Sources, colloidal characteristics, and separation technologies for highly hazardous waste nanoemulsions.

Nanoemulsions play a crucial role in various industries. However, their application often results in hazardous waste, posing significant risks to human health and the environment. Effective management and separation of waste nanoemulsions requires special attention and effort. This review provides a comprehensive understanding of waste nanoemulsions, covering their sources, characteristics, and suitable treatment technologies, intending to mitigate their environmental impact. This study examines the evolution of nanoemulsions from beneficial products to hazardous wastes, provides an overview of the production processes, fate, and hazards of waste nanoemulsions, and highlights the critical characteristics that affect their stability. The latest advancements in separating waste nanoemulsions for recovering oil and reusable water resources are also presented, providing a comprehensive comparison and evaluation of the current treatment techniques. This review addresses the significant challenges in nanoemulsion treatment, provides insights into future research directions, and offers valuable implications for the development of more effective strategies to mitigate the hazards associated with waste nanoemulsions.

Innovative methodology for comprehensive utilization of arsenic-bearing neutralization sludge.

Arsenic-bearing neutralization (ABN) sludge is a classical hazardous waste commonly found in nonferrous metallurgy. However, the current storage of these hazardous wastes not only has to pay costly hazardous waste taxes but also poses significant risks to both the environment and human health. To address these issues and achieve the comprehensive utilization and minimization of ABN sludge, this study proposes a new combined process. The process involves selective reduction roasting, leaching, and carbonation, through which, the arsenate and gypsum in the ABN sludge were recovered in the form of As(s), high-purity CaCO3, and H2S. The selective reduction behaviors of arsenate and gypsum were investigated through thermodynamic analysis and roasting experiments. The results indicated that the 95.35 % arsenate and 96.55 % gypsum in the sludge were selectively reduced to As4(g) and CaS at 950 °C by carbothermic reduction. The As4(g) was condensed to As(s) and enriched in the dust (As, 96.78 wt %). In the leaching process, H2S gas was adopted to promote the leaching of CaS, and resulted in 97.41 % of CaS in the roasted product was selectively leached in the form of Ca(HS)2, leading to a 74.11 % reduction in the weight of the ABN sludge. Then, the Ca(HS)2 was subjected to capture CO2 for the separation of Ca2+ and S2-. The result depicted that 99.69 % of Ca2+ and 99.12 % of S2- were separated as high-purity (99.12 wt %) CaCO3 and H2S (24.89 vol %) by controlling the terminal carbonation pH to below 6.55. The generated H2S can be economically converted to sulfur by the Clause process. The whole process realized the comprehensive resource recovery and the minimization of the sludge, which provides an alternative solution for the clean treatment of hazardous ABN waste.

Biomedical waste generation at Ayurveda hospitals in South Asia: A mini review of the composition, quantities and characteristics.

Ayurveda hospitals generate biomedical wastes (BMW). However, details on composition, quantities and characteristics are very scarce, details which are important to formulate a proper waste management plan for subsequent implementation and continual improvement. Therefore, this article presents a mini review of the composition, quantities and characteristics of BMW generated from Ayurveda hospitals. Additionally, this article presents some best possible treatment and disposal procedures. Most of the information was gleaned from peer-reviewed journals, although some information was collected by the author and from grey literature available to the author; 70-99% (by wet weight) of the solid waste is non-hazardous; biodegradables contributing to 44-60% by wet weight due to more used Kizhi (medicinal bags for fomentation) and other medicinal/pharmaceutical wastes (excluding waste medicated oils, which is 12-15% of the liquid medicinal waste stream and are not readily biodegradable) largely derived from plants. The hazardous waste component includes infectious wastes, sharps, blood as pathological wastes (from Raktamoksha - bloodletting), heavy metal containing pharmaceutical wastes, chemical wastes and heavy metal rich wastes. Quantities of infectious wastes followed by sharps and blood form a major portion of hazardous wastes. Most of the infectious waste material contaminated with blood or other body fluids and sharps from Raktamoksha are very similar (appearance, moisture content and bulk density) to what is generated from hospitals practicing Western medicine. However, hospital-specific waste studies are required in future to better understand the sources, areas of generation, types, quantities and characteristics of BMW, and hence to formulate more accurate waste management plans.

Recovery of Pure Lead-Tin Alloy from Recycling Spent Lead-Acid Batteries.

Spent lead-acid batteries have become the primary raw material for global lead production. In the current lead refining process, the tin oxidizes to slag, making its recovery problematic and expensive. This paper aims to present an innovative method for the fire refining of lead, which enables the retention of tin contained in lead from recycled lead-acid batteries. The proposed method uses aluminium scrap to remove impurities from the lead, virtually leaving all of the tin in it. The results of the conducted experiments indicate the high efficiency of the proposed method, which obtained a pure Pb-Sn alloy. This alloy is an ideal base material for the production of battery grids. This research was carried out on an industrial scale, which confirms the possibility of facile implementation of the method in almost every lead-acid battery recycling plant in the world.

Mineral phase transition characteristics and its effects on the stabilization of heavy metals in industrial hazardous wastes incineration (IHWI) fly ash via microwave-assisted hydrothermal treatment.

Toxic heavy metals in industrial hazardous waste incineration (IHWI) fly ash can be effectively stabilized by using microwave-assisted hydrothermal technology. However, few works have focused on the relationship between mineralogical conversion and stability of heavy metals of fly ash during hydrothermal process. This study investigated the effect of mineral phase transition process on the stabilization and migration behavior of heavy metals in IHWI fly ash using coal fly ash as silicon­aluminum additive. Mineral composition analysis reveals that after microwave-assisted hydrothermal treatment (MAHT) of IHWI fly ash, zeolite-like minerals (e.g., tobermorite, katoite and sodalite), secondary aluminosilicate minerals (e.g., prehnite and anorthite) and other newly-formed minerals (e.g., wollastonite, pectolite and larnite) were found. The leaching concentrations of heavy metals (Cr, Ni, Cu, Zn, Cd and Pb) in IHWI fly ash decrease sharply after MAHT with the most obvious decreases in Cu, Pb and Zn. Spearman correlation analysis show significantly negative correlation between the content of zeolite-like minerals and the leaching concentrations of most heavy metals (e.g., Ni, Cu, Zn, Cd and Pb). These results suggest that the immobilization effects of heavy metals in IHWI fly ash can be effectively enhanced by promoting the formation of zeolite-like minerals during the MAHT. This study is expected to further promote the development of IHWI fly ash harmless treatment technology.

Metal mobility and bioaccessibility from cyanide leaching heaps in a historical mine site.

Unlike acidic sulfide mine wastes, where metal/loid mobility and bioaccessibility has been widely studied, less attention has been paid to alkaline cyanide heap leaching wastes. Thus, the main goal of this study is to evaluate the mobility and bioaccessibility of metal/loids in Fe-rich (up to 55%) mine wastes resulting from historical cyanide leaching activities. Wastes are mainly composed of oxides/oxyhydroxides (i.e. goethite and hematite), oxyhydroxisulfates (i.e. jarosite), sulfates (i.e., gypsum, evaporitic sulfate salts), carbonates (i.e., calcite, siderite) and quartz, with noticeable concentrations of metal/loids (e.g., 1453-6943 mg/kg of As, 5216-15,672 mg/kg; of Pb, 308-1094 mg/kg of Sb, 181-1174 mg/kg of Cu, or 97-1517 mg/kg of Zn). The wastes displayed a high reactivity upon rainfall contact associated to the dissolution of secondary minerals such as carbonates, gypsum, and other sulfates, exceeding the threshold values for hazardous wastes in some heap levels for Se, Cu, Zn, As, and sulfate leading to potential significant risks for aquatic life. High concentrations of Fe, Pb, and Al were released during the simulation of digestive ingestion of waste particles, with average values of 4825 mg/kg of Fe, 1672 mg/kg of Pb, and 807 mg/kg of Al. Mineralogy may control the mobility and bioaccessibility of metal/loids under rainfall events. However, in the case of the bioaccessible fractions different associations may be observed: i) the dissolution of gypsum, jarosite and hematite would mainly release Fe, As, Pb, Cu, Se, Sb and Tl; ii) the dissolution of an un-identified mineral (e.g., aluminosilicate or Mn oxide) would lead to the release of Ni, Co, Al and Mn and iii) the acid attack of silicate materials and goethite would enhance the bioaccessibility of V and Cr. This study highlights the hazardousness of wastes from cyanide heap leaching, and the need to adopt restoration measures in historical mine sites.

Recovery of zinc and extraction of calcium and sulfur from zinc-rich gypsum residue by selective reduction roasting combined with hydrolysis.

A novel process that includes selective reduction roasting followed by hydrolysis was proposed in this work to recover zinc, and efficiently extract calcium and sulfur from hazardous zinc-rich gypsum residue (ZGR) waste for high-purity of CaCO3 and sulfur production. The selective reduction behaviors of ZGR during the reduction roasting were investigated in detail based on thermodynamic analysis and roasting experiments. The effect of roasting temperature, carbon dosage and time on the selective reduction of ZGR was comprehensively investigated, and the results indicated that ZnO and CaSO4 in the ZGR can be selectively reduced to Zn(g) and CaS, respectively. The volatile Zn(g) was oxidized to ZnO and enriched in the dust, which can be used as a secondary zinc resource. Moreover, the hydrolysis behaviors and leaching kinetic of CaS during hydrolysis were studied intensively. Results depicted that in the H2S-H2O system, the CaS in the roasted product can be selectively and efficiently dissolved into the leachate. Furthermore, the kinetic analysis revealed that the hydrolysis of CaS conformed to the internal diffusion reaction control model in the shrinking core model and the apparent activation energy Ea = -12.02 kJ/mol. The obtained hydrolysate with low impurities could be used to capture CO2 for the production of high-purity sulfur and CaCO3. Iron and other impurities in the roasted product were concentrated into the leaching slag in the form of metallic iron and akermanite. The whole process realized the recovery of zinc, and the selective and effective extraction of calcium and sulfur, which could provide an alternative process for the large-scale treatment of these hazardous wastes.

Biodegradability of polyethylene by efficient bacteria from the guts of plastic-eating waxworms and investigation of its degradation mechanism.

Polyethylene (PE) has been regarded as non-biodegradable for decades, and the evidence for its degradation by bacteria remains unclear in the literature. Waxworms have recently gained attention for their ability to degrade natural long-chain polymers and synthetic plastic. This study aims to explore the potential of low-density polyethylene (LDPE)-degrading bacteria from the gut symbionts of lesser waxworm (Achroia grisella) larvae for the effective biodegradation of LEDP. Two bacterial isolates (LDPE-DB1 and LDPE-DB2) exhibited the greatest reduction in tensile strength among all isolates (P < 0.0001), reaching 51.3% and 58.3%, respectively. The bacterial strains LDPE-DB1 and LDPE-DB2 stand for molecularly identified species, Citrobacter freundii and Bacillus sp., respectively. After 5 days of incubation, the cell density of LDPE-DB1 and LDPE-DB2 reached 2.20 × 108 and 1.8 × 108 CFU/mL, respectively. However, after 30 days of incubation, the cell density reached 7.3 × 108 and 5.9 × 108, respectively. The formed cavities indicate the high activity of the isolated bacteria from Achroia grisella larvae where the cavities reach a depth of up to 1.2 µm. The findings of this study demonstrated the presence of LDPE-degrading bacteria in Achroia grisella and provide promising evidence for the biodegradation of plastic waste management in the environment.

Green Conversion of the Hazardous Cathode Ray Tube and Red Mud into Radiation Shielding Concrete.

The present investigation was aimed at the utilization of alternate materials, emphasizing hazardous industrial products (red mud and cathode ray tubes), as constituents of radiation shielding concrete. The usage of these hazardous industrial products improves the sustainability and performance of the radiation shielding concrete. Five concrete blocks were cast and their density, compressive strength, gamma shielding factors, radiation absorption ratio, and transmission factor were explored. For this purpose, gamma-ray shielding measurements were done with the help of an HPGe detector. Mix-1, with zero contents of red mud and CRTs, had the lowest LAC. The LAC results demonstrated that the shielding performance of the current concretes would be better with the increase in red mud and cathode ray tube glass. The Transmission factor (TF) for the prepared concretes with a thickness of 2 cm varied between 11.9-26.1% at 0.06 MeV, while it varied between 4-13% for a thickness of 3 cm. The TF results showed that the composites with a thickness of 2, 3, or 5 cm are good shields against lower energy radiation. The radiation absorption ratio (RAR) for the prepared concretes is high at low energy, suggesting that these new composites can absorb most of the low-energy photons. The RAR results emphasize that the increase in CRTs in the new composites enhanced the radiation shielding features, and when the CRT glass is at a maximum, more attenuation was achieved.

Characteristics and factors that influence heavy metal leaching from spent catalysts.

With the extensive use of nonferrous metals and metal catalysts, solid wastes containing heavy metals release metal ions into soil and surface water through erosion and leaching. This is one of the major threats to the global environment and human health. Studying the characteristics and impact factors of heavy metal leaching from solid waste is a critical part of managing spent catalysts and environmental risk. In this work, the characteristics of and factors that influence leaching and seepage release from typical spent catalysts and lead-zinc smelting slag were studied. The results indicated that metal ions leached more easily in an acidic environment (pH 4.5) and an environment with DOM than in a neutral environment (pH 7.0). Metal ion leaching was favored by a liquid-to-solid ratio of 20:1. The concentrations of metal ions released from the spent catalysts in sequential leaching experiments were higher than those in column leaching experiments. Leaching of metal ions in the presence of different leaching agents and from different spent catalysts can be described by different controlling models of the shrinking core model, but changes in the liquid-to-solid ratio showed no obvious correlation with changes in the metal release mechanism. These results provide important information for spent catalyst management and risk prevention and control.

Fungal community diversity of heavy metal contaminated soils revealed by metagenomics.

The inappropriate disposal of toxic compounds generated by industrial activity has been impacting the environment considerably. Microbial communities inhabiting contaminated sites may represent interesting ecological alternatives for the decontamination of environments. The present work aimed to investigate the fungal diversity and its functionality contained in stream sediments with industrial waste contaminated with heavy metals by using metagenomic approach. A total of 12 fungal orders were retrieved from datasets and, at phylum level, Ascomycota was the most abundant, followed by Basidiomycota, Chytridiomycota and Blastocladiomycota. Higher abundance of sequences was encountered within the less contaminated site, while the lower abundance was found in the sample with the higher contamination with lead. Gene sequences related to DNA repair and heavy metals biosorption processes were found in the four samples analyzed. The genera Aspergillus and Chaetomium, and Saccharomycetales order were highly present within all samples, showing their potential to be used for bioremediation studies. The present work demonstrated the importance of using the metagenomic approach to understand the dynamics and the possible metabolic pathways associated with fungal communities related to environmental samples containing heavy metals, as well as evidenced the importance of improving culturomics techniques for isolating strains with potential application in bioremediation processes of environments contaminated with heavy metals.

Degradation of urea-formaldehyde resin residues by a hydrothermal oxidation method into recyclable small molecular organics.

Urea-formaldehyde (UF) resin residues and the related product wastes as organic hazardous wastes are difficult to be biodegraded or recycled. In this research, a hydrothermal oxidation method using hydrogen peroxide (H2O2) solution has been developed for the degradation and recycling of UF resin residues. The effects of solution concentration, temperature, and time on the degradation efficiency and products of UF resin residues were studied. Under optimal conditions, i.e., 140 °C and 5 wt% H2O2 solution, over 75% of UF resin residues was degraded after 3 h. The degradation efficiency is much higher than that of the traditional hydrothermal treatment or acid hydrolysis method. In addition, results from Fourier transform infrared spectroscopy (FTIR), gas chromatography-mass spectroscopy (GC-MS), nuclear magnetic resonance spectroscopy (NMR), and X-ray diffraction (XRD) confirmed that H2O2 solution degrades UF resin residues to low molecular compounds, such as alcohols, methylal, and amides. This research provides a novel and high-efficient hydrothermal oxidization process for the degradation of UF resin residues, which might be a promising environmentally friendly and low-cost method for the disposal and recycling of industrial UF resin residues.

Effect of interactions during co-combustion of organic hazardous wastes on thermal characteristics, kinetics, and pollutant emissions.

Thermal disposal of organic hazardous wastes (OHWs) in a rotary kiln is an effective method to destroy organic pollutants and reduce the volume, but the complex interactions between various OHWs may result in sharp degradation on combustion performance and the increase in gaseous pollutants emission. Herein, three typical types of OHWs (i.e., pesticide waste, dyeing waste, and organic resin waste, labeled as HW1, HW2, and HW3, respectively) were chosen and thermally co-treated, and the co-combustion characteristics, kinetics, and gas evolutions were systematically studied. A strong positive interaction between HW1 and HW2 was found between 440 and 680 °C possibly due to the catalytic effect of Fe (III) and alkali metals in HW1. The experimental DTG peaks of mixtures at 480 °C were advanced by 60 °C compared with the calculated ones, resulting from the volatiles combustion of HW2 and the catalytic effect from Fe2O3 formed during the combustion. The decrease of ignition temperature of mixtures was found helpful for stable combustion, while the decrease of burnout temperature during co-combustion of HW2 and HW3 exhibited the potential to reduce the clinker ignition loss.

Qualitative and quantitative assessment of waste generation in a refrigerator-manufacturing plant based on a waste tree and mass balance.

In this study, wastes originating at each production station during refrigerator manufacturing were identified and classified based on a waste tree. A mass balance study revealed a total waste production factor of 0.046 kg/kg of a product of which 75.3%, 23.9%, and 0.8% were non-hazardous wastes (NHWs), packaging wastes (PWs), and hazardous wastes (HWs), respectively. Wastes produced during refrigerator manufacturing were grouped under 35 different waste codes. Waste codes that contributed more than 5% by weight were 15 02 02 (contaminated absorbent material), 15 01 10 (contaminated packaging), 16 02 13 (electronic cards), 07 02 14 (polyol) and 08 05 01 (isocyanates), 19 08 13 (treatment sludge), 16 02 15 (capacitors), and 13 01 13 (hydraulic oil) for HWs, 12 01 01 (ferrous metal), and 16 02 16 (components) for NHWs, and, finally, 15 01 03 (wooden), 15 01 01 (paper&cardboard), and 15 01 02 (plastic) for PWs over 5 years. Scrap costs were used as a surrogate to determine production stages that generated high amounts of metal and plastic wastes. Logarithmically, increasing and decreasing trends were observed for PWs and NHWs over the study period, respectively. HW amounts did not exhibit a statistically significant trend. Twenty-eight BATs (best available techniques) were identified that could be applied in refrigerator manufacturing for waste minimization and management. Among those, 8 of them were proposed for further improvement for waste management in the facility.

A study on pyro-hydrometallurgical process for selective recovery of Pb, Sn and Sb from lead dross.

This study is to propose a pyro-hydrometallurgical process for recovering Pb, Sn, and Sb from lead dross (LD), incorporating stages of roasting, leaching, and precipitation. The LD, containing 67.2% of Pb, 4.0% of Sn, and 1.4% of Sb, was first roasted at 750 °C for 2 h to oxidise the sulphide metals. Approximately 90% of Pb was oxidised from the first roasting. The LD was second roasted by mixing with 95% H2SO4 for sulphatising at 300 °C for 3 h to break the complex oxide structure of the oxyplumboromeite (Pb2Sb2O7). After the two-step roasting process, over 99% of Pb was oxidised and Sb was separated. The calcine obtained was desulphurised by 2 M Na2CO3 solution for insoluble PbSO4 to PbCO3 for selective leaching. The residue was then leached in 2.5 M HNO3 at 50 °C for 3 h and over 99% of Pb dissolved into the solution while Sn and Sb remained in the solid residue. The Pb containing solution was neutralised at pH 8 using 2 M Na2CO3 and over 99% Pb was precipitated as PbCO3 and Pb hydroxides. A residue containing Sn and Sb was leached in 7 M NaOH at 95 for 1 h and over 99% Sn was leached selectively. Sn in the solution was precipitated at pH 7 using 2 M H2SO4 as SnO2. Sb was recovered as Sb2O3 in solid reside from Sn leaching. The overall recovery rates of Pb, Sn, and Sb from the LD were 99.5%, 95.4%, and 86.3%, respectively. The proposed process is expected to contribute to recycling Pb and other metal values from LD by minimising hazardous waste emissions.

Abatement of hazardous materials and biomass waste via pyrolysis and co-pyrolysis for environmental sustainability and circular economy.

The remarkable journey of progression of mankind has created various impacts in the form of polluted environment, amassed heavy metals and depleting resources. This alarming situation demands sustainable energy resources and approaches to deal with these environmental hazards and power deficit. Pyrolysis and co-pyrolysis address both energy and environmental issues caused by civilization and industrialization. The processes use hazardous waste materials including waste tires, plastic and medical waste, and biomass waste such as livestock waste and agricultural waste as feedstock to produce gas, char and pyrolysis oil for energy production. Usage of hazardous materials as pyrolysis and co-pyrolysis feedstock reduces disposal of harmful substances into environment, reducing occurrence of soil and water pollution, and substituting the non-renewable feedstock, fossil fuels. As compared to combustion, pyrolysis and co-pyrolysis have less emission of air pollutants and act as alternative options to landfill disposal and incineration for hazardous materials and biomass waste. Hence, stabilizing heavy metals and solving the energy and waste management problems. This review discusses the pyrolysis and co-pyrolysis of biomass and harmful wastes to strive towards circular economy and eco-friendly, cleaner energy with minimum waste disposal, reducing negative impact on the planet and creating future possibilities.

Radiation Shielding Concrete with alternate constituents: An approach to address multiple hazards.

Radiation Shielding Concrete (RSC) is a superior alternative to many conventional and modern shields against gamma and neutron radiation hazards. The present work is the first comprehensive review on utilization of alternate materials, emphasizing hazardous industrial byproducts, as constituents of RSC. Such usage enhances the performance, sustainability, and affordability of RSC. Added advantages are the immobilization of wastes and the conservation of natural resources for RSC. The review analyses incorporation of ferrous and non-ferrous slags, mines wastes, plastics, red mud, cathode ray tube's glass, metallic wastes, fly ash, silica fume, and miscellaneous residues. Besides, utilization of fibers, nanoparticles, and calcined clay is investigated. The influence on shielding efficiency is adjudged by scrutinizing changes in parameters such as half-value layer and linear attenuation coefficients. Similarly, variations in mechanical and durability properties are investigated and compared. The underlying responsible factors related to the physical, chemical and morphological characteristics of materials and their consequences on RSC's behavior are correlated. In association with alternatives, the advantages, disadvantages, and possible treatment methods are discussed. The country-wise, material-specific, and progressive research trends are revealed to facilitate future work in this upcoming field. Finally, conclusions are drawn with exposition of current bottlenecks and scope of future research.

The use of Atlantic hagfish (Myxine glutinosa) as a bioindicator species for studies on effects of dumped chemical warfare agents in the Skagerrak. 1: Liver histopathology.

Within the framework of the international project DAIMON (Decision Aid for Marine Munitions), the impact of dumped chemical munitions on fish health was investigated. The Skagerrak Straight (North Sea, at 600 m depth) contains munitions with chemical warfare agents (CWA), scuttled after the end of World War II. Studies of liver histopathology in Atlantic hagfish (Myxine glutinosa) were carried out at three sampling sites: at a wreck with CWA in the Skagerrak (n = 82), a Skagerrak reference site considered to be free of CWA (n = 14) and at a reference site in the northern North Sea outside the Skagerrak (n = 17). Liver lesions were diagnosed and categorized according to standardized ICES and BEQUALM protocols and OSPAR guidelines. Non-specific liver lesions were found in 87.6% of 113 hagfish examined. The prevalence of pre-neoplastic lesions was 7.1% and of neoplastic lesions 6.2%. There was no statistically significant difference in prevalence between hagfish samples from the wreck site and from the reference site near the wrecks. However, at the reference site in the northern North Sea, the prevalence of non-specific lesions was low and neither pre-neoplastic nor neoplastic lesions were observed.

A review on phytoremediation of mercury contaminated soils.

Mercury (Hg) and its compounds are one of the most dangerous environmental pollutants and Hg pollution exists in soils in different degrees over the world. Phytoremediation of Hg-contaminated soils has attracted increasing attention for the advantages of low investment, in-situ remediation, potential economic benefits and so on. Searching for the hyperaccumulator of Hg and its application in practice become a research hotspot. In this context, we review the current literatures that introduce various experimental plant species for accumulating Hg and aided techniques improving the phytoremediation of Hg-contaminated soils. Experimental plant species for accumulating Hg and accumulation or translocation factor of Hg are listed in detail. The translocation factor (TF) is greater than 1.0 for some plant species, however, the bioaccumulation factor (BAF) is greater than 1.0 for Axonopus compressus only. Plant species, soil properties, weather condition, and the bioavailability and heterogeneity of Hg in soils are the main factors affecting the phytoremediation of Hg-contaminated soils. Chemical accelerator kinds and promoting effect of chemical accelerators for accumulating and transferring Hg by various plant species are also discussed. Potassium iodide, compost, ammonium sulphate, ammonium thiosulfate, sodium sulfite, sodium thiosulfate, hydrochloric acid and sulfur fertilizer may be selected to promote the absorption of Hg by plants. The review introduces transgenic gene kinds and promoting effect of transgenic plants for accumulating and transferring Hg in detail. Some transgenic plants can accumulate more Hg than non-transgenic plants. The composition of rhizosphere microorganisms of remediation plants and the effect of rhizosphere microorganisms on the phytoremediation of Hg-contaminated soils are also introduced. Some rhizosphere microorganisms can increase the mobility of Hg in soils and are beneficial for the phytoremediation.

Exposure status of sea-dumped chemical warfare agents in the Baltic Sea.

About 50 000 tons of chemical weapons (CW) were dumped to the Baltic Sea after the Second World War. Munitions are located in the deep areas of the Baltic Sea, and there they act as a point source of contamination to the ecosystem. Corroded munitions release chemical warfare agents (CWAs) to nearby water and sediments. In this study we investigated known dumpsites (Bornholm, Gotland and Gdansk Deep) and dispersed chemical munitions, to evaluate the extent of contamination of nearby sediments, as well as to assess the degradation process of released CWA. It was found that CWA-related phenylarsenic chemicals (Clark I, Clark II and Adamsite) and sulfur mustard are released to the sediments and undergo environmental degradation to chemicals, of which some remain toxic. The extent of pollution of released CWAs and their corresponding degradation products reaches more than 250 m from the CW objects, and seem to follow a power curve decrease of concentration from the source. Bornholm Deep is characterised with the highest concentration of CWAs in sediments, but occasional concentration peaks are also observed in the Gdansk Deep and close to dispersed munitions. Detailed investigation of spreading pattern show that the range of pollution depends on bottom currents and topography.