Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN
Autor(a) principal: | |
---|---|
Data de Publicação: | 2015 |
Tipo de documento: | Dissertação |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/5539 |
Resumo: | In this paper was performed a characterization of the solar protectors avobenzone and octyl methoxycinnamate and the assignments of its second order coupling. The avobenzone photostability was evaluated in different types of solvents, concentrations and time exposition to UV light. Nevertheless, it was measured the radiation absorption on near and medium infrared in four commercial solar protectors, wherein only one of them claims in its package the guarantee of such protection. The characterization of the solar protector sctructure was made by ¹H NMR using a Bucker Avance III 500 spectrometer. It was used a Gaussian 09 program to calculate and optimize the most stable molecule structure and the coupling constants of protons and the WinDNMR to simulate the theoretical spectra from the data obtained by the calculations. The photostability of the avobenzone was determined by irradiating for 5, 10, 15 and 20 minutes, under a UV lamp, solutions of avobenzone in chloroform, methanol, acetone and acetonitrile in concentrations of 5,32x10-2 mol/L and 1,6x10-3 mol/L, monitoring the alterations occurred by 1H NMR. The absorption in the near and middle infrared regions was made in a PerkinElmer Frontier Dual Range FT spectrometer, where the sample was directly deposited into the equipment, without the need of previous treatment. The theoretical calculation showed itself an important tool to the attribution of second order systems, given that is not possible to manually determine the coupling constant values in this kind of system. The avobenzone presented itself photoinstable in the solution with concentration 1,6 x 103 mol/L, and in acetonitrile. On other solvents the photoinstability wasn’t observed. In the others commercial solar protectors showed similar absorption on the near and middle infrared, not existing significative difference between the product that declared having as a selling point this kind of absorption and the rest, being possible to assert that this information is used in its label for commercial reasons, not being characteristic of quality among the other products. |
id |
UFG-2_ed1771d6bc1040d87f9aa759c4e3cd93 |
---|---|
oai_identifier_str |
oai:repositorio.bc.ufg.br:tede/5539 |
network_acronym_str |
UFG-2 |
network_name_str |
Repositório Institucional da UFG |
repository_id_str |
|
spelling |
Queiroz Júnior, Luiz Henrique Kenghttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4141331D0Queiroz Júnior, Luiz Henrique KengLacerda Júnior, ValdemarVaz, Boniek Gontijohttp://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4268397D5Sousa, Renato Ribeiro de2016-05-06T11:10:17Z2015-08-28SOUSA, R. R. Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN. 2015. 70 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2015.http://repositorio.bc.ufg.br/tede/handle/tede/5539In this paper was performed a characterization of the solar protectors avobenzone and octyl methoxycinnamate and the assignments of its second order coupling. The avobenzone photostability was evaluated in different types of solvents, concentrations and time exposition to UV light. Nevertheless, it was measured the radiation absorption on near and medium infrared in four commercial solar protectors, wherein only one of them claims in its package the guarantee of such protection. The characterization of the solar protector sctructure was made by ¹H NMR using a Bucker Avance III 500 spectrometer. It was used a Gaussian 09 program to calculate and optimize the most stable molecule structure and the coupling constants of protons and the WinDNMR to simulate the theoretical spectra from the data obtained by the calculations. The photostability of the avobenzone was determined by irradiating for 5, 10, 15 and 20 minutes, under a UV lamp, solutions of avobenzone in chloroform, methanol, acetone and acetonitrile in concentrations of 5,32x10-2 mol/L and 1,6x10-3 mol/L, monitoring the alterations occurred by 1H NMR. The absorption in the near and middle infrared regions was made in a PerkinElmer Frontier Dual Range FT spectrometer, where the sample was directly deposited into the equipment, without the need of previous treatment. The theoretical calculation showed itself an important tool to the attribution of second order systems, given that is not possible to manually determine the coupling constant values in this kind of system. The avobenzone presented itself photoinstable in the solution with concentration 1,6 x 103 mol/L, and in acetonitrile. On other solvents the photoinstability wasn’t observed. In the others commercial solar protectors showed similar absorption on the near and middle infrared, not existing significative difference between the product that declared having as a selling point this kind of absorption and the rest, being possible to assert that this information is used in its label for commercial reasons, not being characteristic of quality among the other products.Nesse trabalho foi realizada a caracterização dos filtros solares avobenzona e metoxinamato de octila, e as atribuições de seus acoplamentos de segunda ordem. A fotoestabilidade da avobenzona foi avaliada em diferentes tipos de solventes, concentrações e tempos de exposições à luz UV. Além disso, foi medida a absorção da radiação no infravermelho próximo e médio em quatro protetores solares comerciais, sendo que, somente um deles declara em sua embalagem a garantia de tal proteção. A caracterização das estruturas dos filtros solares foi feita por RMN de 1H utilizando um espectrômetro Bruker Avance III 500. Utilizou-se os programas Gaussian 09 para calcular e otimizar a estrutura mais estável da molécula e as constantes de acoplamento dos hidrogênios, e o WinDNMR para simular a partir dos dados obtidos pelo cálculo os espectros teóricos. A fotoestabilidade da avobenzona foi determinada irradiando por 5, 10, 15 e 20 minutos, sob uma lâmpada UV, soluções de avobenzona em clorofórmio, metanol, acetona e acetonitrila nas concentrações de 5,32 x 10-2 mol/L e 1,6 x 10-3 mol/L, monitorando as alterações ocorridas por RMN de 1H. Já a absorção na região do infravermelho próximo e médio foi feita em um espectrômetro PerkinElmer Frontier Dual Range FT, onde a amostra foi depositada diretamente no equipamento sem necessidade de tratamento prévio. O cálculo teórico se mostrou uma importante ferramenta para a atribuição de sistemas de segunda ordem, já que não é possível determinar manualmente os valores das constantes de acoplamento nesse tipo de sistema. Já a avobenzona se apresentou fotoinstável na solução de concentração 1,6 x 10-3 mol/L e em acetonitrila. Nos demais solventes a fotoinstabilidade não foi observada. Já os protetores solares comercias apresentaram absorções semelhantes da radiação no infravermelho próximo e médio, não havendo diferença significativa entre o produto que declarou ter como diferencial esse tipo de absorção e os demais, podendo afirmar que essa informação é utilizada em seu rótulo por questões comerciais, não sendo um diferencial de qualidade entre os demais produtos.Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2016-05-05T19:02:00Z No. of bitstreams: 2 Dissertação - Renato Ribeiro de Sousa - 2015.pdf: 3128241 bytes, checksum: bca24056dbea9a9bcc77e3576d3d0d76 (MD5) license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2016-05-06T11:10:17Z (GMT) No. of bitstreams: 2 Dissertação - Renato Ribeiro de Sousa - 2015.pdf: 3128241 bytes, checksum: bca24056dbea9a9bcc77e3576d3d0d76 (MD5) license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5)Made available in DSpace on 2016-05-06T11:10:17Z (GMT). No. of bitstreams: 2 Dissertação - Renato Ribeiro de Sousa - 2015.pdf: 3128241 bytes, checksum: bca24056dbea9a9bcc77e3576d3d0d76 (MD5) license_rdf: 19874 bytes, checksum: 38cb62ef53e6f513db2fb7e337df6485 (MD5) Previous issue date: 2015-08-28Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - CAPESapplication/pdfporUniversidade Federal de GoiásPrograma de Pós-graduação em Química (IQ)UFGBrasilInstituto de Química - IQ (RG)http://creativecommons.org/licenses/by/4.0/info:eu-repo/semantics/openAccessFiltro solarAvobenzonaFotoestabilidadeCálculos teóricosSolar protectorAvobenzonePhotostabilityTheoretical calculationsCIENCIAS EXATAS E DA TERRA::QUIMICACaracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMNinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis663693921325415158600600600600782606674374119727815717003253031171952075167498588264571reponame:Repositório Institucional da UFGinstname:Universidade Federal de Goiás (UFG)instacron:UFGLICENSElicense.txtlicense.txttext/plain; charset=utf-82165http://repositorio.bc.ufg.br/tede/bitstreams/f32852b9-9a28-4951-aac5-cb485caa0793/downloadbd3efa91386c1718a7f26a329fdcb468MD51CC-LICENSElicense_urllicense_urltext/plain; charset=utf-843http://repositorio.bc.ufg.br/tede/bitstreams/aea1641c-052e-484f-9bd3-e675772dc3cb/download321f3992dd3875151d8801b773ab32edMD52license_textlicense_texttext/html; charset=utf-821818http://repositorio.bc.ufg.br/tede/bitstreams/449d9d54-4ca1-44a4-86c4-66d9153cc155/downloadb19767193fa05eb8852808b812c188a0MD53license_rdflicense_rdfapplication/rdf+xml; charset=utf-819874http://repositorio.bc.ufg.br/tede/bitstreams/f2e1f917-ce67-48a3-885d-fc6e2f8ddbd0/download38cb62ef53e6f513db2fb7e337df6485MD54ORIGINALDissertação - Renato Ribeiro de Sousa - 2015.pdfDissertação - Renato Ribeiro de Sousa - 2015.pdfapplication/pdf3128241http://repositorio.bc.ufg.br/tede/bitstreams/2623bda6-2752-4fd2-9e07-e9f10c552cac/downloadbca24056dbea9a9bcc77e3576d3d0d76MD55tede/55392016-05-06 08:10:17.077http://creativecommons.org/licenses/by/4.0/Acesso Abertoopen.accessoai:repositorio.bc.ufg.br:tede/5539http://repositorio.bc.ufg.br/tedeRepositório InstitucionalPUBhttp://repositorio.bc.ufg.br/oai/requesttasesdissertacoes.bc@ufg.bropendoar:2016-05-06T11:10:17Repositório Institucional da UFG - Universidade Federal de Goiás (UFG)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 |
dc.title.por.fl_str_mv |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
title |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
spellingShingle |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN Sousa, Renato Ribeiro de Filtro solar Avobenzona Fotoestabilidade Cálculos teóricos Solar protector Avobenzone Photostability Theoretical calculations CIENCIAS EXATAS E DA TERRA::QUIMICA |
title_short |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
title_full |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
title_fullStr |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
title_full_unstemmed |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
title_sort |
Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN |
author |
Sousa, Renato Ribeiro de |
author_facet |
Sousa, Renato Ribeiro de |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Queiroz Júnior, Luiz Henrique Keng |
dc.contributor.advisor1Lattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4141331D0 |
dc.contributor.referee1.fl_str_mv |
Queiroz Júnior, Luiz Henrique Keng |
dc.contributor.referee2.fl_str_mv |
Lacerda Júnior, Valdemar |
dc.contributor.referee3.fl_str_mv |
Vaz, Boniek Gontijo |
dc.contributor.authorLattes.fl_str_mv |
http://buscatextual.cnpq.br/buscatextual/visualizacv.do?id=K4268397D5 |
dc.contributor.author.fl_str_mv |
Sousa, Renato Ribeiro de |
contributor_str_mv |
Queiroz Júnior, Luiz Henrique Keng Queiroz Júnior, Luiz Henrique Keng Lacerda Júnior, Valdemar Vaz, Boniek Gontijo |
dc.subject.por.fl_str_mv |
Filtro solar Avobenzona Fotoestabilidade Cálculos teóricos |
topic |
Filtro solar Avobenzona Fotoestabilidade Cálculos teóricos Solar protector Avobenzone Photostability Theoretical calculations CIENCIAS EXATAS E DA TERRA::QUIMICA |
dc.subject.eng.fl_str_mv |
Solar protector Avobenzone Photostability Theoretical calculations |
dc.subject.cnpq.fl_str_mv |
CIENCIAS EXATAS E DA TERRA::QUIMICA |
description |
In this paper was performed a characterization of the solar protectors avobenzone and octyl methoxycinnamate and the assignments of its second order coupling. The avobenzone photostability was evaluated in different types of solvents, concentrations and time exposition to UV light. Nevertheless, it was measured the radiation absorption on near and medium infrared in four commercial solar protectors, wherein only one of them claims in its package the guarantee of such protection. The characterization of the solar protector sctructure was made by ¹H NMR using a Bucker Avance III 500 spectrometer. It was used a Gaussian 09 program to calculate and optimize the most stable molecule structure and the coupling constants of protons and the WinDNMR to simulate the theoretical spectra from the data obtained by the calculations. The photostability of the avobenzone was determined by irradiating for 5, 10, 15 and 20 minutes, under a UV lamp, solutions of avobenzone in chloroform, methanol, acetone and acetonitrile in concentrations of 5,32x10-2 mol/L and 1,6x10-3 mol/L, monitoring the alterations occurred by 1H NMR. The absorption in the near and middle infrared regions was made in a PerkinElmer Frontier Dual Range FT spectrometer, where the sample was directly deposited into the equipment, without the need of previous treatment. The theoretical calculation showed itself an important tool to the attribution of second order systems, given that is not possible to manually determine the coupling constant values in this kind of system. The avobenzone presented itself photoinstable in the solution with concentration 1,6 x 103 mol/L, and in acetonitrile. On other solvents the photoinstability wasn’t observed. In the others commercial solar protectors showed similar absorption on the near and middle infrared, not existing significative difference between the product that declared having as a selling point this kind of absorption and the rest, being possible to assert that this information is used in its label for commercial reasons, not being characteristic of quality among the other products. |
publishDate |
2015 |
dc.date.issued.fl_str_mv |
2015-08-28 |
dc.date.accessioned.fl_str_mv |
2016-05-06T11:10:17Z |
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 |
SOUSA, R. R. Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN. 2015. 70 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2015. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/5539 |
identifier_str_mv |
SOUSA, R. R. Caracterização e avaliação da fotoestabilidade do filtro solar butil metoxidibenzoilmetano (avobenzona) através de IV e RMN. 2015. 70 f. Dissertação (Mestrado em Química) - Universidade Federal de Goiás, Goiânia, 2015. |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/5539 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.program.fl_str_mv |
663693921325415158 |
dc.relation.confidence.fl_str_mv |
600 600 600 600 |
dc.relation.department.fl_str_mv |
7826066743741197278 |
dc.relation.cnpq.fl_str_mv |
1571700325303117195 |
dc.relation.sponsorship.fl_str_mv |
2075167498588264571 |
dc.rights.driver.fl_str_mv |
http://creativecommons.org/licenses/by/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by/4.0/ |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Química (IQ) |
dc.publisher.initials.fl_str_mv |
UFG |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Instituto de Química - IQ (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFG instname:Universidade Federal de Goiás (UFG) instacron:UFG |
instname_str |
Universidade Federal de Goiás (UFG) |
instacron_str |
UFG |
institution |
UFG |
reponame_str |
Repositório Institucional da UFG |
collection |
Repositório Institucional da UFG |
bitstream.url.fl_str_mv |
http://repositorio.bc.ufg.br/tede/bitstreams/f32852b9-9a28-4951-aac5-cb485caa0793/download http://repositorio.bc.ufg.br/tede/bitstreams/aea1641c-052e-484f-9bd3-e675772dc3cb/download http://repositorio.bc.ufg.br/tede/bitstreams/449d9d54-4ca1-44a4-86c4-66d9153cc155/download http://repositorio.bc.ufg.br/tede/bitstreams/f2e1f917-ce67-48a3-885d-fc6e2f8ddbd0/download http://repositorio.bc.ufg.br/tede/bitstreams/2623bda6-2752-4fd2-9e07-e9f10c552cac/download |
bitstream.checksum.fl_str_mv |
bd3efa91386c1718a7f26a329fdcb468 321f3992dd3875151d8801b773ab32ed b19767193fa05eb8852808b812c188a0 38cb62ef53e6f513db2fb7e337df6485 bca24056dbea9a9bcc77e3576d3d0d76 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
repository.mail.fl_str_mv |
tasesdissertacoes.bc@ufg.br |
_version_ |
1823229529842253824 |