id paper:paper_02682575_v90_n9_p1665_Cordoba
record_format dspace
spelling paper:paper_02682575_v90_n9_p1665_Cordoba2023-06-08T15:24:11Z Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes Acid Orange II Alizarin Red S Chitosan Peroxidase Supported hematin Alizarin Aromatic compounds Azo dyes Biomimetics Catalyst activity Catalysts Chitin Chitosan Citrus fruits Ketones Silicon compounds Spectrophotometry Surface analysis Acid Orange II Alizarin Red Aminopropyltriethoxysilane Heterogeneous catalyst Peroxidase Response surface analysis Spectro-photometric method Supported hematin Catalyst supports 3 aminopropyltriethoxysilane anthraquinone azo dye chitosan glutaraldehyde hematin iron porphyrin Article atomic emission spectrometry catalyst catalytic efficiency chemical structure decolorization experimental design infrared spectroscopy response surface method stereospecificity ultraviolet spectrophotometry Armoracia rusticana BACKGROUND: Azo and anthraquinone dyes have been successfully decolorized using enzymatic and biomimetic homogeneous systems.1,2 Hematin, a horseradish peroxidase (HRP) biomimetic, immobilized on chitosan via glutaraldehyde coupling was able to decolorize Alizarin Red S and Orange II solutions. A Doehlert experimental design and response surface analysis was applied to determine conditions for optimal mass of catalyst and catalytic efficiency of the immobilization procedure. RESULTS: The catalysts with supported hematin showed 33% activity (relative to homogeneous hematin as 100%) in decolorization reactions. After six reuses the catalytic activity was maintained at 60% of the initial one. Hematin anchoring to chitosan without alteration of the iron-porphyrin ring was confirmed by ICP, FTIR and UV/visible spectrophotometric methods. In addition, the effect on hematin activity in the decolorization of aminopropyltriethoxysilane (APTS) as a 'spacer arm' between hematin-glutaraldehyde and chitosan was studied. CONCLUSIONS: An economical heterogeneous catalyst alternative to HRP has been obtained. The spacer arm improves the catalyst's performance with activities as high as 57% relative to homogeneous hematin. These results support the notion that the activity loss of supported hematin is caused by the restricted access to Fe of the bulky phenolic dyes. © 2014 Society of Chemical Industry. 2015 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_02682575_v90_n9_p1665_Cordoba http://hdl.handle.net/20.500.12110/paper_02682575_v90_n9_p1665_Cordoba
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Acid Orange II
Alizarin Red S
Chitosan
Peroxidase
Supported hematin
Alizarin
Aromatic compounds
Azo dyes
Biomimetics
Catalyst activity
Catalysts
Chitin
Chitosan
Citrus fruits
Ketones
Silicon compounds
Spectrophotometry
Surface analysis
Acid Orange II
Alizarin Red
Aminopropyltriethoxysilane
Heterogeneous catalyst
Peroxidase
Response surface analysis
Spectro-photometric method
Supported hematin
Catalyst supports
3 aminopropyltriethoxysilane
anthraquinone
azo dye
chitosan
glutaraldehyde
hematin
iron
porphyrin
Article
atomic emission spectrometry
catalyst
catalytic efficiency
chemical structure
decolorization
experimental design
infrared spectroscopy
response surface method
stereospecificity
ultraviolet spectrophotometry
Armoracia rusticana
spellingShingle Acid Orange II
Alizarin Red S
Chitosan
Peroxidase
Supported hematin
Alizarin
Aromatic compounds
Azo dyes
Biomimetics
Catalyst activity
Catalysts
Chitin
Chitosan
Citrus fruits
Ketones
Silicon compounds
Spectrophotometry
Surface analysis
Acid Orange II
Alizarin Red
Aminopropyltriethoxysilane
Heterogeneous catalyst
Peroxidase
Response surface analysis
Spectro-photometric method
Supported hematin
Catalyst supports
3 aminopropyltriethoxysilane
anthraquinone
azo dye
chitosan
glutaraldehyde
hematin
iron
porphyrin
Article
atomic emission spectrometry
catalyst
catalytic efficiency
chemical structure
decolorization
experimental design
infrared spectroscopy
response surface method
stereospecificity
ultraviolet spectrophotometry
Armoracia rusticana
Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes
topic_facet Acid Orange II
Alizarin Red S
Chitosan
Peroxidase
Supported hematin
Alizarin
Aromatic compounds
Azo dyes
Biomimetics
Catalyst activity
Catalysts
Chitin
Chitosan
Citrus fruits
Ketones
Silicon compounds
Spectrophotometry
Surface analysis
Acid Orange II
Alizarin Red
Aminopropyltriethoxysilane
Heterogeneous catalyst
Peroxidase
Response surface analysis
Spectro-photometric method
Supported hematin
Catalyst supports
3 aminopropyltriethoxysilane
anthraquinone
azo dye
chitosan
glutaraldehyde
hematin
iron
porphyrin
Article
atomic emission spectrometry
catalyst
catalytic efficiency
chemical structure
decolorization
experimental design
infrared spectroscopy
response surface method
stereospecificity
ultraviolet spectrophotometry
Armoracia rusticana
description BACKGROUND: Azo and anthraquinone dyes have been successfully decolorized using enzymatic and biomimetic homogeneous systems.1,2 Hematin, a horseradish peroxidase (HRP) biomimetic, immobilized on chitosan via glutaraldehyde coupling was able to decolorize Alizarin Red S and Orange II solutions. A Doehlert experimental design and response surface analysis was applied to determine conditions for optimal mass of catalyst and catalytic efficiency of the immobilization procedure. RESULTS: The catalysts with supported hematin showed 33% activity (relative to homogeneous hematin as 100%) in decolorization reactions. After six reuses the catalytic activity was maintained at 60% of the initial one. Hematin anchoring to chitosan without alteration of the iron-porphyrin ring was confirmed by ICP, FTIR and UV/visible spectrophotometric methods. In addition, the effect on hematin activity in the decolorization of aminopropyltriethoxysilane (APTS) as a 'spacer arm' between hematin-glutaraldehyde and chitosan was studied. CONCLUSIONS: An economical heterogeneous catalyst alternative to HRP has been obtained. The spacer arm improves the catalyst's performance with activities as high as 57% relative to homogeneous hematin. These results support the notion that the activity loss of supported hematin is caused by the restricted access to Fe of the bulky phenolic dyes. © 2014 Society of Chemical Industry.
title Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes
title_short Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes
title_full Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes
title_fullStr Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes
title_full_unstemmed Modified chitosan as an economical support for hematin: Application in the decolorization of anthraquinone and azo dyes
title_sort modified chitosan as an economical support for hematin: application in the decolorization of anthraquinone and azo dyes
publishDate 2015
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_02682575_v90_n9_p1665_Cordoba
http://hdl.handle.net/20.500.12110/paper_02682575_v90_n9_p1665_Cordoba
_version_ 1768546113638367232