ANALYTICAL LETTERS
·
2023
·
IF 2
Hongzhuang Chen,Jialin Fan,Xue Chen,Zhenkuan Ma,Ling Zhang,Xuwei Chen
A novel liposomal nanocomposite with biocompatibility and conductivity, Au@ILs-polysome, was fabricated and first utilized as the electrode material to immobilize the redox enzyme glucose oxidase (GOD) for the sensitive determination of glucose. Ionic liquids (ILs)-based polysome (ILs-polysome) was prepared via the radical polymerization of ILs based liposome (ILs-liposome) and improved by ion exchange with chloroauric acid to prepare Au nanoparticles (Au NPs) modified ILs based polysome (Au@ILs-polysome). The morphology, surface properties, and structure of Au@ILs-polysome were characterized; the results suggest that the nanocomposite exhibited excellent stability on the surface of solid electrodes without fusion. Electrochemical impedance spectroscopy (EIS) demonstrated that the nanocomposite had enhanced conductivity. Cyclic voltammetry (CV) shows that the direct electron transfer of GOD was achieved on the GOD/Au@ILs-polysome/GCE electrode since the Au@ILs-polysome provided a biocompatible microenvironment that made the immobilized enzyme stay natural and active. Differential pulse voltammetry (DPV) demonstrates that the GOD/Au@ILs-polysome/GCE electrode exhibited improved electrocatalytic activity compared with the GOD/ILs-polysome/GCE electrode. The electrochemical sensor exhibited a low detection limit of 0.02 mM, high sensitivity of 32.52 µA mM−1 cm−2, high selectivity toward glucose, and good stability. The practical application of the sensor was verified by the determination of glucose in human serum. The multi-component liposomal nanocomposites possess universal significance in protein-based direct electrochemical devices while offering a facile route to fabricating a highly sensitive glucose sensor for practical clinical diagnosis.
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Petroleum Science
·
2023
·
IF 5.6
Bo-Long Jiang,Dong-Xu Zhang,Dan-Dan Yuan,Yan-Guang Chen,Tian-Zhen Hao,Hua Song
Oxidative desulfurization from fuel oil is one of the important methods for deep desulfurization. The development of efficient oxidative desulfurization catalysts is crucial for improving the desulfurization performance. Successful encapsulation of phosphotungstic acid (HPW) and ionic liquid (BMImBr) inside the mesoporous cages of MIL-101(Cr) was accomplished through a combination of “bottle around ship” and “ship in bottle” methods. The obtained BMImPW@MIL-101(Cr) composite was characterized by XRD, FTIR, BET, SEM, XPS and ICP methods. Results indicated that the BMImPW@MIL-101(Cr) composites with PW 3− loading of 23.1–50.7 wt% were obtained, demonstrating that the “bottle around ship” method is beneficial to make full use of nanocages of MIL-101(Cr) to obtain expected high loading of active PW 3 − . The BMImPW@MIL-101(Cr) exhibits excellent reusability with no evidence of leaching of active PW 3 − and BMIm + , and well-preserved structure after successive cycles of regeneration and reuse. The significantly improved stability of BMImPW@MIL-101(Cr) as compared to HPW@MIL-101(Cr) is possibly because the leaching of the active PW 3 − − sites can be greatly suppressed by forming large size of BMImPW owing to introduction of BMIm + cation. The BMImPW@MIL-101(Cr) exhibited excellent catalytic activity for solvent free oxidative desulfurization of refractory sulfides. The enhanced oxidative desulfurization activity as compared to HPW@MIL-101(Cr) can be explained by the intimate contact of sulfides with active PW 3 − sites owing the strong attraction of BMIm + cation with the sulfides.
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JOURNAL OF CHROMATOGRAPHY A
·
2019
·
IF 3.858
Ning Zhang,Lishen Su,Suning Man,Xiaoyun Lei,Ting Huang,Chunling Zhu,Lan Zhang,Xiaoping Wu
A direct immersion solid-phase microextraction (DI-SPME) approach for gas chromatography-mass spectrometry (GC–MS) based on hybrid fiber coating of ionic liquid and polyhedral oligomeric silsesquioxane (POSS) is presented. To fabricate the task-specific coating for the enrichment of polycyclic aromatic hydrocarbons (PAHs), 1-butyl-3-vinylimidazolium bis[(trifluoromethyl)sulfonyl]imide (IL) and POSS were rapidly photoinitiated copolymerized within 5 min on a stainless steel fiber. The high efficient extraction of target analytes can be attributed to a combined result of multiple interactions including the strong C F⋯H C pseudohydrogen bonding, π-π stacking, hydrophobic force, and molecular sieve effect. A wide linear range (0.04–400 ng L −1 ) with low detection limits in the range of 0.004 and 0.5 ng L −1 were obtained for PAHs by GC–MS. The applicability of this coupling method was successfully demonstrated by the analysis of trace PAHs in real river water and soil samples, with satisfied recoveries (84.2–108.6%) and relative standard deviations (<8.1%). Compared to the other commercial fiber-based SPME methods, the IL/POSS hybrid coating-based SPME is much cheaper, thermally stable and capable of eliminating possible deleterious effects as well.
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高影响因子
LANGMUIR
·
2018
·
IF 3.789
S. Y. Chong,T. T. Wang,L. C. Cheng,H. Y. Lv,M. Ji
A novel heterogeneous catalyst, the ionic liquid (IL) of 1-butyl-3-methylimidazolium acetate (BmimOAc) immobilized on MIL-101-NH2, denoted as IL(OAc–)-MIL-101-NH2, was prepared by the “ship-in-a-bottle” strategy. The IL of BmimOAc was prepared in the MIL-101-NH2 nanocages primordially, in which the condensation product of MIL-101-NH2’s amine group with 1,1′-carbonyldiimidazole (CDI) reacted with 1-bromo butane, and then the intermediate exchanged with potassium acetate. The structure and physicochemical properties of IL(OAc–)-MIL-101-NH2 were characterized by powder X-ray diffraction, scanning electron microscopy, Fourier transform infrared spectroscopy, DRS UV–vis, nitrogen adsorption–desorption, and elemental analysis. The results indicated that BmimOAc was anchored in the MIL-101-NH2 skeleton via the acylamino group and confined in the nanocages in the form of a single molecule. The composite material of IL(OAc–)-MIL-101-NH2 exhibited excellent catalytic activity and catalytically synthesized 3-aryl-2-oxazolone in an excellent yield of 92%. It can be reused up to six times without noteworthy loss of its activity and demonstrated distinct size-selective property for substrates. It was conjectured that the diffusion kinetics of reactants could be controlled by the aperture size of the metal–organic framework support.
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2019
·Vol. 411
·期 6
·1261-1271
·
IF 3.286
Sun Ya Kun,Sun Guang-Ying,Jia Man,Yang Jian,Liu Zhao-Sheng,Huang Yan-Ping,Aisa Haji Akber
One of the main challenges in large-scale applications of molecularly imprinted polymers (MIPs) is the significant amount of template needed in polymer preparation. A new strategy based on room-temperature ionic liquids (RTILs) was suggested to solve this problem by reducing the amount of template in the polymerization recipe. The MIP was synthesized with a mixture of dimethyl sulfoxide and RTIL (1-butyl-3-methylimidazolium tetrafluoroborate) as porogen, in which chlorogenic acid (CGA) was used as template, 4-vinylpyridine (4-VP) as functional monomer, and ethylene glycol dimethacrylate (EDMA) as cross-linker. The influence of polymerization variables, including CGA concentrations, and the ratio of 4-VP to EDMA on imprinting effect were investigated comprehensively. Moreover, the properties involving the column permeability, the number of binding sites, and the polymer morphology of the CGA-MIP monoliths were studied thoroughly. The MIP monolith had an excellent column permeability (1.53 × 10 −13 m 2 ) and allowed an ultra-fast on-line SPE, which dramatically shortens the separation time (< 10 min) and improves the separation efficiency. At high flow velocity (5.0 mL min −1 ), 50 μL of the extract from Eucommia ulmoides leaves can be loaded directly on the CGA-MIP monoliths and CGA with high purity can be obtained with a recovery of 89.01 ± 0.05%. As a conclusion, the resulting RTIL-induced approach of preparing MIP may be an effective tool in fabricating MIP in a low-cost way.
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RSC Advances
·
2018
·Vol. 8
·期 34
·18784-18791
·
IF 2.936
Yuyan Xiao,Xirong Huang
Via heating first and then cooling, binary ionic liquid (IL) mixture of N-methyl-2-pyrrolidonium methylsulfonate ([HNMP][CH3SO3]) and 1-butyl-3-methylimidazolium chloride ([Bmim]Cl) could form a liquid at room temperature. The glass-transition temperature (Tg) characterized by DSC depends on its composition with Tg being as low as −63 °C. The physicochemical properties of the binary IL mixtures also vary with the composition. With the increase of the mole fraction of [Bmim]Cl, the hydrogen-bond accepting ability (β) of the binary IL mixture increases, but the hydrogen-bond donating ability (α) deceases. In this binary IL mixture, fructose could be effectively converted into 5-hydroxymethylfurfural (HMF) at room temperature. The HMF yields at a given time are found to be well correlated with the physicochemical properties of the binary mixture, especially the α and β values. Under specified conditions, the present IL mixture as medium for fructose dehydration into HMF is comparable to the medium formed by ILs and alcohol, where the alcohols have negative effect on the HMF formation.
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY
·
2018
·Vol. 410
·期 12
·2921-2935
·
IF 3.307
Wu Jia,Xu Zilin,Pan Yixuan,Shi Yi,Bao Xiujie,Li Jun,Tong Yu,Tang Han,Ma Shuyan,Wang Xuedong,Lyu Jianxin
Herein, a novel magnetic effervescence tablet-assisted microextraction coupled to in situ metathesis reaction of ionic liquid (IS-META-ILDM) is presented for the determination of four endogenous steroids in human urine, pregnant women’s blood, and fetal umbilical cord blood. The magnetic effervescent tablets, which were composed of Fe 3 O 4 nanoparticles, sodium carbonate (alkaline source), and tartaric acid (acidic source), were used to disperse the extractant and for convenient magnetic separation. After the effervescent reaction, in situ reaction between NH 4 PF 6 and [C 6 MIM]BF 4 was adopted to change hydrophilic ionic liquid to hydrophobic liquid, which could be separated from the aqueous phase. The newly developed method has three obvious advantages: (1) combination of effervescent dispersion and magnetic nanoparticles’ retrieval is cost-effective and the dispersion and collection of the extractant can be completed almost simultaneously; (2) as compared to temperature-controlled ionic liquid dispersive microextraction and cold-induced solidified microextraction, this method avoids a heating and cooling process which significantly reduces the extraction time and energy cost; and (3) the combination of adsorption by magnetic nanoparticles with extraction by in situ metathesis reaction easily produces high recoveries for target analytes. The optimized composition of effervescent tablet and experimental parameters are as follows: 0.64 g mixture of sodium carbonate and tartaric acid, 7 mg of Fe 3 O 4 (20 nm) as magnetic sorbents, 40 μL of [C 6 MIM]BF 4 as the extraction solvent, 0.15 g NH 4 PF 6 , and 300 μL of elution solvent. Under the optimized conditions, the newly developed method provided high extraction recoveries (90.0–118.5%) and low LODs (0.14–0.17 μg L −1 ) in urine and blood samples. In total, this IS-META-ILDM method provided high extraction efficiency, fast and convenient separation, and underutilization of any organic solvent, and thus it has great potential for the determination of trace endogenous steroids in complex human fluids.
The newly developed method has three obvious advantages: combination of effervescent dispersion and magnetic nanoparticles’ retrieval is cost-effective and the dispersion and collection of the extractant can be completed almost simultaneously. It avoids a heating and cooling process which significantly reduces the extraction time and energy cost and easily produces high recoveries for target analytes
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CHEMICAL ENGINEERING JOURNAL
·
2018
·
IF 6.735
Ce-Ce Hu,Qiang Gao,Shu Liu,Li-Li Chang,Kai-Sheng Xia,Bo Han,Cheng-Gang Zhou
Recognition, quantification, and selective removal of target heavy metal ion with a single material are of great practical importance, while there still remains a formidable challenge of accomplishing these multiple tasks in pure aqueous media. Herein, we utilized crosslinked poly(ionic liquid) as support of organic probe to devise a new class of multifunctional material for addressing this issue while simultaneously providing some additional benefits. To illustrate this strategy, an imidazolium-type crosslinked poly(ionic liquid) anchored with rhodamine derivative, P(RhBHSA–BVD), was designed and applied for qualitative/quantitative analysis and selective removal of Cu 2+ . In significant contrast from previously reported organic probe/support composites that were typically hydrophobic and usually required use of organic solvent to disperse them before use, the P(RhBHSA–BVD) was highly hydrophilic and readily dispersed in pure water. Moreover, due to the positively charged nature of polymeric backbone, the P(RhBHSA–BVD) had a potential advantage of avoiding non-receptor binding. Observation with naked eye confirmed the highly selective and sensitive response of P(RhBHSA–BVD) to Cu 2+ , and accordingly a convenient colorimetric sensing method for detection of Cu 2+ was successfully established. Furthermore, it was demonstrated that the P(RhBHSA–BVD) could selectively remove Cu 2+ from multi-ions solution with high efficiency and excellent reusability.
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FOOD CHEMISTRY
·
2018
·
IF 4.946
Fang Liu,Xiaoling Yang,Xiaoling Wu,Xuefei Xi,Haixiang Gao,Sanbing Zhang,Wenfeng Zhou,Runhua Lu
A novel dispersive magnetic solid phase microextraction method based on ionic liquid-coated and cyclodextrin-functionalized magnetic core dendrimer nanocomposites has been developed for the determination of pyrethroids in juice samples. The different generation magnetic core dendrimer nanocomposites were successfully synthesized and the nanocomposites possess both the selective retention of guest dendrimer and cyclodextrin molecules and high adsorption capacities of ionic liquids. The extraction efficiencies of different generation magnetic core dendrimer nanocomposites were compared, and the type of nanocomposite with the highest recovery was obtained. Under the optimized experimental conditions, the method showed good linearity in the range of 3.5–500 μg L −1 . The LODs and LOQs were in the ranges of 0.36–1.3 μg L −1 and 1.2–4.3 μg L −1 , respectively. The method also showed acceptable accuracies ranging from 98.2% to 99.4%. The proposed method was demonstrated to broaden the potential applications of dendrimer for the detection of pyrethroid residues in various juice samples.
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Journal of Materials Chemistry C
·
2016
·Vol. 4
·期 15
·3175-3184
·
IF 5.066
Chunxi Xu,Li Yuan,Guozheng Liang,Aijuan Gu
Sustainability urgently asks for low dielectric loss and a low percolation threshold (fc) while developing high dielectric constant (Hi-k) conductor/polymer composites. In this work, a novel hybridized graphene (PIL–TrGO) was first reported using a two-step process, including the decoration of an epoxy functionalized ionic liquid (IL) on the surface of thermally reduced graphene oxide (TrGO) through πcation–π interaction, followed by in situ polymerization of the IL. The DC conductivity of the PIL–TrGO hybrid is as good as that of TrGO. Then, different loadings of PIL–TrGO were added into cyanate ester (CE) to prepare a series of composites; the TrGO/CE composites were also prepared for comparison. Different from TrGO, the PIL has a large amount of epoxy groups, which guarantees good dispersion of the hybridized graphene in CE matrix, and thus provides the base for transferring the outstanding electrical properties of graphene to the composites. When the loading of fillers approaches the percolation threshold (fc), the dielectric constant and loss at 100 Hz of PIL–TrGO/CE composites are about 13 and 0.57 times that of TrGO/CE composites, respectively, while the fc of PIL–TrGO/CE composites is still as low as 0.94 wt%. The dielectric mechanism was studied by discussing and simulating impedance spectra, and the results show that PIL–TrGO/CE composites possess more micro-capacitor structures than TrGO/CE composites; moreover, the cation–anion charge layers on TrGO surfaces enhance the Maxwell–Wagner–Sillars polarization between PIL–TrGO hybrid and the CE matrix, and then markedly increase the dielectric constant of composites. PILs coated on graphene surfaces act as electron insulative layers and thus decrease dielectric loss induced by the leakage current between conductive carbon layers.
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Food Analytical Methods
·
2016
·Vol. 10
·期 6
·1653-1660
·
IF 2.167
Wang Xiaojun,Chen Peng,Cao Liang,Xu Guoliang,Yang Siyu,Fang Ye,Wang Guozhen,Hong Xincheng
A novel and sensitive magnetic ionic liquid-based up-and-down-shaker-assisted dispersive liquid-liquid microextraction (MIL-UDSA-DLLME) was developed for the graphite furnace atomic absorption spectrometric measurement of inorganic selenium speciation from various rice matrixes. In the first microextraction step, the magnetic ionic liquid (1-butyl-3-methylimidazolium tetrachloroferrate, [C 4 mim][FeCl 4 ]) was selected to extract the complex of Se(IV) and 2,3-diaminonaphthalene from aqueous solution by the assistance of up-and-down-shaker vortex agitator. After the microextraction step, the magnetic ionic liquid containing target analytes was collected at the bottom of the tube by applying an external magnetic field around the test tube. Under the optimized conditions, the method present has low detection limit (0.018 μg L −1 ), wide linear dynamic range (0.03–10 μg L −1 ), and good repeatability (<3.0%, n = 10) for Se(IV). The proposed methodology was applied for separation and preconcentration of inorganic selenium in standard reference materials including GBW10010 rice, GBW10043 Liaoning rice, and GBW10045 Hunan rice with satisfactory results. The developed methodology was also successfully used for the speciation of Se(IV) and Se(VI) in different rice samples with the relative recoveries within the acceptable range of 94.9–104.8% for the addition recovery tests.
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JOURNAL OF CHROMATOGRAPHY A
·
2016
·
IF 3.926
Xiudan Hou,Shujuan Liu,Panpan Zhou,Jin Li,Xia Liu,Licheng Wang,Yong Guo
A solid-phase extraction method for the efficient analysis of the excretion-dynamics of flavonoids in urine was established and described. In this work, in situ surface radical chain-transfer polymerization and in situ anion exchange were utilized to tune the extraction performance of poly(1-vinyl-3-hexylimidazolium bromide)-graphene oxide-grafted silica (poly(VHIm + Br − )@GO@Sil). Graphene oxide (GO) was first coated onto the silica using a layer-by-layer fabrication method, and then the anion of poly(VHIm + Br − )@GO@Sil was changed into hexafluorophosphate (PF 6 − ) by in situ anion exchange. The interaction energies between two PILs and four flavonoids were calculated with the Gaussian09 suite of programs. A Box-Behnken design was used for the optimization of four greatly influential parameters after single-factor experiments to obtain more accurate and precise results. Coupled to high performance liquid chromatography, the poly(VHIm + PF 6 − )@GO@Sil method showed acceptable extraction recoveries for the four flavonoids, with limits of detection in the range of 0.1–0.5 μ g L −1 , and wide linear ranges with correlation coefficients (R) ranging from 0.9935 to 0.9987. Under the optimum conditions, the proposed method was applied to analyze the urines collected from a healthy volunteer. The excretion amount-time profiles revealed that 4–15 h was the main excretion time for the detected flavonoids. The results indicated that the newly developed method offered the advantages of being feasible, green and cost-effective, and could be successfully applied to the extraction and enrichment of flavonoids in human body systems allowing the study of the metabolic kinetics.
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