Recovery of silver residues from dental amalgam
Autor(a) principal: | |
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Data de Publicação: | 2010 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1590/S1678-77572010000200005 http://hdl.handle.net/11449/231235 |
Resumo: | Dental amalgam residues are probably the most important chemical residues generated from clinical dental practice because of the presence of heavy metals among its constituents, mainly mercury and silver. Objective: The purpose of this study was to develop an alternative method for the recovery of silver residues from dental amalgam. Material and Methods: The residue generated after vacuum distillation of dental amalgam for the separation of mercury was initially diluted with 32.5% HNO3, followed by precipitation with 20% NaCl. Sequentially, under constant heating and agitation with NaOH and sucrose, the sample was reduced to metallic silver. However, the processing time was too long, which turned this procedure not viable. In another sequence of experiments, the dilution was accomplished with concentrated HNO3 at 90°C, followed by precipitation with 20% NaCl. After washing, the pellet was diluted with concentrated NH4OH, water and more NaCl in order to facilitate the reaction with the reducer. Results: Ascorbic acid was efficiently used as reducer, allowing a fast reduction, thus making the procedure viable. Conclusions: The proposed methodology is of easy application and does not require sophisticated equipment or expensive reagents. |
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Recovery of silver residues from dental amalgamDental amalgamEnvironmentSilverSolid wastesDental amalgam residues are probably the most important chemical residues generated from clinical dental practice because of the presence of heavy metals among its constituents, mainly mercury and silver. Objective: The purpose of this study was to develop an alternative method for the recovery of silver residues from dental amalgam. Material and Methods: The residue generated after vacuum distillation of dental amalgam for the separation of mercury was initially diluted with 32.5% HNO3, followed by precipitation with 20% NaCl. Sequentially, under constant heating and agitation with NaOH and sucrose, the sample was reduced to metallic silver. However, the processing time was too long, which turned this procedure not viable. In another sequence of experiments, the dilution was accomplished with concentrated HNO3 at 90°C, followed by precipitation with 20% NaCl. After washing, the pellet was diluted with concentrated NH4OH, water and more NaCl in order to facilitate the reaction with the reducer. Results: Ascorbic acid was efficiently used as reducer, allowing a fast reduction, thus making the procedure viable. Conclusions: The proposed methodology is of easy application and does not require sophisticated equipment or expensive reagents.Department of Biological Sciences Bauru School Of Dentistry University of São Paulo, Bauru, SPDepartment of Chemistry School of Sciences State University of São Paulo, Bauru, SPUniversidade de São Paulo (USP)Pereira, Heloísa Aparecida Barbosa da SilvaIano, Flávia Godoyda Silva, Thelma Lopesde Oliveira, Rodrigo Cardosode Menezes, Manoel LimaBuzalaf, Marília Afonso Rabelo2022-04-29T08:44:17Z2022-04-29T08:44:17Z2010-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article121-126http://dx.doi.org/10.1590/S1678-77572010000200005Journal of Applied Oral Science, v. 18, n. 2, p. 121-126, 2010.1678-77651678-7757http://hdl.handle.net/11449/23123510.1590/S1678-775720100002000052-s2.0-77953652454Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengJournal of Applied Oral Scienceinfo:eu-repo/semantics/openAccess2024-04-29T18:17:00Zoai:repositorio.unesp.br:11449/231235Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T18:36:32.310305Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Recovery of silver residues from dental amalgam |
title |
Recovery of silver residues from dental amalgam |
spellingShingle |
Recovery of silver residues from dental amalgam Pereira, Heloísa Aparecida Barbosa da Silva Dental amalgam Environment Silver Solid wastes |
title_short |
Recovery of silver residues from dental amalgam |
title_full |
Recovery of silver residues from dental amalgam |
title_fullStr |
Recovery of silver residues from dental amalgam |
title_full_unstemmed |
Recovery of silver residues from dental amalgam |
title_sort |
Recovery of silver residues from dental amalgam |
author |
Pereira, Heloísa Aparecida Barbosa da Silva |
author_facet |
Pereira, Heloísa Aparecida Barbosa da Silva Iano, Flávia Godoy da Silva, Thelma Lopes de Oliveira, Rodrigo Cardoso de Menezes, Manoel Lima Buzalaf, Marília Afonso Rabelo |
author_role |
author |
author2 |
Iano, Flávia Godoy da Silva, Thelma Lopes de Oliveira, Rodrigo Cardoso de Menezes, Manoel Lima Buzalaf, Marília Afonso Rabelo |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade de São Paulo (USP) |
dc.contributor.author.fl_str_mv |
Pereira, Heloísa Aparecida Barbosa da Silva Iano, Flávia Godoy da Silva, Thelma Lopes de Oliveira, Rodrigo Cardoso de Menezes, Manoel Lima Buzalaf, Marília Afonso Rabelo |
dc.subject.por.fl_str_mv |
Dental amalgam Environment Silver Solid wastes |
topic |
Dental amalgam Environment Silver Solid wastes |
description |
Dental amalgam residues are probably the most important chemical residues generated from clinical dental practice because of the presence of heavy metals among its constituents, mainly mercury and silver. Objective: The purpose of this study was to develop an alternative method for the recovery of silver residues from dental amalgam. Material and Methods: The residue generated after vacuum distillation of dental amalgam for the separation of mercury was initially diluted with 32.5% HNO3, followed by precipitation with 20% NaCl. Sequentially, under constant heating and agitation with NaOH and sucrose, the sample was reduced to metallic silver. However, the processing time was too long, which turned this procedure not viable. In another sequence of experiments, the dilution was accomplished with concentrated HNO3 at 90°C, followed by precipitation with 20% NaCl. After washing, the pellet was diluted with concentrated NH4OH, water and more NaCl in order to facilitate the reaction with the reducer. Results: Ascorbic acid was efficiently used as reducer, allowing a fast reduction, thus making the procedure viable. Conclusions: The proposed methodology is of easy application and does not require sophisticated equipment or expensive reagents. |
publishDate |
2010 |
dc.date.none.fl_str_mv |
2010-01-01 2022-04-29T08:44:17Z 2022-04-29T08:44:17Z |
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://dx.doi.org/10.1590/S1678-77572010000200005 Journal of Applied Oral Science, v. 18, n. 2, p. 121-126, 2010. 1678-7765 1678-7757 http://hdl.handle.net/11449/231235 10.1590/S1678-77572010000200005 2-s2.0-77953652454 |
url |
http://dx.doi.org/10.1590/S1678-77572010000200005 http://hdl.handle.net/11449/231235 |
identifier_str_mv |
Journal of Applied Oral Science, v. 18, n. 2, p. 121-126, 2010. 1678-7765 1678-7757 10.1590/S1678-77572010000200005 2-s2.0-77953652454 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Journal of Applied Oral Science |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
121-126 |
dc.source.none.fl_str_mv |
Scopus reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
|
_version_ |
1808128955464548352 |