Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power

Detalhes bibliográficos
Autor(a) principal: Papaleo, Ricardo Meurer
Data de Publicação: 1996
Outros Autores: Hallen, A., Sundqvist, B.U.R., Araujo, Marco Aurelio de, Johnson, R.E., Farenzena, Lucio Sartori, Livi, Rogerio Pohlmann
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UFRGS
Texto Completo: http://hdl.handle.net/10183/104206
Resumo: Thin poly(phenylene sulphide) foils were bombarded with fast atomic ions (4He, 12C, 16O, 32S, 79Br, 127I) in the energy range between 2.5 to 78 MeV. In order to maintain the same ion track size for all impacting ions, their initial velocity was kept constant at 1.1 cm/ns. Under these conditions the deposited energy density in a single ion track changes as a result of the varying stopping power (dE/dx) of the projectiles in the material. Fourier transform infrared spectroscopy and UV-visible spectroscopy were used to characterize the irradiated targets. Damage cross sections (σ) for different chemical bonds, such as C-S and ring C-C bonds, are extracted from the IR data. For all analyzed IR bands, the values of σ scale roughly with the square of dE/dx (energy density in a single ion track). The absorption of the irradiated samples in the visible and UV region increases as a function of fluence. The rate of increase of absorption at a particular wavelength scales also as (dE/dx)n with n~2. The observed nonlinear dependence of the damage cross sections on the deposited energy density is considered in the light of two models: a statistical model based on the fluctuations of the energy deposited by the primary ions (hit theory) and an activation (thermal spike) model. It is found that the damage cross section is not determined directly by the initial deposited energy density distribution. The best agreement between experiment and theory is obtained when transport of the deposited energy occurs.
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spelling Papaleo, Ricardo MeurerHallen, A.Sundqvist, B.U.R.Araujo, Marco Aurelio deJohnson, R.E.Farenzena, Lucio SartoriLivi, Rogerio Pohlmann2014-10-07T02:11:18Z19960163-1829http://hdl.handle.net/10183/104206000148817Thin poly(phenylene sulphide) foils were bombarded with fast atomic ions (4He, 12C, 16O, 32S, 79Br, 127I) in the energy range between 2.5 to 78 MeV. In order to maintain the same ion track size for all impacting ions, their initial velocity was kept constant at 1.1 cm/ns. Under these conditions the deposited energy density in a single ion track changes as a result of the varying stopping power (dE/dx) of the projectiles in the material. Fourier transform infrared spectroscopy and UV-visible spectroscopy were used to characterize the irradiated targets. Damage cross sections (σ) for different chemical bonds, such as C-S and ring C-C bonds, are extracted from the IR data. For all analyzed IR bands, the values of σ scale roughly with the square of dE/dx (energy density in a single ion track). The absorption of the irradiated samples in the visible and UV region increases as a function of fluence. The rate of increase of absorption at a particular wavelength scales also as (dE/dx)n with n~2. The observed nonlinear dependence of the damage cross sections on the deposited energy density is considered in the light of two models: a statistical model based on the fluctuations of the energy deposited by the primary ions (hit theory) and an activation (thermal spike) model. It is found that the damage cross section is not determined directly by the initial deposited energy density distribution. The best agreement between experiment and theory is obtained when transport of the deposited energy occurs.application/pdfengPhysical review. B, Condensed matter. New York. Vol. 53, n. 5 (Feb. 1996), p. 2303-2313Física da matéria condensadaPolímeros : Energia nuclear : Espectroscopia : Modelos estatisticosChemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping powerEstrangeiroinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UFRGSinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSORIGINAL000148817.pdf000148817.pdfTexto completo (inglês)application/pdf167588http://www.lume.ufrgs.br/bitstream/10183/104206/1/000148817.pdf3ad63b69deaba635518d6f9b5ac8ec24MD51TEXT000148817.pdf.txt000148817.pdf.txtExtracted Texttext/plain55033http://www.lume.ufrgs.br/bitstream/10183/104206/2/000148817.pdf.txtadf4b819a3a8251c16266b6eba3d6020MD5210183/1042062018-06-07 02:32:18.897733oai:www.lume.ufrgs.br:10183/104206Repositório de PublicaçõesPUBhttps://lume.ufrgs.br/oai/requestopendoar:2018-06-07T05:32:18Repositório Institucional da UFRGS - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.pt_BR.fl_str_mv Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
title Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
spellingShingle Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
Papaleo, Ricardo Meurer
Física da matéria condensada
Polímeros : Energia nuclear : Espectroscopia : Modelos estatisticos
title_short Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
title_full Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
title_fullStr Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
title_full_unstemmed Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
title_sort Chemical damage in poly (phenylene sulphide) from fast ions: dependence on the primary-ion stopping power
author Papaleo, Ricardo Meurer
author_facet Papaleo, Ricardo Meurer
Hallen, A.
Sundqvist, B.U.R.
Araujo, Marco Aurelio de
Johnson, R.E.
Farenzena, Lucio Sartori
Livi, Rogerio Pohlmann
author_role author
author2 Hallen, A.
Sundqvist, B.U.R.
Araujo, Marco Aurelio de
Johnson, R.E.
Farenzena, Lucio Sartori
Livi, Rogerio Pohlmann
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Papaleo, Ricardo Meurer
Hallen, A.
Sundqvist, B.U.R.
Araujo, Marco Aurelio de
Johnson, R.E.
Farenzena, Lucio Sartori
Livi, Rogerio Pohlmann
dc.subject.por.fl_str_mv Física da matéria condensada
Polímeros : Energia nuclear : Espectroscopia : Modelos estatisticos
topic Física da matéria condensada
Polímeros : Energia nuclear : Espectroscopia : Modelos estatisticos
description Thin poly(phenylene sulphide) foils were bombarded with fast atomic ions (4He, 12C, 16O, 32S, 79Br, 127I) in the energy range between 2.5 to 78 MeV. In order to maintain the same ion track size for all impacting ions, their initial velocity was kept constant at 1.1 cm/ns. Under these conditions the deposited energy density in a single ion track changes as a result of the varying stopping power (dE/dx) of the projectiles in the material. Fourier transform infrared spectroscopy and UV-visible spectroscopy were used to characterize the irradiated targets. Damage cross sections (σ) for different chemical bonds, such as C-S and ring C-C bonds, are extracted from the IR data. For all analyzed IR bands, the values of σ scale roughly with the square of dE/dx (energy density in a single ion track). The absorption of the irradiated samples in the visible and UV region increases as a function of fluence. The rate of increase of absorption at a particular wavelength scales also as (dE/dx)n with n~2. The observed nonlinear dependence of the damage cross sections on the deposited energy density is considered in the light of two models: a statistical model based on the fluctuations of the energy deposited by the primary ions (hit theory) and an activation (thermal spike) model. It is found that the damage cross section is not determined directly by the initial deposited energy density distribution. The best agreement between experiment and theory is obtained when transport of the deposited energy occurs.
publishDate 1996
dc.date.issued.fl_str_mv 1996
dc.date.accessioned.fl_str_mv 2014-10-07T02:11:18Z
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dc.relation.ispartof.pt_BR.fl_str_mv Physical review. B, Condensed matter. New York. Vol. 53, n. 5 (Feb. 1996), p. 2303-2313
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