Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Journal of applied polymer science 2013-09, Vol.129 (5), p.2399-2403
Main Authors: Yang, Peng Fei, Li, Tian Duo
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803
cites cdi_FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803
container_end_page 2403
container_issue 5
container_start_page 2399
container_title Journal of applied polymer science
container_volume 129
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
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1365217247</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2989213291</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803</originalsourceid><addsrcrecordid>eNp1kE1LxDAURYMoOH4s_AcFEXTRMa9JmtedMugoDDqLGRQ3IU1TrNZ2TDpo_fVGq-5cvcU99zy4hBwAHQOlyalercYMM4kbZAQ0kzFPE9wko5BBjFkmtsmO90-UAgiajsjZ0tnuUTc2clabrmqb6LlqbFcZH7VllK-7kBVVW_vI6E7X_YctoryPHtyxNtqc8D2yVera2_2fu0uWlxeLyVU8u51eT85nsUmQYpxjDjZFBGR5-FxkRS4KY3NkEgUFznmBmkGKAnhmUFgmJUt0CRwFDwa2Sw4H78q1r2vrO_XUrl0TXipgqUhAJlwG6mSgjGu9d7ZUK1e9aNcroOprIBUGUt8DBfbox6i90XXpdGMq_1dIJE8BaBK404F7q2rb_y9U5_P5rzkeGpXv7PtfQ7tnlUomhbq7mapFinN5T6mask8ix4CN</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1365217247</pqid></control><display><type>article</type><title>Urethane reaction kinetics of butanediols catalyzed by Zr(acac)4</title><source>Wiley</source><creator>Yang, Peng Fei ; Li, Tian Duo</creator><creatorcontrib>Yang, Peng Fei ; Li, Tian Duo</creatorcontrib><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><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&amp;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>
fulltext fulltext
identifier ISSN: 0021-8995
ispartof Journal of applied polymer science, 2013-09, Vol.129 (5), p.2399-2403
issn 0021-8995
1097-4628
language eng
recordid cdi_proquest_journals_1365217247
source Wiley
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T06%3A42%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Urethane%20reaction%20kinetics%20of%20butanediols%20catalyzed%20by%20Zr(acac)4&rft.jtitle=Journal%20of%20applied%20polymer%20science&rft.au=Yang,%20Peng%20Fei&rft.date=2013-09-05&rft.volume=129&rft.issue=5&rft.spage=2399&rft.epage=2403&rft.pages=2399-2403&rft.issn=0021-8995&rft.eissn=1097-4628&rft.coden=JAPNAB&rft_id=info:doi/10.1002/app.38978&rft_dat=%3Cproquest_cross%3E2989213291%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2808-b8b1e688183b150d9db5dceb8378501444d8a31685149c85e37732af148542803%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1365217247&rft_id=info:pmid/&rfr_iscdi=true