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101.
Desulfurization of flue gas: SO(2) absorption by an ionic liquid 总被引:7,自引:0,他引:7
102.
For the fist time the preparation of a mostly solid-state high efficiem electro-conductive material comprising 1-methyl-3-propylimidazolium iodide (MPII), benzimidazole (BI), iodine and lithium iodide was reported. In this electrolyte, BI acts as not only additives but also gelators. With its significant electrochemical properties, an overall efficiency of 3.07% was achieved under AM 1.5 (100 mW/cm^2). 相似文献
103.
Joan Fraga-DubreuilJean Pierre Bazureau 《Tetrahedron》2003,59(32):6121-6130
The first report of the use of task-specific ionic liquid as synthetic equivalent of ionic liquid-phase matrice for the preparation of a small library of 4-thiazolidinones is reported in this paper. The starting (ethyleneglycol)ionic liquid-phase is functionalized in good yields with 4-(formylphenoxy)butyric acid by using usual esterification reaction conditions (DCC/DMAP as catalyst). The synthesis of the ionic liquid-phase bound 4-thiazolidinones was performed by a one-pot three-component condensation under microwave dielectric heating. The final cleavage under microwave/catalysis strategy provides the expected 4-thiazolidinones in high purity after flash-chromatography purification. According to the ionic liquid-phase organic synthesis (IoLiPOS) methodology, it was found that optimized reaction conditions were performed by standard analytical methods (NMR, TLC). The 1H, 13C NMR spectrum of some representative 4-thiazolidinones and ionic liquid-phase bound benzaldehyde are also reported. 相似文献
104.
Romm F 《Advances in colloid and interface science》2002,95(1):73-82
In this review, existing theoretical models of vibrational phenomena in liquids are analyzed and compared. Most attention is paid to sonoluminescence, sonolysis and related phenomena. The criteria of selection of the optimal theoretical model involve analyzing experimental results, its usefulness for evaluation of thermodynamic and other parameters of the liquid under vibration, simplicity of the mathematical solution and the time needed for computing. It is concluded that, according to these criteria, the optimal (between existing models) is the chemical model of vibration in liquid, while the best perspectives are for its combinations with other models. 相似文献
105.
In this work we address the optimization of mixed conductivity in fluorite compounds based on zirconia. Phase relations of the new systems YbO1.5-NbO2.5-ZrO2, and CaO-NbO2.5-ZrO2 are presented. The limit of the cubic defect fluorite phase in YbO1.5-NbO2.5-ZrO2 closely resembles that of the system YO1.5-NbO2.5-ZrO2, whilst in CaO-NbO2.5-ZrO2 is narrow extending to include composition Ca0.255Nb0.15Zr0.595O1.82 at 1500°C. The influence of dopant ion size, charge and composition on ionic conduction is assessed and parallels are drawn with the systems YO1.5-NbO2.5-ZrO2 and YO1.5-TiO2-ZrO2. Comparison of these results with published data on the Ti containing systems CaO-TiO2-ZrO2, GdO1.5-TiO2-ZrO2 shows that the highest mixed conducting compositions can only be offered in the system YO1.5-TiO2-ZrO2 out of all the systems here studied. 相似文献
106.
Bradley Y.W. Man 《Tetrahedron letters》2005,46(44):7641-7645
The rate of the substitution reaction of (R)-3-chloro-3,7-dimethyloctane (1) with either methanol or benzyl alcohol in mixtures containing the ionic liquid [Bmim][N(CF3SO2)2] was monitored using 35Cl NMR spectroscopy. The enantiomeric excess of the product, (S)-3-methoxy-3,7-dimethyloctane (2a), was analyzed using chiral gas chromatography. This product showed a decreasing enantiomeric excess with increasing concentration of ionic liquid. The rate of reaction of substrate 1 in each case varied with the concentration of the ionic liquid. Polarity measurements of the solvent mixtures were undertaken by standard methods, which are compared both to each other and to the observed rates. Solvent reorganization and selective solvation are also each proposed as contributing to the difference in the observed rates of reaction. 相似文献
107.
108.
综述了近8年来液相平行合成和组合合成中应用的不同技术, 包括可溶性载体、氟合成技术、离子液体、固相试剂树脂以及低聚乙烯二醇(OEG)衍生物的应用等几方面内容. 论述了它们的基本原理以及相关的应用实例, 并着重强调了目标化合物的分离纯化方法. 相似文献
109.
Alessandro?De?Robertis Concetta?De?Stefano Demetrio?Milea Silvio?SammartanoEmail author 《Journal of solution chemistry》2005,34(10):1211-1226
Complex formation constants were determined potentiometrically (by a ISE-H+, glass electrode) in the systems, M2+ – Lz – H+ [M2+ = (C2H5)2Sn2+, Lz = malonate, glycinate and ethylenediamine] at t = 25 ∘C and 0.1 mol-L−1≤ I/ ≤ 1 mol-L−1 in NaClaq (0.1 mol-L−1 ≤ I ≤ 0.75 mol-L−1 for the ethylenediamine system). Thermodynamic values of formation constants, at infinite dilution, are [± 95% confidence
interval, Tβpqr refer to the equilibrium, pM2+ + qLz + rH+ = MpLqHr(2+z+r)]: for malonate, log10 Tβ110 = (5.47 ± 0.10); for glycinate, log10 Tβ110 = (9.54 ± 0.08), log10 Tβ111 = (12.97 ± 0.10); and for ethylenediamine, log10 Tβ110 = (10.47 ± 0.10), log10 Tβ120 = (16.17 ± 0.12) and log10 Tβ111 = (15.46 ± 0.10). The dependence on ionic strength of the formation constants was modeled by a simple Debye–Hückel type equation
and by the SIT approach. By analyzing the stability of the species in the three different systems we found a simple additivity
rule that can be expressed by the relationship: log10 K = 6.46 nN + 3.96 nO − 0.60 (nN2+ nO2), with a mean deviation, ε(log10 K) = 0.15 (K = equilibrium constant for the interaction of the organometal cation with the unprotonated or protonated ligand, nN = number of amino groups and nO = number of carboxylic groups of the ligand(s) involved in the formation reaction of complex species). 相似文献
110.
A room temperature ionic liquid N‐butylpyridinium hexafluorophosphate (BPPF6) was used as a binder to make an ionic liquid modified carbon paste electrode (IL‐CPE), which showed good characteristics such as simple preparation procedure, fast electrochemical response and good conductivity. The electrochemical oxidation of ascorbic acid (AA) on the new IL‐CPE was carefully studied. The oxidation peak potential of AA on the IL‐CPE appeared at 109 mV (vs. SCE), which was about 338 mV decrease of the overpotential compared to that obtained on the traditional carbon paste electrode (CPE) and the oxidation peak current was increased for about four times. The electrochemical parameters of AA on the IL‐CPE were calculated with the charge transfer coefficient (α) and the electrode reaction rate constant (ks) as 0.87 and 0.800 s?1, respectively. Based on the relationship of the oxidation peak current and the concentration of AA a sensitive analytical method was established with cyclic voltammetry. The linear range for AA determination was in the range from 1.0×10?5 to 3.0×10?3 mol/L with the linear regression equation as Ip (μA)=?2.52–0.064C (μmol/L) (n=13, γ=0.9942) and the detection limit was calculated as 8.0×10?6 mol/L (3σ). The proposed method was free of the interferences of coexisting substances such as dopamine (DA) and amino acids etc., and successfully applied to the vitamin C tablets determination. 相似文献