Mckennasalling0879

In the current study, improved exposure control and measurements were applied for the aquatic toxicity testing of a highly hydrophobic organic compound. The aim was to reliably determine the ecotoxicity of the model compound dodecylbenzene (DDB, Log KOW = 8.65) by applying passive dosing for aquatic toxicity testing exactly at the solubility limit. Methodologically, silicone O-rings were saturated by immersion in pure liquid DDB (i.e., "loading by swelling") and then used as passive dosing donors. Daphnia immobilization and fish embryo toxicity tests were successfully conducted and provide, together with recently reported algal growth inhibition data, a full base-set of ecotoxicological data according to REACH. All tests were conducted in closed test systems to avoid evaporative losses, and exposure concentrations were measured throughout test durations. The Daphnia test was optimized by placing the O-rings in cages to prevent direct contact between daphnids and the passive dosing donor. Toxicologically, Daphnia magna immobilization was 19.3 ± 8% (mean ± 95% CI; 6 tests) within 72 h, whereas Danio rerio fish embryos did not show any significant lethal or sublethal toxic responses within 96 h. Growth rate inhibition for the algae Raphidocelis subcapitata was previously reported to be 13 ± 5% in a first and 8 ± 3% in a repeated test. These results for aquatic organisms, spanning three trophic levels, demonstrate toxicity of a highly hydrophobic compound and suggest that improvements of the current ecotoxicological standard tests are needed for these "difficult-to-test" chemicals. Furthermore, the obtained toxicity results significantly question the existence of a generic Log KOW cut-off in baseline toxicity. A detailed mechanistic investigation of the hydroxyl radical (•OH) formation and organic pollutant degradation over transition metal-doped and undoped TiO2 photocatalysts was performed by the quantitative measurement of •OH and the identification of intermediate products under various experimental conditions. The Fe-doped TiO2 as a typical subject was prepared, characterized and used to degrade an azo dye Acid Orange 7 (AO7). It is indicated that the enhanced photocatalytic activity of Fe-doped TiO2 for AO7 degradation was attributed to the increase in surface area, the facilitated charge transfer via Fe-dopant, and a red shift of absorbable wavelength, maintaining a great formation of •OH under visible irradiation. The oxidation of H2O by holes was estimated as the major pathway of •OH formation rather than the reduction of dissolved O2 by electrons, and their formation trends reached to approximately 75% and 25%, respectively. Meanwhile the synergistic effect of Fe-dopant produced nearly 10% of extra •OH by visible light photoactivation. The intermediate products and pathways of AO7 degradation varied greatly with different photocatalysts and conditions of the process, involving several reaction mechanisms such as the azo bond cleaving, naphthalene oxidation, desulfonation, and hydroxylated products generation. Through the quantification of •OH-reacted efficiency we proposed, a stoichiometry of •OH affecting overall reaction mechanisms in the TiO2-assisted photodegradation of AO7 was further established. This study can provide new insights on how to better clarify the variation regularity of organic pollutant degradation from different treatments of the •OH-based advanced oxidation processes. The demand for high quality recycled polymers in the European plastic industry is on the increase, likely due to the EU's Plastic Strategy intended to implement the circular economy model in this sector. The problem is that there is not enough recycled plastic in the market. In terms of volume, post-consumer plastic waste could be key to meet the current and future demand. Nevertheless, a high level of contamination originated during the product's life cycle restricts its use. The first step to change this must be identifying the undesired substances in post-consumer plastics and performing an effective risk assessment. The acquired knowledge will be fundamental for the development of innovative decontamination technologies. In this study, 134 substances including volatile and semi-volatile compounds have been identified in recycled LDPE and HDPE from domestic waste. NVP-BEZ235 Headspace and solvent extraction followed by GC/MS were used. The possible origin of each substance was studied. The main groups were additives, polymer and additives breakdown products, and contamination from external sources. The results suggest that recycled LDPE contains a broader number of additives and their degradation products. Some of them may cause safety concerns if reused in higher added value applications. Regarding recycled HDPE, the contaminants from the use phase are predominant creating problems such as intense odors. To reduce the number of undesired substances, it is proposed to narrow the variety of additives used in plastic manufacturing and to opt for separate waste collection systems to prevent cross-contamination with organic waste. Thermal modification was simply performed on molybdenite to enhance the adsorption of Pb(II) in aqueous solutions, and the root of this phenomenon was well studied in this work. link2 Various thermal modification temperatures at 300 °C, 400 °C and 500 °C were applied to modify the surface property of molybdenite, producing different degrees of edge defect and surface wettability in molybdenite samples. Contact angle tests, atomic force microscopy (AFM) observations and adsorption tests illustrated that molybdenite thermally modified at 400 °C contained most edge defects and achieved a 147.846 mg/g Pb(II) adsorption, which was almost 10 times of that obtained by natural molybdenite. The adsorption experiment also indicated that the increase of surface hydrophilia of molybdenite would slightly benefit the Pb(II) adsorption. The X-ray photoelectron spectroscope (XPS) exhibited that a strong chemical adsorption existed between Pb(II) and S elements. AFM study further demonstrated that the interaction between Pb(II) and S atoms exposed at the triangular edges of molybdenite were the intrinsic reason for the great enhancement of Pb(II) adsorption. This work provides a new insight to absorb Pb(II) in aqueous solutions using natural molybdenite. Sewage sludge (SS) char can be potentially applied to De-NOx processes but it should be active enough and the relevant CO emissions should be controlled. In this paper activated SS chars have been prepared by using a simple KOH impregnation-carbonisation method and the activated chars are applied to remove NOx from flue gases within temperature range of 100-250 °C, acting as both reductants and catalysts. Special attention is paid to inhibiting CO emission in the process. Four reductive agents are adopted to check the catalytic effect of the activated SS chars. The results show that the activated SS chars (i.e. SC-KOHs) present a higher adsorption-reduction ability with much lower CO emission than that of non-activated SS chars (i.e. SC-Raws). SC-KOH produced at 800 °C (SC-KOH-800) shows obvious chemical adsorption behaviors, its adsorption capacity for NO is higher than 8.06 mg.L-1, superior to the coal-based activated carbon. Hydrazine hydrate is found to enhance De-NOx performance with SC-KOHs acting as catalysts, especially at higher temperatures. However, the De-NOx efficiency decreased when ammonia, urea and urea involved reductants were used. The physicochemical structure of the SS chars was characterized to show that the SC-KOHs are more porous with higher BET areas and pore volumes. Simultaneously, the SC-KOHs are crystallized to much lower extent, less graphitised, but have richer O-containing functional groups and zeolite structure on the surface when compared to the SC-Raws, which contributed to their high activities. Moreover, SC-KOH-800 can be recommended as the suitable adsorbent/catalyst for De-NOx within 100-250 °C. Eutrophication of surface water bodies is a global problem in recent years. Dosing polluted water with oxygen releasing compounds (ORCs), especially those that can remove excessive nutrients simultaneously is regarded as one of the most economical and eco-friendly methods of treating eutrophic waters. In this study, a novel Mg-based ORC was synthesized and characterized as a magnesium hydroxide and hydrogen peroxide complex (MHHPC) with Mg to H2O2 ratio of 21. Oxygen-releasing, pH-adjusting and nutrient-removal potentials of MHHPC were evaluated in nano-pure and eutrophic water. The overall performance of MHHPC in preventing the eutrophic water from turning black and odorous was compared with the performance of other ORCs namely, MgO2, CaO2 and the combination of MgCl2 and H2O2. The results showed that MHHPC was capable of constantly releasing oxygen to aqueous phase over a period of one week. Phosphate and ammonia nitrogen in synthetic buffered water can were removed as struvite and other precipitates from the aqueous phase. In the synthetic eutrophic water, all the ORCs tested were able to reduce aqueous ammonia nitrogen below 0.5 mM, while only CaO2 and MHHPC successfully removed the aqueous phosphate. However, CaO2 and MgCl2+H2O2 significantly inhibited microbial activity. The adsorption method is generally considered a promising technique to remove inorganic and organic contaminants in an economically and environmentally friendly superior manner. In this study, organic montmorillonite sodium alginate composites were prepared, in which, montmorillonite and cationic surfactant (cetyltrimethylammonium bromide, CTAB) in different added amounts were coagulated with sodium alginate using CaCl2 as the crosslinking agent. The morphological properties of the composites were characterized thoroughly and employed in three typical target pollutants of polycyclic aromatic hydrocarbons (PAHs) (acenaphthene, fluorene, and phenanthrene) by batch adsorption experiments from aqueous solution. The composites provide an efficient alternative for PAHs removals. The composites could be stably separated and regenerated with methyl alcohol. Furthermore, the adsorption kinetic and isotherm data were well described by the Elovich kinetic and the Freundlich isotherm model, respectively. According to these, the adsorption process occurred via multilayer adsorption on the composite's energetically heterogeneous surface. Moreover, pore diffusion and hydrophobicity played a dominant role in the adsorption mechanism. link3 Overall, our study offers a developed adsorbent that has the advantage of being recyclable, low cost, biodegradable and biocompatible for effectively removing PAHs from aqueous solution. Polymetal dust is a common industrial pollutant. While the use of remediation filters and equipment in lead smelters has reduced pollutant emission, surrounding areas remain contaminated due to the long-term transfer of heavy metals along the food chain. Here we assess the mutagenic potential of the lead-zinc smelter near Plovdiv (Bulgaria) situated in an area that has been contaminated with heavy metals for 60 years. We aimed to evaluate the genomic response of the yellow-necked mouse (A. flavicollis), a biomonitor species, in three sampling sites along the pollution gradient. Mice from Strandzha Natural Park were used as a negative control. The bioaccumulation rate of two non-essential heavy metals, lead (Pb) and cadmium (Cd), in liver tissues was determined by atomic absorption spectroscopy. Genetic alterations attributable to chronic exposure to trace levels of heavy metals were assessed in different blood cell populations using two independent methods a micronucleus test was applied to evaluate the clastogenic and aneugenic alterations in erythrocytes, while a comet assay was used to assess DNA instability, as evidenced by single- and double-stranded breaks and alkali-labile sites, in leucocytes.