Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection

Nickel-layered silicates were electrochemically deposited from acidic bath solutions. Citrate was used as a ligand to stabilize nickel (II) ions in the plating solution. The silicate, montmorillonite, was exfoliated by stirring in aqueous solution over 24 hours. The plating solutions were analyzed f...

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Main Authors: Jeerapan Tientong, Casey R. Thurber, Nandika D’Souza, Adel Mohamed, Teresa D. Golden
Format: Article
Language:English
Published: Wiley 2013-01-01
Series:International Journal of Electrochemistry
Online Access:http://dx.doi.org/10.1155/2013/853869
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author Jeerapan Tientong
Casey R. Thurber
Nandika D’Souza
Adel Mohamed
Teresa D. Golden
author_facet Jeerapan Tientong
Casey R. Thurber
Nandika D’Souza
Adel Mohamed
Teresa D. Golden
author_sort Jeerapan Tientong
collection DOAJ
description Nickel-layered silicates were electrochemically deposited from acidic bath solutions. Citrate was used as a ligand to stabilize nickel (II) ions in the plating solution. The silicate, montmorillonite, was exfoliated by stirring in aqueous solution over 24 hours. The plating solutions were analyzed for zeta-potential, particle size, viscosity, and conductivity to investigate the effects of the composition at various pHs. The solution particles at pH 2.5 (−22.2 mV) and pH 3.0 (−21.9 mV) were more stable than at pH 1.6 (−10.1 mV) as shown by zeta-potential analysis of the nickel-citrate-montmorillonite plating solution. Ecorr for the films ranged from −0.32 to −0.39 V with varying pH from 1.6 to 3.0. The films were immersed in 3.5% NaCl and the open circuit potential monitored for one month. The coatings deposited at pH 3.0 were stable 13 days longer in the salt solution than the other coatings. X-ray diffraction showed a change in the (111)/(200) ratio for the coatings at the various pHs. The scanning electron microscopy and hardness results also support that the electrodeposition of nickel-montmorillonite at pH 3.0 (234 GPa) had improved hardness and morphology compared to pH 2.5 (174 GPa) and pH 1.6 (147 GPa).
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spelling doaj-art-c1d5828737574f52a202e17484d675d42025-02-03T01:02:00ZengWileyInternational Journal of Electrochemistry2090-35292090-35372013-01-01201310.1155/2013/853869853869Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion ProtectionJeerapan Tientong0Casey R. Thurber1Nandika D’Souza2Adel Mohamed3Teresa D. Golden4Department of Chemistry, University of North Texas, 1155 Union Circle No. 305070, Denton, TX 76203, USADepartment of Chemistry, University of North Texas, 1155 Union Circle No. 305070, Denton, TX 76203, USADepartment of Mechanical and Energy Engineering, University of North Texas, Denton, TX 76207, USACenter for Advanced Materials, Qatar University, P.O. Box 2713, Doha, QatarDepartment of Chemistry, University of North Texas, 1155 Union Circle No. 305070, Denton, TX 76203, USANickel-layered silicates were electrochemically deposited from acidic bath solutions. Citrate was used as a ligand to stabilize nickel (II) ions in the plating solution. The silicate, montmorillonite, was exfoliated by stirring in aqueous solution over 24 hours. The plating solutions were analyzed for zeta-potential, particle size, viscosity, and conductivity to investigate the effects of the composition at various pHs. The solution particles at pH 2.5 (−22.2 mV) and pH 3.0 (−21.9 mV) were more stable than at pH 1.6 (−10.1 mV) as shown by zeta-potential analysis of the nickel-citrate-montmorillonite plating solution. Ecorr for the films ranged from −0.32 to −0.39 V with varying pH from 1.6 to 3.0. The films were immersed in 3.5% NaCl and the open circuit potential monitored for one month. The coatings deposited at pH 3.0 were stable 13 days longer in the salt solution than the other coatings. X-ray diffraction showed a change in the (111)/(200) ratio for the coatings at the various pHs. The scanning electron microscopy and hardness results also support that the electrodeposition of nickel-montmorillonite at pH 3.0 (234 GPa) had improved hardness and morphology compared to pH 2.5 (174 GPa) and pH 1.6 (147 GPa).http://dx.doi.org/10.1155/2013/853869
spellingShingle Jeerapan Tientong
Casey R. Thurber
Nandika D’Souza
Adel Mohamed
Teresa D. Golden
Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection
International Journal of Electrochemistry
title Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection
title_full Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection
title_fullStr Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection
title_full_unstemmed Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection
title_short Influence of Bath Composition at Acidic pH on Electrodeposition of Nickel-Layered Silicate Nanocomposites for Corrosion Protection
title_sort influence of bath composition at acidic ph on electrodeposition of nickel layered silicate nanocomposites for corrosion protection
url http://dx.doi.org/10.1155/2013/853869
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