TY - JOUR
T1 - Effect of additives on electrodeposition of zn∑zr oxide composite from dispersed particles-free solution
AU - Hara, Yosuke
AU - Ueda, Daiki
AU - Oue, Satoshi
AU - Nakano, Hiroaki
N1 - Publisher Copyright:
© 2018 The Japan Institute of Metals and Materials
PY - 2018
Y1 - 2018
N2 - Electrodeposition of ZnZr oxide composite was performed from an unagitated sulfate solution containing Zn2+, Zr ions and additives such as NO3 ions and polyethylene glycol(PEG)at pH 2 and 313 K under galvanostatic conditions, and the effect of additives on the codeposition of Zr oxide and polarization property and micro structure of deposits was investigated. Zr content in deposits obtained at all the current densities increased significantly with addition of 2.0 g・dm3 of NaNO3. ZnZr oxide deposited from the solution containing NaNO3 showed massive structure composed of fine crystals without Zn platelets crystals, and a lot of large cracks occurred between the massive crystals. EDX analysis revealed that Zr codeposited on the massive crystals as fine concavoconvex oxide. The corrosion current density of ZnZr oxide deposited from the solution containing NaNO3 was almost same as that of pure Zn deposits, showing no improvement of corrosion resistance with codeposition of Zr oxide. On the other hand, Zr content in deposits obtained from the solution containing PEG increased significantly with increasing current density above 1000 A・m2. With addition of 1000 mg・dm3 of PEG, the Zn platelets crystals disappeared, and the deposits were composed of fine meshlike crystals with preferred orientation {1010}Zn plane, resulting in smooth surface. The cathodic current density for the reduction of dissolved oxygen on the ZnZr oxide deposited from the solution containing PEG was smaller than that of pure Zn deposits, as a result, the corrosion current density of ZnZr oxide deposits was smaller than that of pure Zn deposits. The increase in Zr content in deposits with NO3 ions and PEG is attributed to acceleration of hydrolysis reaction of Zr ions.
AB - Electrodeposition of ZnZr oxide composite was performed from an unagitated sulfate solution containing Zn2+, Zr ions and additives such as NO3 ions and polyethylene glycol(PEG)at pH 2 and 313 K under galvanostatic conditions, and the effect of additives on the codeposition of Zr oxide and polarization property and micro structure of deposits was investigated. Zr content in deposits obtained at all the current densities increased significantly with addition of 2.0 g・dm3 of NaNO3. ZnZr oxide deposited from the solution containing NaNO3 showed massive structure composed of fine crystals without Zn platelets crystals, and a lot of large cracks occurred between the massive crystals. EDX analysis revealed that Zr codeposited on the massive crystals as fine concavoconvex oxide. The corrosion current density of ZnZr oxide deposited from the solution containing NaNO3 was almost same as that of pure Zn deposits, showing no improvement of corrosion resistance with codeposition of Zr oxide. On the other hand, Zr content in deposits obtained from the solution containing PEG increased significantly with increasing current density above 1000 A・m2. With addition of 1000 mg・dm3 of PEG, the Zn platelets crystals disappeared, and the deposits were composed of fine meshlike crystals with preferred orientation {1010}Zn plane, resulting in smooth surface. The cathodic current density for the reduction of dissolved oxygen on the ZnZr oxide deposited from the solution containing PEG was smaller than that of pure Zn deposits, as a result, the corrosion current density of ZnZr oxide deposits was smaller than that of pure Zn deposits. The increase in Zr content in deposits with NO3 ions and PEG is attributed to acceleration of hydrolysis reaction of Zr ions.
UR - http://www.scopus.com/inward/record.url?scp=85052686274&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85052686274&partnerID=8YFLogxK
U2 - 10.2320/jinstmet.J2018027
DO - 10.2320/jinstmet.J2018027
M3 - Article
AN - SCOPUS:85052686274
SN - 0021-4876
VL - 82
SP - 366
EP - 371
JO - Nippon Kinzoku Gakkaishi/Journal of the Japan Institute of Metals
JF - Nippon Kinzoku Gakkaishi/Journal of the Japan Institute of Metals
IS - 9
ER -