Thermal and hydrometallurgical recovery methods of heavy metals from municipal solid waste fly ash

Heavy metals in fly ash from municipal solid waste incinerators are present in high concentrations. Therefore fly ash must be treated as a hazardous material. On the other hand, it may be a potential source of heavy metals. Zinc, lead, cadmium, and copper can be relatively easily removed during the thermal treatment of fly ash, e.g. in the form of chlorides. In return, wet extraction methods could provide promising results for these elements including chromium and nickel. The aim of this study was to investigate and compare thermal and hydrometallurgical treatment of municipal solid waste fly ash. Thermal treatment of fly ash was performed in a rotary reactor at temperatures between 950 and 1050 °C and in a muffle oven at temperatures from 500 to 1200 °C. The removal more than 90% was reached by easy volatile heavy metals such as cadmium and lead and also by copper, however at higher temperature in the muffle oven. The alkaline (sodium hydroxide) and acid (sulphuric acid) leaching of the fly ash was carried out while the influence of temperature, time, concentration, and liquid/solid ratio were investigated. The combination of alkaline-acidic leaching enhanced the removal of, namely, zinc, chromium and nickel.     

Cyclodextrin‐enhanced remediation of organic and metal contaminants in porous media and groundwater

Heavy metals and toxic organic contaminants are found at numerous industrial and military sites. The generally poor performance of conventional pump‐and‐treat schemes has made the development of improved methods for contaminated site remediation a significant environmental priority. One such innovative method is cyclodextrin‐enhanced flushing of the contaminated porous media and groundwater. Cyclodextrin is a glucose‐based molecule that is produced on industrial scales by microorganisms. Over the last years, several cyclodextrin derivatives have received extensive research interest. It was shown that cyclodextrins can significantly enhance the solubility of toxic organics, and in some cases, heavy metals and radioactive isotopes. As a sugar, cyclodextrin is considered relatively non‐toxic to humans, plants, and soil microbes. Thus, there are minimal health‐related concerns associated with the injection of cyclodextrin into the subsurface, which is an inherent advantage for use of cyclodextrins as a remediation agent. This paper provides a review of the available literature concerning use of cyclodextrin for remediation of groundwater and soil.     

Thermal desorption of PCB-contaminated waste at the waukegan harbor superfund site

In June 1992, SoilTech ATP Systems, Inc., completed the soil treatment phase of the Waukegan Harbor Superfund Project in Waukegan, Illinois, after approximately five months of operation. SoilTech successfully treated 12,700 tons of sediment contaminated with polychlorinated hiphenyls (PCBs) using a transportable SoilTech anaerobic thermal processor (ATP) system nominally rated at ten tons per hour throughput capacity. The SoilTech ATP technology anaerobically desorbs contaminants such as PCBs from solids and sludges at temperatures over 1,000° F. Principal products of the process are clean, treated solids and an oil condensate containing the hydrocarbon contaminants. At the Waukegan Harbor Superfund site, PCB concentrations in the sediments excavated and dredged from a ditch, lagoon, and harbor slip averaged 10,400 parts per million (ppm) (1.04 percent) and were as high as 23,000 ppm (2.3 percent). Treated soil was backfilled in an on-site containment cell. The removal efficiency of PCBs from the soil averaged 99.98 percent, relative to the project performance specification of 97 percent, and treated soil PCB concentrations were measured below 2 ppm. Approximately 30,000 gallons of PCB oil, desorbed from the feed material, were returned to the owner for subsequent off-site disposal. After modifications to the emissions control equipment, compliance with the 99.9999 percent destruction and removal efficiency (DRE) for PCBs in stack emissions required by the U.S. Environmental Protection Agency was achieved.     

Remediation with cyclodextrin: Recovery of the remedial agent by membrane filtration

Cyclodextrin‐enhanced flushing of contaminants from the subsurface is a promising innovative remediation technology. It will become more economically viable at more sites if methods can be developed to recover and reconcentrate the cyclodextrin solution after it has been flushed through an aquifer. The goal of this study was to determine if membrane technology is capable of meeting that need. Five membranes with different material properties were tested for this purpose in the laboratory. The results of these tests indicate that there are large differences both in the efficiency of these membranes to extract hydroxpropyl‐β‐cyclodextrin (HPCD) and their stability when exposed to trichloroethylene (TCE) at concentrations near aqueous solubility. Not only does the molecular weigh cutoff (MWCO) of a membrane determine if HPCD can be retained, but crucial selection criteria are the membrane's resistance and compatibility with TCE. Of the five membrane materials tested, only two (polymer composite membrane and polysulfone) met both these requirements. The polymer composite membrane (MPF‐44) showed reliable and stable HPCD recoveries (>95 percent) even when exposed to high TCE concentrations. The polysulfone membrane showed high HPCD recoveries, 88.5 ± 0.4 percent to 97 percent ±1 percent for ultrafiltration and nanofiltration membranes, respectively. However, membrane swelling and deterioration became a problem at high TCE concentrations (>1,000 mg/L). These problems diminished when the TCE concentration was less than 1 mg/L. Field tests demonstrated that batch mode treatment by ultrafiltration doubled the cyclodextrin concentration from 5 to 10 percent within three hours at a constant operating pressure of 13 psi. Under continuous single‐pass treatment conditions, cyclodextrin concentration also increased, although the rate of increase was much smaller than in batch mode. Overall, these tests showed that cyclodextrin recovery is possible under field conditions. © 2007 Wiley Periodicals, Inc.     

Recovery of metals from waste printed circuit boards by supercritical water pre-treatment combined with acid leaching process

Waste printed circuit boards (PCBs) contain a large number of metals such as Cu, Sn, Pb, Cd, Cr, Zn, and Mn. In this work, an efficient and environmentally friendly process for metals recovery from waste PCBs by supercritical water (SCW) pre-treatment combined with acid leaching was developed. In the proposed process, waste PCBs were pre-treated by SCW, then the separated solid phase product with concentrated metals was subjected to an acid leaching process for metals recovery. The effect of SCW pre-treatment on the recovery of different metals from waste PCBs was investigated. Two methods of SCW pre-treatment were studied: supercritical water oxidation (SCWO) and supercritical water depolymerization (SCWD). Experimental results indicated that SCWO and SCWD pre-treatment had significant effect on the recovery of different metals. SCWO pre-treatment was highly efficient for enhancing the recovery of Cu and Pb, and the recovery efficiency increased significantly with increasing pre-treatment temperature. The recovery efficiency of Cu and Pb for SCWO pre-treatment at 420 °C was 99.8% and 80%, respectively, whereas most of the Sn and Cr were immobilized in the residue. The recovery of all studied metals was enhanced by SCWD pre-treatment and increased along with pre-treatment temperature. Up to 90% of Sn, Zn, Cr, Cd, and Mn could be recovered for SCWD pre-treatment at 440 °C.     

用CO_2改性碱渣废水强化炼油废水的硝化效能

针对炼油废水缺乏碱度而硝化效能受限问题,以CO_2曝气处理后的改性碱渣废水为碱度补充剂,按一定配比加入炼油废水好氧阶段以强化硝化效能。实验结果表明:经流量为1 L/min的CO_2连续曝气处理5 h后,碱渣废水p H可降至7.2~7.8,钙元素质量浓度可降低90.65%,并去除了部分汞、砷等有毒重金属;将该改性碱渣废水以1∶99的体积比加入炼油废水并进行生化处理,COD去除率可达90.2%;相较于未补充碱渣的炼油废水,出水ρ(NO3--N)提高25%~30%,硝化细菌菌群密度增加52%,污泥絮体形态结构未发生改变。     

Olive mill solid residues as heavy metal sorbent material: a preliminary study

Biosorption of heavy metals is an innovative and alternative technology to remove these pollutants from aqueous solutions using inactive and dead biomasses such as agricultural and industrial wastes, algae and bacteria. In this study olive mill solid residue was used as heavy metal adsorbent material for its wide availability as agricultural waste and also for its cellulosic matrix, rich of potential metal binding active sites. Preliminary studies concerned with the removal of different heavy metals (Hg, Pb, Cu, Zn and Cd), the effect of pre-treatments by water and n-hexane and the regeneration possibility. Olive mill solid residue resulted able to remove heavy metals from aqueous solutions with an affinity series reflecting the hydrolytic properties of the metallic ions, but also a particular affinity for copper. It can be supposed that biosorption phenomenon occur by a general ion exchange mechanism combined with a specific complexation reaction for copper ions. Water pre-treatment is sufficient to reduce COD release in the effluent according to the law limit, while n-hexane pre-treatment strongly reduces also the adsorption properties of this material. Experimental isotherms obtained under different operating conditions were fitted using a non linear regression method for the estimation of the Langmuir parameters. Moreover a simple Scatchard plot analysis was performed for a preliminary investigation of the active sites, showing the presence of two different site affinities depending on the metal concentration, according to the previous hypothesis of two kinds of uptake mechanisms for copper biosorption. Regeneration tests gave good results in terms of yield of regeneration and also concentration ratios.     

Sewage sludge ash to phosphorus fertiliser: variables influencing heavy metal removal during thermochemical treatment

The aim of this study was to improve the removal of heavy metals from sewage sludge ash by a thermochemical process. The resulting detoxified ash was intended for use as a raw material rich in phosphorus (P) for inorganic fertiliser production. The thermochemical treatment was performed in a rotary kiln where the evaporation of relevant heavy metals was enhanced by additives. The four variables investigated for process optimisation were treatment temperature, type of additive (KCl, MgCl(2)) and its amount, as well as type of reactor (directly or indirectly heated rotary kiln). The removal rates of Cd, Cr, Cu, Ni, Pb, Zn and of Ca, P and Cl were investigated. The best overall removal efficiency for Cd, Cu, Pb and Zn could be found for the indirectly heated system. The type of additive was critical, since MgCl(2) favours Zn- over Cu-removal, while KCl acts conversely. The use of MgCl(2) caused less particle abrasion from the pellets in the kiln than KCl. In the case of the additive KCl, liquid KCl - temporarily formed in the pellets - acted as a barrier to heavy metal evaporation as long as treatment temperatures were not sufficiently high to enhance its reaction or evaporation.     

Metal mobilization from municipal solid waste incineration bottom ash through metal complexation with organic and inorganic ligands

As a first step in the development of ligand-assisted removal of heavy metals from municipal solid waste incineration bottom ash under alkaline conditions, ammonium nitrate, ammonium sulfate, ammonium acetate, ammonium oxalate, ammonium citrate, urea, and mixtures of ammonium salts and urea were examined to find which ligands could promote the leachability of elements, including heavy metals, and which elements could be mobilized through complexation. Ammonium citrate promoted the mobilization of Cr, Cu, Mn, P, Sb, and especially Fe. Ammonium nitrate accelerated Mg leachability significantly. Under the conditions used in this study, counter anions seemed to contribute mainly to the complexation. When a mixture of ammonium citrate and urea was utilized, a coexistence effect appeared on Fe mobilization. Although the correlation analysis of leaching test results showed a strong correlation among Cr, Cu, Fe, Mn, and P, X-ray diffraction analysis partially supported the correlation between Fe and Mn only.     

Treatment of Stormwater using Fibre Filter Media

In this study, a high-rate fibre filter was used as a pre-treatment to stormwater in conjunction with in-line flocculation. The effect of operating the fibre filter with different packing densities (105, 115 and 125 kg/m³) and filtration velocities (20, 40, 60 m/h) with and without in-line flocculation was investigated. In-line flocculation was provided using 5, 10 and 15 mg/L of ferric chloride (FeCl₃·6H₂O). The filter performance was studied in terms of pressure drop (ΔP), solids removal efficiency, heavy metals (total) removal efficiency and total organic carbon (TOC) removal efficiency. It is found that the use of in-line flocculation at a dose of 15 mg/L improved the performance of fibre filter as measured by turbidity removal (95%), total suspended solids reduction (98%), colour removal efficiency (99%), TOC removal (reduced by 30–40 %) and total coliform removal (93%). The modified fouling index reduced from 750–950 to 12 s/L² proving that fibre filter can be an excellent pre-treatment to membrane filtration that may be consider as post-treatment. The removal efficiency of heavy metal was variable as their concentration in raw water was small. Even though the concentration of some of these metals such as iron, aluminium, copper and zinc were reduced, others like nickel, chromium and cadmium showed lower removal rates.     

复合重金属污染高岭土的电动修复

根据电子废弃物拆解场地的污染特征,以复合重金属(Cu,Cd,Pb)污染高岭土为研究对象,考察了电动技术对污染土壤的修复效果。实验结果表明:在电压梯度为1 V/cm、阳极液为自来水、阴极液为柠檬酸-柠檬酸钠缓冲液(pH=5)、靠近阴极设置活性炭渗透反应墙(PRB)的条件下电动修复96 h后,Cu,Cd,Pb的平均去除率分别可达79.93%,99.43%,39.36%;土壤的酸碱性对电动修复效果影响显著,通过在阴极添加缓冲液维持土壤偏酸性条件,有利于重金属污染物的电动去除;在靠近阴极设置活性炭PRB可富集重金属,减少阴极液的污染;迁移率大的酸可提取态重金属较易去除,残渣态重金属稳定性强,去除率较低。     

The adsorption characteristics of heavy metals by various particle sizes of MSWI bottom ash

The incineration rate of municipal solid waste (MSW) has been increased because of difficulty in securing a proper disposal site for MSW in Korea. The advantage of incineration is reduction of the volume of waste; however, significant amounts of bottom ash and fly ash were generated in the incineration process. Their treatment has attracted growing interest because of the potential toxicity of hazardous heavy metals. Generally, heavy metals are less released from bottom ash than from fly ash. In this study the adsorption characteristics of heavy metals were investigated using various particle sizes of MSWI bottom ash. Since bottom ash has a broad particle size distribution, it was sieved to size classes of +20, -20, -48, -80, -100 mesh. Cation exchange capacity (CEC) was analyzed by the ammonium acetate method to evaluate the potential as an adsorbent. The CEC values and surface areas increase as the range of particle size becomes finer. The adsorption experiment was conducted using synthetic (Cu and Ni) and plating rinse water as a function of reaction time (10-180 min), liquid/solid ratio (2-100) and particle size (+20 to -100 mesh), respectively. The adsorption rate increased with decreasing particle size and with increasing liquid/solid ratio; however, the removal efficiency of Cu was higher than that of Ni. In the case of plating rinse water, the adsorption rate decreased sharply at high liquid/solid ratio, and it showed over 80% of adsorption rates for Cu and Ni at an initial pH of 3.     

Electrochemical remediation of heavy metal contaminated soils

Over the years, many soils have been contaminated with toxic heavy metals as a result of a variety of industrial and military activities. Electrokinetic soil treatment is an emerging technology that could prove to be very effective in the remediation of these sites. “Real-world” heavy metal contaminated (Pb(II), Cd(II), and Cr(III)) soils from three military sites with varying soil properties were subjected to electrokinetic treatment in the laboratory. Metal extractants (chelating agents and acids) were studied and found to be effective in enhancing the electrokinetic process. Results indicated that heavy metal removal efficiencies varied in the three soils tested. In one case, removal efficiencies of 90 percent and 60 percent were obtained for Cd and Cr, respectively, for the nitric acid amended experiments. For another case, over 60 percent of the total Pb in the system was deposited near the cathode for the non-amended and the citric-acid amended tests. Conversely, in the third case, the electrokinetic soil-washing treatment process failed to produce significant removal of any metal contaminant. The discrepancies that exist between the metal removal results of the three soils were attributed to the different physiochemical characteristics of each soil.     

Heavy metal removal from contaminated sludge for land application: a review

In recent years, various methods for heavy metal removal from sewage sludge have been extensively studied in order to minimize the prospective health risks of sludge during land application. In this paper, a comparative review and critical analysis of the application of chemical extraction, bioleaching, electroreclamation, and supercritical fluid extraction (SFE), in removing heavy metals from contaminated sludges is presented. Moreover, speciation studies, which can indicate ease of leachability of the different forms of heavy metals in sludge, are also presented. Experimental studies revealed a broad range in metal extraction efficiencies of the different extraction technologies. Acid treatment seemed to effectively remove Cd, attaining as much as 100% removal for some studies, as compared to bioleaching. SFE also gave higher removal efficiency than bioleaching. Cr, Pb and Ni seemed to be also effectively removed by the acid treatment. For the removal of Cu, Mn and Zn, the bioleaching process seemed to be appropriate with maximum removal efficiencies of 91%, 93% and 96% for the three metals, respectively, and as high as 64% minimum removal efficiency for Zn. The SFE process also gave good results for Cu, Mn and Zn removal. Electroreclamation exhibited better removal efficiency for Mn, but is still inferior to acid treatment and bioleaching processes. For chemical extraction, because of the adverse impacts that can result from the use of inorganic acids and complexing agents, interest can be directed more toward utilizing organic acids as extracting agents because of their biodegradability and capability to remove metals at mildly acidic condition, hence requiring less acid. The bioleaching process, although it seems to give a higher yield of metal extraction with lower chemical cost than chemical extraction, may be limited by the inability of the system to cope with the natural environmental conditions, requires strict monitoring of aeration rate and temperature and has applicability to only low sludge solids concentration. A full-scale study would be useful to better assess the efficiency of the process. The electroreclamation technology is limited by its relatively higher energy consumption and limited applicability to sludge. The SFE method, on the other hand, is limited by the complexity of the process and the cost of ligands suitable for effective metal extraction. Both of these technologies are still in their early stage of application and hence there is a need for further basic and applied studies. Finally, the common advantage for almost all treatment technologies studied is that the extraction efficiencies for some metals are high enough to remove metals from sludge to levels suitable for land application.     

Treatment of tar pond sludge in a circulating fluidized bed combustor

A series of tests to burn mixtures of tar pond sludge and coal was carried out using a mini‐circulating fluidized bed combustor (mini‐CFBC). During the tests, carbon dioxide, oxygen, carbon monoxide, sulfur dioxide, and nitrogen oxides in the flue gas were monitored continuously. Stack gas sampling was carried out for hydrochloric acid, metals, particulate matter, volatile organic compounds (VOCs), total hydrocarbons, semivolatile organic compounds (SVOCs), dioxins and furans (PCDD/Fs), and polychlorinated biphenyls (PCBs). Results showed that hydrochloric acid, mercury, particulate matter, PCDD/F, and metal concentrations were all below both the current limits and the gas‐release limits to be implemented in 2008 in Canada. The new 2008 emissions limits will reduce the maximum allowable concentrations of most pollutants by half. Thus, the maximum concentration for particulate matter will be 5 mg/m³ (from the current maximum concentration of 10 mg/m³);the maximum concentration for hydrochloric acid will be 5 mg/m³ (from 10 mg/m³); and the‐maximum concentration for dioxins and furans will be 0.032 ng/m toxic equivalent (from 0.08 ng/mcurrently). Sulfur capture efficiency was 89–91 percent. The percentage of fuel nitrogen converted to nitrogen oxides was of the order of 4.7 to 6.1, which is significantly lower than that of conventional pulverized coal‐fired boilers and well within the normal range for fluidized bed combustors (FBCs). PCB and polycyclic aromatic hydrocarbon (PAH) emissions levels were comparable or lower than levels reported in the literature for industrial‐scale FBCs. VOC concentrations were low except for benzene, for which the concentration was higher than that reported for pulverized coal‐fired utility boilers. In addition, carbon monoxide concentration was high at 1,200 to 2,200 parts per million. However, these carbon monoxide concentrations are typical of the mini‐CFBC firing coal. The trials showed that for 10 percent by weight tar pond sludge mixed with 90 percent by weight coal, the combustion was both stable and efficient. The tests demonstrated that CFBC technology is an environmentally sound option for eliminating tar pond waste sludge. © 2005 Wiley Periodicals, Inc.     

Removal of manganese and zinc from Kahrizak landfill leachate using daily cover soil and lime

The possibility of in situ removal of heavy metals found in leachate generated at municipal solid waste landfills was studied through amendment of daily cover soil. Kahrizak landfill, which receives the waste generated at Tehran, was selected as the source of leachate and soil samples. Manganese and zinc were selected in this study. The soil sample taken from the Kahrizak site contained about 17% clay, which was presumed to have significant capability for removing manganese and zinc. This capability was assumed to be enhanced further through the addition of lime and consequently to improve the potential for chemical precipitation of the selected metals. The in situ removal experiment was accomplished through a set of seven columns filled with the sampled soil with varying contents of lime (i.e., from 0% to 6% by dry weight). Fresh leachate of low pH was added to the columns on a daily basis. Concentrations of manganese and zinc were measured in the influent and effluent during 40 days when biological clogging resulted in a condition of almost no outflow in the columns. The results indicated a substantial increase in removal efficiency through the addition of lime to the daily cover soil. Desorption resulting from the low pH of fresh leachate occurs at later stages compared to the column with no lime addition.     

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.     

Improving sustainable recovery of metals from waste printed circuit boards by the primary copper smelter process

In this paper, utilizing the existing primary copper smelter process for the recovery of metals from waste printed circuit boards (PCBs) is proposed as an alternative to the current backyard operations in developing countries. The Model for Evaluating Metal Recycling Efficiency from Complex Scraps (MEMRECS) concept is introduced as a tool for the evaluation of the eco-efficiency of metals recovery from waste PCBs. Based on the MEMRECS approach, the relative contribution of every metal fraction to the recyclability of the whole product is estimated. Thereby, gold content is identified as a key factor strongly influencing the efficiency of metals recovery from waste PCBs. Furthermore, it could be used as an indicator for the categorization of waste PCBs before feeding them into the recycling process. Finally, an integrated process is proposed to optimize the eco-efficiency of metals recovery from waste PCBs in developing countries.     

Remediation of PCB‐Contaminated Soil Using Extraction and Destruction: Bench‐Scale Test

Polychlorinated biphenyls (PCBs) are a persistent environmental issue worldwide. This study summarizes the results obtained from a bench‐scale test of remediating PCB‐impacted soil. The research aimed to evaluate the effectiveness of extracting the PCB Aroclor 1260 from soil, transferring it to a liquid matrix, and then treating the PCB‐containing liquid using an Activated Metal Treatment System, a technology developed by NASA based on zero valent magnesium (ZVMg). The soil was from a former electrical plant area impacted by PCBs. The initial concentration of untreated soil contained an average of 4.7 ± 0.15 mg/kg of Aroclor 1260. The results showed that the mass transfer phenomena is possible using ethanol as a liquid matrix, reaching transfer results up to 93 percent. The ZVMg enabled the destruction of the Aroclor 1260, which reached 20 percent without any buildup of undesirable by‐products, such as less chlorinated PCBs.  ©2016 Wiley Periodicals, Inc.     

Reducing salinity and organic contaminants in the Pearl Harbor dredged material using soil amendments and plants

Phytoremediation is an emerging technique that can be used to economically remediate sites contaminated with trace elements and/or man‐made organic contaminants. This technique was used on Pearl Harbor (Oahu, Hawaii) dredged material (PHDM) containing polycyclic aromatic hydrocarbons (PAHs) and some heavy metals. The dredged material was first amended with a high‐calcium soil (Waialua Mollisol) and a biosolids‐based compost at different proportions to yield varying salinity levels. A mixture that yielded an electrical conductivity (EC, a measure of salinity) of the saturated paste extract of 15 to 20 dS/m was identified and used to evaluate the salt tolerance of five plant species. Relative germination and one‐month‐old biomass indicated that common bermuda grass (Cynodon dactylon), seashore paspalum (Paspalum vaginatum), beach pea (Vigna marina), and cow pea (Vigna unguiculata) can produce at least 40 percent of biomass of the control at an EC of approximately 18 dS/m, suggesting the four plants are relatively salt tolerant. In contrast, Desmodium intortum either did not germinate or died within two weeks after germination at the same salinity level. A subsequent greenhouse experiment, using mixtures of the PHDM (0 or 25 percent dry weight), organic amendments (10 percent leucaena green manure or biosolids‐based compost), and a Mollisol (65 or 90 percent dry weight) in 6‐liter pots containing 4 kilograms of material yielded the following results: (1) A combination of transplanted seashore paspalum, seeded bermuda grass, and seeded beach pea was effective in taking up sodium (Na), thereby reducing salinity and making the medium more amenable to diversified microbes and plants, which may be effective PAH degraders; (2) total PAH concentration was reduced by about 30 percent after three months of active plant growth, but degradation of individual PAH members varied significantly, however; (3) leguminous green manure, as a soil amendment, was more effective than compost for use in bio‐ and/or phytoremediations; and (4) soil amendments, when applicable, could supplement living plants in reducing organic contaminants, such as PAHs. © 2002 Wiley Periodicals, Inc.