Ionic Phase Research Articles

Influence of ionic liquid film thickness and flow rate on macrocyclization efficiency and selectivity in supported ionic liquid-liquid phase catalysis.

Supported ionic-liquid phase (SILP) technology in a biphasic setting with n-heptane as the transport phase was applied to the Ru-alkylidene-N-heterocyclic carbene (NHC) catalyzed macrocyclization of α,ω-dienes to elucidate the effect of ionic liquid (IL)-film thickness, flow rate as well as substrate and product concentration on macrocyclization efficiency, and Z-selectivity. To understand the molecular-level behavior of the substrates and products at the n-heptane/IL interphase, atomistic molecular dynamics simulations were conducted and correlated with experimental observations. The thickness of the IL layer strongly influences the Z/E ratio of the products in that a thin IL layer favors higher Z/E ratios by confining the catalyst between the pore wall and the liquid-liquid interphase whereas a thick IL layer favors formation of the E-product and Ru-hydride catalyzed isomerization reactions. Also, macrocyclization efficiency, expressed by the ratio of oligomers/macromonocycle (O/MMC), is influenced both by the flow rate and the thickness of the IL layer.

Experimental and theoretical investigation of a novel multi-amino-functionalized ionic phase change absorbent for highly efficient CO2 capture

A great potential for CO2 capture is that combining the advantages of both the structural tunability of functionalized ionic liquids and low energy consumption of phase change absorbent. In this study, a novel multi-amino groups functionalized ionic liquids [TEPAH][Lys] was synthesized and dissolved in NPA and H2O to achieve high absorption loading with low energy consumption. The experimental results demonstrated that the [TEPAH][Lys]/NPA/H2O exhibited a remarkable CO2 absorption loading of 2.93 mol CO2 ·mol absorbent−1 with 97.54 % of the CO2 products were concentrated in the lower phase, while the volume fraction was only 38 %. Meanwhile, the lower phase displayed low viscosity and excellent fluidity. The first desorption efficiency was as high as 81.19 % when the volume ratio of the added upper phase to the lower phase is 26.32 %, and the recycling efficiency could maintain above 81.15 % after fifth absorption–desorption cycles.13C NMR analysis revealed that the [TEPAH][Lys]/NPA/H2O absorbent was able to react with CO2, the CO2 products of carbamate, protonated amine, and propyl carbonates were presented only in the lower phase while the upper phase was almost exclusively NPA. The quantum chemical calculations revealed that CO2 products have greater polarity and density, resulting in higher solubility in water than NPA. The energy consumption was estimated as 2.60 GJ·ton-1 CO2, which was approximately 33.50 % lower than that of 30 % MEA (3.91 GJ·ton-1 CO2) under similar conditions. Overall, [TEPAH][Lys]/NPA/H2O phase change absorbent exhibits high CO2 absorption loading and low energy consumption, making it extremely potential for industrial carbon capture applications.

Enhancing Li4Ti5O12 Anodes for High‐Performance Batteries: Ti3+ Induction via Plasma‐Enhanced Chemical Vapor Deposition and Dual Carbon/LLZO Coatings

AbstractLithium titanium oxide (LTO) is a promising anode material due to its ability to store lithium through intercalation reactions. However, its electrochemical performance is limited by poor electron conductivity and side reactions with the electrolyte. In this study, plasma‐enhanced chemical vapor deposition (PECVD) is employed to introduce oxygen vacancies and self‐doped Ti3+ into LTO to improve the internal conductivity. Subsequent carbon coating and aluminum‐doped lithium lanthanum zirconate garnet (LLZO) layers resulted in a multi‐layered composite denoted as LTO−L‐x. Morphological analyses using SEM and TEM demonstrated the successful growth of Al‐doped LLZO on carbon‐coated LTO. Aluminum ions in LLZO cubic structure are crucial for stabilizing the high ionic conductive phase during cooling, as confirmed by X‐ray diffraction. The dual coating layers have a significant impact on the rate capability, reducing polarization gaps and enabling higher capacities at various current rates. Long‐term cycling tests reveal the robustness of the composite, with LTO−L‐1.0 retaining 90.8 % capacity after 4000 cycles at 1.0 A g−1. This underscores the sustained high electronic and ionic conductivity facilitated by the dual coating layers. The study contributes to the design of advanced anode materials for lithium‐ion batteries, emphasizing the importance of tailored coating strategies to address conductivity and stability challenges.

A Comprehensive Comparison Analysis between Ammonium-Based and Phosphonium-Based Bifunctional Ionic Liquids for Metal Extraction and Separation Processes.

A phosphonium-based bifunctional ionic liquid (IL) Cyp-IL was synthesized to recover molybdenum and vanadium from industrial waste resources, such as the spent hydrodesulfurization catalysts. In comparison with the reported versatile Aliquat 336-based ionic liquid, the developed ionic liquid Cyp-IL was investigated for its potential application recovery of vanadium and molybdenum from industrial wastes. To assess the efficiency of the comparative extraction process, a comprehensive comparison analysis was conducted between the ammonium-based bifunctional ionic liquid Aliquat 336 and the developed phosphonium-based bifunctional ionic liquid Cyp-IL. Vanadium and molybdenum in the ionic liquid-loaded phases were selectively precipitated using NH4Cl and BaCl2 solutions in a basic medium. Compared to Aliquat 336-based Ali-IL, Cyp-IL exhibited superior performance in the extraction and separation processes of molybdenum and vanadium such as a recovery rate of Mo 91% and V 82.5% vs Mo 85% and V 72% by the ammonium-based bifunctional ionic liquid Ali-IL. The recovered components, such as molybdenum and vanadium, were characterized by energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), and scanning electron microscopy (SEM). This method capacitates the sustainable recovery of pure vanadium and molybdenum compounds while minimizing the environmental impact.

A Green Chemo-Enzymatic Approach for CO2 Capture and Transformation into Bis(cyclic carbonate) Esters in Solvent-Free Media.

A sustainable approach for CO2 capture and chemo-enzymatic transformation into bis(cyclic carbonate) esters from CO2, glycidol, and organic anhydrides under solvent-free conditions has been demonstrated. The chemo-enzymatic process is based on two consecutive catalytic steps, which can be executed through separated operations or within a one-pot combo system, taking advantage of the synergic effects that emerge from integrating ionic liquid (IL) technologies and biocatalysts. In a first step, lipase-catalyzed transesterification and esterification reactions of different diacyl donors (e.g., glutaric anhydride, succinic anhydride, dimethyl succinate, etc.) with glycidol in solvent-free under mild reaction conditions (70 °C, 6 h) produce the corresponding diglycidyl ester derivatives in up to 41% yield. By a second step, the synthesis of bis(cyclic carbonate) esters was carried out as a result of the cycloaddition reaction of CO2 (from an exhausted gas source, 15% CO2 purity) on these diglycidyl esters, catalyzed by the covalently attached 1-decyl-2-methylimidazolium IL (supported ionic liquid-like phase, SILLP), in solvent-free condition, leading up to 65% yield after 8 h at 45 °C and 1 MPa CO2 pressure. Both key elements of the reaction system (biocatalyst and SILLP) were successfully recovered and reused for at least 5 operational cycles. Finally, different metrics have been applied to assess the greenness of the solvent-free chemo-enzymatic synthesis of bis(cyclic carbonate) esters here reported.

Improving the Stability of 75Li2S·25P2S5 Glass-Ceramic Electrolytes Against Lithium Metals Through Li2O Doping

The chemical and electrochemical stability between solid-state electrolytes (SSEs) and lithium metals is one of the crucial factors in the performance of all-solid-state lithium batteries (ASSLBs). Doping modification has been shown to improve the ionic conductivity and air stability of SSEs, but further research is needed to demonstrate its effectiveness in enhancing stability with lithium metal. In this work, a series of Li2O-doped 75Li2S·25P2S5 glass-ceramic electrolytes have been successfully synthesized using ball milling method. Powder X-ray diffraction (pXRD) and 7Li magic angle spinning nuclear magnetic resonance (MAS NMR) spectroscopy results revealed that Li2O doping effectively reduced the percentage of residual Li2S in the ball milling stage and generated a high ionic conductivity phase Li7P3S11 during annealing. The electrolyte has the highest ionic conductivity (1.5 × 10−4 S cm−1 at room temperature) when doped with 1 mol% Li2O. Various electrochemical characterizations have shown that all doped electrolytes can effectively slow/suppress lithium dendrite formation while being chemically and electrochemically stable to some extent. Among these, 1 mol% Li2O-doped electrolyte performs the best, as the Li|1Li2O|Li cell maintains voltage and resistance nearly unchanged after 1000 h and 900 cycles, with no noticeable degradation in the material structure.

Advanced Compressive Sensing and Dynamic Sampling for 4D-STEM Imaging of Interfaces.

Interfaces in energy materials and devices often involve beam-sensitive materials such as fast ionic, soft, or liquid phases. 4D scanning transmission electron microscopy (4D-STEM) offers insights into local lattice, strain charge, and field distributions, but faces challenges in analyzing beam-sensitive interfaces at high spatial resolutions. Here, a 4D-STEM compressive sensing algorithm is introduced that significantly reduces data acquisition time and electron dose. This method autonomously allocates probe positions on interfaces and reconstructs missing information from datasets acquired via dynamic sampling. This algorithm allows for the integration of various scanning schemes and electron probe conditions to optimize data integrity. Its data reconstruction employs a neural network and an autoencoder to correlate diffraction pattern features with measured properties, significantly reducing training costs. The accuracy of the reconstructed 4D-STEM datasets is verified using a combination of explicitly and implicitly trained parameters from atomic resolution datasets. This method is broadly applicable for 4D-STEM imaging of any local features of interest and will be available on GitHub upon publication.

Application of zwitterionic ionic liquid-based capsule phase microextraction for the HPLC-UV determination of doxycycline in human urine samples

Herein, we describe the utilization of an ionic liquid (IL)/Carbowax 20 M−functionalized sol–gel sorbent for the capsule phase microextraction of doxycycline in authentic human urine samples. This green sample preparation method combines stirring and filtration in a single, standalone sample preparation device, streamlining the sample preparation process. Additionally, it provides rapid extraction kinetics and high extraction efficiency. The experimental conditions (i.e. sorbent type, sample pH and volume, extraction time, ionic strength, elution solvent, and volume) affecting the extraction efficiency of the analyte were studied and optimized. The method was linear in the range of 0.1 – 5.0 μg/mL with a coefficient of determination higher than 0.995. The achieved LOD was found to be 0.02 μg/mL while the lower limit of quantitation (LLOQ) was 0.1 μg/mL. The IL/Carbowax 20 M−functionalized microextraction capsules were reusable at least 30 times for urine samples. The relative recoveries (% RR) ranged between 93.4 – 115.9 % while the precision (expressed as % RSD) was better than 8.1 % in all cases. The robustness of the microextraction procedure and the instrumental HPLC method were separately investigated using Plackett-Burman experimental designs. The analytical protocol demonstrated cost-effectiveness, ease of handling, and speed, leading to increased sample throughput. The green character of the developed method was evaluated using the Green Analytical Procedure Index (GAPI) and Blue Applicability Grade Index (BAGI). Finally, the method’s applicability was demonstrated by analyzing authentic human urine samples after oral administration of a doxycycline-containing pharmaceutical formulation.

Preparation of ionic gel-modified stationary phase for RPLC/HILIC/IC separation and its application in per aqueous liquid chromatography

In this study, we synthesized and employed an ionic gel-functionalized silica stationary phase for high-performance liquid chromatography. The successful fabrication of the stationary phase was confirmed through attenuated total reflection-Fourier transform infrared spectroscopy (ATR-FTIR), X-ray photoelectron spectroscopy (XPS), zeta-potential measurements, and elemental analysis (EA). Comparative performance evaluation against a commercial column demonstrated the prepared column's effectiveness in the mixed mode of reversed-phase liquid chromatography (RPLC), hydrophilic interaction liquid chromatography (HILIC), and ion chromatography (IC). Moreover, the stationary phase exhibited exceptional retention repeatability in per aqueous liquid chromatography, showcasing its potential as an environmentally friendly analytical method. Mechanistic investigations unveiled multiple solute-stationary phase interactions, including π-π interactions, hydrogen bonding, and ion exchange. Finally, we applied the developed stationary phase for the precise detection of preservatives in carbonated beverages and jelly, achieving high levels of accuracy and recovery rates.

Structural stability and electrochemical response of 3D printed and reactively sintered Ga-doped Li7La3Zr2O12 electrolytes

Cubic Ga-doped Li7La3Zr2O12 (LLZO) tubes with one closed end were produced by a 3D printing-reactive sintering process. For the first time, the structural stability of Ga-doped LLZO tubes (relative density: ∼88 %, cubic LLZO fraction > 90 %) was evaluated after immersion in eutectic PbLi, a candidate molten breeder, at 350 and 450 °C. The high ionic conductivity cubic LLZO phase was maintained after immersion at 350 °C for 100 h, while secondary phase formation and conversion of cubic LLZO to the tetragonal polymorph was observed after 6 h at 450 °C. Li was successfully pumped through the tubes during linear voltage sweeps at 350 °C, indicating that Ga-doped LLZO is a possible candidate for hydrogen isotope extraction in PbLi via direct electrolysis.

Facile synthesis of magnetic ionic covalent organic framework and dispersive magnetic solid phase extraction of aromatic amino acid oxidation products in thermally processed foods

Aromatic amino acid oxidation products (AAAOPs) are newly discovered risk substances of thermal processes. Due to its significant polarity and trace level in food matrices, there are no efficient pre-treatment methods available to enrich AAAOPs. Herein, we proposed a magnetic cationic covalent organic framework (Fe3O4@EB-iCOF) as an adsorbent for dispersive magnetic solid-phase extraction (DMSPE). Benefiting from the unique charged characteristics of Fe3O4@EB-iCOF, AAAOPs can be enriched through electrostatic interaction and π-π interactions. Under the optimal DMSPE conditions, the combined HPLC-MS/MS method demonstrated good linearity (R2 ≥ 0.990) and a low detection limit (0.11–7.5 μg·kg−1) for AAAOPs. In addition, the method was applied to real sample and obtained satisfactory recoveries (86.8 % ∼ 109.9 %). Especially, we applied this method to the detection of AAAOPs in meat samples and conducted a preliminarily study on its formation rules, which provides a reliable basis for assessing potential dietary risks.

In-Column Dehydration Benzyl Alcohols and Their Chromatographic Behavior on Pyridinium-Based Ionic Liquids as Gas Stationary Phases.

At present, stationary phases based on ionic liquids are a promising and widely used technique in gas chromatography, yet they remain poorly studied. Unfortunately, testing of "new" stationary phases is often carried out on a limited set of test compounds (about 10 compounds) of relatively simple structures. This study represents the first investigation into the physicochemical patterns of retention of substituted (including polysubstituted) aromatic alcohols on two stationary phases of different polarities: one based on pyridinium-based ionic liquids and the other on a standard polar phase. The retention order of the studied compounds on such stationary phases compared to the standard polar phase, polyethylene glycol (SH-Stabilwax), was compared and studied. It was shown that pyridinium-based ionic liquids stationary phase has a different selectivity compared to the SH-Stabilwax. Using a quantitative structure-retention relationships (QSRR) study, the differences in selectivity of the two stationary phases were interpreted. Using CHERESHNYA software, the importance of descriptors on different stationary phases was evaluated for the same data set. Different selectivity of the stationary phases correlates with different contributions of descriptors for the analytes under study. For the first time, we show that in-column dehydration is observed for some compounds (mostly substituted benzyl alcohols). This effect is worthy of further investigation and requires attention when analyzing complex mixtures. It suggests that when testing "new" stationary phases, it is necessary to conduct tests on a large set of different classes of compounds. This is because, in the case of using ionic liquids as an stationary phase, a reaction between the analyte and the stationary phase is possible.

Quantitative structure-retention relationships for pyridinium-based ionic liquids used as gas chromatographic stationary phases: convenient software and assessment of reliability of the results

Ionic liquids, i.e., organic salts with a low melting point, can be used as gas chromatographic liquid stationary phases. These stationary phases have some advantages such as peculiar selectivity, high polarity, and thermostability. Many previous works are devoted to such stationary phases. However, there are still no large enough retention data sets of structurally diverse compounds for them. Consequently, there are very few works devoted to quantitative structure-retention relationships (QSRR) for ionic liquid-based stationary phases. This work is aimed at closing this gap. Three ionic liquids with substituted pyridinium cations are considered. We provide large enough data sets (123–158 compounds) that can be used in further works devoted to QSRR and related methods. We provide a QSRR study using this data set and demonstrate the following. The retention index for a polyethylene glycol stationary phase (denoted as RI_PEG), predicted using another model, can be used as a molecular descriptor. This descriptor significantly improves the accuracy of the QSRR model. Both deep learning-based and linear models were considered for RI_PEG prediction. The ability to predict the retention indices for ionic liquid-based stationary phases with high accuracy is demonstrated. Particular attention is paid to the reproducibility and reliability of the QSRR study. It was demonstrated that adding/removing several compounds, small perturbations of the data set can considerably affect the results such as descriptor importance and model accuracy. These facts have to be considered in order to avoid misleading conclusions. For the QSRR research, we developed a software tool with a graphical user interface, which we called CHERESHNYA. It is intended to select molecular descriptors and construct linear equations connecting molecular descriptors with gas chromatographic retention indices for any stationary phase. The software allows the user to generate several hundred molecular descriptors (one-dimensional and two-dimensional). Among them, predicted retention indices for popular stationary phases such as polydimethylsiloxane and polyethylene glycol are used as molecular descriptors. Various methods for selecting (and assessing the importance of) molecular descriptors have been implemented, in particular the Boruta algorithm, partial least squares, genetic algorithms, L1-regularized regression (LASSO) and others. The software is free, open-source and available online: https://github.com/mtshn/chereshnya.

Mechanistic insight into the impact of dry-state prelithiated SiOx thin-film anode toward extremely fast-charging and long-term stability

Silicon suboxides (SiOx) have achieved partial success in commercialization as high-capacity anode materials to replace graphite because of optimal electrochemical properties over silicon. Unfortunately, the further development has been sluggish, jeopardizing the urgent need of green energy. The daunting challenges to tackle include low initial coulombic efficiency (ICE) and low charging rate due to poor electron and ionic conductivity. In the context of thin film microbattery, we propose to precisely control the chemical states of SiOx films through varying sputtering power followed by dry-state pre-lithiation through Li-metal thermal evaporation, superior to the current pre-lithiation approaches for SiOx thin-film anodes. We addressed the leading roles of the surface chemical states of the as-deposited SiOx in the formation of the high ionic conductive Li4SiO4 phase as the pre-solid electrolyte interphase during the proposed dry-state prelithiation process. Ultimately, the prelithiated SiOx successfully mitigated the most confronted issues as low ICE and C-rate limitation, achieving an unprecedented rate performance of 72.8 % at 20 C, and ultra-long-cycle retention of 54.2 % over 5000 cycles at 10 C. These results strongly prove that appropriate pre-lithiation provides tremendous advantages to SiOx thin film anode not only in prolonging electrode stability but also promoting a significant fast-cycling.

Numerical study of electrode permeability influence on planar SOFC performance

A solid oxide fuel cell (SOFC) is a clean and very efficient electrochemical conversion device, which generates electricity directly from fuel electrochemical oxidation. In this paper, a three dimensional numerical model has been developed in order to analyse the role of some thermophysical and morphological parameters on the performance of the SOFC cell. In particular, we studied the effect of the variation of permeability of the electrodes: fuel distribution, ionic and electric current density, pressure and diffusion flux are analyzed and compared. The volume fraction of the ionic and electronic phase in the electrodes is studied using a parametric study. It was shown that the current density enhanced by decreasing the permeability, up to a defined value, and it diminished with very small permeability. A remarkable influence of pressure and diffusion of species on the performance of the cell, with the variation of permeability, has been recognized. Varying the permeability in the active layer of electrodes has a large impact on the current density, connected to the volume fraction of ionic phase. This study permits to comprehend the relationship between the performance and microstructure of SOFCs. Meanwhile, it furnishes theoretical guidance for an optimum design of the electrode permeability.

An ion specific continuum model on ionic surfactant's binary phase diagram in aqueous solution

A continuum aggregation model is proposed to account for specific ion effects, enabling accurate phase diagrams calculations for the micellar, cylindrical and lamellar aggregates of sodium/potassium carboxylate surfactants in aqueous solution across a range of temperatures. Three groups of concentrations at distinctive temperatures are fitted to build empirical temperature dependence given the limited availability of relevant experimental measurements. The specific ion effects are manifested in the aggregates' surface tension as well as in the distributions of counter-ions' concentrations in the vicinity of the aggregates. The aggregates' geometric sizes are well-reproduced. The differential evolution algorithm is applied to address boundary conditions of the electrostatic potential, aggregate size optimization as well as the equilibrium of monomers transferring between the aggregate and aqueous region.

Microwave enhanced demulsification of metal ion extraction emulsions: From permittivity modeling to proof of concept for solvent extraction processes

The demulsification by microwaves of liquid-liquid systems for metal recycling was experimentally and numerically investigated. Strongly ionic aqueous phases with high conductivities and typical organic phases, both representative of industrial ones, were used. Experimental microwave demulsification was achieved in both the W/O and O/W systems at the laboratory scale showing the rapidity and the efficiency of the process. The dielectric properties of these representative emulsions were measured and modeled using the permittivities measured in the separate phases and the phase fractions. Taking into account the direction of the emulsion, permittivities were predicted over a wide range of frequencies, along with microwave penetration depths in the whole range of phase fractions. Numerical simulations of the electric field distribution and penetration depths calculations at several frequencies demonstrated that microwave heating is relevant and possible in both W/O and O/W dense packed emulsions, which should rapidly lead to demulsification, including on a large industrial scale.

A new concept of ternary aqueous electrolytes based on lithium 4,5-dicyanoimidazolate hydrates

A new concept of aqueous electrolytes based on heterocyclic anions (hydrated anionic triplet electrolyte, HATE) has been presented. Structural studies showed that dimeric lithium 4,5-dicyanoimidazolate (LiTDI) dihydrate molecules, in the presence of acetonitrile, form an ionic system preserved in high concentrations and solid states. X-ray diffraction measurements show that electroneutral dihydrate units can coordinate additional lithium cations acting as charge carriers. The crystalline ionic phase was characterized using spectroscopic, thermal, and electrochemical methods and was used to prepare model electrolytes based on LiTDI hydrates. Linear sweep voltammetry and impedance spectroscopy measurements show, in this system, the depletion of water activity, high conductivity, and reversible cycling of full cells comprising examined electrolytes. We will prove that a concentrated triplet solution acts similarly to the anhydrous electrolyte; regardless of the concentration, it reaches high ionic conductivity values (12–16 mS/cm at room temperature) and is electrochemically stable.

Preparation and post-modified of dicationic ionic liquid stationary phase and their application in mixed-mode liquid chromatography

This work prepared two dicationic ionic liquid stationary phases for mixed-mode chromatography via thioe-ene click reaction, one of which was post-modified by p-tolyl isocyanate. The successful synthesis of two stationary phases was demonstrated by several characterizations. The separation of a wide range of substances, including nucleosides and bases, alkylbenzene, polycyclic aromatic hydrocarbons, anilines, phenols, inorganic anions and organic acids, shows that homemade stationary phases can not only be applie to RPLC/HILIC/IEC mixed-mode chromatography, but also has better separation selectivity than commercial column. Therefore, the post-modification of p-tolyl isocyanate can greatly improve the separation effect in RPLC mode, which proves that this modification method is of research significance. The retention mechanisms of two stationary phases were investigated by varying the chromatographic conditions and linear solvation energy relationships (LSER). In addition, the stationary phase is able to detect preservatives in foods quickly and accurately. In actual sample testing, the limit of detection ≤ 0.074mg·L−1 and the inter-day precision was not more than 3.33 %.

Dicationic imidazole ionic liquid stationary phase for preservative detection and its application under mixed mode of HILIC/RPLC/IEC

BackgroundFood safety has always been a great concern, and the detection of additives is vital to ensuring food safety. Therefore, there is a necessity to develop a method that can quickly and efficiently separate and detect additives in food. High performance liquid chromatography is widely used in the analysis and testing of food additives. Ionic liquids have attracted wide attention in the preparation of high performance liquid chromatography stationary phases owing to their high stability, low vapor pressure and adjustable structure. ResultsWe developed a novel dicationic imidazole ionic liquid stationary phase for the simultaneous determination of organic preservatives (sodium benzoate, potassium sorbate) and inorganic preservatives (nitrate and nitrite) in foodstuffs under mixed-mode chromatography. The method had the advantages of easy operation, high reproducibility, good linearity and precision. In the detection of these four preservatives, the limit of detection ≤0.4740 mg⋅L−1 and the limit of quantification ≤1.5800 mg⋅L−1. The intra-day and inter-day precision were less than 4.02%, and the recovery rate was 95.90∼100.19 %. At the same time, we also characterized the stationary phase, explored the mechanism and evaluated the chromatographic performance. The stationary phase was able to operate under the mixed mode of reversed phase/hydrophilic interaction/ion exchange chromatography, and it was capable of separating hydrophilic substances, hydrophobic substances, acids, and inorganic anionic substances with good separation efficiency and had high column efficiency. SignificanceIn summary, the stationary phase has a promising application in the routine analysis of organic and inorganic preservatives in food. In addition, the stationary phase has good separation ability for hydrophilic, hydrophobic, ionic substances and complex samples, making it a prospective material for chromatographic separation.