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Herein we demonstrate the formation of new stimuli-responsive aqueous biphasic systems (ABS), able to respond simultaneously to temperature and pH, or just to one stimulus, therefore allowing the design of more sustainable separation processes. This dual behavior is achieved with ABS formed by mono- or dicationic protic ionic liquids as phase-forming components, being defined by the ionic liquid cation chemical structure or its basicity. While ABS comprising monocationic ionic liquids only respond to the effect of temperature, systems comprising dicationic ionic liquids are simultaneously affected by both temperature and pH variations. Dicationic ionic liquids are here identified as the key to unlock a double response to stimuli, which is due to the presence of two pKa values afforded by the cation. The reported findings contribute to increase the customizability of double stimuli-responsive ABS based on ionic liquids, whose development was up to date limited to ionic liquids bearing pH-responsive anions, opening the door towards the development of more sustainable separation processes.
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http://dx.doi.org/10.1002/chem.202403605 | DOI Listing |
Environ Health (Wash)
December 2024
Institute of Environmental Research at Greater Bay Area, Key Laboratory for Water Quality and Conservation of the Pearl River Delta, Ministry of Education, Guangzhou University, Guangzhou 510006, China.
The rational design of molecules with the desired functionality presents a significant challenge in chemistry. Moreover, it is worth noting that making chemicals safe and sustainable is crucial to bringing them to the market. To address this, we propose a novel deep learning framework developed explicitly for inverse design of molecules with both functionality and biocompatibility.
View Article and Find Full Text PDFJ Colloid Interface Sci
December 2024
College of Chemistry and Materials Engineering, Bohai University, Jinzhou 121013, China. Electronic address:
The unique structure and strong interaction of multiphase hybrid materials have garnered significant attention as prospective candidates for electrode materials in the realm of energy storage. The present study presents a rational design of a functional NiSe-CoSe/N, B double-doped carbon hybrid composite (NCS/C), resulting in the emergence of various novel cooperative regulatory mechanisms involving: (i) the heterogeneous structure of NiSe and CoSe generates built-in electric fields to increase electron mobility; (ii) the incorporation of polyatomic double-doped carbon (N, and B) expedites electron transfer rate; intriguingly, (iii) ionic liquids not only serve as polyatomic dopants in the reaction system but also influence the microstructure of the composite. Benefiting from these synergistic effects, the NCS/C hybrid exhibits remarkable charge storage capacity and rapid electrochemical kinetics, driven by its multi-fold hollow structure and multicomponent cooperative modulation.
View Article and Find Full Text PDFSpectrochim Acta A Mol Biomol Spectrosc
December 2024
Department of Chemistry, Presidency University, Kolkata 700073, India. Electronic address:
Pyrene fluorescence in aqueous solutions of two surface active ionic liquids, namely, 1-decyl-3-methylimidazolium chloride, and 1-hexadecyl-3-methylimidazolium chloride was investigated in presence of a biopolymer sodium alginate. The principal objective of this study was to explore the influence of the length of the hydrocarbon tails of these surface active ionic liquids on the possible location of the probe (pyrene) molecules in presence of the additive. While an abrupt decrease in the values of the ratio of the intensity of the first vibronic band to that of the third band of pyrene emission spectrum with concentration was observed for 1-hexadecyl-3-methylimidazolium chloride in presence of sodium alginate like the polymer-free case reported earlier, there was a peculiar reversal for 1-decyl-3-methylimidazolium chloride + sodium alginate.
View Article and Find Full Text PDFJ Phys Chem B
December 2024
Department of Chemistry, Eszterházy Károly Catholic University, Leányka utca 12, H-3300 Eger, Hungary.
In this work, we carry out a systematic computer simulation investigation of the single particle dynamics at the free surface of imidazolium-based room temperature ionic liquids by applying intrinsic surface analysis. Besides assessing the effect of the potential model and temperature, we focus in particular on the effect of changing the anion type, and, hence, their shape and size. Further, we also address the role of the length of the cation alkyl chains, known to protrude into the vapor phase, on the surface dynamics of the ions.
View Article and Find Full Text PDFRSC Adv
December 2024
C2CNT LLC A4 188 Triple Diamond Blvd, North Venice FL 34275 USA
Beryllium carbonate has the highest capacity to bind and release the greenhouse gas CO compared to amines, ionic liquids, CaCO or LiCO. The thermodynamic equilibrium for CO and BeO from BeCO is calculated. TGA of BeCO is used to determine the stepwise mechanism of its CO release, and the low melting point Li/Sr/BeCO is demonstrated.
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