Loading…

Blocking and Deblocking of Diisocyanate to Synthesize Polyurethanes

Diisocyanates, particularly toluene diisocyanate (TDI), are useful for the preparation of various polyurethanes with specific applications as leather-like materials, adhesives and insoles, etc. Blocking agents can be used for the operational simplicity and to reduce the hazards of TDI. In this paper...

Full description

Saved in:
Bibliographic Details
Published in:Polymers 2021-08, Vol.13 (17), p.2875
Main Authors: Jana, Sourita, Samanta, Debasis, Fahad, Mir Muhammad, Jaisankar, Sellamuthu N., Kim, Hongdoo
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-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3
cites cdi_FETCH-LOGICAL-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3
container_end_page
container_issue 17
container_start_page 2875
container_title Polymers
container_volume 13
creator Jana, Sourita
Samanta, Debasis
Fahad, Mir Muhammad
Jaisankar, Sellamuthu N.
Kim, Hongdoo
description Diisocyanates, particularly toluene diisocyanate (TDI), are useful for the preparation of various polyurethanes with specific applications as leather-like materials, adhesives and insoles, etc. Blocking agents can be used for the operational simplicity and to reduce the hazards of TDI. In this paper, we reported the use of 3-(4-bromo-phenyl)-1H-pyrazole to block toluene diisocyanate (TDI). FTIR, NMR, thermogravimetric analysis, contact angle analysis and differential scanning calorimetry (DSC) were used for the characterization. The effectiveness of the blocking was confirmed by spectroscopic techniques. The DSC thermogram showed that blocked adducts deblock at 240 °C, causing the regeneration of TDI, and causing the diisocyanates to react with polyols of different molecular weights, forming polyurethanes. The characterization of the polyurethanes was performed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, thermogravimetric analysis, differential scanning calorimetry and a contact angle study.
doi_str_mv 10.3390/polym13172875
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8434501</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2571466322</sourcerecordid><originalsourceid>FETCH-LOGICAL-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3</originalsourceid><addsrcrecordid>eNpdkU1LAzEQhoMoVmqP3he8eFnNd3YvgrZ-QUFBPYfsbrZN3SY12RXWX29qq1jnMpOZhzfzMgCcIHhOSA4vVq7pl4gggTPB9sARhoKklHC4_6cegFEICxiDMs6ROAQDQhnEOWJHYHzduPLN2FmibJVMdPHzdHUyMSa4sldWtTppXfLc23aug_nUyVP8uPO6nSurwzE4qFUT9Gibh-D19uZlfJ9OH-8exlfTtCQYtylGucgKhDDjFawIyzivGKZ5RiCPXZgpTjTXRCAhKK9VVRUcZUTkHGpKi5oMweVGd9UVS12V2rZeNXLlzVL5Xjpl5O7EmrmcuQ-Z0bVhFAXOtgLevXc6tHJpQqmbJrpwXZCYCZRjJPgaPf2HLlznbbT3TVHOo6dIpRuq9C4Er-vfZRCU6wvJnQuRL-VagYQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2571466322</pqid></control><display><type>article</type><title>Blocking and Deblocking of Diisocyanate to Synthesize Polyurethanes</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Jana, Sourita ; Samanta, Debasis ; Fahad, Mir Muhammad ; Jaisankar, Sellamuthu N. ; Kim, Hongdoo</creator><creatorcontrib>Jana, Sourita ; Samanta, Debasis ; Fahad, Mir Muhammad ; Jaisankar, Sellamuthu N. ; Kim, Hongdoo</creatorcontrib><description>Diisocyanates, particularly toluene diisocyanate (TDI), are useful for the preparation of various polyurethanes with specific applications as leather-like materials, adhesives and insoles, etc. Blocking agents can be used for the operational simplicity and to reduce the hazards of TDI. In this paper, we reported the use of 3-(4-bromo-phenyl)-1H-pyrazole to block toluene diisocyanate (TDI). FTIR, NMR, thermogravimetric analysis, contact angle analysis and differential scanning calorimetry (DSC) were used for the characterization. The effectiveness of the blocking was confirmed by spectroscopic techniques. The DSC thermogram showed that blocked adducts deblock at 240 °C, causing the regeneration of TDI, and causing the diisocyanates to react with polyols of different molecular weights, forming polyurethanes. The characterization of the polyurethanes was performed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, thermogravimetric analysis, differential scanning calorimetry and a contact angle study.</description><identifier>ISSN: 2073-4360</identifier><identifier>EISSN: 2073-4360</identifier><identifier>DOI: 10.3390/polym13172875</identifier><identifier>PMID: 34502915</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Adducts ; Blocking ; Contact angle ; Differential scanning calorimetry ; Heat measurement ; Infrared analysis ; Infrared spectroscopy ; Insoles ; Leather ; NMR spectroscopy ; Phenols ; Polyethylene glycol ; Polyols ; Polyurethane ; Pyrazole ; Regeneration ; Solvents ; Temperature ; Thermogravimetric analysis ; Toluene ; Toluene diisocyanates</subject><ispartof>Polymers, 2021-08, Vol.13 (17), p.2875</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3</citedby><cites>FETCH-LOGICAL-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3</cites><orcidid>0000-0002-3043-8033 ; 0000-0001-5961-2691</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2571466322/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2571466322?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids></links><search><creatorcontrib>Jana, Sourita</creatorcontrib><creatorcontrib>Samanta, Debasis</creatorcontrib><creatorcontrib>Fahad, Mir Muhammad</creatorcontrib><creatorcontrib>Jaisankar, Sellamuthu N.</creatorcontrib><creatorcontrib>Kim, Hongdoo</creatorcontrib><title>Blocking and Deblocking of Diisocyanate to Synthesize Polyurethanes</title><title>Polymers</title><description>Diisocyanates, particularly toluene diisocyanate (TDI), are useful for the preparation of various polyurethanes with specific applications as leather-like materials, adhesives and insoles, etc. Blocking agents can be used for the operational simplicity and to reduce the hazards of TDI. In this paper, we reported the use of 3-(4-bromo-phenyl)-1H-pyrazole to block toluene diisocyanate (TDI). FTIR, NMR, thermogravimetric analysis, contact angle analysis and differential scanning calorimetry (DSC) were used for the characterization. The effectiveness of the blocking was confirmed by spectroscopic techniques. The DSC thermogram showed that blocked adducts deblock at 240 °C, causing the regeneration of TDI, and causing the diisocyanates to react with polyols of different molecular weights, forming polyurethanes. The characterization of the polyurethanes was performed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, thermogravimetric analysis, differential scanning calorimetry and a contact angle study.</description><subject>Adducts</subject><subject>Blocking</subject><subject>Contact angle</subject><subject>Differential scanning calorimetry</subject><subject>Heat measurement</subject><subject>Infrared analysis</subject><subject>Infrared spectroscopy</subject><subject>Insoles</subject><subject>Leather</subject><subject>NMR spectroscopy</subject><subject>Phenols</subject><subject>Polyethylene glycol</subject><subject>Polyols</subject><subject>Polyurethane</subject><subject>Pyrazole</subject><subject>Regeneration</subject><subject>Solvents</subject><subject>Temperature</subject><subject>Thermogravimetric analysis</subject><subject>Toluene</subject><subject>Toluene diisocyanates</subject><issn>2073-4360</issn><issn>2073-4360</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNpdkU1LAzEQhoMoVmqP3he8eFnNd3YvgrZ-QUFBPYfsbrZN3SY12RXWX29qq1jnMpOZhzfzMgCcIHhOSA4vVq7pl4gggTPB9sARhoKklHC4_6cegFEICxiDMs6ROAQDQhnEOWJHYHzduPLN2FmibJVMdPHzdHUyMSa4sldWtTppXfLc23aug_nUyVP8uPO6nSurwzE4qFUT9Gibh-D19uZlfJ9OH-8exlfTtCQYtylGucgKhDDjFawIyzivGKZ5RiCPXZgpTjTXRCAhKK9VVRUcZUTkHGpKi5oMweVGd9UVS12V2rZeNXLlzVL5Xjpl5O7EmrmcuQ-Z0bVhFAXOtgLevXc6tHJpQqmbJrpwXZCYCZRjJPgaPf2HLlznbbT3TVHOo6dIpRuq9C4Er-vfZRCU6wvJnQuRL-VagYQ</recordid><startdate>20210827</startdate><enddate>20210827</enddate><creator>Jana, Sourita</creator><creator>Samanta, Debasis</creator><creator>Fahad, Mir Muhammad</creator><creator>Jaisankar, Sellamuthu N.</creator><creator>Kim, Hongdoo</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3043-8033</orcidid><orcidid>https://orcid.org/0000-0001-5961-2691</orcidid></search><sort><creationdate>20210827</creationdate><title>Blocking and Deblocking of Diisocyanate to Synthesize Polyurethanes</title><author>Jana, Sourita ; Samanta, Debasis ; Fahad, Mir Muhammad ; Jaisankar, Sellamuthu N. ; Kim, Hongdoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Adducts</topic><topic>Blocking</topic><topic>Contact angle</topic><topic>Differential scanning calorimetry</topic><topic>Heat measurement</topic><topic>Infrared analysis</topic><topic>Infrared spectroscopy</topic><topic>Insoles</topic><topic>Leather</topic><topic>NMR spectroscopy</topic><topic>Phenols</topic><topic>Polyethylene glycol</topic><topic>Polyols</topic><topic>Polyurethane</topic><topic>Pyrazole</topic><topic>Regeneration</topic><topic>Solvents</topic><topic>Temperature</topic><topic>Thermogravimetric analysis</topic><topic>Toluene</topic><topic>Toluene diisocyanates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jana, Sourita</creatorcontrib><creatorcontrib>Samanta, Debasis</creatorcontrib><creatorcontrib>Fahad, Mir Muhammad</creatorcontrib><creatorcontrib>Jaisankar, Sellamuthu N.</creatorcontrib><creatorcontrib>Kim, Hongdoo</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Polymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jana, Sourita</au><au>Samanta, Debasis</au><au>Fahad, Mir Muhammad</au><au>Jaisankar, Sellamuthu N.</au><au>Kim, Hongdoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Blocking and Deblocking of Diisocyanate to Synthesize Polyurethanes</atitle><jtitle>Polymers</jtitle><date>2021-08-27</date><risdate>2021</risdate><volume>13</volume><issue>17</issue><spage>2875</spage><pages>2875-</pages><issn>2073-4360</issn><eissn>2073-4360</eissn><abstract>Diisocyanates, particularly toluene diisocyanate (TDI), are useful for the preparation of various polyurethanes with specific applications as leather-like materials, adhesives and insoles, etc. Blocking agents can be used for the operational simplicity and to reduce the hazards of TDI. In this paper, we reported the use of 3-(4-bromo-phenyl)-1H-pyrazole to block toluene diisocyanate (TDI). FTIR, NMR, thermogravimetric analysis, contact angle analysis and differential scanning calorimetry (DSC) were used for the characterization. The effectiveness of the blocking was confirmed by spectroscopic techniques. The DSC thermogram showed that blocked adducts deblock at 240 °C, causing the regeneration of TDI, and causing the diisocyanates to react with polyols of different molecular weights, forming polyurethanes. The characterization of the polyurethanes was performed by infrared spectroscopy, nuclear magnetic resonance spectroscopy, thermogravimetric analysis, differential scanning calorimetry and a contact angle study.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34502915</pmid><doi>10.3390/polym13172875</doi><orcidid>https://orcid.org/0000-0002-3043-8033</orcidid><orcidid>https://orcid.org/0000-0001-5961-2691</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2073-4360
ispartof Polymers, 2021-08, Vol.13 (17), p.2875
issn 2073-4360
2073-4360
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8434501
source Publicly Available Content Database; PubMed Central
subjects Adducts
Blocking
Contact angle
Differential scanning calorimetry
Heat measurement
Infrared analysis
Infrared spectroscopy
Insoles
Leather
NMR spectroscopy
Phenols
Polyethylene glycol
Polyols
Polyurethane
Pyrazole
Regeneration
Solvents
Temperature
Thermogravimetric analysis
Toluene
Toluene diisocyanates
title Blocking and Deblocking of Diisocyanate to Synthesize Polyurethanes
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-03T09%3A51%3A49IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Blocking%20and%20Deblocking%20of%20Diisocyanate%20to%20Synthesize%20Polyurethanes&rft.jtitle=Polymers&rft.au=Jana,%20Sourita&rft.date=2021-08-27&rft.volume=13&rft.issue=17&rft.spage=2875&rft.pages=2875-&rft.issn=2073-4360&rft.eissn=2073-4360&rft_id=info:doi/10.3390/polym13172875&rft_dat=%3Cproquest_pubme%3E2571466322%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c322t-21978b11256d0d35866d5249830611208a63e6e3717746faddb61837960e44bf3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2571466322&rft_id=info:pmid/34502915&rfr_iscdi=true