Search Results (6)

Composite materials based on diatomite (DT) with the addition of biochar (BC), dolomite (DL), and bentonite (BN) were developed. The effect of chemical modification on the chemical structure of the resulting composites was investigated, and their influence on heavy metal immobilization and the ecotoxicity of post-flotation sediments was evaluated. It was demonstrated that the chemical modifications resulted in notable alterations to the chemical properties of the composites compared to pure DT and mixtures of DT with BC, DL, and BN. An increase in negative charge was observed in all variants. The addition of BC introduced valuable chemically and thermally resistant organic components into the composite. Among the chemical modifications, composites with the addition of perlite exhibited the lowest values of negative surface charge, which was attributed to the dissolution and transformation of silicon compounds and traces of kaolinite during their initial etching with sodium hydroxide. The materials exhibited varying efficiencies in metal immobilization, which is determined by both the type of DT additive and the type of chemical modification applied. The greatest efficacy in reducing the mobility of heavy metals was observed in the PFS with the addition of DT and BC without modification and with the addition of DT and BC after the modification of H₂SO₄ and H₂O₂: Cd 8% and 6%; Cr 71% and 69%; Cu 12% and 14%; Ni 10% and Zn 15%; and 4% and 5%. In addition, for Zn and Pb, good efficacy in reducing the content of mobile forms of these elements was observed for DT and DL without appropriate modification: 4% and 20%. The highest reduction in ecotoxicity was observed in the PFS with the addition of DT and BC, followed by BN and DL, which demonstrated comparable efficacy to materials with DT and BN. Full article

Soil contaminated with petroleum substances is classified as hazardous, i.e., particularly harmful to the proper functioning of environmental ecosystems. It is therefore necessary to take measures to restore the homeostasis and ecological potential of degraded areas. The study aim was to determine the impact of bentonite, compost, and calcium oxide (CaO) on trace element content in the maize grown on diesel oil (DO)-contaminated soil. Increasing doses of the petroleum substance increased the accumulation of chromium (Cr), lead (Pb), copper (Cu), nickel (Ni), manganese (Mn), cobalt (Co), and cadmium (Cd) in maize. The largest increases were found for Cu (by 76%), Co (by 73%), and Pb (by 42%). All soil amendments proved useful for in situ stabilization of anthropogenically transformed soils. Bentonite reduced Cr (by 94%), Cu (by 84%), and Mn content (by 53%), while compost reduced the contents of Cu (by 75%), Mn (by 44%), and iron (Fe—by 29%) in maize. CaO significantly reduced the levels of Cr (by 94%), Cu (by 84%), Ni (by 66%), Mn (by 32%), Co (by 72%), zinc (Zn—by 30%), and Cd (by 22%) in maize. The effects of compost and bentonite on maize chemical composition were smaller than that achieved with CaO, and the direction of changes in elements content depended on the DO dose and the element type. Full article

The purpose of this research is to identify the radiation shielding capability of ceramics adding CuO, CdO, and Bi₂O₃ with diverse wt (%). The chemical compositions of the raw ceramics were documented through Energy Dispersive X-ray “EDX” techniques. For aesthetic appeal and solidification, CuO has been chosen to be added to ceramic. Moreover, in the interest of increasing the radiation shielding ability, the high atomic number and density of both CdO and Bi₂O₃ were suggested for the raw ceramics. To obtain the morphological features of the prepared ceramic samples, a Scanning Electron Microscope, or SEM, was utilized. To verify the experimental results, the MCA value obtained from the Phy-X software was compared to the experimental value collected from the HPGe detector. At energies 0.06 MeV, 0.662 MeV, 1.173 MeV, and 1.333 MeV the linear and mass attenuation coefficients of the prepared ceramics have been measured using a high purity germanium “HPGe” detector as well as three different point sources. Moreover, the relationship between ln(I) and the thickness of the ceramics has been presented here, and the comparison between the LAC of the prepared ceramics with other materials has also been displayed. Bentonite ceramic containing CuO (15 mol %)-CdO (15 mol %)-Bi₂O₃ (20 mol %) with density 3.6 showed the lowest HVL, MFP, and TVL at all studied energies, yet pure Bentonite ceramic containing only CuO (50 mol %), having density 3.4, presented the greatest values. Hence, it can be concluded that the addition of CdO and Bi₂O₃ enhances the radiation shielding ability. Full article

A CuO/bentonite composite photocatalyst was prepared to fully utilize the adsorption capacity of bentonite and the photocatalytic activity of CuO. CuO and bentonite were chosen as a photocatalyst due to the excellent optical property of CuO and large specific surface area of bentonite, together with their high stability and low production cost. The sample was characterized by XRD, SEM, and BET. The effects of several factors on degradation process were investigated such as dosage of H₂O₂, irradiation time, pH of the solution, and dosage of catalyst. The optimum conditions for decolorization of methylene blue solution by CuO/bentonite were determined. Under optimal conditions, the decolorization efficiency of methylene blue by a 1.4% CuO/bentonite (400 °C) composite photocatalyst under visible irradiation at 240 min reached 96.98%. The degradation process follow edpseudo-second-order kinetics. The photocatalytic mechanism is discussed in detail. This composite structure provides a new solution to the cycle and aggregation of the photocatalyst in water. Full article

Dissolution rates of nanomaterials can be decisive for acute in vivo toxicity (via the released ions) and for biopersistence (of the remaining particles). Continuous flow systems (CFSs) can screen for both aspects, but operational parameters need to be adjusted to the specific physiological compartment, including local metal ion saturation. CFSs have two adjustable parameters: the volume flow-rate and the initial particle loading. Here we explore the pulmonary lysosomal dissolution of nanomaterials containing the metals Al, Ba, Zn, Cu over a wide range of volume flow-rates in a single experiment. We identify the ratio of particle surface area (SA) per volume flow-rate (SA/V) as critical parameter that superimposes all dissolution rates of the same material. Three complementary benchmark materials—ZnO (quick dissolution), TiO₂ (very slow dissolution), and BaSO₄ (partial dissolution)—consistently identify the SA/V range of 0.01 to 0.03 h/μm as predictive for lysosomal pulmonary biodissolution. We then apply the identified method to compare against non-nanoforms of the same substances and test aluminosilicates. For BaSO₄ and TiO₂, we find high similarity of the dissolution rates of their respective nanoform and non-nanoform, governed by the local ion solubility limit at relevant SA/V ranges. For aluminosilicates, we find high similarity of the dissolution rates of two Kaolin nanoforms but significant dissimilarity against Bentonite despite the similar composition. Full article

Silicic, mafic and alkali intra-seam tonsteins have been known from SW China for a number of years. This paper reports on the geochemical compositions of coals and tonsteins from three seam sections of the Songzao Coalfield, SW China, and evaluates the geological factors responsible for the chemical characteristics of the coal seams, with emphasis on the influence from different types of volcanic ashes. The roof and floor samples of the Songzao coal seams mostly have high TiO₂ contents, consistent with a high TiO₂ content in the detrital sediment input from the source region, namely mafic basalts from the Kangdian Upland on the western margin of the coal basin. The coals from the Songzao Coalfield generally have high ash yields and are highly enriched in trace elements including Nb, Ta, Zr, Hf, rare earth elements (REE), Y, Hg and Se; some variation occurs among different seam sections due to input of geochemically different volcanic ash materials. The geochemistry of the Songzao coals has also been affected by the adjacent tonstein/K-bentonite bands. The relatively immobile elements that are enriched in the altered volcanic ashes also tend to be enriched in the adjacent coal plies, possibly due to leaching by groundwaters. The coals near the alkali tonstein bands in the Tonghua and Yuyang sections of the Songzao Coalfield are mostly high in Nb, Ta, Zr, Hf, Th, U, REE and Y. Coal samples overlying the mafic K-bentonite in the Tonghua section are high in V, Cr, Zn and Cu. The Datong coal, which has neither visible tonstein layers nor obvious volcanogenic minerals, has high TiO₂, V, Cr, Ni, Cu and Zn concentrations in the intervals between the coal plies affected by mafic and alkaline volcanic ashes. This is consistent with the suggestion that a common source material was supplied to the coal basin, derived from the erosion of mafic basaltic rocks of the Kangdian Upland. Although the Songzao coal is generally a high-sulfur coal, most of the chalcophile trace elements show either poor or negative correlations with total iron sulfide contents. The absence of traditional pyrite-metal associations may reflect wide variations in the concentrations of these elements in individual pyrite/marcasite components, or simply poor retention of these elements in the pyrite/marcasite of the relevant coals. Full article