Characterisation of secondary metal-bearing phases in used dental amalgam and assessment of gastric solubility

Detailed SEM/EDS investigation of used dental amalgams was carried out in order to characterise morphology and chemical composition of secondary metal-bearing phases resulting from long-term exposure of dental amalgam to oral environment, and assess their solubility in gastric environment. The investigation revealed numerous secondary phases, represented by compositionally and morphologically complex Hg-, Cu-, Sn-, Ag-, Zn-bearing sulphides and oxides/hydroxides, while sulphates and phosphates are scarce. Secondary metal-bearing phases mostly occur at the amalgam/tooth interface; however, some phases were found only on the occlusal surfaces of amalgam. Secondary phases mostly form porous aggregates of minute crystallites and micro- or nanocrystalline crusts. In oral environment, these phases are mostly stable and represent trapping media for dissolved potentially toxic metals released during amalgam corrosion. Simplified PHREEQC calculations of solubility of secondary metal-bearing phases in aqueous environment under conditions similar to those in gastric environment showed that secondary phases are more soluble in gastric environment than in oral solutions, which is mostly due to their forms of occurrence. Secondary phases in gastric environment thus act as secondary sources of potentially toxic metals, particularly Sn, Zn and also Cu, which are released both under reducing and oxidising conditions especially in acidic environment. Only very small amounts of Hg are potentially released and should not represent serious threat. Secondary phases that contribute the most to bioaccessibility of these metals are Sn hydroxychlorides, Sn oxides/hydroxides, Sn sulphates/hydroxysulphates, Sn oxides, Zn sulphides and Cu sulphides (Cu₂S).

     

Polychlorinated dibenzo-p-dioxins/furans and dioxin-like polychlorinated biphenyls in food and feed in the Lithuanian market

Foods and feeds were analyzed during the period of 2007–2014 employing validated and accredited methods based on gas chromatography–high-resolution mass spectrometry. Sampling has been carried out in-line with national monitoring programs as well as during import controls into Lithuania. Food samples such as eggs, milk, beef, pork, poultry, fats of plant and animal origin, fish, cod liver, and feed samples such as premixes, feeds of plant origin, compound feed, mineral feed, vegetable oil, and fish meals were analyzed. Most of the samples exhibited concentrations below maximum limits, except cod liver. Health impacts were assessed in respect to human daily intakes. Data between groups are compared.     

兰坪铅锌矿区不同污染梯度下优势植物的重金属累积特征

对兰坪铅锌矿区污染程度不同的3个样地(云南松林、魁蒿群落和马桑灌丛)进行植被调查,选择其中9种共有的自然生长的优势草本植物为研究对象,测定了土壤及植物体的重金属含量。结果显示,3个样地土壤Cu、Cd、Pb和Zn等4种重金属含量均表现为马桑灌丛>魁蒿群落>云南松林;植物体内重金属积累呈现出随着土壤污染程度增加而增加的趋势;所选择的9种植物均不符合超富集植物的标准,依据不同的耐性机制将9种植物分为3类,野棉花能较强吸收土壤中重金属,并转移到地上部分,属于富集型植物;西南金丝梅、倒提壶、长籽柳叶菜、魁蒿、翻白叶和四脉金茅吸收的重金属主要积累在根部,属于根部囤积型植物;尼泊尔蓼和中华山蓼体内重金属含量较低,属于规避型植物。讨论了利用这些植物进行矿山治理。     

煤粉炉掺烧干化污泥的污染物排放研究

结合某电厂420 t/h四角煤粉炉掺烧污泥项目的实验室分析测试,了解煤粉掺烧不同含水率不同比例的干化污泥条件下烟气中污染物和灰渣中重金属的排放特性。结果表明,在实验研究配比和燃烧的条件下,大部分重金属元素Pb、Cu、Cr和Ni残留在灰渣中,Zn、Cd部分残留在灰渣中,As、Hg和Se等易挥发元素释放到烟气中,在灰渣中的含量很小。掺烧污泥后,灰渣中的重金属含量较单烧单煤都有了一定幅度的升高,Zn的含量是单煤的2倍,其余重金属是单煤的1.1~1.2倍。3种不同的掺混比例之间的污染气体排放浓度基本相似。烟气中主要污染物及重金属浓度可以满足现行国家标准。与单烧单煤相比,CO、HCl以及其他有机气体排放浓度基本相同;NH3的排放浓度较单煤有所升高;SO2、NOx和CO2排放浓度略有降低;飞灰浓度有所升高。烟气中的重金属,Hg含量升高了30%,Pb含量约为单煤的4.3~4.8倍。以上研究结果可为环保达标和飞灰利用提供基础数据。     

Plant species richness of riverbed elevations—the Pripyat river valley case study

Flora of the still unchanged or slightly modified floodplains is particularly valuable. Such are the natural, periodically flooded riparian ecosystems within the Mid-Pripyat river valley in Belarus. Distinctive elements of that area are ‘periodic islands’, which arise from the most elevated parts of the riverbed during flooding and have a specific microtopography. The aim of the research was to recognize floristic composition and ecological conditions of the ‘islands.’ Noted plants were mainly photophilous, by clearly varied in soil moisture, acidity and fertility requirements.     

Impact of industrial pollution on Scots pine (Pinus sylvestris L.) radial growth in the areas of mineral fertilizer factory “Achema”

The aim of research was to assess the changes of annual radial increment of Scots pine forests in the vicinity of intensive and moderate industrial pollution of “Achema” factory producing mineral fertilizers. Our results indicate that the radial growth of the pine tree can be divided into three different periods: growth promotion, growth inhibition and growth recovery. Low levels of nitrogen emissions were beneficial for tree growth: the radial increment in the intensive and moderate pollution zones increased by 15–25% and 10%, respectively compared to control. During the growth inhibition period, the total annual industrial emission was 37–40 kt, and 40–45% radial growth loss was observed for the closest and 15–20% for the most distant stands. The radial growth decrease slowed down and the recovery of damaged stands began in 1990–1992 then air pollution was considerably reduced. The rate of forest recovery was high for the most damaged stands: their radial growth was close to control in 2000–2011.     

Highly active photocatalytic coatings prepared by a low-temperature method

Photocatalytic properties of titanium (IV) oxide (TiO₂) in anatase form can be used for various purposes, including photocatalytic purification of water. For such an application, suspended or fixed photocatalytic reactors are used. Those with fixed phase seem to be preferred due to some advantages, one of which is the avoidance of photocatalyst filtration. To avoid leaching and exfoliation of the fixed phase, an immobilization procedure leading to a good adhesion of a catalyst to a substrate is crucial. Within this work, we present physical and photocatalytic characterization results of five commercially available TiO₂ photocatalysts (P25, P90, PC500, KRONOClean 7000, VPC-10) and one pigment (Hombitan LO-CR-S-M), which were successfully immobilized on glass slides by a “sol suspension” procedure. Different mechanical tests and characterization methods were used to evaluate the stability and morphology of the layers. Evaluation of photocatalytic activity was done by tests under UVA and UV–vis irradiation, using a method based on the detection of the fluorescent oxidation product of terephthalic acid (TPA), i.e., hydroxyterephthalic acid (HTPA). Aeroxide® P90 incorporated into the silica-titania binder was the most photocatalytically active layer and, unlike the others, showed significant increase of photocatalytic activity through the entire range of tested UVA irradiation intensities (2.3 mW/cm²–6.1 mW/cm²). The high mechanical stability of some photocatalytic layers allows using them in water photocatalytic purification reactions.     

Forest Die-Back Modified Plankton Recovery from Acidic Stress

We examined long-term data on water chemistry of Lake Rachelsee (Germany) following the changes in acidic depositions in central Europe since 1980s. Despite gradual chemical recovery of Rachelsee, its biological recovery was delayed. In 1999, lake recovery was abruptly reversed by a coincident forest die-back, which resulted in elevated terrestrial export of nitrate and ionic aluminum lasting ~5 years. This re-acidification episode provided unique opportunity to study plankton recovery in the rapidly recovering lake water after the abrupt decline in nitrate leaching from the catchment. There were sudden changes both in lake water chemistry and in plankton biomass structure, such as decreased bacterial filaments, increased phytoplankton biomass, and rotifer abundance. The shift from dominance of heterotrophic to autotrophic organisms suggested their substantial release from severe phosphorus stress. Such a rapid change in plankton structure in a lake recovering from acidity has, to the best of our knowledge, not been previously documented.     

Dioxin-like activity in sediments from Tai Lake, China determined by use of the H4IIE-luc bioassay and quantification of individual AhR agonists

Deterioration of the general ecosystem and specifically quality of the water in Tai Lake (Ch: Taihu), the third largest freshwater in China, is of great concern. However, knowledge on status and trends of dioxin-like compounds in Tai Lake was limited. This study investigated AhR-mediated potency and quantified potential aryl hydrocarbon receptor (AhR) agonists in sediments from four regions (Meiliang Bay, Zhushan Lake, Lake Center, Corner of Zhushan Lake, and Meiliang Bay) of Tai Lake by use of the in vitro H4IIE-luc, cell-based, transactivation, reporter gene assay, and instrumental analysis. Concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin equivalents (Bio-TEQs) in sediments ranged from less than the limit of detection to 114.5 pg/g, dry weight, which indicated that organic extracts of sediments exhibited significant AhR-mediated potencies. Results of the potency balance analysis demonstrated that acid-labile, dioxin-like compounds represented a greater proportion of concentrations of Bio-TEQs in sediments from Tai Lake. Concentrations of 2,3,7,8-tetrachlorodibenzo-p-dioxin equivalents calculated as the sum of the product of concentrations of individual congeners and their respective relative potencies (Chem-TEQs) based on polycyclic aromatic hydrocarbons and/or polychlorinated biphenyls represented no more than 10 % of the total concentrations of Bio-TEQs.     

Photocatalytic degradation of acetaminophen in modified TiO2 under visible irradiation

This study investigated the photocatalytic degradation of acetaminophen (ACT) in synthetic titanium dioxide (TiO₂) solution under a visible light (λ >440 nm). The TiO₂ photocatalyst used in this study was synthesized via sol–gel method and doped with potassium aluminum sulfate (KAl(SO₄)₂) and sodium aluminate (NaAlO₂). The influence of some parameters on the degradation of acetaminophen was examined, such as initial pH, photocatalyst dosage, and initial ACT concentration. The optimal operational conditions were also determined. Results showed that synthetic TiO₂ catalysts presented mainly as anatase phase and no rutile phase was observed. The results of photocatalytic degradation showed that LED alone degraded negligible amount of ACT but with the presence of TiO₂/KAl(SO₄)₂, 95 % removal of 0.10-mM acetaminophen in 540-min irradiation time was achieved. The synthetic TiO₂/KAl(SO₄)₂ presented better photocatalytic degradation of acetaminophen than commercially available Degussa P-25. The weak crystallinity of synthesized TiO₂/NaAlO₂ photocatalyst showed low photocatalytic degradation than TiO₂/KAl(SO₄)₂. The optimal operational conditions were obtained in pH 6.9 with a dose of 1.0 g/L TiO₂/KAl(SO₄)₂ at 30 °C. Kinetic study illustrated that photocatalytic degradation of acetaminophen fits well in the pseudo-first order model. Competitive reactions from intermediates affected the degradation rate of ACT, and were more obvious as the initial ACT concentration increased.