Minimizing transient microenvironment-associated variability for analysis of environmental anthropogenic contaminants via ambient ionization
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The NOAA IR serves as an archival repository of NOAA-published products including scientific findings, journal articles, guidelines, recommendations, or other information authored or co-authored by NOAA or funded partners. As a repository, the NOAA IR retains documents in their original published format to ensure public access to scientific information.
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Minimizing transient microenvironment-associated variability for analysis of environmental anthropogenic contaminants via ambient ionization

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  • Journal Title:
    Science of The Total Environment
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  • Description:
    The rapid and quantitative analysis of anthropogenic contaminants in environmental matrices is crucial for regulatory testing and to elucidate the environmental fate of these pollutants. Direct ambient mass spectrometry (AMS) methodologies greatly increase sample throughput, can be adapted for onsite analysis and are often regarded as semi-quantitative by most developed protocols. One of the limitations of AMS, especially for on site analysis applications, is the irreproducibility of the measurements related to the occurrence of transient microenvironments (TME) and variable background interferences. In this work we report an effective strategy to minimize these effects by hyphenating, for the first time, solid phase microextraction (SPME) arrow to mass spectrometry via a thermal desorption unit (TDU) and direct analysis in real time (DART) source. The developed method was optimized for the extraction and analysis of pesticides and pharmaceuticals from surface water. It was demonstrated that the hyphenation of the SPME and TDU-DART resulted in reduced background contamination, indicating the suitability of the method for onsite analysis even in variable and non-ideal environments. Model analytes were quantitated in the low μg/L range with a total analysis time of less than 5 min, linear dynamic ranges (LDR) and interday reproducibility for most compounds being 2.5–500 μg/L and lower than 10%, respectively. The developed approach provides an excellent analytical tool that can be applied for the onsite high-throughput analysis of water samples as well as air and aereosols. Considering the tunability of our extraction process, time-resolved environmental monitoring can be achieved onsite within minutes.
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  • Source:
    Science of The Total Environment, 775, 145789
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  • ISSN:
    0048-9697
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    Accepted Manuscript
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    Library
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