Ecotoxicological assessment and evaluation of a pine bark biosorbent treatment of five landfill leachates

When selecting a landfill leachate treatment method the contaminant composition of the leachate should be considered in order to obtain the most cost-effective treatment option. In this study the filter material pine bark was evaluated as a treatment for five landfill leachates originating from different cells of the same landfill in Sweden. The objective of the study was to determine the uptake, or release, of metals and dissolved organic carbon (DOC) during a leaching test using the pine bark filter material with the five different landfill leachates. Furthermore the change of toxicity after treatment was studied using a battery of aquatic bioassays assessing luminescent bacteria (Vibrio fischeri) acute toxicity (30-min Microtox®), immobility of the crustacean Daphnia magna, growth inhibition of the algae Pseudokirchneriella subcapitata and the aquatic plant Lemna minor; and genotoxicity with the bacterial Umu-C assay. The results from the toxicity tests and the chemical analysis were analyzed in a Principal Component Analysis and the toxicity of the samples before and after treatment was evaluated in a toxicity classification. The pine bark filter material reduced the concentrations of metal contaminants from the landfill leachates in the study, with some exceptions for Cu and Cd. The Zn uptake of the filter was high for heavily contaminated leachates (≥73%), although some desorption of zinc occurred in less contaminated waters. Some of the leachates may require further treatment due to discharge into a natural recipient in order to reduce the risk of possible biological effects. The difference in pH changes between the different leachates was probably due to variations in buffering capacity, affected by physicochemical properties of the leachate. The greatest desorption of phenol during filtration occurred in leachates with high conductivity or elevated levels of metals or salts. Generally, the toxicity classification of the leachates implies that although filter treatment with pine bark removes metal contaminants from the leachates effectively, it does not alter leachate toxicity noticeably. The leachates with the highest conductivity, pH and metal concentrations are most strongly correlated with an increased toxic response in the score plots of both untreated and treated leachates. This is in line with the toxicity classification of the leachate samples. The results from this study highlight the importance of evaluating treatment efficiency from the perspective of potential recipient effects, rather than in terms of residual concentrations of individual contaminants when treating waters with a complex contamination matrix, such as landfill leachates.     

Field investigation of the quality of fresh and aged leachates from selected landfills receiving e-waste in an arid climate

The management of electronic waste (e-waste) is a serious problem worldwide and much of it is landfilled. A survey of four selected landfills in an arid region of South Australia was conducted to determine the proportion of e-waste in municipal waste and the properties of each landfill site. Leachate and groundwater samples were collected upgradient and downgradient of the landfills for analysis of polybrominated diphenyl ethers (PBDEs) and 14 metals and metalloids, including Al, As, Ba, Be, Cd, Co, Cr, Cu, Fe, Ni, Pb, Sb, V and Zn. Our data demonstrate that the selected landfills in South Australia continue to receive municipal waste containing in excess of 6%, or 25,000 tonnes per year, of e-waste. The leachates and groundwater collected from the landfills contained significantly elevated concentrations of Pb with the highest concentration in groundwater of 38 μg/l, almost four times higher than the Australian drinking water guideline of 10 μg/l. The presence of PBDEs was detected in both leachate and groundwater samples. Total PBDEs values of 2.13–59.75 ng/l in leachate samples were 10 times higher than in groundwater samples, which recorded a range of 0.41–6.53 ng/l at all sites. Moreover, the concentrations of metals and metalloids in sampled groundwater contained elevated levels of Al, As, Fe, Ni and Pb that exceeded Australian drinking water guideline values. For these reasons potential leaching of these contaminants is of concern and while difficult to attribute elevated contaminant levels to e-waste, we do not recommend continued disposal of e-waste in old landfills that were not originally designed to contain leachates. The survey also revealed temporal variation in the electrical conductivity and concentrations of As, Cd and Pb present in leachates of landfills in arid Mediterranean climates. These results are consistent with the marked variations in rainfall patterns observed for such climates. The solute concentration (EC and other ions including As, Cd and Pb) declines in the leachates during wet winter months (June to September), in contrast to tropical countries where such changes are observed during wet summer months.     

Batch tests on mineral deposit formation due to co-mingling of leachates derived from municipal solid wastes and waste-to-energy combustion residues

Deposit formation in leachate collection systems can be problematic for landfill operations. Deposits from municipal solid waste (MSW) derived leachates are impacted by microbial activity and biofilm development, whereas leachates generated from co-disposal of MSW with combustion residues (CR) from waste-to-energy (WTE) facilities and other mineral-rich waste materials are more prone to forming dense mineral deposits dominated by calcium carbonate. In this study, leachates from laboratory lysimeters containing either WTE-CR or shredded MSW were mixed at different volumetric ratios. The mixed leachates were incubated for 5 weeks in batch tests to evaluate the potential for formation of precipitates. Although mineral precipitates have been reported to form in landfills with no co-disposal practices, in this study mineral precipitates did not form in either the WTE-CR derived leachate or the MSW derived leachate, but formed in all leachate mixtures. Mineral precipitates consisted of calcium carbonate particles, with the highest yield from a 1:1 combination of the WTE-CR derived leachate mixed with the MSW derived leachate. The introduction of gaseous carbon dioxide or air into WTE-CR derived leachate resulted in the production of particles of similar chemical composition but different morphology. Operation of landfills to prevent co-mingling of mineral-rich leachates with microbially active leachates and/or to control leachate exposure to sources of carbon dioxide may help to prevent this type of precipitate formation in leachate collection systems.     

Behavior of endocrine-disrupting chemicals in leachate from MSW landfill sites in Japan

Endocrine-disrupting chemicals (EDCs) in landfill leachates and the effluent from leachate treatment facilities have been analyzed by many researchers. However, seasonal and yearly variations and the influence of landfill age are still not clear. In this study, leachate was sampled on four occasions each, at different seasons, from two MSW landfills which receive different waste material. Then, the quantities of alkylphenols (APs), bisphenol A (BPA), phthalic acid esters (PAEs) and organotin compounds (OTs) in leachate were determined. By sampling leachate from landfill cells of different age, the long-term behavior of EDCs was studied. Furthermore, leachate was also sampled at different points in the process of a leachate treatment system, and then the behavior of EDCs in the facility was studied. The concentrations of APs were as low as in surface waters, and OTs were not detected (detection limit was 0.01 microg/l), while BPA and DEHP, which were the most abundant of the four substances measured as PAEs, were found in all the leachates that were measured. Concentrations of BPA and DEHP were almost constant regardless of season, except for a couple of low concentrations observed for BPA. The varying composition of landfilled waste did not influence BPA and DEHP in leachate. Concentration of BPA in raw leachate tends to decrease as the years go by, but the concentration of DEHP was observed to remain at a constant level. BPA was considerably degraded by aeration for leachates from the two landfills, except when the leachate temperature was low. Aeration, coagulation/sedimentation, and biological treatment could not remove DEHP.     

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     

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.     

Pilot-scale experiment on anaerobic bioreactor landfills in China

Developing countries have begun to investigate bioreactor landfills for municipal solid waste management. This paper describes the impacts of leachate recirculation and recirculation loadings on waste stabilization, landfill gas (LFG) generation and leachate characteristics. Four simulated anaerobic columns, R1-R4, were each filled with about 30 tons of waste and recirculated weekly with 1.6, 0.8 and 0.2m(3) leachate and 0.1m(3) tap water. The results indicated that the chemical oxygen demand (COD) half-time of leachate from R1 was about 180 days, which was 8-14 weeks shorter than that of R2-R4. A large amount of LFG was first produced in R1, and its generation rate was positively correlated to the COD or volatile fatty acid concentrations of influent leachates after the 30th week. By the 50th week of recirculation, the waste in R1 was more stabilized, with 931.2 kg COD or 175.6 kg total organic carbon released and with the highest landfill gas production. However, this contributed mainly to washout by leachate, which also resulted in the reduction of LFG generation potential and accumulation of ammonia and/or phosphorus in the early stage. Therefore, the regimes of leachate recirculation should be adjusted to the phases of waste stabilization to enhance efficiency of energy recovery. Integrated with the strategy of in situ leachate management, extra pre-treatment or post-treatment methods to remove the nutrients are recommended.     

Physico-chemical treatment of Merida landfill leachate for chemical oxygen demand reduction by coagulation.

In order to determine the optimal dosage and type of coagulant for the physico-chemical treatment of leachate from the sanitary landfill of Merida, Mexico, a total of 864 jar tests were performed. Four metallic coagulants (ferric chloride, ferric sulphate, aluminium polychloride and aluminium sulphate) with doses ranging between 50 and 300 mg L(-1) and two polyelectrolytes (high-density anionic and cationic reagents) with doses from 2 to 12 mg L(-1) were tested. Neither an adequate type of coagulant nor an optimal dose could be found. The removal of contaminants was measured as total and dissolved chemical oxygen demand (COD). Soluble COD removal efficiencies were low, from 0 to 47%, with a 4% average value only. These low values of organic material removal were attributed to the particular characteristics of the Merida landfill leachate (low suspended solids concentration), so even with sweep-floc coagulation (300 mg L(-1) dose) only low COD removal efficiencies were obtained. A study of the suspended particle size distribution of the leachate was conducted in order to explain the poor performance. The particle size distribution ranged from 0.375 to 948.2 microm, with an average value of 22.97 microm. In a second step the optimal pH for physico-chemical treatment of these leachates was determined. Finally a greater than 90% removal of organic material, measured as suspended COD, was obtained at pH 2, which was considered as the optimal value.     

Fungal and enzymatic treatment of mature municipal landfill leachate

The aim of our study was to evaluate biotreatability of mature municipal landfill leachate by using white rot fungus and its extracellular enzymes. Leachates were collected in one active and one closed regional municipal landfill. Both chosen landfills were operating for many years and the leachates generated there were polluted by organic and inorganic compounds. The white rot fungus Dichomitus squalens was able to grow in the mature leachate from the closed landfill and as it utilizes present organic matter as a source of carbon, the results were showing 60% of DOC and COD removal and decreased toxicity to the bacterium Aliivibrio fischeri. On the other hand, growth of the fungus was inhibited in the presence of the leachate from the active landfill. However, when the leachate was introduced to a crude enzyme filtrate containing extracellular ligninolytic enzymes, removal levels of COD and DOC reached 61% and 44%, respectively. Furthermore, the treatment led to detoxification of the leachate to the bacterium Aliivibrio fischeri and to reduction of toxicity (42%) to the plant Sinapis alba. Fungal and enzymatic treatment seems to be a promising biological approach for treatment of mature landfill leachates and their application should be further investigated.     

Acute toxicity test of leachates from traditional and sustainable landfills using luminescent bacteria

Landfilling is a fundamental step in any waste management strategy, but it can constitute a hazard for the environment for a long time. The need to protect the environment from potential landfill emissions makes risk assessment a decision tool of extreme necessity. The heterogeneity of wastes and the complexity of physical, chemical and biological processes that occur in the body of a landfill need specific procedures in order to evaluate the groundwater risk for the environment. Given the complexity of the composition of landfill leachates, the exact contribution of each potential toxic substance cannot be known precisely. Some reference contaminants that constitute the hazard (toxicity) of leachate have to be found to perform the risk assessment. A preliminary ecotoxicological investigation with luminescent bacteria has been carried out on different leachates from traditional and sustainable landfills in order to rank the chemicals that better characterize the leachate (heavy metals, ammonia and dissolved organic content). The attention has been focused on ammonia because it is present in high concentration and can last for centuries and can seriously contaminate the groundwater. The results showed that the toxicity of the leachate might reliably depend on the ammonia concentration and that the leachate toxicity is considerably lower in sustainable landfills where the ammonia had been degraded. This has an important consequence because if the containment system fails (as usually occur within 30-50yr), the risk of groundwater contamination will be calculated easier only in terms of the probability that the ammonia concentration is higher than a reference concentration.     

Factors affecting the concentration of bisphenol A in leachates from solid waste disposal sites and its fate in treatment processes

 The concentrations of bisphenol A (BPA) contained in landfill leachates from solid waste disposal sites were measured. The concentrations of BPA contained in leachates from industrial waste sites were in the range below the detection limit to 2800 μg/l, while those from municipal sites were in the range 26–8400 μg/l. The leachates from ash-rich sites contained relatively lower concentrations of BPA compared with organic-rich leachates. It is suggested that BPA concentration increases with time after the completion of reclamation in the case of ash-rich sites, whereas the concentration of BPA decreases with time in the case of organic-rich sites. A 7-year survey on a site in Japan showed neither a decrease nor an increase in the concentration of BPA during on-going reclamation. A leachate from a site in the Philippines contained high concentrations of BPA. A slight positive correlation was found between BPA concentrations and total organic carbon (TOC). A major portion of the BPA in leachates was found in dissolved and organic unassociated fractions, which cannot be precipitated by coagulation. More than 99.9% of the BPA contained in raw leachates was removed by a conventional series of treatment processes consisting of biological treatment, coagulation, sedimentation, sand filtration, and activated carbon adsorption. Received: May 29, 2002 / Accepted: October 17, 2002     

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.     

Polybrominated diphenyl ethers in e-waste: Level and transfer in a typical e-waste recycling site in Shanghai,Eastern China

Very few data for polybrominated diphenyl ethers (PBDEs) were available in the electronic waste (e-waste) as one of the most PBDEs emission source. This study reported concentrations of PBDEs in e-waste including printer, rice cooker, computer monitor, TV, electric iron and water dispenser, as well as dust from e-waste, e-waste dismantling workshop and surface soil from inside and outside of an e-waste recycling plant in Shanghai, Eastern China. The results showed that PBDEs were detected in the majority of e-waste, and the concentrations of ΣPBDEs ranged from not detected to 175 g/kg, with a mean value of 10.8 g/kg. PBDEs were found in TVs made in China after 1990. The mean concentrations of ΣPBDEs in e-waste made in Korea, Japan, Singapore and China were 1.84 g/kg, 20.5 g/kg, 0.91 g/kg, 4.48 g/kg, respectively. The levels of ΣPBDEs in e-waste made in Japan far exceed the threshold limit of RoHS (1.00 g/kg). BDE-209 dominated in e-waste, accounting for over 93%. The compositional patterns of PBDEs congeners resembled the profile of Saytex 102E, indicating the source of deca-BDE. Among the samples of dust and surface soil from a typical e-waste recycling site, the highest concentrations of Σ₁₈PBDEs and BDE-209 were found in dust in e-waste, ranging from 1960 to 340,710 ng/g and from 910 to 320,400 ng/g, which were 1–2 orders of magnitude higher than other samples. It suggested that PBDEs released from e-waste via dust, and then transferred to surrounding environment.     

Effect of an uncontrolled fire and the subsequent fire fight on the chemical composition of landfill leachate

Landfill leachates sampled during and after an accidental landfill fire were analysed and the levels of selected metals and chemical compounds compared to those occurring in the leachate under normal conditions. The fire at the landfill site was put out by excavation and cooling by use of water. The investigation during the fire and fire fight revealed a moderate increase in the level of nitrogen and also in pH and conductivity. Heavy metals and COD in the leachate showed considerably increased levels. In general, the determined variables appeared to normalise within one week after the fire was extinguished. It can be concluded that landfill fires extinguished by excavation may lead to elevated leachate levels of especially COD and heavy metals, but that this is only a short-term effect.     

Fate of saline ions in a planted landfill site with leachate recirculation

Recirculation of leachate on a covered landfill site planted with willows or other highly evapotranspirative woody plants is an inexpensive option for leachate management. In our study, a closed landfill leachate recirculation system was established on a rehabilitated municipal solid waste landfill site with planted landfill cover. The main objective of the study was to evaluate the sustainability of the system with regard to high hydraulic loads of the landfill leachate on the landfill cover and high concentrations of saline ions, especially potassium (K⁺), sodium (Na⁺) and chloride (Cl^?), in leachate.The results of intensive monitoring, implemented during May 2004 and September 2007, including leachate, soil and plant samples, showed a high sustainability of the system regarding saline ions with the precipitation regime of the studied region. Saline ion concentrations in leachates varied between 132 and 2592 mg Cl^? L^?1, 69 and 1310 mg Na⁺ L^?1 and between 66 and 2156 mg K⁺ L^?1, with mean values of 1010, 632 and 686 mg L^?1, respectively. Soil salinity, measured as soil electrical conductivity (EC), remained between 0.17 and 0.38 mS cm^?1 at a depth between 0 and 90 cm. An average annual precipitation of 1000 mm provided sufficient leaching of saline ions, loaded by irrigation with landfill leachate, from the soil of the landfill cover and thus prevented possible salinity shocks to the planted willows.     

Testing Stability Of Chlorophenols And Lindane (γ-HCH) In Different Leachates Originating From Anaerobic Municipal Waste Decomposition

The degradation potential of landfill leachates for several chlorinated phenols and a pesticide (lindane) was investigated. Acidogenic and methanogenic model leachates from a laboratory waste lysimeter, as well as methanogenic leachate from a disposal site, were examined. In the assays with acidogenic leachates only lindane was metabolized completely within 60 days. In the methanogenic leachates, lindane and chlorophenols were metabolized immediately. No lindane metabolites could be detected. Detected chlorophenol metabolites pointed at reductive dehalogenation as the dominant degradation process, whereby ortho-dechlorination was strictly preferred. Transformation reactions were confined to samples which were biologically active.     

DETERMINATION OF ORGANIC PARAMETERS IN WASTE AND LEACHATES FROM THE HAZARDOUS WASTE LANDFILL OF RAINDORF; GERMANY

Extensive investigations of leachates and solid waste samples for organic sum parameters and environmentally relevant organic compounds were carried out at the hazardous waste landfill of Raindorf, which is operated in accordance with German Technical Instructions on Waste (TI Waste). The measurements showed that the majority of the waste samples contained only minor amounts of phenols, highly volatile chlorinated organic compounds (VCHC), benzene, toluene, ethylbenzene and xylene (BTEX), polychlorinated biphenyls (PCB) and polycyclic aromatic hydrocarbons (PAH). The concentrations ranged from less than 100μg/kg⁻¹up to 1000μg/kg⁻¹of dry substance. Only hydrocarbons were detected in higher concentrations (mg to g kg⁻¹of dry substance). In most leachate and gas samples taken at the landfill, the concentrations of the abovementioned parameters were close to or even below the detection limit. The measurement of organic single compounds underlined the usefulness of the sum parameters, adsorbable organic halogen compounds and phenol index, for the estimation of the total amount of these substances. A comparison of organic sum parameter concentrations measured in leachates from landfills of differing ages indicates that the application of TI Waste leads to a reduction of the organic load in the leachate.     

Toxicological evaluation of the chemical oxidation methods for landfill stabilization

As the stabilization criteria for landfill sites, only chemical criteria for the leachate discharges from the landfill sites have been used in Japan and many other countries. Recently, chemical oxidation has been developed as a method for the early-stabilization of landfills. However, by-products that are difficult to detect by chemical analysis can be produced by this method. Therefore, toxicity tests are useful tools for detecting the changes of leachate quality after application of this method. The heat source in the A landfill was analyzed by organic position inquiry technology, and ozone-treated leachate was sprayed back to the heat source in the landfill. Toxicity changes of the leachate after the spray were monitored using Microtoxtrade mark, ToxScreen-II, and DaphTox tests. The hardly-degradable organic matter was efficiently removed and toxicities of the leachate in the heat source decreased after the application. These toxicity results were significantly related to chemical oxygen demand (COD) changes. Thus, it was concluded that the toxicity tests were effective for monitoring the leachate quality after applying the chemical oxidation method for landfill stabilization, and its incorporation to establish the criteria for early-stabilization of landfill sites needs to be considered.     

Advanced physico-chemical treatment experiences on young municipal landfill leachates

In this study, Membrane Filtration (UF+RO), Struvite (MAP) precipitation and ammonia stripping alternatives were studied on biologically pre-treated Landfill Leachate. The results indicated that the system including the Upflow Anaerobic Sludge Blanket Reactor (UASBR) and Membrane Reactors (UF+RO) has been offered as an appropriate treatment alternative for young landfill leachates. This system provided high removals of COD, colour and conductivity (>98-99%). For ammonia removal, struvite precipitation was applied at the stoichiometric ratio (Mg:NH4:PO4=1:1:1) to anaerobically pre-treated raw landfill leachate effluent having an influent ammonium concentration of 2240 mg/l. Maximum ammonium nitrogen removal was observed as 85% at pH of 9.2. In ammonia stripping following 2 h of aeration, the removal was 72% at pH=12 while the removals were around 20% at pH=10 and pH=11. When membrane reactor, and struvite precipitation or ammonia stripping was applied to anaerobically pre-treated effluents, the results indicated that each system could be used as an appropriate post-treatment option for young landfill leachates. In economic aspect, ammonia stripping was found as the cheapest alternative with high ammonium removal. However, when both high COD and ammonium removals were to be achieved membrane technology such as UF+RO (SW) could be considered as the most appropriate system due to the fact that COD removal could be obtained very low by ammonia stripping.     

Occurrence of phenols in leachates from municipal solid waste landfill sites in Japan

The concentrations of 41 phenols in leachates from 38 municipal solid waste (MSW) landfill sites in Japan were measured. The main phenols detected in leachates were phenol, three cresols, 4-tert-butylphenol, 4-tertoctylphenol, 4-nonylphenol, bisphenol A, and some chlorophenols. The concentration levels of phenols were affected by the pH values of the leachates and the different types of landfill waste. The origins of phenol and p-cresol were considered to be incineration residues, and the major origin of 4-tert-butylphenol, bisphenol A, and 2,4,6-trichlorophenol was considered to be solidified fly ash. In contrast, the major origins of 4-tert-octylphenol and 4-nonylphenol were considered to be incombustibles. The discharge of leachates to the environment around MSW landfill sites without water treatment facilities can cause environmental pollution by phenols. In particular, the disposal of incineration residues including solidified fly ash and the codisposal of solidified fly ash and incombustibles might raise the possibility of environmental pollution. Moreover, the discharge of leachates at pH values of 9.8 or more could pollute the water environment with phenol. However, phenol, 4-nonylphenol, and bisphenol A can be removed to below the con centration levels that impact the environment around landfill sites by a series of conventional water treatment processes.