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Investigation of poly(phenylacetylene) derivatives for carbon precursor with high carbon yield and good solubility
[Display omitted] •Synthesis of p-conjugated poly(phenylacetylene) derivatives for carbon precursors.•Poly(PA-A) shows 90% C-yield but poor solubility.•Poly(PA-PA) shows 80% C-yield, good solubility, and facile thermal transformation.•Smooth dark-red poly(PA-PA) fibers were prepared using electrospi...
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Published in: | European polymer journal 2021-03, Vol.147 (C), p.110289, Article 110289 |
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container_title | European polymer journal |
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creator | Sengeh, Joseph Vandy Agboola, Olumide D. Li, Houxiang Zhu, Wei Mike Chung, T.C. |
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•Synthesis of p-conjugated poly(phenylacetylene) derivatives for carbon precursors.•Poly(PA-A) shows 90% C-yield but poor solubility.•Poly(PA-PA) shows 80% C-yield, good solubility, and facile thermal transformation.•Smooth dark-red poly(PA-PA) fibers were prepared using electrospinning.•The resulting carbon fibers exhibit a desirable polymorphous morphology.
This paper investigates a family of poly(phenylacetylene) derivatives with a p-electrons conjugated polymer backbone and side groups containing only sp2 and sp carbons. The objective is to identify the suitable carbon precursor that is processible and can be transformed to carbonaceous material with high carbon yield by a simple (one-step) thermal transformation process (without any external reagent). Poly(phenylacetylene) with para-substituted acetylene group poly(PA-A) shows an exceptionally high C-yield (~90%) in one-step heating from ambient temperature to 1000 °C under N2 atmosphere. Unfortunately, this poly(PA-A) polymer is quite sensitive to heat and light with very limited solubility. On the other hand, poly(phenylacetylene) with para-substituted phenylacetylene group, i.e. poly(PA-PA), offers a relatively high C-yield (~80%) and also good solubility in common organic solvents, such as toluene and tetrahydrofuran (THF). Several uniform dark-red poly(PA-PA) fibers with smooth surface and fiber diameter in the range of 3–6 μm were prepared from 30 wt% poly(PA-PA)/THF solution using electrospinning technique. The resulting precursor fibers were converted to the corresponding carbon structure in a one-step thermal heating process under N2 atmosphere. Both X-ray and Raman spectra show the polymorphous carbon morphology with the graphene crystalline domains. |
doi_str_mv | 10.1016/j.eurpolymj.2021.110289 |
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•Synthesis of p-conjugated poly(phenylacetylene) derivatives for carbon precursors.•Poly(PA-A) shows 90% C-yield but poor solubility.•Poly(PA-PA) shows 80% C-yield, good solubility, and facile thermal transformation.•Smooth dark-red poly(PA-PA) fibers were prepared using electrospinning.•The resulting carbon fibers exhibit a desirable polymorphous morphology.
This paper investigates a family of poly(phenylacetylene) derivatives with a p-electrons conjugated polymer backbone and side groups containing only sp2 and sp carbons. The objective is to identify the suitable carbon precursor that is processible and can be transformed to carbonaceous material with high carbon yield by a simple (one-step) thermal transformation process (without any external reagent). Poly(phenylacetylene) with para-substituted acetylene group poly(PA-A) shows an exceptionally high C-yield (~90%) in one-step heating from ambient temperature to 1000 °C under N2 atmosphere. Unfortunately, this poly(PA-A) polymer is quite sensitive to heat and light with very limited solubility. On the other hand, poly(phenylacetylene) with para-substituted phenylacetylene group, i.e. poly(PA-PA), offers a relatively high C-yield (~80%) and also good solubility in common organic solvents, such as toluene and tetrahydrofuran (THF). Several uniform dark-red poly(PA-PA) fibers with smooth surface and fiber diameter in the range of 3–6 μm were prepared from 30 wt% poly(PA-PA)/THF solution using electrospinning technique. The resulting precursor fibers were converted to the corresponding carbon structure in a one-step thermal heating process under N2 atmosphere. Both X-ray and Raman spectra show the polymorphous carbon morphology with the graphene crystalline domains.</description><identifier>ISSN: 0014-3057</identifier><identifier>EISSN: 1873-1945</identifier><identifier>DOI: 10.1016/j.eurpolymj.2021.110289</identifier><language>eng</language><publisher>Oxford: Elsevier Ltd</publisher><subject>Acetylene ; Ambient temperature ; Carbon ; Carbon fibers ; Carbon Materials ; Carbon Precursor ; Carbon Yield ; Carbonaceous materials ; Copolymers ; Electrospinning ; Graphene ; Heating ; Morphology ; Poly(phenylacetylene) Derivatives ; Polymerization ; Polymers ; Polyphenylacetylene ; Precursors ; Raman spectra ; Reagents ; Solubility ; Studies ; Substitutes ; Tetrahydrofuran ; Thermal transformations ; Toluene ; Wet-Spinning</subject><ispartof>European polymer journal, 2021-03, Vol.147 (C), p.110289, Article 110289</ispartof><rights>2021 Elsevier Ltd</rights><rights>Copyright Elsevier BV Mar 15, 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c419t-3617b54259cf279257f423305490dac5a5d43e927ccca6bbcdae560f14883e053</citedby><cites>FETCH-LOGICAL-c419t-3617b54259cf279257f423305490dac5a5d43e927ccca6bbcdae560f14883e053</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.osti.gov/biblio/1775731$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Sengeh, Joseph Vandy</creatorcontrib><creatorcontrib>Agboola, Olumide D.</creatorcontrib><creatorcontrib>Li, Houxiang</creatorcontrib><creatorcontrib>Zhu, Wei</creatorcontrib><creatorcontrib>Mike Chung, T.C.</creatorcontrib><title>Investigation of poly(phenylacetylene) derivatives for carbon precursor with high carbon yield and good solubility</title><title>European polymer journal</title><description>[Display omitted]
•Synthesis of p-conjugated poly(phenylacetylene) derivatives for carbon precursors.•Poly(PA-A) shows 90% C-yield but poor solubility.•Poly(PA-PA) shows 80% C-yield, good solubility, and facile thermal transformation.•Smooth dark-red poly(PA-PA) fibers were prepared using electrospinning.•The resulting carbon fibers exhibit a desirable polymorphous morphology.
This paper investigates a family of poly(phenylacetylene) derivatives with a p-electrons conjugated polymer backbone and side groups containing only sp2 and sp carbons. The objective is to identify the suitable carbon precursor that is processible and can be transformed to carbonaceous material with high carbon yield by a simple (one-step) thermal transformation process (without any external reagent). Poly(phenylacetylene) with para-substituted acetylene group poly(PA-A) shows an exceptionally high C-yield (~90%) in one-step heating from ambient temperature to 1000 °C under N2 atmosphere. Unfortunately, this poly(PA-A) polymer is quite sensitive to heat and light with very limited solubility. On the other hand, poly(phenylacetylene) with para-substituted phenylacetylene group, i.e. poly(PA-PA), offers a relatively high C-yield (~80%) and also good solubility in common organic solvents, such as toluene and tetrahydrofuran (THF). Several uniform dark-red poly(PA-PA) fibers with smooth surface and fiber diameter in the range of 3–6 μm were prepared from 30 wt% poly(PA-PA)/THF solution using electrospinning technique. The resulting precursor fibers were converted to the corresponding carbon structure in a one-step thermal heating process under N2 atmosphere. Both X-ray and Raman spectra show the polymorphous carbon morphology with the graphene crystalline domains.</description><subject>Acetylene</subject><subject>Ambient temperature</subject><subject>Carbon</subject><subject>Carbon fibers</subject><subject>Carbon Materials</subject><subject>Carbon Precursor</subject><subject>Carbon Yield</subject><subject>Carbonaceous materials</subject><subject>Copolymers</subject><subject>Electrospinning</subject><subject>Graphene</subject><subject>Heating</subject><subject>Morphology</subject><subject>Poly(phenylacetylene) Derivatives</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Polyphenylacetylene</subject><subject>Precursors</subject><subject>Raman spectra</subject><subject>Reagents</subject><subject>Solubility</subject><subject>Studies</subject><subject>Substitutes</subject><subject>Tetrahydrofuran</subject><subject>Thermal transformations</subject><subject>Toluene</subject><subject>Wet-Spinning</subject><issn>0014-3057</issn><issn>1873-1945</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNqFkc1u3CAUhVHVSp1O-wxFzSZdeMKPMeNlFKVNpEjZpGuE4XqM5YAD9kR--2K5zTYbkOC7R-fcg9B3Sg6U0OqqP8AcxzAsz_2BEUYPlBJ2rD-gHT1KXtC6FB_RjhBaFpwI-Rl9SaknhEhe8R2K9_4MaXInPbngcWjxKnU5duCXQRuYlgE8_MQWojtnJsO4DREbHZvMjxHMHFN-eHVThzt36v5_LQ4Gi7W3-BSCxSkMc-MGNy1f0adWDwm-_bv36M-v26ebu-Lh8ff9zfVDYUpaTwWvqGxEyURtWiZrJmRbMp4jlDWx2ggtbMmhZtIYo6umMVaDqEhLy-ORAxF8j35suiHnU8m4CUxngvdgJkWlFJLTDF1s0BjDy5w3ofowR599KSby7jit87FHcqNMDClFaNUY3bOOi6JErS2oXr21oNYW1NZCnrzeJiEnPTuIqxHwBqyLqw8b3LsafwFyK5al</recordid><startdate>20210315</startdate><enddate>20210315</enddate><creator>Sengeh, Joseph Vandy</creator><creator>Agboola, Olumide D.</creator><creator>Li, Houxiang</creator><creator>Zhu, Wei</creator><creator>Mike Chung, T.C.</creator><general>Elsevier Ltd</general><general>Elsevier BV</general><general>Elsevier</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><scope>OTOTI</scope></search><sort><creationdate>20210315</creationdate><title>Investigation of poly(phenylacetylene) derivatives for carbon precursor with high carbon yield and good solubility</title><author>Sengeh, Joseph Vandy ; Agboola, Olumide D. ; Li, Houxiang ; Zhu, Wei ; Mike Chung, T.C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c419t-3617b54259cf279257f423305490dac5a5d43e927ccca6bbcdae560f14883e053</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Acetylene</topic><topic>Ambient temperature</topic><topic>Carbon</topic><topic>Carbon fibers</topic><topic>Carbon Materials</topic><topic>Carbon Precursor</topic><topic>Carbon Yield</topic><topic>Carbonaceous materials</topic><topic>Copolymers</topic><topic>Electrospinning</topic><topic>Graphene</topic><topic>Heating</topic><topic>Morphology</topic><topic>Poly(phenylacetylene) Derivatives</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Polyphenylacetylene</topic><topic>Precursors</topic><topic>Raman spectra</topic><topic>Reagents</topic><topic>Solubility</topic><topic>Studies</topic><topic>Substitutes</topic><topic>Tetrahydrofuran</topic><topic>Thermal transformations</topic><topic>Toluene</topic><topic>Wet-Spinning</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sengeh, Joseph Vandy</creatorcontrib><creatorcontrib>Agboola, Olumide D.</creatorcontrib><creatorcontrib>Li, Houxiang</creatorcontrib><creatorcontrib>Zhu, Wei</creatorcontrib><creatorcontrib>Mike Chung, T.C.</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>OSTI.GOV</collection><jtitle>European polymer journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sengeh, Joseph Vandy</au><au>Agboola, Olumide D.</au><au>Li, Houxiang</au><au>Zhu, Wei</au><au>Mike Chung, T.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Investigation of poly(phenylacetylene) derivatives for carbon precursor with high carbon yield and good solubility</atitle><jtitle>European polymer journal</jtitle><date>2021-03-15</date><risdate>2021</risdate><volume>147</volume><issue>C</issue><spage>110289</spage><pages>110289-</pages><artnum>110289</artnum><issn>0014-3057</issn><eissn>1873-1945</eissn><abstract>[Display omitted]
•Synthesis of p-conjugated poly(phenylacetylene) derivatives for carbon precursors.•Poly(PA-A) shows 90% C-yield but poor solubility.•Poly(PA-PA) shows 80% C-yield, good solubility, and facile thermal transformation.•Smooth dark-red poly(PA-PA) fibers were prepared using electrospinning.•The resulting carbon fibers exhibit a desirable polymorphous morphology.
This paper investigates a family of poly(phenylacetylene) derivatives with a p-electrons conjugated polymer backbone and side groups containing only sp2 and sp carbons. The objective is to identify the suitable carbon precursor that is processible and can be transformed to carbonaceous material with high carbon yield by a simple (one-step) thermal transformation process (without any external reagent). Poly(phenylacetylene) with para-substituted acetylene group poly(PA-A) shows an exceptionally high C-yield (~90%) in one-step heating from ambient temperature to 1000 °C under N2 atmosphere. Unfortunately, this poly(PA-A) polymer is quite sensitive to heat and light with very limited solubility. On the other hand, poly(phenylacetylene) with para-substituted phenylacetylene group, i.e. poly(PA-PA), offers a relatively high C-yield (~80%) and also good solubility in common organic solvents, such as toluene and tetrahydrofuran (THF). Several uniform dark-red poly(PA-PA) fibers with smooth surface and fiber diameter in the range of 3–6 μm were prepared from 30 wt% poly(PA-PA)/THF solution using electrospinning technique. The resulting precursor fibers were converted to the corresponding carbon structure in a one-step thermal heating process under N2 atmosphere. Both X-ray and Raman spectra show the polymorphous carbon morphology with the graphene crystalline domains.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><doi>10.1016/j.eurpolymj.2021.110289</doi><oa>free_for_read</oa></addata></record> |
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subjects | Acetylene Ambient temperature Carbon Carbon fibers Carbon Materials Carbon Precursor Carbon Yield Carbonaceous materials Copolymers Electrospinning Graphene Heating Morphology Poly(phenylacetylene) Derivatives Polymerization Polymers Polyphenylacetylene Precursors Raman spectra Reagents Solubility Studies Substitutes Tetrahydrofuran Thermal transformations Toluene Wet-Spinning |
title | Investigation of poly(phenylacetylene) derivatives for carbon precursor with high carbon yield and good solubility |
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