In-situ biological treatment of vinyl acetate-contaminated soil: An emergency response action

In-situ biological solid-phase (or land) treatment was cost-effectively used to remediate 1,500 cubic yards (1,100 m³) of contaminated soil within three months of field operation following spillage of an estimated 12,000 gallons (45,000 L) of vinyl acetate from a railroad tank car onto surface soil. The vinyl acetate rapidly hydrolyzed to acetate and acetaldehyde with concentrations ranging up to 22,000 and 3,000 mg/kg, respectively. Ethanol, a metabolic intermediate, was found to accumulate in soil to concentrations as high as 280 mg/kg. The estimate for excavation, transportation, and disposal of the contaminated soil as a special waste, and for backfilling of the excavated area, was $850,000. The cost for biological remediation of the contaminated soil was $400,000, which was less than half the cost of excavation. In-situ biological treatments have been used to readily remove contaminants, such as acrylonitrile, styrene, butylcellosolve, ethylacrylate, and n-butylacrylate, at other sites involving railroad incidents.     

Enhanced land treatment of petroleum-contaminated soils using solid peroxygen materials

A pilot field study evaluated whether adding solid peroxygen materials during land treatment could cost effectively accelerate cleanup at a site contaminated with petroleum-related compounds. Five test cells were constructed containing approximately five cubic yards of soil contaminated with 300–400 mg/kg of total petroleum hydrocarbons (TPH). Three cells received treatment with solid peroxygen materials (either MgO₂ or CaO₂), while the other two cells served as controls (no peroxygen amendment). Adding solid peroxygen compounds effectively reduced the hydrocarbon contamination in the soils and decreased the treatment time. During this time, the concentration of TPH in soil in the three treatment cells decreased. In contrast, there was little loss of TPH from the two control cells simulating traditional land treatment. Adding the solid peroxygen materials reduced the total site remediation time, thereby reducing the overall costs.     

Remediation of the Radioactive Waste Landfill and Chemical Disposal Pits Sites at Sandia National Laboratories

Sandia National Laboratories' Environmental Restoration (ER) Project remediated the Radioactive Waste Landfill and Chemical Disposal Pits (RWL/CDPs) sites located in Albuquerque, New Mexico. The remediation was conducted in 1996 using conventional excavation, as well as hybrid remote robotic manipulation technology at a cost of approximately $3 million. Wastes generated included approximately 73 cubic meters (m³) of debris (including thermal batteries, spark gap tubes, radioactive sources, weapons components, and some classified material), 535 m³ of plutonium-contaminated soil, and 2,294 m³ of soil contaminated with thorium, cesium, uranium, and tritium. The remediation was successful since the project goal of risk reduction was accomplished and no injuries or negative occurrences resulted. This cleanup is one example of the Department of Energy's (DOE's) accelerated approach to environmental restoration. The remediation was performed as a voluntary corrective measure to reduce schedule and budget, compared with the traditional approach following Resource Conservation and Recovery Act (RCRA) regulations.     

Combined thermal and zero‐valent iron In Situ soil mixing remediation technology

Thermal remediation of contaminated soils and groundwater by injection of hot air and steam using large‐diameter auger in situ soil mixing effectively remediates volatile and semivolatile organic compounds. This technology removes large amounts of contamination during the early treatment stages, but extended treatment times are needed to achieve high removal percentages. Combining thermal treatment with another technology that can be injected and mixed into the soil, and that continues to operate after removal of the drilling equipment, improves removal efficiency, and reduces cost. Using field‐determined pseudo first‐order removal rates, the cost of the combined remediation of chlorinated volatile organic compounds (CVOCs) by thermal treatment followed by reductive dechlorination by iron powder has been estimated as 57 percent of the cost of thermal treatment alone. This analysis was applied to a case‐study remediation of 48,455 cubic yards, which confirmed the cost estimate of the combined approach and showed over 99.8 percent removal of trichloroethene and other chlorinated VOCs. © 2010 Wiley Periodicals, Inc.     

Hydrogen peroxide for physicochemically degrading petroleum-contaminated soils

Catalyzed hydrogen peroxide was applied to contaminated soil at an equipment storage yard in Reno, Nevada, that had also been used as a dump for motor oil and diesel fuel for twenty years. The site is only a quarter mile from the Truckee River—a principal source of Reno's drinking water. This article details hydrogen peroxide's advantages, disadvantages, costs, and treatment for reducing to below the 100 mg/kg Nevada action level the petroleum hydrocarbons in the yard's arid soil, which is characterized by low organic carbon content and low manganese oxide content.     

A research note on the assessment of optimum conditions for preparing soils for bioremediation feasibility testing

In this applied study, the effects of short‐term storage at 22°C, 6°C, and ?25°C on the numbers of microorganisms enumerated were examined with soils collected from a petrochemical contaminated soil containing multiple contaminants including phenol, polycyclic aromatic hydrocarbons, and petroleum hydrocarbons. Short term storage of soils at refrigerator temperature did not significantly change the number of microorganisms compared to those in the fresh soil (0 days of storage); however, at ?25°C there was a slight decrease in the phenol utilizers and total viable count (TVC). Long‐term storage caused a significant decrease in the number of phenol utilizers in the petrochemical‐contaminated soil samples. Chemical dispersing agents were used in an attempt to increase the extraction of microorganisms from naphthalene contaminated soil which were predominantly clay soils. These did not significantly change the enumeration of naphthalene utilizers or TVC. While these results are not unexpected from current research and knowledge of microbial community succession in laboratory environments, the results from the applied nature of this study confirm that it is best practice to keep soil samples designated for bacterial enumeration for the shortest possible time, and not longer than 1–2 weeks, and at refrigerated temperature (6°C) in preference to room (22°C) or deep freezer (?18°C) temperatures.     

Stabilization and a multimedia cap for a doe mixed waste site

Closure often of the eleven waste management units covering almost seventy-five acres at the U.S. Department of Energy's Oak Ridge Y-12 Plant has been completed. Costing about $47 million, DOE's accelerated Closure and Post Closure Program (CAPCA) has involved structural waste stabilization and installation of a multimedia cap to contain ferrous metals, salts, uranium, solvents, ethylenediamine tetraacetic acid (EDTA), oils and coolants, asbestos, and material contaminated with radioisotopes. Designs for closure of the remaining waste unit—used for disposing depleted uranium chips, metals, oxides, organic and caustic chemicals, aged ethers, and more—are being prepared now; they will address the potentially explosive and pyrophoric nature of these wastes. This article describes CAPCA's innovative design and construction methods, as well as how its management coordinated the tight schedules mandated by agreements with federal and state regulatory agencies.     

ERI evaluation of injectates used at a dry‐cleaning site

A former dry‐cleaning site in Jackson, Tennessee, has undergone remediation to treat dense nonaqueous‐phase liquid (trichloroethene [TCE] and tetrachloroethene [PCE]) contamination in the subsurface. The dry cleaning operation closed in 1977. In 2002, a series of injections were made at the site consisting of corn syrup, vegetable oils, and Simple Green®. In 2004, approximately 200 cubic yards of contaminated soil were excavated, and the bottom of the excavation was covered with sodium lactate. In 2009, the site was characterized using proprietary electrical resistivity imaging (ERI; commercially available as Aestus GeoTrax Surveys^TM). Follow‐up confirmation soil borings targeted anomalies detected via the geophysical work. The results indicate an extremely electrically conductive (less than 1 ohm‐m) vadose zone downgradient from the injection wells, and extremely electrically resistive areas (greater than 10,000 ohm‐m) in the phreatic zone near the injection area. The sample data indicate that the electrically resistive anomalous zones contain moderate to high concentrations of undegraded dry‐cleaning compounds. Electrically conductive anomalous zones are interpreted to be areas of biological activity generated by the amendments injected into the subsurface based on the extreme conductivity values detected, the chemical composition (i.e., PCE degradates are present), and the dominant vadose‐zone location of the conductive zones. © 2012 Wiley Periodicals, Inc.     

Challenges of soil mixing using catalyzed hydrogen peroxide with rotating dual axis blending technology

Although known to be one of the most effective oxidants for treatment of organic contaminants, catalyzed hydrogen peroxide (CHP) is typically not used for soil mixing applications because of health and safety concerns related to vapor generation and very rapid rates of reaction in open excavations. In likely the first large‐scale in situ CHP soil mixing application, an enhanced CHP, modified Fenton's reagent (MFR), was applied during soil mixing at the Kearsarge Metallurgical Superfund Site in New Hampshire. An innovative rotating dual‐axis blender (DAB) technology was used to safely mix the MFR into low‐plasticity silt and clay soils to remediate residual 1,1,1‐trichloroethane (111TCA); 1,1‐dichloroethene (11DCE); and 1,4‐dioxane (14D). It was expected that the aggressive treatment approach using relatively “greener” hydrogen peroxide (HP) chemistry would effectively treat Site contaminants without significant byproduct impacts to groundwater or the adjacent pond. The remediation program was designed to treat approximately 3,000 cubic yards of residual source area soil in situ by aggressively mixing MFR into the soils. The subsurface interval treated was from 7 to 15 feet below ground surface. To accurately track the soil mixing process and MFR addition, the Site was divided into 109 10‐foot square treatment cells that were precisely located, dosed, and mixed using the DAB equipped with an on‐board GPS system. The use of stabilizing agents along with careful calculation of the peroxide dose helped to ensure vapor‐free conditions in the vicinity of the soil mixing operation. Real‐time sampling and monitoring were critical in identifying any posttreatment exceedences of the cleanup goals. This allowed retreatment and supplemental testing to occur without impacting the soil mixing/in situ chemical oxidation (ISCO) schedule. Posttreatment 24‐hr soil samples were collected from 56 random locations after ensuring that the HP had been completely consumed. The posttreatment test results showed that 111TCA and 11DCE concentrations were reduced to nondetect (ND) or below the cleanup goals of 150 μg/kg for 111TCA and 60 μg/kg for 11DCE. Supplemental posttreatment soil samples, collected six months after treatment, showed 100 percent compliance with the soil treatment goals. Groundwater samples collected one year after the MFR soil mixing treatment program showed either ND or low concentrations for 111TCA, 11DCE, and 14D. Successful stabilization and site restoration was performed after overcoming considerable challenges associated with loss of soil structure, high liquid content, and reduced bearing capacity of the blended soils.     

In Situ solidification—A case study at a former manufactured gas plant in Macon,Georgia

In situ solidification (ISS) is a reliable, EPA‐recognized technology for the treatment of industrial and waste sites. ISS was employed at a former manufactured gas plant (MGP) site in Macon, Georgia, for the treatment of approximately 33,000 cubic yards of coal tar residues in the saturated zone soil. The site is regulated by the Georgia Environmental Protection Division (EPD) under the Hazardous Site Rehabilitation Act (HSRA) and is located approximately four blocks from downtown Macon. This article will review the technical and regulatory basis for the successful use of this technology, provide an overview of the treatability and pilot testing used to develop the design and implementation of the treatment process, and present the results of the application of ISS to an MGP site. The results of groundwater monitoring, pre and postremediation, will also be discussed. © 2004 Wiley Periodicals, Inc.     

Soil washing for volume reduction of radioactively contaminated soils

The Office of Radiation and Indoor Air of the U.S. Environmental Protection Agency has demonstrated a soil washing plant for the treatment of radioactively contaminated soils from two Superfund sites in New Jersey. The plant employs unit operations that are widely used in the processing of minerals and coal. These operations were examined and tested to determine how they would apply to volume reduction of these contaminated soils. In this context, they are considered to be innovative candidates for remediation of other sites with large volumes of soil contaminated with low-level radioactivity. Laboratory testing of soil characteristics and behavior in unit processes is used to assess the applicability of volume reduction/chemical extraction (VORCE) technology to specific sites.     

Successful solid-phase bioremediation of petroleum-contaminated soil

Biological processes have been used to remediate petroleum hydrocarbons, pesticides, chlorinated solvents, and halogenated aromatic hydrocarbons. Biological treatment of contaminated soils may involve solid-phase, slurry-phase, or in situ treatment techniques. This article will review the general principle of solid-phase bioremediation and discuss the application of this technique for the cleanup of total petroleum hydrocarbons on two sites. These remedial programs will reduce total petroleum hydrocarbon contamination from the mean concentration of 2,660 ppm to under the 200-ppm cleanup criteria for soil and under the 15-ppm cleanup criteria for groundwater. Over 32,000 yards of soil have been treated by solid-phase treatment to date. The in situ system operation is effectively producing biodegradation in the subsurface. The project is approximately one-third complete.     

The Use of Zero‐Valent Iron (ZVI) Technology to Promote DDT and Dieldrin Degradation at Point Pelee National Park

Point Pelee National Park (PPNP) is highly contaminated with dichlorodiphenyltrichloroethane (DDT) and dieldrin due to the historical use of these two persistent organochlorine pesticides. Zero‐valent iron (ZVI) technology with and without amendments has been successfully used in the past to promote organochlorine pesticides degradation in several locations in North America and Europe. In this study, the use of two commercially available ZVI products, DARAMEND^® and EHC^®, to promote DDT and dieldrin degradation in PPNP's soil and groundwater were investigated. DARAMEND^® was applied to PPNP's soil in a laboratory experiment and in an in situ pilot‐scale plot. In both cases, DARAMEND^® did not significantly increase DDT or dieldrin degradation in treated soils. The effectiveness of EHC^® was tested in a laboratory experiment that simulated the park's groundwater environment using PPNP's pesticide contaminated soil. The result was consistent with the one reported for DARAMEND^®, in that there was no significant increase in DDT or dieldrin degradation in any of the samples treated with EHC^®. These results demonstrate that both of these ZVI commercially available products are not suitable for in situ remediation at PPNP.  ©2017 Wiley Periodicals, Inc.     

Remediation and review: Developing groundwater strategy at the hanford site

The U.S. Department of Energy's (US DOE's) environmental challenges include remediation of the Hanford Site in Washington State. The site's legacy from nuclear weapons “production” activities includes approximately 80 square miles of contaminated groundwater, containing radioactive and other hazardous substances at levels above drinking water standards. In 1998, the U.S. General Accounting Office (US GAO), the auditing arm of Congress, concluded that groundwater remediation at Hanford should be integrated with a comprehensive understanding of the “vadose zone,” the soil region between the ground surface and groundwater. The US DOE's Richland Operations Office adjusted its program in response, and groundwater/vadose‐zone efforts at Hanford have continued to develop since that time. Hanford provides an example of how a federal remediation program can be influenced by reviews from the US GAO and other organizations, including the US DOE itself. © 2008 Wiley Periodicals, Inc.     

Nuclear waste disposition and site remediation: U.S. department of energy,state governments,and other stakeholders dialogue

Remediation responsibilities of the U.S. Department of Energy (DOE) encompass a vast national complex of highly contaminated former weapons facilities. During the mid‐1990s, DOE announced its intentions to consolidate some waste types at specific sites. At about the same time, organizations and public officials around DOE sites urged a National Dialogue, designed to develop comprehensive solutions to the Department's needs for waste disposition ( transportation, treatment, and storage). Recent opposition from citizens and elected officials in Nevada and Washington State has presented obstacles to DOE's plans. Additionally, chairs of nine site‐specific advisory boards recommended that DOE support a National Stakeholder Forum, similarly designed to develop solutions to disposition needs. This article reviews the chronology of DOE's disposition efforts, along with public and state reactions and recommendations. © 2006 Wiley Periodicals, Inc.     

To Dredge or Not

The streams, rivers, freshwater lakes, and coastal and open ocean waters of the world have been used for centuries for the disposal of municipal and industrial wastes. During the twentieth century, the range and quantities of waste materials discharged to the world's fresh and salt waters have grown progressively, increasing the potential ecological and human health impacts. The types and quantities of organic and inorganic wastes reaching the surface waters and associated sediments have increased in proportion to a region's or nation's population and industrial growth. Many of the contaminaants deliberately or inadvertently discharged to waterways are hydrophobic, are not biodegradable, or are highly resistant to degradation resulting in the accumulation of organic and inorganic substances in the waters, bottom, and suspended sediments of impacted waterways. Because of their persistence, these compounds and trace metals bioaccumulate and bioconcentreate in the aquatic organisms that occupy the affected waterway. Because many of the discharged waste materials are relatively insoluble and readily sorb to particles, the bottom and suspended sediments will commonly have higher contaminant concentrations than the associated overlying waters. Concentrations will normally decrease downstream of the contaminant source areas due to inputs and dilution by sediments and waters from cleaner tributaries. Although the sediments will normally have the higher concentrations, considerable quantities of contaminants may be found in the aqueous phase requiring not only removal of the solids, but treatment of the associated water as well. This is particularly the case when the water to solids recovered during dredging may approach 10:1. Many of the persistent contaminants impacting a nation's waterways are readily sorbed to the finer‐grained, organic rich sediments. Reaches of rivers and streams, or areas amenable to deposition of organic rich clays and silts, result in the creation of “hot spots” of contamination, localized areas where higher contaminant concentrations are found. It is these “hot spots” that are at the center of a debate over whether to dredge or leave the contaminated sediments undisturbed to allow natural attenuation to work. It is well recognized that dredging is not able to remove all of the contaminated sediments; some portion of the resuspended sediments created during the dredgirg will be dispersed downstream. The issue is whether to physically removeportions of the mass of contaminants impacting waterwa‐ys or rely on natural attenuation. Environmental dredging is expensive and many argue not worth the effort because of the lack of effective technologies that will prevent redistribution of the material resuspended as apart oJthe dredging process and management of associated water. Opponents of dredging cite natural attenuation and burial by cleaner sediments as eflective mechanisms to reduce the concentration of contaminants. Dredgingproponents argue the contaminant sources and accumulated hot spots must be removed in order to accelerate ecological recovery of the impacted waterway as well as reduce impacts to the environment and to public heulth. During thc next several years, decisions will be made by the U.S. Environmental Protection Agemy (USEPA) on whether to dredge major and minor waterways involving millions of cubic yards of contaminatedsedinaents requiring expenditures of hundreds of millions oj‐dollars by the responsible parties. © 2000 John Wiley & Sons, Innc.     

Treatment of MTBE‐Contaminated Waters with Fenton's Reagent

Methyl tertiary‐butyl ether (MTBE) is commonly used as a fuel additive because of its many favorable properties that allow it to improve fuel combustion and reduce resulting concentrations of carbon monoxide and unburnt hydrocarbons. Unfortunately, increased production and use have led to its introduction into the environment. Of particular concern is its introduction into drinking water supplies. Accordingly, research studies have been initiated to investigate the treatment of MTBE‐contaminated soil and groundwater. The summer 2000 issue of Remediation reported the results of an initial study conducted by the authors to evaluate the treatment of MTBE using Fenton's reagent. In this follow‐up study, experiments were conducted to further demonstrate the effectiveness of using Fenton's reagent (H₂O₂:Fe⁺²) to treat MTBE‐contaminated groundwater. The concentration of MTBE was reduced from an initial concentration of 1,300 μg/l (14.77 μ moles) to the regulatory level of 20 μg/l (0.23 μ moles) at a H₂O₂:Fe⁺² molar ratio of 1:1, with ten minutes of contact time and an optimum pH of 5. The by‐products, acetone and tertiary butyl alcohol, which are always present in MTBE in trace amounts, were not removed even after 60 minutes of reaction time. © 2002 Wiley Periodicals, Inc. *     

Removal and recovery of creosote sludge at a wood treatment plant

Off-site reclamation and incineration of residues proved to be the most efficient and cost-effective solution for remediation of the Broderick Wood Products Superfund site, a closed-down wood-preserving plant outside of Denver, Colorado. More than 3,200 cubic yards of hazardous K001 creosote sludge were removed and recovered at a total cost of only $3.1 million.     

Natural attenuation of a low mobility chlorinated insecticide in low-level and high-level contaminated soil: A feasibility study

Endosulfan is an economically important insecticide and widespread environmental pollutant, originating from a wide range of agricultural activities. The major implication from the feasibility study described was that endosulfan I can be remediated by natural attenuation processes in cotton-farming soil, in which concentrations were relatively low, as well as heavily contaminated soil, from an agricultural chemical waste (evaporation) pit. Endosulfan I, the major isomer of endosulfan, was present in agricultural soils with low (2.2 mg/kg) and high (417 mg/kg) concentrations of technical-grade endosulfan. The half-lives of the major isomer of endosulfan were 94 and greater than 350 days in the low-level (cotton farming soil) and high-level (contaminated soil), respectively. Even under conditions of minimal intervention, as in the current study, endosulfan concentrations in contaminated soils can be substantially reduced. The nonbiological process of soil binding was predominantly responsible for the natural attenuation of endosulfan I in both soils. Low levels of mineralization of the chlorinated ring ¹⁴C-labelled carbons were also reported, but mineralization did not play an important role in natural attenuation of endosulfan I in either soil studied.