A new practical application of the unique sorption abilities of Diatomaceous Earth (DE) or diatomite, a widely accessible and promising natural mineral, has been studied. By analyzing aqueous extracts of natural diatomite, it was shown that DE probably contains various inorganic salts, which are released into the solution in the form of ions, such as Cl-, SO42-, Na+, Ca2+, Mg2+, K+ and, apparently, others. Diatomite was able to exchange these ions with the environment, exhibiting the properties of a natural ion exchanger. Studying the kinetics of ion release from diatomite showed that the ion desorption process continues for 4‒5 h until the surrounding solution is saturated with ions, after which it is dynamically balanced by the sorption process. In order to significantly reduce the ionic content of diatomite, DE samples were processed in a technologically simple and environmentally friendly way. Thus, as a result of deionization, the content of ions released from diatomite significantly decreases. Deionized diatomite was applied to study the adsorption of sodium and chloride ions from aqueous solutions. The maximum adsorption was 50.2 mg/g, and the maximum degree of extraction, corresponding to the concentration range of 5‒100 mg/l, was 53.9%. The observed effect was also applicable for increasing the resistance of plants to salt stress, improving the germination and growth of wheat samples. The developed method can be used in the manufacturing of filters for water desalination, both drinking and technological; in ecology; in agriculture to reduce salt stress of plants, as well as for the restoration of lands contaminated by salt.
In this study, the mechano-chemical properties of aromatic polymer polyetheretherketone (PEEK) samples, irradiated by high energy electrons at 200 and 400 kGy doses, were investigated by Nanoindentation, Brillouin light scattering spectroscopy and Fourier-transform infrared spectroscopy (FTIR). Irradiating electrons penetrated down to a 5 mm depth inside the polymer, as shown numerically by the monte CArlo SImulation of electroN trajectory in sOlids (CASINO) method. The irradiation of PEEK samples at 200 kGy caused the enhancement of surface roughness by almost threefold. However, an increase in the irradiation dose to 400 kGy led to a decrease in the surface roughness of the sample. Most likely, this was due to the processes of erosion and melting of the sample surface induced by high dosage irradiation. It was found that electron irradiation led to a decrease of the elastic constant C11, as well as a slight decrease in the sample’s hardness, while the Young’s elastic modulus decrease was more noticeable. An intrinsic bulk property of PEEK is less radiation resistance than at its surface. The proportionality constant of Young’s modulus to indentation hardness for the pristine and irradiated samples were 0.039 and 0.038, respectively. In addition, a quasi-linear relationship between hardness and Young’s modulus was observed. The degradation of the polymer’s mechanical properties was attributed to electron irradiation-induced processes involving scission of macromolecular chains.
In this paper, we demonstrate a new, highly efficient method of crosslinking multilayer graphene, and create nanopores in it by its irradiation with low-energy argon cluster ions. Irradiation was performed by argon cluster ions with an acceleration energy E ≈ 30 keV, and total fluence of argon cluster ions ranging from 1 × 109 to 1 × 1014 ions/cm2. The results of the bombardment were observed by the direct examination of traces of argon-cluster penetration in multilayer graphene, using high-resolution transmission electron microscopy. Further image processing revealed an average pore diameter of approximately 3 nm, with the predominant size corresponding to 2 nm. We anticipate that a controlled cross-linking process in multilayer graphene can be achieved by appropriately varying irradiation energy, dose, and type of clusters. We believe that this method is very promising for modulating the properties of multilayer graphene, and opens new possibilities for creating three-dimensional nanomaterials.
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