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Precipitation and surface adsorption of metal complexes during electropolishing. Theory and characterization with X-ray nanotomography and surface tension isotherms
被引:4
作者:
Nave, Maryana I.
[1
]
Chen-Wiegart, Yu-chen Karen
[2
]
Wang, Jun
[2
]
Kornev, Konstantin G.
[1
]
机构:
[1] Clemson Univ, Dept Mat Sci & Engn, Clemson, SC 29634 USA
[2] Brookhaven Natl Lab, Photon Sci Directorate, Upton, NY 11973 USA
关键词:
AQUEOUS SALT-SOLUTIONS;
SCANNING-TUNNELING-MICROSCOPY;
ENHANCED RAMAN-SPECTROSCOPY;
TUNGSTEN TIPS;
THERMODYNAMIC PARAMETERS;
ELECTROLYTE-SOLUTIONS;
FUNDAMENTAL-ASPECTS;
INTERFACES;
OXIDATION;
HYDROGELS;
D O I:
10.1039/c5cp03431k
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Electropolishing of metals often leads to supersaturation conditions resulting in precipitation of complex compounds. The solubility diagrams and Gibbs adsorption isotherms of the electropolishing products are thus very important to understand the thermodynamic mechanism of precipitation of reaction products. Electropolishing of tungsten wires in aqueous solutions of potassium hydroxide is used as an example illustrating the different thermodynamic scenarios of electropolishing. Electropolishing products are able to form highly viscous films immiscible with the surrounding electrolyte or porous shells adhered to the wire surface. Using X-ray nanotomography, we discovered a gel-like phase formed at the tungsten surface during electropolishing. The results of these studies suggest that the electropolishing products can form a rich library of compounds. The surface tension of the electrolyte depends on the metal oxide ions and alkali-metal complexes.
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页码:23121 / 23131
页数:11