution standards. However, research on AQ has predominantly focused on high-income countries and densely populated cities, neglecting low- and middle-income countries, particularly Pacific Island Countries, Territories, and States (PICTS). This systematic review compiles existing peer-reviewed literature on AQ research in PICTS to assess the current state of knowledge and emphasize the need for further investigation. A systematic literature search yielded 40 papers from databases including Web of Science, Scopus, and Embase. Among the 26 PICTS, only 6 (Hawai'i, Fiji, Papua New Guinea, New Caledonia, Republic of Marshall Islands, and Pacific) have been subject to AQ-related research, with 4 considering the World Health Organization (WHO) parameters and 26 addressing non-WHO parameters. Analysis reveals AQ parameters often exceed 2021 WHO guidelines for PM2.5, PM10, SO2, and CO, raising concerns among regional governments. Studies primarily focused on urban, agricultural, rural, and open ocean areas, with 15 based on primary data and 14 on both primary and secondary sources. Research interests and funding sources dictated the methods used, with a predominant focus on environmental risks over social, economic, and technological impacts. Although some papers addressed health implications, further efforts are needed in this area. This review underscores the urgent need for ongoing AQ monitoring efforts in PICTS to generate spatially and temporally comparable data. By presenting the current state of AQ knowledge, this work lays the foundation for coordinated regional monitoring and informs national policy development.

Stability of volatile sulfur compounds (VSCs) in sampling bags - impact of temperature.

Volatile sulfur compounds (VSCs) are a major component of odorous emissions that can cause annoyance to local populations surrounding wastewater, waste management and agricultural practices. Odour collection and storage using sample bags can result in VSC losses due to sorption and leakage. Stability within 72 hour storage of VSC samples in three sampling bag materials (Tedlar, Mylar, Nalophan) was studied at three temperatures: 5, 20, and 30 °C. The VSC samples consisted of hydrogen sulfide (H2S), methanethiol (MeSH), ethanethiol (EtSH), dimethyl sulfide (DMS), tert-butanethiol (t-BuSH), ethylmethyl sulfide (EMS), 1-butanethiol (1-BuSH), dimethyl disulfide (DMDS), diethyl disulfide (DEDS), and dimethyl trisulfide (DMTS). The results for H2S showed that higher loss trend was clearly observed (46-50% at 24 hours) at 30 °C compared to the loss at 5 °C or 20 °C (of up to 27% at 24 hours) in all three bag materials. The same phenomenon was obtained for other thiols with the relative recoveries after a 24 hour period of 76-78% at 30 °C and 80-93% at 5 and 20 °C for MeSH; 77-80% at 30 °C and 79-95% at 5 and 20 °C for EtSH; 87-89% at 30 °C and 82-98% at 5 and 20 °C for t-BuSH; 61-73% at 30 °C and 76-98% at 5 and 20 °C for 1-BuSH. Results for other sulfides and disulfides (DMS, EMS, DMDS, DEDS) indicated stable relative recoveries with little dependency on temperature (83-103% after 24 hours). DMTS had clear loss trends (with relative recoveries of 74-87% in the three bag types after 24 hours) but showed minor differences in relative recoveries at 5, 20, and 30 °C.

Investigation of PM10 sources in Santa Catarina, Brazil through graphical interpretation analysis combined with receptor modelling.

Epidemiological studies have documented that elevated airborne particulate matter (PM) concentrations, especially those with an aerodynamic diameter less than 10 microm (PM10), are associated with adverse health effects. Two receptor models, UNMIX and positive matrix factorization (PMF), were used to identify and quantify the sources of PM10 concentrations in Tubarão and Capivari de Baixo, Santa Catarina, Brazil. This region is known for its high pollution levels due to intense industrial activity and exploitation of natural resources. PM10 samples were collected using high volume samplers at two sites in the region and statistical exploratory analysis techniques were applied to identify and assess PM10 sources. The two primary PM10 sources were identified as soil re-suspension/road dust emissions and coal burning emissions, contributing 65-75% and 15-25% of the PM10, respectively. The study confirmed the significance of the influence of local PM10 emissions (power plants, soil re-suspension and road dust emissions) on regional air quality, although no violations of the Brazilian PM10 standards (limit of 150 microg/m3) were observed, with a mean concentration of 27.6 microg/m3 measured in this study. This study demonstrated the usefulness of statistical exploratory analysis techniques in assessing the validity of modelling results and contributing to the interpretation of ambient air quality data.

Removal of trace organic chemical contaminants by a membrane bioreactor.

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.

Demonstrating ultra-filtration and reverse osmosis performance using size exclusion chromatography.

Advanced water treatment plants employing ultrafiltration (UF) and reverse osmosis (RO) membrane processes are frequently implemented for the production of high-quality recycled water. It is important that process performance is able to be quantified and assessed to ensure it is fit for purpose. This research utilizes size exclusion chromatography with organic carbon, organic nitrogen and UV(254) detection to determine the change in both DOC concentration and character through a UF/3 stage-RO pilot plant. It was determined that 97% of the influent DOC was removed on average to produce a water of less than 0.5 mg L(-1) as C. The UF process removed more than half of the biopolymer fraction, equating to 4.5% DOC removal, while the RO process generally removed all DOC except a small proportion of the low MW humics and acids and low MW neutral fraction. While not changing significantly in concentration, the Stage 3 RO permeate typically contained low concentrations of humic fraction, indicating a change in character and therefore a change in rejection mechanism. Overall, it was determined that while TOC monitoring is important in advanced water treatment systems, improved understanding of the character of the TOC present lends greater insight into the assessment of process performance.

Probabilistic analysis of fluorescence signals for monitoring dual reticulation water recycling schemes.

Improved techniques are required for the detection of inadvertent cross-connections between recycled water and potable water systems in dual reticulation schemes. The aim of this research was to assess the potential for fluorescence spectroscopy to be developed as a tool to distinguish recycled water from potable water. Weekly grab samples of recycled and potable water were obtained over 12 weeks from within an Australian dual reticulation site and analysed for fluorescence excitation-emission matrix (EEM), dissolved organic carbon (DOC), electrical conductivity (EC), and pH. Probabilistic techniques including distribution function fitting and Monte Carlo simulation were used to assess the ability to distinguish between recycled water and potable water sample pairs and the reliability of doing so. Fluorescence EEM spectroscopy was determined to be the most effective for the reliable differentiation by monitoring the protein-like fluorescence at peak T(1)--an excitation-emission wavelength pair of λ(ex/em)=300/350 nm. While EC could distinguish between recycled and potable water, it was shown to be less sensitive and less reliable than peak T(1) fluorescence.

Fluorescence monitoring for cross-connection detection in water reuse systems: Australian case studies.

A rapid, highly sensitive method for detection of cross-connections between recycled and potable water in dual reticulation systems is required. The aim of this research was to determine the potential of fluorescence spectroscopy as a monitoring tool at three Australian dual distribution (drinking and recycled water) systems. Weekly grab samples of recycled and potable water were obtained over 12 weeks at each site and analysed for fluorescence excitation-emission matrix (EEM) spectroscopy, UV(254), dissolved organic carbon (DOC), electrical conductivity and pH. Fluorescence EEM spectroscopy was able to differentiate between recycled and potable water at each site by monitoring the protein-like fluorescence at peak T-an excitation-emission wavelength pair of lambda(ex/em) = 300/350 nm. While electrical conductivity was also able to distinguish between recycled and potable water, the differentiation was greatest when using fluorescence. For example, the peak T fluorescence in recycled water was up to 10 times that of potable water in comparison with electrical conductivity that had a maximum 5 times differentiation. Furthermore, by comparing the protein-like fluorescence at peak T and humic-like fluorescence at peak A (lambda(ex/em) = 235/426 nm), the three different recycled water systems were able to be differentiated. Overall, fluorescence shows promise as a monitoring tool for detecting cross-connections.

The application of membrane bioreactors as decentralised systems for removal of endocrine disrupting chemicals and pharmaceuticals.

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. Samples 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.

Fate and levels of steroid oestrogens and androgens in waste stabilisation ponds: quantification by liquid chromatography-tandem mass spectrometry.

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. Samples 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.

Conceptual analysis of the UASB/polishing pond system regarding the removal of surfactants, micropollutants and control of gaseous emissions.

A conceptual and integrated analysis of the UASB/Polishing Pond system is presented in relation to the removal of specific constituents not normally covered in the pond's literature, namely surfactants (linear alkylbenzene sulphonate, LAS), micropollutants (phthalates and bisphenol A) and sulfide. Experimental studies carried out on a small full-scale UASB/PP system have shown limited overall removal efficiencies for some constituents (53% to 70% for phthalates and 50% for LAS), but excellent removal levels for bisphenol A (around 99%) and sulfide (no trace concentrations were detected in the second and third ponds of the series). Further research is needed to investigate possible limitations and to identify means to improve the performance of the UASB/PP system.

Fluorescence as a potential monitoring tool for recycled water systems: a review.

A rapid, highly sensitive and selective detector is urgently required to detect contamination events in recycled water systems - for example, cross-connection events in dual reticulation pipes that recycle advanced treated sewage effluent - as existing technologies, including total organic carbon and conductivity monitoring, cannot always provide the sensitivity required. Fluorescence spectroscopy has been suggested as a potential monitoring tool given its high sensitivity and selectivity. A review of recent literature demonstrates that by monitoring the fluorescence of dissolved organic matter (DOM), the ratios of humic-like (Peak C) and protein-like (Peak T) fluorescence peaks can be used to identify trace sewage contamination in river waters and estuaries, a situation analogous to contamination detection in recycled water systems. Additionally, strong correlations have been shown between Peak T and biochemical oxygen demand (BOD) in rivers, which is indicative of water impacted by microbial activity and therefore of sewage impacted systems. Hence, this review concludes that the sensitive detection of contamination events in recycled water systems may be achieved by monitoring Peak T and/or Peak C fluorescence. However, in such systems, effluent is treated to a high standard resulting in much lower DOM concentrations and the impact of these advanced treatment processes on Peaks T and C fluorescence is largely unknown and requires investigation. This review has highlighted that further work is also required to determine (a) the stability and distinctiveness of recycled water fluorescence in relation to the treatment processes utilised, (b) the impact of matrix effects, particularly the impact of oxidation, (c) calibration issues for online monitoring, and (d) the advanced data analytical techniques required, if any, to improve detection of contamination events.

Distinguishing Stage 1 and 2 reverse osmosis permeates using fluorescence spectroscopy.

Fluorescence excitation-emission matrix (EEM) spectroscopy was used to distinguish between two stages of reverse osmosis (RO) permeates as the first step towards investigating the potential application of fluorescence as a monitoring tool for membrane performance. The signal response of several fluorescence peaks present in Stage 1 and Stage 2 RO permeates of an advanced water treatment plant were compared. The humic-like fluorescence region was found to have the largest percentage difference between stages and therefore was the most appropriate for enabling differentiation. Increases in humic-like fluorescence did not correlate with increases in conductivity or dissolved organic carbon measurements. This suggests that fluorescence is a more selective and sensitive method for monitoring the organic composition of RO permeates than established methods. Fluorescence is therefore a promising tool for improved water quality monitoring of RO permeates.

Enhanced real-time cyanobacterial fluorescence monitoring through chlorophyll-a interference compensation corrections.

In situ fluorometers can be used as a real-time cyanobacteria detection tool to maintain safe drinking and recreational water standards. However, previous studies into fluorometers have established issues arising mainly from measurement inaccuracies due to green algae interference. Therefore, this study focusses on developing correction factors from a systematic study on the impact of green algae as an interference source. This study brings a novel technique where the chlorophyll-a (Chl-a) and phycocyanin measurements are used to correct the fluorometer output for interference bias; four fluorometers were tested against three key cyanobacterial species and the relationship between phycocyanin output, green algae and cyanobacteria concentrations were investigated. Good correlation (R2 > 0.9, p-value < 0.05) was found between the fluorometer phycocyanin output and increasing green algae concentration. The optimal correction method was selected for each of the fluorometer and cyanobacteria species pairs by validating against data from the investigation of green algae as an interference source. The correction factors determined in this study reduced the measurement error for almost all the fluorometers and species tested by 21%-99% depending on the species and fluorometer, compared to previous published correction factors in which the measurement error was reduced by approximately 11%-81%. Field validation of the correction factors showed reduction in fluorometer measurement error at sites in which cyanobacterial blooms were dominated by a single species.