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  • Validation of Sample Extraction and Analysis Techniques for Simultaneous Determination of Legacy and Insensitive Munitions (IM) Constituents

    Abstract: Currently, no standardized method exists for the analysis of insensitive munitions (IM) in environmental matrices such as water, soils, and tis-sues. However, standardized methods, such as United States Environmental Protection Agency (EPA) 8330B, exist for legacy munitions for water and soil matrices. The lack of standardized methods for IM analysis leads researchers to use a wide variety of incomplete and overlapping analytical methodologies. The overall project’s first phase, Strategic Environmental Research and Development Program (SERDP) Environmental Restoration (ER)–2722, was to develop and optimize methods to address these methodological gaps by creating analytical methods for simultaneous analysis of IM and legacy munitions in water, soil, and tissue matrices. The main objective of the current project phase, Environmental Security Technology Certification Program (ESTCP) ER19-5078, is to build upon the previous work in phase one and to focus on the validation of the newly developed methods. Synergizing with the main objective of the overall project, the methods were validated and submitted to the EPA for inclusion as a possible addendum to EPA 8330B.
  • Cut and Capture System Technology for Demilitarization of Underwater Munitions

    Abstract: Munitions are encountered in a variety of underwater environments as unexploded ordnance (UXO) or munitions and explosives of concern (MEC). These items can cause unacceptable explosive risks to critical infrastructure, recreational divers, and fishermen. The primary goal of the demonstrations was to validate an underwater suite of tools that can be used to render underwater UXO and MEC safe in shallow water (i.e., up to 100 ft). US Navy underwater ranges in the Gulf of Mexico, south of the Naval Support Activity–Panama City, were selected for the first two demonstrations to fully display the integrated system by processing inert munitions, such as the Navy 5 in./38 cal and the Army 105 mm High Explosive (HE) M1 projectile. The third demonstration, however, occurred at the Naval Surface Warfare Center (NSWC), Crane, Lake Glendora Test Facility, in Sullivan, Indiana. Twenty US Army 105 mm HE M1 projectiles filled with TNT were successfully processed. Overall, this project showed that Gradient Technology’s high-pressure waterjet demilitarization technology can be reliably operated underwater at depths less than 100 ft of seawater when the supporting equipment is located on the deck of a vessel or floating pier system.
  • Environmental Monitoring of Munitions Constituents During a Demonstration of the Underwater Cut-and-Capture System Demilitarization Technology

    PURPOSE: The presence of underwater military munitions (UWMM) in aquatic environments may present explosive blast risks and potentially affect the environment because of the release of munitions constituents (MC). Therefore, in situ demilitarization of UWMM is highly desirable. This technical note presents the results of environmental monitoring measuring water and sediment contamination resulting from the demonstration of an in situ technology that uses high-pressure water jets to render UWMM safe.
  • Methods for Simultaneous Determination of 29 Legacy and Insensitive Munition (IM) Constituents in Aqueous, Soil-Sediment, and Tissue Matrices by High-Performance Liquid Chromatography (HPLC)

    Abstract: Standard methods are in place for analysis of 17 legacy munitions compounds and one surrogate in water and soil matrices; however, several insensitive munition (IM) and degradation products are not part of these analytical procedures. This lack could lead to inaccurate determinations of munitions in environmental samples by either not measuring for IM compounds or using methods not designed for IM and other legacy compounds. This work seeks to continue expanding the list of target analytes currently included in the US Environmental Protection Agency (EPA) Method 8330B. This technical report presents three methods capable of detecting 29 legacy, IM, and degradation products in a single High Performance Liquid Chromatography (HPLC) method with either ultraviolet (UV)-visible absorbance detection or mass spectrometric detection. Procedures were developed from previously published works and include the addition of hexahydro-1-nitroso-3,5-dinitro-1,3,5-triazine (MNX); hexahydro-1,3-dinitroso-5-nitro-1,3,5-triazine (DNX); hexahydro-1,3,5-trinitroso-1,3,5-triazine (TNX); 2,4-diamino-6-nitrotoluene (2,4-DANT); and 2,6-diamino-4-nitrotoluene (2,6-DANT). One primary analytical method and two secondary (confirmation) methods were developed capable of detecting 29 analytes and two surrogates. Methods for high water concentrations (direct injection), low-level water concentrations (solid phase extraction), soil (solvent extraction), and tissue (solvent extraction) were tested for analyte recovery of the new compounds.
  • Long-Term Stability and Efficacy of Historic Activated Carbon (AC) Deployments at Diverse Freshwater and Marine Remediation Sites

    Abstract: A number of sites around the United States have used activated carbon (AC) amendments to remedy contaminated sediments. Variation in site-specific characteristics likely influences the long-term fate and efficacy of AC treatment. The long-term effectiveness of an AC amendment to sediment is largely unknown, as the field performance has not been monitored for more than three years. As a consequence, the focus of this research effort was to evaluate AC’s long-term (6–10 yr) performance. These assessments were performed at two pilot-scale demonstration sites, Grasse River, Massena, New York and Canal Creek, Aberdeen Proving Ground (APG), Aberdeen, Maryland, representing two distinct physical environments. Sediment core samples were collected after 6 and 10 years of remedy implementation at APG and Grasse River, respectively. Core samples were collected and sectioned to determine the current vertical distribution and persistence of AC in the field. The concentration profile of polychlorinated biphenyls (PCBs) in sediment pore water with depth was measured using passive sampling. Sediment samples from the untreated and AC-treated zones were also assessed for bioaccumulation in benthic organisms. The data collected enabled comparison of AC distribution, PCB concentrations, and bioaccumulation measured over the short- and long-term (months to years).
  • PUBLICATION NOTICE: Autonomous QUerying And PATHogen Threat Agent Sensor System (AQUA PATH): Monitoring Source Waters with Geospatially Wirelessly Networked Distributed Sensing Systems

    Abstract: Contaminants serve as health risks to recreational water, potable water, and marine life that result in undocumented effects on population exposure. In many areas of the world, the concern lies in contaminated drinking water, which would immediately effect social and economic order. As research advances for innovative solutions, the deployment of automated systems for source water monitoring could reduce the risk of exposure. Water quality monitoring typically involves sample collection and analyses that are performed in a laboratory setting. These results are normally presented after an 18−48 hr period. This report details the prototyped Autonomous QUerying And PATHogen threat agent sensor (AQUA PATH) geoenabled system that is able to detect the presence/absence of pathogenic bacteria indicators in source waters and report these values in the field, in less than 30 minutes. The AQUA PATH system establishes rapid field data collection and reports assessment of source waters bacterial loads at near shore inner coastal locations, which makes a leap forward compared to current presence/absence tests standards established by the EPA.
  • PUBLICATION NOTICE: High-Performance Photocatalytic Degradation of Model Contaminants with Iron Oxide–Based Colloidal Solutions under Broad-Spectrum Illumination

    Abstract:  Small molecule contaminants, such as compounds from pharmaceuticals, personal care products, and pesticides, persist through traditional wastewater treatment processes. Heterogeneous photocatalysis with transition metal oxides (TMOs) is an emerging technology for removing these recalcitrant contaminants from wastewater. To leverage this technology, we selectively combined three different TMOs with bandgap energies in different regions of the solar spectrum as a means of harvesting multiple wavelengths of incident radiation to increase the degradation rate of model and real contaminants. Specifically, we combined zincite (ZnO, ultraviolet active), hematite (α-Fe2O3, visible active), and tenorite (CuO, near-infrared active). The combination of tenorite and hematite (2:1 mass ratio) was the most effective, degrading methyl orange with a rate constant of 40±1E-03 min−1. When applied to multicontaminant solutions using laboratory illumination, our multispectral photocatalyst degrades real-world contaminants, methyl orange, carbamazepine, and nitrobenzene, with rate constants of 30±1E-03, 24±1E-03, and 6±1E-03 min−1, respectively. In addition, the material degrades contaminants with a greater efficiency under outdoor solar illumination, with Collector Area per Order values of 4.0, 6.1 and 14.5 kWh/order/m³, for methyl orange, carbamazepine, and nitrobenzene, respectively. These results demonstrate the effectiveness of this approach to purify water for strategic applications.