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91.
Ionic liquids as electrolytes 总被引:5,自引:0,他引:5
Salts having a low melting point are liquid at room temperature, or even below, and form a new class of liquids usually called room temperature ionic liquids (RTIL). Information about RTILs can be found in the literature with such key words as: room temperature molten salt, low-temperature molten salt, ambient-temperature molten salt, liquid organic salt or simply ionic liquid. Their physicochemical properties are the same as high temperature ionic liquids, but the practical aspects of their maintenance or handling are different enough to merit a distinction. The class of ionic liquids, based on tetraalkylammonium cation and chloroaluminate anion, has been extensively studied since late 1970s of the XX century, following the works of Osteryoung. Systematic research on the application of chloroaluminate ionic liquids as solvents was performed in 1980s. However, ionic liquids based on aluminium halides are moisture sensitive. During the last decade an increasing number of new ionic liquids have been prepared and used as solvents. The general aim of this paper was to review the physical and chemical properties of RTILs from the point of view of their possible application as electrolytes in electrochemical processes and devices. The following points are discussed: melting and freezing, conductivity, viscosity, temperature dependence of conductivity, transport and transference numbers, electrochemical stability, possible application in aluminium electroplating, lithium batteries and in electrochemical capacitors. 相似文献
92.
93.
Liang Xu Lei Su Hongjie Wang Min Niu Lei Zhuang Kang Peng Xingyu Fan Hongfei Gao De Lu 《Journal of the American Ceramic Society》2022,105(8):5490-5500
Pursuing novel thermal barrier–coating materials with lower thermal conductivity and high-temperature stability can simultaneously improve the working efficiency and service temperature of a gas turbine. In this study, a series of high-entropy RE2(Y0.2Yb0.2Nb0.2Ta0.2Ce0.2)2O7 (RE = La, Nd, Sm, Gd, Dy, and Er) oxides were prepared though solid-state reaction. Through tuning the rare-earth cations, an order–disorder transition occurs from certain partially ordered weberite structure (C2221) to disordered defective fluorite structure (Fm m). All the high-entropy RE2(Y0.2Yb0.2Nb0.2Ta0.2Ce0.2)2O7 oxides possess low thermal conductivity in the range of 0.91–1.34 W m−1 K−1 at room temperature, which can be attributed to increased lattice anharmonicity and disorder, resulting in additional phonon scattering. Herein, we proved that the incorporation of heterovalent cations at B-sites in high-entropy A2B2O7 crystals is an effective strategy to reduce the thermal conductivity without compromising the decrease of oxygen vacancy. Moreover, the high-entropy RE2(Y0.2Yb0.2Nb0.2Ta0.2Ce0.2)2O7 oxides show the relatively higher thermal expansion coefficients of 10.3–10.7 × 10−6°C−1 and excellent phase stability at elevated temperatures. 相似文献
94.
95.
Nanocomposites of iron oxide (Fe3O4) with a sulfonated polyaniline, poly(aniline‐co‐aminonaphthalenesulfonic acid) [SPAN(ANSA)], were synthesized through chemical oxidative copolymerization of aniline and 5‐amino‐2‐naphthalenesulfonic acid/1‐amino‐5‐naphthalenesulfonic acid in the presence of Fe3O4 nanoparticles. The nanocomposites [Fe3O4/SPAN(ANSA)‐NCs] were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), X‐ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, elemental analysis, UV–visible spectroscopy, thermogravimetric analysis (TGA), superconductor quantum interference device (SQUID), and electrical conductivity measurements. The TEM images reveal that nanocrystalline Fe3O4 particles were homogeneously incorporated within the polymer matrix with the sizes in the range of 10–15 nm. XRD pattern reveals that pure Fe3O4 particles are having spinel structure, and nanocomposites are more crystalline in comparison to pristine polymers. Differential thermogravimetric (DTG) curves obtained through TGA informs that polymer chains in the composites have better thermal stability than that of the pristine copolymers. FTIR spectra provide information on the structure of the composites. The conductivity of the nanocomposites (~ 0.5 S cm?1) is higher than that of pristine PANI (~ 10?3 S cm?1). The charge transport behavior of the composites is explained through temperature difference of conductivity. The temperature dependence of conductivity fits with the quasi‐1D variable range hopping (quasi‐1D VRH) model. SQUID analysis reveals that the composites show ferromagnetic behavior at room temperature. The maximum saturation magnetization of the composite is 9.7 emu g?1. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci, 2007 相似文献
96.
97.
Ahmed H. Ashour Naeem M. El‐Sawy Mahmoud A. Abdel Ghaffar Gamil A. El‐Shobaky 《应用聚合物科学杂志》2005,97(3):867-871
Grafted copolymer of poly(tetrafluoroethylene ethylene) (ET) with acrylic acid (AAc) was prepared by direct radiation method. The obtained films were modified by treating with small amounts of Co2+ and K+ ions (1.0 wt %). The effects of such treatment on the thermal stability and electrical conductivity of these films were studied. Cobalt treatment did not much affect the thermal degradation of the films. The results obtained revealed that k+ treatment enhanced the thermal degradation of ET‐g‐PAAc, which started 273 K lower than that observed in the case of the untreated and Co2+‐treated films. Potassium and cobalt treatment of the investigated films increased their electrical conductivity (σ) and decreased the activation energy ΔEσ. The increase in σ values was, however, more pronounced in the case of K+‐treated film. These results were discussed in terms of the effective increase in the hydrophilicity of the films, especially those treated with potassium. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 97: 867–871, 2005 相似文献
98.
用于测定钢液低氧含量的双层固体电解质研究 总被引:1,自引:0,他引:1
采用“毛坯浆料法”在ZrO2(9%摩尔含量MgO)管状固体电解质基体表面制备了厚度为1-4μm的ZrO2(10%摩尔含量Y2O3)固体电解质涂层,并分别对此在本实验室和美国LeedsandNorthrup公司进行了钢液低氧含量测试,结果表明:涂层没有破坏基体的抗热震性:氧浓差电池电动势的重现性偏差由原来的±2mV;电动势的绝对值提高10mV左右;而比日本Toray公司的同类产品提高35mV,这说明 相似文献
99.
Highly densified W2B5/C composites with W2B5 content from 30 to 70 vol% were fabricated by reaction hot pressing of the powder mixture of B4C, WC and carbon black. The reaction products were identified by XRD analysis to consist of only W2B5 and carbon, regardless of carbon content. The reaction formed composites have excellent mechanical properties (the maximum flexural strength and fracture toughness of 786 MPa and 8.9 MPa m1/2 respectively), electrical conductivity (the highest electrical conductivity of 1.64 × 106 Ω−1 m−1), and resistance to both wear and oxidation because of the presence of the plate-like W2B5 grains. In this paper, the preparation, microstructure and properties of this new composite are investigated, and the strengthening, toughening, conduction mechanisms are discussed. 相似文献
100.
The effect of the reaction kinetics on the ionic conductivity for a comblike‐type polyether (MEO) electrolyte with lithium bis(trifluoromethane sulfonyl)imide (LiTFSI) was characterized by DSC, complex impedance measurements, and 1H pulse NMR spectroscopy. The ionic conductivity of these electrolytes was affected by the reaction condition of the methacrylate monomer and revealed by the glass transition temperature (Tg), spin–spin relaxation time (T2), steric effects of the terminal groups, and the number of charge carriers indicated by the VTF kinetic parameter. In this system, the electrolytes prepared by the reaction heating rate of 10°C/min of MEO–H and 15°C/min of MEO–CH3 showed maximum ionic conductivity, σi, two to three times higher in magnitude than that of the σi of the others at room temperature. As experimental results, the reaction kinetic rate affected the degree of conversion, the ionic conductivity, and the relaxation behaviors of polyether electrolytes. © 2003 Wiley Periodicals, Inc. J Appl Polym Sci 89: 2149–2156, 2003 相似文献