Distribution of Pb, V, Cr, Ni, Cd, Cu and Fe in particles formed from the combustion of waste oils

The determination of Pb, V, Cr, Ni, Cd, Cu and Fe in particles of different size obtained from the combustion of waste oils has been carried out. The study consists of the separation of several fractions according to the size of particles, the wet digestion and the individual analysis by graphite furnace atomic absorption spectrometry of the mentioned metals. Taking into account the volatilization temperature of different compounds containing the metals and their distribution on the size fractions, the mineral speciation of metals is proposed.     

Changes in speciation and leaching behaviors of heavy metals in dredged sediment solidified/stabilized with various materials

Solidification/stabilization (S/S) of sediments is frequently used to treat contaminants in dredged sediments. In this study, sediment collected from the Pearl River Delta (China) was solidified/stabilized with three different kinds of functional materials: cement, lime and bentonite. Lime primarily acted via induced increases in pH, while cements stabilization occurred through their silicate-based systems and the main function of bentonite was adsorption. The speciation and leaching behaviors of specific heavy metals before and after S/S were analyzed and the results showed that the residual speciation of Cd, Cr, Ni, Pb and Zn increased in all treatments except for Cu, as the exchangeable speciation, carbonate-bound speciation and Fe-Mn-oxide-bound speciation of Cu (all of which could be stabilized) were less than 2 % of the total amount. Pb leaching only decreased when pH increased, while the mobility of Cr and Ni only decreased in response to the silicate-based systems. The leached portion of the Fe-Mn-oxide-bound speciation followed the order Zn?>?Cu?>?Ni/Cd?>?Pb?>?Cr. The leached portion of organic-matter-bound species was less than 4 % for Cd, Cr, Ni and Pb, but 35.1 % and 20.6 % for Cu and Zn, respectively.     

Solid speciation and mobility of potentially toxic elements from natural and contaminated soils: a combined approach

The study area (Szklary Massif, SW Poland) comprises three sites of different soil provenance: (1) natural serpentine Cambisol, (2) anthroposol situated on waste dump and (3) cultivated Inceptisol developed on glacial tills next to the dump. Potentially toxic elements (PTE) have either lithogenic or anthropogenic origins in these sites. The chemical partitioning of Co, Cr, Cu, Ni, Pb and Zn among solid forms was determined by sequential extractions coupled with direct mineral identifications (SEM, electron microprobe analysis - EMPA, and XRD). Examination of solid residues after several extraction steps was conducted in order to discuss the indirect speciation obtained by the extraction method. Total concentrations of PTE having anthropogenic origin greatly exceed those of lithogenic origin. Mobility of studied PTE is variable in the different environments except for Cr which is always mostly found in residual fractions of extractions. Cu and Pb are more mobile than Cr and Co in all soils. Zn is more stable (Cu>Pb>Ni>Co>Zn>Cr) in the serpentine soil and cultivated epipedon (Pb>Cu>Zn>Ni>Co>Cr) than in the anthroposol (Zn>CuPb>Ni>Co>Cr). PTE of lithogenic origin are generally less mobile than those from anthropogenic origin except Ni which is more mobile in the serpentine soil. Nonetheless, mineral forms of metals better determine their mobility than metal origin. Identification by direct methods of the PTE mineral form was not possible for metals present at low concentrations (Cu, Pb). However, direct mineralogical examinations of the solid residues of several extractions steps improved the assessment of the PTE solid speciation and mobility, particularly for Cr, Ni and Zn.     

Behaviour of metals following intensive pig slurry applications to a natural field treatment process in Brittany (France)

It is well-known that heavy metals brought by intensive pig slurry applications accumulate in the soil; because of their potential impact on the environment, studying their behaviour is of utmost interest. The Solepur process has been developed in Brittany (France) where pig farming causes serious environmental problems; it enables the soil to be used as a treatment medium to process pig slurry. Numerous pig slurry applications were performed from 1991 to 1995 on an experimental hydrologically-isolated field specially equipped to recover all the leachate. These applications approximately corresponded to the amount which might have been spread over one century. The Solepur process can be considered as a simulation model for what happens to metals in pig slurry under normal field conditions over a long period of time. This work measured the concentrations of Cu, Zn, Mn, Co, Fe and Cd in pig slurry, in soil and in drainage water, and the results are discussed. Total concentrations and speciation data within the three different compartments were analysed and showed that Cu and Zn accumulate in the surface layer, whereas other metals, such as Mn and Co, dissolve and are washed away in the leachate. The increase in the bioavailability and toxicity of these metals as well as their impact on the environment are discussed.     

焦化废水处理过程外排污泥中重金属形态特征及其潜在环境风险

焦化废水处理过程所排放污泥中重金属的含量及化学形态是否构成环境风险将直接影响污泥处置方法的选择,为此,实验采用BCR顺序提取法分析了焦化废水处理站外排污泥中重金属(Cd、Hg、Pb、Cr、As、Ni、Zn、Cu和Mn)的形态特征,并采用地累积指数(Igeo)和潜在生态危害指数(RI)评价了重金属对土壤的潜在环境风险。研究结果表明:除Ni主要以可氧化态存在外,焦化废水外排污泥中其他几种重金属元素主要存在于残渣态,重金属元素的含量低于《城镇污水处理厂污染物排放标准(GB18918—2002)》中的控制限值;与城市污泥相比,焦化废水外排污泥具有低Pb、Cr、Zn、Cu含量,而高Cd、Hg、Mn含量的特点;基于Igeo和RI的评价结果,Cd和Hg是外排污泥中具有一定环境风险的元素,需要考虑其下游去向。焦化废水处理外排污泥中主要存在残渣态重金属成分,不表现为很高的环境风险,其处置应重点考虑其中有机污染物特别是POPs。     

Impact of sewage sludge spreading on heavy metal speciation in tropical soils (Réunion, Indian Ocean)

This study was designed to evaluate the impact of sewage sludge spreading on tropical soilborne heavy metal speciation. Sludgeborne heavy metal speciation was also assessed, and the potential mobility of the elements was classified as follows: Zn>Ni>Cu approximately Cr. Two sequential extraction procedures were applied to study Cr, Cu, Ni and Zn speciation in control soils and sludge-amended soils. We demonstrated that sewage sludge spreading over a 2-year period did not have an impact on soilborne heavy metal concentrations but affected speciation of the most mobile fractions of Ni and Zn. Both protocols were consistent for the organic matter fractions, with an increase in Cu, Zn and Cr concentrations in the amended soil as compared to the control soil. In addition, we highlighted that the two protocols characterized different pools of organic matter and that organic compounds remained in the solid matrix after extraction. With respect to the reducible fraction, completely opposite results were obtained with the two protocols and the solid residue study revealed that the two schemes were ineffective in characterizing iron and manganese fractions.     

Mercury in the Mediterranean. Part 2: processes and mass balance

Mass balance of contaminants can provide useful information on the processes that influence their concentrations in various environmental compartments. The most important sources, sinks and the equilibrium or non-equilibrium state of the contaminant in individual environmental compartments can also be identified. Using the latest mercury speciation data, the results of numerical models and the results of recent studies on mercury transport and transformation processes in the marine environment, we have re-evaluated the total mercury (HgT) mass balance in the Mediterranean Sea. New calculations have been performed employing three distinct marine layers: the surface layer, the thermocline and the deep sea. New transport mechanisms, deep water formation and density-driven sinking and upwelling, were included in the mass balance calculations. The most recent data have even enabled the calculation of an approximate methylmercury (MeHg) mass balance. HgT is well balanced in the entire Mediterranean, and the discrepancies between inputs and outputs in individual layers do not exceed 20 %. The MeHg balance shows larger discrepancies between gains and losses due to measurement uncertainties and gaps in our knowledge of Hg species transformation processes. Nonetheless, the main sources and sinks of HgT (deposition and evasion) and MeHg (fluxes from sediment, outflow through the Gibraltar Strait) are in accordance with previous studies on mercury in the Mediterranean Basin. Mercury in the Mediterranean fish harvest is the second largest MeHg sink; about 300 kg of this toxic substance is consumed annually with sea food.     

Chemical speciation and bioavailability of rare earth elements (REEs) in the ecosystem: a review

Rare earths (RE), chemically uniform group of elements due to similar physicochemical behavior, are termed as lanthanides. Natural occurrence depends on the geological circumstances and has been of long interest for geologist as tools for further scientific research into the region of ores, rocks, and oceanic water. The review paper mainly focuses to provide scientific literature about rare earth elements (REEs) with potential environmental and health effects in understanding the research. This is the initial review of RE speciation and bioavailability with current initiative toward development needs and research perceptive. In this paper, we have also discussed mineralogy, extraction, geochemistry, analytical methods of rare earth elements. In this study, REEs with their transformation and vertical distribution in different environments such as fresh and seawater, sediments, soil, weathering, transport, and solubility have been reported with most recent literature along key methods of findings. Speciation and bioavailability have been discussed in detail with special emphasis on soil, plant, and aquatic ecosystems and their impacts on the environment. This review shows that REE gained more importance in last few years due to their detrimental effects on living organisms, so their speciation, bioavailability, and composition are much more important to evaluate their health risks and are discussed thoroughly as well.     

An environmental fate, exposure and risk assessment of ethylene oxide from diffuse emissions

Ethylene oxide (EO) is mainly used as a chemical intermediate and as a fumigant and sterilizing agent. Through its manufacturing and intended uses, EO may be released into the environment. Therefore, an assessment of the environmental significance of those potential emissions was conducted. Data were collected describing pertinent physical properties, degradation and other loss mechanisms that control the fate of EO in the environment. Available aquatic and terrestrial ecotoxicity data were assembled and used as the basis of calculating critical toxicity values to characterize hazard. Environmental compartment concentrations of EO were calculated using Level III fugacity-based modeling. Six scenarios were developed to account for different climatic conditions in various portions of the US. Finally, potential regional-scale risks to aquatic and terrestrial wildlife were determined. In the conceptual model that was developed in this assessment, EO diffuses into air, partitions between environmental compartments, is transported out of the different compartments via advection, and undergoes abiotic and biological degradation within each compartment. All known emissions within the continental USA were assumed to enter a modeled region roughly the size of the State of Ohio. Organisms (receptors) were assumed to dwell in both terrestrial and aquatic compartments. Receptors were assumed to include small mammals, soil invertebrates, water column (pelagic) organisms, and sediment benthos. The goal of this assessment was to characterize any potential adverse risks to terrestrial and aquatic wildlife populations. Hazard Quotients (HQ) were calculated by dividing predicted concentrations of EO in air, water, sediment, and soil by their critical toxicity values. Maximum calculated HQ values in air were 1.52x10(-7), in water were 1.17x10(-5), in sediment were 2.25x10(-4), and in soil were 1.37x10(-5). The results of this assessment suggest that EO as currently manufactured and used does not pose adverse risks to aquatic or terrestrial wildlife. In all cases, the HQ values were much less than the maximum desired HQ value of 1.0 (4,400-6,600,000 times), indicating that the potential for diffuse emissions of EO to pose adverse environmental risks is quite low.     

Hydroxylated polychlorinated biphenyls in the environment: sources,fate, and toxicities

Hydroxylated polychlorinated biphenyls (OH-PCBs) are produced in the environment by the oxidation of PCBs through a variety of mechanisms, including metabolic transformation in living organisms and abiotic reactions with hydroxyl radicals. As a consequence, OH-PCBs have been detected in a wide range of environmental samples, including animal tissues, water, and sediments. OH-PCBs have recently raised serious environmental concerns because they exert a variety of toxic effects at lower doses than the parent PCBs and they are disruptors of the endocrine system. Although evidence about the widespread dispersion of OH-PCBs in various compartments of the ecosystem has accumulated, little is currently known about their biodegradation and behavior in the environment. OH-PCBs are, today, increasingly considered as a new class of environmental contaminants that possess specific chemical, physical, and biological properties not shared with the parent PCBs. This article reviews recent findings regarding the sources, fate, and toxicities of OH-PCBs in the environment.     

Bioremediation of industrial effluents containing heavy metals using brewing cells of <Emphasis Type="Italic">Saccharomyces cerevisiae</Emphasis> as a green technology: a review

The release of heavy metals into the environment, mainly as a consequence of anthropogenic activities, constitutes a worldwide environmental pollution problem. Unlike organic pollutants, heavy metals are not degraded and remain indefinitely in the ecosystem, which poses a different kind of challenge for remediation. It seems that the “best treatment technologies” available may not be completely effective for metal removal or can be expensive; therefore, new methodologies have been proposed for the detoxification of metal-bearing wastewaters. The present work reviews and discusses the advantages of using brewing yeast cells of Saccharomyces cerevisiae in the detoxification of effluents containing heavy metals. The current knowledge of the mechanisms of metal removal by yeast biomass is presented. The use of live or dead biomass and the influence of biomass inactivation on the metal accumulation characteristics are outlined. The role of chemical speciation for predicting and optimising the efficiency of metal removal is highlighted. The problem of biomass separation, after treatment of the effluents, and the use of flocculent characteristics, as an alternative process of cell–liquid separation, are also discussed. The use of yeast cells in the treatment of real effluents to bridge the gap between fundamental and applied studies is presented and updated. The convenient management of the contaminated biomass and the advantages of the selective recovery of heavy metals in the development of a closed cycle without residues (green technology) are critically reviewed.     

Currently used organophosphate and brominated flame retardants in the environment of China and other developing countries (2000–2016)

This review summarizes the environmental occurrence of new brominated flame retardants (NBFRs) and organophosphate compounds (OPs) in the environment of developing countries since 2000. The ban on the production and use of commercial formulations of polybrominated diphenyl ethers (PBDEs) have paved the way for the high use of NBFRs and OPs in consumer products to fulfill the fire safety regulations. Recent studies have shown that the ever increasing production volumes and extensive use of these chemicals as additive FRs and plasticizers have resulted into their ubiquitous occurrence in all environmental compartments. Although presumed to be safe for use and the environment, recent studies on their occurrence and persistence in the environment have raised questions. Due to the lack of awareness, research interest, and availability of technical facilities, limited scientific data is available on the occurrence of these chemicals in developing countries. In this study, we collected reported data and provide an overview of environmental occurrence of NBFRs and OPs in abiotic and biotic matrices of different developing countries. Finally, research gaps were identified with recommendations for future research work and would be useful towards the environmental management of these toxic chemicals.     

Applying waste management scenarios in the Peloponnese region in Greece: a critical analysis in the frame of life cycle assessment

The aim of this paper is to apply life cycle assessment in the waste management sector, in order to compare the environmental performance of different waste management methods. The methods that are studied are: landfilling, aerobic and anaerobic biological treatment, incineration and recycling, focusing on mass and energy balances and the environmental performance of each applied scenario. The Peloponnese Region in Greece was selected as a case for the application of this methodology and more specifically its largest municipalities, where a significant amount of waste is presented. The conducted LCA study proves the necessity of the adoption of an integrated waste management system and indicates its principal objectives by measuring environmental impacts. Thermal scenario contributes significant to the mitigation on the Greenhouse Gases. On the other hand, separation at source and recycling practices provides significant benefits to the abiotic depletion impact.     

Challenge of the Future

ABSTRACT

The separation of Cr(III) from collagen in chromium-tanned leather (wet-blue) is achieved by a combination of the protein (collagen) stabilization (protective cross-linking) and a subsequent labilization of the Cr(III) species bound to the protein. During the separation collagen retains the tertiary triple helical and higher (fibril) structures. The model proposed for the protective cross-linking involves inter- rather than intramolecular bridging, that is, a supramolecular bridging. The process of chromium removal takes place in a restricted aqueous environment, and it can be characterized as semihomogeneous or semiheterogeneous.     

Speciation of zinc in contaminated soils

The chemical speciation of zinc in soil solutions is critical to the understanding of its bioavailability and potential toxic effects. We studied the speciation of Zn in soil solution extracts from 66 contaminated soils representative of a wide range of field conditions in both North America and Europe. Within this dataset, we evaluated the links among the dissolved concentrations of zinc and the speciation of Zn(2+), soil solution pH, total soil Zn, dissolved organic matter (DOM), soil organic matter (SOM) and the concentrations of different inorganic anions. The solid-liquid partitioning coefficient (K(d)) for Zn ranged from 17 to 13,100Lkg(-1) soil. The fraction of dissolved Zn bound to DOM varied from 60% to 98% and the soil solution free Zn(2+) varied from 40% to 60% of the labile Zn. Multiple regression equations to predict free Zn(2+), dissolved Zn and the solid-liquid partitioning of Zn are given for potential use in environmental fate modeling and risk assessment. The multiple regressions also highlight some of the most important soil properties controlling the solubility and chemical speciation of zinc in contaminated soils.     

Speciation of arsenic and chromium metal ions by reversed phase high performance liquid chromatography

The speciation of arsenic [As(III) and As(V)] and chromium [Cr(III) and Cr(VI)] was carried out by high performance liquid chromatography. The column used was Econosil C18 (250 x 4.6 mm i.d., particle size 10 microm). The mobile phases consisted of water-acetonitrile (80:20, v/v) for arsenic and 10 mM ammonium acetate buffer (6.0 pH)-acetonitrile (10:90, v/v) for chromium speciation separately and respectively. The detection was carried out by UV-Vis at 410 nm and atomic absorption spectrometer (AAS) respectively and separately. The values of alpha and Rs of As(III) and As(V) species were 1.4 and 1.5 respectively while the values of alpha and Rs for Cr(III) and Cr(VI) were 1.35 and 0.2 respectively. The effect of the acetonitrile percentages was also carried out on the speciation of arsenic only. The relative standard deviation and limit of detection were in the range of 0.01-0.02 and 0.4-1.0 microg/ml respectively.     

环境中有机锡化合物形态分析方法进展

本文综述了国内外近２０年来环境样品中有机锡化合物的分析技术。对有机锡样品的衍生技术进行了评价：系统介绍了检测有机锡化合物的气相色谱（ＧＣ）联用技术、高效液相色谱（ＨＰＬＣ）联用技术以及超临界流体液相色谱（ＳＦＣ）联用技术。     

Recent advances in mercury speciation analysis with focus on spectrometric methods and enriched stable isotope applications

This paper discusses some recent advances in spectrometric methods and approaches for mercury speciation analysis of environmental samples with focus on isotope dilution techniques for determination of mercury species' concentrations in gaseous samples and reaction rates in soils and sediments. Such analytical data is important inter alia in fundamental research on mercury biogeochemistry and for risk assessments of mercury-contaminated soils and sediments and for designing effective remedial actions. The paper describes how the use of enriched stable isotope tracers in mercury speciation analysis can improve the traceability and accuracy of results, facilitate rational method developments, and be useful for studying biogeochemical processes, i.e. rate of reactions and fluxes, of mercury species. In particular the possibilities to study and correct for unwanted species transformation reactions during sample treatment and to study "natural" transformations of species in environmental samples, or micro- and mesocosm ecosystems, during incubations are highlighted. Important considerations to generate relevant data in isotope tracer experiments as well as reliability and quality assurance of mercury speciation analysis in general are also discussed.     

规划环境影响评价指标体系及评价方法浅析

对规划环境影响评价的内容作出了概述性的介绍，并根据规划环境影响评价的特点，得出规划环境影响评价的指标体系应包括自然环境指标、生态环境指标、资源利用指标、能源利用指标和社会经济指标5大体系。列举了当前适用于规划环境影响评价的技术方法，并对其进行简单的对比分析。