Hexavalent chromium release from lignite fly ash and related ecotoxic effects

Hexavalent chromium Cr(VI) is a pollutant of immense concern due to its high mobility to water sources and highly toxic properties. In most cases, Cr(VI) could be released from lignite fly ash in aquatic environment when fly ash comes into contact with water. In this study, the contribution of the leaching patterns and bioavailability of Cr(VI) from lignite fly ash to the overall ecotoxic properties of fly ash leachates was originally examined and leaching procedures were evaluated in this context. A series of customized leaching tests were conducted and a battery of ecotoxicity tests including the crustacean Daphnia magna and the photobacterium Vibrio fischeri was applied. The leaching of Cr(VI) was pH and liquid to solid (L/S) ratio dependent, exhibiting the highest releases at pH values between 7 and 8. At the liquid to solid ratio (L/S) equal to 100 L/kg, the (CrVI) release reached a plateau, implying the presence of diffusion constrains and/or solubility hindrances. The toxic effect of the leachates obtained under leaching at pH 7 towards D. magna was relatively high (TU = 28.6 (23.8-35.7) at L/S = 10 L/kg). Interestingly, the toxicity of the leachates towards D. magna not only was significantly correlated to Cr(VI) (r = 0.961, P < 0.01), but the toxicity of the leachates (in absolute values) was matching the toxicity of the Cr(VI) revealing its remarkable contribution to the overall effect. In addition, the lower sensitivity of the bacteria V. fischeri when exposed to the leachates, along with the time dependence of the toxicity profiles supported the interpretation of the results obtained in this study

A PREVIOUSLY UNRECOGNIZED SPECIES OF SENEGALIA (FABACEAE) FROM NORTHEASTERN BRAZIL

Volume: 6Start Page: 397End Page: 40

Nanoscale zero-valent iron supported on mesoporous silica: Characterization and reactivity for Cr(VI) removal from aqueous solution

MCM-41-supported nanoscale zero-valent iron (nZVI) was sytnhesized by impregnating the mesoporous silica martix with ferric chloride, followed by chemical reduction with NaHB4. The samples were studied with a combination of characterization techniques such as powder X-ray diffraction (XRD), Fourier-transform infrared (FT-IR) and Mössbauer spectroscopy, N2 adsorption measurements, transmission electron microscopy (TEM), magnetization measurements, and thermal analysis methods. The experimental data revealed development of nanoscale zero-valent iron particles with an elliptical shape and a maximum size of ~80nm, which were randomly distributed and immobilized on the mesoporous silica surface. Surface area measurements showed that the porous MCM-41 host matrix maintains its hexagonal mesoporous order structure and exhibits a considerable high surface area (609m2/g). Mössbauer and magnetization measurements confirmed the presence of core-shell iron nanoparticles composed of a ferromagnetic metallic core and an oxide/hydroxide shell. The kinetic studies demonstrated a rapid removal of Cr(VI) ions from the aqueous solutions in the presence of these stabilized nZVI particles on MCM-41, and a considerably increased reduction capacity per unit mass of material in comparison to that of unsupported nZVI. The results also indicate a highly pH-dependent reduction efficiency of the material, whereas their kinetics was described by a pseudo-first order kinetic model. © 2013 Elsevier B.V

THREE NEW SPECIES OF SENEGALIA (FABACEAE) FROM BRAZIL

Volume: 8Start Page: 61End Page: 6

Magnetic Carbon Nanocages: An Advanced Architecture with Surface- and Morphology-Enhanced Removal Capacity for Arsenites

Magnetic carbon nanocages (Mag@CNCs) were synthesized via a green one-step process using pine resin and iron nitrate salt as a carbon and iron source, respectively. To produce Mag@CNCs, pristine materials have been carbonized at high temperature under inert atmosphere. The structural, textural, and surface properties of as-synthesized Mag@CNCs were studied employing microscopic, spectroscopic, and surface physicochemical methods. The obtained results showed that the new Mag@CNCs have significant surface area (177 m² g^–1) with both microporosity and mesoporosity. Moreover, the material exhibits a homogeneous distribution of core–shell-type magnetic nanoparticles within the carbon matrix, formed by iron carbide (Fe₃C) and metallic iron (α-Fe), with sizes of 20–100 nm, surrounded by a few graphitic layers-walls. Most importantly, Mag@CNCs were tested as absorbents for As­(III) removal from aqueous solutions, showing a total of 263.9 mg As­(III)-uptake capacity per gram of material at pH = 7, a record sorption capacity value among all previously tested iron-based materials and one of highest values among all reported sorbents so far. The adsorbed As­(III) species are anchored at the surface of Mag@CNCs, as demonstrated by high-resolution transmission electron microscopy and X-ray photoelectron spectroscopy measurements. The pH-edge As­(III)-adsorption experiments combined with theoretical surface complexation modeling allowed a detailed understanding of the interfacial properties of Mag@CNCs, and hence the As­(III) uptake mechanism. The analysis revealed that As­(III) binds on two types of surface sites of Mag@CNCs, i.e., on carbon-surface species (C_<i>x</i>OH₂) and on Fe-oxide layer (FeOH₂) of nanoparticles. This exemplifies that the advanced morphology- and surface-driven synergistic properties of the Mag@CNCs material are crucial for its As­(III)-uptake performance

SARS-CoV-2 wastewater monitoring using a novel PCR-based method rapidly captured the Delta-to-Omicron ΒΑ.1 transition patterns in the absence of conventional surveillance evidence

Conventional SARS-CoV-2 surveillance based on genotyping of clinical samples is characterized by challenges related to the available sequencing capacity, population sampling methodologies, and is time, labor, and resource-demanding. Wastewater-based variant surveillance constitutes a valuable supplementary practice, since it does not require extensive sampling, and provides information on virus prevalence in a timely and cost-effective manner. Consequently, we developed a sensitive real-time RT-PCR-based approach that exclusively amplifies and quantifies SARS-CoV-2 genomic regions carrying the S:Δ69/70 deletion, indicative of the Omicron BA.1 variant, in wastewater. The method was incorporated in the analysis of composite daily samples taken from the main Wastewater Treatment Plant of Thessaloniki, Greece, from 1 December 2021. The applicability of the methodology is dependent on the epidemiological situation. During Omicron BA.1 global emergence, Thessaloniki was experiencing a massive epidemic wave attributed solely to the Delta variant, according to genomic surveillance data. Since Delta does not possess the S:Δ69/70, the emergence of Omicron BA.1 could be monitored via the described methodology. Omicron BA.1 was detected in sewage samples on 19 December 2021 and a rapid increase of its viral load was observed in the following 10-day period, with an estimated early doubling time of 1.86 days. The proportion of the total SARS-CoV-2 load attributed to BA.1 reached 91.09 % on 7 January, revealing a fast Delta-to-Omicron transition pattern. The detection of Omicron BA.1 subclade in wastewater preceded the outburst of reported (presumable) Omicron cases in the city by approximately 7 days. The proposed wastewater surveillance approach based on selective PCR amplification of a genomic region carrying a deletion signature enabled rapid, real-time data acquisition on Omicron BA.1 prevalence and dynamics during the slow remission of the Delta wave. Timely provision of these results to State authorities readily influences the decision-making process for targeted public health interventions, including control measures, awareness, and preparedness. © 2022 Elsevier B.V