CHEMICAL ENGINEERING JOURNAL
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2024
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IF 13.3
Qingyun Zhao,Xiaohui Liu,Shuo Deng,Xianghong Zheng,Birong Zeng,Xinyu Liu,Yiting Xu,Conghui Yuan,Lizong Dai
A composited flame-retardant phosphorus-containing polyimine vitrimer films (Ionic-PIs) were synthesized by using ionic liquid BMIM∙PF 6 containing flame retardant elements N, P and F as the regulator. The effects of the addition amount of BMIM∙PF 6 on the mechanical properties, degradation, recycling, and flame retardancy were investigated. Compared to intrinsically phosphorus-containing polyimine film (PI), the composited Ionic-PIs exhibited better mechanical strength and toughness. Hydrogen bonding interactions between BMIM∙PF 6 and polyimine network greatly increased Ionic-PI’s mechanical strength at a low addition of 1 wt%, and the microphase separation caused by the aggregation of BMIM∙PF 6 drastically enhanced their toughness as the addition increased. Ionic-PIs exhibited excellent reprocessability at 85 °C and degradable recyclability under acidic conditions. In addition, due to the synergistic effect of condensed-phase and gas-phase flame-retardant mechanisms, the Ionic-PIs possessed good flame retardancy with LOI above 27 % and a UL-94 test reaching VTM-0 grade, which was important for the high-fire safety of polyimine vitrimer. This work is helpful to provide a simple and feasible strategy to modulate the comprehensive properties of cross-linked polyimine vitrimer film and to expand their applications in many fields.
研究领域:
材料科学
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高分子化学
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DOI
高影响因子
GREEN CHEMISTRY
·
2019
·Vol. 21
·期 3
·597-605
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IF 9.405
Shaoqi Yang,Xingmei Lu,Haoyu Yao,Jiayu Xin,Junli Xu,Ying Kang,Yongqing Yang,Guangming Cai,Suojiang Zhang
Selective catalytic hydrotreatment of lignin-derived phenols and dimeric ethers into alkanes is crucial for utilization of lignin and its fragments. Herein, we developed an efficient catalytic system with well-dispersed metal nanoparticles supported on SBA-15 synergistic with an ionic liquid. The catalytic system could catalyze the hydrodeoxygenation (HDO) of various monomeric and dimeric lignin-derived phenols into the corresponding alkanes under acid free conditions. The synergistic [Bmim]PF6-Ru/SBA-15 (1-butyl-3-methylimidazolium hexafluorophosphate) catalysis exhibited the best HDO activity for lignin-derived phenols and dimeric ethers with >99.0% conversion and maximum >98.0% selectivity of the corresponding alkanes. The yield of cyclohexane from diphenyl ether was 97.7% with 100% conversion under 2 MPa H2 at 130 °C for 6 h. The mechanism investigation confirmed that the Ru/SBA-15 catalyst and the anion of [Bmim]PF6 played crucial roles in the hydrogenation process and deoxidization process, respectively. The catalytic system was reused six times for HDO of diphenyl ether to test its stability.
研究领域:
化学工程
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可再生能源
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DOI
高影响因子
JOURNAL OF MOLECULAR STRUCTURE
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2023
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IF 3.8
Yuxiu Fu,Xiaoli Song,Yaming Pang,Yinan Zheng,Liguo Gao
In this paper, a green solvent [BMIM] [PF 6 ] ionic liquid was selected for the extraction and separation of quinoline from simulated wash oil. The effects of extraction temperature, extraction time, and solvent oil ratio on the extraction of quinoline from wash oil were studied. The optimal process parameters were obtained by changing single factor conditions and optimizing the experiment using response surface methodology. When the temperature is 71 ℃, the time is 60 min, and the solvent oil ratio is 3:5, the extraction efficiency can reach 67%. The ionic liquids were recovered and their properties were investigated by infrared spectroscopy. The mechanism of quinoline extraction by ionic liquids was analyzed using infrared spectroscopy and GROMACS kinetic simulation calculations.
研究领域:
化学工程
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环境科学
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DOI
高影响因子
JOURNAL OF CHEMICAL AND ENGINEERING DATA
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2021
·
IF 2.694
Lixia Yang,Yuexia Han,Zhen Jiao
To obtain the basic data for the recovery of 1-methylimidazole from wastewater by extraction, the ternary liquid–liquid phase equilibrium data of the water (1) + 1-methylimidazole (2) + 1-butyl-3-methylimidazolium hexafluorophosphate ([Bmim][PF6]) (3) system were determined using an equilibrium autoclave at the temperatures of 303.15 to 323.15 K and 101.32 kPa. The solute distribution coefficient (D) and the selectivity (S) of the ternary system were calculated in accordance with the experimental data. Their values were up to 1.39 and 41.17, respectively, which showed that the ionic liquid can extract 1-methylimidazole effectively. The experimental results showed that the temperature had a slight effect on the liquid–liquid equilibrium behavior. Meanwhile, the calculated results revealed that the selectivity coefficient decreased with the enhancing concentration of 1-methylimidazole in the ternary system and the increasing temperature. In addition, the nonrandom two liquid (NRTL) model was used for correlation of the ternary systems. The root-mean-square deviation value of 0.0218 indicated that the calculated results using the model were in good agreement with the experimental data and were reliable to apply to practice.
研究领域:
化学工程
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环境科学
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DOI
高影响因子
CHROMATOGRAPHIA
·
2018
·Vol. 81
·期 4
·595-610
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IF 1.401
Liu Wei,Quan Ji
In this work, a quantitative structure–property relationship (QSPR) model based on atom-type electrotopological state (E-state) indices has been developed for predicting the dispersive liquid–liquid microextraction (DLLME) enrichment effect for aromatic organics by using 1-octyl-3-methylimidazolium hexafluorophosphate ([OMIM][PF 6 ]) ionic liquid as extractant. The enrichment factors of the aromatic organics obtained through DLLME-IL process were used as the dependent variable of the multiple linear regression (MLR) equation. The E-state indices of those organic compounds which combined together both electronic and topological characteristics of the analyzed molecules were used as molecular structure descriptors and the independent variable of the equation. The squared correlation coefficient R 2 for the MLR was 0.992 for the training set of 33 compounds. For the test set of 8 compounds, the linear regression coefficient was R 2 = 0.985. The results of this study showed that it can successfully predict enrichment factors of [OMIM][PF 6 ] in DLLME by using atom-type E-state indices, which can provide one more way for predicting the ability of ionic liquid to extract organic compounds based on their molecular structures.
研究领域:
分析化学
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环境科学
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
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2026
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IF 2.6
Mengjia Sheng,Xiang Zhang,Zhen Song,Hongye Cheng,Zhiwen Qi
The rapid development of dye industry has led to a significant amount of wastewater discharged. As a widely-used dye, toxic and non-degradable methylene blue is becoming a serious threat to our ecosystem. Thus, wastewater containing methylene blue must be treated properly. Considering the strengths of ionic liquid (IL) and metal organic framework (MOF) in molecular separation, a convenient solution strategy is proposed in this work for designing and preparing IL@MOF composite adsorbent in order to efficiently remove methylene blue from water. As a kind of water-stable MOFs, UiO-66 was synthesized by a one-pot method under very mild conditions using deep eutectic solvent (DES) as reaction media instead of conventional organic solvents. The easily obtained UiO-66-DES has superior MB adsorption kinetics but limited adsorption capacity. To mitigate this weakness, a computational and systematic IL screening framework is developed. [EtOHMIM][PF6] is eventually selected from 3569 candidates and incorporated into the UiO-66-DES. The resulted IL@MOF composite maintains the fast MB adsorption while importantly increasing the adsorption capacity from 45.85 mg/g to 227.57 mg/g. Given 10 mg/L MB solution, the removal rate is improved from 34% to 91% in 5 minutes. Meanwhile, the adsorption capacity is almost unchanged after 5 regeneration cycles, which offers great potentials for practical applications. Finally, the detailed mechanism analysis reveals that the loaded IL introduces new adsorption sites with stronger interactions with MB. These results show that the [EtOHMIM][PF6]@UiO-66-DES composite resulted from DES-assisted MOF synthesis and IL-based post-synthesis is a promising material for efficient MB wastewater treatment.
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高影响因子
International Journal of Analytical Chemistry
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2018
·
IF 1.479
Xiaoshan Huang,Mingxin Guan,Zhuliangzi Lu,Yiping Hang
A new sensitive method for antimony (III) determination by graphite furnace atomic absorption spectrometry (GFAAS) has been developed by using N-benzoyl-N-phenylhydroxylamine (BPHA) and 1-butyl-3-methylimidazolium hexafluorophosphate ([C4mim][PF6]) single drop microextraction. The single drop microextraction (SDMM) system is more competitive compared with other traditional extraction methods. Under the optimized conditions, the limit of detection (signal-to-noise ratio is 3) and the enrichment factor of antimony (III) are 0.01 μg·L−1 and 112, respectively. The relative standard deviation of the 0.5 μg·L−1 antimony (III) is 4.2% (n=6). The proposed method is rather sensitive to determinate trace antimony (III) in water.
研究领域:
分析化学
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环境科学
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产品关联
DOI
PubMed
高影响因子
FOOD CHEMISTRY
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2024
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IF 8.5
Li Zhang,Yu Han,Ming Sun,Shaobin Li
In this study, we developed an electrochemical sensor utilizing a composite material consisting of zirconium‑copper bimetallic metal-organic framework functionalized with ionic liquid [BMIM][PF 6 ]. This composite material was fabricated by simple wet impregnation method, which not only maintains excellent electrocatalytic activity but also enhances electron transfer rate and electroactive surface area . The ZrCu-MOF-818/ILs composite modified electrode has been demonstrated as an effective tool for the detection of nitrite. The electrode exhibited a remarkable limit of detection (LOD) of 0.148 μM and wide linear ranges of 6–3000 μM and 3000–5030 μM. It is worth noting that the sensor displayed excellent reproducibility and repeatability, with relative standard deviation (RSD) values of 1.06% and 1.37%, respectively. Furthermore, the proposed method was successfully applied for the detection of nitrite in tap water and pickle juice.
研究领域:
分析化学
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食品科学
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产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING SCIENCE
·
2023
·
IF 4.7
Qiang Sun,Jia Xiong,Hongxia Gao,Wilfred Olson,Zhiwu Liang
Catalytic CO 2 desorption from rich amine solution is a practical approach to reducing energy consumption for amine regeneration. In this study, for the first time, the catalytic effect of environmentally friendly, imidazole series ionic liquids ([Bmim]PF 6 , [Bmim]BF 4 , [Bmim]HSO 4 , [Bmim]NO 3 , [Bmim]CH 3 COOH, [Bmim]Cl, [Bmim]Br, and [Bmim]I) is evaluated in terms of CO 2 desorption rate, amount of CO 2 released, and heat duty. Overall, the [Bmim]PF 6 catalyst shows excellent catalytic activity for CO 2 desorption, increasing the quantity of CO 2 released by 21.35% and reducing the relative heat duty by 17.59%. In addition, the catalytic applicability of [Bmim]PF 6 for secondary and tertiary amine systems was evaluated. Of note, the homogeneous [Bmim]PF 6 catalyst presents good stability during 5 cycles. The catalyst/MEA (monoethanolamine) solution ratio of 3 wt% retained about 94% of the catalytic performance after five cycling tests without any reactivation step, showing the potential application of this desorption technology for CO 2 capture with lower heat duty.
研究领域:
化学工程
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环境科学
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催化
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碳捕集与封存
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2025
·Vol. 49
·期 9
·3526-3535
·
IF 2.5
Shuang Meng,Yan Zhuang,Xue Yang,Dongxuan Guo,Jinlong Li
Volatile organic compounds (VOCs) emitted from industrial activities and transportation pose significant health risks to humans and contribute to environmental issues. As a result, there has been growing interest in developing effective technologies for VOC removal. This study investigates the removal of low-concentration VOCs from air using a membrane catalytic process that combines a supported ionic liquid membrane (SILM) with a novel visible light-driven photocatalyst. The system, consisting of a 1-butyl-3-methylimidazolium hexafluorophosphate ([BMIM]PF6) SILM and N-doped La–TiO2 photocatalysts, achieves a mineralization rate of 40%–60% and a removal efficiency of approximately 75% for VOCs under visible light exposure for 10 hours. The synergistic effects of membrane separation and photocatalytic degradation significantly enhance the overall VOC removal efficiency compared to using either method alone. The membrane catalytic system demonstrates particular applicability and stability for various organic compounds, including toluene, acetone, chloroform, benzene, and xylene. Overall, this work presents a promising approach for the removal and mineralization of VOCs.
研究领域:
环境科学
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化学工程
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DOI
高影响因子
Nano Energy
·
2024
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IF 16.8
Qiang Liu,Yi-Hu Feng,Xu Zhu,Mengting Liu,Lianzheng Yu,Guang-Xu Wei,Xin-Yu Fan,Xiao Ji,Peng-Fei Wang,Hanshen Xin
Sodium-ion batteries (SIBs) operating under high-voltages suffer from unstable cathode-electrolyte interphase (CEI) formed on the cathode surface , resulting in continuous electrolyte decomposition, surface reconstruction, transition metal dissolution, and eventually capacity decay. Therefore, designing high-voltage electrolyte and constructing the robust CEI are critical for high-energy SIBs. Herein, a localized high-concentration electrolyte (LHCE) is fabricated by dissolving sodium hexafluorophosphate in methyl ethyl carbonate, fluorinated ethylene carbonate and 1,1,2,2-tetrafluoroethyl-2,2,3,3-tetrafluoropropyl ether, which demonstrates oxidative stability exceeding 6 V relative to Na + /Na. The dense and homogeneous inorganics-rich CEIs are generated by the preferential decomposition of PF 6 − anions during the electrochemical charge to 4.4 V, which lower interface impedance, facilitate Na + transportation and suppress subsequent side reactions. Consequently, the cell integrating high-voltage P2-Na 0.7 Li 0.03 Mg 0.03 Ni 0.27 Mn 0.6 Ti 0.07 O 2 cathode and Na anode exhibits a capacity retention of 87.3% after 200 cycles and a high-rate discharge capacity of 84 mA h g −1 at 20 C under a high cut-off voltage of 4.4 V. This work offers a feasible pathway to tailor electrolyte chemistry and interphase properties for practical next generation high-voltage SIBs.
研究领域:
电化学
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储能
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材料科学
·
电池技术
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DOI
高影响因子
BIORESOURCE TECHNOLOGY
·
2016
·
IF 4.917
Yu-Cai He,Zhi-Cheng Tao,Jun-Hua Di,Liang Chen,Lin-Bing Zhang,Dan-Ping Zhang,Gang-Gang Chong,Feng Liu,Yun Ding,Chun-Xia Jiang,Cui-Luan Ma
It was the first report that the concentrated hydrolyzates from the enzymatic hydrolysis of dilute NaOH (3 wt%)-soaking rice straw at 30 °C was used to form [Bmim]PF 6 -hydrolyzate (50:50, v/v) media for bioconverting ethyl 4-chloro-3-oxobutanoate (COBE) into ethyl ( R )-4-chloro-3-hydroxybutanoate [( R )-CHBE] (>99% e.e. ) with recombinant E. coli CCZU-A13. Compared with pure glucose, the hydrolyzates could promote both initial reaction rate and the intracellular NADH content. Furthermore, emulsifier OP-10 (20 mM) was employed to improve the reductase activity. Moreover, Hp-β-cyclodextrin (0.01 mol Hp-β-cyclodextrin/mol COBE) was also added into this bioreaction system for enhancing the biosynthesis of ( R )-CHBE from COBE by E. coli CCZU-A13 whole-cells. The yield of ( R )-CHBE (>99% e.e. ) from 800 mM COBE was obtained at 100% in the [Bmim]PF 6 -hydrolyzate (50:50, v/v) media by supplementation of OP-10 (20 mM) and Hp-β-CD (8 mM). In conclusion, an effective strategy for the biosynthesis of ( R )-CHBE was successfully demonstrated.
研究领域:
生物化学
·
微生物学
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DOI
高影响因子
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