TL;DR: In this paper, the state of the art in using passive sampling technology for environmental monitoring of waterborne organic and inorganic pollutants is reviewed, and strategies for sampler design, calibration, in situ sampling and quality control issues are discussed.
Abstract: We review the state of the art in using passive sampling technology for environmental monitoring of waterborne organic and inorganic pollutants. We discuss strategies for sampler design, calibration, in situ sampling and quality-control issues, and advantages and challenges associated with passive sampling in aqueous environments. We then review typical applications of passive samplers in assessing the aquatic environment.
TL;DR: A passive in situ sampling device that integratively concentrates trace levels of complex mixtures of hydrophilic environmental contaminants, enables the determination of their time-weighted average water concentrations, and provides a method of estimating the potential exposure of aquatic organisms to the complex mixture of waterborne contaminants is developed.
Abstract: Increasingly it is being realized that a holistic hazard assessment of complex environmental contaminant mixtures requires data on the concentrations of hydrophilic organic contaminants including new generation pesticides, pharmaceuticals, personal care products, and many chemicals associated with household, industrial, and agricultural wastes. To address this issue, we developed a passive in situ sampling device (the polar organic chemical integrative sampler [POCIS]) that integratively concentrates trace levels of complex mixtures of hydrophilic environmental contaminants, enables the determination of their time-weighted average water concentrations, and provides a method of estimating the potential exposure of aquatic organisms to the complex mixture of waterborne contaminants. Using a prototype sampler, linear uptake of selected herbicides and pharmaceuticals with log K(ow)s < 4.0 was observed for up to 56 d. Estimation of the ambient water concentrations of chemicals of interest is achieved by using appropriate uptake models and determination of POCIS sampling rates for appropriate exposure conditions. Use of POCIS in field validation studies targeting the herbicide diuron in the United Kingdom resulted in the detection of the chemical at estimated concentrations of 190 to 600 ng/L. These values are in agreement with reported levels found in traditional grab samples taken concurrently.
TL;DR: The main milestones in the development of passive techniques for sampling and/or extraction of analytes, and in biomonitors used in environmental analysis, are summarized in this review.
Abstract: The current state-of-the-art of passive sampling and/or extraction methods for long-term monitoring of pollutants in different environmental compartments is discussed in this review. Passive dosimeters that have been successfully used to monitor organic and inorganic contaminants in air, water, sediments, and soil are presented. The application of new approaches to the determination of pollutants at the sampling stage is discussed. The main milestones in the development of passive techniques for sampling and/or extraction of analytes, and in biomonitors used in environmental analysis, are summarized in this review. Passive samplers and biomonitors are compared.
TL;DR: Overall, POCIS has been applied to a wide range of sampling environments and scenarios and has been proven to be a useful screening tool, however, a more mechanistic approach is required to increase understanding and thus improve the quantitative nature of the measurements.
Abstract: The implementation of strict environmental quality standards for polar organic priority pollutants poses a challenge for monitoring programs. The polar organic chemical integrative sampler (POCIS) may help to address the challenge of measuring low and fluctuating trace concentrations of such organic contaminants, offering significant advantages over traditional sampling. In the present review, the authors evaluate POCIS calibration methods and factors affecting sampling rates together with reported environmental applications. Over 300 compounds have been shown to accumulate in POCIS, including pesticides, pharmaceuticals, hormones, and industrial chemicals. Polar organic chemical integrative sampler extracts have been used for both chemical and biological analyses. Several different calibration methods have been described, which makes it difficult to directly compare sampling rates. In addition, despite the fact that some attempts to correlate sampling rates with the properties of target compounds such as log K(OW) have been met with varying success, an overall model that can predict uptake is lacking. Furthermore, temperature, water flow rates, salinity, pH, and fouling have all been shown to affect uptake; however, there is currently no robust method available for adjusting for these differences. Overall, POCIS has been applied to a wide range of sampling environments and scenarios and has been proven to be a useful screening tool. However, based on the existing literature, a more mechanistic approach is required to increase understanding and thus improve the quantitative nature of the measurements.
TL;DR: A new sampling system has been developed for the measurement of time-averaged concentrations of organic micropollutants in aquatic environments based on the diffusion of targeted organic compounds through a rate-limiting membrane and the subsequent accumulation of these species in a bound, hydrophobic, solid-phase material.
Abstract: A new sampling system has been developed for the measurement
of time-averaged concentrations of organic micropollutants in aquatic
environments. The system is based on the diffusion of targeted organic compounds
through a rate-limiting membrane and the subsequent accumulation of these
species in a bound, hydrophobic, solid-phase material. It provides a novel
and robust solution to the problem of monitoring in situations where large
temporal fluctuations in pollutant levels may occur. Accumulation rates are
regulated by choice of diffusion-limiting membrane and bound solid-phase
material and have been found to be dependent on the physico-chemical properties
of individual target analytes. Two separate prototype systems are described:
one suitable for the sampling of non-polar organic species with log octanol/water
partition coefficient (log P) values greater than 4, the other
for more polar species with log P values between 2 and 4.
Both systems use the same solid-phase material (47 mm C18
Empore™
disk) as a receiving phase but are fitted with different
rate-limiting membrane materials (polysulfone for the polar and polyethylene
for the non-polar analytes). The two systems complement each other and
together can be used for sampling a wider range of organic analytes than generally
possible using current passive sampling techniques. Calibration data are presented
for both devices. In each case, linear uptake kinetics were sustained, under
constant conditions, for deployment periods of between 1 and 9 days.
The effects of water temperature and turbulence on sampling rates have been
quantitatively assessed. The performance of the system was further investigated
by means of field exposures for one and two weeks in marine environments where
calibrated samplers were used to determine the time-averaged concentrations
of the polar biocides diuron and irgarol 1051. The quantitative results obtained
using the passive sampler were compared with those obtained using spot sampling.