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Ionic Liquid
ACS Omega · 2018 · IF 0

Ionic-Liquid-Assisted One-Step Synthesis of CoO Nanosheets as Electrocatalysts for Oxygen Evolution Reaction

Anning Jiang,Nagapradeep Nidamanuri,Chenyun Zhang,Zhonghao Li

The sluggish oxygen evolution reaction (OER) hinders the development of electrocatalytic water splitting for energy conversion and storage. Therefore, it is imperative to explore the cost-effective and highly efficient noble-metal-free electrocatalysts for OER. Herein, we are introducing such OER electrocatalyst based on Co, fabricated through an ionic-liquid-assisted one-step synthesis, where ionic liquid played a dual role as solvent cum structure-directing agent. Besides possessing large-accessible surface area and numerous active sites, the as-prepared stable CoO nanosheets exhibited excellent electrochemical activity through establishing an extensive contact with the electrolyte. Under alkaline conditions, the overpotential to achieve a current density of 10 mA cm–2 is only 320 mV, and the Tafel slope is as small as 70 mV dec–1. Thus, our work provides a new pathway for designing and engineering the highly efficient non-noble metal OER electrocatalysts by using ionic liquids.

CAS / MDL: 21679-46-9
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POLYMER · 2018 · IF 3.483

Ionic liquid embedded polyimides with ultra-foldability, ultra-flexibility, ultra-processability and superior optical transparency

Ning-Bo Li,Meng Wang,Ling-Xiang Guo,Bao-Ping Lin,Hong Yang

New generation spacecraft technology requires more and more deployable, light-weight, thin polymer films , in particular novel polyimide materials with high optical transparency, excellent foldability and superior flexibility. In this work, we develop a highly transparent, ultra-foldable, ultra-flexible and ultra-processable polyimide composite material by incorporating 5–8 wt% of ionic liquid 1-ethyl-3-methylimidazolium bis((trifluoromethyl)sulfonyl)imide into colorless polyimide matrices. This 23-μm-thick polyimide composite film exhibits a high optical transmittance of 90.4% even at 450 nm wavelength and an incredibly low cutoff wavelength of 273 nm. It is an extremely strong and flexible material, with a tensile modulus of 844.6 MPa, a tensile strength of 48.2 MPa, a high elongation at break of 108.4%, and an extraordinary minimum bend radius of 1  μ m. It can be easily folded in half 4 times or twisted by 900° without any crack damages. Moreover, it has a low expense cost and good film processability for industrialization manufacturing. All of these superior performances render this ionic liquid/polyimide composite an ideal structural material for solar sails, solar arrays and thin-film photovoltaics , etc.

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POLYMER ENGINEERING AND SCIENCE · 2013 ·Vol. 54 ·期 1 ·59-63 · IF 1.243

Synthesis of new crosslinked porous ammonium-based poly(ionic liquid) and application in CO2 adsorption

Guangren Yu,Qingzeng Li,Na Li,Ziwei Man,Chenghao Pu,Charles Asumana,Xiaochun Chen

A new poly(ionic liquid) of N , N -methylenebisacrylamide (MBA)-crosslinked-poly(4-vinylbenzyltriethylammonium hexafluorophosphate)(MBA-crosslinked-P[VBTEA][PF 6 ]) is prepared through the ion exchange of KPF 6 with the precursor of MBA-crosslinked-P[VBTEA][Cl]; the precursor is synthesized by 4-vinylbenzyltriethylammonium chloride and MBA via inverse suspension polymerization. MBA-crosslinked-P[VBTEA][PF 6 ] is a thermally stable (decomposes at nearly 300°C) and porous (apparent porosity of 64.3% and specific surface of 39.12 m 2 /g) polymer particle with high purity, as indicated by Fourier transformed infrared, energy dispersive spectroscopy, thermogravimetric, scanning electron microscopy, and porous analyses. It is observed that MBA-crosslinked-P[VBTEA][PF 6 ] has good CO 2 adsorption capability of 14.04 mg/g at 0.2 MPa and 25°C, and can be recovered by desorption at vacuum and 80°C, and reused with 99% CO 2 adsorption after four cycles. POLYM. ENG. SCI., 54:59–63, 2014. © 2013 Society of Plastics Engineers

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JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL · 2012 · IF 2.947

The effect of vinyl-containing ionic liquid on the photocatalytic activity of iron-doped TiO2

Fang Deng,Xubiao Luo,Ke Li,Xinman Tu,Shenglian Luo,Lixia Yang,Ninghui Zhou,Hongying Shu

Visible light responsive iron-doped TiO 2 (Fe 3+ /TiO 2 -IL) was synthesized by sol–gel method using 1-vinyl-3-propylimidazolium iodide (VPIM + I − ) as a reaction medium. VPIM + I − not only made the morphological and structural changes of Fe 3+ /TiO 2 -IL, but also extended its absorption edge to the visible light region. The photocatalytic activity of Fe 3+ /TiO 2 -IL was tested in the degradation of 2-nitrophenol under simulated solar light irradiation. The photocatalytic activity of Fe 3+ /TiO 2 -IL was higher than the samples prepared in the reaction medium without VPIM + I − . Moreover, the effect of pH and H 2 O 2 on the photocatalytic activity of Fe 3+ /TiO 2 -IL was also investigated. Fe 3+ /TiO 2 -IL showed high photocatalytic activity in acidic environment, and H 2 O 2 had a dual effect on the photocatalytic activity Fe 3+ /TiO 2 -IL.

CAS / MDL: 88-75-5
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JOURNAL OF MOLECULAR CATALYSIS B-ENZYMATIC · 2014 · IF 2.745

Ionic liquid as a recyclable and efficient medium for lipase-catalyzed asymmetric cross aldol reaction

Yang Zhang,Na Wang,Zong-Bo Xie,Long-Hua Zhou,Xiao-Qi Yu

PPL (lipase from porcine pancreas) was found to catalyze asymmetric cross aldol reactions of aromatic and heteroaromatic aldehydes with various ketones in ionic liquid ([BMIM][PF 6 ]) for the first time. Interestingly, PPL exhibited high catalytic activity and excellent stereoselectivity in this efficient and recyclable room temperature ionic liquid in the presence of moderate water, similar to the results obtained in organic solvents. High yields of up to 99%, excellent enantioselectivities of up to 90% ee, and good diastereoselectivities of up to >99:1 dr were achieved.

CAS / MDL: 98-10-2
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INORGANICA CHIMICA ACTA · 2015 · IF 2.046

Commercially available ammonium salt-catalyzed efficient dehydration of fructose to 5-hydroxymethylfurfural in ionic liquid

Hui Liu,Chun Hua,Changhua Song,Shifeng Dai,Hongwei Wang,Wenshuai Zhu,Huaming Li

Some sulfur oxyacid salts with weak acidity or alkalinity, including Na 2 SO 4 , (NH 4 ) 2 SO 4 , (NH 4 ) 2 S 2 O 3 and Na 2 S 2 O 3 , were applied to the conversion of fructose to 5-hydroxymethylfurfural. The results indicated that (NH 4 ) 2 S 2 O 3 had excellent catalytic performance for the conversion of fructose. A desired HMF yield of 81.6% was obtained with only 5   mg (NH 4 ) 2 S 2 O 3 as the catalyst in [Bmim]Cl at 120   °C for 50   min. Furthermore, the HMF yield remained at 76.6% with 60   wt% water in the IL–water mixture solvent. In addition, the system of (NH 4 ) 2 S 2 O 3 and [Bmim]Cl exhibited a constant stability and activity, and a good HMF yield was maintained after nine recycles.

CAS / MDL: 7783-18-8
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Polymer Chemistry · 2013 ·Vol. 5 ·期 3 ·882-891 · IF 5.231

Poly(ionic liquid)s-based nanocomposite polyelectrolytes with tunable ionic conductivity prepared via SI-ATRP

Ping Wang,Yin-Ning Zhou,Jiang-Shui Luo,Zheng-Hong Luo

In this study, a novel kind of organic–inorganic core–shell SiO2-poly(p-vinylbenzyl) trimethylammonium tetrafluoroborate (SiO2–P[VBTMA][BF4]) nanoparticle was well designed and successfully synthesized via surface-initiated atom transfer radical polymerization (SI-ATRP). Fourier transform infrared spectroscopy (FT-IR), 1H nuclear magnetic resonance (1H NMR), X-ray photoelectron spectroscopy (XPS), dynamic light scattering (DLS) and scanning electron microscopy (SEM) were used to confirm the formation of the core–shell nanoparticles and the surface modification. In order to overcome the challenge of the characterization of the number average molecular weight of poly(ionic liquid)s, “sacrificial initiator” method was used here employing a trimethylsilyl (TMS)-labeled initiator as the NMR marker for integration. In addition, good thermal stability of the new hybrid polyelectrolyte was proved by thermogravimetric analysis. The electrochemical impedance measurements revealed that the room temperature conductivity reached 10−4 S cm−1, which is much higher than that of the pure poly(ionic liquid)s and varies with the amount of the grafted polymer and the test temperature. The X-ray diffraction (XRD) tests further investigated the crystal structure of the nanocomposite and pure P[VBTMA][BF4]. The temperature dependence of ionic conductivity conforms to Arrhenius behavior for both of the nanocomposites and the pure polymer. The results indicated that the SI-ATRP approach provided a simple and versatile route to tune the ionic conductivity of the hybrid nanoparticles by changing the chain length of the grafted polymer, which can be potentially used in a variety of electrochemical devices.

CAS / MDL: 13755-29-8 2916-68-9
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SPECTROSCOPY LETTERS · 2013 · IF 0.667

Fluorescence Spectrometric Studies on the Binding of an Amino-Functionalized Ionic Liquid to Cytochrome c

Yun-Chang Fan,Xue-Yun Gong,Jing Li,Lei Zhang,Chun-Jia Sun

The interaction of an amino-functionalized ionic liquid, 1-(2-aminoethyl)-3-butylimidazolium bromide ([NH2C2C4im]Br), with cytochrome c (cyt c) at pH 7.4 was investigated using fluorescence and UV-Vis absorption spectroscopic techniques. From the experimental results, it is found that cyt c has a strong ability to quench the intrinsic fluorescence of [NH2C2C4im]Br and the quenching mechanism is considered as a static quenching process. The binding constants and the number of binding sites (n) were calculated at different temperatures. The thermodynamic parameters such as free energy change (ΔG), enthalpy change (ΔH), and entropy change (ΔS) were calculated by thermodynamic equations. According to the results, the values of ΔG, ΔH, and ΔS are all negative, suggesting that interaction between [NH2C2C4im]Br and cyt c is spontaneous and mainly driven by hydrogen bonding and van der Waals forces.

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NEW JOURNAL OF CHEMISTRY · 2017 ·Vol. 41 ·期 19 ·10598-10606 · IF 3.269

Solubilization of seven hydrophobic pesticides in quaternary ammonium based eco-friendly ionic liquid aqueous systems

Chong Chen,Fengmao Liu,Tengfei Fan,Qizhen Zhou,Qingrong Peng

In this work, quaternary ammonium based ionic liquids (ILs) are proven to be good candidates to act as green solvents/solubilizers for pesticide formulations. The surface activity of six ionic liquids ([M3CnN]X; M = CH3; n = 10, 12, 14; X = Cl, Br) was tested, along with the corresponding critical aggregation concentration (CAC), lowest surface tension (γCAC), maximum surface excess concentration (Γmax), minimum area per molecule (Amin) and higher adsorption efficiency (pC20), which were measured using several methods, including surface tension measurements, electrical conductivity measurements, steady-state fluorescence measurements and 1H NMR. The thermodynamic parameters of micellization, the viscosities and the activation energies of the six ILs in 30% aqueous solutions, over the temperature range of 288–308 K, were determined and calculated. The results indicated that the solubilities of representative pesticides (metolachlor, acetochlor, clethodim, thiamethoxam, prochloraz, acetamiprid and fosthiazate) in different concentrations of these ILs were significantly higher than in pure water, especially for prochloraz (e.g., 137.2 g L−1 in 30% C10Br, 4035 times higher than in pure water). The microenvironment existing between the pesticide and micelle was investigated using 1H NMR techniques, revealing that micelle localization of pesticide molecules and a change in micelle conformation occurred in the dissolving process.

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JOURNAL OF SOLUTION CHEMISTRY · 2016 ·Vol. 45 ·期 3 ·359-370 · IF 1.256

Structural Heterogeneities in Solutions of Triethylamine Nitrate Ionic Liquid: 1H NMR and LC Model Study

Zhu Xiao,Zhang Huan,Xu Yingjie

In order to uncover the micro-structural heterogeneities in solutions of ammonium based ionic liquids, triethylamine nitrate (N 222 NO 3 ) has been synthesized using acid–base neutralization and the 1 H NMR spectra of two binary mixtures, namely N 222 NO 3 /dimethyl sulfoxide (DMSO) and N 222 NO 3 /acetone at different concentrations, have been measured at 298.15 K. The internal reference method was adopted to obtain the concentration-dependent chemical shifts of –CH 3 in N 222 NO 3 , which have been correlated using the 1 H NMR local composition (LC) model to obtain the local mole fractions. It has been revealed that within N 222 NO 3 rich region, self-association of the ionic liquid was predominant instead of N 222 NO 3 –solvent interactions. However, in the solvent rich region, N 222 NO 3 mainly interacts with solvent molecules, indicating that the self-association network of N 222 NO 3 has been greatly destroyed by solvents. In addition, the different influences of DMSO and acetone have been detected. DMSO molecules more effectively destroy the original network of the ionic liquid, due to its higher dielectric constant. Also, LC behavior in N 222 NO 3 /DMSO systems is more significant than in N 222 NO 3 /acetone, indicating that DMSO can induce more obvious heterogeneities in DMSO/N 222 NO 3 mixtures, which is consistent with physicochemical properties and cellulose solubility of solutions.

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JOURNAL OF CHEMICAL THERMODYNAMICS · 2016 · IF 2.196

Physicochemical properties of binary mixtures of 1,1,3,3-tetramethylguanidine imidazolide ionic liquid with water and alcohols

Fangfang Ye,Jiahong Zhu,Keke Yu,Ruyu Zhu,Yingjie Xu,Jiayi Chen,Lingxiao Chen

In this work, densities and viscosities of aqueous solution of 1,1,3,3-tetramethylguanidine imidazolide ([TMG]IM) ionic liquid were measured at temperatures from T   =   (293.15 to 313.15)   K. Volumetric properties including excess molar volumes V E , apparent molar volumes, partial molar volumes, and excess partial molar volumes were calculated from the experimental density. Viscosity deviations Δ η , Gibbs energy and excess Gibbs energy of activation for viscous flow were deduced from the viscosity. Moreover, electrical conductivities κ and refractive indices of binary mixtures of [TMG]IM with water and alcohols were determined at 298.15   K. The results show that V E values of {[TMG]IM (1)   +   water (2)} mixture are negative over the whole composition range, while Δ η and refractive index deviations Δ n D values exhibit positive deviations, indicating that the hydrogen bonding interaction between [TMG]IM and water is dominant. The absolute values of V E and Δ η of the mixture decrease with the increasing temperature. The V E , Δ η , and Δ n D can be fitted by the Redlich–Kister equation with satisfactory results. The concentration-dependent κ of the studied systems are fitted to Casteel–Amis equation, showing that the κ values of {[TMG]IM (1)   +   water (2)} mixture are much higher than those of {[TMG]IM (1)   +   ethanol (2)} mixture.

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JOURNAL OF MATERIALS SCIENCE · 2017 ·Vol. 52 ·期 24 ·13992-14003 · IF 2.599

An efficient phosphonate-based ionic liquid on flame retardancy and mechanical property of epoxy resin

Xiao Fei,Wu Kun,Luo Fubin,Guo Yuyue,Zhang Shiheng,Du Xiangxiang,Zhu Qingqing,Lu Mangeng

In order to develop a highly efficient flame-retardant system, a phosphonate-based ionic liquid named 1-vinyl-3-(diethoxyphosphoryl)-propylimidazolium bromide (IL) was synthesized and introduced into epoxy resin (EP). With only 4 wt% loading, EP/IL composite passed UL-94 V-0 rating, and its limiting oxygen index value increased to 34.9% from 25.9% for neat epoxy resin. The char yield of EP/IL-2 (2 wt%) was improved by 58.3%, and its peak of heat release rate was reduced by 65% compared with that of neat EP. The reason is that the presence of IL promoted the forming of a compact and stable phosphorus-rich residual chars. Unlike traditional additive-type flame retardant, it is very interesting that the introduction of IL changed the color and transparency of EP few and enhanced mechanical property of neat EP remarkably. Owing to the excellent compatibility and steric effect between IL and EP matrix, tensile strength was increased to 108.6 MPa for EP/IL sample from 84.9 MPa for neat EP, indicating the outstanding reinforcement effect of IL on EP composites.

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