Journal
AICHE JOURNAL
Volume 55, Issue 3, Pages 783-796Publisher
WILEY
DOI: 10.1002/aic.11698
Keywords
ionic liquid; electrodeposition; aluminium; stainless steel; nucleation; orientation
Categories
Funding
- National Natural Science Foundation of China [20776140, 20973152]
- National Science Found for Distinguished Young Scholars of China [20625618]
- National 863 Program of China [2006AA06Z317, 2006AA06Z371]
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A promising method for aluminium deposition was proposed by using AlCl3/[bmim]Cl (1-butyl-3-methylimidazolium chloride) ionic liquid as electrolyte. By using this novel method, the volatile and flammable organic solvent systems and the high corrosive inorganic molten salts with high temperature can be substituted, and the deposit microstructure can be easily adjusted by changing the current density, temperature and electrolyte composition. The study was performed by means of galvano-static electrolysis and the optimum operating conditions were determined based oil the systematic studies of the effects of current density, temperature, molar ratio of AlCl3 to [bmim]Cl, stirring speed and deposition time Oil the quality of deposited coatings. The electrical conductivities of electrolytes were also investigated as a function of temperature (298-358 K) and molar ratio of AlO3 to [bmim]Cl (from 0.1:1 to 2.0:1). Dense, bright and adherent aluminium coatings were obtained over a wide range of temperature (298-348 K), current densities (8-44 mA/cm(2)) and molar ratio (1.6:1-2.0:1). Results from the analysis of crystal structure shou, that all of the electrodeposits exhibit a preferred (200) crystallographic orientation. Temperature has significant influence on the crystallographic orientation and there does not appear to he an apparent impact of current density oil it. Analyses of the chronoamperograms indicate that the deposition process of aluminium on stainless steel was controlled by three-dimension nucleation with diffusion-controlled growth and there is a conversion from progressive nucleation to instantaneous nucleation. (c) 2009 American Institute of Chemical Engineers AIChE J, 55: 783-796, 2009
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