Remediation techniques for mitigating vapor intrusion from sewer systems to indoor air

Investigations at former dry cleaning sites in Denmark show that sewer systems often are a major vapor intrusion pathway for chlorinated solvents to indoor air. In more than 20 percent of the contaminated drycleaner sites in Central Denmark Region, sewer systems were determined to be a major vapor intrusion pathway. Sewer systems can be a major intrusion pathway if contaminated groundwater intrudes into the sewer and contamination is transported within the sewer pipe by water flow in either free phase or dissolved states. Additionally, the contamination can volatilize from the water phase or soil gas can intrude the sewer system directly. In the sewer, the gas phase can migrate in any direction by convective transport or diffusion. Indications of the sewer as a major intrusion pathway are:

• higher concentrations in the upper floors in buildings,
• higher concentrations in indoor air than expected from soil gas measurements,
• higher concentrations in bathrooms/kitchen than in living rooms,
• chlorinated solvents in the sewer system, and
• a pressure gradient from the sewer system to indoor air.

Measurements to detect whether or not the sewer system is an intrusion pathway are simple. In Central Denmark Region, the concentrations of contaminants are routinely measured in the indoor air at all floors, the outdoor air, behind the water traps in the building, and in the manholes close to the building. The indoor and outdoor air concentration, as well as concentrations in manholes, are measured by passive sampling on sorbent samplers over a 14‐day period, and the measurements inside the sewer system are carried out by active sampling using carbon tubes (sorbent samplers). Furthermore, the pressure gradient over the building slab and between the indoor air and the sewer system are also measured. A simple test is depressurization of the sewer system. Using this technique, the pressure gradient between the sewer system and the indoor air is altered toward the sewer system—the contamination cannot enter the indoor air through the sewer system. If the sewer system is a major intrusion pathway, the effect of the test can be observed immediately in the indoor air. Remediation of a sewer transported contamination can be:

• prevention of the contaminants from intruding into the sewer system or
• prevention of the contaminated gas in the sewer system from intruding into the indoor air.

Remediation techniques include the following:

• lining of the sewer piping to prevent the contamination from intruding into the sewer;
• sealing the sewer system in the building to prevent the contamination from the sewer system to intrude the indoor air;
• venting of manholes; and
• depressurizing the sewer system.

     

Addressing soil gas vapor intrusion using sustainable building solutions

Soil gas vapor intrusion (VI) emerged in the 1990s as one of the most important problems in the investigation and cleanup of thousands of sites across the United States. A common practice for sites where VI has been determined to be a significant pathway is to implement interim building engineering controls to mitigate exposure of building occupants to VI while the source of contamination in underlying soil and groundwater is assessed and remediated. Engineering controls may include passive barriers, passive or active venting, subslab depressurization, building pressurization, and sealing the building envelope. Another recent trend is the emphasis on “green” building practices, which coincidentally incorporate some of these same engineering controls, as well as other measures such as increased ventilation and building commissioning for energy conservation and indoor air quality. These green building practices can also be used as components of VI solutions. This article evaluates the sustainability of engineering controls in solving VI problems, both in terms of long‐term effectiveness and “green” attributes. Long‐term effectiveness is inferred from extensive experience using similar engineering controls to mitigate intrusion of radon, moisture, mold, and methane into structures. Studies are needed to confirm that engineering controls to prevent VI can have similar long‐term effectiveness. This article demonstrates that using engineering controls to prevent VI is “green” in accelerating redevelopment of contaminated sites, improving indoor air quality, and minimizing material use, energy consumption, greenhouse gas emissions, and waste generation. It is anticipated that engineering controls can be used successfully as sustainable solutions to VI problems at some sites, such as those deemed technically impracticable to clean up, where remediation of underlying soil or groundwater contamination will not be completed in the foreseeable future. Furthermore, green buildings to be developed in areas of potential soil or groundwater contamination may be designed to incorporate engineering controls to prevent VI. © 2009 Wiley Periodicals, Inc.     

High‐Frequency Continuous Monitoring to Track Vapor Intrusion Resulting From Naturally Occurring Pressure Dynamics

Vapor intrusion characterization efforts can be challenging due to complexities associated with background indoor air constituents, preferential subsurface migration pathways, and response time and representativeness limitations associated with conventional low‐frequency monitoring methods. For sites experiencing trichloroethylene (TCE) vapor intrusion, the potential for acute risks poses additional challenges, as the need for rapid response to exposure exceedances becomes critical in order to minimize health risks and associated liabilities. Continuous monitoring platforms have been deployed to monitor indoor and subsurface concentrations of key volatile constituents, atmospheric pressure, and pressure differential conditions that can result in advective transport. These systems can be comprised of multiplexed laboratory‐grade analytical components integrated with telemetry and geographical information systems for automatically generating time‐stamped renderings of observations and time‐weighted averages through a cloud‐based data management platform. Integrated automatic alerting and responses can also be engaged within one minute of risk exceedance detection. The objectives at a site selected for testing included continuous monitoring of vapor concentrations and related surface and subsurface physical parameters to understand exposure risks over space and time and to evaluate potential mechanisms controlling risk dynamics which could then be used to design a long‐term risk reduction strategy. High‐frequency data collection, processing, and automated visualization efforts have resulted in greater understanding of natural processes such as dynamic contaminant vapor intrusion risk conditions potentially influenced by localized barometric pumping induced by temperature changes. For the selected site, temporal correlation was observed between dynamic indoor TCE vapor concentration, barometric pressure, and pressure differential. This correlation was observed with a predictable daily frequency even for very slight diurnal changes in barometric pressure and associated pressure differentials measured between subslab and indoor regimes and suggests that advective vapor transport and intrusion can result in elevated indoor TCE concentrations well above risk levels even with low‐to‐modest pressure differentials. This indicates that vapor intrusion can occur in response to diurnal pressure dynamics in coastal regions and suggests that similar natural phenomenon may control vapor intrusion dynamics in other regions, exhibiting similar pressure, geochemical, hydrogeologic, and climatic conditions. While dynamic indoor TCE concentrations have been observed in this coastal environment, questions remain regarding whether this hydrogeologic and climatic setting represent a special case, and how best to determine when continuous monitoring should be required to most appropriately minimize exposure durations as early as possible. ©2017 Wiley Periodicals, Inc.     

Vapor intrusion risk evaluation using automated continuous chemical and physical parameter monitoring

Vapor intrusion risk characterization efforts are challenging due to complexities associated with background indoor air constituents, preferential subsurface migration pathways, and representativeness limitations associated with traditional randomly timed time‐integrated sampling methods that do not sufficiently account for factors controlling concentration dynamics. The U.S. Environmental Protection Agency recommends basing risk related decisions on the reasonable maximum exposure (RME). However, with very few exceptions, practitioners have not been applying this criterion. The RME will most likely occur during upward advective flux conditions. As such, for RME determinations, it is important to sample when upward advective flux conditions are occurring. The most common vapor intrusion assessment efforts include randomly timed sample collection events, and therefore do not accurately yield RME estimates. More specifically, researchers have demonstrated that randomly timed sampling schemes can result in false negative determinations of potential risk corresponding to RMEs. For sites experiencing trichloroethylene (TCE) vapor intrusion, the potential for acute risks poses additional challenges, as there is a critical need for rapid response to exposure exceedances to minimize health risks and liabilities. To address these challenges, continuous monitoring platforms have been deployed to monitor indoor concentrations of key volatile constituents, atmospheric pressure, and pressure differential conditions that can result in upward toxic vapor transport and entry into overlying buildings. This article demonstrates how vapor intrusion RME‐based risks can be successfully and efficiently determined using continuous monitoring of concentration and parameters indicating upward advective chemical flux. Time series analyses from multiple selected 8‐ and 24‐hr time increments during upward advective TCE flux conditions were performed to simulate results expected from the most commonly employed sampling methods. These analyses indicate that, although most of the selected time increments overlap within the same 24‐hr window, results and conclusions vary. As such, these findings demonstrate that continuous monitoring of concentration and parameters such as differential pressure and determination of a time‐weighted concentration average over a selected duration when upward advective flux is occurring can allow for a realistic RME‐based risk estimate.     

Recycling building demolition waste in hot-mix asphalt concrete: a case study in Kuwait

Building demolition waste constitutes a major component of municipal solid waste in Kuwait. Over 90% of this waste is currently land-filled, causing extreme pressure on the available land-fill sites. At the same time, the sources of natural aggregates are almost depleted, and there is an increasing demand because of the increased construction and maintenance activities. This article presents the results of a technical feasibility study into meeting this need by recycling the aggregates obtained from building demolition waste for asphalt concrete. The Marshall test, the immersion compression test, the loss of stability test, and the wheel track test were performed to evaluate the asphalt concrete made with recycled aggregate. The results showed that the asphalt concrete produced using an aggregate of demolition waste met all the requirements of local specifications.     

ART in‐well air stripping—An innovative technology succeeds where other technologies have failed

Accelerated Remediation Technologies LLC (ART) developed a proprietary (patent‐pending) effective remediation technology that is based on verified and established concepts. The ART technology combines in‐situ air stripping, air sparging, soil vapor extraction, enhanced bioremediation/oxidation, and Dynamic Subsurface Circulation^TM in an innovative wellhead system. The system is designed to accommodate a 4‐inch well and is cost‐effective when compared with other remediation technologies. The air‐sparging component results in lifting the water table. This lifting of the water in the well causes a net reduction in head at the well location. Vacuum pressure (the vapor‐extraction component) is applied on top of the well point to extract vapor from the subsurface. The negative pressure from the vacuum extraction results in water suction that creates additional water lifting (mounding). A submersible pump is placed at the bottom of the well to recirculate water to the top for downward discharge through a spray head. The water cascades down the interior of the well similar to what occurs in an air‐stripping tower. Enhanced stripping via air sparging near the bottom of the well occurs simultaneously. In essence, the well acts as a subsurface air‐stripping tower. The pumped‐and‐stripped, highly oxygenated water flows down well annulus and over the “mounded” water back in to the aquifer, which creates a circulation zone around the well to further enhance cleanup. The ART technology has been implemented at several sites nationwide, including industrial laundry facilities, manufacturing plants, and service stations, and has achieved significant reductions in contaminant concentrations. Specifically, a concentration of tetrachloroethene (PCE) decreased from 2,700 to 240 μg/l, in 13 days. In less than three months, the concentrations dropped further to 79 μg/l, which is within the range of background levels. Other sites utilizing the technology have exhibited similar reduction trends in complex subsurface environments. © 2002 Wiley Periodicals, Inc.     

PFAS Experts Symposium: Statements on regulatory policy,chemistry and analytics,toxicology, transport/fate,and remediation for per‐ and polyfluoroalkyl substances (PFAS) contamination issues

Sixty leading members of the scientific, engineering, regulatory, and legal communities assembled for the PFAS Experts Symposium in Arlington, Virginia on May 20 and 21, 2019 to discuss issues related to per‐ and polyfluoroalkyl substances (PFAS) based on the quickly evolving developments of PFAS regulations, chemistry and analytics, transport and fate concepts, toxicology, and remediation technologies.  The Symposium created a venue for experts with various specialized skills to provide opinions and trade perspectives on existing and new approaches to PFAS assessment and remediation in light of lessons learned managing other contaminants encountered over the past four decades. The following summarizes several consensus points developed as an outcome of the Symposium:

• Regulatory and policy issues: The response by many states and the US Environmental Protection Agency (USEPA) to media exposure and public pressure related to PFAS contamination is to relatively quickly initiate programs to regulate PFAS sites. This includes the USEPA establishing relatively low lifetime health advisory levels for PFAS in drinking water and even more stringent guidance and standards in several states. In addition, if PFAS are designated as hazardous substances at the federal level, as proposed by several Congressional bills, there could be wide‐reaching effects including listing of new Superfund sites solely for PFAS, application of stringent state standards, additional characterization and remediation at existing sites, reopening of closed sites, and cost renegotiation among PRPs.
• Chemistry and analytics: PFAS analysis is confounded by the lack of regulatory‐approved methods for most PFAS in water and all PFAS in solid media and air, interference with current water‐based analytical methods if samples contain high levels of suspended solids, and sample collection and analytical interference due to the presence of PFAS in common consumer products, sampling equipment, and laboratory materials.
• Toxicology and risk: Uncertainties remain related to human health and ecological effects for most PFAS; however, regulatory standards and guidance are being established incorporating safety factors that result in part per trillion (ppt) cleanup objectives. Given the thousands of PFAS that may be present in the environment, a more appropriate paradigm may be to develop toxicity criteria for groups of PFAS rather than individual PFAS.
• Transport and fate: The recalcitrance of many perfluoroalkyl compounds and the capability of some fluorotelomers to transform into perfluoroalkyl compounds complicate conceptual site models at many PFAS sites, particularly those involving complex mixtures, such as firefighting foams. Research is warranted to better understand the physicochemical properties and corresponding transport and fate of most PFAS, of branched and linear isomers of the same compounds, and of the interactions of PFAS with other co‐contaminants such as nonaqueous phase liquids. Many PFAS exhibit complex transport mechanisms, particularly at the air/water interface, and it is uncertain whether traditional transport principles apply to the ppt levels important to PFAS projects. Existing analytical methods are sufficient when combined with the many advances in site characterization techniques to move rapidly forward at selected sites to develop and test process‐based conceptual site models.
• Existing remediation technologies and research: Current technologies largely focus on separation (sorption, ion exchange, or sequestration). Due to diversity in PFAS properties, effective treatment will likely require treatment trains. Monitored natural attenuation will not likely involve destructive reactions, but be driven by processes such as matrix diffusion, sorption, dispersion, and dilution.

The consensus message from the Symposium participants is that PFAS present far more complex challenges to the environmental community than prior contaminants. This is because, in contrast to chlorinated solvents, PFAS are severely complicated by their mobility, persistence, toxicological uncertainties, and technical obstacles to remediation—all under the backdrop of stringent regulatory and policy developments that vary by state and will be further driven by USEPA. Concern was expressed about the time, expense, and complexity required to remediate PFAS sites and whether the challenges of PFAS warrant alternative approaches to site cleanups, including the notion that adaptive management and technical impracticability waivers may be warranted at sites with expansive PFAS plumes. A paradigm shift towards receptor protection rather than broad scale groundwater/aquifer remediation may be appropriate.     

Forest Ecosystem Responses to Atmospheric Pollution: Linking Comparative With Experimental Studies

The impact on an ecosystem of an environmental stress, such as climate change or air pollution, can be studied through experimentation, through comparisons of sites across a gradient of the stress, through long-term studies at a single site, or through theoretical or modelling approaches. Although the former three techniques often are used to develop and test models, it is much rarer to explicitly link experimental, comparative or long-term studies together. Here we present a concept for combining experimental and comparative research to assess the direction and rate of change, the expected long-term state, and the rate at which the long-term state is achieved after an ecosystem is exposed to an environmental stress. We do this by comparing the response of a forest in Denmark to experimentally increased N deposition with the expected long-term response based on a European database of forests exposed to different levels of N deposition over long time periods. The analysis suggests that if N deposition were to increase by 3-fold to about 50 kg N ha^-1 a^-1 at the Danish site, and remain at this level, the N concentration in needles would respond within 2–4 yr after the onset of the enhanced N deposition, and would rapidly plateau to an expected mean value of 18.0 mg N g^-1 dry mass (95% confidence interval ± 2.5 mg g^-1). The N concentration of new litter also would respond rapidly (1–2 yr) to reach an expected value of 16.6 mg N kg^-1 dry mass (± 3). The N concentration of the organic layer in the soil would increase much more slowly, but a significant increase would be expected within 5–10 yr. Mineral soil pH would take more than 7 yr to change. Finally, the flux of dissolved inorganic N in leachate wouldbegin to increase immediately, but would take many years to reach the expected level of 22.4 kg N ha^-1 a^-1(± 4).