Decolorization of orange II by catalytic oxidation using iron (III) phthalocyanine-tetrasulfonic acid
Orange II, C.I. Acid Orange 7 (AO7), is oxidatively decolorized via catalytic oxidation by iron(III) phthalocyanine-tetrasulfonic acid (Fe(III)-PcTS) as a biomimetic catalyst and KHSO 5 as an oxygen donor. The nature of the decolorization of AO7 was investigated in the catalyst concentration range o...
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creator | Rismayani, Sinta Fukushima, Masami Ichikawa, Hiroyasu Tatsumi, Kenji |
description | Orange II, C.I. Acid Orange 7 (AO7), is oxidatively decolorized via catalytic oxidation by iron(III) phthalocyanine-tetrasulfonic acid (Fe(III)-PcTS) as a biomimetic catalyst and KHSO
5 as an oxygen donor. The nature of the decolorization of AO7 was investigated in the catalyst concentration range of 10–50
μM, in which the initial concentration of AO7 was 417
mg
l
−1. A 99.6% decolorization was observed at [KHSO
5] = 2.5
mM and [Fe(III)-PcTS] = 20
μM after a 3-h reaction period. However, the fact that only 4.9% of the TOC was removed indicated that the conversion to CO
2 was incomplete. The results of a total organic nitrogen analysis of the reaction mixture showed that the nitrogen in the azo chain was mainly converted to N
2 gas. In addition, 38.6% of the AO7 was converted to 1,2-dihydroxynaphthalene, and 21.4% to
p-phenolsulfonic acid. These results indicate that the degradation via this catalytic system involves the conversion of AO7 to phenolic compounds, followed by N
2 production. In addition, a Microtox test showed that toxicity of the solution increased as a result of AO7 oxidation using this catalytic system. |
doi_str_mv | 10.1016/j.jhazmat.2004.08.006 |
format | Article |
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5 as an oxygen donor. The nature of the decolorization of AO7 was investigated in the catalyst concentration range of 10–50
μM, in which the initial concentration of AO7 was 417
mg
l
−1. A 99.6% decolorization was observed at [KHSO
5] = 2.5
mM and [Fe(III)-PcTS] = 20
μM after a 3-h reaction period. However, the fact that only 4.9% of the TOC was removed indicated that the conversion to CO
2 was incomplete. The results of a total organic nitrogen analysis of the reaction mixture showed that the nitrogen in the azo chain was mainly converted to N
2 gas. In addition, 38.6% of the AO7 was converted to 1,2-dihydroxynaphthalene, and 21.4% to
p-phenolsulfonic acid. These results indicate that the degradation via this catalytic system involves the conversion of AO7 to phenolic compounds, followed by N
2 production. In addition, a Microtox test showed that toxicity of the solution increased as a result of AO7 oxidation using this catalytic system.</description><identifier>ISSN: 0304-3894</identifier><identifier>EISSN: 1873-3336</identifier><identifier>DOI: 10.1016/j.jhazmat.2004.08.006</identifier><identifier>PMID: 15511589</identifier><identifier>CODEN: JHMAD9</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Applied sciences ; Azo Compounds - chemistry ; Azo Compounds - toxicity ; Azo dyestuff ; Benzenesulfonates - chemistry ; Benzenesulfonates - toxicity ; Catalysis ; Chromatography, Ion Exchange ; Color ; Coloring Agents - chemistry ; Coloring Agents - toxicity ; Decolorization ; Exact sciences and technology ; Ferric Compounds - chemistry ; Gas Chromatography-Mass Spectrometry ; Hydrogen-Ion Concentration ; Indicators and Reagents ; Iron(III) phthalocyanine-tetrasulfonic acid ; Kinetics ; Luminescent Measurements ; Metalloporphyrins - chemistry ; Nitrogen - chemistry ; Orange II ; Oxidation ; Oxidation-Reduction ; Pollution ; Toxicity ; Toxicity Tests</subject><ispartof>Journal of hazardous materials, 2004-10, Vol.114 (1), p.175-181</ispartof><rights>2004 Elsevier B.V.</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c519t-d635fc9b19dc3e3fa795c8dbe3947f88363ff83022a2f70c83db8e947217a5cb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0304389404004145$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,65309</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16232796$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15511589$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rismayani, Sinta</creatorcontrib><creatorcontrib>Fukushima, Masami</creatorcontrib><creatorcontrib>Ichikawa, Hiroyasu</creatorcontrib><creatorcontrib>Tatsumi, Kenji</creatorcontrib><title>Decolorization of orange II by catalytic oxidation using iron (III) phthalocyanine-tetrasulfonic acid</title><title>Journal of hazardous materials</title><addtitle>J Hazard Mater</addtitle><description>Orange II, C.I. Acid Orange 7 (AO7), is oxidatively decolorized via catalytic oxidation by iron(III) phthalocyanine-tetrasulfonic acid (Fe(III)-PcTS) as a biomimetic catalyst and KHSO
5 as an oxygen donor. The nature of the decolorization of AO7 was investigated in the catalyst concentration range of 10–50
μM, in which the initial concentration of AO7 was 417
mg
l
−1. A 99.6% decolorization was observed at [KHSO
5] = 2.5
mM and [Fe(III)-PcTS] = 20
μM after a 3-h reaction period. However, the fact that only 4.9% of the TOC was removed indicated that the conversion to CO
2 was incomplete. The results of a total organic nitrogen analysis of the reaction mixture showed that the nitrogen in the azo chain was mainly converted to N
2 gas. In addition, 38.6% of the AO7 was converted to 1,2-dihydroxynaphthalene, and 21.4% to
p-phenolsulfonic acid. These results indicate that the degradation via this catalytic system involves the conversion of AO7 to phenolic compounds, followed by N
2 production. In addition, a Microtox test showed that toxicity of the solution increased as a result of AO7 oxidation using this catalytic system.</description><subject>Applied sciences</subject><subject>Azo Compounds - chemistry</subject><subject>Azo Compounds - toxicity</subject><subject>Azo dyestuff</subject><subject>Benzenesulfonates - chemistry</subject><subject>Benzenesulfonates - toxicity</subject><subject>Catalysis</subject><subject>Chromatography, Ion Exchange</subject><subject>Color</subject><subject>Coloring Agents - chemistry</subject><subject>Coloring Agents - toxicity</subject><subject>Decolorization</subject><subject>Exact sciences and technology</subject><subject>Ferric Compounds - chemistry</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Hydrogen-Ion Concentration</subject><subject>Indicators and Reagents</subject><subject>Iron(III) phthalocyanine-tetrasulfonic acid</subject><subject>Kinetics</subject><subject>Luminescent Measurements</subject><subject>Metalloporphyrins - chemistry</subject><subject>Nitrogen - chemistry</subject><subject>Orange II</subject><subject>Oxidation</subject><subject>Oxidation-Reduction</subject><subject>Pollution</subject><subject>Toxicity</subject><subject>Toxicity Tests</subject><issn>0304-3894</issn><issn>1873-3336</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkUtv1DAUhS1ERYfCTwBlA4JFgh9xYq8QKo9GqtQNrC3Hvu54lIkH20FMf309mkhddnUt3e-ca52D0DuCG4JJ92XX7Lb6Ya9zQzFuGywajLsXaENEz2rGWPcSbTDDbc2EbC_R65R2GGPS8_YVuiScE8KF3CD4DiZMIfoHnX2Yq-CqEPV8D9UwVOOxMjrr6Zi9qcJ_b8_Mkvx8X_lYnp-GYfhcHbZ5q6dgjnr2M9QZctRpmVyYi04bb9-gC6enBG_XeYX-_Pzx-_qmvr37NVx_u60NJzLXtmPcGTkSaQ0D5nQvuRF2BCbb3gnBOuacYJhSTV2PjWB2FFB2lPSam5FdoY9n30MMfxdIWe19MjBNeoawJEUlEbyX4lmQFE_KOlpAfgZNDClFcOoQ_V7HoyJYnYpQO7UWoU5FKCxUKaLo3q8HlnEP9km1Jl-ADyugk9GTK6Ebn564cpv28mT09cxBye2fh6iS8TAbsD6CycoG_8xXHgGDn6ox</recordid><startdate>20041018</startdate><enddate>20041018</enddate><creator>Rismayani, Sinta</creator><creator>Fukushima, Masami</creator><creator>Ichikawa, Hiroyasu</creator><creator>Tatsumi, Kenji</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>C1K</scope><scope>SOI</scope><scope>8FD</scope><scope>FR3</scope><scope>KR7</scope></search><sort><creationdate>20041018</creationdate><title>Decolorization of orange II by catalytic oxidation using iron (III) phthalocyanine-tetrasulfonic acid</title><author>Rismayani, Sinta ; Fukushima, Masami ; Ichikawa, Hiroyasu ; Tatsumi, Kenji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c519t-d635fc9b19dc3e3fa795c8dbe3947f88363ff83022a2f70c83db8e947217a5cb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Applied sciences</topic><topic>Azo Compounds - chemistry</topic><topic>Azo Compounds - toxicity</topic><topic>Azo dyestuff</topic><topic>Benzenesulfonates - chemistry</topic><topic>Benzenesulfonates - toxicity</topic><topic>Catalysis</topic><topic>Chromatography, Ion Exchange</topic><topic>Color</topic><topic>Coloring Agents - chemistry</topic><topic>Coloring Agents - toxicity</topic><topic>Decolorization</topic><topic>Exact sciences and technology</topic><topic>Ferric Compounds - chemistry</topic><topic>Gas Chromatography-Mass Spectrometry</topic><topic>Hydrogen-Ion Concentration</topic><topic>Indicators and Reagents</topic><topic>Iron(III) phthalocyanine-tetrasulfonic acid</topic><topic>Kinetics</topic><topic>Luminescent Measurements</topic><topic>Metalloporphyrins - chemistry</topic><topic>Nitrogen - chemistry</topic><topic>Orange II</topic><topic>Oxidation</topic><topic>Oxidation-Reduction</topic><topic>Pollution</topic><topic>Toxicity</topic><topic>Toxicity Tests</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rismayani, Sinta</creatorcontrib><creatorcontrib>Fukushima, Masami</creatorcontrib><creatorcontrib>Ichikawa, Hiroyasu</creatorcontrib><creatorcontrib>Tatsumi, Kenji</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Civil Engineering Abstracts</collection><jtitle>Journal of hazardous materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rismayani, Sinta</au><au>Fukushima, Masami</au><au>Ichikawa, Hiroyasu</au><au>Tatsumi, Kenji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decolorization of orange II by catalytic oxidation using iron (III) phthalocyanine-tetrasulfonic acid</atitle><jtitle>Journal of hazardous materials</jtitle><addtitle>J Hazard Mater</addtitle><date>2004-10-18</date><risdate>2004</risdate><volume>114</volume><issue>1</issue><spage>175</spage><epage>181</epage><pages>175-181</pages><issn>0304-3894</issn><eissn>1873-3336</eissn><coden>JHMAD9</coden><abstract>Orange II, C.I. Acid Orange 7 (AO7), is oxidatively decolorized via catalytic oxidation by iron(III) phthalocyanine-tetrasulfonic acid (Fe(III)-PcTS) as a biomimetic catalyst and KHSO
5 as an oxygen donor. The nature of the decolorization of AO7 was investigated in the catalyst concentration range of 10–50
μM, in which the initial concentration of AO7 was 417
mg
l
−1. A 99.6% decolorization was observed at [KHSO
5] = 2.5
mM and [Fe(III)-PcTS] = 20
μM after a 3-h reaction period. However, the fact that only 4.9% of the TOC was removed indicated that the conversion to CO
2 was incomplete. The results of a total organic nitrogen analysis of the reaction mixture showed that the nitrogen in the azo chain was mainly converted to N
2 gas. In addition, 38.6% of the AO7 was converted to 1,2-dihydroxynaphthalene, and 21.4% to
p-phenolsulfonic acid. These results indicate that the degradation via this catalytic system involves the conversion of AO7 to phenolic compounds, followed by N
2 production. In addition, a Microtox test showed that toxicity of the solution increased as a result of AO7 oxidation using this catalytic system.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>15511589</pmid><doi>10.1016/j.jhazmat.2004.08.006</doi><tpages>7</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Applied sciences Azo Compounds - chemistry Azo Compounds - toxicity Azo dyestuff Benzenesulfonates - chemistry Benzenesulfonates - toxicity Catalysis Chromatography, Ion Exchange Color Coloring Agents - chemistry Coloring Agents - toxicity Decolorization Exact sciences and technology Ferric Compounds - chemistry Gas Chromatography-Mass Spectrometry Hydrogen-Ion Concentration Indicators and Reagents Iron(III) phthalocyanine-tetrasulfonic acid Kinetics Luminescent Measurements Metalloporphyrins - chemistry Nitrogen - chemistry Orange II Oxidation Oxidation-Reduction Pollution Toxicity Toxicity Tests |
title | Decolorization of orange II by catalytic oxidation using iron (III) phthalocyanine-tetrasulfonic acid |
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