Difference between revisions of "User:Jhurley/sandbox"

From Enviro Wiki
Jump to: navigation, search
(Introduction)
(Introduction)
 
(240 intermediate revisions by the same user not shown)
Line 1: Line 1:
==Transition of Aqueous Film Forming Foam (AFFF) Fire Suppression Infrastructure Impacted by Per and Polyfluoroalkyl Substances (PFAS)==
+
==Assessing Vapor Intrusion (VI) Impacts in Neighborhoods with Groundwater Contaminated by Chlorinated Volatile Organic Chemicals (CVOCs)==  
[[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS)|Per and polyfluoroalkyl substances (PFAS)]] contained in [[wikipedia:Firefighting foam |Class B aqueous film-forming foams (AFFFs)]] are known to accumulate on wetted surfaces of many fire suppression systems after decades of exposure<ref name="LangEtAl2022">Lang, J.R., McDonough, J., Guillette, T.C., Storch, P., Anderson, J., Liles, D., Prigge, R., Miles, J.A.L., Divine, C., 2022. Characterization of per- and polyfluoroalkyl substances on fire suppression system piping and optimization of removal methods. Chemosphere, 308(Part 2), 136254. [https://doi.org/10.1016/j.chemosphere.2022.136254 doi: 10.1016/j.chemosphere.2022.136254]&nbsp;&nbsp;[[Media:LangEtAl2022.pdf | Open Access Article]]</ref>. When replacement PFAS-free firefighting formulations are added to existing infrastructure, PFAS can rebound from the wetted surfaces into the new formulations at high concentrations<ref name="RossStorch2020">Ross, I., and Storch, P., 2020. Foam Transition: Is It as Simple as "Foam Out / Foam In?". The Catalyst (Journal of JOIFF, The International Organization for Industrial Emergency Services Management), Q2 Supplement, 20 pages. [[Media:Catalyst_2020_Q2_Sup.pdf | Industry Newsletter]]</ref><ref>Kappetijn, K., 2023. Replacement of fluorinated extinguishing foam: When is clean clean enough? The Catalyst (Journal of JOIFF, The International Organization for Industrial Emergency Services Management), Q1 2023, pp. 31-33. [[Media:Catalyst_2023_Q1.pdf | Industry Newsletter]]</ref>. Effective methods are needed to properly transition to PFAS-free firefighting formulations in existing fire suppression infrastructure. Considerations in the transition process may include but are not limited to locating, identifying, and evaluating existing systems and AFFF, fire engineering evaluations, system prioritization, cost/downtime analyses, sampling and analysis, evaluation of risks and hazards to human health and the environment, transportation, and disposal.
+
The VI Diagnosis Toolkit<ref name="JohnsonEtAl2020">Johnson, P.C., Guo, Y., Dahlen, P., 2020. The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Mitigating Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes. ESTCP Project ER-201501, Final Report. [https://serdp-estcp.mil/projects/details/a0d8bafd-c158-4742-b9fe-5f03d002af71 Project Website]&nbsp;&nbsp; [//www.enviro.wiki/images/2/28/ER-201501.pdf  Final Report.pdf]</ref> is a set of tools that can be used individually or in combination to assess vapor intrusion (VI) impacts at one or more buildings overlying regional-scale dissolved chlorinated solvent impacted groundwater plumes. The strategic use of these tools can lead to confident and efficient neighborhood-scale VI pathway assessments.
 +
 
 
<div style="float:right;margin:0 0 2em 2em;">__TOC__</div>
 
<div style="float:right;margin:0 0 2em 2em;">__TOC__</div>
  
 
'''Related Article(s):'''
 
'''Related Article(s):'''
*[[Perfluoroalkyl and Polyfluoroalkyl Substances (PFAS)]]
+
 
*[[PFAS Sources]]
+
*[[Vapor Intrusion (VI)]]
*[[PFAS Ex Situ Water Treatment]]
+
*[[Vapor Intrusion – Sewers and Utility Tunnels as Preferential Pathways]]
*[[Supercritical Water Oxidation (SCWO)]]
 
*[[PFAS Treatment by Electrical Discharge Plasma]]
 
  
 
'''Contributor(s):'''  
 
'''Contributor(s):'''  
*Dr. Johnsie Ray Lang
+
 
*Dr. Jonathan Miles
+
*Paul C. Johnson, Ph.D.
*John Anderson
+
*Paul Dahlen, Ph.D.
*Dr. Theresa Guillette
+
*Yuanming Guo, Ph.D.
*[[Craig E. Divine, Ph.D., PG|Dr. Craig Divine]]
 
*[[Dr. Stephen Richardson]]
 
  
 
'''Key Resource(s):'''
 
'''Key Resource(s):'''
*Department of Defense (DoD) performance standard for PFAS-free firefighting formulation:  [https://media.defense.gov/2023/Jan/12/2003144157/-1/-1/1/MILITARY-SPECIFICATION-FOR-FIRE-EXTINGUISHING-AGENT-FLUORINE-FREE-FOAM-F3-LIQUID-CONCENTRATE-FOR-LAND-BASED-FRESH-WATER-APPLICATIONS.PDF Military Specification MIL-PRF-32725]<ref name="DoD2023">US Department of Defense, 2023. Performance Specification for Fire Extinguishing Agent, Fluorine-Free Foam (F3) Liquid Concentrate for Land-Based, Fresh Water Applications. Mil-Spec MIL-PRF-32725, 18 pages. [[Media: MilSpec32725.pdf | Military Specification Document]]</ref>
+
 
*[[Media:LangEtAl2022.pdf | Characterization of per- and polyfluoroalkyl substances on fire suppression system piping and optimization of removal methods]]<ref name="LangEtAl2022"/>
+
*The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes, ESTCP Project ER-201501, Final Report<ref name="JohnsonEtAl2020" />
 +
 
 +
*CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment, ESTCP Project ER-201501, Technical Report<ref name="JohnsonEtAl2021">Johnson, P.C., Guo, Y., Dahlen, P., 2021.  CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment. ESTCP ER-201501, Technical Report. [https://serdp-estcp.mil/projects/details/a0d8bafd-c158-4742-b9fe-5f03d002af71 Project Website]&nbsp;&nbsp; [//www.enviro.wiki/images/c/c7/ER-201501_Technical_Report.pdf  Technical_Report.pdf]</ref>
 +
 
 +
*VI Diagnosis Toolkit User Guide, ESTCP Project ER-201501<ref name="JohnsonEtAl2022">Johnson, P.C., Guo, Y., and Dahlen, P., 2022. VI Diagnosis Toolkit User Guide, ESTCP ER-201501, User Guide. [https://serdp-estcp.mil/projects/details/a0d8bafd-c158-4742-b9fe-5f03d002af71 Project Website]&nbsp;&nbsp; [//www.enviro.wiki/images/2/22/ER-201501_User_Guide.pdf  User_Guide.pdf]</ref>
  
 
==Introduction==
 
==Introduction==
[[File:LangFig1.png | thumb |400px|Figure 1. (A) Schematic of a typical PFAS molecule demonstrating the hydrophobic fluorinated tail in green and the hydrophilic charged functional group in blue, (B) a PFAS bilayer formed with the hydrophobic tails facing inward and the charged functional groups on the outside, and (C) multiple bilayers of PFAS assembled on the wetted surfaces of fire suppression piping.]]PFAS are a class of synthetic fluorinated compounds which are highly mobile and persistent within the environment<ref>Giesy, J.P., Kannan, K., 2001. Global Distribution of Perfluorooctane Sulfonate in Wildlife. Environmental Science and Technology 35(7), pp. 1339-1342. [https://doi.org/10.1021/es001834k doi: 10.1021/es001834k]</ref>. Due to the surfactant properties of PFAS, these compounds self-assemble at any solid-liquid interface forming resilient bilayers during prolonged exposure<ref>Krafft, M.P., Riess, J.G., 2015. Selected physicochemical aspects of poly- and perfluoroalkylated substances relevant to performance, environment and sustainability-Part one. Chemosphere, 129, pp. 4-19. [https://doi.org/10.1016/j.chemosphere.2014.08.039 doi: 10.1016/j.chemosphere.2014.08.039]</ref>. Solid phase accumulation of PFAS has been proposed to be influenced by both [[wikipedia: Hydrophobic effect|hydrophobic]] and electrostatic interactions with fluorinated carbon chain length as the dominant feature influencing sorption<ref>Higgins, C.P., Luthy, R.G., 2006. Sorption of Perfluorinated Surfactants on Sediments. Environmental Science and Technology, 40(23), pp. 7251-7256. [https://doi.org/10.1021/es061000n doi: 10.1021/es061000n]</ref>. While the majority of previous research into solid phase sorption typically focused on water treatment applications or subsurface porous media<ref>Brusseau, M.L., 2018. Assessing the Potential Contributions of Additional Retention Processes to PFAS Retardation in the Subsurface. Science of the Total Environment, 613-614, pp. 176-185. [https://doi.org/10.1016/j.scitotenv.2017.09.065 doi: 10.1016/j.scitotenv.2017.09.065]&nbsp;&nbsp;[https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5693257Open Access Manuscript]</ref>, recently PFAS accumulations have been demonstrated on the wetted surfaces of fire suppression infrastructure exposed to aqueous film forming foam (AFFF)<ref name="LangEtAl2022"/> (see Figure 1).
+
Most federal, state, and local regulatory guidance for assessing and mitigating the [[Vapor Intrusion (VI) | vapor intrusion]] pathway reflects USEPA’s ''Technical Guide for Assessing and Mitigating the Vapor Intrusion Pathway from Subsurface Vapor Sources to Indoor Air''<ref name="USEPA2015">USEPA, 2015. OSWER Technical Guide for Assessing and Mitigating the Vapor Intrusion Pathway from Subsurface Vapor Sources to Indoor Air. U.S. Environmental Protection Agency, Office of Solid Waste and Emergency Response, OSWER Publication No. 9200.2-154, 267 pages. [https://www.epa.gov/vaporintrusion/technical-guide-assessing-and-mitigating-vapor-intrusion-pathway-subsurface-vapor USEPA Website]&nbsp;&nbsp; [//www.enviro.wiki/images/0/06/USEPA2015.pdf  Report.pdf]</ref>. The paradigm outlined by that guidance includes: 1) a preliminary and mostly qualitative analysis that looks for site conditions that suggest vapor intrusion might occur (e.g., the presence of vapor-forming chemicals in close proximity to buildings); 2) a multi-step and more detailed quantitative screening analysis that involves site-specific data collection and their comparison to screening levels to identify buildings of potential VI concern; and 3) selection and design of mitigation systems or continued monitoring, as needed. With respect to (2), regulatory guidance typically recommends consideration of “multiple lines of evidence” in decision-making<ref name="USEPA2015" /><ref>NJDEP, 2021. Vapor Intrusion Technical Guidance, Version 5.0. New Jersey Department of Environmental Protection, Trenton, NJ. [https://dep.nj.gov/srp/guidance/vapor-intrusion/vig/ Website]&nbsp;&nbsp; [//www.enviro.wiki/images/e/ee/NJDEP2021.pdf Guidance Document.pdf]</ref>, with typical lines-of-evidence being groundwater, soil gas, sub-slab soil gas, and/or indoor air concentrations. Of those, soil gas measurements and/or measured short-term indoor air concentrations can be weighted heavily, and therefore decision making might not be completed without them. Effective evaluation of VI risk from sub-slab and/or soil gas measurements would require an unknown building-specific attenuation factor, but there is also uncertainty as to whether or not indoor air data is representative of maximum and/or long-term average indoor concentrations. Indoor air data can be confounded by indoor contaminant sources because the number of samples is typically small, indoor concentrations can vary with time, and because a number of household products can emit the chemicals being measured. When conducting VI pathway assessments in neighborhoods where it is impractical to assess all buildings, the EPA recommends following a “worst first” investigational approach.  
     
 
Fire suppression systems with potential PFAS impacts include fire fighting vehicles that carried AFFF and fixed suppression systems in buildings containing large amounts of flammable materials such as aircraft hangars (Figure 2). PFAS residue on the wetted surfaces of existing infrastructure can rebound into replacement PFAS-free firefighting formulations if not removed during the transition process<ref name="RossStorch2020"/>. Simple surface rinsing with water and low-pressure washing has been proven to be inefficient for removal of surface bound PFAS from piping and tanks that contained fluorinated AFFF<ref name="RossStorch2020"/>
 
[[File:LangFig2.png | thumb|left|600px|Figure 2. Fixed fire suppression system for an aircraft hangar, with storage tank on left and distribution piping on right.]]
 
  
In&nbsp;addition&nbsp;to&nbsp;proper methods for system cleaning to remove residual PFAS, transition to PFAS-free foam may also include consideration of compliance with state and federal regulations, selection of the replacement PFAS free firefighting formulation, a cost benefit analysis for replacement of the system components versus cleaning, and PFAS verification testing. Foam transition should be completed in a manner which minimizes the volume of waste generated as well as preventing any PFAS release into the environment.
+
The limitations of this approach, as practiced, are the following:
  
==PFAS Assembly on Solid Surfaces==
+
*Decisions are rarely made without indoor air data and generally, seasonal sampling is required, delaying decision making.
The self-assembly of [[Wikipedia: Amphiphile | amphiphilic]] molecules into supramolecular bilayers is a result of their structure and how it interacts with the bulk water of a solution. Single chain hydrocarbon based amphiphiles can form [[Wikipedia: Micelle | micelles]] under relatively dilute aqueous concentrations, however for hydrocarbon based surfactants the formation of more complex organized system such as [[Wikipedia: Vesicle (biology and chemistry) | vesicles]] is rarely seen, requiring double chain amphiphiles such as phospholipids. Associations of single chain cationic and anionic hydrocarbon based amphiphiles into stable supramolecular structures such as vesicles has however been demonstrated<ref>Fukuda, H., Kawata, K., Okuda, H., 1990. Bilayer-Forming Ion-Pair Amphiphiles from Single-Chain Surfactants. Journal of the American Chemical Society, 112(4), pp. 1635-1637. [https://doi.org/10.1021/ja00160a057 doi: 10.1021/ja00160a057]</ref>, with the ion pairing of the polar head groups mimicking the a double tail situation. The behavior of single chain fluorosurfactant amphiphiles has been demonstrated to be significantly different from similar hydrocarbon based analogues. Not only are [[Wikipedia: Critical micelle concentration | critical micelle concentrations (CMC)]] of fluorosurfactants typically two orders of magnitude lower than corresponding hydrocarbon surfactants but self-assembly can occur even when fluorosurfactants are dispersed at low concentrations significantly below the CMC in water and other solvents<ref name="Krafft2006">Krafft, M.P., 2006. Highly fluorinated compounds induce phase separation in, and nanostructuration of liquid media. Possible impact on, and use in chemical reactivity control. Journal of Polymer Science Part A: Polymer Chemistry, 44(14), pp. 4251-4258. [https://doi.org/10.1002/pola.21508 doi: 10.1002/pola.21508]&nbsp;&nbsp;[[Media:Krafft2006.pdf | Open Access Article]]</ref>. The assembly of fluorinated amphiphiles structurally similar to those found in AFFF have been shown to readily form stable, complex structures including vesicles, fibers, and globules at concentrations as low as 0.5% w/v in contrast to their hydrocarbon analogues which remained fluid at 30% w/v<ref>Krafft, M.P., Guilieri, F., Riess, J.G., 1993. Can Single-Chain Perfluoroalkylated Amphiphiles Alone form Vesicles and Other Organized Supramolecular Systems? Angewandte Chemie International Edition in English, 32(5), pp. 741-743. [https://doi.org/10.1002/anie.199307411 doi: 10.1002/anie.199307411]</ref><ref name="KrafftEtAl_1994">Krafft, M.P., Guilieri, F., Riess, J.G., 1994. Supramolecular assemblies from single chain perfluoroalkylated phosphorylated amphiphiles. Colloids and Surfaces A: Physicochemical and Engineering Aspects, 84(1), pp. 113-119. [https://doi.org/10.1016/0927-7757(93)02681-4 doi: 10.1016/0927-7757(93)02681-4]</ref>.  
+
*The collection of a robust indoor air data set that adequately characterizes long term indoor air concentrations could take years given the typical frequency of data collection and the most common methods of sample collection (e.g., 24-hour samples).  Therefore, indoor air sampling might continue indefinitely at some sites.
 +
*The “worst first” buildings might not be identified correctly by the logic outlined in USEPA’s 2015 guidance and the most impacted buildings might not even be located over a groundwater plume. Recent studies have shown [[Vapor Intrusion – Sewers and Utility Tunnels as Preferential Pathways |VI impacts in homes as a result of sewer and other subsurface piping connections]], which are not explicitly considered nor easily characterized through conventional VI pathway assessment<ref> Beckley, L, McHugh, T., 2020. A Conceptual Model for Vapor Intrusion from Groundwater Through Sewer Lines. Science of the Total Environment, 698, Article 134283. [https://doi.org/10.1016/j.scitotenv.2019.134283 doi: 10.1016/j.scitotenv.2019.134283]&nbsp;&nbsp; [//www.enviro.wiki/images/4/4e/BeckleyMcHugh2020.pdf  Open Access Article]</ref><ref name="GuoEtAl2015">Guo, Y., Holton, C., Luo, H., Dahlen, P., Gorder, K., Dettenmaier, E., Johnson, P.C., 2015. Identification of Alternative Vapor Intrusion Pathways Using Controlled Pressure Testing, Soil Gas Monitoring, and Screening Model Calculations. Environmental Science and Technology, 49(22), pp. 13472–13482. [https://doi.org/10.1021/acs.est.5b03564 doi: 10.1021/acs.est.5b03564]</ref><ref name="McHughEtAl2017">McHugh, T., Beckley, L., Sullivan, T., Lutes, C., Truesdale, R., Uppencamp, R., Cosky, B., Zimmerman, J., Schumacher, B., 2017. Evidence of a Sewer Vapor Transport Pathway at the USEPA Vapor Intrusion Research Duplex.  Science of the Total Environment, pp. 598, 772-779. [https://doi.org/10.1016/j.scitotenv.2017.04.135 doi: 10.1016/j.scitotenv.2017.04.135]&nbsp;&nbsp; [//www.enviro.wiki/images/6/63/McHughEtAl2017.pdf Open Access Manuscipt]</ref><ref name="McHughBeckley2018">McHugh, T., Beckley, L., 2018. Sewers and Utility Tunnels as Preferential Pathways for Volatile Organic Compound Migration into Buildings: Risk Factors and Investigation Protocol. ESTCP ER-201505, Final Report. [https://serdp-estcp.mil/projects/details/f12abf80-5273-4220-b09a-e239d0188421 Project Website]&nbsp;&nbsp; [//www.enviro.wiki/images/5/55/2018b-McHugh-ER-201505_Conceptual_Model.pdf  Final Report.pdf]</ref><ref name="RiisEtAl2010">Riis, C., Hansen, M.H., Nielsen, H.H., Christensen, A.G., Terkelsen, M., 2010. Vapor Intrusion through Sewer Systems: Migration Pathways of Chlorinated Solvents from Groundwater to Indoor Air. Seventh International Conference on Remediation of Chlorinated and Recalcitrant Compounds, May, Monterey, CA. Battelle Memorial Institute. ISBN 978-0-9819730-2-9. [https://www.battelle.org/conferences/battelle-conference-proceedings Website]&nbsp;&nbsp; [//www.enviro.wiki/images/9/95/2010-Riis-Migratioin_pathways_of_Chlorinated_Solvents.pdf  Report.pdf]</ref>.
 +
*The presumptive remedy for VI mitigation (sub-slab depressurization) may not be effective for all VI scenarios (e.g., those involving vapor migration to indoor spaces via sewer connections).
 +
 +
The '''VI Diagnosis Toolkit''' components were developed considering these limitations as well as more recent knowledge gained through research, development, and validation projects funded by SERDP and ESTCP.
  
Krafft found that fluorinated amphiphiles formed bilayer membranes with phospholipids, and that the resulting vesicles were more stable than those made of phospholipids alone<ref name="KrafftEtAl_1998">Krafft, M.P., Riess, J.G., 1998. Highly Fluorinated Amphiphiles and Collodial Systems, and their Applications in the Biomedical Field. A Contribution. Biochimie, 80(5-6), pp. 489-514. [https://doi.org/10.1016/S0300-9084(00)80016-4 doi: 10.1016/S0300-9084(00)80016-4]</ref>. The similarities in amphiphilic properties between phospholipids and the hydrocarbon-based surfactants in AFFF suggests that bilayer vesicles may form between these and the fluorosurfactants also present in the concentrate. Krafft demonstrated that both the permeability of resulting mixed vesicles and their propensity to fuse with each other at increasing ionic strength was reduced as a result of the creation of an inert hydrophobic and lipophobic film within the membrane, and also suggested that the fluorinated amphiphiles increased [[Wikipedia: van der Waals force | van der Waals interactions]] in the hydrocarbon region<ref name="KrafftEtAl_1998"/>. Thus this low permeability may allow vesicles formed by the surfactants present in AFFF to act as long term repositories of PFAS not only as part of the bilayer itself but also solvated within the vesicle. This prediction is supported by the observation that supramolecular structures formed from single chain fluorinated amphiphiles have been demonstrated to be stable at elevated temperature (15 min at 121&deg;C) and have been shown to be stable over periods of months, even increasing in size over time when stored at environmentally relevant temperatures<ref name="KrafftEtAl_1994"/>.
+
==The VI Diagnosis Toolkit Components==
 +
[[File:DahlenFig1.png|thumb|450px|Figure 1. Vapor intrusion pathway conceptualization considering “alternate VI pathways”, including “pipe flow
 +
VI” and “sewer VI” pathways<ref name="JohnsonEtAl2020" />.]]
 +
The primary components of the VI Diagnosis Toolkit and their uses include:
  
Formation of complex structures at relatively low solute concentrations requires the monomer molecules to be well ordered to maintain tight packing in the supramolecular structure<ref>Ringsdorf, H., Schlarb, B., Venzmer, J., 1988. Molecular Architecture and Function of Polymeric Oriented Systems: Models for the Study of Organization, Surface Recognition, and Dynamics of Biomembranes. Angewandte Chemie International Edition in English, 27(1), pp. 113-158. [https://doi.org/10.1002/anie.198801131 doi: 10.1002/anie.198801131]</ref>. This order results from electrostatic forces, hydrogen bonding, and in the case of fluorinated amphiphiles, hydrophobic interactions. The geometry of the amphiphile also potentially contributes to the type of supramolecular aggregation<ref>Israelachvili, J.N., Mitchell, D.J., Ninham, B.W., 1976. Theory of Self-Assembly of Hydrocarbon Amphiphiles into Micelles and Bilayers. Journal of the Chemical Society, Faraday Transactions 2: Molecular and Chemical Physics, 72, pp. 1525-1568. [https://doi.org/10.1039/F29767201525 doi: 10.1039/F29767201525]</ref>. Surfactants which adopt a conical shape (such as a typical hydrocarbon based surfactant with a large polar head group and a single alkyl chain as a tail) tend to form micelles more easily. Increasing the bulk of the tail makes the surfactant more cylindrically shaped which makes assembly into bilayers more likely.  
+
*'''External VI source strength screening''' to identify buildings most likely to be impacted by VI at levels warranting building-specific testing.
 +
*'''Indoor air source screening''' to locate and remove indoor air sources that might confound building specific VI pathway assessment.
 +
*'''Controlled pressurization method (CPM)''' testing to quickly (in a few days or less) measure the worst-case indoor air impact likely to be caused by VI under natural conditions in specific buildings. CPM tests can also be used to identify the presence of indoor air sources and diagnose active VI pathways.
 +
*'''Passive indoor sampling''' for determining long-term average indoor air concentrations under natural VI conditions and/or for verifying mitigation system effectiveness in buildings that warrant VI mitigation.
 +
*'''Comprehensive VI conceptual model development and refinement''' to ensure that appropriate monitoring, investigation, and mitigation strategies are being selected (Figure 1).
  
Perfluoroalkyl chains are significantly more bulky than their hydrocarbon based analogues both in cross sectional area (28-30 Å<sup>2</sup> versus 20 Å<sup>2</sup>, respectively) and mean volume (CF<sub>2</sub> and CF<sub>3</sub> estimated as 38 Å<sup>3</sup> and 92 Å<sup>3</sup> compared to 27 Å<sup>3</sup> and 54 Å<sup>3</sup> for CH<sub>2</sub> and CH<sub>3</sub>)<ref name="KrafftEtAl_1998"/><ref name="Krafft2006"/>. Structural studies on linear PFOS have shown that the molecule adopts an unusual helical structure<ref>Erkoç, Ş., Erkoç, F., 2001. Structural and electronic properties of PFOS and LiPFOS. Journal of Molecular Structure: THEOCHEM, 549(3), pp. 289-293. [https://doi.org/10.1016/S0166-1280(01)00553-X doi:10.1016/S0166-1280(01)00553-X]</ref><ref name="TorresEtAl2009">Torres, F.J., Ochoa-Herrera, V., Blowers, P., Sierra-Alvarez, R., 2009. Ab initio study of the structural, electronic, and thermodynamic properties of linear perfluorooctane sulfonate (PFOS) and its branched isomers. Chemosphere 76(8), pp. 1143-1149. [https://doi.org/10.1016/j.chemosphere.2009.04.009 doi: 10.1016/j.chemosphere.2009.04.009]</ref> in aqueous and solvent phases to alleviate steric hindrance. This arrangement results from the carbon chain starting in the planar all anti conformation and then successively twisting all the CC-CC dihedrals by 15&deg;-20&deg; in the same direction<ref>Abbandonato, G., Catalano, D., Marini, A., 2010. Aggregation of Perfluoroctanoate Salts Studied by <sup>19</sup>F NMR and DFT Calculations: Counterion Complexation, Poly(ethylene glycol) Addition, and Conformational Effects. Langmuir 26(22), pp. 16762-16770. [https://doi.org/10.1021/la102578k  doi: 10.1021/la102578k].</ref>. The conformation also minimizes the electrostatic repulsion between fluorine atoms bonded to the same side of the carbon backbone by maximizing the interatomic distances between them<ref name="TorresEtAl2009"/>.
+
Expanded discussions for each of these are given below.
  
A consequence of the helical structure is that there is limited carbon-carbon bond rotation within the perfluoroalkyl chain giving them increased rigidity compared to alkyl chains<ref>Barton, S.W., Goudot, A., Bouloussa, O., Rondelez, F., Lin, B., Novak, F., Acero, A., Rice, S., 1992. Structural transitions in a monolayer of fluorinated amphiphile molecules. The Journal of Chemical Physics, 96(2), pp. 1343-1351. [https://doi.org/10.1063/1.462170 doi: 10.1063/1.462170]</ref>. The bulkiness of the perfluoroalkyl chain confers a cylindrical shape on the fluorosurfactant amphiphile and therefore favors the formation of bilayers and vesicles the aggregation of which is further assisted by the rigidity of the molecules which allow close packing in the supramolecular structure. Fluorosurfactants therefore cannot be regarded as more hydrophobic analogues of hydrogenated surfactants. Their self-assembly behavior is characterized by a strong tendency to form vesicles and lamellar phases rather than micelles, due to the bulkiness and rigidity of the perfluoroalkyl chain that tends to decrease the curvature of the aggregates they form in solution<ref>Barton, C.A., Butler, L.E., Zarzecki, C.J., Flaherty, J., Kaiser, M., 2006. Characterizing Perfluorooctanoate in Ambient Air near the Fence Line of a Manufacturing Facility: Comparing Modeled and Monitored Values. Journal of the Air and Waste Management Association, 56, pp. 48-55. [https://doi.org/10.1080/10473289.2006.10464429 doi: 10.1080/10473289.2006.10464429]&nbsp;&nbsp;[https://www.tandfonline.com/doi/epdf/10.1080/10473289.2006.10464429?needAccess=true Open Access Article]</ref>. The larger tail cross section of fluorinated compared to hydrogenated amphiphiles tends to favor the formation of aggregates with lesser surface curvature, therefore rather than micelles they form bilayer membranes, vesicles, tubules and fibers<ref>Krafft, M.P., Guilieri, F., Riess, J.G., 1993. Can Single-Chain Perfluoroalkylated Amphiphiles Alone form Vesicles and Other Organized Supramolecular Systems? Angewandte Chemie International Edition in English, 32(5), pp. 741-743. [https://doi.org/10.1002/anie.199307411 doi: 10.1002/anie.199307411]</ref><ref>Furuya, H., Moroi, Y., Kaibara, K., 1996. Solid and Solution Properties of Alkylammonium Perfluorocarboxylates. The Journal of Physical Chemistry, 100(43), pp. 17249-17254[https://doi.org/10.1021/jp9612801 doi: 10.1021/jp9612801]</ref><ref>Giulieri, F., Krafft, M.P., 1996. Self-organization of single-chain fluorinated amphiphiles with fluorinated alcohols. Thin Solid Films, 284-285, pp. 195-199. [https://doi.org/10.1016/S0040-6090(95)08304-9 doi: 10.1016/S0040-6090(95)08304-9]</ref><ref>Gladysz, J.A., Curran, D.P., Horvath, I.T., 2004. Handbook of Fluorous Chemistry. WILEY-VCH Verlag GmbH & Co. KGaA,, Weinheim, Germany. ISBN: 3-527-30617-X</ref>. Rojas ''et al.'' (2002) demonstrated that perfluorooctyl sulphonamide formed a contiguous bilayer at 50 mg/L with self-assembled aggregates present at concentrations as low as 10 mg/L<ref name="RojasEtAl2002">Rojas, O.J., Macakova, L., Blomberg, E., Emmer, A., and Claesson, P.M., 2002. Fluorosurfactant Self-Assembly at Solid/Liquid Interfaces. Langmuir, 18(21), pp. 8085-8095. [https://doi.org/10.1021/la025989c doi: 10.1021/la025989c]</ref>.     
+
'''External VI source strength screening''' identifies those buildings that warrant more intrusive building-specific assessments, using data collected exterior to the buildings. The use of groundwater and/or soil gas concentration data for building screening has been part of VI pathway assessments for some time and their use is discussed in many regulatory guidance documents. Typically, the measured concentrations are compared to relevant screening levels derived via modeling or empirical analyses from indoor air concentrations of concern.   
  
==Thermodynamics of PFAS Accumulations on Solid Surfaces==
+
More recently it has been discovered that VI impacts can occur via sewer and other subsurface piping connections in areas where vapor migration through the soil would not be expected to be significant, and this could also occur in buildings that do not sit over contaminated groundwater<ref name="RiisEtAl2010" /><ref name="GuoEtAl2015" /><ref name="McHughEtAl2017" /><ref name="McHughBeckley2018" />.  
The thermodynamics of formation of amphiphiles into supramolecular species requires consideration of both hydrophobic and hydrophilic interactions resulting from the amphoteric nature of the molecule. The hydrophilic portions of the molecule are driven to maximize their solvation interaction with as many water molecules as possible, whereas the hydrophobic portions of the molecule are driven to aggregate together thus minimizing interaction with the bulk water. Both of these processes change the enthalpy and entropy of the system.
 
  
In aqueous solution, the hydrophilic portions of an amphiphile form hydrogen bonds (4 - 120 kJ/mol) and van der Waals interactions (<5 kJ/mol) with water molecules and surfaces, and electrostatic interactions (5 – 300 kJ/mol) can also occur where the amphiphile is ionic<ref name="LombardoEtAl2015">Lombardo, D., Kiselev, M.A., Magazù, S., Calandra, P., 2015. Amphiphiles Self-Assembly: Basic Concepts and Future Perspectives of Supramolecular Approaches. Advances in Condensed Matter Physics, vol. 2015, article ID 151683, 22 pages. [https://doi.org/10.1155/2015/151683 doi: 10.1155/2015/151683]&nbsp;&nbsp;[[Media: LombardoEtAl2015.pdf | Open Access Article]]</ref>. These interactions, although weak compared to intramolecular covalent bonds within a molecule are energetically favorable and increase the enthalpy of the combined solute-solvent system. Thus, the hydrophilic portion of an amphiphile will look to maximize enthalpic gain through hydrogen bond interactions with the bulk water.
+
Therefore, in addition to groundwater and soil gas sampling, external data collection that includes and extends beyond the area of concern should include manhole vapor sampling (e.g., sanitary sewer, storm sewer, land-drain). Video surveys from sanitary sewers, storm sewers, and/or land-drains can also be used to identify areas of groundwater leakage into utility corridors and lateral connections to buildings that are conduits for vapor transport. During these investigations, it is important to recognize that utility corridors can transmit both impacted water and vapors beyond groundwater plume boundaries, so extending investigations into areas adjacent to groundwater plume boundaries is necessary.
  
The hydrophobic portion of an amphiphile cannot form hydrogen bonds with the bulk solution, and its presence disrupts the hydrogen bond interactions between individual water molecules within the bulk water matrix. This disruption lowers the entropy of the system by reducing the degrees of translational rotational freedom available to the bulk water. The second law of thermodynamics dictates that a system will arrange itself to maximize its entropy. With hydrophobic species this can be achieved by their spontaneous aggregation, as the reduction in solution entropy of the aggregated system is less than that which would occur if the component parts were solvated individually. These hydrophobic and hydrophilic interactions are weak, and the individual entropy gain per amphiphile upon aggregation is very small. However, taken together the overall effect on the entropy of the aggregate is sufficient to maintain it in solution, and moreover these interactions make the aggregates resistant to minor perturbations while retaining the reversibility of the self-assembled structure<ref name="LombardoEtAl2015"/>.
+
Using projected indoor air concentrations from modeling and empirical data analyses, and distance screening approaches, external source screening can identify areas and buildings that can be ruled out, or conversely, those that warrant building-specific testing.  
  
==Regulatory Drivers for Transition to PFAS Free Firefighting Formulations==
+
Demonstration of neighborhood-scale external VI source screening using groundwater, depth, sewer, land drain, and video data is documented in the ER-201501 final report<ref name="JohnsonEtAl2020" />.  
Regulations restricting the use and release of PFAS are being proposed and promulgated worldwide, with several enacted regulations addressing the use of aqueous film forming foams (AFFF) containing PFAS<ref name="Queensland2016">Queensland (Australia) Department of Environment and Heritage Protection, 2016. Operational Policy - Environmental Management of Firefighting Foam. 16 pages. [https://environment.des.qld.gov.au/assets/documents/regulation/firefighting-foam-policy.pdf Free Download]</ref><ref>U.S. Congress, 2019. S.1790 - National Defense Authorization Act for Fiscal Year 2020. United States Library of Congress.&nbsp;&nbsp;[https://www.congress.gov/bill/116th-congress/senate-bill/1790 Text and History of Law].</ref><ref>Arizona State Legislature, 2019. Title 36, Section 1696. Firefighting foam; prohibited uses; exception; definitions. [https://www.azleg.gov/viewdocument/?docName=https://www.azleg.gov/ars/36/01696.htm Text of Law]</ref><ref>California Legislature, 2020. Senate Bill No. 1044, Chapter 308, Firefighting equipment and foam: PFAS chemicals. [https://leginfo.legislature.ca.gov/faces/billTextClient.xhtml?bill_id=201920200SB1044 Text and History of Law]</ref><ref>Arkansas General Assembly, 2021. An Act Concerning the Use of Certain Chemicals in Firefighting Foam; and for Other Purposes. Act 315, State of Arkansas. [https://trackbill.com/bill/arkansas-house-bill-1351-concerning-the-use-of-certain-chemicals-in-firefighting-foam/2008913/ Text and History of Law].</ref><ref>Espinosa, Summers, Kelly, J., Statler, Hansen, Young, 2021. Amendment to Fire Prevention and Control Act. House Bill 2722. West Virginia Legislature. [https://trackbill.com/bill/west-virginia-house-bill-2722-prohibiting-the-use-of-class-b-fire-fighting-foam-for-testing-purposes-if-the-foam-contains-a-certain-class-of-fluorinated-organic-chemicals/2047674/ Text and History of Law]</ref><ref>Louisiana Legislature, 2021. Act No. 232. [https://trackbill.com/bill/louisiana-house-bill-389-fire-protect-fire-marshal-provides-relative-to-the-discharge-or-use-of-class-b-fire-fighting-foam-containing-fluorinated-organic-chemicals/2092535/  Text and History of Law]</ref><ref>Vermont Legislature, 2021b. Act No. 36, PFAS in Class B Firefighting Foam. [https://trackbill.com/bill/vermont-senate-bill-20-an-act-relating-to-restrictions-on-perfluoroalkyl-and-polyfluoroalkyl-substances-and-other-chemicals-of-concern-in-consumer-products/1978963/  History and Text of Law]</ref>. In addition to regulated usage, firefighting formulation users are transitioning to PFAS-free firefighting formulations to reduce environmental liability in the event of a release, to reduce the cost of expensive containment systems and management of generated waste streams, and to avoid reputational damage. In 2016, Queensland, Australia was one of the first governments to ban PFAS use in firefighting foam<ref name="Queensland2016"/>. The US 2020 National Defense Authorization Act specifies immediate prohibition of controlled releases of AFFF containing PFAS and requires the Secretary of the Navy to publish a specification for PFAS-free firefighting formulation use and ensure it is available for use by the Department of Defense (DoD) by October 1, 2023<ref>U.S. Congress, 2021. S.2792 - National Defense Authorization Act for Fiscal Year 2021. United States Library of Congress.&nbsp;&nbsp;[https://www.congress.gov/bill/117th-congress/senate-bill/2792/ Text and History of Law].</ref>. The National Fire Protection Association (NFPA) recently removed the requirement for AFFF containing PFAS from their Standard on Aircraft Hangars and added two new chapters to allow users to determine if AFFF containing PFAS is needed at their facility<ref name="NFPA2022">National Fire Protection Association (NFPA), 2022. Codes and Standards, 409: Standard on Aircraft Hangars. [https://www.nfpa.org/codes-and-standards/4/0/9/409?l=42 NFPA Website]</ref>.
 
  
==Selection of Replacement PFAS Free Firefighting Formulations==       
+
'''Indoor air source screening''' seeks to locate and remove indoor air sources<ref>Doucette, W.J., Hall, A.J., Gorder, K.A., 2010. Emissions of 1,2-Dichloroethane from Holiday Decorations as a Source of Indoor Air Contamination. Ground Water Monitoring and Remediation, 30(1), pp. 67-73. [https://doi.org/10.1111/j.1745-6592.2009.01267.x doi: 10.1111/j.1745-6592.2009.01267.x] </ref> that might confound building specific VI pathway assessment. Visual inspections and written surveys might or might not identify significant indoor air sources, so these should be complemented with use of portable analytical instruments<ref>McHugh, T., Kuder, T., Fiorenza, S., Gorder, K., Dettenmaier, E., Philp, P., 2011. Application of CSIA to Distinguish Between Vapor Intrusion and Indoor Sources of VOCs. Environmental Science and Technology, 45(14), pp. 5952-5958. [https://doi.org/10.1021/es200988d doi: 10.1021/es200988d]</ref><ref name="BeckleyEtAl2014">Beckley, L., Gorder, K., Dettenmaier, E., Rivera-Duarte, I., McHugh, T., 2014. On-Site Gas Chromatography/Mass Spectrometry (GC/MS) Analysis to Streamline Vapor Intrusion Investigations. Environmental Forensics, 15(3), pp. 234–243. [https://doi.org/10.1080/15275922.2014.930941 doi: 10.1080/15275922.2014.930941]</ref>.
Since they first entered the market in the 2000s, the operational capabilities of PFAS free firefighting formulations have grown<ref>Allcorn, M., Bluteau, T., Corfield, J., Day, G., Cornelsen, M., Holmes, N.J.C., Klein, R.A., McDowall, J.G., Olsen, K.T., Ramsden, N., Ross, I., Schaefer, T.H., Weber, R., Whitehead, K., 2018. Fluorine-Free Firefighting Foams (3F) – Viable Alternatives to Fluorinated Aqueous Film-Forming Foams (AFFF). White Paper prepared for the IPEN by members of the IPEN F3 Panel and associates, POPRC-14, Rome. [https://ipen.org/sites/default/files/documents/IPEN_F3_Position_Paper_POPRC-14_12September2018d.pdf Free Download].</ref> and numerous companies are now manufacturing and delivering PFAS-free firefighting formulations for fixed systems and AFFF vehicles<ref>Ansul (Company), Ansul NFF-331 3%x3% Non-Fluorinated Foam Concentrate (Commercial Product). [https://docs.johnsoncontrols.com/specialhazards/api/khub/documents/1nbeVfynU1IW~eJcCOA0Bg/content Product Data Sheet].</ref><ref>BioEx (Company), Ecopol A+ (Commercial Product). [https://www.bio-ex.com/en/our-products/product/ecopol-aplus/  Website]</ref><ref>National Foam (Company), 2020. Avio F3 Green KHC 3%, Fluorine Free Foam Concentrate (Commercial Product). [https://nationalfoam.com/wp-content/uploads/sites/4/NMS515-Avio-Green-KHC-3-FF.pdf Safety Data Sheet]</ref>. Key factors in the selection of a PFAS-free firefighting formulations product are compatibility of the new formulation with the existing system (as confirmed by a fire protection engineer) and environmental certifications (i.e., verifying the absence of organic fluorine or PFAS or the absence of other non-fluorine environmental contaminants).
 
  
In January 2023, the US Department of Defense (DoD) published the Performance Specification for Fire Extinguishing Agent, Fluorine-Free Foam (F3) Liquid Concentrate for Land-Based, Fresh Water Applications<ref name="DoD2023"/>. This Military Performance Specification (Mil-Spec) allows PFAS free firefighting formulations to be certified as meeting certain standardized operational goals for use in military settings. In addition to Mil-Spec requirements, PFAS free firefighting formulations can also be certified through Underwriters Laboratories Standard for Safety, Foam Equipment and Liquid Concentrates, UL 162, which requires the new firefighting formulations be investigated for suitability and compatibility with the specific equipment with which they are intended to be used<ref>Underwriters Laboratories Inc., 2018. UL162, UL Standard for Safety, Foam Equipment and Liquid Concentrates, 8th Edition, Revised 2022. 40 pages. [https://global.ihs.com/doc_detail.cfm?document_name=UL%20162&item_s_key=00096960 Website]</ref>. Several PFAS-free foams have been certified under various parts of EN1568, the European Standard which specifies the necessary foam properties and performance requirements<ref>CSN EN 1568-1 ed. 2, 2018. Fire extinguishing media - Foam concentrates - Part 1: Specification for medium expansion foam concentrates for surface application to water-immiscible liquids. 48 pages. [https://www.en-standard.eu/csn-en-1568-1-ed-2-fire-extinguishing-media-foam-concentrates-part-1-specification-for-medium-expansion-foam-concentrates-for-surface-application-to-water-immiscible-liquids/ European Standards Website.]</ref>. Both ESTCP and SERDP have supported (and continue to support) the development and field validation of PFAS free firefighting formulations (e.g. WP22-7456, WP21-3461, WP20-1535, WP20-1524). Both the US Federal Aviation Administration (FAA) and National Fire Protection Association (NFPA) have performed a variety of foam certification tests on numerous PFAS-free firefighting formulations<ref>Back, G.G., Farley, J.P., 2020. Evaluation of the Fire Protection Effectiveness of Fluorine Free Firefighting Foams. National Fire Protection Association, Fire Protection Research Foundation. [https://www.iafc.org/docs/default-source/1safehealthshs/effectivenessofflourinefreefoam.pdf Free Download].</ref><ref>Casey, J., Trazzi, D., 2022. Fluorine-Free Foam Testing. Federal Aviation Administration (FAA) Final Report. [https://www.airporttech.tc.faa.gov/DesktopModules/EasyDNNNews/DocumentDownload.ashx?portalid=0&moduleid=3682&articleid=2882&documentid=3054  Open Access Article]</ref>.
+
The advantage of portable analytical tools is that they allow practitioners to expeditiously test indoor air concentrations under natural conditions in each room of the building. Concentrations in any room in excess of relevant screening levels trigger more sampling in that room to identify if an indoor source is present in that room. Removal of a suspected source and subsequent room testing can identify if that object or product was the source of the previously measured concentrations.  
  
==Selection of Flushing Agent==
+
'''Building-specific controlled pressurization method (CPM) testing''' directly measures the worst case indoor air impact, but it can also be used to determine contributing VI pathways and to identify indoor air sources<ref>McHugh, T.E., Beckley, L., Bailey, D., Gorder, K., Dettenmaier, E., Rivera-Duarte, I., Brock, S., MacGregor, I.C., 2012. Evaluation of Vapor Intrusion Using Controlled Building Pressure. Environmental Science and Technology, 46(9), pp. 4792–4799. [https://doi.org/10.1021/es204483g doi: 10.1021/es204483g]</ref><ref name="BeckleyEtAl2014" /><ref name="GuoEtAl2015" /><ref name="HoltonEtAl2015">Holton, C., Guo, Y., Luo, H., Dahlen, P., Gorder, K., Dettenmaier, E., Johnson, P.C., 2015. Long-Term Evaluation of the Controlled Pressure Method for Assessment of the Vapor Intrusion Pathway. Environmental Science and Technology, 49(4), pp. 2091–2098.  [https://doi.org/10.1021/es5052342 doi: 10.1021/es5052342]</ref><ref name="JohnsonEtAl2020" /><ref name="GuoEtAl2020a">Guo, Y., Dahlen, P., Johnson, P.C., 2020a. Development and Validation of a Controlled Pressure Method Test Protocol for Vapor Intrusion Pathway Assessment.  Environmental Science and Technology, 54(12), pp. 7117-7125. [https://dx.doi.org/10.1021/acs.est.0c00811 doi: 10.1021/acs.est.0c00811]</ref>. In CPM testing, blowers/fans installed in a doorway(s) or window(s) are set-up to exhaust indoor air to outdoor, which causes the building to be under pressurized relative to the atmosphere. This induces air movement from the subsurface into the test building via openings in the foundation and/or subsurface piping networks with or without direct connections to indoor air. This is similar to what happens intermittently under natural conditions when wind, indoor-outdoor temperature differences, and/or use of appliances that exhaust air from the structure (e.g. dryer exhaust) create an under-pressurized building condition.  
General industry guidance has typically recommended several rinses with water to remove PFAS from impacted equipment. Owing to the unique physical and chemical properties of PFAS, the use of room temperature water to remove PFAS from impacted equipment has not been very effective. To address these recalcitrant accumulations, companies are developing new methods to remove self-assembled PFAS bilayers from existing fire-fighting infrastructure so that it can be successfully transitioned to PFAS-free formulations. Arcadis developed a non-toxic cleaning agent, Fluoro Fighter<sup>TM</sup>, which has been demonstrated to be effective for removal of PFAS from equipment by disrupting the accumulated layers of PFAS coating the AFFF-wetted surfaces.  
 
  
Laboratory studies have supported the optimization of this PFAS removal method in fire suppression system piping obtained from a commercial airport hangar in Sydney, Australia<ref name="LangEtAl2022"/>. Prior to removal from the hangar, the stainless-steel pipe held PFAS-containing AFFF for more than three decades. Results indicated that Fluoro Fighter<sup>TM</sup>, as well as flushing at elevated temperatures, removed more surface associated PFAS in comparison to equivalent extractions using methanol or water at room temperature. ESTCP has supported (and continues to support) the development and field validation of best practices for methodologies to clean foam delivery systems (e.g. ER20-5364, ER20-5361, ER20-5369, ER21-7229).
+
The blowers/fans can also be used to blow outdoor air into the building, thereby creating a building over-pressurization condition. A positive pressure difference CPM test suppresses VI pathways; therefore, chemicals detected in indoor air above outdoor air concentrations during this condition are attributed to indoor contaminant sources which facilitates the identification of any such indoor air sources.
  
==PFAS Verification Testing==
+
Data collected during CPM testing, when combined with screening level VI modeling, can be used to identify which VI chemical migration pathways are significant contributors to indoor air impacts<ref name="GuoEtAl2015" />. CPM testing guidelines were developed and validated under ESTCP Project ER-201501<ref name="GuoEtAl2020a" /><ref name="JohnsonEtAl2021" />.
In general, PFAS sampling techniques used to support firefighting formulation transition activities are consistent with conventional sampling techniques used in the environmental industry, but special consideration is made regarding high concentration PFAS materials, elevated detection levels, cross-contamination potential, precursor content, and matrix interferences. The analytical method selected should be appropriate for the regulatory requirements in the site area.
 
  
==Rinsate Treatment==
+
'''Passive samplers''' can be used to measure long term average indoor air concentrations under natural conditions and during VI mitigation system operation. They will provide more confident assessment of long term average concentrations than an infrequent sequence of short term grab samples. Long term average concentrations can also be determined by long term active sampling (e.g., by slowly pulling air through a thermal desorption (TD) tube). However, passive sampling has the advantage that additional equipment and expertise is not required for sampler deployment and recovery.
Numerous technologies for treatment of PFAS-impacted water sources, including rinsates, have been and are currently being developed. These include separation technologies such as foam fractionation, nanofiltration, sorbents/flocculants, ion exchange resins, reverse osmosis. and destructive technologies such as [PFAS Treatment by Electrical Discharge Plasma |enhanced contact plasma], [Supercritical Water Oxidation (SCWO |supercritical water oxidation (SCWO)], electrochemical oxidation, hydrothermal alkaline treatment, and sonolysis. Many of these technologies have rapidly developed from bench-scale (e.g., microcosms, columns, single reactors) to commercially available field-scale units capable of managing PFAS-impacted waters of varying waste volumes and PFAS compositions and concentrations. Ongoing field research continues to improve the treatment efficiency, reliability, and versatility of these technologies, both individually and as coupled treatment solutions (e.g., treatment train). ESTCP has supported (and continues to support) the development and field validation of separation and destructive technologies for treatment of PFAS-impacted water sources, including rinsates (e.g. ER20-5370, ER20-5369, ER20-5350, ER20-5355).  
 
  
Remedy selection for treatment of rinsates involves several key factors. It is critical that environmental practitioners have up-to-date technical and practical knowledge on the suitability of these remedial options for different site conditions, treatment volumes, PFAS composition (e.g., presence of precursors, co-contaminants), PFAS concentrations, safety considerations, potential for undesired byproducts (e.g., perchlorate, disinfection byproducts), and treatment costs (e.g., energy demand, capital costs, operational labor).
+
Use of passive samplers in indoor air under time-varying concentration conditions was demonstrated and validated by comparing against intensive active sampling in ESTCP Project ER-201501<ref name="JohnsonEtAl2020" /><ref name="GuoEtAl2021">Guo, Y., O’Neill, H., Dahlen, P., and Johnson, P.C.  2021.  Evaluation of Passive Diffusive-Adsorptive Samplers for Use in Assessing Time-Varying Indoor Air Impacts Resulting from Vapor Intrusion.  Groundwater Monitoring and Remediation, 42(1), pp. 38-49.  [https://doi.org/10.1111/gwmr.12481 doi: 10.1111/12481]</ref>.
 +
 
 +
The purpose of maintaining an evergreen '''comprehensive VI conceptual model''' is to ensure that the most complete and up-to-date understanding of the site is informing decisions related to future sampling, data interpretation, and the need for and design of mitigation systems. The VI conceptual model can also serve as an effective communication tool in stakeholder discussions.
 +
 
 +
Use of these tools for residential neighborhoods and in non-residential buildings overlying chlorinated solvent groundwater plumes is documented comprehensively in a series of peer reviewed articles<ref name="JohnsonEtAl2020" /><ref name="JohnsonEtAl2021" /><ref name="JohnsonEtAl2022" /><ref name="GuoEtAl2015" /><ref name="GuoEtAl2020a" /><ref name="GuoEtAl2020b">Guo, Y., Dahlen, P., Johnson, P.C. 2020b. Temporal variability of chlorinated volatile organic compound vapor concentrations in a residential sewer and land drain system overlying a dilute groundwater plume. Science of the Total Environment, 702, Article 134756.  [https://doi.org/10.1016/j.scitotenv.2019.134756 doi: 10.1016/j.scitotenv.2019.134756]&nbsp;&nbsp; [//www.enviro.wiki/images/e/e5/GuoEtAl2020b.pdf  Open Access Manuscript]</ref><ref name="GuoEtAl2021" /><ref name="HoltonEtAl2015" />.
 +
 
 +
==Summary==
 +
In summary, the VI Diagnosis Toolkit provides a set of tools that can lead to quicker, more confident, and more cost effective neighborhood-scale VI pathway and impact assessments. Toolkit components and their use can complement conventional methods for assessing and mitigating the vapor intrusion pathway.
  
 
==References==
 
==References==
Line 73: Line 83:
  
 
==See Also==
 
==See Also==
 +
 +
*[https://papers.ssrn.com/sol3/papers.cfm?abstract_id=4000681 Evaluation of Radon and Building Pressure Differences as Environmental Indicators for Vapor Intrusion Assessment]
 +
*[https://pubs.acs.org/doi/10.1021/es4024767 Temporal Variability of Indoor Air Concentrations under Natural Conditions in a House Overlying a Dilute Chlorinated Solvent Groundwater Plume]
 +
*[https://serdp-estcp.mil/projects/details/e0d00662-c333-4560-8ae7-60f20b0e714b Integrated Field-Scale, Lab-Scale, and Modeling Studies for Improving Our Ability to Assess the Groundwater to Indoor Air Pathway at Chlorinated Solvent Impacted Sites]

Latest revision as of 22:25, 18 July 2024

Assessing Vapor Intrusion (VI) Impacts in Neighborhoods with Groundwater Contaminated by Chlorinated Volatile Organic Chemicals (CVOCs)

The VI Diagnosis Toolkit[1] is a set of tools that can be used individually or in combination to assess vapor intrusion (VI) impacts at one or more buildings overlying regional-scale dissolved chlorinated solvent impacted groundwater plumes. The strategic use of these tools can lead to confident and efficient neighborhood-scale VI pathway assessments.

Related Article(s):

Contributor(s):

  • Paul C. Johnson, Ph.D.
  • Paul Dahlen, Ph.D.
  • Yuanming Guo, Ph.D.

Key Resource(s):

  • The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes, ESTCP Project ER-201501, Final Report[1]
  • CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment, ESTCP Project ER-201501, Technical Report[2]
  • VI Diagnosis Toolkit User Guide, ESTCP Project ER-201501[3]

Introduction

Most federal, state, and local regulatory guidance for assessing and mitigating the vapor intrusion pathway reflects USEPA’s Technical Guide for Assessing and Mitigating the Vapor Intrusion Pathway from Subsurface Vapor Sources to Indoor Air[4]. The paradigm outlined by that guidance includes: 1) a preliminary and mostly qualitative analysis that looks for site conditions that suggest vapor intrusion might occur (e.g., the presence of vapor-forming chemicals in close proximity to buildings); 2) a multi-step and more detailed quantitative screening analysis that involves site-specific data collection and their comparison to screening levels to identify buildings of potential VI concern; and 3) selection and design of mitigation systems or continued monitoring, as needed. With respect to (2), regulatory guidance typically recommends consideration of “multiple lines of evidence” in decision-making[4][5], with typical lines-of-evidence being groundwater, soil gas, sub-slab soil gas, and/or indoor air concentrations. Of those, soil gas measurements and/or measured short-term indoor air concentrations can be weighted heavily, and therefore decision making might not be completed without them. Effective evaluation of VI risk from sub-slab and/or soil gas measurements would require an unknown building-specific attenuation factor, but there is also uncertainty as to whether or not indoor air data is representative of maximum and/or long-term average indoor concentrations. Indoor air data can be confounded by indoor contaminant sources because the number of samples is typically small, indoor concentrations can vary with time, and because a number of household products can emit the chemicals being measured. When conducting VI pathway assessments in neighborhoods where it is impractical to assess all buildings, the EPA recommends following a “worst first” investigational approach.

The limitations of this approach, as practiced, are the following:

  • Decisions are rarely made without indoor air data and generally, seasonal sampling is required, delaying decision making.
  • The collection of a robust indoor air data set that adequately characterizes long term indoor air concentrations could take years given the typical frequency of data collection and the most common methods of sample collection (e.g., 24-hour samples). Therefore, indoor air sampling might continue indefinitely at some sites.
  • The “worst first” buildings might not be identified correctly by the logic outlined in USEPA’s 2015 guidance and the most impacted buildings might not even be located over a groundwater plume. Recent studies have shown VI impacts in homes as a result of sewer and other subsurface piping connections, which are not explicitly considered nor easily characterized through conventional VI pathway assessment[6][7][8][9][10].
  • The presumptive remedy for VI mitigation (sub-slab depressurization) may not be effective for all VI scenarios (e.g., those involving vapor migration to indoor spaces via sewer connections).

The VI Diagnosis Toolkit components were developed considering these limitations as well as more recent knowledge gained through research, development, and validation projects funded by SERDP and ESTCP.

The VI Diagnosis Toolkit Components

Figure 1. Vapor intrusion pathway conceptualization considering “alternate VI pathways”, including “pipe flow VI” and “sewer VI” pathways[1].

The primary components of the VI Diagnosis Toolkit and their uses include:

  • External VI source strength screening to identify buildings most likely to be impacted by VI at levels warranting building-specific testing.
  • Indoor air source screening to locate and remove indoor air sources that might confound building specific VI pathway assessment.
  • Controlled pressurization method (CPM) testing to quickly (in a few days or less) measure the worst-case indoor air impact likely to be caused by VI under natural conditions in specific buildings. CPM tests can also be used to identify the presence of indoor air sources and diagnose active VI pathways.
  • Passive indoor sampling for determining long-term average indoor air concentrations under natural VI conditions and/or for verifying mitigation system effectiveness in buildings that warrant VI mitigation.
  • Comprehensive VI conceptual model development and refinement to ensure that appropriate monitoring, investigation, and mitigation strategies are being selected (Figure 1).

Expanded discussions for each of these are given below.

External VI source strength screening identifies those buildings that warrant more intrusive building-specific assessments, using data collected exterior to the buildings. The use of groundwater and/or soil gas concentration data for building screening has been part of VI pathway assessments for some time and their use is discussed in many regulatory guidance documents. Typically, the measured concentrations are compared to relevant screening levels derived via modeling or empirical analyses from indoor air concentrations of concern.

More recently it has been discovered that VI impacts can occur via sewer and other subsurface piping connections in areas where vapor migration through the soil would not be expected to be significant, and this could also occur in buildings that do not sit over contaminated groundwater[10][7][8][9].

Therefore, in addition to groundwater and soil gas sampling, external data collection that includes and extends beyond the area of concern should include manhole vapor sampling (e.g., sanitary sewer, storm sewer, land-drain). Video surveys from sanitary sewers, storm sewers, and/or land-drains can also be used to identify areas of groundwater leakage into utility corridors and lateral connections to buildings that are conduits for vapor transport. During these investigations, it is important to recognize that utility corridors can transmit both impacted water and vapors beyond groundwater plume boundaries, so extending investigations into areas adjacent to groundwater plume boundaries is necessary.

Using projected indoor air concentrations from modeling and empirical data analyses, and distance screening approaches, external source screening can identify areas and buildings that can be ruled out, or conversely, those that warrant building-specific testing.

Demonstration of neighborhood-scale external VI source screening using groundwater, depth, sewer, land drain, and video data is documented in the ER-201501 final report[1].

Indoor air source screening seeks to locate and remove indoor air sources[11] that might confound building specific VI pathway assessment. Visual inspections and written surveys might or might not identify significant indoor air sources, so these should be complemented with use of portable analytical instruments[12][13].

The advantage of portable analytical tools is that they allow practitioners to expeditiously test indoor air concentrations under natural conditions in each room of the building. Concentrations in any room in excess of relevant screening levels trigger more sampling in that room to identify if an indoor source is present in that room. Removal of a suspected source and subsequent room testing can identify if that object or product was the source of the previously measured concentrations.

Building-specific controlled pressurization method (CPM) testing directly measures the worst case indoor air impact, but it can also be used to determine contributing VI pathways and to identify indoor air sources[14][13][7][15][1][16]. In CPM testing, blowers/fans installed in a doorway(s) or window(s) are set-up to exhaust indoor air to outdoor, which causes the building to be under pressurized relative to the atmosphere. This induces air movement from the subsurface into the test building via openings in the foundation and/or subsurface piping networks with or without direct connections to indoor air. This is similar to what happens intermittently under natural conditions when wind, indoor-outdoor temperature differences, and/or use of appliances that exhaust air from the structure (e.g. dryer exhaust) create an under-pressurized building condition.

The blowers/fans can also be used to blow outdoor air into the building, thereby creating a building over-pressurization condition. A positive pressure difference CPM test suppresses VI pathways; therefore, chemicals detected in indoor air above outdoor air concentrations during this condition are attributed to indoor contaminant sources which facilitates the identification of any such indoor air sources.

Data collected during CPM testing, when combined with screening level VI modeling, can be used to identify which VI chemical migration pathways are significant contributors to indoor air impacts[7]. CPM testing guidelines were developed and validated under ESTCP Project ER-201501[16][2].

Passive samplers can be used to measure long term average indoor air concentrations under natural conditions and during VI mitigation system operation. They will provide more confident assessment of long term average concentrations than an infrequent sequence of short term grab samples. Long term average concentrations can also be determined by long term active sampling (e.g., by slowly pulling air through a thermal desorption (TD) tube). However, passive sampling has the advantage that additional equipment and expertise is not required for sampler deployment and recovery.

Use of passive samplers in indoor air under time-varying concentration conditions was demonstrated and validated by comparing against intensive active sampling in ESTCP Project ER-201501[1][17].

The purpose of maintaining an evergreen comprehensive VI conceptual model is to ensure that the most complete and up-to-date understanding of the site is informing decisions related to future sampling, data interpretation, and the need for and design of mitigation systems. The VI conceptual model can also serve as an effective communication tool in stakeholder discussions.

Use of these tools for residential neighborhoods and in non-residential buildings overlying chlorinated solvent groundwater plumes is documented comprehensively in a series of peer reviewed articles[1][2][3][7][16][18][17][15].

Summary

In summary, the VI Diagnosis Toolkit provides a set of tools that can lead to quicker, more confident, and more cost effective neighborhood-scale VI pathway and impact assessments. Toolkit components and their use can complement conventional methods for assessing and mitigating the vapor intrusion pathway.

References

  1. ^ 1.0 1.1 1.2 1.3 1.4 1.5 1.6 Johnson, P.C., Guo, Y., Dahlen, P., 2020. The VI Diagnosis Toolkit for Assessing Vapor Intrusion Pathways and Mitigating Impacts in Neighborhoods Overlying Dissolved Chlorinated Solvent Plumes. ESTCP Project ER-201501, Final Report. Project Website   Final Report.pdf
  2. ^ 2.0 2.1 2.2 Johnson, P.C., Guo, Y., Dahlen, P., 2021. CPM Test Guidelines: Use of Controlled Pressure Method Testing for Vapor Intrusion Pathway Assessment. ESTCP ER-201501, Technical Report. Project Website   Technical_Report.pdf
  3. ^ 3.0 3.1 Johnson, P.C., Guo, Y., and Dahlen, P., 2022. VI Diagnosis Toolkit User Guide, ESTCP ER-201501, User Guide. Project Website   User_Guide.pdf
  4. ^ 4.0 4.1 USEPA, 2015. OSWER Technical Guide for Assessing and Mitigating the Vapor Intrusion Pathway from Subsurface Vapor Sources to Indoor Air. U.S. Environmental Protection Agency, Office of Solid Waste and Emergency Response, OSWER Publication No. 9200.2-154, 267 pages. USEPA Website   Report.pdf
  5. ^ NJDEP, 2021. Vapor Intrusion Technical Guidance, Version 5.0. New Jersey Department of Environmental Protection, Trenton, NJ. Website   Guidance Document.pdf
  6. ^ Beckley, L, McHugh, T., 2020. A Conceptual Model for Vapor Intrusion from Groundwater Through Sewer Lines. Science of the Total Environment, 698, Article 134283. doi: 10.1016/j.scitotenv.2019.134283   Open Access Article
  7. ^ 7.0 7.1 7.2 7.3 7.4 Guo, Y., Holton, C., Luo, H., Dahlen, P., Gorder, K., Dettenmaier, E., Johnson, P.C., 2015. Identification of Alternative Vapor Intrusion Pathways Using Controlled Pressure Testing, Soil Gas Monitoring, and Screening Model Calculations. Environmental Science and Technology, 49(22), pp. 13472–13482. doi: 10.1021/acs.est.5b03564
  8. ^ 8.0 8.1 McHugh, T., Beckley, L., Sullivan, T., Lutes, C., Truesdale, R., Uppencamp, R., Cosky, B., Zimmerman, J., Schumacher, B., 2017. Evidence of a Sewer Vapor Transport Pathway at the USEPA Vapor Intrusion Research Duplex. Science of the Total Environment, pp. 598, 772-779. doi: 10.1016/j.scitotenv.2017.04.135   Open Access Manuscipt
  9. ^ 9.0 9.1 McHugh, T., Beckley, L., 2018. Sewers and Utility Tunnels as Preferential Pathways for Volatile Organic Compound Migration into Buildings: Risk Factors and Investigation Protocol. ESTCP ER-201505, Final Report. Project Website   Final Report.pdf
  10. ^ 10.0 10.1 Riis, C., Hansen, M.H., Nielsen, H.H., Christensen, A.G., Terkelsen, M., 2010. Vapor Intrusion through Sewer Systems: Migration Pathways of Chlorinated Solvents from Groundwater to Indoor Air. Seventh International Conference on Remediation of Chlorinated and Recalcitrant Compounds, May, Monterey, CA. Battelle Memorial Institute. ISBN 978-0-9819730-2-9. Website   Report.pdf
  11. ^ Doucette, W.J., Hall, A.J., Gorder, K.A., 2010. Emissions of 1,2-Dichloroethane from Holiday Decorations as a Source of Indoor Air Contamination. Ground Water Monitoring and Remediation, 30(1), pp. 67-73. doi: 10.1111/j.1745-6592.2009.01267.x
  12. ^ McHugh, T., Kuder, T., Fiorenza, S., Gorder, K., Dettenmaier, E., Philp, P., 2011. Application of CSIA to Distinguish Between Vapor Intrusion and Indoor Sources of VOCs. Environmental Science and Technology, 45(14), pp. 5952-5958. doi: 10.1021/es200988d
  13. ^ 13.0 13.1 Beckley, L., Gorder, K., Dettenmaier, E., Rivera-Duarte, I., McHugh, T., 2014. On-Site Gas Chromatography/Mass Spectrometry (GC/MS) Analysis to Streamline Vapor Intrusion Investigations. Environmental Forensics, 15(3), pp. 234–243. doi: 10.1080/15275922.2014.930941
  14. ^ McHugh, T.E., Beckley, L., Bailey, D., Gorder, K., Dettenmaier, E., Rivera-Duarte, I., Brock, S., MacGregor, I.C., 2012. Evaluation of Vapor Intrusion Using Controlled Building Pressure. Environmental Science and Technology, 46(9), pp. 4792–4799. doi: 10.1021/es204483g
  15. ^ 15.0 15.1 Holton, C., Guo, Y., Luo, H., Dahlen, P., Gorder, K., Dettenmaier, E., Johnson, P.C., 2015. Long-Term Evaluation of the Controlled Pressure Method for Assessment of the Vapor Intrusion Pathway. Environmental Science and Technology, 49(4), pp. 2091–2098. doi: 10.1021/es5052342
  16. ^ 16.0 16.1 16.2 Guo, Y., Dahlen, P., Johnson, P.C., 2020a. Development and Validation of a Controlled Pressure Method Test Protocol for Vapor Intrusion Pathway Assessment. Environmental Science and Technology, 54(12), pp. 7117-7125. doi: 10.1021/acs.est.0c00811
  17. ^ 17.0 17.1 Guo, Y., O’Neill, H., Dahlen, P., and Johnson, P.C. 2021. Evaluation of Passive Diffusive-Adsorptive Samplers for Use in Assessing Time-Varying Indoor Air Impacts Resulting from Vapor Intrusion. Groundwater Monitoring and Remediation, 42(1), pp. 38-49. doi: 10.1111/12481
  18. ^ Guo, Y., Dahlen, P., Johnson, P.C. 2020b. Temporal variability of chlorinated volatile organic compound vapor concentrations in a residential sewer and land drain system overlying a dilute groundwater plume. Science of the Total Environment, 702, Article 134756. doi: 10.1016/j.scitotenv.2019.134756   Open Access Manuscript

See Also