Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine
Autor(a) principal: | |
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Data de Publicação: | 2007 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042007000400001 |
Resumo: | Compared to pure zinc plating, zinc alloys provide several advantages. A zinc alloy generally offers superior sacrificial protection to steel since it corrodes more slowly than pure zinc. A search for a non-cyanide zinc plating bath resulted on the development of a zinc nickel sulphamate bath. To obtain better quality zinc-nickel deposits, triethanolamine was added to the bath. In this paper the influence of triethanolamine in zinc-nickel plating from sulphamate bath has been investigated through current efficiency measurements, cyclic voltammetry, scanning electron microscope, and X-ray diffraction techniques. In the presence of triethanolamine in the zinc-nickel sulphamate bath the current efficiency of alloy deposition increased to a maximum of 99% at the current density of 1.5 Adm-2 and thereafter decreased. TEA adsorbed on the electrode surface obeying Henrys isotherm. On mild steel surfaces, uniform smooth slate gray deposit with smaller crystallites was produced, in presence of TEA in solution, and the electrodeposits exhibited additional Zn(OH)2 and g-Ni3Zn22 phases. Hydrogen evolution was suppressed by TEA and thereby current efficiency is increased for alloy deposition. |
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Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolaminecyclic voltammetryelectrodepositiontriethanolamineXRDZn-NiCompared to pure zinc plating, zinc alloys provide several advantages. A zinc alloy generally offers superior sacrificial protection to steel since it corrodes more slowly than pure zinc. A search for a non-cyanide zinc plating bath resulted on the development of a zinc nickel sulphamate bath. To obtain better quality zinc-nickel deposits, triethanolamine was added to the bath. In this paper the influence of triethanolamine in zinc-nickel plating from sulphamate bath has been investigated through current efficiency measurements, cyclic voltammetry, scanning electron microscope, and X-ray diffraction techniques. In the presence of triethanolamine in the zinc-nickel sulphamate bath the current efficiency of alloy deposition increased to a maximum of 99% at the current density of 1.5 Adm-2 and thereafter decreased. TEA adsorbed on the electrode surface obeying Henrys isotherm. On mild steel surfaces, uniform smooth slate gray deposit with smaller crystallites was produced, in presence of TEA in solution, and the electrodeposits exhibited additional Zn(OH)2 and g-Ni3Zn22 phases. Hydrogen evolution was suppressed by TEA and thereby current efficiency is increased for alloy deposition.Sociedade Portuguesa de Electroquímica2007-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articletext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042007000400001Portugaliae Electrochimica Acta v.25 n.4 2007reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042007000400001Ravindran,V.Muralidharan,V.S.info:eu-repo/semantics/openAccess2024-02-06T17:06:53Zoai:scielo:S0872-19042007000400001Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:20:03.030349Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
title |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
spellingShingle |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine Ravindran,V. cyclic voltammetry electrodeposition triethanolamine XRD Zn-Ni |
title_short |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
title_full |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
title_fullStr |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
title_full_unstemmed |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
title_sort |
Zinc-Nickel Alloy Electrodeposition: Influence of Triethanolamine |
author |
Ravindran,V. |
author_facet |
Ravindran,V. Muralidharan,V.S. |
author_role |
author |
author2 |
Muralidharan,V.S. |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Ravindran,V. Muralidharan,V.S. |
dc.subject.por.fl_str_mv |
cyclic voltammetry electrodeposition triethanolamine XRD Zn-Ni |
topic |
cyclic voltammetry electrodeposition triethanolamine XRD Zn-Ni |
description |
Compared to pure zinc plating, zinc alloys provide several advantages. A zinc alloy generally offers superior sacrificial protection to steel since it corrodes more slowly than pure zinc. A search for a non-cyanide zinc plating bath resulted on the development of a zinc nickel sulphamate bath. To obtain better quality zinc-nickel deposits, triethanolamine was added to the bath. In this paper the influence of triethanolamine in zinc-nickel plating from sulphamate bath has been investigated through current efficiency measurements, cyclic voltammetry, scanning electron microscope, and X-ray diffraction techniques. In the presence of triethanolamine in the zinc-nickel sulphamate bath the current efficiency of alloy deposition increased to a maximum of 99% at the current density of 1.5 Adm-2 and thereafter decreased. TEA adsorbed on the electrode surface obeying Henrys isotherm. On mild steel surfaces, uniform smooth slate gray deposit with smaller crystallites was produced, in presence of TEA in solution, and the electrodeposits exhibited additional Zn(OH)2 and g-Ni3Zn22 phases. Hydrogen evolution was suppressed by TEA and thereby current efficiency is increased for alloy deposition. |
publishDate |
2007 |
dc.date.none.fl_str_mv |
2007-01-01 |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042007000400001 |
url |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042007000400001 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-19042007000400001 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
Sociedade Portuguesa de Electroquímica |
publisher.none.fl_str_mv |
Sociedade Portuguesa de Electroquímica |
dc.source.none.fl_str_mv |
Portugaliae Electrochimica Acta v.25 n.4 2007 reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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1799137289836691456 |