ELECTROCHEMICAL-BEHAVIOR OF YTTRIUM ION IN LICL-KCL-NACL EUTECTIC MELT

The electrochemical reduction of yttrium ion on a molybdenum electrode in a LiCl-KCl-NaCl eutectic melt at 723 K was found to be almost reversible and to proceed by a one-step three electron reaction. The diffusion coefficient D of the Y(III) ion was measured to be (3.3 +/- 0.4) x 10(-6) cm2 s-1 by cyclic voltammetry, (5.0 +/- 0.9) x 10(-6) cm2 s-1 by the rotating disk electrode method, and (7.1 +/- 0.7) x 10(-6) cm2 s-1 by chronopotentiometry. The D values obtained by the latter two methods are in fairly good agreement with each other. The rather low D value obtained by cyclic voltammetry might be attributed to the fact that yttrium metal can dissolve slightly in the chloride melt. The standard potential of Y(III)/Y(0) couple was determined to be (-3.174 +/- 0.006) V (vs. Cl2/Cl-) by open-circuit potentiometry, (-3.15 +/- 0.02) V (vs. Cl2/Cl-) by the rotating disk electrode method and (-3.16 +/- 0.02) V (vs. Cl2/Cl) by chronopotentiometry. These three values are in good agreement with each other. Several types of Ni-Y intermetallic compounds were found to be formed on a nickel electrode.

SURFACE TENSION AND DENSITY OF NaCl-NaF-RE2O8 MELTS

Surface tension and density of NaCl-NaF-RE2O, melts have been measured by means of maximum buble pressure and Archimedes methods. The results are expressed by two mathematic models. Mass fraction of RE2O5 in the melts from 0.0 to 0.6% and that of NaF/NaCl, 50-90%. This investigation shows that there might be com plexes in the melts. The information obtained can be used as a reference in the preparation of Al-RE alloys.

金属镧、钕分别在KCl+NaCl熔盐中的溶解行为

金属溶解于熔盐中的行为表现为溶解的金属与熔盐中的离子发生了不同程度的相互作用。稀土金属在含有自身熔盐中的溶解,前人已作了一些研究,其溶解机理归结起来主要有以下几种:生成了低价稀土离子;体系形成了胶体溶液以及离子-电子液

NaCl-NaF-RE_2O_3体系的表面张力和密度

以NaCl-NaF体系为还原介质,以RE_2O_3,REOCl,或RE_2(CO_3)_3为原料,以铝为还原剂,在铝熔融过程中直接制备Al-RE应用合金已获得了应用.结果表明,这一方法使用简单,操作方便,不需额外设备,容易为工厂采用.本工作是为这一工艺开展的基础研究工作. 资料对LaCl_3-碱金属氯化物,碱土金属氯化物的表面张力和密度进行了专门总结,对NaCl-NaF-RE_2O_3体系未见报导。

流动注射-ICP-AES多元素同时分析及NaCl基体干扰效应的研究

本文研究了以流动注射进样的ICP-AES分析方法和NaCl的基体效应。0.25-2.5%NaCl对11个元素的影响结果表明,FI进样可克服常规连续雾化的信号漂移,从而改善了测量精度。不同功率下的NaCl基体的影响不同。结果表明,NaCl的基体效应主要存在于气溶胶微粒在ICP中的蒸发—原子化—激发过程。

电化学方法研究ZnAl、ZnAlRE合金在NaCl溶液中的腐蚀行为

用电化学方法研究了锌中掺入不同量Al、RE的锌合金在NaCl溶液中的耐蚀性能、硬度以及电化学行为的变化,并试图从合金结构上给予解释。

La在KCl-NaCl和LaCl_3-KCl-NaCl熔体中的溶解行为

本文利用透明槽技术、电化学循环V-A法及量子化学EHMO三种方法,研究了La在KCl-NaCl(1:1mol)及LaCl_3-KCl-NaCl熔体中的溶解行为。初步认为:溶解在KCl-NaCl熔体中的La是以中性金属状态存在。在LaCl_3-KCl-NaCl熔体中,溶解的La与La~(3+)作用生成低价La~(2+)离子,La~(2+)又与周围的La~(3+)作用形成原子簇离子La_m~(n+)赋存于熔体之中。

Electrochemical impedance spectroscopy analysis for oxygen reduction reaction in 3.5% NaCl solution

The electrochemical impedance spectroscopy (EIS) at different potentials has been used to study the oxygen reduction reaction (ORR) in 3.5% NaCl solution on glassy carbon (GC) electrode in this work. Results show that ORR consists of three two-electron reaction steps and both superoxide ion (O-2(-)) and hydrogen peroxide (H2O2), which are produced by ORR, obstruct the diffusion of oxygen to the surface of the electrode and make the EIS results change into a transmissive finite diffusion process with the real part contraction and a reflective finite diffusion process from a semi-infinite diffusion process. The values of electron transfer resistance (R-t) and diffusion resistance (R-d) were calculated from EIS. O-2(-) influenced strongly on the Rt values and induced a maximum at -0.45 V.

Epoxidation of propylene on NaCl-modified silver catalysts with air as the oxidant

Propylene epoxidation by air was carried out on NaCl-modified silver (NaCl/Ag) catalysts, and the catalysts were characterized by X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). The effects of NaCl loadings, propylene to oxygen ratio, and the reaction time on the catalytic performance were investigated. It was found that the addition of NaCl to silver significantly increases the propylene oxide (PO) selectivity. The PO yield has a maximum when the NaCl loading is about 10 wt.%. Also 12.4% conversion of propylene and 31.6% selectivity to PO are obtained on the NaCl/Ag (10 wt.%) catalyst at 350 degreesC, space velocity 1.8 x 10(4) h(-1) and C3H6:O-2 = 1:2. XPS and XRD characterizations show that AgCl formed on the silver catalyst was favorable to propylene epoxidation. A compound with highly oxidized Ag ion was also found, which may be effective for the reaction. (C) 2002 Elsevier Science B.V. All rights reserved.