Investigating the Use of Iron Reducing Bacteria for the Removal of Arsenic from Contaminated Soils

Clean-up techniques, which were developed for removing cationic heavy metals from contaminated soils, are inappropriate for the metalloid As, which is a common and highly toxic pollutant. Because arsenic is mainly found associated with the hydrous ferric oxides of the soil, a possible mechanism for the mobilisation of this element is the reductive dissolution of Fe(III) oxyhydroxides. In this paper we investigate the possibility to mobilise arsenic, using the Fe(III)-reducing bacterium Desulfuromonas Palmitatis. The initial experiments were carried out using a crystalline ferric arsenate as model compound, i.e. scorodite (FeAsO₄.2H₂O). D. palmitatis was found able to reduce the trivalent iron of scorodite at a percentage of 80% within 16 days, but arsenic remained in the pentavalent state, and reprecipitated with Fe(II) in the form of low solubility ferrous arsenates. To avoid the precipitation of ferrous arsenates the subsequent experiments with soil were conducted by combining the reducing ability of D. palmitatis with the chelating strength of EDTA (ethylenediamine tetracetic acid), which can form strong aqueous complexes with Fe(II). Approximately 60% of Fe and 75% of As were recovered in the aqueous solution in the presence of EDTA, while in the simple biological treatment no Fe was dissolved and only a 3% of As was mobilised.     

Chemical immobilisation of arsenic in contaminated soils using iron(II)sulphate—advantages and pitfalls

Chemical immobilisation of inorganic contaminants by increasing the sorption capacity of soils and/or promoting the formation of sparingly soluble precipitates may be a cost-effective approach to counteract groundwater pollution. This study focuses on the enhanced retention of arsenic in two contaminated soils by addition of solid iron(II)sulphate. Four lab-scale column experiments were performed under unsaturated conditions with subsoil material sampled at a former timber preservation site and a pigment production plant. Arsenic effluent concentrations indicated 89.9 to 99.8% immobilisation in the treated columns. Sequential extractions showed a shift in contaminant binding forms towards the iron(hydr)oxide and residual fractions. Possible immobilisation mechanisms are the precipitation of FeAs phases, the formation of inner sphere complexes, and/or the occlusion of arsenic in newly formed amorphous/crystalline iron oxides. Bromide breakthrough curves point to the fact that the addition of iron(II)sulphate only moderately affects soil hydraulic properties. In contrast to reduced emissions of arsenic, increased seepage water concentrations were observed for other trace elements (e.g., cobalt, nickel, zinc). Mass balances indicate that this effect is primarily related to the temporary pH-drop caused by the oxidation of ferrous iron. The results show that chemical immobilisation using iron(II)sulphate is a promising way to protect groundwater quality at sites contaminated with timber preservation and pigment production remnants. As a prerequisite, optimum amendment levels need to be established and practical/field tests should be accompanied by a monitoring for a broad range of relevant trace elements.     

In situ Measurement of Daphnia longispina Grazing on Algae and Bacteria in a High Mountain Lake (Lake Paione Superiore,Northern Italy) using Fluorescently Labeled Cells

Grazing impact of Daphnia longispina on phytoplankton and bacteria in Lake Paione Superiore (Northern Italy) was evaluated using fluorescently labeled cells in short-term in situ experiments. Structure and size distribution of Daphnia were studied weekly from its appearance in July to its decline in September. Relative importance of algae and bacteria in the diet varied over time, as did consequently the relative impact of Daphnia on the phytoplankton and bacteria populations. Biomass of bacteria in the diet of Daphnia varied from 1 to 42%, and was highest at the beginning of population development when young individuals dominated. The percent biomass of algae in the diet increased with population development, ranging from 58 to 99%. Daphnia population consumed per hour 0.04–1.8% of bacteria and 0.3–17.6% of phytoplankton abundances.     

Preparation and performance of arsenate (V) adsorbents derived from concrete wastes

Solid adsorbent materials, prepared from waste cement powder and concrete sludge were assessed for removal of arsenic in the form of arsenic (As(V)) from water. All the materials exhibited arsenic removal capacity when added to distilled water containing 10–700 mg/L arsenic. The arsenic removal isotherms were expressed by the Langmuir type equations, and the highest removal capacity was observed for the adsorbent prepared from concrete sludge with heat treatment at 105 °C, the maximum removal capacity being 175 mg-As(V)/g. Based on changes in arsenic and calcium ion concentrations, and solution pH, the removal mechanism for arsenic was considered to involve the precipitation of calcium arsenate, Ca₃(AsO₄)₂. The enhanced removal of arsenic for the adsorbent prepared from concrete sludge with heat treatment was thought to reflect ion exchange by ettringite. The prepared adsorbents, derived from waste cement and concrete using simple procedures, may offer a cost effective approach for arsenic removal and clean-up of contaminated waters, especially in developing countries.     

Phytoremediation of arsenic‐contaminated soil as affected by the chelating agent CDTA and different levels of soil pH

Elevated levels of arsenic can pose a major threat to both human health and the environment. The phytoremediation of heavy metals from soil is emerging as a cost‐effective technology for the remediation of contaminated soils. The present greenhouse study was undertaken to identify plants capable of tolerating and accumulating high concentrations of arsenic. Asparagus fern and rye grass were found to tolerate and accumulate more than 1,100 ppm of arsenic in plant tissue. Arsenic uptake as affected by different levels of the chelating agent trans‐1, 2‐ cyclohexylenedinitrilotetraacetic acid (CDTA) and soil pH were also studied. The application of 5 mmol kg^?1 of CDTA to arsenic‐contaminated medium loam field soil enhanced the accumulation of arsenic by the test plants. Under these conditions, plants accumulated up to 1,400 ppm of arsenic as compared to 950 ppm by the plants grown in soil containing 1,200 ppm of arsenic but without any amendment of the chelating agent. Plants grown in field soil of pH 5 containing 300 ppm of arsenic absorbed higher concentrations of arsenic than at other tested pH levels. Corresponding reductions in arsenic content of soil after plant harvests were observed. © 2001 John Wiley & Sons, Inc.     

Arbuscular mycorrhizal fungi involvement in zinc and cadmium speciation change and phytoaccumulation

Over the past few years, there has been a greater study and understanding of the application of phytoremediation to remediate contaminated soil. The enhancement of phytoaccumulation of heavy metals—zinc (Zn), cadmium (Cd), arsenic (As), and selenium (Se)—in plants has been shown by inoculation of roots using arbuscular mycorrhizal fungi (AMF). This article presents the results of in vitro lab experiments conducted to verify the effects of AMF ( Glomus intraradices) hyphae on speciation of essential Zn and nonessential Cd heavy metals in order to change these metals from a water‐ insoluble carbonate to a soluble and phytoavailable form. Results show that in the presence of heavy metals in a nonavailable form to plants, endomycorrhizal hyphae can change the metal from carbonate to a water‐ soluble species. This phenomenon is more apparent with a nonessential (Cd) than with an essential metal (Zn). Zn saturation is reached in the G. intraradices colonized roots at around 400 ppm, independently of initial ZnCO₃ concentrations. Cd saturation is not reached; in the lower Cd treatment, the plant/media metal ratio is 3:1, and in the higher treatment, the ratio is 1:1. © 2005 Wiley Periodicals, Inc.     

Evaluation of synthetic adsorbents for cleanup of herbicide-laden wastewater

Small-and large-scale farm operators and applicators urgently need user-friendly and cost-effective on-site methods to treat dilute-formulated herbicide-laden wastewater (i.e., rinsate). In this study, we investigated solvent-regenerable synthetic adsorbents, Ambersorb® 563 adsorbent, Ambersorb 572 adsorbent, and Ambersorb 575 adsorbent, as alternatives to activated carbon (Filtrasorb ® 400) for cleanup of water containing Dual 8E (a.i., metolachlor [2-chloro-N-(2-ethyl-6-methylphenyl)-N-(2-methoxy-1-methylethyl)acetamide]) or Banvel 4L (a.i., dicamba [3,6-dichloro-2-methoxybenzoic acid]). Batch-type adsorption experiments were conducted to compare adsorptive capacities of the various adsorbents. Adsorption maxima, obtained from adsorption isotherms, indicated that of the Ambersorb adsorbents tested, Ambersorb 572 adsorbent generally exhibited the highest adsorptive capacities for the herbicides tested and was comparable to Filtrasorb 400. Solvent (methanol) regenerability studies demonstrated that herbicide was readily recovered from Ambersorb 572 adsorbent and Filtrasorb 400. In general, metolachlor was more readily recoverable than dicamba. In fixed-bed column studies, Ambersorb 572 adsorbent exhibited twice the adsorptive capacity of Filtrasorb 400. Fixed-bed columns were more effective in removing metolachlor from herbicide containing water regardless of the adsorbent used. Multicycling of Ambersorb 572 adsorbent resulted in 30% loss of adsorptive capacity for dicamba as Banvel 4L and no loss of adsorptive capacity for metolachlor as Dual 8E. Working capacity was reached after three adsorption-regeneration cycles. Fixed-bed columns packed with solvent-regenerable adsorbents may prove useful as part of an on-site wastewater disposal system.     

Kinetic Study of Naphthalene Biodegradation in Aerobic Slurry Phase Microcosms for the Optimisation of the Process

The research was focused on the slurry-phase biodegradation of naphthalene. The biodegradation process was optimised with preliminary experiments in slurry aerobic microcosms. From soil samples collected on a contaminated site, a Pseudomonas putida strain, called M8, capable to degrade naphthalene was selected. Microcosms were prepared with M8 strain by mixing non-contaminated soil and mineral M9 medium. Different experimental conditions were tested varying naphthalene concentration, soil:water ratio and inoculum density. The disappearance of hydrocarbon, the production of carbon dioxide, and the ratio of total heterotrophic and naphthalene-degrading bacteria were monitored at different incubation times. The kinetic equation that best fitted the disappearance of contaminant with time was determined. The results showed that the isolated strain enhanced the biodegradation rate with respect to the natural biodegradation.     

Bacterioplankton Community Structure and Dynamics in Enclosures During Bioremediation Experiments in an Acid Mining Lake

In an acid mining lake (pH 2.6) enclosure experiments wereperformed with the addition of different concentrations oforganic carbon, nitrogen and phosphorus. SSCP-communityfingerprints, based on 16S rRNA gene amplicons, were performed tomonitor changes in the structure of the total bacterialcommunity and the sulfate reducing bacteria (SRB) in themesocosms. Total bacterial cell counts, as assessed byepifluorescence microscopy, were increased in the mesocosmsamended with organic carbon. The addition of carbon alsoincreased the number of abundant bacterial taxa substantiallyalong depth. Sulfate reducing bacteria (SRB) could be detected inall enclosures and all parts of the water column. These SRBbelonged to genus Desulfobacter as indicated bycoroborating molecular data.     

Spatial Distribution of Geobacteraceae and Sulfate‐Reducing Bacteria During In Situ Bioremediation of Uranium‐Contaminated Groundwater

Analysis of the physiological status of subsurface microbial communities generally relies on the study of unattached microorganisms in the groundwater. These approaches have been employed in studies on bioremediation of uranium‐contaminated groundwater at a study site in Rifle, Colorado, in which Geobacter species typically account for over 90 percent of the microbial community in the groundwater during active uranium reduction. However, to develop efficient in situ bioremediation strategies it is necessary to know the status of sediment‐associated microorganisms as well. In order to evaluate the distribution of the natural community of Geobacter during bioremediation of uranium, subsurface sediments were packed into either passive flux meters (PFMs) or sediment columns deployed in groundwater monitoring wells prior to acetate injection during in situ biostimulation field trials. The trials were performed at the Department of Energy's (DOE's) Rifle Integrated Field Research Challenge site. Sediment samples were removed either during the peak of Fe(III) reduction or the peak of sulfate reduction over the course of two separate field experiments and preserved for microscopy. Direct cell counts using fluorescence in situ hybridization (FISH) probes targeting Geobacter species indicated that the majority of Geobacter cells were unattached during Fe(III) reduction, which typically tracks with elevated rates of uranium reduction. Similar measurements conducted during the sulfate‐reducing phase revealed the majority of Geobacter to be attached following exhaustion of more readily bioavailable forms of iron minerals. Laboratory sediment column studies confirmed observations made with sediment samples collected during field trials and indicated that during Fe(III) reduction, Geobacter species are primarily unattached (90 percent), whereas the majority of sulfate‐reducing bacteria and Geobacter species are attached to sediment surfaces when sulfate reduction is the predominant form of metabolism (75 percent and 77 percent, respectively). In addition, artificial sediment experiments showed that pure cultures of Geobacter uraniireducens, isolated from the Rifle site, were primarily unattached once Fe(III) became scarce. These results demonstrate that, although Geobacter species must directly contact Fe(III) oxides in order to reduce them, cells do not firmly attach to the sediments, which is likely an adaptive response to sparsely and heterogeneously dispersed Fe(III) minerals in the subsurface. © 2013 Wiley Periodicals, Inc.     

Evaluation of algal phytoremediation of light extractable petroleum hydrocarbons in subarctic climates

The presence of an organic mat in a hydrocarbon‐impacted creek in Whitehorse, Yukon Territory, Canada was examined for contributions to in situ remediation of petroleum‐contaminated water. This article investigates the role of algae, found in the organic mat, in the remediation of light extractable petroleum hydrocarbons (LEPHs) at the site and in the laboratory. During the study, LEPH concentrations were reduced by 16.8 percent in the presence of algae alone (algal solution) and 30.4 percent in the combined organic mat solution containing microbial consortia. The study results indicate that algal species at the site did not directly phytoremediate hydrocarbons. Rather, they were part of the total biological degradation taking place. © 2009 Wiley Periodicals, Inc.     

Removal of copper,chromium, and arsenic from CCA-C treated wood by EDTA extraction

Ethylenediaminetetracetic acid (EDTA) is one of the most common chelators used to bind the metal ions in extremely stable complexes in heavy metal contaminated soils and thus to remediate such substrates. EDTA forms water soluble complexes with many metal ions and it is used to release the various metals. In this study, EDTA extraction of copper, chromium, and arsenic from chromated copper arsenate (CCA-C) treated wood was evaluated using batch leaching experiments. CCA-treated wood samples were extracted with eight different concentrations of EDTA for 4, 8, 18, and 24 h at room temperature. Exposing CCA-treated chips and sawdust to EDTA extraction enhanced removal of CCA components compared with extraction by deionized water. Grinding CCA-treated wood chips into 40-mesh sawdust provided greater access to and removal of CCA components. Extraction with 1% EDTA solution for 24 h removed 60% copper, 13% chromium, and 25% arsenic from treated chips. EDTA extraction of treated sawdust samples resulted in 93% copper, 36% chromium, and 38% arsenic removal. CCA leaching from treated wood blocks was also evaluated according to modified AWPA E11-99 standard test method of determining the leachability of wood preservatives. Leaching of CCA components from treated wood blocks with 1% EDTA solution for 14 days caused more copper leaching compared to leaching with deionized water. Leaching with 1% EDTA for 14 days removed 53% copper from the blocks whereas 14% copper was leached from the blocks with deionized water. The results suggest that EDTA extraction removes significant quantities of copper from CCA-treated wood. Thus, EDTA could be important in the remediation of wood waste treated with the newest formulations of organometalic copper compounds and other water-borne wood preservatives containing copper.     

In situ remediation of arsenic in contaminated soils

In situ chemical fixation represents a promising and potentially cost‐effective treatment alternative for metal‐contaminated soils. This article presents the findings of the use of iron‐bearing soil amendments to reduce the leachability and bioaccessibility of arsenic in soils impacted by stack fallout from a zinc smelter. The focus of this investigation was to reduce the lead bioaccessibility of the soils through addition with phosphorus‐bearing amendments. However, as phosphorus addition was expected to increase arsenic mobility, the fixation strategy also incorporated use of iron‐bearing amendments to offset or reverse these effects. The findings of this investigation demonstrated that inclusion of iron‐bearing chemicals in the amendment formulation reduced arsenic leachability and bioaccessibility without compromising amendment effectiveness for reducing lead bioaccessibility. These results suggest that in situ chemical fixation has the potential to be an effective strategy for treatment of the impacted soils. © 2003 Wiley Periodicals, Inc.     

Enhanced phytoremediation: A study of mycorrhizoremediation of heavy metal–contaminated soil

Arbuscular mycorrhizal fungi (AMF) are microscopic fungi that occur naturally in soil and form a symbiosis with plant roots. By colonizing the roots, the fungus increases plant growth by making soil essential elements like zinc and phosphorus more accessible. AMF can play a role in the phytoremediation of heavy metal–contaminated soil (mycorrhizoremediation). Two research experiments were conducted to evaluate the impact of AMF on the extraction of different heavy metals (arsenic, cadmium, lead, selenium, and zinc) in contaminated soil. A grass mixture composed of Festuca rubra, Festuca eliator, Agropyron repens, and Trifolium repens was used in the experiments, and four different types of AMF were investigated: Glomus intraradices, Glomus mosseae, Glomus etunicatum, and Gigaspora gigantea. The results of the study showed that heavy metal extraction by Glomus intraradices colonized plants was the highest of all four AMF tested and was generally higher than nonmycorrhizal plants, depending on the heavy metal concentration in soil and whether it interacted with other metals in soil. However, metal extraction by AMF colonized grasses reached a plateau after an approximately two‐month period showing no further phytoaccumulation. © 2006 Wiley Periodicals, Inc.     

油脂工业废水的回用

以某油脂化工厂排放的达标废水为研究对象,提出了微絮凝-直接过滤、二级活性炭吸附、二氧化氯氧化消毒串连的深度处理工艺,并在小试基础上进行了油脂废水再生回用的工业化试验研究,处理规模为400m^3／d。处理后出水中COD、浊度、色度、阴离子表面活性剂（LAS）含量、细菌总数等均满足市政供水水质标准。回用水可作为碱化车间和油脂预处理车间的生产补充用水。     

In‐Situ and Ex‐Situ Bioremediation Options for Treating Perchlorate in Groundwater

Perchlorate has been identified as a water contaminant in 14 states, including California, Nevada, New Mexico, Arizona, Utah, and Texas, and current estimates suggest that the compound may affect the drinking water of as many as 15 million people. Biological treatment represents the most‐favorable technology for the effective and economical removal of perchlorate from water. Biological fluidized bed reactors (FBRs) have been tested successfully at the pilot scale for perchlorate treatment at several sites, and two full‐scale FBR systems are currently treating perchlorate‐contaminated groundwater in California and Texas. A third full‐scale treatment system is scheduled for start‐up in early 2002. The in‐situ treatment of perchlorate through addition of specific electron donors to groundwater also appears to hold promise as a bioremediation technology. Recent studies suggest that perchlorate‐reducing bacteria are widely occurring in nature, including in groundwater aquifers, and that these organisms can be stimulated to degrade perchlorate to below the current analytical reporting limit (< 4 μg/l) in many instances. In this article, in‐situ and ex‐situ options for biological treatment of perchlorate‐contaminated groundwater are discussed and results from laboratory and field experiments are presented. © 2002 Wiley Periodicals, Inc.     

Phytoremediation of zinc and cadmium: A study of arbuscular mycorrhizal hyphae

Arbuscular mycorrhizal fungi (AMF) are microscopic fungi naturally occurring in soil that form a symbiosis with plant roots, producing a highly elaborated hyphal mycelium network in soil.In vitro lab experiments were conducted to determine whether extraradical mycorrhizal hyphae are directly involved in sequestration and uptake of essential zinc and nonessential cadmium by plant roots under toxic concentrations. The research is a continuation of an initial study presented in the Spring 2005 issue of Remediation that focused on the specific role of AMF in the speciation of heavy metals. Thus, this article presents a more expanded view. Results show that zinc and cadmium heavy metals are sequestered and translocated to plant roots via extraradical AMF hyphae. Root/growth media accumulation factors reached 5:1 and 18:1 for zinc and cadmium, respectively. Phytoremediation of heavy metal–contaminated soils can be enhanced by mycorrhizal inoculation. © 2005 Wiley Periodicals, Inc.     

用钢渣处理含砷废水

对用钢渣处理含硫废水进行了试验，用配水探讨了钢渣投加量，水样，ＰＨ，混合时间等因素对除砷效果的影响，结果表明，钢渣具有较好的除砷效果。     

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。     

Kinetics and thermodynamics of copper ions removal from wastewater by use of zeolite.

Natural Bulgarian zeolite was tested for its ability to remove Cu2+ from model wastewater. Influence of process variables was investigated. It was found that the optimum wastewater to zeolite ratio is 100:1 and the optimum pH value of water to be treated is 5.5 to 7.5. Zeolite with finer particles shows a higher uptake capacity. The simultaneous presence of Ca2+ and Mg2+ in concentrations similar to their concentrations in Bulgarian natural water does not significantly influence the uptake of Cu2+. Zeolite modification by treating it with NaCl, CH3COONa and NaOH increases its uptake ability. Copper ions are strongly immobilized by modified zeolite and secondary pollution of water caused by its contact with preloaded zeolite is very low (1.5-2.5% of Cu2+ preliminary immobilized have been released back into acidified water). Contacting with 2 mol dm(-3) NaCl can easily regenerate loaded zeolite; best results were obtained for zeolite modified with NaCl. Requirements of Bulgarian standards for industrial wastewater can be met by a one-stage process for an initial Cu2+ concentration of 10 mg dm(-3), and by a two stage process for an initial Cu2+ concentration of 50 mg dm(-3). Uptake of Cu2+ by zeolite from neutral wastewater has proved to be as effective as Cu2+ removal by precipitation of copper hydroxide. The process of Cu2+ uptake by natural zeolite is best described by the kinetic equation for adsorption. This fact, together with the correlation found between the Cu2+ uptake and the amount of Na+, Ca2+ and K+ released into solution by zeolite shows that the ion exchange sorption plays the basic role in Cu2+ uptake by natural zeolite. The value obtained for the apparent activation energy (26.112 kJ mol(-1) implies that the process can be easily carried out with a satisfactory rate. The uptake equilibrium is best described by the Langmuir adsorption isotherm, with Langmuir constants KL= 6.4 x 10(-2) dm3 mg(-1) and M = 6.74 mg g(-1). The apparent equilibrium constant found shows moderate affinity of zeolite for Cu2+. Values of deltaG degrees and deltaH degrees found show the spontaneous and endothermic nature of the process of Cu2+ uptake by natural zeolite.