Dechlorination of Polyvinyl Chloride via Solvothermal Treatment with Glycerol
Solvothermal treatment using glycerol effectively removes chlorine from polyvinyl chloride (PVC). Additive-free PVC was dechlorinated by treatment with glycerol in an autoclave at 200–240 °C. Liquid glycerol was coexistent with a red powder after the reaction at 200 °C. At reaction temperatures of 2...
Gespeichert in:
Veröffentlicht in: | Processes 2022-10, Vol.10 (10), p.2047 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 10 |
container_start_page | 2047 |
container_title | Processes |
container_volume | 10 |
creator | Kusakabe, Katsuki Nagai, Anna Leong, Wai Hong Yamasaka, Kouki Nakaaki, Takuro Uemura, Yoshimitsu Ikenaga, Kazutoshi |
description | Solvothermal treatment using glycerol effectively removes chlorine from polyvinyl chloride (PVC). Additive-free PVC was dechlorinated by treatment with glycerol in an autoclave at 200–240 °C. Liquid glycerol was coexistent with a red powder after the reaction at 200 °C. At reaction temperatures of 220 and 240 °C, the liquid glycerol disappeared, and carbonization proceeded to form a black powder. In this reaction, the glycerol was directly converted into glycidol. Epichlorohydrin was also produced from the glycerol via 1,3-dichloro-2-propanol as an intermediate. The PVC was converted into the polyethylene oxide structure, following the generation of the polyene structure by zip-elimination. Finally, the converted PVC was resinified by an epoxidation reaction with the glycidol and epichlorohydrin. Thus, glycerol acted as a useful reaction medium for this reaction system. The analysis of the decomposition ratio and dechlorination yield showed that the PVC was converted into solid products in high yields via chlorine release, and 30% of the glycerol was solidified by resinification at 240 °C. The effects of the additives on dechlorination were investigated using commercially available PVC sheets. Elemental analysis showed that the calorific value of the solid product dechlorinated at 240 °C was found to be higher than that of standard bituminous coal. |
doi_str_mv | 10.3390/pr10102047 |
format | Article |
fullrecord | <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_journals_2728515376</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A744992960</galeid><sourcerecordid>A744992960</sourcerecordid><originalsourceid>FETCH-LOGICAL-c334t-816137756e72c43cd4f09159a976b3ac61065837d140469f875622ae3f62b2583</originalsourceid><addsrcrecordid>eNpNUE1LAzEQDaJgqb34CwLehK352mRzLFWrUFGwnpc0m9iU7KZm08r-e6MVdOYww7z3ZoYHwCVGU0olutlFjDAiiIkTMCKEiEIKLE7_9edg0vdblENiWpV8BJ5ujd74EF2nkgsdDBa-BD8cXDd4OP9BGgMPTsHX4A8hbUxslYeraFRqTZfgp0sbuPCDNjH4C3Bmle_N5LeOwdv93Wr-UCyfF4_z2bLQlLJUVJhjKkTJjSCaUd0wmx8qpZKCr6nSHCNeVlQ0mCHGpa0ylRBlqOVkTTIyBlfHvbsYPvamT_U27GOXT9ZEkKrEJRU8s6ZH1rvypnadDSkqnbMxrdOhM9bl-UwwJiWRHGXB9VGgY-j7aGy9i65Vcagxqr8trv8spl_Hlmwr</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2728515376</pqid></control><display><type>article</type><title>Dechlorination of Polyvinyl Chloride via Solvothermal Treatment with Glycerol</title><source>MDPI - Multidisciplinary Digital Publishing Institute</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Kusakabe, Katsuki ; Nagai, Anna ; Leong, Wai Hong ; Yamasaka, Kouki ; Nakaaki, Takuro ; Uemura, Yoshimitsu ; Ikenaga, Kazutoshi</creator><creatorcontrib>Kusakabe, Katsuki ; Nagai, Anna ; Leong, Wai Hong ; Yamasaka, Kouki ; Nakaaki, Takuro ; Uemura, Yoshimitsu ; Ikenaga, Kazutoshi</creatorcontrib><description>Solvothermal treatment using glycerol effectively removes chlorine from polyvinyl chloride (PVC). Additive-free PVC was dechlorinated by treatment with glycerol in an autoclave at 200–240 °C. Liquid glycerol was coexistent with a red powder after the reaction at 200 °C. At reaction temperatures of 220 and 240 °C, the liquid glycerol disappeared, and carbonization proceeded to form a black powder. In this reaction, the glycerol was directly converted into glycidol. Epichlorohydrin was also produced from the glycerol via 1,3-dichloro-2-propanol as an intermediate. The PVC was converted into the polyethylene oxide structure, following the generation of the polyene structure by zip-elimination. Finally, the converted PVC was resinified by an epoxidation reaction with the glycidol and epichlorohydrin. Thus, glycerol acted as a useful reaction medium for this reaction system. The analysis of the decomposition ratio and dechlorination yield showed that the PVC was converted into solid products in high yields via chlorine release, and 30% of the glycerol was solidified by resinification at 240 °C. The effects of the additives on dechlorination were investigated using commercially available PVC sheets. Elemental analysis showed that the calorific value of the solid product dechlorinated at 240 °C was found to be higher than that of standard bituminous coal.</description><identifier>ISSN: 2227-9717</identifier><identifier>EISSN: 2227-9717</identifier><identifier>DOI: 10.3390/pr10102047</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>Additives ; Analysis ; Biodiesel fuels ; Bituminous coal ; Calorific value ; Chlorides ; Chlorine ; Dechlorination ; Decomposition ; Decomposition reactions ; Dioxins ; Epichlorohydrin ; Epoxidation ; Epoxy resins ; Glycerin ; Glycerol ; Methods ; Polyethylene oxide ; Polyvinyl chloride ; Propanol</subject><ispartof>Processes, 2022-10, Vol.10 (10), p.2047</ispartof><rights>COPYRIGHT 2022 MDPI AG</rights><rights>2022 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><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c334t-816137756e72c43cd4f09159a976b3ac61065837d140469f875622ae3f62b2583</citedby><cites>FETCH-LOGICAL-c334t-816137756e72c43cd4f09159a976b3ac61065837d140469f875622ae3f62b2583</cites><orcidid>0000-0002-6226-4074</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>Kusakabe, Katsuki</creatorcontrib><creatorcontrib>Nagai, Anna</creatorcontrib><creatorcontrib>Leong, Wai Hong</creatorcontrib><creatorcontrib>Yamasaka, Kouki</creatorcontrib><creatorcontrib>Nakaaki, Takuro</creatorcontrib><creatorcontrib>Uemura, Yoshimitsu</creatorcontrib><creatorcontrib>Ikenaga, Kazutoshi</creatorcontrib><title>Dechlorination of Polyvinyl Chloride via Solvothermal Treatment with Glycerol</title><title>Processes</title><description>Solvothermal treatment using glycerol effectively removes chlorine from polyvinyl chloride (PVC). Additive-free PVC was dechlorinated by treatment with glycerol in an autoclave at 200–240 °C. Liquid glycerol was coexistent with a red powder after the reaction at 200 °C. At reaction temperatures of 220 and 240 °C, the liquid glycerol disappeared, and carbonization proceeded to form a black powder. In this reaction, the glycerol was directly converted into glycidol. Epichlorohydrin was also produced from the glycerol via 1,3-dichloro-2-propanol as an intermediate. The PVC was converted into the polyethylene oxide structure, following the generation of the polyene structure by zip-elimination. Finally, the converted PVC was resinified by an epoxidation reaction with the glycidol and epichlorohydrin. Thus, glycerol acted as a useful reaction medium for this reaction system. The analysis of the decomposition ratio and dechlorination yield showed that the PVC was converted into solid products in high yields via chlorine release, and 30% of the glycerol was solidified by resinification at 240 °C. The effects of the additives on dechlorination were investigated using commercially available PVC sheets. Elemental analysis showed that the calorific value of the solid product dechlorinated at 240 °C was found to be higher than that of standard bituminous coal.</description><subject>Additives</subject><subject>Analysis</subject><subject>Biodiesel fuels</subject><subject>Bituminous coal</subject><subject>Calorific value</subject><subject>Chlorides</subject><subject>Chlorine</subject><subject>Dechlorination</subject><subject>Decomposition</subject><subject>Decomposition reactions</subject><subject>Dioxins</subject><subject>Epichlorohydrin</subject><subject>Epoxidation</subject><subject>Epoxy resins</subject><subject>Glycerin</subject><subject>Glycerol</subject><subject>Methods</subject><subject>Polyethylene oxide</subject><subject>Polyvinyl chloride</subject><subject>Propanol</subject><issn>2227-9717</issn><issn>2227-9717</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpNUE1LAzEQDaJgqb34CwLehK352mRzLFWrUFGwnpc0m9iU7KZm08r-e6MVdOYww7z3ZoYHwCVGU0olutlFjDAiiIkTMCKEiEIKLE7_9edg0vdblENiWpV8BJ5ujd74EF2nkgsdDBa-BD8cXDd4OP9BGgMPTsHX4A8hbUxslYeraFRqTZfgp0sbuPCDNjH4C3Bmle_N5LeOwdv93Wr-UCyfF4_z2bLQlLJUVJhjKkTJjSCaUd0wmx8qpZKCr6nSHCNeVlQ0mCHGpa0ylRBlqOVkTTIyBlfHvbsYPvamT_U27GOXT9ZEkKrEJRU8s6ZH1rvypnadDSkqnbMxrdOhM9bl-UwwJiWRHGXB9VGgY-j7aGy9i65Vcagxqr8trv8spl_Hlmwr</recordid><startdate>20221001</startdate><enddate>20221001</enddate><creator>Kusakabe, Katsuki</creator><creator>Nagai, Anna</creator><creator>Leong, Wai Hong</creator><creator>Yamasaka, Kouki</creator><creator>Nakaaki, Takuro</creator><creator>Uemura, Yoshimitsu</creator><creator>Ikenaga, Kazutoshi</creator><general>MDPI AG</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>LK8</scope><scope>M7P</scope><scope>PDBOC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><orcidid>https://orcid.org/0000-0002-6226-4074</orcidid></search><sort><creationdate>20221001</creationdate><title>Dechlorination of Polyvinyl Chloride via Solvothermal Treatment with Glycerol</title><author>Kusakabe, Katsuki ; Nagai, Anna ; Leong, Wai Hong ; Yamasaka, Kouki ; Nakaaki, Takuro ; Uemura, Yoshimitsu ; Ikenaga, Kazutoshi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c334t-816137756e72c43cd4f09159a976b3ac61065837d140469f875622ae3f62b2583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Additives</topic><topic>Analysis</topic><topic>Biodiesel fuels</topic><topic>Bituminous coal</topic><topic>Calorific value</topic><topic>Chlorides</topic><topic>Chlorine</topic><topic>Dechlorination</topic><topic>Decomposition</topic><topic>Decomposition reactions</topic><topic>Dioxins</topic><topic>Epichlorohydrin</topic><topic>Epoxidation</topic><topic>Epoxy resins</topic><topic>Glycerin</topic><topic>Glycerol</topic><topic>Methods</topic><topic>Polyethylene oxide</topic><topic>Polyvinyl chloride</topic><topic>Propanol</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kusakabe, Katsuki</creatorcontrib><creatorcontrib>Nagai, Anna</creatorcontrib><creatorcontrib>Leong, Wai Hong</creatorcontrib><creatorcontrib>Yamasaka, Kouki</creatorcontrib><creatorcontrib>Nakaaki, Takuro</creatorcontrib><creatorcontrib>Uemura, Yoshimitsu</creatorcontrib><creatorcontrib>Ikenaga, Kazutoshi</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>ProQuest Natural Science Collection</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection (ProQuest)</collection><collection>Natural Science Collection (ProQuest)</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>ProQuest Biological Science Collection</collection><collection>Biological 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><jtitle>Processes</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kusakabe, Katsuki</au><au>Nagai, Anna</au><au>Leong, Wai Hong</au><au>Yamasaka, Kouki</au><au>Nakaaki, Takuro</au><au>Uemura, Yoshimitsu</au><au>Ikenaga, Kazutoshi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dechlorination of Polyvinyl Chloride via Solvothermal Treatment with Glycerol</atitle><jtitle>Processes</jtitle><date>2022-10-01</date><risdate>2022</risdate><volume>10</volume><issue>10</issue><spage>2047</spage><pages>2047-</pages><issn>2227-9717</issn><eissn>2227-9717</eissn><abstract>Solvothermal treatment using glycerol effectively removes chlorine from polyvinyl chloride (PVC). Additive-free PVC was dechlorinated by treatment with glycerol in an autoclave at 200–240 °C. Liquid glycerol was coexistent with a red powder after the reaction at 200 °C. At reaction temperatures of 220 and 240 °C, the liquid glycerol disappeared, and carbonization proceeded to form a black powder. In this reaction, the glycerol was directly converted into glycidol. Epichlorohydrin was also produced from the glycerol via 1,3-dichloro-2-propanol as an intermediate. The PVC was converted into the polyethylene oxide structure, following the generation of the polyene structure by zip-elimination. Finally, the converted PVC was resinified by an epoxidation reaction with the glycidol and epichlorohydrin. Thus, glycerol acted as a useful reaction medium for this reaction system. The analysis of the decomposition ratio and dechlorination yield showed that the PVC was converted into solid products in high yields via chlorine release, and 30% of the glycerol was solidified by resinification at 240 °C. The effects of the additives on dechlorination were investigated using commercially available PVC sheets. Elemental analysis showed that the calorific value of the solid product dechlorinated at 240 °C was found to be higher than that of standard bituminous coal.</abstract><cop>Basel</cop><pub>MDPI AG</pub><doi>10.3390/pr10102047</doi><orcidid>https://orcid.org/0000-0002-6226-4074</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2227-9717 |
ispartof | Processes, 2022-10, Vol.10 (10), p.2047 |
issn | 2227-9717 2227-9717 |
language | eng |
recordid | cdi_proquest_journals_2728515376 |
source | MDPI - Multidisciplinary Digital Publishing Institute; EZB-FREE-00999 freely available EZB journals |
subjects | Additives Analysis Biodiesel fuels Bituminous coal Calorific value Chlorides Chlorine Dechlorination Decomposition Decomposition reactions Dioxins Epichlorohydrin Epoxidation Epoxy resins Glycerin Glycerol Methods Polyethylene oxide Polyvinyl chloride Propanol |
title | Dechlorination of Polyvinyl Chloride via Solvothermal Treatment with Glycerol |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T15%3A41%3A28IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Dechlorination%20of%20Polyvinyl%20Chloride%20via%20Solvothermal%20Treatment%20with%20Glycerol&rft.jtitle=Processes&rft.au=Kusakabe,%20Katsuki&rft.date=2022-10-01&rft.volume=10&rft.issue=10&rft.spage=2047&rft.pages=2047-&rft.issn=2227-9717&rft.eissn=2227-9717&rft_id=info:doi/10.3390/pr10102047&rft_dat=%3Cgale_proqu%3EA744992960%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2728515376&rft_id=info:pmid/&rft_galeid=A744992960&rfr_iscdi=true |