IPMC的制备及其电极结构的表征

由聚乙烯-乙烯醇(EVOH)和1,3-丙烷磺酸内酯合成了EVOH磺酸钾离子聚合物(EVOH-SO3K),并用2,4-甲苯二异氰酸酯(TDI)对其进行了交联改性,得到TDI改性EVOH磺酸钾离子聚合物(EVOH-TSO3K),通过EVOH-TSO3K溶液的铸膜和化学沉积制得离子聚合物膜金属复合材料(IPMC).采用傅立叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)分别对EVOH-TSO3K及其IPMC进行了结构表征.结果表明,EVOH-TSO3K形成了交联结构,银金属电极均匀沉积在聚合物膜表面.通过三次化学沉积,IPMC表面电阻可达到8×10-1Ω/mm2,从而在外加负载电压下(3V)实现了电形变,电形变角度达到36°.     

胃、肠消化后猪肝酱中铁和锌的形态分析

研究胃、肠消化对猪肝酱中Fe和Zn的形态影响。采用体外全仿生消化技术模拟猪肝酱在胃、肠中消化,利用0.45 μm微孔滤膜分离悬浮态和可溶态,通过D101大孔树脂实现无机态和有机态的分离。通过单因素试验,确定Fe最佳测定条件为乙炔流量80 L/h,燃烧器高度5 mm;Zn最佳测定条件为乙炔流量90 L/h,燃烧器高度6 mm。在此条件下,测定猪肝酱中Fe含量为112.56 μg/g,Zn含量为41.38 μg/g。胃、肠消化后除悬浮态Fe和Zn,其他各形态Fe和Zn的含量都所有增加,生物可给性变大,这表明胃、肠消化都是将一部分悬浮态Fe和Zn消化成可溶态Fe和Zn,其中以有机态Fe和Zn为主。     

COSMO-RS:An ionic liquid prescreening tool for gas hydrate mitigation

Recently ionic liquids(ILs) are introduced as novel dual function gas hydrate inhibitors. However, no desired gas hydrate inhibition has been reported due to poor IL selection and/or tuning method. Trial error as well as selection based on existing literature are the methods currently employed for selecting and/or tuning ILs. These methods are probabilistic, time consuming, expensive and may not result in selecting high performance ILs for gas hydrate mitigation. In this work, COSMO-RS is considered as a prescreening tool of ILs for gas hydrate mitigation by predicting the hydrogen bonding energies(E_(HB)) of studied IL inhibitors and comparing the predicted E_(HB) to the depression temperature(?) and induction time. Results show that, predicted EHBand chain length of ILs strongly relate and significantly affect the gas hydrate inhibition depression temperature but correlate moderately(R = 0.70) with average induction time in literature. It is deduced from the results that, ? increases with increasing IL EHBand/or decreases with increasing chain length. However, the cation–anion pairing of ILs also affects IL gas hydrate inhibition performance. Furthermore, a visual and better understanding of IL/water behavior for gas hydrate inhibition in terms of hydrogen bond donor and acceptor interaction analysis is also presented by determining the sigma profile and sigma potential of studied IL cations and anions used for gas hydrate mitigation for easy IL selection.     

Novel composite electrolyte membranes consisting of fluorohydrogenate ionic liquid and polymers for the unhumidified intermediate temperature fuel cell

Novel composite electrolyte membranes consisting of [EMIm](FH)_nF (EMIm = 1-ethyl-3-methylimidazolium, n = 1.3 and 2.3) ionic liquids and fluorinated polymers were synthesized and their physical and electrochemical properties were measured under unhumidified conditions for their application to the intermediate temperature fuel cells. The ionic conductivities of composite membrane, P(VdF-co-HFP)/s-DFBP-HFDP/[EMIm](FH)_2.3F (1/0.3/1.75 in weight ratio), were 11.3 and 34.7 mS cm⁻¹ at 25 and 130 °C, respectively. The open circuit voltage (OCV) observed for the single cell using [EMIm](FH)_2.3F composite electrolyte was ∼1.0 V at 130 °C for over 5 h. The maximum power density of 20.2 mW cm⁻² was observed under the current of 60.1 mA cm⁻² at 120 °C. From the high thermal stability and high ionic conductivity, the fluorohydrogenate ionic liquid composite membranes are regarded as promising candidates for the electrolytes of the unhumidified intermediate temperature fuel cells.     

A novel PEO-based composite polymer electrolyte with absorptive glass mat for Li-ion batteries

A novel PEO (polyethylene oxide)-based composite polymer electrolyte (CPE) using absorptive glass mat (AGM) as filler was prepared and characterized. Scanning electronic micrograph (SEM) images showed that the addition of Li salt and modified AGM may improve the surface morphology of CPE. The results of Fourier-transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and differential scanning calorimeters (DSC) indicated that the inclusion of LiClO₄ salt and the addition of AGM filler can reduce the crystallinity of PEO. It was concluded that the addition of AGM plays two roles in PEO-based CPEs, namely, interruption of the PEO recrystallization and reinforcement of CPEs, accordingly enhancing room temperature ionic conductivity of CPEs and improving its mechanical strength and electrochemical stability at high temperatures.     

Ionic liquid based periodic mesoporous organosilica: An efficient support for removal of sunset yellow from aqueous solutions under ultrasonic conditions

The efficiency of an ionic liquid based periodic mesoporous organosilica (PMO-IL) in the removal of sunset yellow from aqueous solutions using ultrasonic assisted adsorption method was investigated. The PMO-IL was first characterized by nitrogen sorption and TEM techniques. The optimized conditions (0.013 g of adsorbent, 32 mg L⁻¹ of sunset yellow at 2 min of sonication time and pH 7) were obtained by central composite design (CCD). Fitting the equilibrium data show the suitability of the Langmuir model with second-order equation to control the kinetic of the adsorption process and good reusability (5 cycles) of PMO-IL for adsorption of dye.     

Increasing ionic conductivity and mechanical strength of a plastic electrolyte by inclusion of a polymer

In this contribution we present a soft matter solid electrolyte which was obtained by inclusion of a polymer (polyacrylonitrile, PAN) in LiClO₄/LiTFSI-succinonitrile (SN), a semi-solid organic plastic electrolyte. Addition of the polymer resulted in considerable enhancement in ionic conductivity as well as mechanical strength of LiX-SN (X = ClO₄, TFSI) plastic electrolyte. Ionic conductivity of 92.5%-[1 M LiClO₄-SN]:7.5%-PAN (PAN amount as per SN weight) composite at 25 °C recorded a remarkably high value of 7 × 10⁻³ Ω⁻¹ cm⁻¹, higher by few tens of order in magnitude compared to 1 M LiClO₄-SN. Composite conductivity at sub-ambient temperature is also quite high. At −20 °C, the ionic conductivity of (100 − x)%-[1 M LiClO₄-SN]:x%-PAN composites are in the range 3 × 10⁻⁵-4.5 × 10⁻⁴ Ω⁻¹ cm⁻¹, approximately one to two orders of magnitude higher with respect to 1 M LiClO₄-SN electrolyte conductivity. Addition of PAN resulted in an increase of the Young's modulus (Y) from Y → 0 for LiClO₄-SN to a maximum of 0.4 MPa for the composites. Microstructural studies based on X-ray diffraction, differential scanning calorimetry and Fourier transform infrared spectroscopy suggest that enhancement in composite ionic conductivity is a combined effect of decrease in crystallinity and enhanced trans conformer concentration.     

Ionic conductivity studies of poly(ethylene oxide)-lithium salt electrolytes in high-pressure carbon dioxide

We have measured ionic conductivity of PEO-LiX [anion X=N(CF₃SO₂)₂ (TFSI), ClO₄, CF₃SO₃, BF₄, NO₃, and CH₃SO₃] polymer electrolytes in CO₂ at pressures varied from 0.1 to 20 MPa. From the temperature dependence in supercritical CO₂, a large increase in the conductivity for PEO-LiBF₄ and LiCF₃SO₃ electrolytes has been observed. Permeation of the CO₂ molecules gave rise to the plasticization for crystal domains in the electrolytes, which is related to the reduction in transition point of the Arrhenius plot corresponding to the melting of crystal PEO. Relation between the conductivity and CO₂ reduced density revealed that the electrolytes containing fluorinated anions such as ‘CO₂-philic’ BF₄ and CF₃SO₃ increase in the conductivity with increasing the density. This indicates that the salt dissociation was promoted by the CO₂ permeation and the Lewis acid-base interactions between fluorinated anions and CO₂ molecules.     

Electrodeposition of PtZn in a Lewis acidic ZnCl2-1-ethyl-3-methylimidazolium chloride ionic liquid

The electrodeposition of PtZn from a Lewis acidic 40-60 mol% zinc chloride-1-ethyl-3-methylimidazolium chloride ionic liquid containing PtCl₂ was investigated at polycrystalline tungsten substrates at 90 °C. Cyclic voltammetric data indicates that Pt(II) was reduced at a potential slightly more positive than Zn(II) was. The Pt-Zn electrodeposits exhibited multiple anodic stripping waves. The Zn-dominant deposits were stripped at a potential less positive than that of the Pt-dominant deposits. Energy-dispersive spectroscopy and scanning electron microscopy data indicated that the composition and morphology of the electrodeposited Pt-Zn alloys were affected by the deposition potential and the Pt(II) concentration in the plating solution. The electrodeposition of Zn at a Pt substrate also produced surface Pt-Zn alloys. The Pt of the electrochemically prepared Pt-Zn alloys was easier to oxidize than the bulk Pt substrate.     

Design and optimization of an integrated process for the purification of propylene oxide and the separation of propylene glycol by-product

It is difficult to separate the methanol and hydrocarbons in the propylene oxide (PO) purification process due to their forming azeotrope. As for this, a novel PO separation process, in that the deionized water is employed as extractant and 1,2-propylene glycol (MPG) that is formed from the PO hydrolysis reaction is recovered, is presented in this work. The salient feature of this process is that both the non-catalyzed reactions of PO hydrolysis to form MPG and dipropylene glycol (DPG) are simultaneously considered and MPG by-product with high purity is obtained in virtue of the deionized water as reflux liquid and side take-off in MPG column. In addition, the ionic liquid (IL) extractant is screened through the conductor-like screening model for segment activity coefficient (COSMO-SAC) and the comparisons of separation efficiency between the IL and normal octane (nC₈) extractant for the separation of PO and 2-methylpentane are made. With the non-random two-liquid (NRTL) thermodynamic model, the simulation and optimization design for the full flow sheet are performed and the effects of the key operation parameters such as solvent ratio, theoretical stages, feeding stage etc. on separation efficiency are detailedly discussed. The results show that the mass purity and the mass yield of PO can be up to 99.99% and 99.0%, and the condenser duty, reboiler duty and PO loss in the process with IL extractant can be decreased by 69.66%, 30.21% and 78.86% compared to ones with nC₈. The total annual cost (TAC) calculation also suggests that the TAC would be significantly reduced if using IL in replace of nC₈ for the investigated process. The presented results would provide a useful guide for improving the quality of PO product and the economic efficiency of industrial plant.