The Ionic State of Molybdenum in Sulfuric Uterine Solutions of Rhenium Sorption and its Extraction

results of studies of the forms of finding and methods of extracting molybdenum from acidic solutions with a high concentration of sulfuric acid are presented. Ion-exchange resins of various modifications were tested to determine the most effective for molybdenum during its sorption from a sulfuric acid solution.

Odstraňování rtuti z kyselých roztoků chloridu rtuťnatého sorbenty připravenými katalyzovanou vulkanizací rostlinných olejů

Mercury is a metallic element, dangerous and toxic for the environment. Presently, the incineration of municipal solid waste (MSW) belongs to important sources of Hg emissions. Methods of conversion of metallic mercury and mercury compounds from soluble and toxic forms into water insoluble/non-toxic form (HgS) are sought after. Gaseous HCl and a significant part of HgCl2 vapors present in flue gas from incineration of MSW can be removed there by absorption in hot water. Efficiencies of Hg2+ removal from acidic water solutions by means of sorbents prepared by catalyzed reaction of sulfur with vegetable oils (inverse vulcanization) were studied. These kinds of sorbents were tested and found to be exploitable for selective removal of mercury ions from aqueous solutions, particularly from acidic solutions containing HCl at higher temperatures (50–75 °C). Presence of relatively high concentrations of salts of some other metallic elements (Fe, Zn, Ca) had only very small effects on Hg-sorption. Mercury adsorbed on such sorbents converts relatively quickly into a non-toxic form (HgS). Reactive sulfides and SH‑groups present on the surface of the sorbent particles contribute to a faster sorption of mercury and its conversion to HgS. Leaching of zinc from the catalyst (Zn‑diethyldithiocarbamate) present in the vulcanized sorbents is negligible at neutral conditions and small (about 10 %) at acidic conditions (pH = 1.5).

Kinetic control concept for the diffusion processes of paracetamol active molecules across affinity polymer membranes from acidic solutions

Background Paracetamol compound remains the most used pharmaceutical as an analgesic and antipyretic for pain and fever, often identified in aquatic environments. The elimination of this compound from wastewater is one of the critical operations carried out by advanced industries. Our work objective was to assess studies based on membrane processes by using two membranes, polymer inclusion membrane and grafted polymer membrane containing gluconic acid as an extractive agent for extracting and recovering paracetamol compound from aqueous solutions. Result The elaborated membrane characterizations were assessed using Fourier-transform infrared spectroscopy (FTIR) and scanning electron microscopy (SEM). Kinetic and thermodynamic models have been applied to determine the values of macroscopic (P and J0), microscopic (D* and Kass), activation and thermodynamic parameters (Ea, ΔH#, ΔS#, ΔH#diss, and ΔH#th). All results showed that the PVA–GA was more performant than its counterpart GPM–GA, with apparent diffusion coefficient values (107D*) of 41.807 and 31.211 cm2 s−1 respectively, at T = 308 K. In addition, the extraction process for these membranes was more efficient at pH = 1. The relatively low values of activation energy (Ea), activation association enthalpy (ΔH≠ass), and activation dissociation enthalpy (ΔH≠diss) have indicated a kinetic control for the oriented processes studied across the adopted membranes much more than the energetic counterpart. Conclusion The results presented for the quantification of oriented membrane process ensured clean, sustainable, and environmentally friendly methods for the extraction and recovery of paracetamol molecule as a high-value substance.

Synthesis of porous γ-Fe2O3 from scorodite synthesized using ultrasound irradiation and evaluation of its battery performance

The effect of 200 kHz ultrasound on scorodite synthesis at 70 °C and 3 h reaction conditions was investigated using sulfuric acidic solutions of various pH (3.0, 2.0, 1.5, 1.0, and 0.0). In contrast to the case of only O2 gas flow without ultrasound irradiation, oxidizing radicals generated by ultrasound irradiation promote Fe(II) oxidation in solution and precursor, allowing scorodite to synthesize with high crystallinity (>99%), which relates to low solubility, even in strong acid solution at pH 1.0. During synthesis, particle shape was changed to polyhedral or spindle type depending on the pH of 0.0 to 3.0. The spindle-shaped scorodite was probably formed by the decrease of precursor amount produced in initial stage of the synthesis. Furthermore, porous maghemite obtained by alkali treatment of scorodite showed initial discharge capacities of 146 mAh/g (polyhedron) and 167 mAh/g (spindle), indicating that its potential use as a cathode material for lithium-ion batteries.

Structure and properties of two new heteroleptic bismuth(III) dithiocabamates of the general composition Bi(S2CNH2)2X (X = Cl, SCN)

The title compounds were prepared by precipitation from acidic solutions of the reactants in acetone/water. Bi(S2CNH2)2Cl (1) crystallizes in the non-centrosymmetric trigonal space group P32 with a = 8.6121(3) and c = 11.1554(4) Å, Z = 3; Bi(S2NH2)2SCN (2) in P21/c (monoclinic) with a = 5.5600(2), b = 14.3679(5), c = 12.8665(4) Å, and β = 90.37(3)°. In the crystal structure of 1 Bi3+ is in a sevenfold coordination of two bidentate and one monodentate S2CHNH2 − anions with an asymmetric coordination pattern of five Bi–S and two Bi–Cl− bonds. The linkage of these polyhedra via common Cl–S edges leads to a 1D polymeric structure with undulated chains propagating in the direction [001]. These chains are linked by strong and medium strong hydrogen bonds forming the 3D crystal structure. In the crystal structure of 2 the Bi3+ cation is in an eightfold coordination. The polyhedron can be described as a significantly distorted tetragonal anti-prism, capped by an additional S atom. Two of these prisms share a common quadrilateral face to form a “prism-double” (Bi2S10N2). These building units are linked by common edges, and the resulting 1D infinite angulated chains propagate along [100]. By contrast to organo-dithiocarbamate compounds, where C–H···X bridges are dominant, the interchain connections in the crystal structures of 1 and 2 are formed exclusively via N–H···S, N–H···Cl, and N–H···N interactions, generating the 3D networks. A significant eccentricity of the Bi3+ cation in the crystal structures of both complexes is observed. Both compounds emit light in the orange range of the electromagnetic spectrum.

Studies on the Formation of Catalytically Active PGM Nanoparticles from Model Solutions as a Basis for the Recycling of Spent Catalysts

The paper presents basic studies on the precipitation of platinum, palladium, rhodium, and ruthenium nanoparticles from model acidic solutions using sodium borohydride, ascorbic acid, and sodium formate as reducing agents and polyvinylpyrrolidone as a stabilizing agent. The size of the obtained PGM particles after precipitation with NaBH4 solution does not exceed 55 nm. NaBH4 is an efficient reducer; the precipitation yields for Pt, Pd, Ru, Rh are 75, 90, 65 and 85%, respectively. By precipitation with ascorbic acid, it is possible to efficiently separate Pt, Rh, and Ru from Pd from the two-component mixtures. The obtained Pt, Pd, and Rh precipitates have the catalytic ability of the catalytic reaction of p-nitrophenol to p-aminophenol. The morphological characteristic of the PGM precipitates was analyzed by AFM, SEM-EDS, and TEM.

Corrosion Inhibition in Acidic Environments: Key Interfacial Insights with Photoelectron Spectroscopy

In many engineering scenarios, surface-active organic species are added to acidic solutions to inhibit the corrosion of metallic components. Given suitable selection, such corrosion inhibitors are highly effective, preventing significant...

A new "on-off-on" g-C3N4 nanosheets fluorescent sensor for 5-Br-PADAP and Co2+ under acidic condition

Scientists were still working on developing a "turn-on" fluorescence sensor for Co2+, especially in acidic solutions. A novel "on-off-on" fluorescence sensor based on g-C3N4 nanosheets was designed and prepared in...