Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process
Autor(a) principal: | |
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Data de Publicação: | 2004 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Materials research (São Carlos. Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392004000400017 |
Resumo: | Several techniques have been utilized for the preparation of hydroxyapatite (HA) and other calcium phosphates for the development of biomaterials. It is vital to know the reaction kinetics to be able to control the material obtained by the aqueous solution route. In the present work, HA has been produced by different wet precipitation processes and different experimental conditions. Calcium hydroxide, calcium phosphate, ammonium phosphate and phosphoric acid were used as reagents. The precipitate was dried at 100 °C overnight and then some samples were treated at 900 °C for 2 h. The powder samples were characterized by scanning electron microscopy (SEM), X-ray fluorescence (XRF) and X-ray diffraction (XRD) analyses. SEM photomicrographs showed an aggregate powder, granular to dense and suggested typical columnar particles. Qualitative XRF showed that the main components of HA powders were calcium and phosphorus. Pure HA and other phases according to processing parameters were observed by XRD analysis. |
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Synthesis control and characterization of hydroxyapatite prepared by wet precipitation processhydroxyapatitesynthesis parametersX-ray diffractionbioceramicSeveral techniques have been utilized for the preparation of hydroxyapatite (HA) and other calcium phosphates for the development of biomaterials. It is vital to know the reaction kinetics to be able to control the material obtained by the aqueous solution route. In the present work, HA has been produced by different wet precipitation processes and different experimental conditions. Calcium hydroxide, calcium phosphate, ammonium phosphate and phosphoric acid were used as reagents. The precipitate was dried at 100 °C overnight and then some samples were treated at 900 °C for 2 h. The powder samples were characterized by scanning electron microscopy (SEM), X-ray fluorescence (XRF) and X-ray diffraction (XRD) analyses. SEM photomicrographs showed an aggregate powder, granular to dense and suggested typical columnar particles. Qualitative XRF showed that the main components of HA powders were calcium and phosphorus. Pure HA and other phases according to processing parameters were observed by XRD analysis.ABM, ABC, ABPol2004-12-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392004000400017Materials Research v.7 n.4 2004reponame:Materials research (São Carlos. Online)instname:Universidade Federal de São Carlos (UFSCAR)instacron:ABM ABC ABPOL10.1590/S1516-14392004000400017info:eu-repo/semantics/openAccessSantos,Maria HelenaOliveira,Marise deSouza,Luciana Palhares de FreitasMansur,Herman SanderVasconcelos,Wander Luizeng2005-11-08T00:00:00Zoai:scielo:S1516-14392004000400017Revistahttp://www.scielo.br/mrPUBhttps://old.scielo.br/oai/scielo-oai.phpdedz@power.ufscar.br1980-53731516-1439opendoar:2005-11-08T00:00Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)false |
dc.title.none.fl_str_mv |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
title |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
spellingShingle |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process Santos,Maria Helena hydroxyapatite synthesis parameters X-ray diffraction bioceramic |
title_short |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
title_full |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
title_fullStr |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
title_full_unstemmed |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
title_sort |
Synthesis control and characterization of hydroxyapatite prepared by wet precipitation process |
author |
Santos,Maria Helena |
author_facet |
Santos,Maria Helena Oliveira,Marise de Souza,Luciana Palhares de Freitas Mansur,Herman Sander Vasconcelos,Wander Luiz |
author_role |
author |
author2 |
Oliveira,Marise de Souza,Luciana Palhares de Freitas Mansur,Herman Sander Vasconcelos,Wander Luiz |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Santos,Maria Helena Oliveira,Marise de Souza,Luciana Palhares de Freitas Mansur,Herman Sander Vasconcelos,Wander Luiz |
dc.subject.por.fl_str_mv |
hydroxyapatite synthesis parameters X-ray diffraction bioceramic |
topic |
hydroxyapatite synthesis parameters X-ray diffraction bioceramic |
description |
Several techniques have been utilized for the preparation of hydroxyapatite (HA) and other calcium phosphates for the development of biomaterials. It is vital to know the reaction kinetics to be able to control the material obtained by the aqueous solution route. In the present work, HA has been produced by different wet precipitation processes and different experimental conditions. Calcium hydroxide, calcium phosphate, ammonium phosphate and phosphoric acid were used as reagents. The precipitate was dried at 100 °C overnight and then some samples were treated at 900 °C for 2 h. The powder samples were characterized by scanning electron microscopy (SEM), X-ray fluorescence (XRF) and X-ray diffraction (XRD) analyses. SEM photomicrographs showed an aggregate powder, granular to dense and suggested typical columnar particles. Qualitative XRF showed that the main components of HA powders were calcium and phosphorus. Pure HA and other phases according to processing parameters were observed by XRD analysis. |
publishDate |
2004 |
dc.date.none.fl_str_mv |
2004-12-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392004000400017 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392004000400017 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1516-14392004000400017 |
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 |
ABM, ABC, ABPol |
publisher.none.fl_str_mv |
ABM, ABC, ABPol |
dc.source.none.fl_str_mv |
Materials Research v.7 n.4 2004 reponame:Materials research (São Carlos. Online) instname:Universidade Federal de São Carlos (UFSCAR) instacron:ABM ABC ABPOL |
instname_str |
Universidade Federal de São Carlos (UFSCAR) |
instacron_str |
ABM ABC ABPOL |
institution |
ABM ABC ABPOL |
reponame_str |
Materials research (São Carlos. Online) |
collection |
Materials research (São Carlos. Online) |
repository.name.fl_str_mv |
Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR) |
repository.mail.fl_str_mv |
dedz@power.ufscar.br |
_version_ |
1754212657778393088 |