Difference between revisions of "User:Jhurley/sandbox"

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The persistent release of residual contaminants from low hydraulic conductivity (low ''k'') zones prevents many chlorinated solvent sites from reaching groundwater cleanup goals. Low ''k'' aquifer settings limit the effectiveness of many conventional remediation technologies that rely on extraction, recirculation, or amendment delivery and distribution to achieve contact between the residual contaminants and the reagents, contact which is necessary for subsequent contaminant transformation or destruction. Alternative methods are needed to effectively distribute remedial amendments, to control contaminants leaving low ''k'' source zones, and to enhance natural attenuation processes. Two innovative remediation technologies for the treatment of chlorinated solvents and other contaminants in low ''k'' media are introduced, along with operational and performance results from recent field demonstrations.
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==Estimating PCE/TCE Abiotic First-Order Reductive Dechlorination Rate Constants in Clayey Soils Under Anoxic Conditions==
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The U.S. Department of Defense (DoD) faces many challenges in restoring aquifers at contaminated sites, often due to back-diffusion of tetrachloroethene (PCE) and trichloroethene (TCE) from low-permeability clay zones. The uptake, storage, and subsequent long-term release of these dissolved contaminants from clays are key processes in understanding the longevity, intensity, and risks associated with many persistent chlorinated ethene groundwater plumes. Although naturally occurring abiotic and biotic dechlorination processes in clays may reduce stored contaminant mass and significantly aid natural attenuation, no standardized field method currently exists to verify or quantify these reactions. It is critical to remediation design efforts to demonstrate and validate a cost-effective in situ approach for assessing these dechlorination processes using first-order rate constants. An approach was developed and applied across eight DoD sites to support Remedial Project Managers (RPMs) and regulators in evaluating natural attenuation potential in clay-rich environments.
 
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'''Related Article(s):'''
 
'''Related Article(s):'''
* [[Bioremediation - Anaerobic | Anaerobic Bioremediation]]
 
* [[Chemical Oxidation (In Situ - ISCO) | In Situ Chemical Oxidation]]
 
* [[Chemical Reduction (In Situ - ISCR) | In Situ Chemical Reduction]]
 
  
'''CONTRIBUTOR(S): '''
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*[[Monitored Natural Attenuation (MNA)]]
* [[Stephen D. Richardson, Ph.D., PE]]
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*[[Monitored Natural Attenuation (MNA) of Chlorinated Solvents]]
* [[Craig E. Divine, Ph.D., PG]]
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*[[Monitored Natural Attenuation - Transitioning from Active Remedies]]
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*[[Matrix Diffusion]]
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*[[REMChlor - MD]]
  
'''Key Resource(s):'''
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'''Contributors:''' Dani Tran, Dr. Charles Schaefer, Dr. Charles Werth
* The Horizontal Reactive Media Treatment Well (HRX Well<sup>&reg;</sup>) for Passive In-Situ Remediation<ref name="Divine2018a">Divine, C. E., Roth, T, Crimi, M., DiMarco, A.C., Spurlin, M., Gillow, J., and Leone, G., 2018. The Horizontal Reactive Media Treatment Well (HRX Well<sup>&reg;</sup>) for Passive In-Situ Remediation. Groundwater Monitoring & Remediation, 38(1), pp. 56–65.  [https://doi.org/10.1111/gwmr.12252 DOI: 10.1111/gwmr.12252]</ref>
 
  
* The Horizontal Reactive Media Treatment Well (HRX Well<sup>&reg;</sup>) for Passive In Situ Remediation: Design, Implementation, and Sustainability Considerations<ref name="Divine2018">Divine, C.E., Wright, J., Wang, J., McDonough, J., Kladias, M., Crimi, M., Nzeribe, B.N., Devlin, J.F., Lubrecht, M., Ombalski, D., Hodge, B., Voscott, H., and Gerber, K., 2018. The Horizontal Reactive Media Treatment Well (HRX Well<sup>&reg;</sup>) for Passive In Situ Remediation: Design, Implementation, and Sustainability Considerations. Remediation, 28(4), pp. 5-16.  [https://doi.org/10.1002/rem.21571 DOI: 10.1002/rem.21571]&nbsp;&nbsp; Also available from: [https://www.researchgate.net/publication/327487096_The_horizontal_reactive_media_treatment_well_HRX_WellR_for_passive_in_situ_remediation_Design_implementation_and_sustainability_considerations ResearchGate]</ref>
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'''Key Resource:'''
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*Schaefer, C.E, Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils (3)
  
* New Application of A Geotechnical Technology to Remediate Low-Permeability Contaminated Media – Final Technical Report<ref name="Richardson2020">Richardson, S.D., Hart, D.M., Long, J.A., and Newell, C.J., 2020. New Application of A Geotechnical Technology to Remediate Low-Permeability Contaminated Media – Final Technical Report. ER-201627, Environmental Security Technology Certification Program (ESTCP). [https://www.serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-201627/ Project Overview]</ref>
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==Introduction==
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Cost-effective methods are needed to verify the occurrence of natural dechlorination processes and quantify their dechlorination rates in clays under ambient in situ conditions in order to reliably predict their long-term influence on plume longevity and mass discharge. However, accurately determining these rates is challenging due to slow reaction kinetics, the transient nature of transformation products, and the interplay of biotic and abiotic mechanisms within the clay matrix or at clay-sand interfaces. Tools capable of quantifying these reactions and assessing their role in mitigating plume persistence would be a significant aid for long-term site management.
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For reductive abiotic dechlorination under anoxic conditions, a 1% hydrochloric acid (HCl) extraction of a sample of native clay coupled with X-ray diffraction (XRD) data can be used as a screening level tool to estimate reductive dechlorination rate constants. These rate constants can be inserted into fate and transport models such as [[REMChlor - MD]]<ref>Falta, R., and Wang, W., 2017. A semi-analytical method for simulating matrix diffusion in numerical transport models. Journal of Contaminant Hydrology, 197, pp. 39-49. [https://doi.org/10.1016/j.jconhyd.2016.12.007 doi: 10.1016/j.jconhyd.2016.12.007]&nbsp; [[Media: FaltaWang2017.pdf | Open Access Manuscript]]</ref><ref>Kulkarni, P.R., Adamson, D.T., Popovic, J., Newell, C.J., 2022. Modeling a well-charactized perfluorooctane sulfate (PFOS) source and plume using the REMChlor-MD model to account for matrix diffusion. Journal of Contaminant Hydrology, 247, Article 103986. [https://doi.org/10.1016/j.jconhyd.2022.103986 doi: 10.1016/j.jconhyd.2022.103986]&nbsp; [[Media: KulkarniEtAl2022.pdf | Open Access Manuscript]]</ref> to quantify abiotic dechlorination impacts within clay aquitards on chlorinated solvent plumes. Thus, determination of the abiotic reductive dechlorination rate constant for a particular clayey soil can be readily utilized to provide a more accurate assessment of aquifer cleanup timeframes for groundwater plumes that are being sustained by contaminant back-diffusion.
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==Recommended Approach==
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[[File: TranFig1.png | thumb | 600 px | Figure 1: First-order rate constants for abiotic reductive dechlorination of TCE under anaerobic conditions (data from this study and prior research)]]
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[[File: TranFig2.png | thumb | 600 px | Figure 2: Flowchart diagram of field screening procedures]]
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The recommended approach builds upon the methodology and findings of a recent study<ref name="SchaeferEtAl2025">Schaefer, C.E., Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils. Groundwater Monitoring and Remediation, 45(2), pp. 31-39. [https://doi.org/10.1111/gwmr.12709 doi: 10.1111/gwmr.12709]</ref>, emphasizing field-based and analytical techniques to quantify abiotic first-order reductive dechlorination rate constants for PCE and TCE in clayey soils under anoxic conditions. Key components of this evaluation are listed below:
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#<u>Zone Identification:</u> The focus of the investigation should be to delineate clayey zones adjacent to hydraulically conductive zones.
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#<u>Ferrous Mineral Quantification:</u> Assess ferrous mineral context in clay via 1% HCl extraction at ambient temperature over a 10-minute interval.
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#<u>Mineralogical Characterization:</u> Conduct XRD analysis with the specific intent of identifying the presence of pyrite and biotite.
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#<u>Reduced Gas Analysis:</u> Measurement of reduced gases such as acetylene, ethene, and ethane concentrations in clay samples. Gas-tight sampling devices (e.g., En Core® soil samplers by En Novative Technologies, Inc.)  should be used to ensure sample integrity during collection and transport. 
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Clay samples should be collected within a few centimeters of the high-permeability interface, with optional additional sampling further inward. For mineralogical analysis, a defined interval may be collected and subsequently subsampled. To preserve sample integrity, exposure to air should be minimized during collection, transport, and handling. Homogenization should occur within an anaerobic chamber, and if subsamples are required for external analysis, they must be shipped in gas-tight, anaerobic containers.
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Estimation of the abiotic reductive first-order rate constant for PCE and TCE is based on the “reactive” ferrous content in the clay. Reactive ferrous content (Fe(II)<sub>r</sub>) is estimated as shown in Equation 1:
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::'''Equation 1:'''&nbsp;&nbsp;&nbsp;&nbsp;&nbsp;&nbsp; <big>''Fe(II)<sub><small>r</small></sub> = DA + XRD<sub><small>pyr</small></sub> - XRD<sub><small>biotite</small></sub>''</big>
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where ''DA'' is the ferrous content from the dilute acid (1% HCl) extraction, ''XRD<sub><small>pyr</small></sub>'' is the pyrite content from XRD analysis, and ''XRD<sub><small>biotite</small></sub>'' is the biotite content from XRD analysis<ref name="SchaeferEtAl2025"/>.
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Abiotic dechlorination is unlikely to contribute to mitigating contaminant back-diffusion when reactive ferrous iron (Fe(II)<sub><small>r</small></sub>) concentrations are below 100 mg/kg (Figure 1). For Fe(II)<sub><small>r</small></sub> above 100 mg/kg, the first-order rate constant for PCE and TCE reductive dechlorination can be estimated using the correlation shown in Figure 1<ref name="SchaeferEtAl2018">Schaefer, C.E., Ho, P., Berns, E., Werth, C., 2018. Mechanisms for abiotic dechlorination of trichloroethene by ferrous minerals under oxic and anoxic conditions in natural sediments. Environmental Science and Technology, 52(23), pp.13747-13755. [https://doi.org/10.1021/acs.est.8b04108 doi: 10.1021/acs.est.8b04108]</ref><ref>Borden, R.C., Cha, K.Y., 2021. Evaluating the impact of back diffusion on groundwater cleanup time. Journal of Contaminant Hydrology, 243, Article 103889. [https://doi.org/10.1016/j.jconhyd.2021.103889 doi: 10.1016/j.jconhyd.2021]&nbsp; [[Media: BordenCha2021.pdf | Open Access Manuscript]]</ref>. The rate constant exhibits a strong positive correlation with the logarithm of reactive Fe(II) content (Pearson’s ''r'' = 0.82), with a slope of 4.7 × 10⁻⁸ L g⁻¹ d⁻¹ (log mg kg⁻¹)⁻¹.
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Figure 2 presents a decision flowchart designed to evaluate the significance and extent of abiotic reductive dechlorination. By applying Equation 1 to the dilute acid extractable Fe(II) plus measured mineral species data from clay samples, the reactive ferrous iron content (Fe(II)<sub><small>r</small></sub>) can be quantified, enabling a streamlined assessment of the extent to which abiotic processes are contributing to the mitigation of contaminant back-diffusion.
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==Study Design Considerations==
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===Diagnostic Resin Treatments===
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Several commercially available resins have been verified for use in the iTIE system. Investigators can select resins based on stressor classes of interest at each site. Each resin selectively removes a CoC class from site water prior to organism exposure.
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*[https://www.dupont.com/products/ambersorb560.html DuPont Ambersorb 560] for removal of 1,4-dioxane and other organic chemicals<ref>Woodard, S., Mohr, T., Nickelsen, M.G., 2014. Synthetic media: A promising new treatment technology for 1,4-dioxane. Remediation Journal, 24(4), pp. 27-40. [https://doi.org/10.1002/rem.21402 doi: 10.1002/rem.21402]</ref>
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*C18 for nonpolar organic chemicals
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*[https://www.bio-rad.com/en-us Bio-Rad] [https://www.bio-rad.com/en-us/product/chelex-100-resin?ID=6448ab3e-b96a-4162-9124-7b7d2330288e Chelex] for metals
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*Granular activated carbon for metals, general organic chemicals, sulfide<ref>Lemos, B.R.S., Teixeira, I.F., de Mesquita, J.P., Ribeiro, R.R., Donnici, C.L., Lago, R.M., 2012. Use of modified activated carbon for the oxidation of aqueous sulfide. Carbon, 50(3), pp. 1386-1393. [https://doi.org/10.1016/j.carbon.2011.11.011 doi: 10.1016/j.carbon.2011.11.011]</ref>
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*[https://www.waters.com/nextgen/us/en.html Waters] [https://www.waters.com/nextgen/us/en/search.html?category=Shop&isocode=en_US&keyword=oasis%20hlb&multiselect=true&page=1&rows=12&sort=best-sellers&xcid=ppc-ppc_23916&gad_source=1&gad_campaignid=14746094146&gbraid=0AAAAAD_uR00nhlNwrhhegNh06pBODTgiN&gclid=CjwKCAiAtLvMBhB_EiwA1u6_PsppE0raci2IhvGnAAe5ijciNcetLaGZo5qA3g3r4Z_La7YAPJtzShoC6LoQAvD_BwE Oasis HLB] for general organic chemicals<ref name="SteigmeyerEtAl2017"/>
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*[https://www.waters.com/nextgen/us/en.html Waters] [https://www.waters.com/nextgen/us/en/search.html?category=All&enableHL=true&isocode=en_US&keyword=Oasis%20WAX%20&multiselect=true&page=1&rows=12&sort=most-relevant Oasis WAX] for PFAS, organic chemicals of mixed polarity<ref>Iannone, A., Carriera, F., Di Fiore, C., Avino, P., 2024. Poly- and Perfluoroalkyl Substance (PFAS) Analysis in Environmental Matrices: An Overview of the Extraction and Chromatographic Detection Methods. Analytica, 5(2), pp. 187-202. [https://doi.org/10.3390/analytica5020012 doi: 10.3390/analytica5020012]&nbsp; [[Media: IannoneEtAl2024.pdf | Open Access Article]]</ref>
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*Zeolite for ammonia, other organic chemicals
  
==Introduction==
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Resins must be adequately conditioned prior to use. Otherwise, they may inadequately adsorb toxicants or cause stress to organisms. New resins should be tested for efficacy and toxicity before being used in an iTIE system.   
[[File:Richardson1w2Fig1.png | thumb | 400px | Figure 1. Examples of low ''k'' geology. Upper left: bay muds, Oakland, California; lower left: weathered siltstone, Denver, Colorado; right: tailings slimes, central New Mexico<ref name="Horst2019"/>.]]
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[[File:Richardson1w2Fig2.png | thumb | 400px | Figure 2. Contaminant back diffusion (“Matrix Diffusion”) from low ''k'' zones<ref name="NRC2005">National Research Council, 2005. Contaminants in the Subsurface: Source Zone Assessment and Remediation. National Academies Press, Washington, DC, pp. 372. [https://doi.org/10.17226/11146 DOI: 10.17226/11146]&nbsp;&nbsp; [[Media: NRC2005.pdf | Book.pdf]]</ref>.]]
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===Test Organism Species and Life Stages===
A critical challenge preventing many chlorinated solvent sites from achieving groundwater cleanup goals is the long term release of residual contaminants from low hydraulic conductivity (low ''k'') zones such as silts, clays, glacial till, over-bank deposits, marine deposits, tailings “slimes”, saprolite and bedrock (see Figure 1)<ref name ="Horst2019">Horst, J., Divine, C., Schnobrich, M., Oesterreich, R., and Munholland, J., 2019. Groundwater Remediation in Low-Permeability Settings: The Evolving Spectrum of Proven and Potential. Groundwater Monitoring & Remediation, 39(1), pp. 11-19. [https://doi.org/10.1111/gwmr.12316 DOI: 10.1111/gwmr.12316]</ref><ref name ="Sale2008">Sale, T., C. Newell, H. Stroo, R. Hinchee, and Johnson, P., 2008. Frequently Asked Questions Regarding Management of Chlorinated Solvents in Soils and Groundwater. Environmental Security Technology Certification Program (ESTCP) Project ER-0530, 38 pp. [[Media:2008-Sale-Frequently_Asked_Questions_Regarding_Management_of_Chlorinated_Solvent_in_Soils_and_Groundwater.pdf  | Report.pdf]]&nbsp;&nbsp; [https://serdp-estcp.org/Program-Areas/Environmental-Restoration/Contaminated-Groundwater/Persistent-Contamination/ER-200530/(language)/eng-US Project overview]</ref>. Such sites may be dominated by matrix diffusion processes (see Figure 2) which can significantly prolong restoration and site management timeframes. Residual contaminants residing in low permeability zones slowly diffuse from the low ''k'' matrix back into higher permeability zones, becoming a persistent source that is very difficult to remediate. One of the side effects of matrix diffusion is concentration rebound after an ''in situ'' treatment is applied. This is commonly observed at sites treated with chemical oxidation<ref name="McGuire2006">McGuire, T.M., McDade, J.M., and Newell, C.J., 2006. Performance of DNAPL Source Depletion Technologies at 59 Chlorinated Solvent-Impacted Sites. Groundwater Monitoring & Remediation. Volume 26, Issue 1, pp. 73-84. [https://doi.org/10.1111/j.1745-6592.2006.00054.x DOI: 10.1111/j.1745-6592.2006.00054.x]&nbsp;&nbsp; [https://www.provectusenvironmental.com/marketing/p-ox1/McGuire%20et%20al%202006.pdf Free download.pdf]</ref><ref name="Krembs2010">Krembs, F., Siegrist, R., Crimi, M., Furrer, R., and Petri, B., 2010. ISCO for Groundwater Remediation: Analysis of Field Applications and Performance. Groundwater Monitoring & Remediation, 30(4), pp. 42-53.  [https://doi.org/10.1111/j.1745-6592.2010.01312.x DOI: 10.1111/j.1745-6592.2010.01312.x]</ref> and has the potential to occur at ''in situ'' bioremediation sites after the depletion of electron donors<ref name="Adamson2011">Adamson, D., McGuire, T., Newell, C., and Stroo, H., 2011. Sustained Treatment: Implications for Treatment Timescales Associated with Source-Depletion Technologies. Remediation, 21(2), pp. 27-50.  [https://doi.org/10.1002/rem.20280 DOI: 10.1002/rem.20280]</ref>.
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Practitioners can also select different organism species and life stages for use in the iTIE system, depending on site characteristics and study goals. The iTIE system can accommodate various small test organisms, including embryo-stage fish and most macroinvertebrates. The following common toxicity tests can be adapted for application within iTIE systems<ref>U.S. Environmental Protection Agency, Office of Solid Waste and Emergency Response, 1994. Catalogue of Standard Toxicity Tests for Ecological Risk Assessment. ECO Update, 2(2), 4 pages. Publication No. 9345.0.05I [https://www.epa.gov/sites/default/files/2015-09/documents/v2no2.pdf Free Download]&nbsp; [[Media: usepa1994.pdf | Report.pdf]]</ref>.
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<ul><u>Freshwater acute toxicity:</u></ul>
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*[[Wikipedia: Daphnia magna | ''Daphnia magna'']] or [[Wikipedia: Daphnia pulex | ''Daphnia pulex'']] 24-, 48-, and 96-hour survival
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<ul><u>Freshwater chronic toxicity:</u></ul>
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*[[Wikipedia: Ceriodaphnia dubia | ''Ceriodaphnia dubia'']]  7-day survival and reproduction
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*''D. magna'' 7-day survival and reproduction
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*[[Wikipedia: Fathead minnow | ''Pimephales promelas'']] 7-day embryo-larval survival and teratogenicity
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*[[Wikipedia: Hyalella azteca | ''Hyalella Azteca'']] 10- or 30-day survival and reproduction
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<ul><u>Marine acute toxicity:</u></ul>
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*[[Wikipedia: Americamysis bahia | ''Americamysis bahia'']] 24- and 48-hour survival
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<ul><u>Marine chronic toxicity:</u></ul>
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*''Americamysis'' survival, growth and fecundity
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*[[Wikipedia: Topsmelt silverside | ''Atherinops affinis'']] embryo-larval survival and growth
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Acute toxicity is quantifiable via organism survival rates immediately following the termination of an iTIE system field deployment. Chronic toxicity can be quantified by continuing to culture and observe test organisms in-lab. Common chronic endpoints include stunted growth, altered development such as teratogenicity in larval fish, decreased reproduction rates, and changes in gene expression.  
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Several gene expression endpoints have been detectable in bioassays following an iTIE system deployment and in-lab culturing period. Steigmeyer ''et al.''<ref name="SteigmeyerEtAl2017"/> were able to detect changes in the expression of two genes in ''D. magna'' after a 24-hour exposure to bisphenol A. In a separate study, Nichols<ref>Nichols, E., 2023. Methods for Identification and Prioritization of Stressors at Impaired Sites. Masters thesis, University of Michigan. University of Michigan Library Deep Blue Documents. [https://deepblue.lib.umich.edu/bitstream/handle/2027.42/176142/Nichols_Elizabeth_thesis.pdf?sequence=1 Free Download]&nbsp; [[Media: Nichols2023.pdf | Report.pdf]]</ref> found a significant decline in acetylcholinesterase activity in ''H. azteca'' after a 24-hour exposure to chlorpyrifos. These results indicate a potential to adapt other gene expression bioassays for use in conjunction with iTIE system field exposures to prove stressor-causality linkages.
  
Currently, there are limited remediation options available to treat residual contamination trapped in low ''k'' zones. Low ''k'' settings limit the applicability and effectiveness of conventional remediation technologies due to the constraint on fluid introduction and recovery. As such, methods relying on extraction, recirculation, or reagent delivery and distribution are often limited in their effectiveness. For the long lived, difficult to treat sites, innovative technologies are needed that will reliably address mass flux limitations of contaminants leaving low ''k'' source zones, and also increase the actual treatment of the contaminants leaving these low ''k'' zones by enhancing natural attenuation processes. Two innovative technologies investigated by ESTCP are summarized below.
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===Cost Effectiveness Study===
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Burton ''et al.''<ref name="BurtonEtAl2020"/> conducted a cost effectiveness study comparing the iTIE technology with the traditional US EPA Phase 1 TIE method. Comparisons were based on the estimated time required to complete various sub-tasks within each method. Sub-tasks included organism care, equipment preparation, mobilization and deployment, test maintenance, test termination, demobilization, and test termination analyses. It was ultimately estimated that the iTIE protocol requires 47% less time (67 fewer hours) to complete than the Phase 1 TIE method, with the largest time differences in equipment preparation, deployment, test maintenance, and demobilization. It is important to note that the iTIE method may require additional initial costs for equipment and training.
  
==“Grout Bomber”==
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==Field Application==
===Technology Description===  
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[[File: CraneFig6.png | thumb | left | 400px | Figure 6. iTIES deployment at the Rouge River, Detroit, MI.  In the foreground is the iTIE Cooler Sub-System, which contains iTIE resin treatments and test organism groups, as well as the oxygenation coil and sample collection bottles. Next to the iTIE Cooler are the two pump cases. The Trident can be seen above the pump cases, installed in the river channel near shore.]]
[[File:Richardson1w2Fig3.png | thumb | 400px | Figure 3. a) Grout Bomber equipment; b) hopper for mixing and delivery of grout to the “stitcher”; and c) grout exiting the mandrel]]
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The&nbsp;iTIE&nbsp;system&nbsp;has&nbsp;been successfully deployed at a variety of marine and freshwater sites during the proof-of-concept phase of prototype development. One example is the 2024 iTIE system deployment completed near the mouth of the Rouge River in Detroit, MI (Figure 6). The Rouge River watershed has a long history of industrialization, with a legacy of chemical dumping, channelization, damming, and urban runoff<ref>Ridgway, J., Cave, K., DeMaria, A., O’Meara, J., Hartig, J. H., 2018. The Rouge River Area of Concern—A multi-year, multi-level successful approach to restoration of Impaired Beneficial Uses. Aquatic Ecosystem Health and Management, 21(4), pp. 398-408. [https://doi.org/10.1080/14634988.2018.1528816 doi: 10.1080/14634988.2018.1528816]</ref>. This has led to degraded environmental conditions, with previous detections of a wide range of chemicals including heavy metals and various organics.
[[File:Richardson1w2Fig4.png | thumb | 400px | Figure 4. Application of the Bomber technology for contaminated sites in low ''k'' materials.]]
 
[[File:Richardson1w2Fig5.png | thumb | 400px | Figure 5. Chlorinated ethene concentrations at well pair (CMT-1 and IS17MW04).]]
 
The geotechnical industry offers a variety of well-established techniques for quickly and efficiently accessing the subsurface for the purposes of ground stabilization, foundation rehabilitation, porewater drainage, and structural support. The speed and efficiency of these techniques can also be a major advantage for emplacement of remedial amendments into the subsurface. One promising approach is the Grout Bomber, a larger adaptation of conventional cement or compaction grouting techniques for subsurface stabilization. The technology uses an excavator equipped with specialized equipment (a “stitcher”) to quickly push a mandrel (3.5 in. diameter hollow cylindrical rod) into the subsurface and subsequently fill the hole and subsurface voids with cement grout (from bottom to top) using an in-line grout delivery system. The typical arrangement of the Grout Bomber technology includes the installation rig (excavator with the “stitcher” mast; see Figure 3a) and an on-site grout mixing and delivery unit consisting of mixing hopper, pumps, hosing, and power supply. Raw materials are loaded into the mixing hopper (see Figure 3b) where it is mixed to the appropriate consistency, then pumped to the Bomber rig at a rate of approximately 0.25 cubic feet per pump stroke. At the exit end of the Bomber mandrel (see Figure 3c), the grout flows in a continuous and uniform manner, allowing the columns to be emplaced with grout while the mandrel (which was pushed into the subsurface) is lifted to the surface.  Hundreds of closely spaced vertical grout columns can be installed per day using this technology.
 
  
For environmental applications, the Grout Bomber approach can be “repurposed” as a means to improve delivery of remediation amendments into contaminated treatment zones in low ''k'' materials. The remedial amendment (e.g., mixture of zero-valent iron (ZVI), sand, neat oil) can replace the grout and be directly placed into the subsurface from bottom to top (not injected into the surrounding formation), creating hundreds of reaction columns. The Bomber technology offers the following benefits:
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[[File: CraneFig7.png | thumb | 300px | Figure 7. Survival and healthy development of ''P. promelas'' embryos and larvae following a 48-hour iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater as embryos for 48 hours and cultured post-exposure for an additional 5 days.]]
* '''Reduces uncertainty: '''
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[[File: CraneFig8.png | thumb | 300px | Figure 8. Survival of ''C. dilutus'' larvae after an iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater for 48 hours and cultured post-exposure for an additional 5 days. Error bars show standard deviation.]]
The Bomber technology circumvents the “delivery problem” associated with conventional injection-based remediation approaches, particularly in low ''k'' zones. The closely spaced nature of the reaction columns (2-3 ft spacing) reduces the diffusion lengths out of low ''k'' zones and also the uncertainty associated with amendment delivery because contaminants are always < 1 - 1.5 ft from an active treatment zone (see Figure 4).  
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An&nbsp;iTIE&nbsp;system&nbsp;deployment&nbsp;was designed and completed to determine which chemical classes are most responsible for causing toxicity at the site. Resin treatments included glass wool (inert, non-fractionating substance), Chelex (metals sorption), Oasis HLB (general organics sorption), and Oasis WAX (organics sorption, with a high affinity for PFAS). The study utilized fathead minnow (''P. promelas'') embryos, due to their relative sensitivity to metals and PAHs, as well as second-instar midge ([[Wikipedia: Chironomus |''Chironomus dilutus'']]) larvae due to their relative sensitivity to PFAS.  
  
* '''Rapid installation of reaction columns: '''
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The test organisms were exposed to fractionated porewater ''in situ'' for 48 hours. Following exposure, organisms were cultured for an additional five days, and survival was recorded (Figures 7 and 8). Moderate declines in survival were seen in both species in the glass wool treatment, indicating toxicity at the site. For ''P. promelas'', the highest proportion of healthy development occurred in the Chelex treatment, supporting the hypothesis that metals are a dominant cause of toxicity. ''C. dilutus'' had the greatest survival in the Oasis WAX treatment, suggesting that an organic stressor class like PFAS is also present at harmful concentrations in the river.
The Grout Bomber can install 100+ reaction columns per day to depths of 40-50 ft below ground surface (bgs) to encourage contaminant degradation in source zones. Since the Grout Bomber is a direct push technique, it is better suited to silts and clays with blow counts < 35. Consolidated materials with higher blow counts will require additional equipment to pre-drill the columns prior to amendment emplacement. In general, this technology represents a much simpler, less intensive, and easier to install version of complete soil mixing.  
 
  
* '''Accommodates various amendment types: '''
+
Water chemical analyses of fractionated and unfractionated water samples were completed to support biological results. Analyses were conducted for a range of stressor classes including metals, PAHs, PCBs, an organophosphate pesticide (chlorpyrifos), a PFAS compound (PFOS) and a pyrethroid insecticide (permethrin). Of these analytes, only heavy metals and PFOS were detected. Some chemical classes including PAHs and PCBs were not detected at the site.
In one example<ref name="Richardson2020"/>, vertical reaction columns containing a mixture of ZVI, vegetable oil, sand and minor amounts of water were installed to a depth of 30 ft bgs in a low ''k'' treatment area consisting primarily of silts, sandy clays, and lean clays<ref name="Divine2018"/>.  The ZVI-sand-oil mixture was designed to have a similar consistency (or viscosity) to cement grout, thus requiring no major alterations to the existing Bomber equipment for the project. Recommended practices to ensure uninterrupted flow of amendments to the Bomber mandrel include:  
+
To reach similar conclusions using traditional Phase 1 TIE methods, one would need to complete the following tests: baseline toxicity, filtration, aeration, EDTA, C18 SPE, and methanol elution of C18 SPE. The iTIE method allows the same conclusions to be drawn with significantly less time and effort required.
** Conduct simple pumping pilot studies with amendments of varying consistencies,  
 
** Consult with a well trained pump operator, and  
 
** Minimize the length of hosing between mixing hopper pump and Bomber mandrel.  
 
  
* '''Cost effective source zone treatment: '''
+
==Summary==
Estimated treatment costs associated with emplacement of amendments with the Grout Bomber are ~$35 per cubic yard of source zone treated (including contractor labor, equipment, and materials). This is generally less than the reported unit cost for ''in situ'' biodegradation ($20-$80/yd<sup>3</sup>) and significantly less than chemical oxidation ($125/yd<sup>3</sup>) and thermal remediation (median $200/yd<sup>3</sup>)<ref name="McDade2005">McDade, J.M., T.M. McGuire, and Newell, C.J., 2005. Analysis of DNAPL Source Depletion Costs at 36 Field Sites, Remediation, 15(2), pp. 9-18.  [https://doi.org/10.1002/rem.20039 DOI: 10.1002/rem.20039]</ref>.
+
The ''in situ'' Toxicity Identification Evaluation technology and protocol is a powerful tool that investigators can use to strengthen causal linkages between chemical stressors and ecological toxicity. By fractionating sampled water and exposing test organisms ''in situ'', investigators can gather toxicity response data while minimizing sample manipulation and accurately representing environmental conditions.
 +
<br clear="right"/>
  
===Operational Approach & Results===
+
==References==
A field demonstration was conducted at Site 17, Naval Support Facility Indian Head, Maryland. The treatment area consists primarily of silts, sandy clays, and lean clays with TCE concentrations in soil and groundwater of up to 250 mg/kg and 400 mg/L, respectively. Eight hundred reaction columns (consisting of ZVI/sand or oil/sand), were installed 2-3 ft apart, to a depth of 30 ft bgs at the site. Approximately 100 reaction columns were installed per day, with the most productive day totaling 180 columns. During operation, installation time for each reaction column was on the order of 1-2 minutes. Overall, 77,000 lbs of ZVI and 650 gallons of vegetable oil were emplaced within the source area of ~5,000 ft<sup>2</sup>.
+
<references />
  
===Performance Results===
+
==See Also==
Ongoing post installation monitoring of treatment area groundwater has found moderate reductions in TCE in site monitoring wells and that key degradation products that serve as indicators for both abiotic and biotic mechanisms (i.e., acetylene, ethene/ethane) are present. Samples from Continuous Multilevel Tubing (CMT) wells installed within reaction columns (anulus filled with ZVI amendment) have demonstrated 1-3 orders of magnitude reductions in TCE relative to the surrounding formation water (see Figure 5). These results provide evidence that the reaction columns are creating steep concentration gradients that could drive contaminants out of low permeability zones. Further, gaseous products (e.g., propane, propene, i-butane, n-butane, n-pentane, n-hexane) were detected in the unsaturated zone of several reaction columns further supporting abiotic TCE degradation. Results of this full scale project were very promising and, although several operational improvements were identified (e.g., improved pumpability of ZVI/sand mixture; minor equipment modifications; improved site prep practices), the Bomber technology has the potential to be an important remediation alternative for hard-to-treat chlorinated source zones, particularly ones with large, persistent matrix diffusion sources over large areas.
 

Latest revision as of 15:58, 14 April 2026

Estimating PCE/TCE Abiotic First-Order Reductive Dechlorination Rate Constants in Clayey Soils Under Anoxic Conditions

The U.S. Department of Defense (DoD) faces many challenges in restoring aquifers at contaminated sites, often due to back-diffusion of tetrachloroethene (PCE) and trichloroethene (TCE) from low-permeability clay zones. The uptake, storage, and subsequent long-term release of these dissolved contaminants from clays are key processes in understanding the longevity, intensity, and risks associated with many persistent chlorinated ethene groundwater plumes. Although naturally occurring abiotic and biotic dechlorination processes in clays may reduce stored contaminant mass and significantly aid natural attenuation, no standardized field method currently exists to verify or quantify these reactions. It is critical to remediation design efforts to demonstrate and validate a cost-effective in situ approach for assessing these dechlorination processes using first-order rate constants. An approach was developed and applied across eight DoD sites to support Remedial Project Managers (RPMs) and regulators in evaluating natural attenuation potential in clay-rich environments.

Related Article(s):

Contributors: Dani Tran, Dr. Charles Schaefer, Dr. Charles Werth

Key Resource:

  • Schaefer, C.E, Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils (3)

Introduction

Cost-effective methods are needed to verify the occurrence of natural dechlorination processes and quantify their dechlorination rates in clays under ambient in situ conditions in order to reliably predict their long-term influence on plume longevity and mass discharge. However, accurately determining these rates is challenging due to slow reaction kinetics, the transient nature of transformation products, and the interplay of biotic and abiotic mechanisms within the clay matrix or at clay-sand interfaces. Tools capable of quantifying these reactions and assessing their role in mitigating plume persistence would be a significant aid for long-term site management.

For reductive abiotic dechlorination under anoxic conditions, a 1% hydrochloric acid (HCl) extraction of a sample of native clay coupled with X-ray diffraction (XRD) data can be used as a screening level tool to estimate reductive dechlorination rate constants. These rate constants can be inserted into fate and transport models such as REMChlor - MD[1][2] to quantify abiotic dechlorination impacts within clay aquitards on chlorinated solvent plumes. Thus, determination of the abiotic reductive dechlorination rate constant for a particular clayey soil can be readily utilized to provide a more accurate assessment of aquifer cleanup timeframes for groundwater plumes that are being sustained by contaminant back-diffusion.

Recommended Approach

File:TranFig1.png
Figure 1: First-order rate constants for abiotic reductive dechlorination of TCE under anaerobic conditions (data from this study and prior research)
File:TranFig2.png
Figure 2: Flowchart diagram of field screening procedures

The recommended approach builds upon the methodology and findings of a recent study[3], emphasizing field-based and analytical techniques to quantify abiotic first-order reductive dechlorination rate constants for PCE and TCE in clayey soils under anoxic conditions. Key components of this evaluation are listed below:

  1. Zone Identification: The focus of the investigation should be to delineate clayey zones adjacent to hydraulically conductive zones.
  2. Ferrous Mineral Quantification: Assess ferrous mineral context in clay via 1% HCl extraction at ambient temperature over a 10-minute interval.
  3. Mineralogical Characterization: Conduct XRD analysis with the specific intent of identifying the presence of pyrite and biotite.
  4. Reduced Gas Analysis: Measurement of reduced gases such as acetylene, ethene, and ethane concentrations in clay samples. Gas-tight sampling devices (e.g., En Core® soil samplers by En Novative Technologies, Inc.) should be used to ensure sample integrity during collection and transport.

Clay samples should be collected within a few centimeters of the high-permeability interface, with optional additional sampling further inward. For mineralogical analysis, a defined interval may be collected and subsequently subsampled. To preserve sample integrity, exposure to air should be minimized during collection, transport, and handling. Homogenization should occur within an anaerobic chamber, and if subsamples are required for external analysis, they must be shipped in gas-tight, anaerobic containers.

Estimation of the abiotic reductive first-order rate constant for PCE and TCE is based on the “reactive” ferrous content in the clay. Reactive ferrous content (Fe(II)r) is estimated as shown in Equation 1:

Equation 1:       Fe(II)r = DA + XRDpyr - XRDbiotite

where DA is the ferrous content from the dilute acid (1% HCl) extraction, XRDpyr is the pyrite content from XRD analysis, and XRDbiotite is the biotite content from XRD analysis[3].

Abiotic dechlorination is unlikely to contribute to mitigating contaminant back-diffusion when reactive ferrous iron (Fe(II)r) concentrations are below 100 mg/kg (Figure 1). For Fe(II)r above 100 mg/kg, the first-order rate constant for PCE and TCE reductive dechlorination can be estimated using the correlation shown in Figure 1[4][5]. The rate constant exhibits a strong positive correlation with the logarithm of reactive Fe(II) content (Pearson’s r = 0.82), with a slope of 4.7 × 10⁻⁸ L g⁻¹ d⁻¹ (log mg kg⁻¹)⁻¹.

Figure 2 presents a decision flowchart designed to evaluate the significance and extent of abiotic reductive dechlorination. By applying Equation 1 to the dilute acid extractable Fe(II) plus measured mineral species data from clay samples, the reactive ferrous iron content (Fe(II)r) can be quantified, enabling a streamlined assessment of the extent to which abiotic processes are contributing to the mitigation of contaminant back-diffusion.

Study Design Considerations

Diagnostic Resin Treatments

Several commercially available resins have been verified for use in the iTIE system. Investigators can select resins based on stressor classes of interest at each site. Each resin selectively removes a CoC class from site water prior to organism exposure.

  • DuPont Ambersorb 560 for removal of 1,4-dioxane and other organic chemicals[6]
  • C18 for nonpolar organic chemicals
  • Bio-Rad Chelex for metals
  • Granular activated carbon for metals, general organic chemicals, sulfide[7]
  • Waters Oasis HLB for general organic chemicals[8]
  • Waters Oasis WAX for PFAS, organic chemicals of mixed polarity[9]
  • Zeolite for ammonia, other organic chemicals

Resins must be adequately conditioned prior to use. Otherwise, they may inadequately adsorb toxicants or cause stress to organisms. New resins should be tested for efficacy and toxicity before being used in an iTIE system.

Test Organism Species and Life Stages

Practitioners can also select different organism species and life stages for use in the iTIE system, depending on site characteristics and study goals. The iTIE system can accommodate various small test organisms, including embryo-stage fish and most macroinvertebrates. The following common toxicity tests can be adapted for application within iTIE systems[10].

    Freshwater acute toxicity:
    Freshwater chronic toxicity:
    Marine acute toxicity:
    Marine chronic toxicity:
  • Americamysis survival, growth and fecundity
  • Atherinops affinis embryo-larval survival and growth

Acute toxicity is quantifiable via organism survival rates immediately following the termination of an iTIE system field deployment. Chronic toxicity can be quantified by continuing to culture and observe test organisms in-lab. Common chronic endpoints include stunted growth, altered development such as teratogenicity in larval fish, decreased reproduction rates, and changes in gene expression.

Several gene expression endpoints have been detectable in bioassays following an iTIE system deployment and in-lab culturing period. Steigmeyer et al.[8] were able to detect changes in the expression of two genes in D. magna after a 24-hour exposure to bisphenol A. In a separate study, Nichols[11] found a significant decline in acetylcholinesterase activity in H. azteca after a 24-hour exposure to chlorpyrifos. These results indicate a potential to adapt other gene expression bioassays for use in conjunction with iTIE system field exposures to prove stressor-causality linkages.

Cost Effectiveness Study

Burton et al.[12] conducted a cost effectiveness study comparing the iTIE technology with the traditional US EPA Phase 1 TIE method. Comparisons were based on the estimated time required to complete various sub-tasks within each method. Sub-tasks included organism care, equipment preparation, mobilization and deployment, test maintenance, test termination, demobilization, and test termination analyses. It was ultimately estimated that the iTIE protocol requires 47% less time (67 fewer hours) to complete than the Phase 1 TIE method, with the largest time differences in equipment preparation, deployment, test maintenance, and demobilization. It is important to note that the iTIE method may require additional initial costs for equipment and training.

Field Application

Figure 6. iTIES deployment at the Rouge River, Detroit, MI. In the foreground is the iTIE Cooler Sub-System, which contains iTIE resin treatments and test organism groups, as well as the oxygenation coil and sample collection bottles. Next to the iTIE Cooler are the two pump cases. The Trident can be seen above the pump cases, installed in the river channel near shore.

The iTIE system has been successfully deployed at a variety of marine and freshwater sites during the proof-of-concept phase of prototype development. One example is the 2024 iTIE system deployment completed near the mouth of the Rouge River in Detroit, MI (Figure 6). The Rouge River watershed has a long history of industrialization, with a legacy of chemical dumping, channelization, damming, and urban runoff[13]. This has led to degraded environmental conditions, with previous detections of a wide range of chemicals including heavy metals and various organics.

Figure 7. Survival and healthy development of P. promelas embryos and larvae following a 48-hour iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater as embryos for 48 hours and cultured post-exposure for an additional 5 days.
Figure 8. Survival of C. dilutus larvae after an iTIE exposure near the mouth of the Rouge River. Organisms were exposed to site porewater for 48 hours and cultured post-exposure for an additional 5 days. Error bars show standard deviation.

An iTIE system deployment was designed and completed to determine which chemical classes are most responsible for causing toxicity at the site. Resin treatments included glass wool (inert, non-fractionating substance), Chelex (metals sorption), Oasis HLB (general organics sorption), and Oasis WAX (organics sorption, with a high affinity for PFAS). The study utilized fathead minnow (P. promelas) embryos, due to their relative sensitivity to metals and PAHs, as well as second-instar midge (Chironomus dilutus) larvae due to their relative sensitivity to PFAS.

The test organisms were exposed to fractionated porewater in situ for 48 hours. Following exposure, organisms were cultured for an additional five days, and survival was recorded (Figures 7 and 8). Moderate declines in survival were seen in both species in the glass wool treatment, indicating toxicity at the site. For P. promelas, the highest proportion of healthy development occurred in the Chelex treatment, supporting the hypothesis that metals are a dominant cause of toxicity. C. dilutus had the greatest survival in the Oasis WAX treatment, suggesting that an organic stressor class like PFAS is also present at harmful concentrations in the river.

Water chemical analyses of fractionated and unfractionated water samples were completed to support biological results. Analyses were conducted for a range of stressor classes including metals, PAHs, PCBs, an organophosphate pesticide (chlorpyrifos), a PFAS compound (PFOS) and a pyrethroid insecticide (permethrin). Of these analytes, only heavy metals and PFOS were detected. Some chemical classes including PAHs and PCBs were not detected at the site. To reach similar conclusions using traditional Phase 1 TIE methods, one would need to complete the following tests: baseline toxicity, filtration, aeration, EDTA, C18 SPE, and methanol elution of C18 SPE. The iTIE method allows the same conclusions to be drawn with significantly less time and effort required.

Summary

The in situ Toxicity Identification Evaluation technology and protocol is a powerful tool that investigators can use to strengthen causal linkages between chemical stressors and ecological toxicity. By fractionating sampled water and exposing test organisms in situ, investigators can gather toxicity response data while minimizing sample manipulation and accurately representing environmental conditions.

References

  1. ^ Falta, R., and Wang, W., 2017. A semi-analytical method for simulating matrix diffusion in numerical transport models. Journal of Contaminant Hydrology, 197, pp. 39-49. doi: 10.1016/j.jconhyd.2016.12.007  Open Access Manuscript
  2. ^ Kulkarni, P.R., Adamson, D.T., Popovic, J., Newell, C.J., 2022. Modeling a well-charactized perfluorooctane sulfate (PFOS) source and plume using the REMChlor-MD model to account for matrix diffusion. Journal of Contaminant Hydrology, 247, Article 103986. doi: 10.1016/j.jconhyd.2022.103986  Open Access Manuscript
  3. ^ 3.0 3.1 Schaefer, C.E., Tran, D., Nguyen, D., Latta, D.E., Werth, C.J., 2025. Evaluating Mineral and In Situ Indicators of Abiotic Dechlorination in Clayey Soils. Groundwater Monitoring and Remediation, 45(2), pp. 31-39. doi: 10.1111/gwmr.12709
  4. ^ Schaefer, C.E., Ho, P., Berns, E., Werth, C., 2018. Mechanisms for abiotic dechlorination of trichloroethene by ferrous minerals under oxic and anoxic conditions in natural sediments. Environmental Science and Technology, 52(23), pp.13747-13755. doi: 10.1021/acs.est.8b04108
  5. ^ Borden, R.C., Cha, K.Y., 2021. Evaluating the impact of back diffusion on groundwater cleanup time. Journal of Contaminant Hydrology, 243, Article 103889. doi: 10.1016/j.jconhyd.2021  Open Access Manuscript
  6. ^ Woodard, S., Mohr, T., Nickelsen, M.G., 2014. Synthetic media: A promising new treatment technology for 1,4-dioxane. Remediation Journal, 24(4), pp. 27-40. doi: 10.1002/rem.21402
  7. ^ Lemos, B.R.S., Teixeira, I.F., de Mesquita, J.P., Ribeiro, R.R., Donnici, C.L., Lago, R.M., 2012. Use of modified activated carbon for the oxidation of aqueous sulfide. Carbon, 50(3), pp. 1386-1393. doi: 10.1016/j.carbon.2011.11.011
  8. ^ 8.0 8.1 Cite error: Invalid <ref> tag; no text was provided for refs named SteigmeyerEtAl2017
  9. ^ Iannone, A., Carriera, F., Di Fiore, C., Avino, P., 2024. Poly- and Perfluoroalkyl Substance (PFAS) Analysis in Environmental Matrices: An Overview of the Extraction and Chromatographic Detection Methods. Analytica, 5(2), pp. 187-202. doi: 10.3390/analytica5020012  Open Access Article
  10. ^ U.S. Environmental Protection Agency, Office of Solid Waste and Emergency Response, 1994. Catalogue of Standard Toxicity Tests for Ecological Risk Assessment. ECO Update, 2(2), 4 pages. Publication No. 9345.0.05I Free Download  Report.pdf
  11. ^ Nichols, E., 2023. Methods for Identification and Prioritization of Stressors at Impaired Sites. Masters thesis, University of Michigan. University of Michigan Library Deep Blue Documents. Free Download  Report.pdf
  12. ^ Cite error: Invalid <ref> tag; no text was provided for refs named BurtonEtAl2020
  13. ^ Ridgway, J., Cave, K., DeMaria, A., O’Meara, J., Hartig, J. H., 2018. The Rouge River Area of Concern—A multi-year, multi-level successful approach to restoration of Impaired Beneficial Uses. Aquatic Ecosystem Health and Management, 21(4), pp. 398-408. doi: 10.1080/14634988.2018.1528816

See Also