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Urethane reaction kinetics of butanediols catalyzed by Zr(acac)4
The urethane reaction of isocyanate was carried out with zirconium acetyl acetonate (Zr(acac)4) as catalyst. 1,2‐Butanediol and 1,4‐butanediol were used as model compounds to investigate the reaction kinetics. It was shown that hydroxyl groups in 1,2‐butanediol appeared to have different reaction ra...
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Published in: | Journal of applied polymer science 2013-09, Vol.129 (5), p.2399-2403 |
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creator | Yang, Peng Fei Li, Tian Duo |
description | The urethane reaction of isocyanate was carried out with zirconium acetyl acetonate (Zr(acac)4) as catalyst. 1,2‐Butanediol and 1,4‐butanediol were used as model compounds to investigate the reaction kinetics. It was shown that hydroxyl groups in 1,2‐butanediol appeared to have different reaction rate when reacting with phenyl isocyanate, which was labeled as kfast and kslow. It was very surprising that the reaction rate of 1,4‐butanediol (kcon) was very similar to the value of kslow at the same temperature although there is only primary hydroxyl group in its molecule. Furthermore, activation energy (Ea), activation enthalpy (ΔH), and activation entropy (ΔS) for the reaction were calculated out, from which some catalytic properties of Zr(acac)4 were revealed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013 |
doi_str_mv | 10.1002/app.38978 |
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It was shown that hydroxyl groups in 1,2‐butanediol appeared to have different reaction rate when reacting with phenyl isocyanate, which was labeled as kfast and kslow. It was very surprising that the reaction rate of 1,4‐butanediol (kcon) was very similar to the value of kslow at the same temperature although there is only primary hydroxyl group in its molecule. Furthermore, activation energy (Ea), activation enthalpy (ΔH), and activation entropy (ΔS) for the reaction were calculated out, from which some catalytic properties of Zr(acac)4 were revealed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013</description><identifier>ISSN: 0021-8995</identifier><identifier>EISSN: 1097-4628</identifier><identifier>DOI: 10.1002/app.38978</identifier><identifier>CODEN: JAPNAB</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Applied sciences ; Exact sciences and technology ; kinetics ; Materials science ; Organic polymers ; Physicochemistry of polymers ; Polycondensation ; Polymers ; polyurethanes ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; spectroscopy</subject><ispartof>Journal of applied polymer science, 2013-09, Vol.129 (5), p.2399-2403</ispartof><rights>Copyright © 2013 Wiley Periodicals, Inc.</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803</citedby><cites>FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27461102$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Peng Fei</creatorcontrib><creatorcontrib>Li, Tian Duo</creatorcontrib><title>Urethane reaction kinetics of butanediols catalyzed by Zr(acac)4</title><title>Journal of applied polymer science</title><addtitle>J. Appl. Polym. Sci</addtitle><description>The urethane reaction of isocyanate was carried out with zirconium acetyl acetonate (Zr(acac)4) as catalyst. 1,2‐Butanediol and 1,4‐butanediol were used as model compounds to investigate the reaction kinetics. It was shown that hydroxyl groups in 1,2‐butanediol appeared to have different reaction rate when reacting with phenyl isocyanate, which was labeled as kfast and kslow. It was very surprising that the reaction rate of 1,4‐butanediol (kcon) was very similar to the value of kslow at the same temperature although there is only primary hydroxyl group in its molecule. Furthermore, activation energy (Ea), activation enthalpy (ΔH), and activation entropy (ΔS) for the reaction were calculated out, from which some catalytic properties of Zr(acac)4 were revealed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013</description><subject>Applied sciences</subject><subject>Exact sciences and technology</subject><subject>kinetics</subject><subject>Materials science</subject><subject>Organic polymers</subject><subject>Physicochemistry of polymers</subject><subject>Polycondensation</subject><subject>Polymers</subject><subject>polyurethanes</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>spectroscopy</subject><issn>0021-8995</issn><issn>1097-4628</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp1kE1LxDAURYMoOH4s_AcFEXTRMa9JmtedMugoDDqLGRQ3IU1TrNZ2TDpo_fVGq-5cvcU99zy4hBwAHQOlyalercYMM4kbZAQ0kzFPE9wko5BBjFkmtsmO90-UAgiajsjZ0tnuUTc2clabrmqb6LlqbFcZH7VllK-7kBVVW_vI6E7X_YctoryPHtyxNtqc8D2yVera2_2fu0uWlxeLyVU8u51eT85nsUmQYpxjDjZFBGR5-FxkRS4KY3NkEgUFznmBmkGKAnhmUFgmJUt0CRwFDwa2Sw4H78q1r2vrO_XUrl0TXipgqUhAJlwG6mSgjGu9d7ZUK1e9aNcroOprIBUGUt8DBfbox6i90XXpdGMq_1dIJE8BaBK404F7q2rb_y9U5_P5rzkeGpXv7PtfQ7tnlUomhbq7mapFinN5T6mask8ix4CN</recordid><startdate>20130905</startdate><enddate>20130905</enddate><creator>Yang, Peng Fei</creator><creator>Li, Tian Duo</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20130905</creationdate><title>Urethane reaction kinetics of butanediols catalyzed by Zr(acac)4</title><author>Yang, Peng Fei ; Li, Tian Duo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Applied sciences</topic><topic>Exact sciences and technology</topic><topic>kinetics</topic><topic>Materials science</topic><topic>Organic polymers</topic><topic>Physicochemistry of polymers</topic><topic>Polycondensation</topic><topic>Polymers</topic><topic>polyurethanes</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>spectroscopy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Peng Fei</creatorcontrib><creatorcontrib>Li, Tian Duo</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of applied polymer science</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Peng Fei</au><au>Li, Tian Duo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Urethane reaction kinetics of butanediols catalyzed by Zr(acac)4</atitle><jtitle>Journal of applied polymer science</jtitle><addtitle>J. Appl. Polym. Sci</addtitle><date>2013-09-05</date><risdate>2013</risdate><volume>129</volume><issue>5</issue><spage>2399</spage><epage>2403</epage><pages>2399-2403</pages><issn>0021-8995</issn><eissn>1097-4628</eissn><coden>JAPNAB</coden><abstract>The urethane reaction of isocyanate was carried out with zirconium acetyl acetonate (Zr(acac)4) as catalyst. 1,2‐Butanediol and 1,4‐butanediol were used as model compounds to investigate the reaction kinetics. It was shown that hydroxyl groups in 1,2‐butanediol appeared to have different reaction rate when reacting with phenyl isocyanate, which was labeled as kfast and kslow. It was very surprising that the reaction rate of 1,4‐butanediol (kcon) was very similar to the value of kslow at the same temperature although there is only primary hydroxyl group in its molecule. Furthermore, activation energy (Ea), activation enthalpy (ΔH), and activation entropy (ΔS) for the reaction were calculated out, from which some catalytic properties of Zr(acac)4 were revealed. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/app.38978</doi><tpages>5</tpages></addata></record> |
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subjects | Applied sciences Exact sciences and technology kinetics Materials science Organic polymers Physicochemistry of polymers Polycondensation Polymers polyurethanes Preparation, kinetics, thermodynamics, mechanism and catalysts spectroscopy |
title | Urethane reaction kinetics of butanediols catalyzed by Zr(acac)4 |
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