Chemical characterization of landfill leachates--400 parameters and compounds

A large number of hazardous compounds can be expected to be present in landfill leachates, many of which have not yet been identified. Thus this study screened samples from 12 Swedish municipal landfill sites for 400 parameters and compounds. More than 90 organic and metal organic compounds and 50 inorganic elements were detected, some of which seem to have not been detected before. Compounds detected include halogenated aliphatic compounds, benzene and alkylated benzenes, phenol and alkylated phenols, ethoxylates, polycyclic aromatic compounds, phthalic esters, chlorinated benzenes, chlorinated phenols, PCB, chlorinated dioxins and chlorinated furans, bromated flame-retardants, pesticides, organic tin, methyl mercury and heavy metals. The presence of this large number of hazardous compounds in landfill leachates should have a significant impact on future landfill risk assessments and the development of leachate treatment methods. We propose that future research should pay more attention to the metal-organic and organic compounds detected in this study. We also suggest using leachate sediments as a matrix for detecting hydrophobic compounds, and reflecting on the degradation phase when evaluating results from monitoring studies. The extensive compilation of compounds in this paper can be used to select compounds to search for in future studies.     

Odor compounds in waste gas emissions from agricultural operations and food industries

In the last decades, large-scale agricultural operations and food industries have increased. These operations generate numerous types of odors. The reduction of land areas available for isolation of agricultural and food processing industrial operations from the public area and the increase in sensitivity and demand of the general public for a clean and pleasant environment have forced all of these industries to control odor emissions and toxic air pollutants. To develop environmentally sound, sustainable agricultural and food industrial operations, it is necessary to integrate research that focuses on modern analytical techniques and latest sensory technology of measurement and evaluation of odor and pollution, together with a fundamental knowledge of factors that are the basic units contributing to the production of odor and pollutants. Without a clear understanding of what odor is, how to measure it, and where it originates, it will be difficult to control the odor. The present paper reviews the available information regarding odor emissions from agricultural operations and food industries by giving an overview about odor problems, odor detection and quantification, and identifying the sources and the mechanisms that contribute to the odor emissions. Finally, ways of reducing or controlling the odor problem are discussed.     

Leaching characteristics of the fine fraction from an excavated landfill: physico-chemical characterization

Journal of Material Cycles and Waste Management - Leaching of fine fraction (<10 mm) obtained from landfill mining activities in an Estonian landfill was done. On-site excavation...     

Organometals of tin, lead and mercury compounds in landfill gases and leachates from Bavaria, Germany

Organo-Sn, -Pb and -Hg compounds were monitored in gases and leachates of 11 municipal waste landfills and one hazardous waste landfill from Bavaria, Germany, with the objectives to estimate the methylation of Sn, Pb and Hg and to assess the risk of their release into the adjacent environment. In the gases, tetramethyl Sn predominated (>80% of total gaseous Sn) with concentrations up to 160mug Sn m(-3). Dimethyl-Hg and tetramethyl-Pb were only occasionally detected with concentrations up to 2.9 and 2.1mugm(-3) as Hg or Pb, respectively. In all leachates, trimethyl-Sn dominated with a maximum concentration of 2100ng Sn L(-1). No organo-Pb compounds were found, and monomethyl-Hg was detected in only one leachate. The concentrations of trimethyl-Sn were up to 100-fold higher in the condensate water than in leachates, and the concentrations of organo-Sn compounds were lower in the adjacent groundwater than in the corresponding leachates. The high abundance of methylated Sn species in the gases and leachates indicates Sn methylation, suggesting the landfill as a source for organo-Sn compounds. In comparison, methylation of Hg and Pb was of little importance, probably due to low Hg concentrations and low rates of Pb methylation in the landfill. The risks of organo-Sn compounds release to the adjacent air is low due to flaring of landfill gases. However, there is probable release of organo-Sn compounds, especially trimethyl-Sn, to the adjacent groundwater.     

Uncontrolled methane emissions from a MSW landfill surface: Influence of landfill features and side slopes

Sanitary landfills for Municipal Solid Waste (MSW) disposal have been identified as one of the most important anthropogenic sources of methane (CH₄) emissions; in order to minimize its negative effects on the environment, landfill gas (LFG) recovery is a suitable tool to control CH₄ emissions from a landfill site; further, the measurement of CH₄ emissions can represent a good way to evaluate the effectiveness of LFG recovering systems. In general, LFG will escape through any faults in the landfill capping or in the LFG collection system. Indeed, some areas of the capping can be more permeable than others (e.g. portions of a side slope), especially when considering a temporarily capped zone (covered area that is not expected to receive any further waste for a period of at least 3 months, but for engineering reasons does not have a permanent cap yet). These areas, which are characterized by abnormal emissions, are usually defined as “features”: in particular, a feature is a small, discrete area or an installation where CH₄ emissions significantly differ from the surrounding zones. In the present study, the influence that specific features have on CH₄ emissions has been investigated, based on direct measurements carried out in different seasons by means of a flux chamber to the case study of Palermo (IT) landfill (Bellolampo). The results showed that the flux chamber method is reliable and easy to perform, and the contoured flux maps, obtained by processing the measured data were found to be a suitable tool for identifying areas with abnormal (high) emissions. Further, it was found that a relationship between methane emission rates and landfill side slope can be established. Concerning the influence of the temporary HDPE cover system on CH₄ recovery efficiency, it contributed to a significant decrease of the free surface area available for uncontrolled emissions; this aspect, coupled to the increase of the CH₄ volumes collected by the LFG recovery system, led to a significant increase of the recovery efficiency.     

Greenhouse gas emissions from landfill leachate treatment plants: A comparison of young and aged landfill

With limited assessment, leachate treatment of a specified landfill is considered to be a significant source of greenhouse gas (GHG) emissions. In our study, the cumulative GHG emitted from the storage ponds and process configurations that manage fresh or aged landfill leachate were investigated. Our results showed that strong CH₄ emissions were observed from the fresh leachate storage pond, with the fluxes values (2219–26,489 mg C m^?2 h^?1) extremely higher than those of N₂O (0.028–0.41 mg N m^?2 h^?1). In contrast, the emission values for both CH₄ and N₂O were low for the aged leachate tank. N₂O emissions became dominant once the leachate entered the treatment plants of both systems, accounting for 8–12% of the removal of N-species gases. Per capita, the N₂O emission based on both leachate treatment systems was estimated to be 7.99 g N₂O–N capita^?1 yr^?1. An increase of 80% in N₂O emissions was observed when the bioreactor pH decreased by approximately 1 pH unit. The vast majority of carbon was removed in the form of CO₂, with a small portion as CH₄ (<0.3%) during both treatment processes. The cumulative GHG emissions for fresh leachate storage ponds, fresh leachate treatment system and aged leachate treatment system were 19.10, 10.62 and 3.63 Gg CO₂ eq yr^?1, respectively, for a total that could be transformed to 9.09 kg CO₂ eq capita^?1 yr^?1.     

Sulfide emissions from different areas of a municipal solid waste landfill in China

Degradation of municipal solid waste in landfills generates sulfide compounds, which are considered one of the main sources of odor emissions. Field sampling was conducted at surfaces of operating, inoperative, and soil-covered areas of a landfill site in northern China to characterize the sulfide compounds. The results showed that dimethyl disulfide dominated the sulfide compounds, accounting for up to 73.6% of the total detected sulfide. With the biggest odor concentration of 365, diethyl sulfide was the most significant sulfide compound. The estimated sulfide emission rates at surfaces of operating and soil-covered areas were similar, and the emission rate of dimethyl disulfide at Surface of Operating Area was up to 345.9 μg/m³ h. Dimethyl disulfide could be released from the fresh waste, and its normalized concentration at 0.2 m beneath operating surface was 10.4 times that at 0.4 m.     

Effects of volatile organic compounds on clay landfill liner performance

Clay borrow materials intended for use in a clay liner system were found to be contaminated by low concentrations of volatile organic chemicals (VOCs). The suspected source of contaminants was a nearby Superfund site where similar compounds were found in soil and groundwater. Based on these observations, questions were raised regarding the potential effects of VOCs on the performance of the clay materials as a landfill liner.Laboratory experiments were conducted to evaluate the effects of three levels of soil precontamination and two types of permeants. Atterberg tests showed that the precontaminations (acetone and m-xylene) and the simulated leachate (methylene chloride, trichloroethylene, and toluene), at the concentrations used, did not impact clay-pore fluid interaction. Sedimentation tests showed that the impact of methylene chloride, trichloroethylene, and toluene on sediment volume and rate of settlement was not detectable up to the maximum concentration level of 100 ppm for each chemical.From the permeation tests, acetone in the precontaminated samples was generally flushed out within three pore volumes but m-xylene was not detected (above the detection limit of 0.01 mg 1⁻¹) in the permeant effluent. The stabilized permeabilities of the specimens ranged from 0.2 × 10⁻⁷ to 3.0 × 10⁻⁷ cms⁻¹. It was found that precontamination of the clay at the levels studied did not affect organic chemical leachate transport/adsorption discernibly when compared with clean clay, and no measurable retardation or adsorption of VOCs in clay liners occurred in either clean clay or precontaminated clay.     

Pollutant source identification and allocation: Advances in hydrocarbon fingerprinting

Often liability for environmental damage and cleanup of contaminated sites is made difficult, especially with chemically complex environments containing different pollutants, by the inability to differentiate potential sources (or “owners”) of pollutants from each other. As a result, unnecessary costs may be associated with having to assume financial responsibility for alleged contamination of a site. This article reviews the advances in chemical fingerprinting as a tool in identifying and differentiating sources of hydrocarbon pollutants in chemically complex environments. Appropriate hydrocarbon target analytes and required analytical methods for hydrocarbon fingerprinting are discussed, and new interpretative tools are presented that may be applied to contaminated soil, sediment, and groundwater environmental situations. With these analytical and interpretative techniques, an appropriate allocation of chemical contamination and costs at a site can be made.     

Bioreactor treatment of municipal solid waste landfill leachates: characterization of organic fractions

Quantitative and qualitative changes in organic matter were studied at different stages of treatment in a bioreactor designed to process leachates from a municipal solid waste landfill. The particulate matter (PM) and macromolecular fractions of the dissolved organic matter with solubility properties comparable to humic (acid-insoluble) and fulvic (acid-soluble) acid fractions (AI, AS, respectively) from the incoming black liquid, the bioreactor content, and the final processed effluent were isolated, quantified, and characterized by visible and infrared (IR) spectroscopies. The macromolecular signature either aliphatic (glycopeptides, carbohydrates) or aromatic (coinciding with infrared patterns of lignin, tannins etc.) enabled us to characterize the different organic fractions during the course of microbial transformation. The results reveal significant changes in the nitrogen speciation patterns within the different organic fractions isolated from the wastewater. The final increase in the relative proportions of nitrogen in the least aromatic AS fraction during microbial transformation could be related to protein formation inside the bioreactor. After biological treatment and ultrafiltration, the amount of organic matter was reduced by approximately 70%, whereas aromaticity increased in all fractions, indicating preferential elimination of aliphatic wastewater compounds. Most of the remaining fractions at the end of the process consisted of a yellow residue rich in low molecular weight AS fractions.     

The identification and possible environmental impact of trace gases and vapours in landfill gas

Trace compounds present in gas from six landfill sites have been identified and their concentrations measured. At least 100 components are present including hydrocarbons, esters, terpenes and organic sulphur compounds. In domestic waste sites these varied with the age of the refuse.Industrial waste sites evolved gas much richer in hydrocarbons and solvents including halocarbons. Vinyl chloride and benzene were also present in significant concentrations. A 100-fold dilution would be advisable to eliminate any long-term health hazard. Domestic waste sites do not pose a health hazard due to minor components although a 1,000,000-fold dilution is required to bring some of them below the odour threshold. At most sites, hydrogen sulphide was not a significant contributor to smell.     

Statistical approach for the source identification of boron in leachates from industrial landfills

Boron has been found in high concentrations in leachates from landfills located throughout Japan. However, the source(s) of boron in the leachates, i.e., what kind of waste(s) releases this element into the leachate, has not been clarified. In this study, boron concentrations in leachates from 48 industrial landfills were evaluated, in relation to the categories of waste constituting the landfill in each of the sites, by multiple regression analysis. The multiple regression analyses were carried out using the log-transformed boron concentration as a dependent variable and each of 19 categories of industrial waste (according to the Japanese Waste Disposal and Public Cleansing Law) as independent variables. Stepwise variable selection was employed in the analyses. Although the significant variable(s) selected varied according to the data sets analyzed (viz., data sets from least controlled landfill sites, from controlled landfill sites, and from both), cinders, slag, and waste plastics emerged as wastes with positive partial regression coefficients that significantly explained the boron levels in the leachates. These results indicated that cinders, slag, and waste plastics were the sources of high concentrations of boron in the leachates. The results of the present exploratory statistical analyses warrant a systematic survey of the boron contents of, and leachability from, cinders, slag, and waste plastics. Received: January 17, 2000 / Accepted: July 24, 2000     

Atmospheric emissions and attenuation of non-methane organic compounds in cover soils at a French landfill

In addition to methane (CH(4)) and carbon dioxide (CO(2)), landfill gas may contain more than 200 non-methane organic compounds (NMOCs) including C(2+)-alkanes, aromatics, and halogenated hydrocarbons. Although the trace components make up less than 1% v/v of typical landfill gas, they may exert a disproportionate environmental burden. The objective of this work was to study the dynamics of CH(4) and NMOCs in the landfill cover soils overlying two types of gas collection systems: a conventional gas collection system with vertical wells and an innovative horizontal gas collection layer consisting of permeable gravel with a geomembrane above it. The 47 NMOCs quantified in the landfill gas samples included primarily alkanes (C(2)-C(10)), alkenes (C(2)-C(4)), halogenated hydrocarbons (including (hydro)chlorofluorocarbons ((H)CFCs)), and aromatic hydrocarbons (BTEXs). In general, both CH(4) and NMOC fluxes were all very small with positive and negative fluxes. The highest percentages of positive fluxes in this study (considering all quantified species) were observed at the hotspots, located mainly along cell perimeters of the conventional cell. The capacity of the cover soil for NMOC oxidation was investigated in microcosms incubated with CH(4) and oxygen (O(2)). The cover soil showed a relatively high capacity for CH(4) oxidation and simultaneous co-oxidation of the halogenated aliphatic compounds, especially at the conventional cell. Fully substituted carbons (TeCM, PCE, CFC-11, CFC-12, CFC-113, HFC-134a, and HCFC-141b) were not degraded in the presence of CH(4) and O(2). Benzene and toluene were also degraded with relative high rates. This study demonstrates that landfill soil covers show a significant potential for CH(4) oxidation and co-oxidation of NMOCs.     

Characterization and tropical seasonal variation of leachate: Results from landfill lysimeter studied

This study aims to characterize the leachate and to investigate the tropical climatic influence on leachate characteristics of lysimeter studies under different seasonal variations at KUET campus, Bangladesh. Three different situations of landfill were considered here as well as both the open dump lysimeter-A having a base liner and sanitary landfill lysimeter-B and C at two different types of cap liner were simulated. The leachate characteristics, leachate generation and climatic influence parameter had been continually monitored since June 2008 to May 2010, these periods cover both the dry and rainy season. The leachate generation had followed the rainfall pattern and the open dump lysimeter-A without top cover was recorded to have highest leachate generation. Moreover, the open dump lysimeter-A had lower total kjeldahl nitrogen (TKN), ammonia nitrogen (NH(4)-N) and TKN load, while both the COD concentration and load was higher compared with sanitary landfill lysimeter-B and C. In addition, sanitary landfill lysimeter-B, not only had lowest leachate generation, but also produces reasonable low COD concentration and load compared with open dump lysimeter-A. Result reveals that lysimeter operational mode had direct effect on leachate quality. Finally, it can be concluded that the knowledge of leachate quality will be useful in planning and providing remedial measures of proper liner system in sanitary landfill design and leachate treatment.     

Solidification/stabilization of landfill leachate concentrate using different aggregate materials

The application of reverse osmosis for the treatment of landfill leachate is becoming widespread in Turkey as well as in Europe. A major drawback of this process is the production of concentrate, which could be as much as 30% of the feed stream, and high concentrations of salts and contaminants. The reverse osmosis concentrate is disposed of by using several methods including re-infiltration, drying, incineration and solidification/stabilization. In this study, solidification/stabilization (S/S) technology was studied for the treatment of reverse osmosis concentrate produced from landfill leachate. In order to benefit from its capability to absorb heavy metals, ammonia and some other pollutants, zeolite and different aggregate materials were used in solidification experiments. Main pollutants in the leachate concentrate, TOC, DOC, TDS and ammonia were successfully solidified and approximately 1% of TOC, DOC, TDS and ammonia remained in the eluate water. The results indicated that the landfill disposal limits could be attained by solidification/stabilization process.     

Emissions of organo-metal compounds via the leachate and gas pathway from two differently pre-treated municipal waste materials -- A landfill reactor study

Due to their broad industrial production and use as PVC-stabilisers, agro-chemicals and anti-fouling agents, organo-metal compounds are widely distributed throughout the terrestrial and marine biogeosphere. Here, we focused on the emission dynamics of various organo-metal compounds (e.g., di,- tri-, tetra-methyl tin, di-methyl mercury, tetra-methyl lead) from two different kinds of pre-treated mass waste, namely mechanically-biologically pre-treated municipal solid waste (MBP MSW) and municipal waste incineration ash (MWIA). In landfill simulation reactors, the emission of the organo-metal compounds via the leachate and gas pathway was observed over a period of 5 months simulating different environmental conditions (anaerobic with underlying soil layer/aerated/anaerobic). Both waste materials differ significantly in their initial amounts of organo-metal compounds and their environmental behaviour with regard to the accumulation and depletion rates within the solid material during incubation. For tri-methyl tin, the highest release rates in leachates were found in the incineration ash treatments, where anaerobic conditions in combination with underlying soil material significantly promoted its formation. Concerning the gas pathway, anaerobic conditions considerably favour the emission of organo-metal compounds (tetra-methyl tin, di-methyl mercury, tetra-methyl lead) in both the MBP material and especially in the incineration ash.     

Impact of different plants on the gas profile of a landfill cover

Methane is an important greenhouse gas emitted from landfill sites and old waste dumps. Biological methane oxidation in landfill covers can help to reduce methane emissions. To determine the influence of different plant covers on this oxidation in a compost layer, we conducted a lysimeter study. We compared the effect of four different plant covers (grass, alfalfa + grass, miscanthus and black poplar) and of bare soil on the concentration of methane, carbon dioxide and oxygen in lysimeters filled with compost. Plants were essential for a sustainable reduction in methane concentrations, whereas in bare soil, methane oxidation declined already after 6 weeks. Enhanced microbial activity - expected in lysimeters with plants that were exposed to landfill gas - was supported by the increased temperature of the gas in the substrate and the higher methane oxidation potential. At the end of the first experimental year and from mid-April of the second experimental year, the methane concentration was most strongly reduced in the lysimeters containing alfalfa + grass, followed by poplar, miscanthus and grass. The observed differences probably reflect the different root morphology of the investigated plants, which influences oxygen transport to deeper compost layers and regulates the water content.