PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO
Autor(a) principal: | |
---|---|
Data de Publicação: | 2014 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Biblioteca Digital de Teses e Dissertações da UEPG |
Texto Completo: | http://tede2.uepg.br/jspui/handle/prefix/2133 |
Resumo: | In this work, starch-stabilized silver nanoparticles (AgNPs-Am) were synthesized by reduction of AgNO3 using the NaBH4. The temperature and concentration of reagents of the synthesis were optimized. The formation of AgNPs-Am was monitored by UV-Vis spectroscopy and dynamic light scattering (DLS). The optimum conditions found for the AgNPs-Am synthesis were starch 0.6 % (w/v), 3.6 x 10-3 mol L-1 NaBH4, 0.9 x 10-3 mol L-1 AgNO3 and synthesis in bath ice. The average size of the AgNPs-Am was between 21 and 77 nm. Transmission electron microscopy (TEM) confirmed the AgNPs-Am formation inside and outside of the starch chains, however the smaller sizes were referred to the NPs stabilized by starch. Measurements of Potential zeta indicated stability of the particles, confirmed by DLS monitoring that demonstrated low agglomeration of NPs in a period of 115 days. For the characterization of AgNPs-Am it was also used infrared spectroscopic (FTIR) and X-ray diffraction (XRD). The AgNPs-Am were applied as polyanion for the construction of films by Layer-by-Layer technique (LbL), alternating with polycation 3-n-propylpyridinium-silsesquioxane (SiPy+Cl-). In order to obtain the films, pH and immersion time of the polyelectrolytes were optimized, as well as the concentration of SiPy+Cl-, monitoring the deposition by UV-Vis. The optimum parameters were immersion time 240 seconds, 2 mg/mL SiPy+Cl- pH 6.5 and AgNPs-Am pH 9.0. Atomic force microscopy (AFM) images showed that film thickness increases linearly and the roughness decrease with the bilayers number. FTIR spectra and Raman confirmed the interaction between the polyelectrolytes in the assembly of LbL films. The LbL films with architecture (SiPy+Cl-/AgNPs-Am)n (n = bilayers number) were applied as modified electrodes for iodine detection, using differential pulse voltammetry (DPV). It was verified that interaction of the components in the LbL films improved the current intensity. The film (SiPy+Cl-/AgNPs-Am)n (n=5) showed better current response in phosphate buffered saline (PBS) 0.1 mol L-1 pH 7.0. The instrumental parameters Epulse, and tpulse were optimized by 23 factorial design. It was verified a significant effect for third order interaction for the intensity of iodine redox peak currents, so the instrumentals parameters were evaluated together. The results of optimization were tpulse = 0.05 s, = 40 mV/s e Epulse = 50 mV. Accordingly, the modified electrode obtained a linear response for iodine concentrations ranging from 4.34 x 10-5 to 3.47 x 10-4 mol L-1 (R=0,9936) and from 4.40 x 10-4 to 4.24 x 10-3 mol L-1 (R=0,9938). It was obtained limit of detection (LOD) 5.56 x 10-6 and 1.51 x 10-5 mol L-1 and for limit of quantification (LOQ) 1.85 x 10-5 and 5.04 x 10-5 mol L-1, respectively. The AgNPs-Am synthesized in this work also acted as colorimetric sensor for iodine, with three regions of linearity. Two analytical curves were obtained for iodine concentration range from 2.40 x 10-7 to 9.50 x 10-7 mol L-1 and from 2.40 x 10-6 mol L-1 to 1.60 x 10-5 mol L-1. It was obtained a LOD of 1.71 x 10-8 and 1.06 x 10-6 mol L-1 and LOQ of 5.69 x 10-8 to 3.55 x 10-6 mol L-1, respectively for each range. Color variations obtained in these concentrations correspond to interaction between iodine and silver, which were monitored by UV-Vis band showed in 410 nm. At concentrations above 5.50 x 10-5 mol L-1 there is the appearance of blue color, absorbance in 600 nm, corresponding to the interaction between starch and iodine. It was also obtained a linear relationship for iodine concentration from 5.50 x 10-5 mol L-1 to 9.50 x 10-5 mol L-1. For this concentration range, LOD and LOQ were respectively 1.37 x 10-6 and 4.58 x 10-6 mol L-1. The results presented confirm the potential use of AgNPs-Am for iodine detection, both for the modification of electrodes for electrochemical determination as a colorimetric sensor. |
id |
UEPG_6af61a5498de8fc8ff3072e05b165b53 |
---|---|
oai_identifier_str |
oai:tede2.uepg.br:prefix/2133 |
network_acronym_str |
UEPG |
network_name_str |
Biblioteca Digital de Teses e Dissertações da UEPG |
repository_id_str |
|
spelling |
Pessoa, Christiana AndradeCPF:02089192445http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4792376U2Castro, Eryza Guimarães deCPF:02229472825CASTRO, E. G. deTarley, Cesar Ricardo TeixeiraCPF:20445556897http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4706017U6CPF:07524995997http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4409944Y5Oliveira, Rafaela Daiane de2017-07-24T19:38:14Z2014-11-112017-07-24T19:38:14Z2014-08-22OLIVEIRA, Rafaela Daiane de. PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO. 2014. 96 f. Dissertação (Mestrado em Química) - UNIVERSIDADE ESTADUAL DE PONTA GROSSA, Ponta Grossa, 2014.http://tede2.uepg.br/jspui/handle/prefix/2133In this work, starch-stabilized silver nanoparticles (AgNPs-Am) were synthesized by reduction of AgNO3 using the NaBH4. The temperature and concentration of reagents of the synthesis were optimized. The formation of AgNPs-Am was monitored by UV-Vis spectroscopy and dynamic light scattering (DLS). The optimum conditions found for the AgNPs-Am synthesis were starch 0.6 % (w/v), 3.6 x 10-3 mol L-1 NaBH4, 0.9 x 10-3 mol L-1 AgNO3 and synthesis in bath ice. The average size of the AgNPs-Am was between 21 and 77 nm. Transmission electron microscopy (TEM) confirmed the AgNPs-Am formation inside and outside of the starch chains, however the smaller sizes were referred to the NPs stabilized by starch. Measurements of Potential zeta indicated stability of the particles, confirmed by DLS monitoring that demonstrated low agglomeration of NPs in a period of 115 days. For the characterization of AgNPs-Am it was also used infrared spectroscopic (FTIR) and X-ray diffraction (XRD). The AgNPs-Am were applied as polyanion for the construction of films by Layer-by-Layer technique (LbL), alternating with polycation 3-n-propylpyridinium-silsesquioxane (SiPy+Cl-). In order to obtain the films, pH and immersion time of the polyelectrolytes were optimized, as well as the concentration of SiPy+Cl-, monitoring the deposition by UV-Vis. The optimum parameters were immersion time 240 seconds, 2 mg/mL SiPy+Cl- pH 6.5 and AgNPs-Am pH 9.0. Atomic force microscopy (AFM) images showed that film thickness increases linearly and the roughness decrease with the bilayers number. FTIR spectra and Raman confirmed the interaction between the polyelectrolytes in the assembly of LbL films. The LbL films with architecture (SiPy+Cl-/AgNPs-Am)n (n = bilayers number) were applied as modified electrodes for iodine detection, using differential pulse voltammetry (DPV). It was verified that interaction of the components in the LbL films improved the current intensity. The film (SiPy+Cl-/AgNPs-Am)n (n=5) showed better current response in phosphate buffered saline (PBS) 0.1 mol L-1 pH 7.0. The instrumental parameters Epulse, and tpulse were optimized by 23 factorial design. It was verified a significant effect for third order interaction for the intensity of iodine redox peak currents, so the instrumentals parameters were evaluated together. The results of optimization were tpulse = 0.05 s, = 40 mV/s e Epulse = 50 mV. Accordingly, the modified electrode obtained a linear response for iodine concentrations ranging from 4.34 x 10-5 to 3.47 x 10-4 mol L-1 (R=0,9936) and from 4.40 x 10-4 to 4.24 x 10-3 mol L-1 (R=0,9938). It was obtained limit of detection (LOD) 5.56 x 10-6 and 1.51 x 10-5 mol L-1 and for limit of quantification (LOQ) 1.85 x 10-5 and 5.04 x 10-5 mol L-1, respectively. The AgNPs-Am synthesized in this work also acted as colorimetric sensor for iodine, with three regions of linearity. Two analytical curves were obtained for iodine concentration range from 2.40 x 10-7 to 9.50 x 10-7 mol L-1 and from 2.40 x 10-6 mol L-1 to 1.60 x 10-5 mol L-1. It was obtained a LOD of 1.71 x 10-8 and 1.06 x 10-6 mol L-1 and LOQ of 5.69 x 10-8 to 3.55 x 10-6 mol L-1, respectively for each range. Color variations obtained in these concentrations correspond to interaction between iodine and silver, which were monitored by UV-Vis band showed in 410 nm. At concentrations above 5.50 x 10-5 mol L-1 there is the appearance of blue color, absorbance in 600 nm, corresponding to the interaction between starch and iodine. It was also obtained a linear relationship for iodine concentration from 5.50 x 10-5 mol L-1 to 9.50 x 10-5 mol L-1. For this concentration range, LOD and LOQ were respectively 1.37 x 10-6 and 4.58 x 10-6 mol L-1. The results presented confirm the potential use of AgNPs-Am for iodine detection, both for the modification of electrodes for electrochemical determination as a colorimetric sensor.Neste trabalho foram sintetizadas nanopartículas de prata estabilizadas em amido (AgNPs-Am). A síntese foi realizada por redução do sal AgNO3 utilizando o NaBH4. A temperatura de síntese e concentração dos reagentes foram otimizadas, a formação das AgNPs-Am foi monitorada por espectroscopia na região do UV-Vis e medidas de espalhamento dinâmico da luz (DLS). As condições ótimas encontradas para síntese de AgNPs-Am foram amido 0,6 % (m/v), 3,6.10-3 mol.L-1 de NaBH4, 0,9.10-3 mol.L-1 de AgNO3 e síntese em banho de gelo. O tamanho médio das AgNPs-Am foi entre 21 e 77 nm. Imagens de microscopia eletrônica de transmissão (TEM) confirmaram que houve formação das AgNPs no interior e fora das cadeias de amido, sendo os menores tamanhos referentes às NPs estabilizadas pelo amido. Medidas de Potencial zeta indicaram estabilidade das NPs, confirmada por acompanhamento DLS que demonstrou baixa aglomeração em um período de 115 dias. Para caracterização das AgNPs-Am utilizou-se também espectroscopia na região do infravermelho (FTIR) e difração de raios X (XRD). As AgNPs-Am foram utilizadas como poliânion para construção de filmes pela técnica Layer-by-Layer (LbL), alternando com policátion 3-n-propilpiridínio-silsesquioxano (SiPy+Cl-). Para construção dos filmes, pH e tempo de imersão dos polieletrólitos foram otimizados, assim como concentração de SiPy+Cl-, monitorando a deposição por UV-Vis. Os parâmetros ótimos foram tempo de imersão 240 segundos, solução de 2 mg/mL de SiPy+Cl- pH 6,5 e AgNPs-Am pH 9,0. Imagens de microscopia de força atômica (AFM) mostram que a espessura dos filmes aumenta linearmente e a rugosidade decresce com o número de bicamadas. Espectros FTIR e Raman confirmaram a interação entre os polieletrólitos na montagem dos filmes. Os filmes LbL com configuração (SiPy+Cl-/AgNPs-Am)n (n = número de bicamadas) foram aplicados como eletrodos modificados para detecção de iodo, utilizando-se voltametria de pulso diferencial (VPD). Verificou-se que a interação dos componentes no filme LbL melhorou a intensidade de corrente. O filme (SiPy+Cl-/AgNPs-Am)n (n=5) apresentou melhor resposta de corrente em eletrólito suporte tampão fosfato salino (PBS) 0,1 mol.L-1 pH 7,0. Os parâmetros instrumentais Epulso, e tpulso foram otimizados por planejamento fatorial 23. Verificou-se efeito significativo para interação de terceira ordem para intensidade de corrente do pico de redução do iodo, portanto os parâmetros instrumentais foram avaliados em conjunto. Os resultados da otimização foram tpulso = 0,05 s, = 40 mV/s e Epulso = 50 mV. Nestas condições, o eletrodo modificado obteve resposta linear para concentrações de iodo que variam de 4,34.10-5 a 3,47.10-4 mol.L-1 (R=0,9936) e de 4,40.10-4 a 4,24.10-3 mol.L-1 (R=0,9938). Respectivamente, obteve-se limite de detecção 5,56.10-6 e 1,51.10-5 mol.L-1 e para o limite de quantificação 1,85.10-5 e 5,04.10-5 mol.L-1. As AgNPs-Am sintetizadas neste trabalho também atuaram como sensor colorimétrico de iodo, com três regiões de linearidade. Duas curvas analíticas foram construídas para concentrações de iodo de 2,40.10-7 a 9,50.10-7 mol.L-1 e de 2,40.10-6 mol.L-1 a 1,60.10-5 mol.L-1. Obteve-se LD de 1,71.10-8 e 1,06.10-6 mol.L-1 e LQ de 5,69.10-8 e 3,55.10-6 mol.L-1, respectivamente para cada intervalo. As variações de cores obtidas nestas concentrações correspondem a interação entre o iodo e a prata, as quais foram acompanhadas pela banda UV-Vis apresentada em 410 nm. Em concentrações acima de 5,50.10-5 mol.L-1 observa-se o aparecimento de coloração azul, absorbância em 600 nm, correspondente a interação entre amido e iodo. Obteve-se linearidade para concentrações de 5,50.10-5 mol.L-1 a 9,50.10-5 mol.L-1. Para este intervalo de concentração, os LD e LQ são respectivamente 1,37.10-6 e 4,58.10-6 mol.L-1. Os resultados apresentados confirmam a potencialidade do uso das AgNPs-Am para detecção de iodo, tanto na modificação de eletrodos para determinação eletroquímica, quanto o uso como sensor colorimétrico.Made available in DSpace on 2017-07-24T19:38:14Z (GMT). No. of bitstreams: 1 RAFAELA D OLIVEIRA.pdf: 2756499 bytes, checksum: e1e60d222b6dbe62066658f22ea4de0b (MD5) Previous issue date: 2014-08-22application/pdfporUNIVERSIDADE ESTADUAL DE PONTA GROSSAPrograma de Pós-Graduação em Química AplicadaUEPGBRQuímicananopartículas de pratafilmes Layer-by-Layer3-n-propilpiridínio-silsesquioxanoiodosensores eletroquímicossilver nanoparticlesLayer-by-Layer films3-n-propylpyridinium-silsesquioxaneiodine, electrochemical sensorsCNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICAPREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDOinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisinfo:eu-repo/semantics/openAccessreponame:Biblioteca Digital de Teses e Dissertações da UEPGinstname:Universidade Estadual de Ponta Grossa (UEPG)instacron:UEPGORIGINALRAFAELA D OLIVEIRA.pdfapplication/pdf2756499http://tede2.uepg.br/jspui/bitstream/prefix/2133/1/RAFAELA%20D%20OLIVEIRA.pdfe1e60d222b6dbe62066658f22ea4de0bMD51prefix/21332017-07-24 16:38:14.922oai:tede2.uepg.br:prefix/2133Biblioteca Digital de Teses e Dissertaçõeshttps://tede2.uepg.br/jspui/PUBhttp://tede2.uepg.br/oai/requestbicen@uepg.br||mv_fidelis@yahoo.com.bropendoar:2017-07-24T19:38:14Biblioteca Digital de Teses e Dissertações da UEPG - Universidade Estadual de Ponta Grossa (UEPG)false |
dc.title.por.fl_str_mv |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
title |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
spellingShingle |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO Oliveira, Rafaela Daiane de nanopartículas de prata filmes Layer-by-Layer 3-n-propilpiridínio-silsesquioxano iodo sensores eletroquímicos silver nanoparticles Layer-by-Layer films 3-n-propylpyridinium-silsesquioxane iodine, electrochemical sensors CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
title_short |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
title_full |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
title_fullStr |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
title_full_unstemmed |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
title_sort |
PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO |
author |
Oliveira, Rafaela Daiane de |
author_facet |
Oliveira, Rafaela Daiane de |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Pessoa, Christiana Andrade |
dc.contributor.advisor1ID.fl_str_mv |
CPF:02089192445 |
dc.contributor.advisor1Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4792376U2 |
dc.contributor.referee1.fl_str_mv |
Castro, Eryza Guimarães de |
dc.contributor.referee1ID.fl_str_mv |
CPF:02229472825 |
dc.contributor.referee1Lattes.fl_str_mv |
CASTRO, E. G. de |
dc.contributor.referee2.fl_str_mv |
Tarley, Cesar Ricardo Teixeira |
dc.contributor.referee2ID.fl_str_mv |
CPF:20445556897 |
dc.contributor.referee2Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4706017U6 |
dc.contributor.authorID.fl_str_mv |
CPF:07524995997 |
dc.contributor.authorLattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4409944Y5 |
dc.contributor.author.fl_str_mv |
Oliveira, Rafaela Daiane de |
contributor_str_mv |
Pessoa, Christiana Andrade Castro, Eryza Guimarães de Tarley, Cesar Ricardo Teixeira |
dc.subject.por.fl_str_mv |
nanopartículas de prata filmes Layer-by-Layer 3-n-propilpiridínio-silsesquioxano iodo sensores eletroquímicos |
topic |
nanopartículas de prata filmes Layer-by-Layer 3-n-propilpiridínio-silsesquioxano iodo sensores eletroquímicos silver nanoparticles Layer-by-Layer films 3-n-propylpyridinium-silsesquioxane iodine, electrochemical sensors CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
dc.subject.eng.fl_str_mv |
silver nanoparticles Layer-by-Layer films 3-n-propylpyridinium-silsesquioxane iodine, electrochemical sensors |
dc.subject.cnpq.fl_str_mv |
CNPQ::CIENCIAS EXATAS E DA TERRA::QUIMICA |
description |
In this work, starch-stabilized silver nanoparticles (AgNPs-Am) were synthesized by reduction of AgNO3 using the NaBH4. The temperature and concentration of reagents of the synthesis were optimized. The formation of AgNPs-Am was monitored by UV-Vis spectroscopy and dynamic light scattering (DLS). The optimum conditions found for the AgNPs-Am synthesis were starch 0.6 % (w/v), 3.6 x 10-3 mol L-1 NaBH4, 0.9 x 10-3 mol L-1 AgNO3 and synthesis in bath ice. The average size of the AgNPs-Am was between 21 and 77 nm. Transmission electron microscopy (TEM) confirmed the AgNPs-Am formation inside and outside of the starch chains, however the smaller sizes were referred to the NPs stabilized by starch. Measurements of Potential zeta indicated stability of the particles, confirmed by DLS monitoring that demonstrated low agglomeration of NPs in a period of 115 days. For the characterization of AgNPs-Am it was also used infrared spectroscopic (FTIR) and X-ray diffraction (XRD). The AgNPs-Am were applied as polyanion for the construction of films by Layer-by-Layer technique (LbL), alternating with polycation 3-n-propylpyridinium-silsesquioxane (SiPy+Cl-). In order to obtain the films, pH and immersion time of the polyelectrolytes were optimized, as well as the concentration of SiPy+Cl-, monitoring the deposition by UV-Vis. The optimum parameters were immersion time 240 seconds, 2 mg/mL SiPy+Cl- pH 6.5 and AgNPs-Am pH 9.0. Atomic force microscopy (AFM) images showed that film thickness increases linearly and the roughness decrease with the bilayers number. FTIR spectra and Raman confirmed the interaction between the polyelectrolytes in the assembly of LbL films. The LbL films with architecture (SiPy+Cl-/AgNPs-Am)n (n = bilayers number) were applied as modified electrodes for iodine detection, using differential pulse voltammetry (DPV). It was verified that interaction of the components in the LbL films improved the current intensity. The film (SiPy+Cl-/AgNPs-Am)n (n=5) showed better current response in phosphate buffered saline (PBS) 0.1 mol L-1 pH 7.0. The instrumental parameters Epulse, and tpulse were optimized by 23 factorial design. It was verified a significant effect for third order interaction for the intensity of iodine redox peak currents, so the instrumentals parameters were evaluated together. The results of optimization were tpulse = 0.05 s, = 40 mV/s e Epulse = 50 mV. Accordingly, the modified electrode obtained a linear response for iodine concentrations ranging from 4.34 x 10-5 to 3.47 x 10-4 mol L-1 (R=0,9936) and from 4.40 x 10-4 to 4.24 x 10-3 mol L-1 (R=0,9938). It was obtained limit of detection (LOD) 5.56 x 10-6 and 1.51 x 10-5 mol L-1 and for limit of quantification (LOQ) 1.85 x 10-5 and 5.04 x 10-5 mol L-1, respectively. The AgNPs-Am synthesized in this work also acted as colorimetric sensor for iodine, with three regions of linearity. Two analytical curves were obtained for iodine concentration range from 2.40 x 10-7 to 9.50 x 10-7 mol L-1 and from 2.40 x 10-6 mol L-1 to 1.60 x 10-5 mol L-1. It was obtained a LOD of 1.71 x 10-8 and 1.06 x 10-6 mol L-1 and LOQ of 5.69 x 10-8 to 3.55 x 10-6 mol L-1, respectively for each range. Color variations obtained in these concentrations correspond to interaction between iodine and silver, which were monitored by UV-Vis band showed in 410 nm. At concentrations above 5.50 x 10-5 mol L-1 there is the appearance of blue color, absorbance in 600 nm, corresponding to the interaction between starch and iodine. It was also obtained a linear relationship for iodine concentration from 5.50 x 10-5 mol L-1 to 9.50 x 10-5 mol L-1. For this concentration range, LOD and LOQ were respectively 1.37 x 10-6 and 4.58 x 10-6 mol L-1. The results presented confirm the potential use of AgNPs-Am for iodine detection, both for the modification of electrodes for electrochemical determination as a colorimetric sensor. |
publishDate |
2014 |
dc.date.available.fl_str_mv |
2014-11-11 2017-07-24T19:38:14Z |
dc.date.issued.fl_str_mv |
2014-08-22 |
dc.date.accessioned.fl_str_mv |
2017-07-24T19:38:14Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
OLIVEIRA, Rafaela Daiane de. PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO. 2014. 96 f. Dissertação (Mestrado em Química) - UNIVERSIDADE ESTADUAL DE PONTA GROSSA, Ponta Grossa, 2014. |
dc.identifier.uri.fl_str_mv |
http://tede2.uepg.br/jspui/handle/prefix/2133 |
identifier_str_mv |
OLIVEIRA, Rafaela Daiane de. PREPARAÇÃO, CARACTERIZAÇÃO E APLICAÇÃO DE FILMES LbL COM NANOPARTÍCULAS DE PRATA ESTABILIZADAS EM AMIDO. 2014. 96 f. Dissertação (Mestrado em Química) - UNIVERSIDADE ESTADUAL DE PONTA GROSSA, Ponta Grossa, 2014. |
url |
http://tede2.uepg.br/jspui/handle/prefix/2133 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
UNIVERSIDADE ESTADUAL DE PONTA GROSSA |
dc.publisher.program.fl_str_mv |
Programa de Pós-Graduação em Química Aplicada |
dc.publisher.initials.fl_str_mv |
UEPG |
dc.publisher.country.fl_str_mv |
BR |
dc.publisher.department.fl_str_mv |
Química |
publisher.none.fl_str_mv |
UNIVERSIDADE ESTADUAL DE PONTA GROSSA |
dc.source.none.fl_str_mv |
reponame:Biblioteca Digital de Teses e Dissertações da UEPG instname:Universidade Estadual de Ponta Grossa (UEPG) instacron:UEPG |
instname_str |
Universidade Estadual de Ponta Grossa (UEPG) |
instacron_str |
UEPG |
institution |
UEPG |
reponame_str |
Biblioteca Digital de Teses e Dissertações da UEPG |
collection |
Biblioteca Digital de Teses e Dissertações da UEPG |
bitstream.url.fl_str_mv |
http://tede2.uepg.br/jspui/bitstream/prefix/2133/1/RAFAELA%20D%20OLIVEIRA.pdf |
bitstream.checksum.fl_str_mv |
e1e60d222b6dbe62066658f22ea4de0b |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 |
repository.name.fl_str_mv |
Biblioteca Digital de Teses e Dissertações da UEPG - Universidade Estadual de Ponta Grossa (UEPG) |
repository.mail.fl_str_mv |
bicen@uepg.br||mv_fidelis@yahoo.com.br |
_version_ |
1809460456998305792 |