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Registro Completo |
Biblioteca(s): |
Embrapa Meio-Norte. |
Data corrente: |
09/02/2009 |
Data da última atualização: |
03/01/2024 |
Tipo da produção científica: |
Artigo em Anais de Congresso / Nota Técnica |
Autoria: |
SOUZA, I. G. de B.; DINIZ, F. M.; SOUZA, V. A. B. de; VALENTE, S. E. dos S.; LIMA, P. S. da C. |
Afiliação: |
ISIS GOMES DE SOUZA, CNPq/UFPI; FABIO MENDONCA DINIZ, CPAMN; VALDOMIRO AURELIO BARBOSA DE SOUZA, CPAMN; SÉRGIO EMÍLIO DOS SANTOS VALENTE, UFPI; PAULO SARMANHO DA COSTA LIMA, CPAMN. |
Título: |
Teste de repetibilidade do marcador RAPD em manga. |
Ano de publicação: |
2008 |
Fonte/Imprenta: |
In: CONGRESSO BRASILEIRO DE FRUTICULTURA, 20.; ANNUAL MEETING OF THE INTERAMERICAN SOCIETY FOR TROPICAL HORTICULTURE, 54., 2008, Vitória. Frutas para todos: estratégias tecnologias e visão sustentável: anais. Vitória: INCAPER: Sociedade Brasileira de Fruticultura, 2008. |
Páginas: |
4 p. |
Idioma: |
Português |
Conteúdo: |
O objetivo do trabalho foi testar a repetibilidade da técnica de RAPD em manga. |
Thesagro: |
Fruta Tropical; Marcador Molecular. |
Categoria do assunto: |
X Pesquisa, Tecnologia e Engenharia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/70463/1/TesteRepetibilidadeMarcadorRAPD-090107.pdf
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Marc: |
LEADER 00858nam a2200193 a 4500 001 1070463 005 2024-01-03 008 2008 bl uuuu u00u1 u #d 100 1 $aSOUZA, I. G. de B. 245 $aTeste de repetibilidade do marcador RAPD em manga.$h[electronic resource] 260 $aIn: CONGRESSO BRASILEIRO DE FRUTICULTURA, 20.; ANNUAL MEETING OF THE INTERAMERICAN SOCIETY FOR TROPICAL HORTICULTURE, 54., 2008, Vitória. Frutas para todos: estratégias tecnologias e visão sustentável: anais. Vitória: INCAPER: Sociedade Brasileira de Fruticultura$c2008 300 $a4 p. 520 $aO objetivo do trabalho foi testar a repetibilidade da técnica de RAPD em manga. 650 $aFruta Tropical 650 $aMarcador Molecular 700 1 $aDINIZ, F. M. 700 1 $aSOUZA, V. A. B. de 700 1 $aVALENTE, S. E. dos S. 700 1 $aLIMA, P. S. da C.
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Embrapa Meio-Norte (CPAMN) |
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Registro Completo
Biblioteca(s): |
Embrapa Instrumentação. |
Data corrente: |
28/11/2022 |
Data da última atualização: |
22/01/2024 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
OLIVEIRA, L. R. de; GONÇALVES, D. S.; CAROLINO, A. S.; FACCINATTO, W. M.; MENEZES. D. C.; DIAS, C. O.; COLNAGO, L. A.; RUIZ, Y. L.; IU, S. T.; FONSECA FILHO, H. D.; CHAUDHURI, P.; CAMPELO, P. H.; MASCARENHAS, I. P.; SANCHES, E. A. |
Afiliação: |
LUIZ ALBERTO COLNAGO, CNPDIA. |
Título: |
Head-to-tail and head-to-head molecular chains of poly(p-anisidine): Combined experimental and theoretical evaluation. |
Ano de publicação: |
2022 |
Fonte/Imprenta: |
Molecules, v. 27, a6326, 2022. |
Páginas: |
28 p. |
DOI: |
https://doi.org/10.3390/molecules27196326 |
Idioma: |
Inglês |
Conteúdo: |
: Poly(p-anisidine) (PPA) is a polyaniline derivative presenting a methoxy (?OCH3) group at the para position of the phenyl ring. Considering the important role of conjugated polymers in novel technological applications, a systematic, combined experimental and theoretical investigation was performed to obtain more insight into the crystallization process of PPA. Conventional oxidative polymerization of p-anisidine monomer was based on a central composite rotational design (CCRD).The effects of the concentration of the monomer, ammonium persulfate (APS), and HCl on the percentage of crystallinity were considered. Several experimental techniques such as X-ray Diffraction(XRD), Scanning Electron Microscopy (SEM), multifractal analysis, Nuclear Magnetic Resonance(13C NMR), Fourier-transform Infrared spectroscopy (FTIR), and complex impedance spectroscopyanalysis, in addition to Density Functional Theory (DFT), were employed to perform a systematic investigation of PPA. The experimental treatments resulted in different crystal structures with a percentage of crystallinity ranging from (29.2 ± 0.6)% (PPA1HT) to (55.1 ± 0.2)% (PPA16HT-HH). A broad halo in the PPA16HT-HH pattern from 2θ = 10.0?30.0◦suggested a reduced crystallinity. Needle and globular-particle morphologies were observed in both samples; the needle morphology might have been related to the crystalline contribution. A multifractal analysis showed that the PPA surface became more complex when the crystallinity was reduced. The proposed molecular structures of PPA were supported by the high-resolution 13C NMR results, allowing us to access the percentage of head-to-tail (HT) and head-to-head (HH) molecular structures. When comparing the calculated and experimental FTIR spectra, the most pronounced changes were observed in ν(C?H), ν(N?H), ν(C?O), and ν(C?N?C) due to the influence of counterions on the polymer backbone as well as the different mechanisms of polymerization. Finally, a significant difference in the electrical conductivitywas observed in the range of 1.00 × 10−9 S.cm−1 and 3.90 × 10−14 S.cm−1, respectively, for PPA1HT and PPA16HT-HH. Menos: Poly(p-anisidine) (PPA) is a polyaniline derivative presenting a methoxy (?OCH3) group at the para position of the phenyl ring. Considering the important role of conjugated polymers in novel technological applications, a systematic, combined experimental and theoretical investigation was performed to obtain more insight into the crystallization process of PPA. Conventional oxidative polymerization of p-anisidine monomer was based on a central composite rotational design (CCRD).The effects of the concentration of the monomer, ammonium persulfate (APS), and HCl on the percentage of crystallinity were considered. Several experimental techniques such as X-ray Diffraction(XRD), Scanning Electron Microscopy (SEM), multifractal analysis, Nuclear Magnetic Resonance(13C NMR), Fourier-transform Infrared spectroscopy (FTIR), and complex impedance spectroscopyanalysis, in addition to Density Functional Theory (DFT), were employed to perform a systematic investigation of PPA. The experimental treatments resulted in different crystal structures with a percentage of crystallinity ranging from (29.2 ± 0.6)% (PPA1HT) to (55.1 ± 0.2)% (PPA16HT-HH). A broad halo in the PPA16HT-HH pattern from 2θ = 10.0?30.0◦suggested a reduced crystallinity. Needle and globular-particle morphologies were observed in both samples; the needle morphology might have been related to the crystalline contribution. A multifractal analysis showed that the PPA surface became more complex when the crystallin... Mostrar Tudo |
Palavras-Chave: |
Conjugated polymer; Multifractal analysis; Poly(p-anisidine). |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1148841/1/P-Head-to-Tail-and-Head-to-Head-Molecular-Chains-of.pdf
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Marc: |
LEADER 03197naa a2200337 a 4500 001 2148841 005 2024-01-22 008 2022 bl uuuu u00u1 u #d 024 7 $ahttps://doi.org/10.3390/molecules27196326$2DOI 100 1 $aOLIVEIRA, L. R. de 245 $aHead-to-tail and head-to-head molecular chains of poly(p-anisidine)$bCombined experimental and theoretical evaluation.$h[electronic resource] 260 $c2022 300 $a28 p. 520 $a: Poly(p-anisidine) (PPA) is a polyaniline derivative presenting a methoxy (?OCH3) group at the para position of the phenyl ring. Considering the important role of conjugated polymers in novel technological applications, a systematic, combined experimental and theoretical investigation was performed to obtain more insight into the crystallization process of PPA. Conventional oxidative polymerization of p-anisidine monomer was based on a central composite rotational design (CCRD).The effects of the concentration of the monomer, ammonium persulfate (APS), and HCl on the percentage of crystallinity were considered. Several experimental techniques such as X-ray Diffraction(XRD), Scanning Electron Microscopy (SEM), multifractal analysis, Nuclear Magnetic Resonance(13C NMR), Fourier-transform Infrared spectroscopy (FTIR), and complex impedance spectroscopyanalysis, in addition to Density Functional Theory (DFT), were employed to perform a systematic investigation of PPA. The experimental treatments resulted in different crystal structures with a percentage of crystallinity ranging from (29.2 ± 0.6)% (PPA1HT) to (55.1 ± 0.2)% (PPA16HT-HH). A broad halo in the PPA16HT-HH pattern from 2θ = 10.0?30.0◦suggested a reduced crystallinity. Needle and globular-particle morphologies were observed in both samples; the needle morphology might have been related to the crystalline contribution. A multifractal analysis showed that the PPA surface became more complex when the crystallinity was reduced. The proposed molecular structures of PPA were supported by the high-resolution 13C NMR results, allowing us to access the percentage of head-to-tail (HT) and head-to-head (HH) molecular structures. When comparing the calculated and experimental FTIR spectra, the most pronounced changes were observed in ν(C?H), ν(N?H), ν(C?O), and ν(C?N?C) due to the influence of counterions on the polymer backbone as well as the different mechanisms of polymerization. Finally, a significant difference in the electrical conductivitywas observed in the range of 1.00 × 10−9 S.cm−1 and 3.90 × 10−14 S.cm−1, respectively, for PPA1HT and PPA16HT-HH. 653 $aConjugated polymer 653 $aMultifractal analysis 653 $aPoly(p-anisidine) 700 1 $aGONÇALVES, D. S. 700 1 $aCAROLINO, A. S. 700 1 $aFACCINATTO, W. M. 700 1 $aMENEZES. D. C. 700 1 $aDIAS, C. O. 700 1 $aCOLNAGO, L. A. 700 1 $aRUIZ, Y. L. 700 1 $aIU, S. T. 700 1 $aFONSECA FILHO, H. D. 700 1 $aCHAUDHURI, P. 700 1 $aCAMPELO, P. H. 700 1 $aMASCARENHAS, I. P. 700 1 $aSANCHES, E. A. 773 $tMolecules$gv. 27, a6326, 2022.
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