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The salt of formula [H2EDTA2+][HSO4−]2 (dihydrogen ethylenediaminetetraacetate di(hydrogen sulfate(VI)) was used to examine the physicochemical properties of the resulting Ni layer and evaluate the applicability of the salt as a new additive for Watts-type baths. The Ni coatings deposited from baths containing [H2EDTA2+][HSO4−]2 were compared with those obtained from other baths. The nucleation of nickel on the electrode was proven to occur the slowest in the bath that contained the mixture of [H2EDTA2+][HSO4−]2 and saccharin compared with other baths. The addition of [H2EDTA2+][HSO4−]2 alone (bath III) generated a coating with a morphology similar to that obtained from bath I (without additives). Despite the similar morphology and wettability of the Ni-coated surfaces plated from various baths (all Ni coatings were hydrophilic with contact angles in the range of 68 to 77°), some differences in electrochemical properties were noted. The corrosion resistance for the coatings plated from baths II and IV containing saccharin (Icorr = 1.1 and 1.5 µA/cm2, respectively) and the mixture of saccharin and [H2EDTA2+][HSO4−]2 (Icorr = 0.88 µA/cm2), respectively, was similar or even better than the coating obtained from baths without [H2EDTA2+][HSO4−]2 (Icorr = 9.02 µA/cm2). [ABSTRACT FROM AUTHOR]

The review presents advances in the removal of Cr(III) from the industrial effluents published in the last ten years. Although Cr(III) has low solubility and is less dangerous for the aquatic environment than Cr(VI), it cannot be released into the aquatic environment without limitations and its content in water should be restricted. The development of efficient techniques for the removal of Cr(III) is also a response to the problem of chromium wastewater containing Cr(VI) ions. Very often the first step in dealing with such wastewater is the reduction in chromium content. In some cases, removal of Cr(III) from wastewaters is an important step for pretreatment of solutions to prepare them for subsequent recovery of other metals. In the review, hydrometallurgical operations for Cr(III) removal are presented, including examples of Cr(III) recovery from real industrial effluents with precipitation, adsorption, ion exchange, extraction, membrane techniques, microbial-enhanced techniques, electrochemical methods. The advantages and disadvantages of the operations mentioned are also presented. Finally, perspectives for the future in line with circular economy and low-environmental impact are briefly discussed. [ABSTRACT FROM AUTHOR]

This paper presents Cr(III) removal from nickel sulfate waste solutions as a pretreatment step for the modification of hydrogen storage alloys. Adsorption with two cation exchange resins, Dowex G26 (strongly acidic) and MAC-3 (weakly acidic), and precipitation with various solutions were chosen as simple operations for Cr(III) removal from waste solutions. The adsorption of Cr(III) was investigated for both model and real waste nickel solutions. Dowex G26 appeared to be more efficient in Cr(III) removal (RCr(III) from 43 to 80%) than MAC-3 (RCr(III) from 40 to 53%). However, the adsorption from multi-component solutions (presence of Co(II), Ni(II) and Cr(III)) showed no selectivity in Cr(III) adsorption in comparison to those of Co(II) and Ni(II). Cr(III), Ni(II) and Co(II) were removed at a comparable level (30–36%) from a three-component solution of 10 g/dm3 of each metal ion, and a 56–72% removal of these ions was achieved from the real solution. Therefore, the precipitation of Cr(III) was carried out from a real waste nickel solution to compare its performance with adsorption. The best precipitation solution appeared to be 3 and 30% NaOH due to the quantitative precipitation of Cr(OH)3 at pH 5 and relatively small co-precipitation of Ni(II) and Co(II) hydroxides (PCo(II) = 20–52%, PNi(II) = 0–54%). Based on the results of the research, it can be concluded that precipitation with a NaOH solution is an efficient pretreatment operation of an electrolyte for further steps of the hydrometallurgical process of nickel electrodeposition and appears to be more selective in the elimination of Cr(III) than adsorption with Dowex G26 resin. [ABSTRACT FROM AUTHOR]

The names of Saul's descendants appear in a different form in the books of Chronicles (1 Chr 8:33-34; 9:39-40) as compared to those in the books of Samuel (2 Sam 2-4; 9; 19; 21). In Chronicles the name Eshbaal is used instead of Ishbosheth, and Meribaal instead of Mephibosheth. This article describes the differences between these names in the context of early Hebrew epigraphy. The recalling of the original names of the first Judaean royal dynasty in the books of Chronicles could be explained not only with reference to the original version of the books of Samuel, but also from the oral tradition of Judea or from some documents of the royal archives that survived the Babylonian conquest. [ABSTRACT FROM AUTHOR]

Attempts have been made to find the best procedure for the detection of premature battery capacity loss (the so called "PCL") in AGM-VRLA 48 V batteries operating in telecommunication systems. However, recorded changes in internal resistance and potential did not give clear indications of the beginning of the PCL effect. The obtained correlation between internal resistance and potential derived from used batteries does not show the expected trend in measured parameters. It seems that the application of Electrochemical Impedance Spectroscopy (EIS), which is a faster and non-destructive method, may solve this problem. It is demonstrated that the change in internal resistance (which is an indicator of the state of health (SoH)) can be determined from EIS spectra during continuous operation of 12 V monoblocks in a backup power source of a base transceiver station (BTS). [ABSTRACT FROM AUTHOR]

The influence of selected types of ammonium ionic liquid (AIL) additives on corrosion and functional parameters of lead-acid battery positive electrode was examined. AILs with a bisulfate anion used in the experiments were classified as protic, aprotic, monomeric, and polymeric, based on the structure of their cation. Working electrodes consisted of a lead-calcium-tin alloy utilized in the industry for manufacturing current collectors of positive electrodes in lead-acid batteries (LABs). This alloy was used in the first part of the study for the evaluation of corrosion intensity and stability of electrolyte with AIL additives. In the second part, the grid made of the examined alloy was covered with positive active mass, the composition of which was modified by selected AIL. The selection of an appropriate substance was made based on parameters such as corrosion potential, corrosion current, polarization resistance, and hydrogen and oxygen evolution potentials. Techniques such as linear sweep voltammetry, corrosimetry, and electrochemical impedance spectroscopy were used. The conducted measurements revealed that polymeric AIL additive had an exceptionally positive influence on the inhibition of the corrosion process in LAB and electrochemical window of the electrolyte. The influence of this compound on the specific capacity and resistance of the active mass was also discussed.ᅟ [ABSTRACT FROM AUTHOR]

This paper examines the influence of aprotic solvents on the spectroscopic properties as well as the energy deactivation of two free-base corrole dyes substituted with C6F5 and/or 4-NO2C6H4 groups. Absorption, fluorescence and laser-induced optoacoustic spectroscopy have been used to follow the singlet and triplet states of fluorine corroles belonging to the A2B and A3 type in toluene (TL), chloroform (CL), dimethylformamide (DMF), dimethyl sulfoxide (DMSO) and also in solvent mixtures. Changes in the absorption and fluorescence spectra are influenced by the type of solvent mixture. The fluorescence behaviors of the two investigated corroles were extremely different – fluorescence of the nitro-corrole in TL is dramatically quenched in the presence of DMF. In contrast, fluorescence quenching of fluorine corroles in DMF–TL mixtures is substantially weakened. Absorption, fluorescence, triplet population as well as singlet oxygen generation parameters are evaluated. The spectral experimental data are supported by quantum chemical calculations – time-dependent density functional theory (TD-DFT) and cyclic voltammetry experiments. The presented results are discussed from a viewpoint of aggregation, tautomerization, and deprotonation effects occurring in the corroles. [ABSTRACT FROM AUTHOR]

The content of essential oil and valerenic acids and the yield of roots were analyzed in valerian cultivar 'Polka' and strain no. 4 during the nine following phases: the beginning of vegetation, spring rosette, pedicel development, the beginning of flowering, full bloom, seed harvest, three weeks after the seed harvest, fall rosette, and after the first frost. The yield of valerian roots was different at the investigated phases and in years of cultivation, while tested genotypes produced similar root yields. The highest contents of essential oil and valerenic acids were obtained at different phases by the tested genotypes: strain no. 4 in full bloom (1.3% and 0.266%, respectively) and cultivar 'Polka' three weeks after seed harvest (1.25%) and during seed harvest (0.218%). The lowest contents of the investigated substances were detected at the beginning of growth and after the first frost in both genotypes. The obtained results revealed significant differences in essential oil and valerenic acids content, which depend on genotype, plant age, harvest time and the year of cultivation. The results suggest that higher amounts of valerenic acids could be obtained in the second year of cultivation over the period from full bloom (0.278%) to fall rosette phase (0.316%). [ABSTRACT FROM AUTHOR]