Difference between revisions of "Vapor Intrusion (VI)"

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==See Also==
 
==See Also==
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*[https://www.navfac.navy.mil/content/dam/navfac/Specialty%20Centers/Engineering%20and%20Expeditionary%20Warfare%20Center/Environmental/Restoration/er_pdfs/v/navfac-ev-fs-vi-mit-newbldg-201108.pdf VI mitigation in new buildings]
 
*[https://www.navfac.navy.mil/content/dam/navfac/Specialty%20Centers/Engineering%20and%20Expeditionary%20Warfare%20Center/Environmental/Restoration/er_pdfs/v/navfac-ev-fs-vi-mit-existbldgs-201105.pdf VI mitigation in existing buildings]
 
*[https://www.navfac.navy.mil/content/dam/navfac/Specialty%20Centers/Engineering%20and%20Expeditionary%20Warfare%20Center/Environmental/Restoration/er_pdfs/v/navfac-ev-fs-vi-mit-existbldgs-201105.pdf VI mitigation in existing buildings]
 
*[[Chlorinated Solvents | Chlorinated Solvents]]
 
*[[Chlorinated Solvents | Chlorinated Solvents]]

Revision as of 20:29, 8 May 2018

Vapor intrusion (VI) is a term that describes the migration of sufficiently volatile compounds from subsurface media (such as soil or groundwater) into the indoor air of buildings. VI may result in unacceptable chronic or even acute exposures to occupants (e.g., residents or employees) of buildings near or overlying volatile compound contaminated sites. VI is assessed as a part of investigation and cleanup activities performed under environmental restoration programs, but characterization can be difficult because several consumer products also contain volatile organic compounds (VOCs). VI is typically addressed using a combination of subsurface source remediation and VI mitigation of exposure in buildings. Because of the rapid biodegradation of petroleum hydrocarbon vapors, fewer petroleum hydrocarbon sites have a complete vapor intrusion pathway than sites containing chlorinated solvents.


CONTRIBUTOR(S): Chris Lutes, Dr. Loren Lund with John Lowe


Key Resource(s):

Introduction

VI is the migration of chemical vapors from a subsurface vapor source in soil or groundwater to indoor air. VI is one example of an exposure pathway - a means by which hazardous substances can move through the environment and come into contact with people. Other examples of exposure pathways include groundwater ingestion and direct contact with contaminated soils. Volatile chemicals, including chlorinated compounds such as trichloroethene (TCE) and tetrachloroethene (PCE), are often considered constituents of concern for VI. Petroleum hydrocarbons such as benzene, toluene, ethylbenzene, and xylenes can also cause VI problems, but this occurs less frequently because these compounds readily biodegrade in soil[3][4]. Some inorganic substances such as mercury also might volatilize from the subsurface into indoor air.

Vapor Sources in a Conceptual Site Model

A conceptual site model (CSM) is a simple description of the key processes at a site and is used to support characterizations, risk assessments, remediation planning, and implementation. In general, the CSM for VI consists of vapor sources, subsurface vapor migration potential, driving forces from the subsurface into buildings, and mixing of chemicals in indoor air[5]. A simplified VI CSM is as follows (Fig. 1):

Lutes-Article1w2.Fig 1.PNG

Vapor sources: Two classes of vapor sources may be included in a CSM:

  • Primary releases are located immediately adjacent to former chemical release locations such as underground storage tanks, landfills, or spill sites. Primary releases that are adjacent to or within buildings, such as spills from a vapor degreaser in a shop, have a higher potential for creating a significant VI pathway.
  • Secondary vapor sources are located at a distance from chemical release locations. For example, a volatile chemical plume that has migrated through soil vapor or groundwater away from a spill site (such as a vapor degreaser). The potential for a significant VI pathway from a secondary vapor source depends on the concentrations and depth in soil vapor or groundwater, the properties of the soil underlying the building, and the locations of atypical preferential pathways for vapor migration (e.g., sewer utilities, McHugh, 2016[6]).

Vapor Migration and Driving Forces

Contaminants in groundwater can volatilize into the overlying soil. The tendency for contaminants to volatilize from groundwater to soil depends on their Henry's Law constant, which is the partitioning coefficient between water and air. Volatile compounds migrate through the air-filled porosity in soil primarily via diffusion from areas with higher vapor concentrations (such as near contaminant sources in the subsurface) to lower vapor concentrations (such as inside a building). The tendency for volatile compounds to diffuse through soil depends on their chemical and physical properties (diffusion coefficients in air and water), soil porosity, and the soil moisture content.

As volatile compounds in soil gas migrate toward the surface, they encounter the building’s zone of influence where advective air movement becomes more dominant. advective transport occurs when there is a difference in pressure between the subsurface and indoor spaces. This pressure differential is related to factors such as the stack effect (the movement of air into and out of buildings, chimneys, flue gas stacks, or other containers, resulting from air buoyancy); operation of the heating, ventilation, and air conditioning (HVAC) system; and wind pressure on the building exterior. Buildings when even slightly depressurized relative to the subsurface may be more prone to VI. Vapor entry may occur through openings in floors and walls (such as cracks and foundations gaps). In addition, atypical preferential pathways or entry points like floor drains and utilities can act as vapor conduits and enhance vapor transport into buildings. Examples of pathways for vapor entry into a building are numerous and include floor cracks, floor drains, plumbing penetrations, mortar joints in foundations, etc.

Key references that describe the vertical distribution and temporal variation of VOCs include McHugh et al., 2007[7]; USEPA, 2009[8]; Schumacher et al., 2010[9]; USEPA, 2012b[5], and the Case Studies presented below.

Investigation and Assessment

Based on the tendency for vapor migration, VI guidance generally recommends that buildings within 100 feet of locations known to have chlorinated volatile contaminants above soil and groundwater screening levels undergo a VI evaluation[10][1]). For petroleum hydrocarbons, which more readily undergo biodegradation in soil, this distance is reduced to 30 feet[4][11].

The current approach in most regulatory guidance involves examining the concordance in multiple lines of evidence, which may include groundwater, soil gas, sub-slab and/or indoor air sampling data, building survey and chemical use information, and data from controlled building depressurization testing or other advanced techniques if available, to determine if VI pathways into buildings are complete and significant. In recent years, there has been increased acceptance of longer (14 day) time-weighted sorbent based samplers as an alternative to short-term (1 day) vapor sampling using summa canisters[12][13]. However, some regulators require use of 1-day samples to evaluate TCE due to the controversial concerns regarding potential birth defects associated with short-term exposure.

Guidance for assessing the VI pathway varies from national to state levels; however, most guidance documents follow investigation approaches similar to those, for example, recommended by the EPA, 2015[1][11]; ITRC, 2007[10]; and DoD, 2009[14]. Most VI regulatory guidance recommends assessing VI by applying a tiered investigation approach:

An initial tier of VI investigation (screening assessment) involves collecting groundwater and soil gas samples to trace a pathway for volatile compounds from the contaminant sources to nearby buildings. These results are compared with conservative (highly protective) screening levels, to determine if further investigation of surrounding buildings is warranted.

Subsequent tiers of a VI assessment may involve investigating nearby buildings. Building investigations typically involve collecting sub-slab soil gas samples [15][16][17], which are collected through the building floors, and collecting indoor and outdoor air samples. Building surveys are performed to:

  • Evaluate the characteristics and condition of the building envelope
  • Determine activities and uses within the building that may contribute to observed volatile organic compound (VOC) concentrations
  • Assess operation of the HVAC system and other factors that may dilute VOCs
  • Identify the location of subsurface utilities or other building features that might represent atypical preferential pathways for vapor migration.

Because several consumer products such as some hobby glue, gun cleaners, Christmas ornaments, and spot cleaners can contain VOCs, there is a need to determine if VOCs found in a building originated from the subsurface or from indoor sources. Several diagnostic methods may be employed, such as methods described in these ESTCP projects:

  • controlled building depressurization that attempts to induce VI in an indoor space using a fan or blower-door while changes in VOC concentrations in indoor air are observed under the depressurized conditions using real-time monitoring[18][19];
  • use of portable analyzers ( gas chromatograph/mass spectrometer) to identify sources in buildings[20].

The results of a VI investigation are then assessed to determine if there is a complete VI pathway into a building and if potential exposures to VOCs in indoor air represent a significant health risk to building occupants.

Remediation and Mitigation of VI Pathways

If an exposure and risk assessment of a particular building finds that VI exposures exceed regulatory criteria, then the VI pathway is generally addressed through a combination of:

  • Remediation focused on the environmental media/source (such as a groundwater plume underneath a building) from which the contaminants originate to reduce their concentrations
  • Mitigation, with the objective to reduce or eliminate exposures in the building impacted by VI. Mitigation is generally considered a short to medium term remedy.

In general, mitigation technologies used to control VI are based on the practices originally developed for radon mitigation. Mitigation is most often considered an interim measure to control exposures in VI-impacted buildings during remediation of volatile chemicals in soil and groundwater.

There are two types of building mitigation methods[21][22][23][24]:

  • Passive mitigation methods prevent the entry of chemical vapors into the building by sealing openings (cracks, perforations) or installing sub-slab liners (passive membranes, vapor barriers, and passive venting techniques). These methods are applicable to both existing and future residential and commercial buildings and may be appropriate when residual volatiles in soil gas are unlikely to contribute to indoor air concentrations above target levels. These methods tend to be cheaper but may be less effective and thus require more monitoring. Passive methods are more likely to be successful and economical in new construction, when the floor system is readily accessible and they can be integrated with building features intended to provide moisture protection.
  • Active mitigation methods include mechanical systems that can be implemented in both existing and new construction, and are designed to change the pressure difference between the sub-slab and the inside of the building to keep vapors out. These mitigation methods include sub-slab depressurization and building over-pressurization techniques, sub-slab venting and indoor air treatment. These control methods are typically more expensive and require long-term operation and maintenance, but more effective than passive systems.

Passive and active mitigation technologies are further described in Engineering Issue: Indoor Air Vapor Intrusion Mitigation Approaches[22].

Causing VI Inadvertently via Remediation

Precautions are sometimes required when designing remediation systems to avoid causing or exacerbating a VI situation. In theory technologies such as air sparging, enhanced anaerobic bioremediation, chemical oxidation, or in situ thermal methods can generate additional volatiles in the vadose zone, or change how those volatiles move near or into structures and cause VI problems. To control VI risk from remediation, the following measures can be employed:

  • Engineering controls, such as soil vapor extraction (SVE) systems between targeted remediation zones and structures
  • Judicious selection of technologies to be used in proximity to buildings
  • Understanding the characteristics of buildings near remediation systems that may provide atypical preferential pathways for gas migration
  • Monitoring and if necessary, building mitigation

Despite the theoretical potential, as of 2016 we are not aware of many well-documented cases where remediation has caused or worsened actual VI problems at a site, suggesting that remediation-caused VI problems may be rare or that existing industry precautions have generally been successful in managing the risks.

Research and Technology Development Efforts

VI is a field with a rapid evolution of conceptual and mechanistic understandings of the pathways and tools for assessment and mitigation.

In addition to primary literature studies, a variety of general guidance documents are listed as key resources at the start of this article. Key SERDP/ESTCP VI projects can be found here: Vapor Intrusion

Case Studies

Some of the most important knowledge about VI has been obtained from detailed studies of buildings. Two of the most extensive data sets from individual residential buildings, in broadly similar climates but of varying construction dates are:

  • The Sun Devil Manor VI Research House, where widely varying temporal variability was observed throughout the year with a distinct summer vs. winter pattern[25][26].
  • The Indiana Duplex House where seasonal variations and different VI characterization methods were evaluated[27] [28].

Several multi-building database studies have been conducted of differing populations of buildings that seek to derive general descriptions of vapor intrusion behavior. In particular these databases often compare buildings using attenuation factors which are defined as “The ratio of the indoor air concentration arising from vapor intrusion to the soil gas concentration at the source or a depth of interest in the vapor migration route”[1]. Multi-building analyses are also contained in Song [29]; USEPA, 2012a[30]; Johnston and Gibson, 2013[31]; Yao et al., 2013[32]; Brewer et al., 2014[33]; and DON, 2015[2].

References

  1. ^ 1.0 1.1 1.2 1.3 U.S. Environmental Protection Agency (USEPA), 2015. OSWER Technical guide for assessing and mitigating the vapor intrusion pathway from subsurface vapor source to indoor air. 9200.2-154. Office of Solid Waste and Emergency Response, Washington, D.C. pp 267. Report pdf
  2. ^ 2.0 2.1 Department of the Navy (DON), 2015. A Quantitative Decision Framework for Assessing Navy Vapor Intrusion Sites. Technical Report TR-NAVFAC-EXWC-EV-1603. Report.pdf
  3. ^ U.S. Environmental Protection Agency (USEPA). 2012. Petroleum Hydrocarbons and Chlorinated Solvents Differ in Their Potential for Vapor Intrusion. Office of Underground Storage Tanks. Report.pdf
  4. ^ 4.0 4.1 Interstate Technology and Regulatory Council (ITRC), 2014. Petroleum vapor intrusion: Fundamentals of screening, investigation, and management. PVI-1. Washington, D.C. Petroleum Vapor Intrusion Team. Report.pdf
  5. ^ 5.0 5.1 U.S. Environmental Protection Agency (USEPA), 2012. Conceptual Model Scenarios for the Vapor Intrusion Pathway. USEPA, Washington, DC. EPA-530-R-10-03. Report.pdf
  6. ^ McHugh, T., Loll, P. and Eklund, B., 2017. Recent advances in vapor intrusion site investigations. Journal of Environmental Management, 204, pp.783-792. doi: 10.1016/j.jenvman.2017.02.015
  7. ^ McHugh, T.E., Nickles, T.N. and Brock, S., 2007. Evaluation of spatial and temporal variability in VOC concentrations at vapor intrusion investigation sites. Proceedings of Vapor Intrusion: Learning from the Challenges, Providence, RI, pp.129-142. Report.pdf
  8. ^ U.S. Environmental Protection Agency (USEPA), 2009. Vertical Distribution of VOCs in Soils from Groundwater to the Surface/Subslab U.S. Environmental Protection Agency, 326 pp. Report.pdf
  9. ^ Schumacher, B. A., Zimmerman, J. H, Swanson, G., Elliot, J., Hartman, B., 2010 Temporal Variation of VOCs in Soils from Groundwater to the Surface/Subslab. U.S. Environmental Protection Agency, Washington, DC, EPA/600/R-10/118, 143 pp. Report.pdf
  10. ^ 10.0 10.1 Interstate Technology & Regulatory Council (ITRC), 2007. Vapor intrusion pathway: A practical guide. VI-1. ITRC Vapor Intrusion Team, Washington, D.C. Report pdf
  11. ^ 11.0 11.1 U.S. Environmental Protection Agency (USEPA), 2015. Technical guide for addressing petroleum vapor intrusion at leaking underground storage tank sites. Office of Underground Storage Tanks, Washington, D.C. EPA 510-R-15-001. Report pdf
  12. ^ U.S. Environmental Protection Agency (USEPA). 2014. Passive Samplers for Investigations of Air Quality: Method Description, Implementation, and Comparison to Alternative Sampling Methods. EPA/600/R-14/434. Report.pdf
  13. ^ McAlary, T., 2014. Development of More Cost-Effective Methods for Long-Term Monitoring of Soil Vapor Intrusion to Indoor Air Using Quantitative Passive Diffusive-Adsorptive Sampling. ER-2100830
  14. ^ U.S. Department of Defense (DoD). 2009. DoD Vapor Intrusion Handbook. Prepared by the Tri-Services Environmental Risk Assessment Working Group. Report.pdf
  15. ^ DiGiulio, D., Paul, C., Cody, R., Willey, R., Clifford, S., Kahn, P., Mosley, R., Lee, A. and Christensen, K., 2006. Assessment of vapor intrusion in homes near the Raymark Superfund site using basement and sub-slab air samples. EPA/600/R-05/147. Report.pdf
  16. ^ McAlary, T.A., Nicholson, P., Groenevelt, H. and Bertrand, D., 2009. A Case Study of Soil‐Gas Sampling in Silt and Clay‐Rich (Low‐Permeability) Soils. Groundwater Monitoring & Remediation, 29(1), pp.144-152. doi: 10.1111/j.1745-6592.2009.01223.x
  17. ^ McAlary, T.A., Nicholson, P.J., Yik, L.K., Bertrand, D.M. and Thrupp, G., 2010. High Purge Volume Sampling—A New Paradigm for Subslab Soil Gas Monitoring. Groundwater Monitoring & Remediation, 30(2), pp.73-85. doi: 10.1111/j.1745-6592.2010.01278.x
  18. ^ McHugh, T.E. and Nickels, T.N., 2008. Detailed field investigation of vapor intrusion processes. ER-200423
  19. ^ McHugh, T.E., Beckley, L., Bailey, D., Gorder, K., Dettenmaier, E., Rivera-Duarte, I., Brock, S. and MacGregor, I.C., 2012. Evaluation of vapor intrusion using controlled building pressure. Environmental Science & Technology, 46(9), pp.4792-4799. doi: 10.1021/es204483g
  20. ^ Beckley, L., McHugh, T., Gorder, K., Dettenmaier, E. and Rivera-Duarte, I., 2013. Use of On-Site GC/MS Analysis to Distinguish Between Vapor Intrusion and Indoor Sources of VOCs. ER-201119
  21. ^ Folkes, D.J. and Kurz, D.W., 2002. Efficacy of sub-slab depressurization for mitigation of vapor intrusion of chlorinated organic compounds. Proceedings of Indoor Air. Report.pdf
  22. ^ 22.0 22.1 U.S. Environmental Protection Agency (USEPA). 2008. Engineering Issue: Indoor Air Vapor Intrusion Mitigation Approaches. EPA/600/R-08-115. Report.pdf
  23. ^ Schumacher, B., Zimmerman, J.H., 2015. Assessment of Mitigation Systems on Vapor Intrusion: Temporal Trends, Attenuation Factors, and Contaminant Migration Routes under Mitigated and Non-mitigated Conditions. U.S. Environmental Protection Agency, Washington, DC, EPA/600/R-14/397. Report.pdf
  24. ^ Lutes, C.C., Truesdale, R.S., Cosky, B.W., Zimmerman, J.H. and Schumacher, B.A., 2015. Comparing vapor intrusion mitigation system performance for VOCs and radon. Remediation Journal, 25(4), pp.7-26. doi: 10.1002/rem.21438
  25. ^ Holton, C., Luo, H., Dahlen, P., Gorder, K., Dettenmaier, E. and Johnson, P.C., 2013. Temporal variability of indoor air concentrations under natural conditions in a house overlying a dilute chlorinated solvent groundwater plume. Environmental Science & Technology, 47(23), pp.13347-13354. doi: 10.1021/es4024767
  26. ^ Johnson, P.C., Holton, C., Guo, Y., Dahlen, P., Luo, H., Gorder, K., Dettenmaier, E. and Hinchee, R.E., 2016. Integrated Field Scale, Lab Scale, and Modeling Studies for Improving Our Ability to Assess the Groundwater to Indoor Air Pathway at Chlorinated Solvent Impacted Groundwater Sites. Arizona State University Tempe United States. ER-1686
  27. ^ U.S. Environmental Protection Agency (USEPA). 2012d. Fluctuation of Indoor Radon and VOC Concentrations Due to Seasonal Variations. Office of Research and Development. EPA/600/R/12/673. Report.pdf
  28. ^ United States Environmental Protection Agency (USEPA), 2015d. Simple, Efficient, and Rapid Methods to Determine the Potential for Vapor Intrusion into the Home: Temporal Trends, Vapor Intrusion Forecasting, Sampling Strategies, and Contaminant Migration Routes. U.S. Environmental Protection Agency, Washington, DC, EPA/600/R-15/070, 2015. Report.pdf
  29. ^ Song, S., Ramacciotti, F., Schnorr, B., Bock, M., Stubbs, C., Bock, M.J., Portland, M.E. and Stubbs, C.M., 2011. Evaluation of EPA’s Empirical Attenuation Factor Database
  30. ^ United States Environmental Protection Agency (USEPA), 2012. EPA's Vapor Intrusion Database: Evaluation and Characterization of Attenuation Factors for Chlorinated Volatile Organic Compounds and Residential Buildings. US Environmental Protection Agency, Office of Solid Waste and Emergency Response. EPA-530-R-10-002. Report.pdf
  31. ^ Johnston, J.E. and Gibson, J.M., 2013. Screening houses for vapor intrusion risks: A multiple regression analysis approach. Environmental Science & Technology, 47(11), pp.5595-5602. doi: 10.1021/es4003795
  32. ^ Yao, Y., Shen, R., Pennell, K.G. and Suuberg, E.M., 2013. Examination of the US EPA’s vapor intrusion database based on models. Environmental science & technology, 47(3), pp.1425-1433. doi: 10.1021/es304546f
  33. ^ Brewer, R., Nagashima, J., Rigby, M., Schmidt, M. and O'Neill, H., 2014. Estimation of Generic Subslab Attenuation Factors for Vapor Intrusion Investigations. Groundwater Monitoring & Remediation, 34(4), pp.79-92. doi: 10.1111/gwmr.12086

See Also

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