Ionic Liquid Research Articles

Preparation of Porous Imidazole-based Poly(ionic liquid) Adsorbents and Their Toluene Adsorption Performance

Preparation of Porous Imidazole-based Poly(ionic liquid) Adsorbents and Their Toluene Adsorption Performance

Design of Ionic Liquids for HF/HFC-245fa Superefficient Separation: COSMO-RS Selection and Process Assessment

Design of Ionic Liquids for HF/HFC-245fa Superefficient Separation: COSMO-RS Selection and Process Assessment

A Bubble Column Dehumidifier using Ionic Liquid Desiccant for Low-Humidity Industries: Insights into Transfer Processes Integrating Experiment and CFD Modelling

A Bubble Column Dehumidifier using Ionic Liquid Desiccant for Low-Humidity Industries: Insights into Transfer Processes Integrating Experiment and CFD Modelling

Mechanistic Understanding of the Underlying Energy Storage Mechanism of α‐MnO2‐based Pseudo‐Supercapacitors

AbstractManganese dioxide (α‐MnO2) has attracted significant research interest in supercapacitors recently. However, the reaction mechanism of α‐MnO2 in supercapacitors remains unclear. Therefore, a nano‐supercapacitor using Environmental transmission electron microscopy (ETEM) is conducted and investigated the reaction mechanism of α‐MnO2 based on three ionic liquids (ILs). It found that in the aprotic ionic liquid (AIL) 1‐ethyl‐3‐methylimidazolium trifluoromethanesulfonate (EMIMOTF), α‐MnO2 nanowires (NWs) undergo an oxidation reaction due to the presence of an active proton at the second position (H2) of the imidazole ring. As a result, α‐MnO2 NWs undergo a phase transition and transform into Mn3O4, exhibiting pseudo‐capacitive properties. Furthermore, characterization of the macroscopic α‐MnO2 electrodes after cycling reveals that after the initial charging cycles, the dominant energy storage mechanism of the supercapacitor transitions from pseudo‐capacitance to a dual‐layer capacitance formed by the combination of Mn3O4 and unreacted α‐MnO2. Simultaneously, due to the coexistence of these two energy storage mechanisms, the specific capacitance of the supercapacitor in EMIMOTF electrolyte reaches up to 80 F g−1, and the cycle number reaches as high as 1000 cycles. The results are expected to provide insights into the selection of electrolytes in supercapacitors and offer a fundamental understanding of the internal reaction mechanisms in capacitors.

Modulating the Conductivity of Light-Responsive Ionic Liquid Crystals

Modulating the Conductivity of Light-Responsive Ionic Liquid Crystals

Exploring the Recognition Mechanism of Surfactant–Cyclodextrin Complex Formation: Insights from SPR Studies on Temperature and Ionic Liquid Influence

Exploring the Recognition Mechanism of Surfactant–Cyclodextrin Complex Formation: Insights from SPR Studies on Temperature and Ionic Liquid Influence

Recent Advances in Synthesis, Properties, and Applications of Magnetic Ionic Liquids: A Review

AbstractMagnetic ionic liquids (MILs) are a subclass of ionic liquids that exhibit paramagnetic properties intrinsically, without the need for additional magnetic particles. These properties can be attributed to the cations, anions, or both. Typically, MILs incorporate transition or inner‐transition metals within the anion structure. These adaptable liquids demonstrate remarkable physicochemical properties, notably a robust response to external magnetic fields. The body of research concerning the synthesis, characterization, and practical applications of MILs has expanded swiftly in recent times. This review delves into the latest research on the synthesis, properties, and utilization of MILs across various domains, including catalysis, fluid‐fluid separation, polymer science, and analytical chemistry. Within the realm of analytical chemistry, MILs are pivotal, serving as solvents in various analytical procedures such as dispersive liquid‐liquid micro‐extraction, matrix solid‐phase dispersion, and single‐drop micro‐extraction. Owing to their paramagnetic nature, MILs are instrumental in the separation process, streamlining organic reactions by obviating the need for traditional extraction or centrifugation steps.

1H, 13C, 15N NMR, and DFT Studies on Complex Formation of Zinc(II) Ion with Ethylenediamine in Ionic Liquid [C2mIm][TFSA

¹H, ¹³C, ¹⁵N NMR, and DFT Studies on Complex Formation of Zinc(II) Ion with Ethylenediamine in Ionic Liquid [C₂mIm][TFSA

Regenerated nanofibrous cellulose electrospun from ionic liquid: Tuning properties toward tissue engineering.

Regenerated fibrous cellulose possesses a unique set of properties, including biocompatibility, biodegradability, and high surface area potential, but its applications in the biomedical sector have not been sufficiently explored. In this study, nanofibrous cellulose matrices were fabricated via a wet-electrospinning process using a binary system of the solvent ionic liquid (IL) 1-butyl-3-methylimidazolium acetate (BMIMAc) and co-solvent dimethyl sulfoxide (DMSO). The morphology of the matrices was controlled by varying the ratio of BMIMAc versus DMSO in the solvent system. The most effective ratio of 1:1 produced smooth fibers with diameters ranging from 200 to 400 nm. The nanofibrous cellulose matrix showed no cytotoxicity when tested on mouse fibroblast L929 cells whose viability remained above 95%. Human triple-negative breast cancer MDA-MB-231 cells also exhibited high viability even after 7 days of seeding and were able to penetrate deeper layers of the matrix, indicating high biocompatibility. These properties of nanofibrous cellulose demonstrate its potential for tissue engineering and cell culture applications.

Multifunctional Guanidine Ionic Liquid with Lactate Anion-Assisted Crystallization and Defect Passivation for High-Efficient and Stable Perovskite Solar Cells

Multifunctional Guanidine Ionic Liquid with Lactate Anion-Assisted Crystallization and Defect Passivation for High-Efficient and Stable Perovskite Solar Cells

Ionic Liquid/Deep Eutectic Solvent-Mediated Calcining Synthesis of Cobalt-Based Electrocatalysts for Water Splitting

The recent advancements of ionic liquids (ILs) and deep eutectic solvents (DESs) in the synthesis of cobalt-based catalysts for water splitting is reviewed. ILs and DESs possess unique physical and chemical properties, serving as solvents, templates, and reagents. Combined with calcination techniques, their advantages can be fully leveraged, enhancing the stability and activity of resulted catalysts. In these solvents, not only are they suitable for simple one-step calcination, but also applicable to more complex multi-step calcination, suitable for more complex reaction conditions. The designability of ILs and DESs allows them to participate in the reaction as reactants, providing metal and heteroatoms, simplifying the preparation system of cobalt phosphide, sulfide, and nitride. This work offers insights into design principles for electrocatalysts and practical guidance for the development of efficient and high-performance materials for hydrogen production and energy storage systems.

Ionic liquids based azeotropic separation of refrigerants R410A (R32+R125) and R508B (R23+R116) through hybrid extractive distillation

ABSTRACT The increment in GreenHouse Gases (GHGs) promotes high Global Warming Potential (GWP) due to the production and consumption of hydrofluorocarbons (HFCs) that diverts the aim toward the recycling and reclaiming of refrigerant gases. However, the presence of azeotrope in refrigerant mixtures restricts the recycling process. Therefore, in this work, the refrigerant R410A and R508B have been separated through the hybrid extractive distillation method by using [HMIM][TF2N] and [BMIM][BF4] as a solvent in ASPEN Plus. UNIFAC model has been used for the correlation of ionic liquid in ASPEN Plus. For thermodynamic properties, Cosmotherm has been used with the collaboration of TurbromoleX. The Vapor-liquid Equilibrium (VLE) data has been predicted by using the UNIFAC group contribution method. The Total Annual Cost (TAC) analysis with optimization has been performed. Besides that, the energy analysis has also been performed. In the overall separation process and (TAC) analysis, [BMIM][BF4] proves to be more efficient with high separation efficiency and minimal TAC requirements. Whereas, [HMIM][TF2N]/R508B provides less CO2 emission.

Charge Delocalization for Electrically Detachable Poly(ionic liquids) Ionoadhesives with Ultrahigh Mechanical Robustness

Charge Delocalization for Electrically Detachable Poly(ionic liquids) Ionoadhesives with Ultrahigh Mechanical Robustness

Surface Charge Regulation of Graphene by Fluorine and Chlorine Co-Doping for Constructing Ultra-Stable and Large Energy Density Micro-Supercapacitors.

Settling the structure stacking of graphene (G) nanosheets to maintain the high dispersity has been an intense issue to facilitate their practical application in the microelectronics-related devices. Herein, the co-doping of the highest electronegative fluorine (F) and large atomic radius chlorine (Cl) into G via a one-step electrochemical exfoliation protocol isengineered to actualize the ultralong cycling stability for flexible micro-supercapacitors (MSCs). Density functional theoretical calculations unveiled that the F into G can form the "ionic" C─F bond to increase the repulsive force between nanosheets, and the introduction of Cl can enlarge the layer spacing of G as well as increase active sites by accumulating the charge on pore defects. The co-doping of F and Cl generates the strong synergy to achieve high reversible capacitance and sturdy structure stability for G. The as-constructed aqueous gel-based MSC exhibited the superb cycling stability for 500,000 cycles with no capacitance loss and structure stacking. Furthermore, the ionic liquid gel-based MSC demonstrated a high energy density of 113.9mWhcm-3 under high voltage of up to 3.5V. The current work enlightens deep insights into the design and scalable preparation of high-performance co-doped G electrode candidate in the field of flexible microelectronics.

Nitric oxide shifts the impact of ionic liquid on microbial community structure in rhizosphere of Arabidopsis

ABSTRACT Ionic liquids (ILs) are widely used in various fields due to their excellent properties. Despite their utility, there is limited knowledge regarding the phytotoxic properties of ILs and the mechanisms by which plants develop resistance to them. This is particularly true when considering the role of nitric oxide (NO) in response to ILs stress. Herein, we investigated the mechanism by which endogenous NO reduces the ILs’ phytotoxicity in Arabidopsis from the perspective of rhizosphere microorganisms. We investigated the impact of 1,3-dibutyl imidazole bromide (DIB) on microbial diversity and community in the rhizosphere of Arabidopsis lines with varying endogenous NO levels, using a high throughput sequencing method. DIB did not affect microbial taxon numbers, richness, or evenness; however, it did alter microbial beta diversity and community structure in the rhizosphere of Arabidopsis. Elevated endogenous NO increased fungal richness and evenness, shifted DIB’s impact on microbial community structure, and enriched more resistant species and toxin-decomposing species. These findings suggest a potential mechanism for plants to resist IL stress. Our study not only elucidates the toxicological mechanisms of ILs but also reveals the involvement of NO in plant responses to IL stress, providing valuable insights for future environmental risk assessments and mitigation strategies.

High Strength and Tough Ionogels with Bicontinuous Phase Network Structure Induced by Electrostatic Adsorption Triggered Microphase Separation

AbstractA simple one‐step approach is presented to fabricate high strength and tough ionogels by copolymerizing zwitterionic monomers and monomers rich in functional groups capable of forming hydrogen bonds within an ionic liquid. The electrostatic adsorption of ionic liquid by the polyzwitterionic segment induces the formation of a bicontinuous phase network structure consisting of a polymer‐rich phase and a solvent‐rich phase. Within this structure, a polymer‐rich phase with hydrogen bonds dissipates energy and enhances the toughness of the ionogel, while an elastic solvent‐rich phase facilitates significant strain. The prepared ionogels exhibit high fracture strength (8.89 MPa), toughness (41.12 MJ m−3), and Young's modulus (58.9 MPa). The critical point for triggering the formation of a bicontinuous phase network can be precisely controlled by the maximum adsorption capacity of the zwitterionic monomers for the ionic liquid. Ionogels at the critical point of bicontinuous phase network formation demonstrate excellent fatigue resistance, with residual strain of only ≈25% under 50% to 250% strain conditions, recovering to their original state within 5 s. Due to the widespread presence of electrostatic interactions, this strategy for constructing a bicontinuous phase network structure exhibits excellent adaptability across different ionic liquid systems.

Ionic Liquid Crystals as Chromogenic Materials

Ionic liquid crystals (ILCs), a class of soft matter materials whose properties can be tuned by the wise pairing of the cation and anion, have recently emerged as promising candidates for different applications, combining the characteristics of ionic liquids and liquid crystals. Among those potential uses, this review aims to cover chromogenic ILCs. In this context, examples of photo-, electro- and thermochromism based on ILCs are provided. Furthermore, thermotropic and lyotropic ionic liquid crystals are also summarised, including the most common chemical and phase structures, as well as the advantages of confining these materials. This manuscript also comprises the following main experimental techniques used to characterise ILCs: Differential Scanning Calorimetry (DSC), Polarised Optical Microscopy (POM) and X-Ray Powder Diffraction (XRD). Chromogenic ILCs can be interesting smart materials for energy and health purposes.

Synergic Effects of Ordered Mesoporous Bifunctional Ionic Liquid: A Recyclable Catalyst to Access Chemoselective N-Protected Indoline-2,3-dione Analogous

SBA-15 and organic ionic liquid were incorporated in a post-grafting technique for generating a bifunctional ionic liquid embedded mesoporous SBA-15. The prepared heterogeneous catalyst was employed for the first time to synthesize N-alkylated indoline-2,3-dione at mild conditions to afford excellent yields in a short reaction time. The synthesized DABCOIL@SBA-15 catalyst was meticulously characterized by various techniques, such as FT-IR, solid-state 13C NMR, solid-state 29Si NMR, small-angle X-ray diffraction (XRD), and N2 adsorption–desorption. Further, the morphological behavior of the catalyst was studied by SEM and TEM. The thermal stability and number of active sites were determined by thermogravimetric analysis (TGA). The Hammett equation was used to analyze the synergetic effect of the catalyst and substituent effects on the N-alkylated products of 5-substituted isatin derivatives, which resulted in a negative slope. This negative slope indicates a positive charge in the transition state. Notably, the DABCOIL@SBA-15 catalyst demonstrated its practicality by being reused for seven cycles with consistently high catalytic activity.

BPBSBDM as an influential Brønsted acidic ionic liquid catalyst in preparing bis(pyrazolyl)methanes under mild conditions

BPBSBDM as an influential Brønsted acidic ionic liquid catalyst in preparing bis(pyrazolyl)methanes under mild conditions

Hydrophilicity Dependent Distribution of Water at Ionic Liquids/Metal Interface Monitored by Electrochemical SERS.

The understanding of the interfacial processes is critically important for extending the practical application of ionic liquids, particularly for the role of interfacial water. In the electrochemical system based on ionic liquid electrolytes, small amounts of water at the interface generate a significant change in the electrochemical behaviors of ionic liquids. Therefore, the investigation on the interfacial behavior of water is highly desired in ionic liquids with different anions, water content, and hydrophilicity. Herein, based on the probe strategy, in situ surface enhanced Raman spectroscopy (SERS) combined with electrochemical control (EC-SERS) was developed to investigate the influence of hydrophilicity/hydrophobicity of ionic liquids on the interfacial water. The water-sensitive transformation reaction of 4,4'-dimercaptoazobenzene (DMAB) to para-aminothiophenol (PATP) was employed as a probe reaction for investigating the behavior of interfacial water. The changes of relative SERS intensities of DMAB to PATP served as an indication of the quantity variation of interfacial water. The results show that the transformation reaction efficiencies were critically dependent on the additional water contents, potential, and hydrophilicity of ionic liquids. With a very low molar fraction of additional water (Xw = 0.01), transformation efficiency of DMAB (the amount of interfacial water) followed the sequence of [BMIm]BF4 < [BMIm]PF6 < [BMIm]Tf2N. It was in agreement with the hydrophobicity order of the ionic liquids. With the increase in additional water content, the potential for the full transformation was positively moved, and the efficiency increased significantly. The stronger hydrophobicity allowed more water molecules to migrate to the interface, which was attributed to the difference in interactions between water and the anions of ionic liquids. It demonstrated that the small amount of water tended to gather at the interface in hydrophobic ionic liquids. Compared to traditional cyclic voltammetry, the EC-SERS technique combined with probe reactions is more sensitive to interfacial water. It is anticipated to develop as a promising tool for the investigating water-related issues at interfaces and to provide guidance to screen ionic liquids for practical application.