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Kinetics of the 5-Hydroxymethylfurfural Formation Reaction in Chinese Rice Wine
The kinetics of 5-hydroxymethylfurfural (HMF) formation in Chinese rice wine was investigated under different treatment conditions. Samples I and II were the rough rice wine and outflow fraction of the rice wine from the macroporous resin, respectively. Sample III was the fraction derived from sampl...
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Published in: | Journal of agricultural and food chemistry 2010-03, Vol.58 (6), p.3507-3511 |
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description | The kinetics of 5-hydroxymethylfurfural (HMF) formation in Chinese rice wine was investigated under different treatment conditions. Samples I and II were the rough rice wine and outflow fraction of the rice wine from the macroporous resin, respectively. Sample III was the fraction derived from sample II loaded through ion-exchange resin. The HMF content of the different samples under a range of temperature values from 323.15 to 363.15 K was measured by high-performance liquid chromatography. The results demonstrated that the kinetics of HMF formation in sample I was determined as first-order [C t = C 0 exp(k t)], but those for samples II and III were found to be the zero-order reaction [C t = C 0 + kt]. For all three samples, the relationships of reaction rates (k) and temperature (T) were computed as follows: k 1 = 2.81 × 105 exp(−43.01/RT), k 2 = 2.33 × 1018 exp(−123.90/RT), and k 3 = 1.79 × 1013 exp(−89.16/RT). By applying the Arrhenius equation k = k f exp(−E a/RT), the activation energy was 43.01, 123.90, and 89.16 kJ mol−1, respectively. On the basis of these kinetics equations, weak polar components such as phenolic groups may be involved in HMF formation. |
doi_str_mv | 10.1021/jf904094q |
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Samples I and II were the rough rice wine and outflow fraction of the rice wine from the macroporous resin, respectively. Sample III was the fraction derived from sample II loaded through ion-exchange resin. The HMF content of the different samples under a range of temperature values from 323.15 to 363.15 K was measured by high-performance liquid chromatography. The results demonstrated that the kinetics of HMF formation in sample I was determined as first-order [C t = C 0 exp(k t)], but those for samples II and III were found to be the zero-order reaction [C t = C 0 + kt]. For all three samples, the relationships of reaction rates (k) and temperature (T) were computed as follows: k 1 = 2.81 × 105 exp(−43.01/RT), k 2 = 2.33 × 1018 exp(−123.90/RT), and k 3 = 1.79 × 1013 exp(−89.16/RT). By applying the Arrhenius equation k = k f exp(−E a/RT), the activation energy was 43.01, 123.90, and 89.16 kJ mol−1, respectively. On the basis of these kinetics equations, weak polar components such as phenolic groups may be involved in HMF formation.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf904094q</identifier><identifier>PMID: 20166663</identifier><identifier>CODEN: JAFCAU</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>activation energy ; Biological and medical sciences ; Cereal and baking product industries ; Chemical Aspects of Food Safety ; Fermented food industries ; food composition ; food contamination ; Food industries ; Fundamental and applied biological sciences. Psychology ; Furaldehyde - analogs & derivatives ; Furaldehyde - chemistry ; heat treatment ; hydroxymethylfurfural ; Kinetics ; mathematical models ; Oryza - chemistry ; polar compounds ; reaction kinetics ; resins ; rice wines ; temperature ; Wine - analysis ; wine quality ; winemaking ; Wines and vinegars</subject><ispartof>Journal of agricultural and food chemistry, 2010-03, Vol.58 (6), p.3507-3511</ispartof><rights>Copyright © 2010 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a368t-30f50056e824737feac5aea4e52d8dad98bce597c6755d9488b456bfbd8a4f1d3</citedby><cites>FETCH-LOGICAL-a368t-30f50056e824737feac5aea4e52d8dad98bce597c6755d9488b456bfbd8a4f1d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22546281$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20166663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chen, Lei</creatorcontrib><creatorcontrib>Huang, Huahong</creatorcontrib><creatorcontrib>Liu, Wenbao</creatorcontrib><creatorcontrib>Peng, Ning</creatorcontrib><creatorcontrib>Huang, Xuesong</creatorcontrib><title>Kinetics of the 5-Hydroxymethylfurfural Formation Reaction in Chinese Rice Wine</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>The kinetics of 5-hydroxymethylfurfural (HMF) formation in Chinese rice wine was investigated under different treatment conditions. Samples I and II were the rough rice wine and outflow fraction of the rice wine from the macroporous resin, respectively. Sample III was the fraction derived from sample II loaded through ion-exchange resin. The HMF content of the different samples under a range of temperature values from 323.15 to 363.15 K was measured by high-performance liquid chromatography. The results demonstrated that the kinetics of HMF formation in sample I was determined as first-order [C t = C 0 exp(k t)], but those for samples II and III were found to be the zero-order reaction [C t = C 0 + kt]. For all three samples, the relationships of reaction rates (k) and temperature (T) were computed as follows: k 1 = 2.81 × 105 exp(−43.01/RT), k 2 = 2.33 × 1018 exp(−123.90/RT), and k 3 = 1.79 × 1013 exp(−89.16/RT). By applying the Arrhenius equation k = k f exp(−E a/RT), the activation energy was 43.01, 123.90, and 89.16 kJ mol−1, respectively. On the basis of these kinetics equations, weak polar components such as phenolic groups may be involved in HMF formation.</description><subject>activation energy</subject><subject>Biological and medical sciences</subject><subject>Cereal and baking product industries</subject><subject>Chemical Aspects of Food Safety</subject><subject>Fermented food industries</subject><subject>food composition</subject><subject>food contamination</subject><subject>Food industries</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Furaldehyde - analogs & derivatives</subject><subject>Furaldehyde - chemistry</subject><subject>heat treatment</subject><subject>hydroxymethylfurfural</subject><subject>Kinetics</subject><subject>mathematical models</subject><subject>Oryza - chemistry</subject><subject>polar compounds</subject><subject>reaction kinetics</subject><subject>resins</subject><subject>rice wines</subject><subject>temperature</subject><subject>Wine - analysis</subject><subject>wine quality</subject><subject>winemaking</subject><subject>Wines and vinegars</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNptkEFLwzAUx4Mobk4PfgHtRcRDNUmbNj3KcE4cDKbDY3lNE5fRNlvSgvv2Rje3i-FBHrxffrz8Ebok-J5gSh6WKsMxzuL1EeoTRnHICOHHqI_9MOQsIT105twSY8xZik9Rj2KS-BP10fRVN7LVwgVGBe1CBiwcb0prvja1bBebSnXWF1TByNgaWm2aYCZB_Da6CYYL_9zJYKaFDD58f45OFFROXuzuAZqPnt6H43AyfX4ZPk5CiBLehhFWDGOWSE7jNEqVVzKQEEtGS15CmfFCSJalIkkZK7OY8yJmSaGKkkOsSBkN0O3Wu7Jm3UnX5rV2QlYVNNJ0Lk-jKCUJpZkn77aksMY5K1W-sroGu8kJzn_iy_fxefZqZ-2KWpZ78i8vD9zsAHACKmWhEdodOMrihHLiuestp8Dk8Gk9M3_zlggT_2NC0oMJhMuXprONj-uflb4BkFOMew</recordid><startdate>20100324</startdate><enddate>20100324</enddate><creator>Chen, Lei</creator><creator>Huang, Huahong</creator><creator>Liu, Wenbao</creator><creator>Peng, Ning</creator><creator>Huang, Xuesong</creator><general>American Chemical Society</general><scope>FBQ</scope><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>7X8</scope></search><sort><creationdate>20100324</creationdate><title>Kinetics of the 5-Hydroxymethylfurfural Formation Reaction in Chinese Rice Wine</title><author>Chen, Lei ; Huang, Huahong ; Liu, Wenbao ; Peng, Ning ; Huang, Xuesong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a368t-30f50056e824737feac5aea4e52d8dad98bce597c6755d9488b456bfbd8a4f1d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>activation energy</topic><topic>Biological and medical sciences</topic><topic>Cereal and baking product industries</topic><topic>Chemical Aspects of Food Safety</topic><topic>Fermented food industries</topic><topic>food composition</topic><topic>food contamination</topic><topic>Food industries</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Furaldehyde - analogs & derivatives</topic><topic>Furaldehyde - chemistry</topic><topic>heat treatment</topic><topic>hydroxymethylfurfural</topic><topic>Kinetics</topic><topic>mathematical models</topic><topic>Oryza - chemistry</topic><topic>polar compounds</topic><topic>reaction kinetics</topic><topic>resins</topic><topic>rice wines</topic><topic>temperature</topic><topic>Wine - analysis</topic><topic>wine quality</topic><topic>winemaking</topic><topic>Wines and vinegars</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Lei</creatorcontrib><creatorcontrib>Huang, Huahong</creatorcontrib><creatorcontrib>Liu, Wenbao</creatorcontrib><creatorcontrib>Peng, Ning</creatorcontrib><creatorcontrib>Huang, Xuesong</creatorcontrib><collection>AGRIS</collection><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>MEDLINE - Academic</collection><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Lei</au><au>Huang, Huahong</au><au>Liu, Wenbao</au><au>Peng, Ning</au><au>Huang, Xuesong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Kinetics of the 5-Hydroxymethylfurfural Formation Reaction in Chinese Rice Wine</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2010-03-24</date><risdate>2010</risdate><volume>58</volume><issue>6</issue><spage>3507</spage><epage>3511</epage><pages>3507-3511</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><coden>JAFCAU</coden><abstract>The kinetics of 5-hydroxymethylfurfural (HMF) formation in Chinese rice wine was investigated under different treatment conditions. Samples I and II were the rough rice wine and outflow fraction of the rice wine from the macroporous resin, respectively. Sample III was the fraction derived from sample II loaded through ion-exchange resin. The HMF content of the different samples under a range of temperature values from 323.15 to 363.15 K was measured by high-performance liquid chromatography. The results demonstrated that the kinetics of HMF formation in sample I was determined as first-order [C t = C 0 exp(k t)], but those for samples II and III were found to be the zero-order reaction [C t = C 0 + kt]. For all three samples, the relationships of reaction rates (k) and temperature (T) were computed as follows: k 1 = 2.81 × 105 exp(−43.01/RT), k 2 = 2.33 × 1018 exp(−123.90/RT), and k 3 = 1.79 × 1013 exp(−89.16/RT). By applying the Arrhenius equation k = k f exp(−E a/RT), the activation energy was 43.01, 123.90, and 89.16 kJ mol−1, respectively. On the basis of these kinetics equations, weak polar components such as phenolic groups may be involved in HMF formation.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>20166663</pmid><doi>10.1021/jf904094q</doi><tpages>5</tpages></addata></record> |
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subjects | activation energy Biological and medical sciences Cereal and baking product industries Chemical Aspects of Food Safety Fermented food industries food composition food contamination Food industries Fundamental and applied biological sciences. Psychology Furaldehyde - analogs & derivatives Furaldehyde - chemistry heat treatment hydroxymethylfurfural Kinetics mathematical models Oryza - chemistry polar compounds reaction kinetics resins rice wines temperature Wine - analysis wine quality winemaking Wines and vinegars |
title | Kinetics of the 5-Hydroxymethylfurfural Formation Reaction in Chinese Rice Wine |
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