Synthesis and Characterization of Non-Isocyanate Polyurethanes using Diglycidyl Ether of Bisphenol Acetone (DGEBPA) Epoxy Resin

Present work focuses on synthesis of non-isocyanate polyurethane (NIPU) using the conventional epoxy resin, diglycidyl ether of bisphenol acetone (DGEBPA). The conventional polyurethanes (PUs) are prepared by reaction of the toxic diisocyanates and polyols. The epoxy resin contains two epoxy groups...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Asian journal of chemistry 2022, Vol.34 (8), p.2155-2160
Hauptverfasser: Soni, D.K., Maithani, A., Kamani, P.K.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2160
container_issue 8
container_start_page 2155
container_title Asian journal of chemistry
container_volume 34
creator Soni, D.K.
Maithani, A.
Kamani, P.K.
description Present work focuses on synthesis of non-isocyanate polyurethane (NIPU) using the conventional epoxy resin, diglycidyl ether of bisphenol acetone (DGEBPA). The conventional polyurethanes (PUs) are prepared by reaction of the toxic diisocyanates and polyols. The epoxy resin contains two epoxy groups which are converted to cyclic carbonate groups when reacted with carbon dioxide. In this work, the epoxy resin (ER) was converted into the cyclocarbonated epoxy resin (CCER) using methyltriphenylphosphonium iodide (MePh.I) as the catalyst and ethyl cellsuolve as the reaction medium. The reaction was carried out in a carbon dioxide atmosphere, slightly above the atmospheric pressure, for 20 h. The progress of reaction was monitored by percent oxirane oxygen content (%OOC). The FTIR study confirms the disappearance of epoxy groups at 910 cm-1 and appearance of cyclic carbonate groups at 1800 cm-1. The films of the resulting resin were prepared by curing with diethylamine (DEA), ethylene diamine (EDA) and reactive polyamide resin (70% NV). The formation of urethane linkage was confirmed by FTIR spectrum. The mechanical, chemical and appearance properties of the resulting NIPU were studied. The results were satisfactory, like improvement in adhesion and alkali resistance, but reduction in gloss and colour retention was observed. This eco-friendly route for synthesis of polyurethane can be used easily and variation in properties can be obtained by selecting the suitable epoxy compound as well as curing agent.
doi_str_mv 10.14233/ajchem.2022.23855
format Article
fullrecord <record><control><sourceid>crossref</sourceid><recordid>TN_cdi_crossref_primary_10_14233_ajchem_2022_23855</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_14233_ajchem_2022_23855</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1365-bdee6e4caf9cb3b3e7d887c70e9542b671120003371348305d46e33d088e93b33</originalsourceid><addsrcrecordid>eNotkEtPwzAQhC0EElXpH-DkIxxS_Eji5NhHKJUqqHhI3CLH2TSuUruyU6nhwl8nbdnL7GFmVvshdE_JmIaM8ye5VTXsxowwNmY8iaIrNCCpiIKQie_r804CQYS4RSPvt6SfmEZMsAH6_ehMW4PXHktT4lktnVQtOP0jW20NthV-tSZYeqs6aWQLeG2b7uCgraUBjw9emw2e603TKV12Dc76NneKTbXf12BsgycKWmsAP8wX2XQ9ecTZ3h47_N5fNXfoppKNh9G_DtHXc_Y5ewlWb4vlbLIKFOVxFBQlQAyhklWqCl5wEGWSCCUIpFHIilhQyvqvOBeUhwknURnGwHlJkgTS3s-HiF16lbPeO6jyvdM76bqckvxMMb9QzE8U8zNF_gcM5Wev</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Synthesis and Characterization of Non-Isocyanate Polyurethanes using Diglycidyl Ether of Bisphenol Acetone (DGEBPA) Epoxy Resin</title><source>Alma/SFX Local Collection</source><creator>Soni, D.K. ; Maithani, A. ; Kamani, P.K.</creator><creatorcontrib>Soni, D.K. ; Maithani, A. ; Kamani, P.K.</creatorcontrib><description>Present work focuses on synthesis of non-isocyanate polyurethane (NIPU) using the conventional epoxy resin, diglycidyl ether of bisphenol acetone (DGEBPA). The conventional polyurethanes (PUs) are prepared by reaction of the toxic diisocyanates and polyols. The epoxy resin contains two epoxy groups which are converted to cyclic carbonate groups when reacted with carbon dioxide. In this work, the epoxy resin (ER) was converted into the cyclocarbonated epoxy resin (CCER) using methyltriphenylphosphonium iodide (MePh.I) as the catalyst and ethyl cellsuolve as the reaction medium. The reaction was carried out in a carbon dioxide atmosphere, slightly above the atmospheric pressure, for 20 h. The progress of reaction was monitored by percent oxirane oxygen content (%OOC). The FTIR study confirms the disappearance of epoxy groups at 910 cm-1 and appearance of cyclic carbonate groups at 1800 cm-1. The films of the resulting resin were prepared by curing with diethylamine (DEA), ethylene diamine (EDA) and reactive polyamide resin (70% NV). The formation of urethane linkage was confirmed by FTIR spectrum. The mechanical, chemical and appearance properties of the resulting NIPU were studied. The results were satisfactory, like improvement in adhesion and alkali resistance, but reduction in gloss and colour retention was observed. This eco-friendly route for synthesis of polyurethane can be used easily and variation in properties can be obtained by selecting the suitable epoxy compound as well as curing agent.</description><identifier>ISSN: 0970-7077</identifier><identifier>EISSN: 0975-427X</identifier><identifier>DOI: 10.14233/ajchem.2022.23855</identifier><language>eng</language><ispartof>Asian journal of chemistry, 2022, Vol.34 (8), p.2155-2160</ispartof><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1365-bdee6e4caf9cb3b3e7d887c70e9542b671120003371348305d46e33d088e93b33</citedby><cites>FETCH-LOGICAL-c1365-bdee6e4caf9cb3b3e7d887c70e9542b671120003371348305d46e33d088e93b33</cites><orcidid>0000-0001-7288-3007 ; 0000-0002-3167-3916 ; 0000-0002-1514-3114</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4009,27902,27903,27904</link.rule.ids></links><search><creatorcontrib>Soni, D.K.</creatorcontrib><creatorcontrib>Maithani, A.</creatorcontrib><creatorcontrib>Kamani, P.K.</creatorcontrib><title>Synthesis and Characterization of Non-Isocyanate Polyurethanes using Diglycidyl Ether of Bisphenol Acetone (DGEBPA) Epoxy Resin</title><title>Asian journal of chemistry</title><description>Present work focuses on synthesis of non-isocyanate polyurethane (NIPU) using the conventional epoxy resin, diglycidyl ether of bisphenol acetone (DGEBPA). The conventional polyurethanes (PUs) are prepared by reaction of the toxic diisocyanates and polyols. The epoxy resin contains two epoxy groups which are converted to cyclic carbonate groups when reacted with carbon dioxide. In this work, the epoxy resin (ER) was converted into the cyclocarbonated epoxy resin (CCER) using methyltriphenylphosphonium iodide (MePh.I) as the catalyst and ethyl cellsuolve as the reaction medium. The reaction was carried out in a carbon dioxide atmosphere, slightly above the atmospheric pressure, for 20 h. The progress of reaction was monitored by percent oxirane oxygen content (%OOC). The FTIR study confirms the disappearance of epoxy groups at 910 cm-1 and appearance of cyclic carbonate groups at 1800 cm-1. The films of the resulting resin were prepared by curing with diethylamine (DEA), ethylene diamine (EDA) and reactive polyamide resin (70% NV). The formation of urethane linkage was confirmed by FTIR spectrum. The mechanical, chemical and appearance properties of the resulting NIPU were studied. The results were satisfactory, like improvement in adhesion and alkali resistance, but reduction in gloss and colour retention was observed. This eco-friendly route for synthesis of polyurethane can be used easily and variation in properties can be obtained by selecting the suitable epoxy compound as well as curing agent.</description><issn>0970-7077</issn><issn>0975-427X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNotkEtPwzAQhC0EElXpH-DkIxxS_Eji5NhHKJUqqHhI3CLH2TSuUruyU6nhwl8nbdnL7GFmVvshdE_JmIaM8ye5VTXsxowwNmY8iaIrNCCpiIKQie_r804CQYS4RSPvt6SfmEZMsAH6_ehMW4PXHktT4lktnVQtOP0jW20NthV-tSZYeqs6aWQLeG2b7uCgraUBjw9emw2e603TKV12Dc76NneKTbXf12BsgycKWmsAP8wX2XQ9ecTZ3h47_N5fNXfoppKNh9G_DtHXc_Y5ewlWb4vlbLIKFOVxFBQlQAyhklWqCl5wEGWSCCUIpFHIilhQyvqvOBeUhwknURnGwHlJkgTS3s-HiF16lbPeO6jyvdM76bqckvxMMb9QzE8U8zNF_gcM5Wev</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>Soni, D.K.</creator><creator>Maithani, A.</creator><creator>Kamani, P.K.</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-7288-3007</orcidid><orcidid>https://orcid.org/0000-0002-3167-3916</orcidid><orcidid>https://orcid.org/0000-0002-1514-3114</orcidid></search><sort><creationdate>2022</creationdate><title>Synthesis and Characterization of Non-Isocyanate Polyurethanes using Diglycidyl Ether of Bisphenol Acetone (DGEBPA) Epoxy Resin</title><author>Soni, D.K. ; Maithani, A. ; Kamani, P.K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1365-bdee6e4caf9cb3b3e7d887c70e9542b671120003371348305d46e33d088e93b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Soni, D.K.</creatorcontrib><creatorcontrib>Maithani, A.</creatorcontrib><creatorcontrib>Kamani, P.K.</creatorcontrib><collection>CrossRef</collection><jtitle>Asian journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soni, D.K.</au><au>Maithani, A.</au><au>Kamani, P.K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and Characterization of Non-Isocyanate Polyurethanes using Diglycidyl Ether of Bisphenol Acetone (DGEBPA) Epoxy Resin</atitle><jtitle>Asian journal of chemistry</jtitle><date>2022</date><risdate>2022</risdate><volume>34</volume><issue>8</issue><spage>2155</spage><epage>2160</epage><pages>2155-2160</pages><issn>0970-7077</issn><eissn>0975-427X</eissn><abstract>Present work focuses on synthesis of non-isocyanate polyurethane (NIPU) using the conventional epoxy resin, diglycidyl ether of bisphenol acetone (DGEBPA). The conventional polyurethanes (PUs) are prepared by reaction of the toxic diisocyanates and polyols. The epoxy resin contains two epoxy groups which are converted to cyclic carbonate groups when reacted with carbon dioxide. In this work, the epoxy resin (ER) was converted into the cyclocarbonated epoxy resin (CCER) using methyltriphenylphosphonium iodide (MePh.I) as the catalyst and ethyl cellsuolve as the reaction medium. The reaction was carried out in a carbon dioxide atmosphere, slightly above the atmospheric pressure, for 20 h. The progress of reaction was monitored by percent oxirane oxygen content (%OOC). The FTIR study confirms the disappearance of epoxy groups at 910 cm-1 and appearance of cyclic carbonate groups at 1800 cm-1. The films of the resulting resin were prepared by curing with diethylamine (DEA), ethylene diamine (EDA) and reactive polyamide resin (70% NV). The formation of urethane linkage was confirmed by FTIR spectrum. The mechanical, chemical and appearance properties of the resulting NIPU were studied. The results were satisfactory, like improvement in adhesion and alkali resistance, but reduction in gloss and colour retention was observed. This eco-friendly route for synthesis of polyurethane can be used easily and variation in properties can be obtained by selecting the suitable epoxy compound as well as curing agent.</abstract><doi>10.14233/ajchem.2022.23855</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0001-7288-3007</orcidid><orcidid>https://orcid.org/0000-0002-3167-3916</orcidid><orcidid>https://orcid.org/0000-0002-1514-3114</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0970-7077
ispartof Asian journal of chemistry, 2022, Vol.34 (8), p.2155-2160
issn 0970-7077
0975-427X
language eng
recordid cdi_crossref_primary_10_14233_ajchem_2022_23855
source Alma/SFX Local Collection
title Synthesis and Characterization of Non-Isocyanate Polyurethanes using Diglycidyl Ether of Bisphenol Acetone (DGEBPA) Epoxy Resin
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T07%3A17%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20and%20Characterization%20of%20Non-Isocyanate%20Polyurethanes%20using%20Diglycidyl%20Ether%20of%20Bisphenol%20Acetone%20(DGEBPA)%20Epoxy%20Resin&rft.jtitle=Asian%20journal%20of%20chemistry&rft.au=Soni,%20D.K.&rft.date=2022&rft.volume=34&rft.issue=8&rft.spage=2155&rft.epage=2160&rft.pages=2155-2160&rft.issn=0970-7077&rft.eissn=0975-427X&rft_id=info:doi/10.14233/ajchem.2022.23855&rft_dat=%3Ccrossref%3E10_14233_ajchem_2022_23855%3C/crossref%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true