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− | ==Contaminated Sediment Risk Assessment== | + | ==Munitions Constituents – Sample Extraction and Analytical Techniques== |
− | [[Contaminated Sediments - Introduction | Contaminated sediments]] in rivers and streams, lakes, coastal harbors, and estuaries have the potential to pose ecological and human health risks. The goals of risk assessment applied to contaminated sediments are to characterize the nature and magnitude of the current and potential threats to human health, wildlife and ecosystem functioning posed by contamination; identify the key factors contributing to the potential health and ecological risks; evaluate how implementation of one or more remedy actions will mitigate the risks in the short and long term; and evaluate the risks and impacts from sediment management, both during and after any dredging or other remedy construction activities. | + | Munitions Constituents, including [[Wikipedia: Insensitive munition | insensitive munitions]] (IM), are a broad category of compounds which, in areas where manufactured or used, can be found in a variety of environmental matrices (waters, soil, and tissues). This presents an analytical challenge when a variety of these munitions are to be quantified. This article discusses sample extraction methods for each typical sample matrix (high level water, low level water, soil and tissue) as well as the accompanying [[Wikipedia: High-performance liquid chromatography | HPLC]]-UV analytical method for 27 compounds of interest (legacy munitions, insensitive munitions, and surrogates). |
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| <div style="float:right;margin:0 0 2em 2em;">__TOC__</div> | | <div style="float:right;margin:0 0 2em 2em;">__TOC__</div> |
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| '''Related Article(s):''' | | '''Related Article(s):''' |
− | *[[Contaminated Sediments - Introduction]]
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− | *[[In Situ Treatment of Contaminated Sediments with Activated Carbon]]
| + | *[[Munitions Constituents]] |
− | *[[Sediment Capping]]
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− | *[[Passive Sampling of Sediments]] | |
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| '''Contributor(s):''' | | '''Contributor(s):''' |
− | *Richard J. Wenning
| + | |
− | *Sabine E. Apitz | + | *Dr. Austin Scircle |
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| '''Key Resource(s):''' | | '''Key Resource(s):''' |
− | * Contaminated Sediment Remediation Guidance for Hazardous Waste Sites<ref name="USEPA2005">United States Environmental Protection Agency (USEPA), 2005. Contaminated Sediment Remediation Guidance for Hazardous Waste Sites. Office of Solid Waste and Emergency Response, Washington, D.C. EPA-540-R-05-012. OSWER 9355.0-85. Free download from: [https://semspub.epa.gov/work/HQ/174471.pdf USEPA] [[Media: EPA-540-R-05-012.pdf | Report.pdf]]</ref>
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− | * Principles for Environmental Risk Assessment of the Sediment Compartment<ref name="Tarazona2014">Tarazona, J.V., Versonnen, B., Janssen, C., De Laender, F., Vangheluwe, M. and Knight, D., 2014. Principles for Environmental Risk Assessment of the Sediment Compartment: Proceedings of the Topical Scientific Workshop. 7-8 May 2013. European Chemicals Agency, Helsinki. Document ECHA-14-R-13-EN. Free download from: [https://echa.europa.eu/documents/10162/22816050/environmental_risk_assessment_final_en.pdf/3515b685-6601-40ce-bd48-3f8d5332c0f8 European Chemicals Agency] [[Media: ECHA-14-R-13-EN.pdf | Report.pdf]]</ref> | + | *[https://www.epa.gov/sites/default/files/2015-07/documents/epa-8330b.pdf USEPA Method 8330B]<ref name= "8330B">United States Environmental Protection Agency (USEPA), 2006. EPA Method 8330B (SW-846) Nitroaromatics, Nitramines, and Nitrate Esters by High Performance Liquid Chromatography (HPLC), Revision 2. [https://www.epa.gov/esam/epa-method-8330b-sw-846-nitroaromatics-nitramines-and-nitrate-esters-high-performance-liquid USEPA Website] [[Media: Epa-2006-method-8330b.pdf | EPA Method 8330b]]</ref> |
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− | * Assessing and managing contaminated sediments: | + | *Methods for simultaneous quantification of legacy and insensitive munition (IM) constituents in aqueous, soil/sediment, and tissue matrices<ref name="CrouchEtAl2020">Crouch, R.A., Smith, J.C., Stromer, B.S., Hubley, C.T., Beal, S., Lotufo, G.R., Butler, A.D., Wynter, M.T., Russell, A.L., Coleman, J.G., Wayne, K.M., Clausen, J.L., Bednar, A.J., 2020. Methods for simultaneous determination of legacy and insensitive munition (IM) constituents in aqueous, soil/sediment, and tissue matrices. Talanta, 217, Article 121008. [https://doi.org/10.1016/j.talanta.2020.121008 doi: 10.1016/j.talanta.2020.121008] [[Media: CrouchEtAl2020.pdf | Open Access Manuscript.pdf]]</ref> |
− | :: Part I, Developing an Effective Investigation and Risk Evaluation Strategy<ref name="Apitz2005a">Apitz, S.E., Davis, J.W., Finkelstein, K., Hohreiter, D.W., Hoke, R., Jensen, R.H., Jersak, J., Kirtay, V.J., Mack, E.E., Magar, V.S. and Moore, D., 2005. Assessing and Managing Contaminated Sediments: Part I, Developing an Effective Investigation and Risk Evaluation Strategy. Integrated Environmental Assessment and Management, 1(1), pp. 2-8. [https://doi.org/10.1897/IEAM_2004a-002.1 DOI: 10.1897/IEAM_2004a-002.1] Free access article from: [https://setac.onlinelibrary.wiley.com/doi/epdf/10.1897/IEAM_2004a-002.1 Society of Environmental Toxicology and Chemistry] [[Media: Apitz2005a.pdf | Report.pdf]]</ref>
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− | :: Part II, Evaluating Risk and Monitoring Sediment Remedy Effectiveness<ref name="Apitz2005b">Apitz, S.E., Davis, J.W., Finkelstein, K., Hohreiter, D.W., Hoke, R., Jensen, R.H., Jersak, J., Kirtay, V.J., Mack, E.E., Magar, V.S. and Moore, D., 2005b. Assessing and Managing Contaminated Sediments: Part II, Evaluating Risk and Monitoring Sediment Remedy Effectiveness. Integrated Environmental Assessment and Management, 1(1), pp.e1-e14. [https://doi.org/10.1897/IEAM_2004a-002e.1 DOI: 10.1897/IEAM_2004a-002e.1]</ref>
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| ==Introduction== | | ==Introduction== |
− | Improving the management of [[Contaminated Sediments - Introduction | contaminated sediments]] is of growing concern globally. Sediment processes in both marine and freshwater environments are important to the function of aquatic ecosystems<ref name="Apitz2012">Apitz, S.E., 2012. Conceptualizing the role of sediment in sustaining ecosystem services: Sediment-Ecosystem Regional Assessment (SEcoRA), Science of the Total Environment, 415, pp. 9-30. [https://doi.org/10.1016/j.scitotenv.2011.05.060 DOI:10.1016/j.scitotenv.2011.05.060] Free download from: [https://d1wqtxts1xzle7.cloudfront.net/7588577/Apitz_SEcoRA%202012.pdf?1326618388=&response-content-disposition=inline%3B+filename%3DConceptualizing_the_role_of_sediment_in.pdf&Expires=1637094311&Signature=c2wczG59XxkitPjmBhc9PaODHJ8Vufg3gyzdG8tqGD6~mIVhLoz30E7eQNIghfMlH~jbch3KTVxMqD2AQFMQCSeXghIwqH~lXjGrEP07MJXCEgntzSW-V8Gws~33it5pEm9Ied64fSOvMLJR-PUXVr2OVTsVHQJHurHdGrtEmhUd90bKrC0NNlD28YLGQpkVUOlqa75e0K4sjPngwPUwUxhq18NAH6-1Uc3fQU5g5AjXwGph-VNe7EwzT-0do5OD056AsG-Eg8xIZi0ABJqMsg1wb92tIPpmmNy6ntdklHeN6tq~3IJFB7Tg8XYntQ-CGT8pYV9S7Kz14GhXVm9OQA__&Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA Academia.edu]</ref>, and many organisms rely on certain sediment quality and quantity characteristics for their life cycle<ref name="Hauer2018">Hauer, C., Leitner, P., Unfer, G., Pulg, U., Habersack, H. and Graf, W., 2018. The Role of Sediment and Sediment Dynamics in the Aquatic Environment. In: Schmutz S., Sendzimir J. (ed.s) Riverine Ecosystem Management. Aquatic Ecology Series, vol. 8, pp. 151-169. Springer. [https://doi.org/10.1007/978-3-319-73250-3_8 DOI: 10.1007/978-3-319-73250-3_8] Open access book from: [https://library.oapen.org/bitstream/handle/20.500.12657/27726/1002280.pdf?seque#page=153 SpringerOpen]</ref>. Human health can also be affected by sediment conditions, either via direct contact, as a result of sediment impacts on water quality, or because of the strong influence sediments can have on the quality of fish and shellfish consumed by people<ref name="Greenfield2015">Greenfield, B.K., Melwani, A.R. and Bay, S.M., 2015. A Tiered Assessment Framework to Evaluate Human Health Risk of Contaminated Sediment. Integrated Environmental Assessment and Management, 11(3), pp. 459-473. [https://doi.org/10.1002/ieam.1610 DOI: 10.1002/ieam.1610]</ref>. A common approach to achieving the explicit management goals inherent in different sediment assessment frameworks in North America and elsewhere is the use of the ecological risk assessment (ERA)<ref name="USEPA1997a">US Environmental Protection Agency (USEPA), 1997. The Incidence and Severity of Sediment Contamination in Surface Waters of the United States: Volume 1, National Sediment Quality Survey. EPA-823R-97-006. Washington, DC. [[Media: EPA-823-R-97-006.pdf | Report.pdf]]</ref>. An ERA “evaluates the likelihood and magnitude of adverse effects from exposure to a chemical for organisms, such as animals, plants, or microbes, in the environment”<ref name="SETAC2018">Society of Environmental Toxicology and Chemistry (SETAC), 2018. Technical Issue Paper: Environmental Risk Assessment of Chemicals. SETAC, Pensacola, FL. 5 pp. Free download from: [https://cdn.ymaws.com/www.setac.org/resource/resmgr/publications_and_resources/setac_tip_era.pdf SETAC] [[Media: setac_tip_era2018.pdf | Report.pdf]]</ref>. An ERA provides information relevant to the management decision-making process<ref name="Stahl2001">Stahl, R.G., Bachman, R., Barton, A., Clark, J., deFur, P., Ells, S., Pittinger, C., Slimak, M., Wentsel, R., 2001. Risk Management: Ecological Risk-Based Decision Making. SETAC Press, Pensacola, FL, 222 pp. ISBN: 978-1-880611-26-5</ref>. It should be performed in a scientifically based, defensible manner that is cost-effective and protective of human health and the environment<ref name="CNO1999">Chief of Naval Operations (CNO), 1999. Navy Policy for Conducting Ecological Risk Assessments, Letter 5090, Ser N453E/9U595355, dated 05 April 99. Department of the Navy, Washington, DC. Free download from: [https://www.navfac.navy.mil/content/dam/navfac/Specialty%20Centers/Engineering%20and%20Expeditionary%20Warfare%20Center/Environmental/Restoration/er_pdfs/gpr/cno-ev-pol-era-19990405.pdf the US Navy] [[Media: CNO1999.pdf | Report.pdf]]</ref>. Therefore, science-based methods for assessing sediment quality and use of risk-based decision-making in sediment management are important for identifying conditions suspected to adversely affect ecological and human services provided by sediments, and predicting the likely consequences of different sediment management actions<ref name="Bridges2006">Bridges, T.S., Apitz, S.E., Evison, L., Keckler, K., Logan, M., Nadeau, S. and Wenning, R.J., 2006. Risk‐Based Decision Making to Manage Contaminated Sediments. Integrated Environmental Assessment and Management, 2(1), pp. 51-58. [https://doi.org/10.1002/ieam.5630020110 DOI: 10.1002/ieam.5630020110] Free access article from: [https://setac.onlinelibrary.wiley.com/doi/epdf/10.1002/ieam.5630020110 SETAC]</ref><ref name="Apitz2011">Apitz, S.E., 2011. Integrated Risk Assessments for the Management of Contaminated Sediments in Estuaries and Coastal Systems. In: Wolanski, E. and McLusky, D.S. (eds.) Treatise on Estuarine and Coastal Science, Vol 4, pp. 311–338. Waltham: Academic Press. ISBN: 9780123747112</ref>.
| + | {| class="wikitable mw-collapsible" style="float:left; margin-right:20px; text-align:center;" |
| + | |+Table 1. Analyte list with acronyms and CAS numbers. |
| + | |- |
| + | !Compound |
| + | ! Acronym |
| + | !CAS Number |
| + | |- |
| + | | 1,2-Dinitrobenzene (surrogate) ||'''1,2-DNB (surr.)''' || 528-29-0 |
| + | |- |
| + | | 1,3-Dinitrobenzene || 1,3-DNB || 99-65-0 |
| + | |- |
| + | | 1,3,5-Trinitrobenzene || 1,3,5-TNB || 99-35-4 |
| + | |- |
| + | | 1,4-Dinitrobenzene || '''1,4-DNB (surr.)''' || 100-25-4 |
| + | |- |
| + | | 2-Amino-4,6-dinitrotoluene || 2-Am-4,6-DNT || 35572-78-2 |
| + | |- |
| + | | 2-Nitrophenol || '''2-NP''' || 88-75-5 |
| + | |- |
| + | | 2-Nitrotoluene || 2-NT || 88-72-2 |
| + | |- |
| + | | 2,4-Dinitrophenol || '''2,4-DNP''' || 51-28-5 |
| + | |- |
| + | | 2,4-Dinitrotoluene || 2,4-DNT || 121-14-2 |
| + | |- |
| + | | 2,4,6-Trinitrophenol || '''Picric Acid (PA)''' || 88-89-1 |
| + | |- |
| + | | 2,4,6-Trinitrotoluene || 2,4,6-TNT || 118-96-7 |
| + | |- |
| + | | 2,6-Dinitrotoluene || 2,6-DNT || 606-20-2 |
| + | |- |
| + | | 3-Nitrotoluene || 3-NT || 99-08-1 |
| + | |- |
| + | | 3,5-Dinitroaniline || 3,5-DNA || 618-87-1 |
| + | |- |
| + | | 4-Amino-2,6-dinitrotoluene || 4-Am-2,6-DNT || 19406-51-0 |
| + | |- |
| + | | 4-Nitrophenol || '''4-NP''' || 100-02-7 |
| + | |- |
| + | | 4-Nitrotoluene || 4-NT || 99-99-0 |
| + | |- |
| + | | 2,4-Dinitroanisole || '''DNAN''' || 119-27-7 |
| + | |- |
| + | | Octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine || HMX || 2691-41-0 |
| + | |- |
| + | | Nitrobenzene || NB || 98-95-3 |
| + | |- |
| + | | Nitroglycerine || NG || 55-63-0 |
| + | |- |
| + | | Nitroguanidine || '''NQ''' || 556-88-7 |
| + | |- |
| + | | 3-Nitro-1,2,4-triazol-5-one || '''NTO''' || 932-64-9 |
| + | |- |
| + | | ''ortho''-Nitrobenzoic acid || '''''o''-NBA (surr.)''' || 552-16-9 |
| + | |- |
| + | | Pentaerythritol tetranitrate || PETN || 78-11-5 |
| + | |- |
| + | | Hexahydro-1,3,5-trinitro-1,3,5-triazine || RDX || 121-82-4 |
| + | |- |
| + | | N-Methyl-N-(2,4,6-trinitrophenyl)nitramide || Tetryl || 479-45-8 |
| + | |- |
| + | | colspan="3" style="background-color:white;" | Note: Analytes in '''bold''' are not identified by EPA Method 8330B. |
| + | |} |
| + | [[File: ScircleFig1.png | thumb | 400px | Figure 1. Primary Method labeled chromatograms]] |
| + | [[File: ScircleFig2.png | thumb | 400px | Figure 2. Secondary Method labeled chromatograms]] |
| + | The primary intention of the analytical methods presented here is to support the monitoring of legacy and insensitive munitions contamination on test and training ranges, however legacy and insensitive munitions often accompany each other at demilitarization facilities, manufacturing facilities, and other environmental sites. Energetic materials typically appear on ranges as small, solid particulates and due to their varying functional groups and polarities, can partition in various environmental compartments<ref>Walsh, M.R., Temple, T., Bigl, M.F., Tshabalala, S.F., Mai, N. and Ladyman, M., 2017. Investigation of Energetic Particle Distribution from High‐Order Detonations of Munitions. Propellants, Explosives, Pyrotechnics, 42(8), pp. 932-941. [https://doi.org/10.1002/prep.201700089 doi: 10.1002/prep.201700089]</ref>. To ensure that contaminants are monitored and controlled at these sites and to sustainably manage them a variety of sample matrices (surface or groundwater, process waters, soil, and tissues) must be considered. (Process water refers to water used during industrial manufacturing or processing of legacy and insensitive munitions.) Furthermore, additional analytes must be added to existing methodologies as the usage of IM compounds changes and as new degradation compounds are identified. Of note, relatively new IM formulations containing [[Wikipedia: Nitrotriazolone | NTO]], [[Wikipedia: 2,4-Dinitroanisole | DNAN]], and [[Wikipedia: Nitroguanidine | NQ]] are seeing use in [[Wikipedia: IMX-101 | IMX-101]], IMX-104, Pax-21 and Pax-41 (Table 1)<ref>Mainiero, C. 2015. Picatinny Employees Recognized for Insensitive Munitions. U.S. Army, Picatinny Arsenal Public Affairs. [https://www.army.mil/article/148873/picatinny_employees_recognized_for_insensitive_munitions Open Access Press Release]</ref><ref>Frem, D., 2022. A Review on IMX-101 and IMX-104 Melt-Cast Explosives: Insensitive Formulations for the Next-Generation Munition Systems. Propellants, Explosives, Pyrotechnics, 48(1), e202100312. [https://doi.org/10.1002/prep.202100312 doi: 10.1002/prep.202100312]</ref>. |
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− | Sediment risk assessment is increasingly used by governmental agencies to support sediment management in freshwater, estuarine, and marine environments. Strategies for sediment management encompass a wide variety of actions, from removal, capping or treatment of contaminated sediment to the monitoring of natural processes, including sedimentation, binding, and bio- and photo-degradation that serve to reduce the potential threat to aquatic life over time. It is not uncommon to revisit a sediment risk assessment periodically to check how changed environmental conditions reflected in sediment and biotic sampling work has either reduced or exacerbated the threats identified in the initial assessment.
| + | Sampling procedures for legacy and insensitive munitions are identical and utilize multi-increment sampling procedures found in USEPA Method 8330B Appendix A<ref name= "8330B"/>. Sample hold times, subsampling and quality control requirements are also unchanged. The key differences lie in the extraction methods and instrumental methods. Briefly, legacy munitions analysis of low concentration waters uses a single cartridge reverse phase [[Wikipedia: Solid-phase extraction | SPE]] procedure, and [[Wikipedia: Acetonitrile | acetonitrile]] (ACN) is used for both extraction and [[Wikipedia: Elution | elution]] for aqueous and solid samples<ref name= "8330B"/><ref>United States Environmental Protection Agency (USEPA), 2007. EPA Method 3535A (SW-846) Solid-Phase Extraction (SPE), Revision 1. [https://www.epa.gov/esam/epa-method-3535a-sw-846-solid-phase-extraction-spe USEPA Website] [[Media: epa-3535a.pdf | Method 3535A.pdf]]</ref>. An [[Wikipedia: High-performance_liquid_chromatography#Isocratic_and_gradient_elution | isocratic]] separation via reversed-phase C-18 column with 50:50 methanol:water mobile phase or a C-8 column with 15:85 isopropanol:water mobile phase is used to separate legacy munitions<ref name= "8330B"/>. While these procedures are sufficient for analysis of legacy munitions, alternative solvents, additional SPE cartridges, and a gradient elution are all required for the combined analysis of legacy and insensitive munitions. |
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− | At present, several countries lack common recommendations specific to conducting risk assessment of contaminated sediments<ref name="Bruce2020">Bruce, P., Sobek, A., Ohlsson, Y. and Bradshaw, C., 2020. Risk assessments of contaminated sediments from the perspective of weight of evidence strategies – a Swedish case study. Human and Ecological Risk Assessment, 27(5), pp. 1366-1387. [https://doi.org/10.1080/10807039.2020.1848414 DOI: 10.1080/10807039.2020.1848414] [https://www.tandfonline.com/doi/full/10.1080/10807039.2020.1848414 Website]</ref>. In the European Union, sediment has played a secondary role in the Water Framework Directive (WFD), with most quality standards being focused on water with the option for the development of national standards for sediment and biota for bioaccumulative compounds. The Common Implementation Strategy (CIS) in 2010 provided guidance on the monitoring of contaminants in sediments and biota, but not on risk-based decision-making<ref name="EC2010">European Commission, 2010. Common Implementation Strategy For The Water Framework Directive (2000/60/EC), Technical Report - 2010 – 041; Guidance document No. 25 On Chemical Monitoring Of Sediment And Biota Under The Water Framework Directive. 82pp. ISBN 978-92-79-16224-4. [https://op.europa.eu/en/publication-detail/-/publication/5ff7a8ec-995b-4d90-a140-0cc9b4bf980d Free download]</ref>. There are efforts underway to incorporate guidance for management of contaminated sediment in the Common Implementation Strategy in 2021<ref name="Brils2020">Brils, J., 2020. Including sediment in European River Basin Management Plans: Twenty years of work by SedNet. Journal of Soils and Sediments, 20(12), pp.4229-4237. [https://doi.org/10.1007/s11368-020-02782-1 DOI: 10.1007/s11368-020-02782-1] [https://link.springer.com/content/pdf/10.1007/s11368-020-02782-1.pdf Open Access Article]</ref>. Sediment risk assessment guidance from Norway, Canada, the Netherlands, and the US are most often referenced when assessing the risks from contaminated sediments<ref name="Bruce2020"/><ref name="Birch2018">Birch, G.F., 2018. A review of chemical-based sediment quality assessment methodologies for the marine environment. Marine Pollution Bulletin, 133, pp.218-232. [https://doi.org/10.1016/j.marpolbul.2018.05.039 DOI: 10.1016/j.marpolbul.2018.05.039]</ref><ref name="Kwok2014">Kwok, K.W., Batley, G.E., Wenning, R.J., Zhu, L., Vangheluwe, M. and Lee, S., 2014. Sediment quality guidelines: challenges and opportunities for improving sediment management. Environmental Science and Pollution Research, 21(1), pp. 17-27. [https://doi.org/10.1007/s11356-013-1778-7 DOI: 10.1007/s11356-013-1778-7] Free download from: [https://www.researchgate.net/profile/Graeme-Batley/publication/236836992_Sediment_quality_guidelines_Challenges_and_opportunities_for_improving_sediment_management/links/0c96052b8a8f5ad0c6000000/Sediment-quality-guidelines-Challenges-and-opportunities-for-improving-sediment-management.pdf ResearchGate]</ref>. Some European countries, such as Norway, have focused their risk assessment guidance on the assessment of sediment conditions relative to general chemical thresholds, while in North America, risk assessment guidance focuses on site- or region-specific conditions<ref name="Apitz2008">Apitz, S.E., 2008. Is risk-based, sustainable sediment management consistent with European policy?. Journal of Soils and Sediments, 8(6), p.461-466. [https://doi.org/10.1007/s11368-008-0039-8 DOI: 10.1007/s11368-008-0039-8] Free download from: [https://d1wqtxts1xzle7.cloudfront.net/7081664/apitz%20jss%20risk-based%20europe-with-cover-page-v2.pdf?Expires=1637274548&Signature=KqIoYyQ6VPAFN7lKHJMVC3bbn00RRMCR68bsQNBGrFJ9kbX5BnI-aucFCqRgVUNUb1lu0Q4tzUkCjPXJRGBsTA3OnbH8Ol9sNoXZ001aOwG7tKuV8qEblGiqtQUHh9GdiNAPQsm50f~E1iozL9a6imApWjqK8oFCfdUbcUd1oaW7PCDu28KWN-k5ddefWNZBAzGIdaWt3mBJ1EYeKRrp4F6Codlny3pWCT5MpA~c4c0IKq8L7Uj~-VxH5LXjFDd7cm07JeOY8S5rlxgF1zMoTIggMo5v2M3AS3CO2SAqy7yR3HC-IjUx3RsMqKa5eS2jT1ADiXcqeVygCdCCXza05g__&Key-Pair-Id=APKAJLOHF5GGSLRBV4ZA Academia.edu]</ref>.
| + | Previously, analysis of legacy and insensitive munitions required multiple analytical techniques, however the methods presented here combine the two munitions categories resulting in an HPLC-UV method and accompanying extraction methods for a variety of common sample matrices. A secondary HPLC-UV method and a HPLC-MS method were also developed as confirmatory methods. The methods discussed in this article were validated extensively by single-blind round robin testing and subsequent statistical treatment as part of ESTCP [https://serdp-estcp.mil/projects/details/d05c1982-bbfa-42f8-811d-51b540d7ebda ER19-5078]. Wherever possible, the quality control criteria in the Department of Defense Quality Systems Manual for Environmental Laboratories were adhered to<ref>US Department of Defense and US Department of Energy, 2021. Consolidated Quality Systems Manual (QSM) for Environmental Laboratories, Version 5.4. 387 pages. [https://www.denix.osd.mil/edqw/denix-files/sites/43/2021/10/QSM-Version-5.4-FINAL.pdf Free Download] [[Media: QSM-Version-5.4.pdf | QSM Version 5.4.pdf]]</ref>. Analytes included in the methods presented here are found in Table 1. |
| | | |
− | There is general consensus from a regulatory perspective, globally, on the importance of sediment risk assessment. Technical guidance documents prepared by Canada<ref name="Fletcher2008">Fletcher, R., Welsh, P. and Fletcher, T., 2008. Guidelines for Identifying, Assessing, and Managing Contaminated Sediments in Ontario. Ontario Ministry of the Environment. PIBS6658e. [http://www.ene.gov.on.ca/publications/6658e Website]</ref><ref name="HealthCanada2017">Health Canada, 2017. Supplemental Guidance on Human Health Risk Assessment of Contaminated Sediments: Direct Contact Pathway, Federal Contaminated Site Risk Assessment in Canada. ISBN: 978-0-660-07989-9. Cat.: H144-41/2017E-PDF. Pub. 160382. Free download from: [https://publications.gc.ca/collections/collection_2018/sc-hc/H144-41-2017-eng.pdf Health Canada] [[Media: HealthCanada2117.pdf | Report.pdf]]</ref> , the European Union<ref name="Tarazona2014"/>, and the United States Environmental Protection Agency (USEPA)<ref name="USEPA2005"/> advise a flexible, tiered approach for sediment risk assessment. Sediment quality guidelines in many countries reflect the scientific importance of including certain sediment-specific measurement and biotic assessment endpoints, as well as certain physical sediment processes and chemical transformation processes potentially affecting biotic responses to contaminant exposure in the sediment<ref name="Wenning2005">Wenning, R.J. Batley, G.E., Ingersoll, C.G., and Moore, D.W., (eds), 2005. Use Of Sediment Quality Guidelines And Related Tools For The Assessment Of Contaminated Sediments. SETAC, Pensacola, FL. 815 pp. ISBN 1-880611-71-6.</ref>. New risk assessment methods continue to emerge in the scientific literature<ref name="Benson2018">Benson, N.U., Adedapo, A.E., Fred-Ahmadu, O.H., Williams, A.B., Udosen, E.D., Ayejuyo, O.O. and Olajire, A.A., 2018. A new method for assessment of sediment-associated contamination risks using multivariate statistical approach. MethodsX, 5, pp. 268-276. [https://doi.org/10.1016/j.mex.2018.03.005 DOI: 10.1016/j.mex.2018.03.005] [https://www.sciencedirect.com/science/article/pii/S2215016118300438/pdfft?md5=85b8a3a1062310e4c7c4a06e670e66c4&pid=1-s2.0-S2215016118300438-main.pdf Free Access Article] [[Media: Benson2018.pdf | Report.pdf]]</ref><ref name="Saeedi2015">Saeedi, M. and Jamshidi-Zanjani, A., 2015. Development of a new aggregative index to assess potential effect of metals pollution in aquatic sediments. Ecological Indicators, 58, pp. 235-243. [https://doi.org/10.1016/j.ecolind.2015.05.047 DOI: 10.1016/j.ecolind.2015.05.047] Free download from: [https://www.academia.edu/download/49801572/mRAC_published.pdf Academis.edu]</ref><ref name="Vaananen2018">Väänänen, K., Leppänen, M.T., Chen, X. and Akkanen, J., 2018. Metal bioavailability in ecological risk assessment of freshwater ecosystems: from science to environmental management. Ecotoxicology and Environmental Safety, 147, pp. 430-446. [https://doi.org/10.1016/j.ecoenv.2017.08.064 DOI: 10.1016/j.ecoenv.2017.08.064]</ref>. These new methods, however, are likely to be considered supplemental to the more generalized framework shared globally.
| + | The chromatograms produced by the primary and secondary HPLC-UV methods are shown in Figure 1 and Figure 2, respectively. Chromatograms for each detector wavelength used are shown (315, 254, and 210 nm). |
| | | |
− | ==Cap Design and Materials for Chemical Containment== | + | ==Extraction Methods== |
− | An inert material such as sand can be effective as a capping material where contaminants are strongly associated with solids and where the operative site specific transport mechanisms do not lead to rapid contaminant migration through such a material. Additional contaminant containment can often be achieved through the placement of clean sediment, e.g. dredged material from a nearby location. Other materials as cap layers or amendments may be useful to address particularly mobile contaminants or when particular degradative mechanisms can be exploited. The Anacostia River was the site of a demonstration that first tested “active” or “amended” capping in the field<ref name="Reible2003">Reible, D., Constant, D.W., Roberts, K. and Zhu, Y., 2003. Active capping demonstration project in anacostia DC. In Second International Conference on the Remediation of Contaminated Sediments: October. Free download available from: [https://www.researchgate.net/profile/Danny-Reible/publication/237747790_ACTIVE_CAPPING_DEMONSTRATION_PROJECT_IN_ANACOSTIA_DC/links/0c96053861030b7699000000/ACTIVE-CAPPING-DEMONSTRATION-PROJECT-IN-ANACOSTIA-DC.pdf ResearchGate]</ref><ref name="Reible2006">Reible, D., Lampert, D., Constant, D., Mutch Jr, R.D. and Zhu, Y., 2006. Active Capping Demonstration in the Anacostia River, Washington, DC. Remediation Journal: The Journal of Environmental Cleanup Costs, Technologies and Techniques, 17(1), pp. 39-53. [https://doi.org/10.1002/rem.20111 DOI: 10.1002/rem.20111] Free download available from: [https://www.academia.edu/download/44146457/Remediation_Journal_Paper_2006.pdf Academia.edu]</ref>. Amended caps are often the best option when groundwater upwelling or other advective processes promote significant mobility of contaminants and the addition of sorbents can slow that contaminant migration<ref name="Ghosh2011">Ghosh, U., Luthy, R.G., Cornelissen, G., Werner, D. and Menzie, C.A., 2011. In-situ Sorbent Amendments: A New Direction in Contaminated Sediment Management. Environmental Science and Technology, 45(4), pp. 1163-1168. [https://doi.org/10.1021/es102694h DOI: 10.1021/es102694h] Open access article from: [https://pubs.acs.org/doi/pdf/10.1021/es102694h American Chemical Society] [[Media: Ghosh2011.pdf | Report.pdf]]</ref>. Although a variety of materials have been proposed for sediment caps, a far smaller number of options have been successfully employed in the field.
| + | [[File: ScircleFig3.PNG |thumb|400px|Figure 3. Triple cartridge SPE setup]] |
− |
| + | [[File: ScircleFig4.PNG |thumb|400px|Figure 4. A flow chart of the soil extraction procedure]] |
− | Metals migration is very site dependent due to the potential for many metals to complex with other species in the interstitial water and the specific metal speciation present at a site. Often, the strongly reducing environment beneath a cap renders many common metals unavailable through the formation of metal sulfides. In such cases, a simple sand cap can be very effective. Amended caps to manage metal contaminated sediments may be advantageous when site specific conditions lead to elevated metals mobility, but should be supported with site specific testing<ref name="Viana2008">Viana, P.Z., Yin, K. and Rockne, K.J., 2008. Modeling Active Capping Efficacy. 1. Metal and Organometal Contaminated Sediment Remediation. Environmental Science and Technology, 42(23), pp. 8922-8929. [https://doi.org/10.1021/es800942t DOI: 10.1021/es800942t]</ref>.
| + | ===High Concentration Waters (> 1 ppm)=== |
| + | Aqueous samples suspected to contain the compounds of interest at concentrations detectable without any extraction or pre-concentration are suitable for analysis by direct injection. The method deviates from USEPA Method 8330B by adding a pH adjustment and use of MeOH rather than ACN for dilution<ref name= "8330B"/>. The pH adjustment is needed to ensure method accuracy for ionic compounds (like NTO or PA) in basic samples. A solution of 1% HCl/MeOH is added to both acidify and dilute the samples to a final acid concentration of 0.5% (vol/vol) and a final solvent ratio of 1:1 MeOH/H<sub><small>2</small></sub>O. The direct injection samples are then ready for analysis. |
| + | |
| + | ===Low Concentration Waters (< 1 ppm)=== |
| + | Aqueous samples suspected to contain the compounds of interest at low concentrations require extraction and pre-concentration using solid phase extraction (SPE). The SPE setup described here uses a triple cartridge setup shown in Figure 3. Briefly, the extraction procedure loads analytes of interest onto the cartridges in this order: Strata<sup><small>TM</small></sup> X, Strata<sup><small>TM</small></sup> X-A, and Envi-Carb<sup><small>TM</small></sup>. Then the cartridge order is reversed, and analytes are eluted via a two-step elution, resulting in 2 extracts (which are combined prior to analysis). Five milliliters of MeOH is used for the first elution, while 5 mL of acidified MeOH (2% HCl) is used for the second elution. The particular SPE cartridges used are noncritical so long as cartridge chemistries are comparable to those above. |
| + | |
| + | {| class="wikitable mw-collapsible" style="float:left; margin-right:20px; text-align:center;" |
| + | |+Table 2. Primary HPLC-UV mobile phase gradient method concentrations |
| + | |- |
| + | | colspan="5" style="background-color:white;"| Method run time = 48 minutes; Column temperature = 25°C<br>Injection volume = 50 μL; Flow rate = 1.0 mL/min<br>Detector wavelengths = 210, 254, and 310 nm |
| + | |- |
| + | ! Time<br>(min) |
| + | ! Reagent Water<br>(%) |
| + | ! MeOH<br>(%) |
| + | ! 0.1% TFA/Water<br>(%) |
| + | ! ACN<br>(%) |
| + | |- |
| + | | 0.00 || 89 || 3 || 3 || 5 |
| + | |- |
| + | | 2.00 || 89 || 3 || 3 || 5 |
| + | |- |
| + | | 2.20 || 52 || 40 || 3 || 5 |
| + | |- |
| + | | 12.5 || 52 || 40 || 3 || 5 |
| + | |- |
| + | | 19.0 || 57 ||35 || 3 || 5 |
| + | |- |
| + | | 28.0 || 48 || 44 || 3 || 5 |
| + | |- |
| + | | 32.0 || 48 || 44 || 3 || 5 |
| + | |- |
| + | | 44.0 || 32 || 60 || 3 || 5 |
| + | |- |
| + | | 44.1 || 89 || 3 || 3 || 5 |
| + | |- |
| + | | 48.0 || 89 || 3 || 3 || 5 |
| + | |} |
| | | |
− | For hydrophobic organic contaminants, cap amendments that directly control groundwater upwelling and also sorbents that can remove migrating contaminants from that groundwater have been successfully employed. Examples include clay materials such as AquaBlok<sup>®</sup> for permeability control, sorbents such as [[Wikipedia: Activated carbon | activated carbon]] for truly dissolved contaminants, and [[Wikipedia: Organoclay | organophilic clays]] for separate phase contaminants.
| + | ===Soils=== |
| + | Soil collection, storage, drying and grinding procedures are identical to the USEPA Method 8330B procedures<ref name= "8330B"/>; however, the solvent extraction procedure differs in the number of sonication steps, sample mass and solvent used. A flow chart of the soil extraction procedure is shown in Figure 4. Soil masses of approximately 2 g and a sample to solvent ratio of 1:5 (g/mL) are used for soil extraction. The extraction is carried out in a sonication bath chilled below 20 ⁰C and is a two-part extraction, first extracting in MeOH (6 hours) followed by a second sonication in 1:1 MeOH:H<sub><small>2</small></sub>O solution (14 hours). The extracts are centrifuged, and the supernatant is filtered through a 0.45 μm PTFE disk filter. |
| | | |
− | The placement of clean sediment as an ''in situ'' cap can be difficult when the material is fine grained or has a low density. Capping with a layer of coarse grained material such as clean sand mitigates this issue although clean sands have minimal sorption capacity. Because of this limitation, sand caps may not be sufficient for achieving remedial goals in sites where contamination levels are high or transport rates are fast due to pore water upwelling or tidal pumping effects. Conditions such as these may require the use of “active” amendments to reduce transport rates. | + | The solvent volume should generally be 10 mL but if different soil masses are required, solvent volume should be 5 mL/g. The extraction results in 2 separate extracts (MeOH and MeOH:H<sub><small>2</small></sub>O) that are combined prior to analysis. |
− |
| |
− | Capping with clean sand provides a physical barrier between the underlying contaminated material and the overlying water, stabilizes the underlying sediment to prevent re-suspension of contaminated particles, and can reduce chemical exposure under certain conditions. Sand primarily provides a passive barrier to the downward penetration of bioturbating organisms and the upward movement of sediment or contaminants. Although conventional sandy caps can often be an effective means of managing contaminated sediments, there are conditions when sand caps may not be capable of achieving design objectives. Some factors that reduce the effectiveness of sand caps include:
| |
| | | |
− | *erosion and loss of cap integrity
| + | ===Tissues=== |
− | *high groundwater upwelling rates
| |
− | *mobile (low sorption) contaminants of concern (COCs)
| |
− | *high COC concentrations
| |
− | *unusually toxic COCs
| |
− | *the presence of tidal influences
| |
− | *the presence of non-aqueous phase liquids (NAPLs)
| |
− | *high rates of gas ebullition
| |
| | | |
− | Of these, the first three are common limitations to capping and often control the ability to effectively design and implement a cap as a sediment remedial strategy. In these cases, it may be possible to offset these issues by increasing the thickness of the cap. However, the required thickness can reach infeasible levels in shallow streams or navigable water bodies. In addition, increased construction costs associated with thick caps may become prohibitive. As a result of these issues, caps that use alternative materials (also known as active caps) to reduce the thickness or increase the protectiveness of a cap may be necessary. The materials in active caps are designed to interact with the COCs to enhance the containment properties of the cap.
| + | Tissue matrices are extracted by 18-hour sonication using a ratio of 1 gram of wet tissue per 5 mL of MeOH. This extraction is performed in a sonication bath chilled below 20 ⁰C and the supernatant (MeOH) is filtered through a 0.45 μm PTFE disk filter. |
| | | |
− | [[Wikipedia: Apatite | Apatites]] are a class of naturally occurring minerals that have been investigated as a sorbent for metals in soils and sediments<ref name="Melton2003">Melton, J.S., Crannell, B.S., Eighmy, T.T., Wilson, C. and Reible, D.D., 2003. Field Trial of the UNH Phosphate-Based Reactive Barrier Capping System for the Anacostia River. EPA Grant R819165-01-0</ref><ref name="Reible2003"/><ref name="Knox2012">Knox, A.S., Paller, M.H. and Roberts, J., 2012. Active Capping Technology—New Approaches for In Situ Remediation of Contaminated Sediments. Remediation Journal, 22(2), pp.93-117. [https://doi.org/10.1002/rem.21313 DOI: 10.1002/rem.21313] Free download available from: [https://www.researchgate.net/profile/Anna-Knox-2/publication/233374607_Active_Capping_Technology-New_Approaches_for_In_Situ_Remediation_of_Contaminated_Sediments/links/5a7de4c5aca272a73765c344/Active-Capping-Technology-New-Approaches-for-In-Situ-Remediation-of-Contaminated-Sediments.pdf ResearchGate]</ref>. Apatites consist of a matrix of calcium phosphate and various other common anions, including fluoride, chloride, hydroxide, and occasionally carbonate. Metals are sequestered either through direct ion exchange with the calcium atom or dissolution of hydroxyapatite followed by precipitation of lead apatite. [[Wikipedia: Zeolite | Zeolites]], which are microporous aluminosilicate minerals with a high cationic exchange capacity (CEC), have also been proposed to manage metal species<ref name="Zhan2019">Zhan, Y., Yu, Y., Lin, J., Wu, X., Wang, Y. and Zhao, Y., 2019. Simultaneous control of nitrogen and phosphorus release from sediments using iron-modified zeolite as capping and amendment materials. Journal of Environmental Management, 249, p.109369. [https://doi.org/10.1016/j.jenvman.2019.109369 DOI: 10.1016/j.jenvman.2019.109369]</ref>.
| + | Due to the complexity of tissue matrices, an additional tissue cleanup step, adapted from prior research, can be used to reduce interferences<ref name="RussellEtAl2014">Russell, A.L., Seiter, J.M., Coleman, J.G., Winstead, B., Bednar, A.J., 2014. Analysis of munitions constituents in IMX formulations by HPLC and HPLC-MS. Talanta, 128, pp. 524–530. [https://doi.org/10.1016/j.talanta.2014.02.013 doi: 10.1016/j.talanta.2014.02.013]</ref><ref name="CrouchEtAl2020"/>. The cleanup procedure uses small scale chromatography columns prepared by loading 5 ¾” borosilicate pipettes with 0.2 g activated silica gel (100–200 mesh). The columns are wetted with 1 mL MeOH, which is allowed to fully elute and then discarded prior to loading with 1 mL of extract and collecting in a new amber vial. After the extract is loaded, a 1 mL aliquot of MeOH followed by a 1 mL aliquot of 2% HCL/MeOH is added. This results in a 3 mL silica treated tissue extract. This extract is vortexed and diluted to a final solvent ratio of 1:1 MeOH/H<sub><small>2</small></sub>O before analysis. |
− |
| |
− | It is possible to create a hydrophobic, sorbing layer for non-polar organics by exchanging a cationic surfactant onto the surface of clays such as zeolites and bentonites,. Organoclay is a modified bentonite containing such substitutions that has been evaluated for control of non-aqueous phase NAPLs and other organic contaminants<ref name="Reible2007">Reible, D.D., Lu, X., Moretti, L., Galjour, J. and Ma, X., 2007. Organoclays for the capping of contaminated sediments. AIChE Annual Meeting. ISBN: 978-081691022-9</ref>. An organoclay cap has been implemented for sediment remediation at the McCormick and Baxter site in Portland, OR<ref name="Parrett2005">Parrett, K. and Blishke, H., 2005. 23-Acre Multilayer Sediment Cap in Dynamic Riverine Environment Using Organoclay an Adsorptive Capping Material. Presentation to Society of Environmental Toxicology and Chemistry (SETAC), 26th Annual Meeting.</ref>. A similar organic sorbing phase can be formed by treating zeolites with surfactants but this approach has not been reported for contaminated sediments.
| |
| | | |
− | Activated carbon is a strong sorbent of hydrophobic organic compounds and has been used as a [[In Situ Treatment of Contaminated Sediments with Activated Carbon | treatment for sediments]] or as an active sorbent within a capping layer<ref name="Zimmerman2004">Zimmerman, J.R., Ghosh, U., Millward, R.N., Bridges, T.S. and Luthy, R.G., 2004. Addition of Carbon Sorbents to Reduce PCB and PAH Bioavailability in Marine Sediments: Physicochemical Tests. Environmental Science and Technology, 38(20), pp. 5458-5464. [https://doi.org/10.1021/es034992v DOI: 10.1021/es034992v]</ref><ref name="Werner2005">Werner, D., Higgins, C.P. and Luthy, R.G., 2005. The sequestration of PCBs in Lake Hartwell sediment with activated carbon. Water Research, 39(10), pp. 2105-2113. [https://doi.org/10.1016/j.watres.2005.03.019 DOI: 10.1016/j.watres.2005.03.019]</ref><ref name="Abel2018">Abel, S. and Akkanen, J., 2018. A Combined Field and Laboratory Study on Activated Carbon-Based Thin Layer Capping in a PCB-Contaminated Boreal Lake. Environmental Science and Technology, 52(8), pp. 4702-4710. [https://doi.org/10.1021/acs.est.7b05114 DOI: 10.1021/acs.est.7b05114] Open access article available from: [https://pubs.acs.org/doi/pdf/10.1021/acs.est.7b05114 American Chemical Society] [[Media: Abel2018.pdf | Report.pdf]]</ref><ref name="Payne 2018">Payne, R.B., Ghosh, U., May, H.D., Marshall, C.W. and Sowers, K.R., 2019. A Pilot-Scale Field Study: In Situ Treatment of PCB-Impacted Sediments with Bioamended Activated Carbon. Environmental Science and Technology, 53(5), pp. 2626-2634. [https://doi.org/10.1021/acs.est.8b05019 DOI: 10.1021/acs.est.8b05019]</ref><ref name="Yan2020">Yan, S., Rakowska, M., Shen, X., Himmer, T., Irvine, C., Zajac-Fay, R., Eby, J., Janda, D., Ohannessian, S. and Reible, D.D., 2020. Bioavailability Assessment in Activated Carbon Treated Coastal Sediment with In situ and Ex situ Porewater Measurements. Water Research, 185, p. 116259. [https://doi.org/10.1016/j.watres.2020.116259 DOI: 10.1016/j.watres.2020.116259]</ref>. Placement of activated carbon for sediment capping is difficult due to the near neutral buoyancy of the material but it has been applied in this manner in relatively low energy environments such as Onondaga Lake, Syracuse, NY<ref name="Vlassopoulos2017">Vlassopoulos, D., Russell, K., Larosa, P., Brown, R., Mohan, R., Glaza, E., Drachenberg, T., Reible, D., Hague, W., McAuliffe, J. and Miller, S., 2017. Evaluation, Design, and Construction of Amended Reactive Caps to Restore Onondaga Lake, Syracuse, New York, USA. Journal of Marine Environmental Engineering, 10(1), pp. 13-27. Free download available from: [https://www.researchgate.net/publication/317762995_Evaluation_design_and_construction_of_amended_reactive_caps_to_restore_Onondaga_lake_Syracuse_New_York_USA ResearchGate]</ref>. Alternatives in higher energy environments include placement of activated carbon in a mat such as the CETCO Reactive Core Mat (RCM)<sup>®</sup> or Huesker Tektoseal<sup>®</sup>, or as a composite material such as SediMite<sup>®</sup> or AquaGate<sup>®</sup>. In the case of the mats, powdered or granular activated carbon can be placed in a controlled layer while the density of the composite materials is such that they can be broadcast from the surface and allowed to settle to the bottom. In a sediment treatment application, the composite material would either be worked into the surface or allowed to intermix gradually by bioturbation and other processes. In a capping application, the mat or composite material would typically be combined or overlain with a sand or other capping layer to keep it in place and to provide a chemical isolation layer away from the sediment surface.
| + | ==HPLC-UV and HPLC-MS Methods== |
| + | {| class="wikitable mw-collapsible" style="float:left; margin-right:20px; text-align:center;" |
| + | |+Table 3. Secondary HPLC-UV mobile phase gradient method concentrations |
| + | |- |
| + | | colspan="5" style="background-color:white;" | Method run time = 43 minutes; Column temperature = 25°C<br>Injection volume = 50 μL; Flow rate = 0.8 mL/min<br>Detector wavelengths = 210, 254, and 310 nm |
| + | |- |
| + | ! Time<br>(min) |
| + | ! Reagent Water<br>(%) |
| + | ! MeOH<br>(%) |
| + | ! 0.1% TFA/Water<br>(%) |
| + | ! ACN<br>(%) |
| + | |- |
| + | | 0.00 || 75 || 10 || 10 || 5 |
| + | |- |
| + | | 2.50 || 75 || 10 || 10 || 5 |
| + | |- |
| + | | 2.60 || 39 || 46 ||10 || 5 |
| + | |- |
| + | | 9.00 || 39 || 46 ||10 || 5 |
| + | |- |
| + | | 9.10 || 33.5 || 51.5 || 10 || 5 |
| + | |- |
| + | | 15.00 || 35 || 50 || 10 || 5 |
| + | |- |
| + | | 15.10 || 43 || 42 || 10 || 5 |
| + | |- |
| + | | 33.00 || 30 || 55 || 10 || 5 |
| + | |- |
| + | | 33.10 || 75 || 10 || 10 || 5 |
| + | |- |
| + | | 43.00 || 75 || 10 || 10 || 5 |
| + | |} |
| + | {| class="wikitable mw-collapsible" style="float:right; margin-left:20px; text-align:center;" |
| + | |+Table 4. Ionization source and detector parameters |
| + | |- |
| + | ! Parameter |
| + | ! Value |
| + | |- |
| + | | Ionization Source || APCI |
| + | |- |
| + | | Ionization Mode || Negative |
| + | |- |
| + | | Drying Gas Temperature (°C) || 350 |
| + | |- |
| + | | Vaporizer Temperature (°C) || 325 |
| + | |- |
| + | | Drying Gas Flow (L/min) || 4.0 |
| + | |- |
| + | | Nebulizer Pressure (psig) || 40 |
| + | |- |
| + | | Corona Current (μA) || 10 |
| + | |- |
| + | | Capillary Potential (V) || 1500 |
| + | |- |
| + | | Mass Range || 40 – 400 |
| + | |- |
| + | | Fragmentor || 100 |
| + | |- |
| + | | Gain || 1 |
| + | |- |
| + | | Threshold || 0 |
| + | |- |
| + | | Step Size || 0.20 |
| + | |- |
| + | | Speed (μ/sec) || 743 |
| + | |- |
| + | | Peak Width (min) || 0.06 |
| + | |- |
| + | | Cycle Time (sec/cycle) || 0.57 |
| + | |} |
| | | |
− | As an alternative to a sorptive capping amendment, low-permeability cap amendments have been proposed to enhance cap design life by decreasing pore water advection. Low permeability clays are an effective means to divert upwelling groundwater away from a contaminated sediment area but are difficult to place in the aqueous environment. Bentonite clays can be placed in mats similar to what is done to provide a low permeability liner in landfills. There are also commercial products that can place clays directly such as the composite material AquaBlok<sup>®</sup>, a bentonite clay and polymer based mineral around an aggregate core<ref name="Barth2008">Barth, E.F., Reible, D. and Bullard, A., 2008. Evaluation of the physical stability, groundwater seepage control, and faunal changes associated with an AquaBlok<sup>®</sup> sediment cap. Remediation: The Journal of Environmental Cleanup Costs, Technologies and Techniques, 18(4), pp.63-70. [https://doi.org/10.1002/rem.20183 DOI: 10.1002/rem.20183]</ref>.
| + | The Primary HPLC-UV method uses a Phenomenex Synergi 4 µm Hydro-RP column (80Å, 250 x 4.6 mm), or comparable, and is based on both the HPLC method found in USEPA 8330B and previous work<ref name= "8330B"/><ref name="RussellEtAl2014"/><ref name="CrouchEtAl2020"/>. This separation relies on a reverse phase column and uses a gradient elution, shown in Table 2. Depending on the analyst’s needs and equipment availability, the method has been proven to work with either 0.1% TFA or 0.25% FA (vol/vol) mobile phase. Addition of a guard column like a Phenomenex SecurityGuard AQ C18 pre-column guard cartridge can be optionally used. These optional changes to the method have no impact on the method’s performance. |
− |
| |
− | Sediment caps become colonized by microorganisms from the sediments and surface water and potentially become a zone of pollutant biotransformation over time. Aerobic degradation occurs only near the solids-water interface in which benthic organisms are active and thus there might still be significant benthic organism exposure to contaminants. Biotransformation in the anaerobic zone of a cap, which typically extends well beyond the zone of benthic activity, could significantly reduce the risk of pollutant exposure but successful caps encouraging deep degradation processes have not been demonstrated beyond the laboratory. The addition of materials such as nutrients and oxygen releasing compounds for enhancing the attenuation of contaminants through biodegradation has also been assessed but not applied in the field. Short term improvements in biodegradation rates can be achieved through tailoring of conditions or addition of nutrients but long term efficacy has not been demonstrated<ref name="Pagnozzi2020">Pagnozzi, G., Carroll, S., Reible, D.D. and Millerick, K., 2020. Biological Natural Attenuation and Contaminant Oxidation in Sediment Caps: Recent Advances and Future Opportunities. Current Pollution Reports, pp.1-14. [https://doi.org/10.1007/s40726-020-00153-5 DOI: 10.1007/s40726-020-00153-5]</ref>.
| |
− | [[File: SedCapFig2.png | thumb |600px|Figure 2. A conceptualization of a cap with accompanying habitat layer]]
| |
| | | |
− | ==Cap Design and Materials for Habitat Restoration==
| + | The Secondary HPLC-UV method uses a Restek Pinnacle II Biphenyl 5 µm (150 x 4.6 mm) or comparable column and is intended as a confirmatory method. Like the Primary method, this method can use an optional guard column and utilizes a gradient elution, shown in Table 3. |
− | In addition to providing chemical isolation and containment, a cap can also be used to provide improvements for organisms by enhancing the habitat characteristics of the bottom substrate<ref name="Yozzo2004">Yozzo, D.J., Wilber, P. and Will, R.J., 2004. Beneficial use of dredged material for habitat creation, enhancement, and restoration in New York–New Jersey Harbor. Journal of Environmental Management, 73(1), pp. 39-52. [https://doi.org/10.1016/j.jenvman.2004.05.008 DOI: 10.1016/j.jenvman.2004.05.008]</ref><ref name="Zhang2016">Zhang, C., Zhu, M.Y., Zeng, G.M., Yu, Z.G., Cui, F., Yang, Z.Z. and Shen, L.Q., 2016. Active capping technology: a new environmental remediation of contaminated sediment. Environmental Science and Pollution Research, 23(5), pp.4370-4386. [https://doi.org/10.1007/s11356-016-6076-8 DOI: 10.1007/s11356-016-6076-8]</ref><ref name="Vlassopoulos2017"/>. Often, contaminated sediment environments are degraded for a variety of reasons in addition to the toxic constituents. One way to overcome this is to provide both a habitat layer and chemical isolation or contaminant capping layer. Figure 2 illustrates just such a design providing a more appropriate habitat enhancing substrate, in this case by incorporation additional organic material, vegetation and debris, which is often used by fish species for protection, into the surface layer. In a high energy environment, it should be recognized that it may not be possible to keep a suitable habitat layer in place during high flow events. This would be true of suitable habitat that had developed naturally as well as a constructed habitat layer and it is presumed that if such a habitat is the normal condition of the waterbody that it will recover over time between such high flow events.
| + | |
| + | For instruments equipped with a mass spectrometer (MS), a secondary MS method is available and was developed alongside the Primary UV method. The method was designed for use with a single quadrupole MS equipped with an atmospheric pressure chemical ionization (APCI) source, such as an Agilent 6120B. A majority of the analytes shown in Table 1 are amenable to this MS method, however nitroglycerine (which is covered extensively in USEPA method 8332) and 2-,3-, and 4-nitrotoluene compounds aren’t compatible with the MS method. MS method parameters are shown in Table 4. |
| | | |
| ==Summary== | | ==Summary== |
− | Clean substrate can be placed at the sediment-water interface for the purposes of reducing exposure to and risk from contaminants in the sediments. The cap can consist of simple materials such as sand designed to physically stabilize contaminated sediments and separate the benthic community from those contaminants or may include other materials designed to sequester contaminants even under adverse conditions including strong groundwater upwelling or highly mobile contaminants. The surface of a cap may be designed of coarse material such as gravel or cobble to be stable under high flow events or designed to be more appropriate habitat for benthic and aquatic organisms. As a result of its flexibility, simplicity and low cost relative to its effectiveness, capping is one of the most prevalent remedial technologies for sediments.
| + | The extraction methods and instrumental methods in this article build upon prior munitions analytical methods by adding new compounds, combining legacy and insensitive munitions analysis, and expanding usable sample matrices. These methods have been verified through extensive round robin testing and validation, and while the methods are somewhat challenging, they are crucial when simultaneous analysis of both insensitive and legacy munitions is needed. |
| | | |
| ==References== | | ==References== |
Line 74: |
Line 228: |
| | | |
| ==See Also== | | ==See Also== |
| + | *[[Media: ERDC_TR-21-12.pdf | Preparative, Extraction, and Analytical Methods for Simultaneous Determination of Legacy and Insensitive Munition (IM) Constituents in Aqueous, Soil or Sediment, and Tissue Matrices]] |
| + | *[https://serdp-estcp.mil/focusareas/9f7a342a-1b13-4ce5-bda0-d7693cf2b82d/uxo#subtopics SERDP/ESTCP Focus Areas – UXO – Munitions Constituents] |
| + | *[https://denix.osd.mil/edqw/home/ Environmental Data Quality Workgroup] |
Munitions Constituents – Sample Extraction and Analytical Techniques
Munitions Constituents, including insensitive munitions (IM), are a broad category of compounds which, in areas where manufactured or used, can be found in a variety of environmental matrices (waters, soil, and tissues). This presents an analytical challenge when a variety of these munitions are to be quantified. This article discusses sample extraction methods for each typical sample matrix (high level water, low level water, soil and tissue) as well as the accompanying HPLC-UV analytical method for 27 compounds of interest (legacy munitions, insensitive munitions, and surrogates).
Related Article(s):
Contributor(s):
Key Resource(s):
- Methods for simultaneous quantification of legacy and insensitive munition (IM) constituents in aqueous, soil/sediment, and tissue matrices[2]
Introduction
Table 1. Analyte list with acronyms and CAS numbers.
Compound
|
Acronym
|
CAS Number
|
1,2-Dinitrobenzene (surrogate) |
1,2-DNB (surr.) |
528-29-0
|
1,3-Dinitrobenzene |
1,3-DNB |
99-65-0
|
1,3,5-Trinitrobenzene |
1,3,5-TNB |
99-35-4
|
1,4-Dinitrobenzene |
1,4-DNB (surr.) |
100-25-4
|
2-Amino-4,6-dinitrotoluene |
2-Am-4,6-DNT |
35572-78-2
|
2-Nitrophenol |
2-NP |
88-75-5
|
2-Nitrotoluene |
2-NT |
88-72-2
|
2,4-Dinitrophenol |
2,4-DNP |
51-28-5
|
2,4-Dinitrotoluene |
2,4-DNT |
121-14-2
|
2,4,6-Trinitrophenol |
Picric Acid (PA) |
88-89-1
|
2,4,6-Trinitrotoluene |
2,4,6-TNT |
118-96-7
|
2,6-Dinitrotoluene |
2,6-DNT |
606-20-2
|
3-Nitrotoluene |
3-NT |
99-08-1
|
3,5-Dinitroaniline |
3,5-DNA |
618-87-1
|
4-Amino-2,6-dinitrotoluene |
4-Am-2,6-DNT |
19406-51-0
|
4-Nitrophenol |
4-NP |
100-02-7
|
4-Nitrotoluene |
4-NT |
99-99-0
|
2,4-Dinitroanisole |
DNAN |
119-27-7
|
Octahydro-1,3,5,7-tetranitro-1,3,5,7-tetrazocine |
HMX |
2691-41-0
|
Nitrobenzene |
NB |
98-95-3
|
Nitroglycerine |
NG |
55-63-0
|
Nitroguanidine |
NQ |
556-88-7
|
3-Nitro-1,2,4-triazol-5-one |
NTO |
932-64-9
|
ortho-Nitrobenzoic acid |
o-NBA (surr.) |
552-16-9
|
Pentaerythritol tetranitrate |
PETN |
78-11-5
|
Hexahydro-1,3,5-trinitro-1,3,5-triazine |
RDX |
121-82-4
|
N-Methyl-N-(2,4,6-trinitrophenyl)nitramide |
Tetryl |
479-45-8
|
Note: Analytes in bold are not identified by EPA Method 8330B.
|
Figure 1. Primary Method labeled chromatograms
Figure 2. Secondary Method labeled chromatograms
The primary intention of the analytical methods presented here is to support the monitoring of legacy and insensitive munitions contamination on test and training ranges, however legacy and insensitive munitions often accompany each other at demilitarization facilities, manufacturing facilities, and other environmental sites. Energetic materials typically appear on ranges as small, solid particulates and due to their varying functional groups and polarities, can partition in various environmental compartments[3]. To ensure that contaminants are monitored and controlled at these sites and to sustainably manage them a variety of sample matrices (surface or groundwater, process waters, soil, and tissues) must be considered. (Process water refers to water used during industrial manufacturing or processing of legacy and insensitive munitions.) Furthermore, additional analytes must be added to existing methodologies as the usage of IM compounds changes and as new degradation compounds are identified. Of note, relatively new IM formulations containing NTO, DNAN, and NQ are seeing use in IMX-101, IMX-104, Pax-21 and Pax-41 (Table 1)[4][5].
Sampling procedures for legacy and insensitive munitions are identical and utilize multi-increment sampling procedures found in USEPA Method 8330B Appendix A[1]. Sample hold times, subsampling and quality control requirements are also unchanged. The key differences lie in the extraction methods and instrumental methods. Briefly, legacy munitions analysis of low concentration waters uses a single cartridge reverse phase SPE procedure, and acetonitrile (ACN) is used for both extraction and elution for aqueous and solid samples[1][6]. An isocratic separation via reversed-phase C-18 column with 50:50 methanol:water mobile phase or a C-8 column with 15:85 isopropanol:water mobile phase is used to separate legacy munitions[1]. While these procedures are sufficient for analysis of legacy munitions, alternative solvents, additional SPE cartridges, and a gradient elution are all required for the combined analysis of legacy and insensitive munitions.
Previously, analysis of legacy and insensitive munitions required multiple analytical techniques, however the methods presented here combine the two munitions categories resulting in an HPLC-UV method and accompanying extraction methods for a variety of common sample matrices. A secondary HPLC-UV method and a HPLC-MS method were also developed as confirmatory methods. The methods discussed in this article were validated extensively by single-blind round robin testing and subsequent statistical treatment as part of ESTCP ER19-5078. Wherever possible, the quality control criteria in the Department of Defense Quality Systems Manual for Environmental Laboratories were adhered to[7]. Analytes included in the methods presented here are found in Table 1.
The chromatograms produced by the primary and secondary HPLC-UV methods are shown in Figure 1 and Figure 2, respectively. Chromatograms for each detector wavelength used are shown (315, 254, and 210 nm).
Figure 3. Triple cartridge SPE setup
Figure 4. A flow chart of the soil extraction procedure
High Concentration Waters (> 1 ppm)
Aqueous samples suspected to contain the compounds of interest at concentrations detectable without any extraction or pre-concentration are suitable for analysis by direct injection. The method deviates from USEPA Method 8330B by adding a pH adjustment and use of MeOH rather than ACN for dilution[1]. The pH adjustment is needed to ensure method accuracy for ionic compounds (like NTO or PA) in basic samples. A solution of 1% HCl/MeOH is added to both acidify and dilute the samples to a final acid concentration of 0.5% (vol/vol) and a final solvent ratio of 1:1 MeOH/H2O. The direct injection samples are then ready for analysis.
Low Concentration Waters (< 1 ppm)
Aqueous samples suspected to contain the compounds of interest at low concentrations require extraction and pre-concentration using solid phase extraction (SPE). The SPE setup described here uses a triple cartridge setup shown in Figure 3. Briefly, the extraction procedure loads analytes of interest onto the cartridges in this order: StrataTM X, StrataTM X-A, and Envi-CarbTM. Then the cartridge order is reversed, and analytes are eluted via a two-step elution, resulting in 2 extracts (which are combined prior to analysis). Five milliliters of MeOH is used for the first elution, while 5 mL of acidified MeOH (2% HCl) is used for the second elution. The particular SPE cartridges used are noncritical so long as cartridge chemistries are comparable to those above.
Table 2. Primary HPLC-UV mobile phase gradient method concentrations
Method run time = 48 minutes; Column temperature = 25°C Injection volume = 50 μL; Flow rate = 1.0 mL/min Detector wavelengths = 210, 254, and 310 nm
|
Time (min)
|
Reagent Water (%)
|
MeOH (%)
|
0.1% TFA/Water (%)
|
ACN (%)
|
0.00 |
89 |
3 |
3 |
5
|
2.00 |
89 |
3 |
3 |
5
|
2.20 |
52 |
40 |
3 |
5
|
12.5 |
52 |
40 |
3 |
5
|
19.0 |
57 |
35 |
3 |
5
|
28.0 |
48 |
44 |
3 |
5
|
32.0 |
48 |
44 |
3 |
5
|
44.0 |
32 |
60 |
3 |
5
|
44.1 |
89 |
3 |
3 |
5
|
48.0 |
89 |
3 |
3 |
5
|
Soils
Soil collection, storage, drying and grinding procedures are identical to the USEPA Method 8330B procedures[1]; however, the solvent extraction procedure differs in the number of sonication steps, sample mass and solvent used. A flow chart of the soil extraction procedure is shown in Figure 4. Soil masses of approximately 2 g and a sample to solvent ratio of 1:5 (g/mL) are used for soil extraction. The extraction is carried out in a sonication bath chilled below 20 ⁰C and is a two-part extraction, first extracting in MeOH (6 hours) followed by a second sonication in 1:1 MeOH:H2O solution (14 hours). The extracts are centrifuged, and the supernatant is filtered through a 0.45 μm PTFE disk filter.
The solvent volume should generally be 10 mL but if different soil masses are required, solvent volume should be 5 mL/g. The extraction results in 2 separate extracts (MeOH and MeOH:H2O) that are combined prior to analysis.
Tissues
Tissue matrices are extracted by 18-hour sonication using a ratio of 1 gram of wet tissue per 5 mL of MeOH. This extraction is performed in a sonication bath chilled below 20 ⁰C and the supernatant (MeOH) is filtered through a 0.45 μm PTFE disk filter.
Due to the complexity of tissue matrices, an additional tissue cleanup step, adapted from prior research, can be used to reduce interferences[8][2]. The cleanup procedure uses small scale chromatography columns prepared by loading 5 ¾” borosilicate pipettes with 0.2 g activated silica gel (100–200 mesh). The columns are wetted with 1 mL MeOH, which is allowed to fully elute and then discarded prior to loading with 1 mL of extract and collecting in a new amber vial. After the extract is loaded, a 1 mL aliquot of MeOH followed by a 1 mL aliquot of 2% HCL/MeOH is added. This results in a 3 mL silica treated tissue extract. This extract is vortexed and diluted to a final solvent ratio of 1:1 MeOH/H2O before analysis.
HPLC-UV and HPLC-MS Methods
Table 3. Secondary HPLC-UV mobile phase gradient method concentrations
Method run time = 43 minutes; Column temperature = 25°C Injection volume = 50 μL; Flow rate = 0.8 mL/min Detector wavelengths = 210, 254, and 310 nm
|
Time (min)
|
Reagent Water (%)
|
MeOH (%)
|
0.1% TFA/Water (%)
|
ACN (%)
|
0.00 |
75 |
10 |
10 |
5
|
2.50 |
75 |
10 |
10 |
5
|
2.60 |
39 |
46 |
10 |
5
|
9.00 |
39 |
46 |
10 |
5
|
9.10 |
33.5 |
51.5 |
10 |
5
|
15.00 |
35 |
50 |
10 |
5
|
15.10 |
43 |
42 |
10 |
5
|
33.00 |
30 |
55 |
10 |
5
|
33.10 |
75 |
10 |
10 |
5
|
43.00 |
75 |
10 |
10 |
5
|
Table 4. Ionization source and detector parameters
Parameter
|
Value
|
Ionization Source |
APCI
|
Ionization Mode |
Negative
|
Drying Gas Temperature (°C) |
350
|
Vaporizer Temperature (°C) |
325
|
Drying Gas Flow (L/min) |
4.0
|
Nebulizer Pressure (psig) |
40
|
Corona Current (μA) |
10
|
Capillary Potential (V) |
1500
|
Mass Range |
40 – 400
|
Fragmentor |
100
|
Gain |
1
|
Threshold |
0
|
Step Size |
0.20
|
Speed (μ/sec) |
743
|
Peak Width (min) |
0.06
|
Cycle Time (sec/cycle) |
0.57
|
The Primary HPLC-UV method uses a Phenomenex Synergi 4 µm Hydro-RP column (80Å, 250 x 4.6 mm), or comparable, and is based on both the HPLC method found in USEPA 8330B and previous work[1][8][2]. This separation relies on a reverse phase column and uses a gradient elution, shown in Table 2. Depending on the analyst’s needs and equipment availability, the method has been proven to work with either 0.1% TFA or 0.25% FA (vol/vol) mobile phase. Addition of a guard column like a Phenomenex SecurityGuard AQ C18 pre-column guard cartridge can be optionally used. These optional changes to the method have no impact on the method’s performance.
The Secondary HPLC-UV method uses a Restek Pinnacle II Biphenyl 5 µm (150 x 4.6 mm) or comparable column and is intended as a confirmatory method. Like the Primary method, this method can use an optional guard column and utilizes a gradient elution, shown in Table 3.
For instruments equipped with a mass spectrometer (MS), a secondary MS method is available and was developed alongside the Primary UV method. The method was designed for use with a single quadrupole MS equipped with an atmospheric pressure chemical ionization (APCI) source, such as an Agilent 6120B. A majority of the analytes shown in Table 1 are amenable to this MS method, however nitroglycerine (which is covered extensively in USEPA method 8332) and 2-,3-, and 4-nitrotoluene compounds aren’t compatible with the MS method. MS method parameters are shown in Table 4.
Summary
The extraction methods and instrumental methods in this article build upon prior munitions analytical methods by adding new compounds, combining legacy and insensitive munitions analysis, and expanding usable sample matrices. These methods have been verified through extensive round robin testing and validation, and while the methods are somewhat challenging, they are crucial when simultaneous analysis of both insensitive and legacy munitions is needed.
References
- ^ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 United States Environmental Protection Agency (USEPA), 2006. EPA Method 8330B (SW-846) Nitroaromatics, Nitramines, and Nitrate Esters by High Performance Liquid Chromatography (HPLC), Revision 2. USEPA Website EPA Method 8330b
- ^ 2.0 2.1 2.2 Crouch, R.A., Smith, J.C., Stromer, B.S., Hubley, C.T., Beal, S., Lotufo, G.R., Butler, A.D., Wynter, M.T., Russell, A.L., Coleman, J.G., Wayne, K.M., Clausen, J.L., Bednar, A.J., 2020. Methods for simultaneous determination of legacy and insensitive munition (IM) constituents in aqueous, soil/sediment, and tissue matrices. Talanta, 217, Article 121008. doi: 10.1016/j.talanta.2020.121008 Open Access Manuscript.pdf
- ^ Walsh, M.R., Temple, T., Bigl, M.F., Tshabalala, S.F., Mai, N. and Ladyman, M., 2017. Investigation of Energetic Particle Distribution from High‐Order Detonations of Munitions. Propellants, Explosives, Pyrotechnics, 42(8), pp. 932-941. doi: 10.1002/prep.201700089
- ^ Mainiero, C. 2015. Picatinny Employees Recognized for Insensitive Munitions. U.S. Army, Picatinny Arsenal Public Affairs. Open Access Press Release
- ^ Frem, D., 2022. A Review on IMX-101 and IMX-104 Melt-Cast Explosives: Insensitive Formulations for the Next-Generation Munition Systems. Propellants, Explosives, Pyrotechnics, 48(1), e202100312. doi: 10.1002/prep.202100312
- ^ United States Environmental Protection Agency (USEPA), 2007. EPA Method 3535A (SW-846) Solid-Phase Extraction (SPE), Revision 1. USEPA Website Method 3535A.pdf
- ^ US Department of Defense and US Department of Energy, 2021. Consolidated Quality Systems Manual (QSM) for Environmental Laboratories, Version 5.4. 387 pages. Free Download QSM Version 5.4.pdf
- ^ 8.0 8.1 Russell, A.L., Seiter, J.M., Coleman, J.G., Winstead, B., Bednar, A.J., 2014. Analysis of munitions constituents in IMX formulations by HPLC and HPLC-MS. Talanta, 128, pp. 524–530. doi: 10.1016/j.talanta.2014.02.013
See Also