Interphase distribution of a number of polybasic carboxylic acids in aqueous two-phase systems based on polyethylene glycol-1500

In this work, we studied the interphase distribution of a number of polybasic carboxylic acids, in particular, malic, succinic, glutaric, citric, ascorbic and tartaric in two-phase aqueous systems polyethylene glycol-1500 (PEG-1500) - sodium sulfate - water and PEG-1500 - ammonium sulfate - water. Using the spectrophotometric method of analysis, quantitative characteristics (interfacial distribution and degree of recovery) of the extraction of carboxylic acids were determined. In conclusion, it was found that the considered two-phase aqueous systems are promising in the process of extraction of polybasic carboxylic acids. In particular, the system polyethylene glycol 1500 - sodium sulfate - water has effective extraction properties for succinic malic and ascorbic acids. On the other hand, depending on the composition of the extraction systems, the quantitative characteristics for citric, glutaric and tartaric acids practically do not differ.

Extraction of Eu(III), Gd(III), and Tb(III) in aqueous two-phase systems based on polyethylene glycol 1500-NaNO3-H2O with the addition of extractants (D2EHPA, TBP, TOMAN)

Luminophores that used, for example, in fluorescent lamps, contain a large number of rare earth elements. Therefore, the processing of waste equipment containing luminophores is a rational approach to the obtaining of rare-earth metals, firstly, from the economics point of view, since they have a high cost, and secondly, from the ecological point of view, since environmental pollution will not occur. The cheapest way to extract rare earth elements from waste products is to dissolve them in strong acids and the following reprocessing by liquid extraction methods. In this case, neutral or ion exchange extractants (tributyl phosphate, di(2-ethylhexyl)phosphoric acid and quaternary ammonium salts) are used, which show high extraction ability and, in some cases, selectivity. Their applying is associated with the use of non-polar organic solvents, which contradicts the principles of «green» chemistry. A good and promising alternative to organic solvents can be aqueous two-phase systems, which have already proved themselves as low-toxic, but highly effective systems for the separation of a number of metals. Thus, in this work, we performed an experimental study of the interphase distribution of Eu(III), Gd(III), and Tb(III) in two-phase systems based on water-soluble polymers with or without the introduction of traditional organic extractants as an additive. The possibility of using such ATPS as a «green» solvent for traditional extragents for Eu(III), Gd(III), and Tb(III) extraction has been shown.

Development of aqueous two-phase systems-based approaches for the selective recovery of metalloproteases and phospholipases A2 toxins from Crotalus molossus nigrescens venom

Snake venoms are rich sources of proteins with potential biotechnological and pharmaceutical applications. Among them, metalloproteases (MPs) and phospholipases A2 (PLA2) are the most abundant. Their isolation involves a multistep chromatographic approach, which has proven to be effective, however implies high operating costs and long processing times. In this study, a cost-effective and simple method based on aqueous two-phase systems (ATPS) was developed to recover MPs and PLA2 from Crotalus molossus nigrescens venom. A system with PEG 400 g mol−1, volume ratio (VR) 1, tie line length (TLL) 25% w/w and pH 7 showed the best performance for PLA2 recovery. In systems with PEG 400 g mol−1, VR 1, TLL 15% w/w, pH 7 and 1 and 3% w/w of NaCl, selective recovery of MP subtype P-III was achieved; whereas, in a system with PEG 400 g mol−1, VR 1, TLL 25% w/w and pH 8.5, MP subtypes P-I and P-III were recovered. Due to their low costs, ethanol–salt systems were also evaluated, however, failed to differentially partition PLA2 and MPs. The use of ATPS could contribute to the simplification and cost reduction of protein isolation processes from snake venoms and other toxin fluids, as well as potentially aid their biochemical, proteomic and biological analyses. Graphic Abstract

Hydrogen Bond Arrangement Is Shown to Differ in Coexisting Phases of Aqueous Two-Phase Systems

Analysis by attenuated total reflection–Fourier transform infrared spectroscopy shows that each coexisting phase in aqueous two-phase systems has a different arrangement of hydrogen bonds. Specific arrangements vary for systems formed by different solutes. The hydrogen bond arrangement is shown to correlate with differences in hydrophobic and electrostatic properties of the different phases of five specific systems, four formed by two polymers and one by a single polymer and salt. The results presented here suggest that the arrangement of hydrogen bonds may be an important factor in phase separation.