by Joel Kane, Sr Associate, Fleming Lee Shue
Advancements in in-situ remediation technologies have enabled practitioners to aggressively target even the most persistent environmental contaminants. However, it is critical for environmental professionals to recognize that these technologies may unintentionally alter subsurface geochemistry and mobilize or concentrate non-target compounds. This phenomenon—referred to as Technologically Enhanced Contamination—can present unforeseen challenges during long-term monitoring, site closure, and waste management.
TENORM
One of the clearest examples of this phenomenon involves the concentration of Naturally Occurring Radioactive Materials (NORM)—such as isotopes of uranium, thorium, and radium—which are present in trace amounts in soil and groundwater. When groundwater is extracted and treated in large volumes, trace levels of NORM can accumulate in scale deposits, filter media, and sludge within treatment systems. Over time, these accumulations may exceed background levels and surpass regulatory thresholds, transitioning into Technologically Enhanced Naturally Occurring Radioactive Material (TENORM)1.
This process is well-documented in oil and gas operations, where radium-rich scale forms during initial crude separation. Similarly, coal—a common carrier of radioactive isotopes—can produce TENORM when combusted, with radionuclides concentrating in the resulting coal ash. When such ash is later used as fill material, as historically was the case in much of New York City, a remedial system (such as a pump-and-treat well or recovery trench) can unintentionally accumulate TENORM within filters and piping.2
Although certainly not a concern at every site, properties with specific risk factors — such as historic coal ash fill or long-term groundwater extraction systems — may benefit from evaluation of potential TENORM accumulation within treatment infrastructure. Monitoring of scale, filters, and sediments, and proper waste characterization prior to disposal, may be important steps for mitigating radiological health and safety risks.
ERH and Secondary Contaminant Mobilization
The combined use of Electric Resistance Heating (ERH) and Soil Vapor Extraction (SVE) can significantly enhance the removal of volatile and semi-volatile organic compounds. ERH increases subsurface temperatures, volatilizing contaminants and improving mass transfer to the vapor phase, where they are captured by SVE systems.
However, superheating the subsurface can also inadvertently increase the mobility of otherwise immobile contaminants—such as Polychlorinated Biphenyls (PCBs). Though PCBs have low volatility under ambient conditions, elevated temperatures enhance their partitioning to the vapor phase.3 When combined with the strong advective forces of an SVE system, low-level PCB concentrations can migrate toward extraction points, and potentially concentrate in knock-out drums, vapor treatment vessels, and even within localized areas of the subsurface if not fully extracted by the SVE.
Several studies and post-operation evaluations have identified unexpectedly high PCB concentrations in vapor-phase effluent and condensate, requiring specialized waste handling and disposal.4 While ERH remains a powerful tool, practitioners must anticipate the possibility of mobilizing compounds not originally targeted in the remedial design.
ISCO and Metal Mobilization
In Situ Chemical Oxidation (ISCO) is another widely used remedial technology, wherein strong oxidants—such as sodium persulfate, permanganate—are injected into the subsurface to destroy organic contaminants.
However, these oxidants can often significantly alter the geochemical balance of the aquifer. They may lower pH, increase redox potential, and raise ionic strength—conditions that favor the dissolution of naturally occurring metals previously bound to soil minerals. Following ISCO treatment, it is not uncommon to observe elevated concentrations of iron, manganese, arsenic, and lead within the groundwater monitoring programs.5
Though these metals are not typically the focus of remediation, their mobilization can complicate site closure or regulatory compliance, particularly if they were previously below detection limits. For sites considering ISCO, baseline groundwater chemistry should be evaluated in advance, and post-treatment monitoring should include metals to assess for geochemically driven mobilization.
ERH-Induced Geochemical Shifts and Metals
In addition to contaminant volatilization, ERH can cause broader geochemical shifts within the local affected aquifer. When highly chlorinated solvents—such as PCE or TCE—are thermally degraded, the reaction often generates free chloride ions, which can acidify the groundwater and increase its ionic strength.6
This shift enhances the solubility of subsurface metals, which may then appear in monitoring data as elevated concentrations of iron, manganese, arsenic, or lead. While often transient, these metals spikes can delay regulatory closure or complicate long-term monitoring, especially when concentrations exceed site-specific cleanup criteria.
As with ISCO, pre-treatment geochemical profiling and careful interpretation of post-treatment data are critical for managing unintended consequences.
Implications for Remedial Design and Site Management Monitoring
Modern remedial technologies offer powerful tools to achieve cleanup goals, but it is important to be aware that they may also trigger secondary effects that are not immediately apparent during remedy design. Subsurface heating, oxidation, and even pump & treat can all change the behavior of metals, radionuclides, and semi-volatile organics in ways that can influence both short and long-term outcomes.
To help best anticipate and manage Technologically Enhanced Contamination, environmental professionals may opt to:
- Conduct thorough baseline investigations of groundwater chemistry and geologic conditions
- Develop a robust conceptual site model that considers geochemical responses
- Monitor non-target compounds throughout and after system operation
- Coordinate with regulators early to plan for temporary and/or unexpected byproducts or secondary contaminant mobilization/spikes.
Understanding these site-specific interactions is critical for managing costs, ensuring regulatory compliance, and achieving sustainable site closure.
- U.S. EPA (2022). TENORM in Oil and Gas Production. https://www.epa.gov/radiation/tenorm-oil-and-gas-production-wastes
- NYC Department of Environmental Protection. Historical Fill and Ash Use in NYC.
- Johnson, G. et al. (2009). PCB Behavior in Subsurface Thermal Remediation. Environmental Science & Technology.
- Heron, G., Van Zutphen, M., & Carroll, S. (2009). “Design and performance of an in situ thermal remediation at a former manufacturing facility.” Remediation Journal, 19(3), 5–21. Rogers, R.D., et al. (1999). “Application of electric resistance heating to PCB-contaminated soils.” Journal of Hazardous Materials, 68(3), 235–256.
- Interstate Technology & Regulatory Council (2005). In Situ Chemical Oxidation Guidance Document.
- Lee, T.Y., et al. (2015). Impact of Thermal Remediation on Groundwater Geochemistry. Environmental Science: Processes & Impacts.
The Author:

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Joel Kane is a Senior Associate at Fleming Lee Shue, where he oversees the firm’s technical operations and manages a diverse portfolio of remediation projects across the greater New York Metropolitan Area. He specializes in complex remediation sites and his experience spans both the public and private sectors. Joel works closely with developers, agencies, real estate firms, and legal teams to navigate environmental regulations across local, state, and federal programs—including NEPA, CERCLA, the Brownfield Cleanup Program, E-Designations, petroleum spills, and CEQR/SEQR.
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