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C.I. Reactive Black 5 decolorization by combined sonolysis and ozonation
Decolorization of the azo dye C.I. Reactive Black 5 (RB5) in solution by a combination of sonolysis and ozonation was investigated. The results showed that the optimum pH for the reaction was 11.0, and both lower and higher pH decreased the decolorization rate. Increasing the initial concentration o...
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Published in: | Ultrasonics sonochemistry 2007-03, Vol.14 (3), p.298-304 |
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description | Decolorization of the azo dye C.I. Reactive Black 5 (RB5) in solution by a combination of sonolysis and ozonation was investigated. The results showed that the optimum pH for the reaction was 11.0, and both lower and higher pH decreased the decolorization rate. Increasing the initial concentration of RB5 led to a decreasing decolorization rate. Under the experimental conditions, the decolorization rate increased with an increase in temperature. The decolorization of RB5 followed pseudo-first-order reaction kinetics. Based on the decolorization rate constants obtained at different temperatures within the range 287–338
K and the Arrhenius equation, the apparent activation energy (
E
a) was calculated to be 11.2
kJ
mol
−1. This indicated that the reaction has little dependence on temperature. The color decay was considerably faster than the decrease in total organic carbon (TOC), which was attributed to the ease of chromophore destruction. Hence the efficiency of decolorization was 84% compared with 4% of TOC removal after 5
min reaction. Additionally, muconic acid, (2
Z)-pent-2-enedioic acid and maleic acid were identified as main oxidation products by gas chromatography coupled with mass spectrometry (GC–MS) after 150
min of reaction. |
doi_str_mv | 10.1016/j.ultsonch.2006.09.002 |
format | article |
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K and the Arrhenius equation, the apparent activation energy (
E
a) was calculated to be 11.2
kJ
mol
−1. This indicated that the reaction has little dependence on temperature. The color decay was considerably faster than the decrease in total organic carbon (TOC), which was attributed to the ease of chromophore destruction. Hence the efficiency of decolorization was 84% compared with 4% of TOC removal after 5
min reaction. Additionally, muconic acid, (2
Z)-pent-2-enedioic acid and maleic acid were identified as main oxidation products by gas chromatography coupled with mass spectrometry (GC–MS) after 150
min of reaction.</description><identifier>ISSN: 1350-4177</identifier><identifier>EISSN: 1873-2828</identifier><identifier>DOI: 10.1016/j.ultsonch.2006.09.002</identifier><identifier>PMID: 17067839</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>Apparent activation energy ; Chemistry ; Exact sciences and technology ; General and physical chemistry ; Kinetics ; Ozonation ; Physical chemistry of induced reactions (with radiations, particles and ultrasonics) ; Reactive Black 5 ; Sonolysis ; Ultrasonic chemistry</subject><ispartof>Ultrasonics sonochemistry, 2007-03, Vol.14 (3), p.298-304</ispartof><rights>2006 Elsevier B.V.</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c396t-e114e2b2990ce75d8a7ddbc7592293be3968a90119672e12e53778b6f5b0bb9f3</citedby><cites>FETCH-LOGICAL-c396t-e114e2b2990ce75d8a7ddbc7592293be3968a90119672e12e53778b6f5b0bb9f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18403315$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17067839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>He, Zhiqiao</creatorcontrib><creatorcontrib>Song, Shuang</creatorcontrib><creatorcontrib>Zhou, Huamin</creatorcontrib><creatorcontrib>Ying, Haiping</creatorcontrib><creatorcontrib>Chen, Jianmeng</creatorcontrib><title>C.I. Reactive Black 5 decolorization by combined sonolysis and ozonation</title><title>Ultrasonics sonochemistry</title><addtitle>Ultrason Sonochem</addtitle><description>Decolorization of the azo dye C.I. Reactive Black 5 (RB5) in solution by a combination of sonolysis and ozonation was investigated. The results showed that the optimum pH for the reaction was 11.0, and both lower and higher pH decreased the decolorization rate. Increasing the initial concentration of RB5 led to a decreasing decolorization rate. Under the experimental conditions, the decolorization rate increased with an increase in temperature. The decolorization of RB5 followed pseudo-first-order reaction kinetics. Based on the decolorization rate constants obtained at different temperatures within the range 287–338
K and the Arrhenius equation, the apparent activation energy (
E
a) was calculated to be 11.2
kJ
mol
−1. This indicated that the reaction has little dependence on temperature. The color decay was considerably faster than the decrease in total organic carbon (TOC), which was attributed to the ease of chromophore destruction. Hence the efficiency of decolorization was 84% compared with 4% of TOC removal after 5
min reaction. Additionally, muconic acid, (2
Z)-pent-2-enedioic acid and maleic acid were identified as main oxidation products by gas chromatography coupled with mass spectrometry (GC–MS) after 150
min of reaction.</description><subject>Apparent activation energy</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Kinetics</subject><subject>Ozonation</subject><subject>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</subject><subject>Reactive Black 5</subject><subject>Sonolysis</subject><subject>Ultrasonic chemistry</subject><issn>1350-4177</issn><issn>1873-2828</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqF0MtuEzEUgGELUbWl9BUqb2A3w7Gd8WUHREArVaqEYG35ckY4TMbFnlRKn74uCeqSlb34jo_1E3LFoGfA5IdNv5uWmufwq-cAsgfTA_BX5JxpJTquuX7d7mKAbsWUOiNvat0AgDAcTskZUyCVFuacXK_7m55-RxeW9ID08-TCbzrQiCFPuaRHt6Q8U7-nIW99mjHStjRP-5oqdXOk-THPf81bcjK6qeLl8bwgP79--bG-7m7vvt2sP912QRi5dMjYCrnnxkBANUTtVIw-qMFwboTHhrQzwJiRiiPjOAiltJfj4MF7M4oL8v7w7n3Jf3ZYF7tNNeA0uRnzrlqphRyUWTUoDzCUXGvB0d6XtHVlbxnY54Z2Y_81tM8NLRjbGrbBq-OGnd9ifBk7Rmvg3RG4Gtw0FjeHVF-cXoEQbGju48Fh6_GQsNgaEs4BYyoYFhtz-t9fngDgjZJ5</recordid><startdate>20070301</startdate><enddate>20070301</enddate><creator>He, Zhiqiao</creator><creator>Song, Shuang</creator><creator>Zhou, Huamin</creator><creator>Ying, Haiping</creator><creator>Chen, Jianmeng</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070301</creationdate><title>C.I. Reactive Black 5 decolorization by combined sonolysis and ozonation</title><author>He, Zhiqiao ; Song, Shuang ; Zhou, Huamin ; Ying, Haiping ; Chen, Jianmeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c396t-e114e2b2990ce75d8a7ddbc7592293be3968a90119672e12e53778b6f5b0bb9f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Apparent activation energy</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>General and physical chemistry</topic><topic>Kinetics</topic><topic>Ozonation</topic><topic>Physical chemistry of induced reactions (with radiations, particles and ultrasonics)</topic><topic>Reactive Black 5</topic><topic>Sonolysis</topic><topic>Ultrasonic chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>He, Zhiqiao</creatorcontrib><creatorcontrib>Song, Shuang</creatorcontrib><creatorcontrib>Zhou, Huamin</creatorcontrib><creatorcontrib>Ying, Haiping</creatorcontrib><creatorcontrib>Chen, Jianmeng</creatorcontrib><collection>Pascal-Francis</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Ultrasonics sonochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>He, Zhiqiao</au><au>Song, Shuang</au><au>Zhou, Huamin</au><au>Ying, Haiping</au><au>Chen, Jianmeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>C.I. Reactive Black 5 decolorization by combined sonolysis and ozonation</atitle><jtitle>Ultrasonics sonochemistry</jtitle><addtitle>Ultrason Sonochem</addtitle><date>2007-03-01</date><risdate>2007</risdate><volume>14</volume><issue>3</issue><spage>298</spage><epage>304</epage><pages>298-304</pages><issn>1350-4177</issn><eissn>1873-2828</eissn><abstract>Decolorization of the azo dye C.I. Reactive Black 5 (RB5) in solution by a combination of sonolysis and ozonation was investigated. The results showed that the optimum pH for the reaction was 11.0, and both lower and higher pH decreased the decolorization rate. Increasing the initial concentration of RB5 led to a decreasing decolorization rate. Under the experimental conditions, the decolorization rate increased with an increase in temperature. The decolorization of RB5 followed pseudo-first-order reaction kinetics. Based on the decolorization rate constants obtained at different temperatures within the range 287–338
K and the Arrhenius equation, the apparent activation energy (
E
a) was calculated to be 11.2
kJ
mol
−1. This indicated that the reaction has little dependence on temperature. The color decay was considerably faster than the decrease in total organic carbon (TOC), which was attributed to the ease of chromophore destruction. Hence the efficiency of decolorization was 84% compared with 4% of TOC removal after 5
min reaction. Additionally, muconic acid, (2
Z)-pent-2-enedioic acid and maleic acid were identified as main oxidation products by gas chromatography coupled with mass spectrometry (GC–MS) after 150
min of reaction.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>17067839</pmid><doi>10.1016/j.ultsonch.2006.09.002</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Apparent activation energy Chemistry Exact sciences and technology General and physical chemistry Kinetics Ozonation Physical chemistry of induced reactions (with radiations, particles and ultrasonics) Reactive Black 5 Sonolysis Ultrasonic chemistry |
title | C.I. Reactive Black 5 decolorization by combined sonolysis and ozonation |
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