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Registro Completo |
Biblioteca(s): |
Embrapa Solos. |
Data corrente: |
19/10/2021 |
Data da última atualização: |
19/10/2021 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
MAVROPOULOS, E.; ROSSI, A. M.; COSTA, A. M.; PEREZ, C. A. C.; MOREIRA, J. C.; SALDANHA, M. F. C. |
Afiliação: |
ELENA MAVROPOULOS, CBPF; ALEXANDRE MALTA ROSSI, CBPF; ANDRÉA M. COSTA, CBPF; CARLOS ANDRÉ C. PEREZ, NUCAT; JOSINO C. MOREIRA, FIOCRUZ; MARCELO FRANCISCO COSTA SALDANHA, CNPS. |
Título: |
Studies on the mechanisms of lead immobilization by hydroxyapatite. |
Ano de publicação: |
2002 |
Fonte/Imprenta: |
Environmental Science and Technology, v. 36, n. 7, p. 1625-1629, 2002. |
DOI: |
https://doi.org/10.1021/es0155938 |
Idioma: |
Inglês |
Notas: |
Na publicação: Marcelo Saldanha. |
Conteúdo: |
The sorption of lead by synthetic hydroxyapatite (HA) from solutions containing Pb2+ initial concentrations up to 1770 mg L-1 was studied. X-ray diffractometry (XRD) associated with Rietveld methodology for refining the spectra pattern was used in order to characterize the mechanisms of lead uptake. It is shown that the dissolution of hydroxyapatite is followed by the formation of a solid solution, Pb(10-x)Cax(PO4)6(OH)2, with Pb ions mostly occupying Ca(II) sites. The Ca/Pb molar ratio of this solid solution decreases continuously until it reaches the structure of a pure hydroxypyromorphite. The cell parameters and the crystallite mean size behavior of both mineral phases reinforce the hypothesis that hydroxypyromorphite, PbHA, formation is the end of a process in which Pb(10-x)Cax(PO4)6(OH)2 crystallites are continuously dissolved and recrystallized producing crystals with lower calcium content. Combination of Inductively Coupled Plasma spectrometry (ICP), chemical analysis, and XRD results permitted the conclusion that lead ions are not completely immobilized by precipitating Pb(10-x)Cax(PO4)6(OH)2. Additional surface mechanisms also contribute to Pb2+ uptake. During Pb2+ sorption process, pH variations of the solution phase showed a more complex pattern than previously reported. Contribution of surface mechanisms, in addition to the hydroxyapatite dissolution, could explain this behavior. |
Palavras-Chave: |
Dissolution; Physical and chemical processes. |
Thesaurus Nal: |
Hydroxyapatite; Metals; Sorption. |
Categoria do assunto: |
P Recursos Naturais, Ciências Ambientais e da Terra |
Marc: |
LEADER 02218naa a2200265 a 4500 001 2135443 005 2021-10-19 008 2002 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.1021/es0155938$2DOI 100 1 $aMAVROPOULOS, E. 245 $aStudies on the mechanisms of lead immobilization by hydroxyapatite.$h[electronic resource] 260 $c2002 500 $aNa publicação: Marcelo Saldanha. 520 $aThe sorption of lead by synthetic hydroxyapatite (HA) from solutions containing Pb2+ initial concentrations up to 1770 mg L-1 was studied. X-ray diffractometry (XRD) associated with Rietveld methodology for refining the spectra pattern was used in order to characterize the mechanisms of lead uptake. It is shown that the dissolution of hydroxyapatite is followed by the formation of a solid solution, Pb(10-x)Cax(PO4)6(OH)2, with Pb ions mostly occupying Ca(II) sites. The Ca/Pb molar ratio of this solid solution decreases continuously until it reaches the structure of a pure hydroxypyromorphite. The cell parameters and the crystallite mean size behavior of both mineral phases reinforce the hypothesis that hydroxypyromorphite, PbHA, formation is the end of a process in which Pb(10-x)Cax(PO4)6(OH)2 crystallites are continuously dissolved and recrystallized producing crystals with lower calcium content. Combination of Inductively Coupled Plasma spectrometry (ICP), chemical analysis, and XRD results permitted the conclusion that lead ions are not completely immobilized by precipitating Pb(10-x)Cax(PO4)6(OH)2. Additional surface mechanisms also contribute to Pb2+ uptake. During Pb2+ sorption process, pH variations of the solution phase showed a more complex pattern than previously reported. Contribution of surface mechanisms, in addition to the hydroxyapatite dissolution, could explain this behavior. 650 $aHydroxyapatite 650 $aMetals 650 $aSorption 653 $aDissolution 653 $aPhysical and chemical processes 700 1 $aROSSI, A. M. 700 1 $aCOSTA, A. M. 700 1 $aPEREZ, C. A. C. 700 1 $aMOREIRA, J. C. 700 1 $aSALDANHA, M. F. C. 773 $tEnvironmental Science and Technology$gv. 36, n. 7, p. 1625-1629, 2002.
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Embrapa Solos (CNPS) |
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Biblioteca(s): |
Embrapa Arroz e Feijão. |
Data corrente: |
31/08/2005 |
Data da última atualização: |
09/02/2023 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
FILIPPI, M. C. de; EBBOLE, D.; GONZALEZ, C. |
Afiliação: |
MARTA CRISTINA CORSI DE FILIPPI, CNPAF; DANIEL EBBOLE, TEXAS A&M UNIVERSITY; CARLOS GONZALEZ, TEXAS A&M UNIVERSITY. |
Título: |
Bioactive inhibition of appressorium formation in Magnaporthe grisea. |
Ano de publicação: |
2004 |
Fonte/Imprenta: |
Fitopatologia Brasileira, v. 29, p. S56, ago. 2004. Suplemento, ref. 092, Edição de Resumos do XXXVII Congresso Brasileiro de Fitopatologia, Gramado, RS, ago. 2004. |
Idioma: |
Português |
Palavras-Chave: |
Bioactive. |
Thesaurus NAL: |
Magnaporthe grisea; molecular biology. |
Categoria do assunto: |
H Saúde e Patologia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/208544/1/fb-2004-p56.pdf
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Marc: |
LEADER 00582nam a2200157 a 4500 001 1208544 005 2023-02-09 008 2004 bl uuuu u00u1 u #d 100 1 $aFILIPPI, M. C. de 245 $aBioactive inhibition of appressorium formation in Magnaporthe grisea. 260 $aFitopatologia Brasileira, v. 29, p. S56, ago. 2004. Suplemento, ref. 092, Edição de Resumos do XXXVII Congresso Brasileiro de Fitopatologia, Gramado, RS, ago. 2004.$c2004 650 $aMagnaporthe grisea 650 $amolecular biology 653 $aBioactive 700 1 $aEBBOLE, D. 700 1 $aGONZALEZ, C.
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