Mechanism of the cathode process in the electrolytic boriding in molten salts

Mechanism of the cathode process in the electrolytic boriding in molten salts
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熔盐电解硼阴极过程的机理

DOI:
10.1016/0013-4686(84)89006-4
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发表时间:
1984
影响因子:
6.6
通讯作者:
P. Fellner
P. Fellner
中科院分区:
材料科学2区
文献类型:
--
作者:
M. Makyta;K. Matiašovský;P. Fellner

文献摘要

被引文献

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采用伏安法和计时电位法,研究了LiFKFKBF4和LiFKFB2O3体系中铂电极上电解沉积硼的阴极过程机理。研究发现,在该体系中,LiFKFKBF4硼通过简单的三电子过程直接从四氟硼酸络合物阴离子中还原。在该系统中,LiFKFB2O3 硼氧化物与碱性氟化物电解质反应,形成 BF−4 阴离子和平均氧硼比为 1.66 的未指定的氧氟配合物。 BF−4 阴离子和氧氟络合物中的硼浓度之比约为 0.1。这两种电化学活性物质的硼沉积电位之间的差异约为 0.47 V,有利于 BF−4。 BF−4阴离子的扩散系数值为4.4×10−9m2s−1(700℃)。
The mechanism of the cathode process in the electrolytic deposition of boron on a platinum electrode has been investigated in the systems LiFKFKBF4and LiFKFB2O3by means of the voltametric and chronopotentiometric methods. It was found that in the system LiFKFKBF4boron is reduced directly from the tetrafluoroborate complex anion by a simple 3-electron process. In the system LiFKFB2O3boron oxide reacts with the basic fluoride electrolyte under formation of the BF−4anion and of unspecified oxofluoro complex(es) with a mean oxygen to boron ratio of 1.66. The ratio of boron concentrations in the BF−4anion and in the oxofluoro complex(es) is about 0.1. The difference between the deposition potential of boron from those two electrochemically active species is about 0.47 V in favour of BF−4. The value of the diffusion coefficient of the BF−4anion was found to be 4.4 × 10−9m2s−1(700°C).