Magnetic Ionic Liquid Research Articles

Dispersive solid phase extraction of chloramphenicol and florfenicol in honey sample performed in narrow bore tube with the aid of magnetic ionic liquids prior to HPLC-DAD analysis

The precedence of high levels of antibiotics in animal-derived foods such as honey poses a significant food safety risk. Therefore, the development of an accurate, and reliable method for determining these residues is crucial. In this study, a new extraction method was proposed for the simultaneous determination of chloramphenicol and florfenicol residues in honey samples prior to high performance liquid chromatography analysis. The method involved using amino-functionalized UiO-66 metal–organic framework (NH2-UiO-66) as a sorbent in a narrow bore tube. To begin, the solution was placed into a narrow bore tube and the pH was adjusted to 6. Then, 100 mg of the sorbent was added to the solution. The particles were slowly passed through the solution and collected in the tube bottom. After removing the supernatant phase, 55 µL of 1-butyl-3-methylimidazolium tetrachloroferrate (III) magnetic ionic liquid was used as the elution solvent under sonication for 3 min. The optimized method exhibited low limits of detection (0.19 and 0.44 ng g−1) and quantification (0.63 and 1.4 ng g−1), good extraction recovery (81 and 74 %), and good linearity of the calibration curve (r2 ≥ 0.996) over the ranges of 1.2–500 and 2.4–500 ng g−1 for florfenicol and chloramphenicol, respectively. Precision was satisfactory, with relative standard deviations ≤8.1 % for both intra- and inter-day precisions. The developed method was done on ten honey samples and chloramphenicol was found in five samples.

Phase behavior of aqueous two-phase systems formed with cholinium-based magnetic ionic liquids: Experimental insights and theoretical correlations

In this work, three cholinium-based MILs were synthesized, characterized and successfully applied to construct the magnetically responsive aqueous two-phase system (ATPs). This ATPs combined the advantages of ILs and magnetic responsiveness, and showed great potential in the field of extraction and separation. Phase behavior for the magnetic ionic liquid aqueous two-phase systems (MIL-ATPSs) containing [N 1 1n 2OH] [TEMPO-OSO3] + salts + water was investigated experimentally at different temperatures. Merchuk equation was adopted to fit the experimental binodal data with satisfactory correlation performances. The effects of the structure of MILs, temperature and types of salts on the phase behavior were evaluated. Investigation on the phase separation mechanism showed that the phase formation was affected by the structure and viscosity of MILs. The salting-out effect is recognized as the major force for phase separation, which is closely related to the Gibbs free energy of hydration (ΔhydG) and entropy of hydration (ΔhydS) of salts. In addition, a larger biphasic area was obtained by increasing the temperature, indicating the phase separation process was endothermic and entropically driven. The binodal curve at different temperature confirms that this MIL-ATPs has low critical solution temperature (LCST) phase transition behavior. All these experimentally measured data and the theoretical correlations can provide meaningful and valuable information that may promote further research and application.

Regulating the N-functional hydrogen bond donors over magnetic nanoparticles supported imidazole tribromide zinc ionic liquid for CO2 cycloaddition

The design of catalysts for the mile production of cyclic carbonates by CO2 cycloaddition is of value. Magnetic polymer nanoparticles-supported imidazole tribromide zinc ionic liquid catalysts, incorporating N-functional hydrogen bond donors (HBD), was successfully accomplished. The correlation between the N-functional HBD and catalytic activity was thoroughly investigated through experimental studies and DFT calculations. The catalyst featuring a secondary amine group (NHM) demonstrated remarkable catalytic performance in CO2 cycloaddition reactions. Under optimized conditions, including 0.12 mol% catalyst dose, 100 °C, and nPO:nCO2 = 1:1.2 for 3 h, a complete conversion was achieved. The exceptional performance of the catalyst was attributed to the multicenter synergistic effect, arising from the appropriate electronegativity, minimal spatial site resistance, a balanced distance between the NHM and imidazolium ion, and the presence of multiple active centers (NHM, Zn2+, and Br−). The integration of a magnetic component enabled swift separation and exceptional recovery stability over 8 consecutive cycles.

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.

Effervescence tablets based on magnetic ionic liquids as simple microdevices for the in situ dispersive liquid-liquid microextraction of urinary biomarkers

BackgroundMagnetic ionic liquids (MILs) have been explored in dispersive liquid-liquid microextraction (DLLME). Their usage allows to substitute centrifugation and/or filtration steps by a quick magnetic separation. Besides, effervescence-assisted DLLME is one of the most known options to improve the dispersion of the extractant in the sample, while allowing to avoid the consumption of external energy during dispersion. Despite these interesting features, only one study incorporates MILs containing the tetrachloroferrate anion in effervescence tablets. These MILs are highly viscous and liquid at room temperature, thus compromising the stability of the tablets when used as extraction microdevices in effervescence-assisted DLLME, and only allowing their use in the conventional MIL-DLLME mode. ResultsA new class of effervescence tablets containing a Ni(II)-based MIL, that is solid at room temperature, is here proposed. This type of tablets permits their use, for first time, in the in situ DLLME mode, occurring through the transformation of a water-soluble MIL into a water-insoluble MIL microdroplet. This way, the tablet formulation included: the MIL, the metathesis reagent lithium bis[(trifluoromethyl)sulfonyl]imide, NaH2PO4 and K2CO3 as effervescence precursors salts, and Na2SO4 as salting-out and desiccating agent. The method is combined with high-performance liquid-chromatography and both fluorescence and ultraviolet detection, for the determination of monohydroxylated polycyclic aromatic hydrocarbons (OH-PAHs) and benzophenones (BPs), as biomarkers in urine. The method simply involved the addition of the effervescence tablet to the sample, thus taken place simultaneously the effervescence process and the metathesis reaction, without requiring any external energy consumption. The method presented limits of detection down to 10 ng L−1 for OH-PAHs and to 0.60 μg L−1 for BPs, inter-day relative standard deviations lower than 17 %, and average relative recoveries of 94 % in urine. The determined OH-PAHs contents in urine were between 0.40 and 16 μg L−1, and between 17.8 and 334 μg L−1 for BPs. SignificanceWe have developed the first MIL-based effervescence tablets that are completely solid, thus improving the stability and robustness of these microdevices with respect to previously reported tablets involving MILs, while permitting to perform into the in situ DLLME mode (thus gaining in extraction efficiency). This approach including the MIL-based effervescence tablets constitutes an alternative on-site platform for the analysis of urine, as satisfactory precision, accuracy, and sensitivity are achieved despite not involving any external energy input within the analytical sample preparation setup. This method also constitutes the first application of MIL-based effervescence tablets for bioanalysis.

Cost-effective Phytohormone Extraction of Sargassum swartzii from the Persian Gulf Using Magnetic Ionic Liquid.

Algae extracts are utilized as biofertilizers instead of chemical ferti-lizers in agriculture. Further, algae are known to possess a high content of plant hormones, such as gibberellin, salicylic acid, abscisic acid, and brassinosteroids. The main objective of this study was to increase the extraction yield and simulta-neously extract hormones required for plant growth from Sargassum swartzii using Magnetic recoverable ionic liquid (IL). In this study, extraction was performed by acidic digestion with acetic acid and then alkaline digestion with potassium hydroxide. The results showed the ionic liquid effect in extraction yield by 266 percent. The extracted phytohormones were analyzed using high-performance liquid chromatography (HPLC) methods. High levels of gibberellin, salicylic acid, abscisic acid, and brassinosteroids in improved algae extraction showed that seaweed extract could be used as environmentally friendly liquid bio-fertilizers to replace chemical fertilizers and could play a crucial role in organic farming for sustainable agriculture. Additionally, the recoverability of ionic liquid eight times with negligible leaching proved the introduced procedure to be cost-effective. The reported procedure for algae extraction improved by using an acidic/primary ionic liquid environment. This procedure is economical because of the simple reusability of ionic liquid due to its magnetic features.

Investigation of magnetic ionic liquids for selective and rapid extraction of gallic acid from complex samples using experimental, statistical modeling and density functional theory studies

Given the high antioxidant capacity of gallic acid (GA), there is a great deal of interest in the development of rapid, selective, simple, and easily accessible analytical methods for its determination from complex samples. Consequently, the present study aimed to develop an ultrasonic assisted magnetic ionic liquid-based dispersive liquid microextraction (UA-MIL-DLLME) method for the extraction of GA from various samples prior to its spectrophotometric detection. The method's key variables were optimized through statistical analysis. Four magnetic liquids (MILs) were prepared and tested to extract the GA-Se complex formed in aqueous solution. Both experimental studies and theoretical calculations demonstrated that the most suitable MIL for the phase separation of the relevant complex is [P6,6,6,14][Mn(hfacac)3]. The developed UA-MIL-DLLME method exhibited a wide linear range (5–400 ng mL-1), a remarkable enhancement factor (133), and a low limit of detection (1.6 ng mL-1). Additionally, high extraction recovery (97 ± 1%) with a low relative standard deviation (1.9%) was achieved. The extraction time for the UA-MIL-DLLME method was 8 min. The precision of the method was evaluated through repeatability and reproducibility studies. Finally, the UA-MIL-DLLME method was successfully applied to the extraction of the GA from complex samples using a reference method.

Versatile DNA extraction from diverse plant taxa using ionic liquids and magnetic ionic liquids: a methodological breakthrough for enhanced sample utility

BackgroundThere is a growing demand for fast and reliable plant biomolecular analyses. DNA extraction is the major bottleneck in plant nucleic acid-based applications especially due to the complexity of tissues in different plant species. Conventional methods for plant cell lysis and DNA extraction typically require extensive sample preparation processes and large quantities of sample and chemicals, elevated temperatures, and multiple sample transfer steps which pose challenges for high throughput applications.ResultsIn a prior investigation, an ionic liquid (IL)-based modified vortex-assisted matrix solid phase dispersion approach was developed using the model plant, Arabidopsis thaliana (L.) Heynh. Building upon this foundational study, the present study established a simple, rapid and efficient protocol for DNA extraction from milligram fragments of plant tissue representing a diverse range of taxa from the plant Tree of Life including 13 dicots and 4 monocots. Notably, the approach was successful in extracting DNA from a century old herbarium sample. The isolated DNA was of sufficient quality and quantity for sensitive molecular analyses such as qPCR. Two plant DNA barcoding markers, the plastid rbcL and nuclear ribosomal internal transcribed spacer (nrITS) regions were selected for DNA amplification and Sanger sequencing was conducted on PCR products of a representative dicot and monocot species. Successful qPCR amplification of the extracted DNA up to 3 weeks demonstrated that the DNA extracted using this approach remains stable at room temperature for an extended time period prior to downstream analysis.ConclusionsThe method presented here is a rapid and simple approach enabling cell lysis and DNA extraction from 1.5 mg of plant tissue across a broad range of plant taxa. Additional purification prior to DNA amplification is not required due to the compatibility of the extraction solvents with qPCR. The method has tremendous potential for applications in plant biology that require DNA, including barcoding methods for agriculture, conservation, ecology, evolution, and forensics.

Investigating a new approach for magnetic ionic liquids: Dispersive liquid-liquid microextraction coupled to pyrolysis gas-chromatography-mass spectrometry to determine flame retardants in sewage sludge samples

This study addresses the analysis of emerging contaminants, often using chromatographic techniques coupled to mass spectrometry. However, sample preparation is often required prior to instrumental analysis, and dispersive liquid-liquid microextraction (DLLME) is a viable strategy in this context. DLLME stands out for its ability to reduce sample and solvent volumes. Notably, dispersive liquid-liquid microextraction using magnetic ionic liquids (MILs) has gained relevance due to the incorporation of paramagnetic components in the chemical structure, thereby eliminating the centrifugation step. A pyrolizer was selected in this work to introduce sample onto the GC column, since the MIL is extremely viscous and incompatible with direct introduction through an autosampler. This study is the first to report the use of a DLLME/MIL technique for sample introduction through a pyrolizer in gas chromatography coupled to mass spectrometry (GC–MS). This approach enables the MIL to be compatible with gas chromatography systems, resulting in optimized analytical and instrument performance. The analysis of polybrominated diphenyl ether flame retardants (PBDEs) was focused on the PBDE congeners 28, 47, 99, 100, and 153 in sewage sludge samples. The [P6,6,6,14+]2[MnCl42−] MIL was thoroughly characterized using UV–Vis, Fourier transform infrared spectroscopy (FTIR), and Raman spectroscopy, as well as thermal analysis. In the chromatographic method, a pyrolyzer was used in the sample introduction step (Py-GC–MS), and critical injection settings were optimized using multivariate approaches. Optimized conditions were achieved with a temperature of 220 °C, a pyrolysis time of 0.60 min, and an injection volume of 9.00 μL. DLLME optimization was performed through central compound planning (CCD), and optimized training conditions were achieved with 10.0 mg of MIL, 3.00 μL of acetonitrile (ACN) as dispersive solvent, extraction time of 60 s, and volume of a sample of 8.50 mL. Precision was observed to range from 0.11 % to 12.5 %, with limits of detection (LOD) of 44.4 μg L−1 for PBDE 28, 16.9 μg L−1 for PBDE 47 and PBDE 99, 33.0 μg L−1 for PBDE 100 and 375 μg L−1 for PBDE 153. PBDE 28 was identified and analyzed in the sludge sample at a concentration of 800 μg L−1. The use of MIL in dispersive liquid-liquid microextraction combined with pyrolysis gas chromatography-mass spectrometry enables identification and quantification of PBDEs in sewage sludge samples at concentrations down to the µg L−1 level.

Combination of a magnetic ionic liquid and magnetic particles for the determination of Pb(II) and Sn(IV) using electrothermal atomic absorption spectrometry

A procedure for the determination of traces of lead and tin by electrothermal atomic absorption spectrometry (ETAAS) after complexation with diethyl dithiophosphate and preconcentration by using a microextraction stage with a magnetic ionic liquid (MIL) supported by ferrite particles is presented. After complexation, the analytes are extracted into the ferrite-supported MIL, the solid particles acting as a carrier to facilitate the separation with a magnet. The analytes are released by treating with acetonitrile and the resulting liquid phase is sampled for the ETAAS measurement. The optimal experimental conditions such as pH, appropriate complexing agent, volumes and doses of all reagents used in the procedure are studied to achieve complete separation of both species. Enrichment factors of 195 and 165 and detection limits of 25 and 72 ng L−1 are obtained for Pb and Sn, respectively. The reliability of the procedure is checked by analyzing six certified reference materials and applied to water samples of different origin, the results being in addition confirmed by standard additions (recoveries 97 ± 7% in all cases).

MOF@N–doped carbon dots–based dispersive solid phase extraction combined dispersive liquid–liquid microextraction of several aflatoxins from raw cow’s milk samples prior to HPLC–FLD

A dispersive solid-phase extraction method based on metal–organic framework and nitrogen–doped carbon dot nanocomposite combined with magnetic ionic liquid-based dispersive liquid–liquid microextraction was established for the extraction of aflatoxins from milk samples. For this purpose, the proteins in the sample were precipitated using a zinc sulfate solution. After vortexing (for 5 min) and centrifuging, 35 mg of the sorbent were added into the aqueous phase obtained from previous step, and the mixture was vortexed for five minutes. In the following, the sorbent particles were separated and eluted with methanol in the presence of vortex agitation (4 min). After centrifuging, the eluent phase was mixed with magnetic ionic liquid (1- octyl-3-methylimidazolium tetrachloroferrate) and rapidly injected into deionized water to perform the dispersive liquid–liquid microextraction procedure. Finally, the magnetic solvent was separated in the presence of a magnet and injected into a high-performance liquid chromatography-fluorescence detector after diluting with the mobile phase. Referring to the results, the limits of detection and quantification of the studied aflatoxins were in the ranges of 0.69–1.09 and 2.31–3.63 ng/L, respectively. Extraction recoveries were in the range of 61 to 73 %. At the end, the suggested approach was employed in the analysis of the aflatoxins in the raw cow’s milk samples collected from different regions of East Azarbaijan and AFM1 was found in several samples (34 out of 60 samples). Also, AFB1 was found in three samples.

Theoretical Calculation of Different Side-Chain Lengths [Cnmim]FeCl4 and Factors Influencing Coal Pyrolysis Swelling Modification.

With the increasing requirements for clean and effective utilization, coal swelling pretreatment provides a good theoretical basis for coal molecular structure, application in coal pyrolysis, and liquefaction. Ionic liquids containing magnetic anionic groups were designed, synthesized, and used as solvents to study the effect on swelling pyrolysis performance. Studies have shown magnetism enhancement with the growth of alkyl chains. The growth of the MIL alkyl side chain made the modification effect of coal more obvious, and the swelling degree showed a trend of first increasing and then decreasing with the increase of temperature and time, and at the temperature of 35 °C, the swelling degree is the largest when the modification time is 8 h. Pyrolysis experiments show that magnetic ionic liquid (MIL) pretreatment can significantly reduce the temperature at the maximum weight loss of coal and increase the tar content of pyrolysis, indicating that MIL plays a catalytic cracking role in coal pyrolysis.

Extraction of poly aromatic hydrocarbons (PAHs) using magnetic ionic liquids (MILs) as extractive materials from water samples

Herein two magnetic ionic liquids (MILs), [P66614]2[CoCl4] and [P66614]3 [DyCl6], were synthesized and evaluated as extractive materials in a micro liquid extraction procedure (MLE) to remove polycyclic aromatic hydrocarbons (PAHs) present in water samples. The extraction capacity of evaluated PAHs was studied at different conditions such as pH, extraction time, MIL mass, PAH concentration and ionic strength. Both synthesized MILs demonstrated successful extraction of the five evaluated PAHs. Optimal extraction conditions were achieved at pH = 2, 60 min, and 7.5 % NaCl and 15 mg for [P66614]2[CoCl4] and 10 % NaCl, and 100 mg of [P66614]3[DyCl6] for each of PAH. Finally, recovery and reuse of the MILs was evaluated. In this study, only [P66614]2[CoCl4] was recovered successfully without the presence of any PAH and used successfully in future extractions. Recovered [P66614]2[CoCl4] was used for five consecutive extractions with an extraction efficiency of the Pyrene above 99 %. These MILs effectively extracted five PAHs from aqueous samples and proved to be recyclable for up to five extraction cycles. These MILs have a high potential to be employed as extractive materials for remediation purposes.

Investigation of different solvents for selective, safe and rapid extraction of curcumin from various food and herbal supplement products: Multivariate strategy and assessment of green profile

In the paper, different extraction solvents including magnetic ionic liquids (MILs), deep eutectic solvents, SUPRAS and surfactant were investigated for the fast, reliable and simple extraction of curcumin in the dispersive liquid–liquid microextraction (DLLME) method prior to UV–Vis spectrophotometric analysis. As a result of preliminary studies, the [Co(C8IM)42+]2[Cl−] MIL was selected as the extraction solvent for the extraction of curcumin from various matrix samples. Optimization of essential factors in the DLLME method was carried out with central composite design (CCD). Effective dispersion of the [Co(C8IM)42+]2[Cl−] MIL in the sample solution was achieved by orbital shaking (OS). After the CCD modelling, the OS-MIL-DLLME method provided linearity in the range of 0.5–225 ng mL−1 with a detection limit of 0.15 ng mL−1 for the model solution. The OS-MIL-DLLME method showed a matrix effect of 7.6 % with an enrichment factor of 135. Validation parameters of the OS-MIL-DLLME method such as selectivity, robustness, intraday/interday precision and recovery test were investigated in detail. The green analytical scale of the method was determined using the analytical greenness calculator tool. The OS-MIL-DLLME method was applied to the foods and herbal supplement products together with the reference method, and quantitative recoveries and statistically reliable results were obtained.

Facile synthesis of magnetic ionic liquid with magnetic tuning electrochemical performance

Facile synthesis of magnetic ionic liquid with magnetic tuning electrochemical performance

Exploring a new generation of bimetallic magnetic ionic liquids with ultra-low viscosity in microextraction that enable direct coupling with high-performance liquid-chromatography

BackgroundThe incorporation of bimetallic magnetic ionic liquids (MILs) in microextraction methods is an emerging trend due to the improved magnetic susceptibility offered by these solvents, which relies on the presence of metallic components in both the cation and the anion. This feature favors easy magnetic separation of these solvents in analytical sample preparation strategies. However, reported liquid-phase microextraction methods based on bimetallic MILs still present an important drawback in that the MILs are highly viscous, making a dispersive solvent during the microextraction procedure necessary, while also requiring a tedious back-extraction step prior to the chromatographic analysis. ResultsWe propose for the first time a new generation of ultra-low viscosity bimetallic MILs composed of two paramagnetic Mn(II) complexes characterized by their easy usage in dispersive liquid-liquid microextraction (DLLME). The approach does not require dispersive solvent and the MIL-DLLME setup was directly combined with high-performance liquid chromatography (HPLC) and fluorescence detection (FD), without any back-extraction step. The approach was evaluated for the determination of five monohydroxylated polycyclic aromatic hydrocarbons, as carcinogenic biomarkers, in human urine. Optimum conditions of the MIL-DLLME method included the use of a low MIL volume (75 μL), a short extraction time (5 min), and no need of any dispersive solvent neither NaCl. The method presented limits of detection down to 7.50 ng L−1, enrichment factors higher than 17, and provided inter-day relative standard deviation lower than 11%. Analysis of urine samples was successfully performed, with biomarker content found at levels between 0.24 and 7.8 ng mL−1. SignificanceThis study represents the first liquid-phase microextraction method using the new generation of low-viscous bimetallic MILs. The proposed MIL-DLLME approach represents 2 important advances with respect to previous methods employing bimetallic MILs: 1) no dispersive solvent is required, and 2) direct injection of the MIL in the HPLC is possible after minor dilution (no back extraction steps are required). Therefore, the microextraction strategy is simple, rapid, and consumes very small amounts of energy.

Magnetic Ionic Liquids: Current Achievements and Future Perspectives with a Focus on Computational Approaches.

Magnetic ionic liquids (MILs) stand out as a remarkable subclass of ionic liquids (ILs), combining the desirable features of traditional ILs with the unique ability to respond to external magnetic fields. The incorporation of paramagnetic species into their structures endows them with additional attractive features, including thermochromic behavior and luminescence. These exceptional properties position MILs as highly promising materials for diverse applications, such as gas capture, DNA extractions, and sensing technologies. The present Review synthesizes key experimental findings, offering insights into the structural, thermal, magnetic, and optical properties across various MIL families. Special emphasis is placed on unraveling the influence of different paramagnetic species on MILs' behavior and functionality. Additionally, the Review highlights recent advancements in computational approaches applied to MIL research. By leveraging molecular dynamics (MD) simulations and density functional theory (DFT) calculations, these computational techniques have provided invaluable insights into the underlying mechanisms governing MILs' behavior, facilitating accurate property predictions. In conclusion, this Review provides a comprehensive overview of the current state of research on MILs, showcasing their special properties and potential applications while highlighting the indispensable role of computational methods in unraveling the complexities of these intriguing materials. The Review concludes with a forward-looking perspective on the future directions of research in the field of magnetic ionic liquids.

Experimental and numerical study of the mixed lubrication under the action of magnetic ionic liquid additives

In this paper, the tribological characteristics of an oil-soluble magnetic fluid additive under mixed lubrication are studied by experiments and numerical simulation. [bmim][FeCl4] is dissolved in CF10W-40 lubricating oil as a magnetic liquid additive, and its friction coefficient is tested by a point contact friction tester at different temperatures, rotational speeds and magnetic field intensities. The transition condition of lubrication state is obtained through analyzing the Stribeck curves based on the experiments, and the strength model of boundary film is established accordingly. A mixed lubrication model is established by substituting the boundary film strength model and the surface roughness model into the hydrodynamic lubrication model based on Reynolds equation. The results show that the magnetic solution as an additive can obviously reduce friction and wear, and the effect is more obvious under the condition of magnetic field. The boundary film strength model can accurately reflect the transition characteristics of lubrication state in the presence of boundary film, and the mixed lubrication model based on boundary film strength model can more precisely reflect the tribological characteristics of friction pairs, so this study provides a new theoretical method for the related research on the influence of boundary film on lubrication characteristics.

Simple Magnetic Polymeric Ionic Liquid Nanocomposite Coated Hollow Fiber Membrane for the Determination of Lead (II) and Copper (II) in Water and Fruit Juice with Microinjection Sampling-Flame Atomic Absorption Spectrometry (MIS-FAAS)

A novel and effective adsorbent based on magnetic polymeric ionic liquid nanocomposite-coated hollow fiber membrane (MPILNC-HFM) was developed and applied for magnetic solid phase extraction of Pb (II) and Cu (II) from environmental water and fruit juice samples with microinjection sampling-flame atomic absorption spectrometry (MIS-FAAS). During extraction process, the adsorbent coated on the surface of the hollow fiber can be removed from the solution using tweezers without using a magnet. Additionally, the need to use a centrifuge during adsorption and desorption steps is also eliminated, thereby increasing the speed, simplicity, and efficiency of the extraction process. The nanocomposite characterized through Fourier-transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy-dispersive x-ray (EDX) analyses to ensure its applicability. The experimental parameters were optimized by applying one-variable-at the-time (OVAT) approach. Under optimal conditions, limits of detection were achieved 16.5 µg L−1 for Pb (II) and 20.4 µg L−1 for Cu (II), respectively, with relative standard deviations up to 7.9% and relative recoveries in the range of 91.8%–02.2%.

Critical assessment of interactions between ct-DNA and choline-based magnetic ionic liquids: evidences of compaction.

Ionic liquids (ILs) have become an alternative green solvent for storage and for stability of DNA. However, an in-depth understanding of binding and molecular interactions between ILs and DNA is needed. In this respect, magnetic ILs (MILs) are promising due to their tunable physicochemical properties. Various spectroscopic techniques and molecular simulations have been employed to unravel the critical factors of the strength and binding mechanism of MILs with DNA. UV-vis spectra unravel the multimodal binding of MILs with DNA, and the intrusion of IL molecules into the minor groove of DNA has been observed from dye displacement studies. Fluorescence correlation spectroscopic studies and scanning electron microscopy confirm the compaction of the DNA. ITC and molecular docking studies estimate the binding affinity of DNA with MILs, of ∼7 kcal mol-1. The 1 μs long-MD simulations give insight into the structural changes in the DNA in the MIL environment. Due to strong interaction with choline ions in the close vicinity, DNA helixes bend or squeeze in length and dilate in diameter (elliptical → spherical), leading to compaction. The post-MD parameters suggest a stronger interaction with [Ch]2[Mn] IL than with [Ch][Fe] IL; hence, the former induces DNA compaction to a more significant extent. Furthermore, decompaction is observed with the addition of sodium salts and is characterized using spectroscopic methods.