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.     

Ethanol washing of PAH-contaminated soil and Fenton oxidation of washing solution

As a means to remediate soil contaminated by polycyclic aromatic hydrocarbons, we investigated a combined process involving ethanol washing followed by a Fenton oxidation reaction. Artificial loamy soil was contaminated with various representative polycyclic aromatic hydrocarbons (i.e., fluorene, anthracene, pyrene, benzo(b)fluoranthene, or benzo(a)pyrene) at concentrations ten times higher than regulatory soil standards of The Netherlands or Canada, and then washed four times in ethanol, which reduced the concentration of polycyclic aromatic hydrocarbon contamination to below the regulatory standard. Fenton oxidation of ethanol solutions containing anthracene, benzo(a)pyrene, pyrene, acenaphthylene, acenaphthene, benz(a)anthracene, benzo(j)fluoranthene, or indeno(1,2,3-cd)pyrene showed a removal efficiency of 73.3%–99.0%; by contrast, solutions containing naphthalene, fluorene, fluoranthene, phenanthrene, or benzo(b)fluoranthene showed a removal efficiency of 9.6%–27.6%. Since each of the nonremediated polycyclic aromatic hydrocarbons, excluding benzo(b)fluoranthene, are easily biodegradable, these results indicate that the proposed treatment can be successfully applied to polycyclic aromatic hydrocarbon-contaminated soil that does not contain high concentrations of benzo(b)fluoranthene. The main reaction products resulting from Fenton oxidation of ethanol solutions containing anthracene or benz(a)anthracene were anthraquinon or benz(a)anthracene-7,12-dione, respectively; while 1,8-naphthalic anhydride was produced by solutions of acenaphthylene and acenaphthene, and 9-fluorenone by a fluorene solution. Received: June 9, 1998 / Accepted: March 24, 1999     

Integrated bioremediation of soil and groundwater at a superfund site

The soil and two aquifers under an active lumber mill in Libby, Montana, had been contaminated from 1946 to 1969 by uncontrolled releases of creosote and pentachlorophenol (PCP). In 1983, because the contaminated surface soil and the shallower aquifer posed immediate risks to human health and the natural environment, the U.S. Environmental Protection Agency placed the site on its National Priorities List. Feasibility studies in 1987 and 1988 determined that in situ bioremediation would help clean up this aquifer and that biological treatment would help clean up the contaminated soils. This article outlines the studies that led to a 1988 EPA record of decision and details the EPA-approved remedial plan implemented starting in 1989; EPA estimates a total cost of about $15 million (in 1988 dollars). The plan involves extensive excavation and biological treatment of shallow contaminated soils in two lined and bermed land treatment units, extraction of heavily contaminated groundwater, an aboveground bioreactor treatment system, and injection of oxygenated water to the contaminant source area, as well as to other on-site areas affected by the shallower aquifer's contaminant plume.     

The influence of soil macroinvertebrates on primary biodegradation of starch-containing polyethylene films

The primary biodegradability of polyethylene (PE) films containing different percentages of cornstarch (0–50%) and other additives (prooxidant, oxidized polyethylene) was tested using four species of earthworms (Eisenia fetida, Lumbricus terrestris, Aporectodea trapezoides, Aporectodea tuberculata), three species of cockroaches (Periplaneta americana, Blaberus sp.,Blattella germanica), termites (Reticulotermes flavipes), sowbugs (Porcellio laevis), and crickets (Acheta domesticus). These studies were conducted to elucidate the potential role of soil macroinvertebrates in degrading starch/PE biodegradable plastics. The results of the macroinvertebrate bioassays indicate that crickets, cockroaches, and sowbugs consumed starch-containing PE films most readily. In addition, the degree to which the films were attacked and consumed was directly related to the starch content of the film. Films with oxidized polyethylene and those containing prooxidant (vegetable oil and a transition metal catalyst) were also consumed. None of the four species of earthworms tested or the termites showed any activity toward the starch/polyethylene films. These results have important implications for determining the fate of novel plastic formulations which claim to be biodegradable in natural environments. Studies such as these, coupled with studies on microbial degradation, will help provide the type of information needed to assess the environmental fate of biodegradable starch/PE plastics and fill the voids in the scientific database regarding this rapidly developing field.     

The influence of air inflow on CH4 composition ratio in landfill gas

When landfill gas is collected, air inflow into the landfill can reduce CH₄ productivity. The decline of CH₄ content in landfill gas (LFG) negatively affects energy projects. We studied air inflow rates and LFG characteristics from 699 vertical collection facilities (VCFs) in the 2nd landfill at the Sudokwon Landfill in South Korea. We first determined whether or not N₂ was an effective indicator of air inflow at this site using argon assays. The results of this analysis showed that the denitrification processes could be disregarded and that N₂ was an effective indicator of air inflow. Using the composition of N₂ in LFG samples, we found that air inflow occurred at 73.6 % of the VCFs, and 25.6 % of samples from these facilities showed more than 80 vol% of air inflow. In addition, we observed that the O₂ consumption rate was more than 70 % of the volume in all samples. $ R_{{{\text{CH}}_{ 4} }} $ , which is the ratio of CH₄ to the sum of CH₄ and CO₂, decreased with increasing air inflow. Finally, we found that, as air inflow increased, the variation in $ R_{{{\text{CH}}_{ 4} }} $ values for samples with equal air inflow ratios also increased due to differences in air inflow routes.     

The process and potential of bioremediation

Bioremediation has proven to be a powerful weapon in cleaning up contaminated soils and aquifers. This article gives the perspective of time, cost, and extent of remediation. It warns that disappointment will follow unless adequate site assessments are made and that the support of nutrients and supply of oxygen must be assured. Bioremediation cannot deal with all contaminants and the process is not instantaneous. However, the method is fail safe. In spite of any mistakes we may make, nature will eventually come to our rescue.     

Temporal variability of soil gas composition in landfill covers

In order to assess the temporal variability of the conditions for the microbial oxidation of methane in landfill cover soils and their driving variables, gas composition at non-emissive and strongly emissive locations (hotspots) was monitored on a seasonal, daily and hourly time scale on an old, unlined landfill in northern Germany. Our study showed that the impact of the various environmental factors varied with the mode of gas transport and with the time scale considered. At non-emissive sites, governed by diffusive gas transport, soil gas composition was subject to a pronounced seasonal variation. A high extent of aeration, low methane concentrations and a high ratio of CO₂ to CH₄ were found across the entire depth of the soil cover during the warm and dry period, whereas in the cool and moist period aeration was less and landfill gas migrated further upward. Statistically, variation in soil gas composition was best explained by the variation in soil temperature. At locations dominated by advective gas transport and showing considerable emissions of methane, this pattern was far less pronounced with only little increase in the extent of aeration during drier periods. Here, the change of barometric pressure was found to impact soil gas composition. On a daily scale under constant conditions of temperature, gas transport at both types of locations was strongly impacted by the change in soil moisture. On an hourly scale, under constant conditions of temperature and moisture, gas migration was impacted most by the change in barometric pressure. It was shown that at diffusion-dominated sites complete methane oxidation was achieved even under adverse wintry conditions, whereas at hotspots, even under favorable dry and warm conditions, aerobic biological activity can be limited to the upper crust of the soil.     

Use of lignin degrading fungi in bioremediation

The use of lignin degrading fungi for decomposition of a wide variety of xenobiotics has become an area of intensive research. One distinct advantage of lignin degrading fungi over bacteria is that they do not require preconditioning to a particular pollutant prior to transformation. This degradative ability has been attributed to a nonspecific and nonstereoselective extracellular lignin-degrading enzymatic system (ligninase) which is induced by the fungi under nitrogen or carbon-limiting conditions (Reid, 1979). Ligninases (lignin-peroxidases) are responsible for the initial oxidative attack on lignin and other complex molecules via formation of a free radical thereby leading to depolymerization of complex molecular structures. Potential degradative ability of peroxidases may extend to include (1) sorbed contaminants, (2) high molecular-weight, hydrophobic contaminants, and (3) complex mixtures of chemicals typical of a contaminated site.     

The use of enhanced bioremediation at the Savannah River Site to remediate pesticides and PCBs

Enhanced bioremediation is quickly developing into an economical and viable technology for the remediation of contaminated soils. Until recently, chlorinated organic compounds have proven difficult to bioremediate. Environmentally recalcitrant compounds, such as polychlorinated biphenyls (PCBs) and persistent organic pesticides (POPs) such as dichlorodiphenyl trichloroethane (DDT) have shown to be especially arduous to bioremediate. Recent advances in field‐scale bioremedial applications have indicated that biodegradation of these compounds may be possible. Engineers and scientists at the Savannah River Site (SRS), a major DOE installation near Aiken, South Carolina, are using enhanced bioremediation to remediate soils contaminated with pesticides (DDT and its metabolites, heptachlor epoxide, dieldrin, and endrin) and PCBs. This article reviews the ongoing remediation occurring at the Chemicals, Metals, and Pesticides (CMP) Pits using windrow turners to facilitate microbial degradation of certain pesticides and PCBs. © 2003 Wiley Periodicals, Inc.     

Enhanced intrinsic bioremediation of hydrocarbons using an oxygen-releasing compound

An “oxygen barrier” was formed by depositing an oxygen-releasing compound in a series of wells that were placed perpendicular to the direction of groundwater flow at a site in Belen, New Mexico. The objective was to enhance the intrinsic bioremediation of dissolved phase BTEX contamination in the aquifer and to quantify the results. The oxygen was supplied by a controlled release formulation of magnesium peroxide called Oxygen Release Compound (ORC®), a virtually insoluble powder that is packaged in polyester filter socks. The areal distributions of the initial concentrations of dissolved oxygen and BTEX were measured and compared to the concentration changes at various times in the first 93 days of system operation. The concomitant reduction in BTEX can be seen in a series of contour plots. In 93 days, dissolved oxygen had dispersed at least 20-feet downgradient from the ORC source wells based on the pattern of decreasing BTEX concentrations.     

In-situ bioremediation of an aquifer contaminated with 1,2-dichloroethane

This article describes the application of in-situ bioremediation for the treatment of an aquifer contaminated with 1,2-dichloroethane (DCA). The first step in the process was to properly delineate the contamination and to contain the contaminated groundwater using a pumping well. The second step was to isolate in the groundwater microorganisms able to degrade DCA and to demonstrate the possibility of increasing their efficiency by injecting in-situ nutrients and hydrogen peroxide (H₂O₂) solution. In the third step, after the characterization of the hydrogeology of the aquifer with tracing experiments, the in-situ bioremediation of the groundwater was conducted. The analyses show that 95 percent of DCA was destroyed by this treatment, leading to a DCA concentration around the pumping well of about 0.2 mg/l.     

The influence of atmospheric pressure on landfill methane emissions

Landfills are the largest source of anthropogenic methane (CH4) emissions to the atmosphere in the United States. However, few measurements of whole landfill CH4 emissions have been reported. Here, we present the results of a multi-season study of whole landfill CH4 emissions using atmospheric tracer methods at the Nashua, New Hampshire Municipal landfill in the northeastern United States. The measurement data include 12 individual emission tests, each test consisting of 5-8 plume measurements. Measured emissions were negatively correlated with surface atmospheric pressure and ranged from 7.3 to 26.5 m3 CH4 min(-1). A simple regression model of our results was used to calculate an annual emission rate of 8.4 x 10(6) m3 CH4 year(-1). These data, along with CH4 oxidation estimates based on emitted landfill gas isotopic characteristics and gas collection data, were used to estimate annual CH4 generation at this landfill. A reported gas collection rate of 7.1 x 10(6) m3 CH4 year(-1) and an estimated annual rate of CH4 oxidation by cover soils of 1.2 x 10(6) m3 CH4 year(-1) resulted in a calculated annual CH4 generation rate of 16.7 x 10(6) m3 CH4 year(-1). These results underscore the necessity of understanding a landfill's dynamic environment before assessing long-term emissions potential.     

Nitrate enhancement of in-situ bioremediation of monoaromatic compounds in groundwater

Removal of benzene, toluene, and the isomers of xylene (BTX) from gasoline-contaminated groundwater under denitrifying conditions was investigated. In laboratory microcosms, benzene removal was found to be significantly stimulated by phosphorus addition. For total xylenes, removal followed a similar response, but toluene disappearance was unaffected by phosphorus enrichment. An in-situ bioremediation project was conducted to extend this laboratory work to an actual field-scale cleanup of gasoline-contaminated groundwater. The flow of groundwater from two extraction wells to an infiltration gallery created a mostly closed loop to recycle the groundwater enriched with added nutrients and the electron acceptor (nitrate). The coincident occurrence of BTX loss (greater than 90 percent) in situ, nitrate (as well as phosphorus and ammonia) appearance, and increased levels of denitrifying bacteria at a downgradient well all suggested that denitrification may play a significant role in BTX remediation at this site.     

Technical and economic analyses in the development of bioremediation processes

The very large extent of subsurface and groundwater contamination with toxic organic compounds has prompted research on a number of bioremedial processes. The justification of this research has been to achieve lower overall remedial costs than are incurred by currently existing technologies. Laboratory studies are often undertaken with the notion that a new set of process conditions can reduce reagent consumption or the time for treatment by a significant factor with an attendant reduction in overall remediation costs. Research programs are initiated on the basis of these simple premises. Our work has shown that many research projects have been undertaken for the wrong reasons and that experimental effort has often not been directed toward large-scale implementation. A preliminary process analysis has been shown to be a very valuable component of any research and development program on bioremedial and other innovative technologies. As described in this article, the analysis (1) identifies the critical engineering and cost parameters and (2) provides guidance to the research program in the design of experiments and the collection of data. The methodology is also useful in the review of proposed new technologies and treatment equipment. The article includes an example of a process analysis for an actual development project directed toward the remediation of solids contaminated with chlorinated hydrocarbons to illustrate the benefits and the power of the technique.     

Enhanced anaerobic bioremediation of chlorinated solvents utilizing vegetable oil emulsions

The use of vegetable oil as an electron donor to enhance the reductive dechlorination of chlori‐nated solvents as an in situ remediation technology is gaining significant traction. Vegetable oil is a cost‐effective slow‐release electron donor with greater hydrogen‐release efficiency than other electron‐donor products. However, neat vegetable oil can inhibit distribution in aquifers due to the oil droplets blocking the flow of groundwater through the smaller pore spaces in the aquifer materials. This issue has been partially overcome by applying the vegetable oil as an oil‐water emulsion, which typically is created in the field. However, the field preparation results in a mixture of droplet sizes, including larger droplets that can make the emulsions unstable and reduce the soil permeability by blocking soil‐pore throats with oil. RNAS, Inc., has developed a kinetically sta‐ble soybean oil emulsion (“Newman Zone”) consisting of submicron droplets with less droplet‐size variation than field‐prepared emulsions. This product is composed of a blend of fast‐release (sodium lactate) and slow‐release (soybean oil) electron donors. The emulsion is produced in a stable factory environment in which it is pasteurized and packaged in sterile packaging. This ma‐terial can be utilized as an electron donor without further treatments or amendments in the field. This article discusses factors associated with selecting electron donors and the development of vegetable oil–based products. A case study of an application of Newman Zone at a former adhe‐sives manufacturing facility is then presented. The case study demonstrates the effect of Newman Zone in reducing chlorinated solvent concentrations in groundwater by both rapidly stimulating initial microbial activity and supporting long‐term reductive dechlorination with a slow‐release electron donor. © 2006 Wiley Periodicals, Inc.     

Solvent extraction and soil washing treatment of contaminated soils from wood preserving sites: Bench‐scale studies

Bench‐scale solvent extraction and soil washing studies were performed on soil samples obtained from three abandoned wood preserving sites included in the National Priority List. The soil samples from these sites were contaminated with high levels of polyaromatic hydrocarbons (PAHs), pentachlorophenol (PCP), dioxins, and heavy metals. The effectiveness of the solvent extraction process was assessed using liquefied propane or dimethyl ether as solvents over a range of operating conditions. These studies have demonstrated that a two‐stage solvent extraction process using dimethyl ether as a solvent at a ratio of 1.61 per kg of soil could decrease dioxin levels in the soil by 93.0 to 98.9 percent, and PCP levels by 95.1 percent. Reduction percentages for benzo(a)pyrene (BaP) potency estimate and total detected PAHs were 82.4 and 98.6 percent, respectively. Metals concentrations were not reduced by the solvent extraction treatment. These removal levels could be significantly improved using a multistage extraction system. Commercial scale solvent extraction using liquefied gases costs about $220 per ton of contaminated soil. However, field application of this technology at the United Creosote site, Conroe, Texas, failed to perform to the level observed at bench scale due to the excessive foaming and air emission problem. Soil washing using surfactant solution and wet screening treatability studies were also performed on the soil samples in order to assess remediation strategies for sites. Although aqueous phase solubility of contaminants seemed to be the most important factor affecting removal of contaminants from soil, surfactant solutions (3 percent by weight) having nonionic surfactants with hydrophile‐lipophile balance (HLB) of about 14 (Makon‐12 and Igepal CA 720) reduced the PAH levels by an average of 71 percent, compared to no measurable change when pure deionized water was used. Large fractioza of clay and silt (<0.06mm), high le!ezielsof orgaizic contami‐ nants and hzimic acid can makesoil washing less applicable.     

浅析循环流化床锅炉脱硫效率影响因素

鉴于循环流化床（CFB）锅炉燃烧过程中煤自脱硫能力的充分发挥,CFB锅炉脱硫效率中煤的自脱硫作用具有一定贡献。首先统一了CFB锅炉在添加脱硫剂和不添加脱硫剂时脱硫效率的表达方式,其后在总结CFB锅炉脱硫效率影响因素研究成果的基础上,利用电厂运行和监测的实际数据进一步验证这些规律,以供CFB锅炉实际运行借鉴之用。     

The influence of additives on the steam gasification of PVC waste

This study is concerned with the influence of additives on the steam gasification of polyvinyl chloride (PVC) waste. Three types of PVC waste, namely pipe waste, cable waste, and flooring, were tested. The presence of additives proved to have a profound effect on the carbon-to-gas conversion. Plasticizers and other organic additives caused an increase in carbon-to-gas conversion. Inorganic additives, especially calcium, caused a decrease in carbon-to-gas conversion, resulting in an overall decrease in the yield of syngas for all three types of waste. This decrease is probably caused by the deposition of Ca on the surface of the alumina bed material. In addition, calcium reacts with the HCl formed to give CaCl₂. This results in a decrease in the recovery of hydrochloric acid. Received: July 19, 2000 / Accepted: October 9, 2000     

Application of in-situ bioremediation to a gasoline spill in fractured bedrock

After achieving remediation goals during only thirty-two months of operation, the first full-scale in-situ bioremediation (ISB) system in the state of Missouri was shut down in 1990. In addition to ISB, the system included a combination of soil venting and air stripping to remediate subsurface gasoline contamination at a large manufacturing facility. More than 84,000 pounds of gasoline were degraded or removed from the fractured limestone bedrock aquifer and overburden materials. The successful application of ISB in this complex geologic environment and the fact that this was the first such system to complete remediation in Missouri make this system unique.