The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay
- Autores
- Carlos, Luciano; Pedersen, Brian W.; Ogilby, Peter R.; Martire, Daniel Osvaldo
- Año de publicación
- 2011
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- The effect of humic acid (HA) aggregate formation on the photosensitized generation and subsequent quenching of singlet molecular oxygen O2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic meso-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.
Fil: Carlos, Luciano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina
Fil: Pedersen, Brian W.. University Aarhus; Dinamarca
Fil: Ogilby, Peter R.. University Aarhus; Dinamarca
Fil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina - Materia
-
HUMIC ACIDS
AGGREGATION
SINGLET OXYGEN - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
.jpg)
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/279076
Ver los metadatos del registro completo
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The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decayCarlos, LucianoPedersen, Brian W.Ogilby, Peter R.Martire, Daniel OsvaldoHUMIC ACIDSAGGREGATIONSINGLET OXYGENhttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1The effect of humic acid (HA) aggregate formation on the photosensitized generation and subsequent quenching of singlet molecular oxygen O2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic meso-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.Fil: Carlos, Luciano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaFil: Pedersen, Brian W.. University Aarhus; DinamarcaFil: Ogilby, Peter R.. University Aarhus; DinamarcaFil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; ArgentinaRoyal Society of Chemistry2011-03info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/279076Carlos, Luciano; Pedersen, Brian W.; Ogilby, Peter R.; Martire, Daniel Osvaldo; The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay; Royal Society of Chemistry; Photochemical and Photobiological Sciences; 10; 6; 3-2011; 1080-10861474-905XCONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2011/pp/c1pp00003a/unauthinfo:eu-repo/semantics/altIdentifier/doi/10.1039/C1PP00003Ainfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2026-01-14T11:42:56Zoai:ri.conicet.gov.ar:11336/279076instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982026-01-14 11:42:56.951CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
| dc.title.none.fl_str_mv |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| title |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| spellingShingle |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay Carlos, Luciano HUMIC ACIDS AGGREGATION SINGLET OXYGEN |
| title_short |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| title_full |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| title_fullStr |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| title_full_unstemmed |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| title_sort |
The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay |
| dc.creator.none.fl_str_mv |
Carlos, Luciano Pedersen, Brian W. Ogilby, Peter R. Martire, Daniel Osvaldo |
| author |
Carlos, Luciano |
| author_facet |
Carlos, Luciano Pedersen, Brian W. Ogilby, Peter R. Martire, Daniel Osvaldo |
| author_role |
author |
| author2 |
Pedersen, Brian W. Ogilby, Peter R. Martire, Daniel Osvaldo |
| author2_role |
author author author |
| dc.subject.none.fl_str_mv |
HUMIC ACIDS AGGREGATION SINGLET OXYGEN |
| topic |
HUMIC ACIDS AGGREGATION SINGLET OXYGEN |
| purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
| dc.description.none.fl_txt_mv |
The effect of humic acid (HA) aggregate formation on the photosensitized generation and subsequent quenching of singlet molecular oxygen O2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic meso-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment. Fil: Carlos, Luciano. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina Fil: Pedersen, Brian W.. University Aarhus; Dinamarca Fil: Ogilby, Peter R.. University Aarhus; Dinamarca Fil: Martire, Daniel Osvaldo. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - La Plata. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas. Universidad Nacional de La Plata. Facultad de Ciencias Exactas. Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas; Argentina |
| description |
The effect of humic acid (HA) aggregate formation on the photosensitized generation and subsequent quenching of singlet molecular oxygen O2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) was investigated. Time-resolved O2(a1Dg) phosphorescence traces were obtained from (a) bulk samples of HA dispersions and (b) microscope-based experiments performed upon irradiation of a single HA aggregate. In the bulk experiments, the dependence of the O2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic2(a1Dg) lifetime on the HA concentration yields a critical concentration for the formation of micrometric HA aggregates of 0.58 g L-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1. This value is consistent with that obtained using pyrene as a fluorescent probe (0.38 g L-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic-1). Microscope-based experiments were also performed with HA samples containing added singlet oxygen sensitizers; either the hydrophobic meso-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.-tetraphenylporphyrin (TPP) or the hydrophilic 5,10,15,20-tetrakis(N-methyl-4-pyridyl)- 21H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.H,23H-porphine (TMPyP). Singlet oxygen phosphorescence could only be detected upon irradiation of TMPyP, a molecule which localizes on the exterior part of the HA aggregates. The inability to detect O2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) phosphorescence from HA samples containing TPP is consistent with the model that the O2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment.2(a1Dg) produced in the interior of the aggregate was completely quenched by the high local concentration of HA reactive groups in this environment. |
| publishDate |
2011 |
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2011-03 |
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info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
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article |
| status_str |
publishedVersion |
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http://hdl.handle.net/11336/279076 Carlos, Luciano; Pedersen, Brian W.; Ogilby, Peter R.; Martire, Daniel Osvaldo; The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay; Royal Society of Chemistry; Photochemical and Photobiological Sciences; 10; 6; 3-2011; 1080-1086 1474-905X CONICET Digital CONICET |
| url |
http://hdl.handle.net/11336/279076 |
| identifier_str_mv |
Carlos, Luciano; Pedersen, Brian W.; Ogilby, Peter R.; Martire, Daniel Osvaldo; The role of humic acid aggregation on the kinetics of photosensitized singlet oxygen production and decay; Royal Society of Chemistry; Photochemical and Photobiological Sciences; 10; 6; 3-2011; 1080-1086 1474-905X CONICET Digital CONICET |
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eng |
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eng |
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info:eu-repo/semantics/altIdentifier/url/https://pubs.rsc.org/en/content/articlelanding/2011/pp/c1pp00003a/unauth info:eu-repo/semantics/altIdentifier/doi/10.1039/C1PP00003A |
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info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
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openAccess |
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Royal Society of Chemistry |
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Royal Society of Chemistry |
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dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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