Ionic Liquid Salt Research Articles

Organic Cationic-Coordinated Perfluoropolymer Electrolytes with Strong Li+-Solvent Interaction for Solid State Li-Metal Batteries.

The practical application of solid-state polymer lithium-metal batteries (LMBs) is plagued by the inferior ionic conductivity of the applied polymer electrolytes (PEs), which is caused by the coupling of ion transport with the motion of polymer segments. Here, solvated molecules based on ionic liquid and lithium salt with strong Li+-solvent interaction are inserted into an elaborately engineered perfluoropolymer electrolyte via ionic dipole interaction, extensively facilitating Li+ transport and improving mechanical properties. The intensified formation of solvation structures of contact ion pairs and ionic aggregates, as well as the strong electron-withdrawal properties of the F atoms in perfluoropolymers, give the PE high electrochemical stability and excellent interfacial stability. As a result, Li||Li symmetric cells demonstrate a lifetime of 2500 h and an exceptionally high critical current density above 2.3 mA cm-2, Li||LiFePO4 batteries exhibit consistent cycling for 550 cycles at 10 C, and Li||uncoated LiNi0.8Co0.1Mn0.1O2 cells achieve 1000 cycles at 0.5 C with an average Coulombic efficiency of 98.45 %, one of the best results reported to date based on PEs. Our discovery sheds fresh light on the targeted synergistic regulation of the electro-chemo-mechanical properties of PEs to extend the cycle life of LMBs.

Lubrication and antibacterial performance and mechanism of functionalized ionic liquids in glycerol media with different water contents

Glycerol lubricants face limitations in industrial applications due to their inadequate antimicrobial properties. In this study, a functionalized long-chain quaternary ammonium salt ionic liquid, BTA-16-BTA, was synthesized. The antimicrobial and tribological properties of BTA-16-BTA as a lubricant additive in glycerol media with different water contents were investigated. The results show that the antimicrobial performance of the glycerol medium is positively correlated with the amount of BTA-16-BTA added. At the optimal concentration of 1.5 % BTA-16-BTA dispersion, excellent friction-reducing, anti-wear, and extreme pressure properties were observed. The friction-reducing and anti-wear effects were further enhanced when 1 % water was added to the system. The liquid medium containing BTA-16-BTA can inhibit the growth of Escherichia coli, indicating that BTA-16-BTA possesses antimicrobial properties.

Efficient and selective extraction of gold from acidic leaching solutions using novel guanidinium ionic liquid

As gold is a non-renewable resource, it holds both economic and environmental importance to enhance the recycling of precious metal waste from secondary resources. Herein, a guanidine salt ionic liquid ([DIETMG][NTf2]) with low water solubility and viscosity was synthesized by molecular design of guanidine salt ionic liquid with good biocompatibility and biodegradability, and a solvent-free system of [DIETMG][NTf2]-water was constructed to extract Au(Ⅲ). The findings reveal that the extraction efficiency of Au(Ⅲ) can reach 97.57 % under optimal extraction conditions. Further thermodynamic and kinetic studies revealed that the reaction process is spontaneous and exothermic, with the extraction rate being primarily controlled by interfacial chemical reactions. The system demonstrates remarkable selectivity for Au(Ⅲ) in solutions containing a mix of various metal ions. Finally, ascorbic acid (Vc) was employed as a stripping agent to obtain gold at room temperature. After 8 cycles, [DIETMG][NTf2] still achieved a 90% extraction efficiency. This study provides a new idea and method for recovery of gold from secondary resources.

Enabling room temperature solid-state lithium batteries by blends of copolymers and ionic liquid electrolytes

High lithium-concentration phosphonium ionic liquids electrolytes have shown outstanding properties even overcoming ammonium derivatives in terms of viscosity and transport properties. Consequently, they have been also combined with fluorinated polymers, such as poly(vinylidene fluoride) (PVDF) or poly(ionic liquids), for solid-state batteries with satisfying performance at 50 °C. The aim of this work is to develop highly lithium conducting solid-state electrolyte (≥0.1 mS cm−1) at room temperature but maintaining solid-state properties. For this, polymer electrolytes based on ISOBAM alternating copolymer (isobutylene and maleic anhydride) and ionic liquid (P111i4FSI) were developed. The composition-dependent behavior of the solid electrolytes was studied in terms of electrochemical impedance spectroscopy (EIS), reaching σLi+ of 0.52 mS cm−1; differential scanning calorimetry (DSC) and Fourier-transform infrared spectroscopy (FTIR) under different ionic liquid electrolyte loadings and salt concentration. The polymer electrolytes presented a solid-like behavior in the range of 25 to 90 °C with a storage modulus of 2.3·104 Pa. Finally, the best free-standing membrane electrolytes were tested and compared electrochemically in lithium symmetrical cells and lithium iron phosphate full cells exhibiting an excellent cycling at room temperature.

Effect of pre-hydrolysis on the dissolution of hardwood pulp in double salt ionic liquid

Abstract Ionic liquids (ILs) are potentially alternative solvents for cellulose dissolution. In this article, effect of hemicellulose in cellulose dissolution in ILs and the regeneration process were investigated. Hardwood pulps were produced by kraft (KP) and pre-hydrolysis kraft (PHKP) processes. The α-cellulose and residual pentosan contents were 95.6 % and 4.2 % in PHKP and 84.3 % and 9.9 % in KP, respectively. Both pulps were dissolved in 1-butyl-3-methylimidazolium chloride [C4mim]Cl, 1-butyl-3-methylimidazolium acetate [C4mim]CH3CO2 and their double salt (DSIL), [C4mim](CH3CO2)0.6Cl0.4 at 90 °C. It was observed that PHKP had slightly higher solubility in both ILs and DSIL. The dissolved pulps were regenerated by water and characterized by FTIR, TGA, X-ray diffraction, and viscosity. Regenerated pulp film formed smooth and homogenous surface. The viscosity of regenerated PHKP was higher than the original PHKP, which affected the strength of the produced cellulose film. As observed in FTIR, the regenerated cellulose showed a stronger absorption band at 1,647 cm−1 corresponding to the C–O stretching vibration of C–O–H. The crystalline structures of regenerated KP and PHKP from [C4mim](CH3CO2)0.6Cl0.4 changed to cellulose II form from the original cellulose I form.

Fabrication of Na+-Conducting Ionic Liquids Na[((FSO2)2n) x ((CF3SO2)(FSO2)N)1-X ], and Its Physical and Electrochemical Properties

To achieve low-carbon society in near future, it’s imperative to research and develop high-performance and low-cost batteries. Therefore, sodium-ion batteries (SIBs) are attracting attention owing to their possibility to be composed of elements with no resource scarcity and low cost.To solve the challenge of low energy density in SIBs, it is essential to focus on developing electrodes of the 4V to 5V class. Simultaneously, electrolytes with wide electrochemical window are crucial from in terms of electrolyte decomposition at high operating voltages. Molten salt electrolytes exhibit relatively high ionic conductivity and electrochemical stability. On the other hands, there is an issue that the electrolyte must be heated to a high temperature to maintain molten state of the electrolytes. In this study, with the goal of expanding the melting temperature range of molten salt electrolytes, we precisely mixed relatively low-melting sodium salts Na(FSO2)2N (NaFSA) and Na(CF3SO2)(FSO2)N (NaFTA) and found a composition with a melting point below 100 ℃. As a result, we successfully fabricated novel single-sodium cationic salt ionic liquid. In this presentation, we will report on its bulk properties and electrochemical characteristics. All mixed sodium salts were mixed NaFSA and NaFTA in each molar ratio and stirred during gradually cooling after uniformly melting at 170 ℃ in Ar-filled grove box. The thermal properties of the mixed sodium salts were evaluated by differential scanning calorimetry (DSC). The samples were stored at room temperature for 2~3 days to reach equilibrium state, and then sealed in a high-pressure SUS pan. Ionic conductivity (σ) of the mixed sodium salts were also measured from 60 ℃ to 135 ℃ at each temperature. Symmetrical cells were constructed by put the mixed sodium salt between two SUS or sodium metal electrodes. Ionic conductivity of mixed sodium salts was evaluated by electrochemical impedance spectroscopy (EIS) with SUS electrodes symmetric cells. Na+ transference number was measured by potentiostatic polarization and EIS with sodium metal symmetric cells at 90℃. The binary phase diagram of NaFSA and NaFTA were shown in Fig.1. In the NaFTA-rich composition range (0.1 < x < 0.4), the phase diagram resembles a simple eutectic phase diagram, while, in the NaFTA-rich composition range (0.5 < x < 0.9), the mixed sodium salts exhibited pseudo-single-phase behavior, and the lowest liquid-phase transition temperature (T L) was observed at 90℃ of Na[(FSA)0.8(FTA)0.2].(1) Additionally, in this composition range, glass transition points (T g) were also confirmed, indicating the supercooled behavior.The Arrhenius plot of the ionic conductivity (σ) for Na[(FSA)0.8(FTA)0.2] was shown in Fig.2. At the T L around 90℃, σ was observed to 0.69 mS cm-1. This is attributed to the strong interactions between Na+ and anion in the absence of solvents, causing high viscosity and decreasing mobility. Below the T L, there was no remarkable decrease in σ and Nyquist plots remained non-divergent to 55℃, allowing for the attribution of σ. Moreover, below the T L, the glass transition and crystallization of Na[(FSA)0.8(FTA)0.2] were not observed. The temperature dependence of σ was analyzed by the Vogel-Fulcher-Tamman (VFT) equation.(2) In addition, the σ(T g) at the observed T g from DSC were calculated by VFT equation. Also, the decoupling index (R τ), representing the ratio of ionic conductive relaxation time (τ σ) to structural relaxation time (τ s), were calculated.(3) The value of logR τ value for Na[(FSA)0.8(FTA)0.2] was -0.62 and the low value indicates that τ s is coupled with τ σ.To investigate the Na+ conduction behavior in Na[(FSA)0.8(FTA)0.2], chronoamperograms with an applied potential of 500 mV to the sodium metal symmetric cells were shown in Fig.3(a). Fig.3(b) shows Nyquist plots before and after direct current polarization. The steady current was observed after 8h. Furthermore, there was slightly changes of Nyquist plots before and after direct current (DC) polarization, stable interface between sodium metal and Na[(FSA)0.8(FTA)0.2] was also confirmed. The Na+ transference Number (t Na+) in the Na[(FSA)0.8(FTA)0.2] was estimated to be 0.86. Tatara et al. reported the t Na+ of 0.18 in the 1M NaPF6/PC+0.5vol% FEC.(4) Since molten salts consisting of only cations and anions should not be occurred concentration polarization, it exhibited a considerably higher t Na+ in Na[(FSA)0.8(FTA)0.2] compared to the t Na+ in dilute non-aqueous sodium electrolyte. In the presentation, we will discuss the cycle characteristics obtained by constant current charge-discharge tests of both half-cell and full-cell configurations using generic positive and negative electrode materials.(1) K. Kubota et al., J. Chem. Eng. Data, 55, No. 9, 2010, 3142–3146.(2) H. Vogel., Phys. Z. 1921, 22, 645.(3) C. A. Angell, Annu. Rev. Phys. Chem. 1992, 43, 693.(4) R. Tatara et al., Electrochemistry, 89(6), 2021, 590–596. Figure 1

Acetate-based ionic liquid immobilized Fe-MIL-101-NH2: A highly efficient heterogeneous catalyst for the conversion of CO2 into oxazolidinones with N-aryl epoxy amines

A novel acetate-based ionic liquid immobilized metal organic frameworks catalyst, Fe-MIL-101-N(Bnme2)OAc, was synthesized using a straightforward ion exchange strategy. Initially, Fe-MIL-101-N(Bnme2)Br was prepared by condensing a quaternary ammonium salt ionic liquid (N(BzBnme2)Br) with Fe-MIL-101-NH2. Subsequently, the Br- ions were exchanged with OAc- ions from potassium acetate to produce the desired catalyst. The morphology, structure and physicochemical properties of the catalyst were comprehensively characterized by XRD, SEM, FT-IR, DRS UV−vis, TGA, BET, and EA, which confirmed both the successful preparation of the catalyst and the integrity of the MOFs framework. The heterogeneous catalyst Fe-MIL-101-N(Bnme2)OAc demonstrated high activity in catalyzing the reaction of N-aryl epoxy amines with CO2 to form oxazolidinone compounds under optimal conditions (80 °C, 8 h, 1 mL of MeCN, 1.0 MPa CO2 and 5 mg catalyst), achieving a yield of up to 99 % with almost no production of the by-product cyclic carbonate. Moreover, this catalyst displayed excellent recyclability and extensive substrate applicability, maintaining its catalytic activity for at least five consecutive uses. Substrates with various substituents also produced the corresponding oxazolidinone products in high yields.

Extraction of low-concentration bio-based diols and dicarboxylic acids using ionic liquid-based aqueous two-phase systems: Experimental and theoretical studies

Biochemical pathways to generate renewable and high value-added diols and dicarboxylic acids have attracted increasing interest. However, the diols/dicarboxylic acids usually exist in the form of low-concentration aqueous solution after the bioprocesses, causing the issues of low efficiency and high energy consumption in the separation and recovery of these highly hydrophilic bioproducts. Here, we developed an aqueous two-phase system (ATPS) consisting of ionic liquid (IL) and inorganic salt for efficient extraction of the bio-based diols and dicarboxylic acids. The optimal salt, IL, and extractant to feed volume ratio were K4P2O7, [Bmim][C12H23O2], and 1:4, respectively. The selected IL showed large capacity and good reusability, with the highest dehydration rate reaching up to 97.6%. More importantly, the IL-based ATPS exhibited effectiveness and high efficiency in the separation of various low-concentration diols and dicarboxylic acids, with the recovery exceeding 91.9%. To explore the extraction mechanism, the structural and interactions analyses were conducted by DFT calculations. The strength of hydrogen bond interactions formed between diols/dicarboxylic acids and ILs and those between salts and water largely determines the extraction performance. Moreover, three descriptors that can well represent the H-bond basicity and polarizability/dipolarity of ILs were established to facilitate the IL evaluation and screening.

Polyether-functionalized ionic liquid-assisted Rh-AMPP-catalyzed asymmetric hydrogenation of ketopantoyl lactone to D-(−)-pantolactone

Abstract In this paper, the reaction of chiral Rh-AMPP catalysts for the asymmetric hydrogenation of ketopantoyl lactone to D-(-)pantolactone under a polyether guanidinium salt ionic liquid ([Me(EO)16TMG][OMs])/toluene homogeneous catalytic system was investigated. The impact of polyether ionic liquid doping on the catalytic activity and enantioselectivity was investigated. To separate and recycle chiral Rh-AMPP catalysts, a “homogeneous catalytic-liquid/solid separation” system on the basis of [Me(EO)16TMG][OMs] was constructed. The catalytic system exhibited high catalytic activity, enantioselectivity, and long-term stability, and no obvious reduction in enantioselectivity was found after four cycles.

Effect of Relative Mass on Ion Velocity Cross-Correlations in Ionic Liquids and Molten Salts: Different Perspectives in Different Reference Frames.

In electrolytes, the self- and interdiffusion coefficients, transport numbers, and electrical conductivity can be used to determine velocity cross-correlation coefficients (VCC) that are also accessible through molecular dynamics simulations. In an ionic liquid or molten salt, there are only three, corresponding to correlations between the velocities of distinct ion pairs (cation-anion, cation-cation, and anion-anion) averaged over both the ensemble and time, calculable from experimental ion self-diffusion coefficients and the electrolyte conductivity. Most usually, the mass-fixed frame of reference (with velocities relative to that of the center of mass of the system) is used to discuss the VCC and the distinct diffusion coefficients (DDC) derived from them. Recent work in the literature has suggested a dependence of the DDC on the ratio of the anion to cation mass. Here, we demonstrate, using our own and literature transport property data for a large number of ionic liquids and molten salts, that the trends observed depend on the particular choice of velocity reference frame, mass-, number-, or volume-fixed. The perception of ion-ion interactions may be distorted in the mass- and volume fixed frames when the co-ions have very different masses or volumes, particularly for systems containing light lithium ions.

Dissolution of cellulose in imidazolium-based double salt ionic liquids

The dissolution of cellulose in double salt ionic liquids (DSILs) was studied in detail and compared with the dissolution in individual constituent ionic liquids (ILs). The DSILs, [C4mim](CH3CO2)xCl1-x (x is the mole fraction of the single component ILs), were synthesized using acetate and chloride salts of 1-butyl-3-methylimidazolium. These DSILs were then used for the investigation of the solubility of cellulose in the whole mole fraction range. Commercial cellulose (CC) powder, kraft pulp (KP), and prehydrolysis kraft pulp (PHKP) of jute were chosen as cellulose sources. The solubility of cellulose increased with an increasing temperature for [C4mim](CH3CO2)0.6Cl0.4 and with increasing amount of [C4mim]Cl in DSILs. The maximum solubility of CC powder was 32.8 wt% in [C4mim](CH3CO2)0.6Cl0.4 at 100 °C, while for KP and PHKP, solubilities were 30.1 and 30.5 wt%, respectively under the identical condition. Cellulose could be regenerated from the DSILs using water as an antisolvent. Structure, morphology, and thermal stability of the regenerated cellulosic materials were analyzed. DSILs could be recycled >99 % without a discernible change in structure. This work demonstrates that DSILs display enhanced solubility over ILs system and have potential as a chemical processing methodology.

In situ ionic liquid-assisted mechanochemical extraction and aqueous two-phase system enrichment of hydrophobic flavonoids from rose

An effective in situ ionic liquid-assisted mechanochemical extraction (MCE) and aqueous two-phase system (ATPS) enrichment method was established. An ATPS can be formed to accomplish the enrichment of the compounds while realizing the MCE for medicinal crop, aiming to establish a pretreatment method for quantitative analysis of active compounds in complex matrices. The effects of ionic liquid amount, milling time, salt amount, vortex time and pH value were investigated, and the optimal conditions for the response surface method were obtained as follows: 1-butyl-3-methylimidazolium bromide amount of 250.37 mg, milling time of 1.99 min and salt amount of 4.38 g. After obtaining the optimal conditions, the method has the correlation coefficients of 0.9963–0.9996, and the limits of detection for the analytes were ranged from 0.05 to 0.08 ng/mL. Besides, the recoveries of rose samples were 84–119% at spiked levels of 0.1 and 1 µg/mL. Compared with other extraction methods, this method synchronously combines MCE and ATPS enrichment techniques, which is environmentally friendly and shortens the extraction time, and can effectively extract hydrophobic flavonoids from roses without any organic solvents.

Room Temperature Ionic Liquid Capping Layer for High Efficiency FAPbI3 Perovskite Solar Cells with Long-Term Stability.

Ionic liquid salts (ILs) are generally recognized as additives in perovskite precursor solutions to enhance the efficiency and stability of solar cells. However, the success of ILs incorporation as additives is highly dependent on the precursor formulation and perovskite crystallization process, posing challenges for industrial-scale implementation. In this study, a room-temperature spin-coated IL, n-butylamine acetate (BAAc), is identified as an ideal passivation agent for formamidinium lead iodide (FAPbI3) films. Compared with other passivation methods, the room-temperature BAAc capping layer (BAAc RT) demonstrates more uniform and thorough passivation of surface defects inthe FAPbI3 perovskite. Additionally, it provides better energy level alignment for hole extraction. As a result, the champion n-i-p perovskite solar cell with a BAAc capping layer exhibits a power conversion efficiency (PCE) of 24.76%, with an open-circuit voltage (Voc) of 1.19V, and a Voc loss of ≈330mV. The PCE of the perovskite mini-module with BAAc RT reaches 20.47%, showcasing the effectiveness and viability of this method for manufacturing large-area perovskite solar cells. Moreover, the BAAc passivation layer also improves the long-term stability of unencapsulated FAPbI3 perovskite solar cells, enabling a T80 lifetime of 3500h when stored at 35% relative humidity at room temperature in an air atmosphere.

Efficacy of the Ionic Liquid 1,4-Bis(carboxymethyl)piperazine-1,4-diium Chloride as a Catalyst for Xanthenes/Acridines Synthesis: Spectral Characterization, X-ray Structure, and Nematicidal Activity

In this research paper, a straightforward and efficient approach for synthesizing the 1,4-bis(carboxymethyl)piperazine-1,4-diium chloride [BCMPZ][2Cl] ionic liquid salt (IL) catalyst is introduced. The morphology, thermal stability, and functionality of the synthesized [BCMPZ][2Cl] IL were characterized using spectroscopic, electron microscopy, and thermal analysis. A density functional theory (DFT) study, including infrared spectroscopy (IR), powder X-ray diffraction (PXRD), Thermogravimetric analysis (TGA), and scanning electron microscopy with energy-dispersive X-ray spectroscopy (SEM with EDX), were employed. The well-characterized ionic liquid (IL) assisted as a catalyst in the synthesis reaction involving aldehydes, dimidone, and arylamine to yield 1,8-dioxo-octahydroxanthene and 1,8-dioxo-9-aryl-10-aryl-decahydroacridine derivatives (3a-i and 4a-b) with high yields, getting up to 97%. The structure of the synthesized molecules was confirmed through various physicochemical techniques, including 1H and 13C NMR, IR, elemental analysis, and MS. X-ray single crystal diffraction techniques were also used to elucidate the geometry of one of the synthesized molecules (3f). The heterogeneous catalyst (IL) used in the synthesis of the molecules was successfully recycled and reused without additional treatment of purification. The synthesized xanthines were found to inhibit nematode activity, thus they may act as potential nematicides for crop protection. The present study also identified five different compounds that were effective against Meloidogyne incognita. Compound 3a reduced nematode egg hatching by 65% at a concentration of 2000 ppm, which was the highest efficacy in tested compounds. Compound 3c had a mortality rate of 80% against nematodes. Overall, the developed method has many advantages, including fast reaction time, economic efficiency, and minimal catalyst loading, making it a promising method for future research in the field of heterocycle synthesis and crop protection.

Enhancing the efficiency and stability of ZnSe pure blue quantum dot light-emitting diodes via ionic liquid doping

The novel ionic liquid (IL) salt BMIMPF6 doping TFB elevates the work functions and surface potentials of the TFB HTL, and promotes effective charge transfer within the QDs, resulting in a significant improvement in device performance.

Design of High-Entropy Electrolytes Enabled By the High-Throughput and Autonomous Procedure

Electrolytes in Li-ion batteries play a significant role as they influence different aspects directly related to the battery performance, such as safety, voltage window, electrochemical stability, and the formation of solid-electrolyte interphase (SEI). Conventionally, these electrolytes are composed of a lithium salt dissolved in an organic solvent such as ethylene carbonate and propylene carbonate. Regarding safety, these organic electrolytes can be replaced by room-temperature ionic liquids (RTILs), which present lower vapor pressure and non-flammability.1 Moreover, adding polymer to these liquid electrolytes to form polymer gel electrolytes has proven to be a good strategy to avoid dendritic growth and increase electrolyte stability.2 The properties of RTIL electrolytes containing Li salts have been studied in the last decade. Still, the scope has been limited primarily to simple RTILs consisting of one cationic and one anionic species. Inspired by the success of high-entropy alloys (HEAs) for forming stable solid solutions with excellent mechanical properties,3 the concept of high-entropy materials has been recently transferred to electrolytes, where the effect of mixing multiple Li salts is explored.4 However, the number of compositional combinations increases rapidly when multiple salts, cationic and anionic species are introduced, and the explorable compositional space increases even more when polymers are added to the mixture.Automating the electrolyte preparation and characterization can be the key feature to allow the exploration of all the possible electrolyte combinations. In this work, we explain the first preliminary results obtained from an autonomous preparation and characterization of high-entropy electrolytes composed of a mixture of two different lithium salts in ionic liquids consisting of multiple anionic and cationic species. In addition, the adaptation of the autonomous system of preparation and characterization of liquid electrolytes to polymer gel electrolytes is also proposed and explained. References. (1) Niu, H.; Wang, L.; Guan, P.; Zhang, N.; Yan, C.; Ding, M.; Guo, X.; Huang, T.; Hu, X. Recent Advances in Application of Ionic Liquids in Electrolyte of Lithium Ion Batteries. J. Energy Storage 2021, 40, 102659. https://doi.org/10.1016/j.est.2021.102659.(2) Chen, J.; Wu, J.; Wang, X.; Zhou, A.; Yang, Z. Research Progress and Application Prospect of Solid-State Electrolytes in Commercial Lithium-Ion Power Batteries. Energy Storage Mater. 2021, 35, 70–87. https://doi.org/10.1016/j.ensm.2020.11.017.(3) Yeh, J.-W.; Chen, S.-K.; Lin, S.-J.; Gan, J.-Y.; Chin, T.-S.; Shun, T.-T.; Tsau, C.-H.; Chang, S.-Y. Nanostructured High-Entropy Alloys with Multiple Principal Elements: Novel Alloy Design Concepts and Outcomes. Adv. Eng. Mater. 2004, 6 (5), 299–303. https://doi.org/10.1002/adem.200300567.(4) Wang, Q.; Zhao, C.; Wang, J.; Yao, Z.; Wang, S.; Kumar, S. G. H.; Ganapathy, S.; Eustace, S.; Bai, X.; Li, B.; Wagemaker, M. High Entropy Liquid Electrolytes for Lithium Batteries. Nat. Commun. 2023, 14 (1), 440. https://doi.org/10.1038/s41467-023-36075-1.

Buccal delivery system of active pharmaceutical ingredients-ionic liquid (API-IL): Effects of API-IL loading and gelatin film concentration

Ionic liquid (IL) salt of active pharmaceutical ingredient (API) represents a promising formulation strategy to address low drug solubility and polymorphism prevalent in API solid crystals. The present work developed for the first time a buccal delivery system of API-IL via fast-dissolving API-IL-loaded gelatin films. Imidazolium-based ibuprofen salt was used as the model API-IL. The effects of API-IL loading and gelatin concentration on the film’s (i) mechanical strength, (ii) inter-batch uniformity in the films’ API payload, weight, and thickness, (iii) thermal stability, (iv) API dissolution and solubility enhancement were investigated. The plasticizer role of API-IL was evident, where minimum 30 wt% API-IL loading was needed to produce flexible yet mechanically-strong films. Lower API-IL loading produced brittle films due to insufficient plasticization facilitated by hydrogen bond interactions between API-IL and gelatin. Gelatin concentration influenced films’ mechanical strength, weight/thickness, and API dissolution rate. Depending on the API-IL loading and gelatin concentration, films with API payload (7–30 mg/cm2), thickness (300–900 µm), and weight (20–110 mg/cm2) were produced at nearly 100% efficiency and high inter-batch uniformity. API-IL existed as amorphous liquid in the film exhibiting fast API dissolution (100% in 15 min) and high kinetic solubility (8 times thermodynamic solubility) in simulated saliva fluid.

Influence of TiO2 and SiO2 Nanoparticles on the Properties of Polymer Electrolytes Based on Ionic Liquid and Lithium Salt

Influence of TiO2 and SiO2 Nanoparticles on the Properties of Polymer Electrolytes Based on Ionic Liquid and Lithium Salt

Enhancing aromatics extraction by double salt ionic liquids: Rational screening‐validation and mechanistic insights

AbstractDespite offering remarkable advantages as solvents, double salt ionic liquids (DSILs) have been scarcely studied for extractive dearomatization from hydrocarbons as well as many other applications, thus urging a theoretical guidance method. In this work, a systematic framework combining the rational screening validation and mechanistic analysis is proposed for tailoring DSILs for the o‐xylene/n‐octane separation. From an initial pool of commercially available ionic liquids (ILs), key thermodynamic properties of paired DSILs are predicted by COSMO‐RS while their important physical properties are estimated from those of corresponding parent ILs (retrieved from experimental database or predicted by a deep learning model). Promising DSILs are tested by liquid–liquid equilibrium experiments, wherein the effect of ion ratio is also evaluated. The mechanism underlying the tunability of DSIL thermodynamic properties is disclosed by quantum chemistry calculation and molecular dynamics simulation. This work can be a valuable reference for guiding the design of DSILs for diverse applications.

A new potentiometric method of determining the ionization constant of water based on the ionic liquid salt bridge consisting of N-ethyl-N-heptylpyrrolidinium bis(pentafluoroethanesulfonyl)amide

The ionization constant of water, KW, has been determined potentiometrically by use of an ionic liquid salt bridge (ILSB) consisting of a moderately hydrophobic N-ethyl-N-heptylpyrrolidinium bis(pentafluoroethanesulfonyl)amide at 25°C. The value obtained for pKW = -log10(KW) on the assumption that the liquid junction potential across the ILSB inserted between aqueous ca. 0.001 mol dm−3 solutions of HCl and NaOH is negligible was 13.81 ± 0.01(STDEV), which is smaller than 13.9965, reported about 90 years ago [1,2], based on potentiometry of the cells claimed to be without liquid junction. The present results seem to challenge the unproven assumption of no liquid junction in the so-called Harned cells in that if our Ecell value were greater by 10 mV, pKW would have been in perfect agreement with their 13.99, although it is very difficult to expect such a substantial magnitude of potential difference across the ILSB; logically, one may expect the opposite case, that is, that their value bears ca. 10 mV surplus possibly due to the hidden liquid junctions in the Harned cell.Relevant physicochemical properties of N-ethyl-N-alkylpyrrolidinium+ (alkyl = pentyl, hexyl and heptyl) and its ionic liquids formed in combination with bis(pentafluoroethanesulfonyl)amide− at 25°C are also reported.