Carbonate-based hyper-cross-linked polymers with pendant versatile electron-withdrawing functional groups for CO2 adsorption and separation
The simple and highly efficient preparation of porous hyper-cross-linked polymers (HCPs) with high surface area and manifold functionalities for high-performance CO2 uptake and selective separation has drawn significant attention in the past decade. Herein, three low-cost carbonates rich in electron...
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Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-07, Vol.10 (28), p.15062-15073 |
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description | The simple and highly efficient preparation of porous hyper-cross-linked polymers (HCPs) with high surface area and manifold functionalities for high-performance CO2 uptake and selective separation has drawn significant attention in the past decade. Herein, three low-cost carbonates rich in electron-withdrawing carbonyl and ester groups, fluorine atoms and electron-donating heteroatoms such as N, were used as building blocks to fabricate a series of novel and functional HCPs via the typical one-step Friedel–Crafts alkylation reaction under mild conditions, which has been scarcely reported to date. The resulting functional polymers were permanently microporous and the polymer enriched with nitrogen atoms and carbonyl and ester groups possessed the highest BET surface area of 1367 m2 g−1, Langmuir surface area of up to 2058 m2 g−1, CO2 uptake of 14.61 wt% at 273.15 K/1.00 bar, H2 adsorption of 1.28 wt% at 77.3 K/1.00 bar, and CH4 storage of 1.79 wt% at 273.15 K/1.00 bar. Besides, the structurally accessible functional groups and heteroatoms were able to endow the resultant polymers with improved gas adsorption selectivity for CO2/N2 (20.16) and CO2/CH4 (41.84) at 273.15 K and a low-pressure coverage of less than 0.3 bar according to Henry's law (initial slope ratio). In addition, it was found that by fine tuning the molecular structure of the employed building blocks, the texture property and gas capturing capacity of the obtained polymers can also be rationally tuned, and detailed insight from the viewpoint of structure–property relationships has been provided. |
doi_str_mv | 10.1039/d2ta02774g |
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Herein, three low-cost carbonates rich in electron-withdrawing carbonyl and ester groups, fluorine atoms and electron-donating heteroatoms such as N, were used as building blocks to fabricate a series of novel and functional HCPs via the typical one-step Friedel–Crafts alkylation reaction under mild conditions, which has been scarcely reported to date. The resulting functional polymers were permanently microporous and the polymer enriched with nitrogen atoms and carbonyl and ester groups possessed the highest BET surface area of 1367 m2 g−1, Langmuir surface area of up to 2058 m2 g−1, CO2 uptake of 14.61 wt% at 273.15 K/1.00 bar, H2 adsorption of 1.28 wt% at 77.3 K/1.00 bar, and CH4 storage of 1.79 wt% at 273.15 K/1.00 bar. Besides, the structurally accessible functional groups and heteroatoms were able to endow the resultant polymers with improved gas adsorption selectivity for CO2/N2 (20.16) and CO2/CH4 (41.84) at 273.15 K and a low-pressure coverage of less than 0.3 bar according to Henry's law (initial slope ratio). In addition, it was found that by fine tuning the molecular structure of the employed building blocks, the texture property and gas capturing capacity of the obtained polymers can also be rationally tuned, and detailed insight from the viewpoint of structure–property relationships has been provided.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/d2ta02774g</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Adsorption ; Alkylation ; Carbon dioxide ; Carbonates ; Carbonyl compounds ; Carbonyls ; Crosslinking ; Electrons ; Fluorine ; Functional groups ; Henrys law ; Low pressure ; Methane ; Molecular structure ; Nitrogen atoms ; Polymers ; Selectivity ; Separation ; Surface area ; Surface chemistry</subject><ispartof>Journal of materials chemistry. A, Materials for energy and sustainability, 2022-07, Vol.10 (28), p.15062-15073</ispartof><rights>Copyright Royal Society of Chemistry 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids></links><search><creatorcontrib>Hou, Shuangshuang</creatorcontrib><creatorcontrib>Hu, Jiarui</creatorcontrib><creatorcontrib>Liang, Xueting</creatorcontrib><creatorcontrib>Zhang, Daohong</creatorcontrib><creatorcontrib>Bien Tan</creatorcontrib><title>Carbonate-based hyper-cross-linked polymers with pendant versatile electron-withdrawing functional groups for CO2 adsorption and separation</title><title>Journal of materials chemistry. A, Materials for energy and sustainability</title><description>The simple and highly efficient preparation of porous hyper-cross-linked polymers (HCPs) with high surface area and manifold functionalities for high-performance CO2 uptake and selective separation has drawn significant attention in the past decade. Herein, three low-cost carbonates rich in electron-withdrawing carbonyl and ester groups, fluorine atoms and electron-donating heteroatoms such as N, were used as building blocks to fabricate a series of novel and functional HCPs via the typical one-step Friedel–Crafts alkylation reaction under mild conditions, which has been scarcely reported to date. The resulting functional polymers were permanently microporous and the polymer enriched with nitrogen atoms and carbonyl and ester groups possessed the highest BET surface area of 1367 m2 g−1, Langmuir surface area of up to 2058 m2 g−1, CO2 uptake of 14.61 wt% at 273.15 K/1.00 bar, H2 adsorption of 1.28 wt% at 77.3 K/1.00 bar, and CH4 storage of 1.79 wt% at 273.15 K/1.00 bar. Besides, the structurally accessible functional groups and heteroatoms were able to endow the resultant polymers with improved gas adsorption selectivity for CO2/N2 (20.16) and CO2/CH4 (41.84) at 273.15 K and a low-pressure coverage of less than 0.3 bar according to Henry's law (initial slope ratio). In addition, it was found that by fine tuning the molecular structure of the employed building blocks, the texture property and gas capturing capacity of the obtained polymers can also be rationally tuned, and detailed insight from the viewpoint of structure–property relationships has been provided.</description><subject>Adsorption</subject><subject>Alkylation</subject><subject>Carbon dioxide</subject><subject>Carbonates</subject><subject>Carbonyl compounds</subject><subject>Carbonyls</subject><subject>Crosslinking</subject><subject>Electrons</subject><subject>Fluorine</subject><subject>Functional groups</subject><subject>Henrys law</subject><subject>Low pressure</subject><subject>Methane</subject><subject>Molecular structure</subject><subject>Nitrogen atoms</subject><subject>Polymers</subject><subject>Selectivity</subject><subject>Separation</subject><subject>Surface area</subject><subject>Surface chemistry</subject><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNo9kN1KAzEQhYMoWGpvfIKA19FJsj_JpRT_oNAbvS6zm2y7dU1ikrX0GXxptyjOzZnzHTgMQ8g1h1sOUt8ZkRFEXRfbMzITUAKrC12d_-9KXZJFSnuYRgFUWs_I9xJj4x1myxpM1tDdMdjI2uhTYkPv3icU_HD8sDHRQ593NFhn0GX6NRHM_WCpHWybo3fslJuIh95taTe6NvdT80C30Y8h0c5HulwLiib5GE4ZRWdosgEjnuwVuehwSHbxp3Py9vjwunxmq_XTy_J-xQJXMrOKl0JYkEUDFRc1ytZUyEEjb60UbSexFGClBm1aoRqhodQAXTO9RqmiAjknN7-9IfrP0aa82fsxTpemjag0L6GWSssfIydneg</recordid><startdate>20220719</startdate><enddate>20220719</enddate><creator>Hou, Shuangshuang</creator><creator>Hu, Jiarui</creator><creator>Liang, Xueting</creator><creator>Zhang, Daohong</creator><creator>Bien Tan</creator><general>Royal Society of Chemistry</general><scope>7SP</scope><scope>7SR</scope><scope>7ST</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>C1K</scope><scope>JG9</scope><scope>L7M</scope><scope>SOI</scope></search><sort><creationdate>20220719</creationdate><title>Carbonate-based hyper-cross-linked polymers with pendant versatile electron-withdrawing functional groups for CO2 adsorption and separation</title><author>Hou, Shuangshuang ; Hu, Jiarui ; Liang, Xueting ; Zhang, Daohong ; Bien Tan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p183t-61522e034b06127a3cd6a109a1ce32cf3a520e3909dc28b2905900fb027884603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Adsorption</topic><topic>Alkylation</topic><topic>Carbon dioxide</topic><topic>Carbonates</topic><topic>Carbonyl compounds</topic><topic>Carbonyls</topic><topic>Crosslinking</topic><topic>Electrons</topic><topic>Fluorine</topic><topic>Functional groups</topic><topic>Henrys law</topic><topic>Low pressure</topic><topic>Methane</topic><topic>Molecular structure</topic><topic>Nitrogen atoms</topic><topic>Polymers</topic><topic>Selectivity</topic><topic>Separation</topic><topic>Surface area</topic><topic>Surface chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hou, Shuangshuang</creatorcontrib><creatorcontrib>Hu, Jiarui</creatorcontrib><creatorcontrib>Liang, Xueting</creatorcontrib><creatorcontrib>Zhang, Daohong</creatorcontrib><creatorcontrib>Bien Tan</creatorcontrib><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environment Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><collection>Environment Abstracts</collection><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hou, Shuangshuang</au><au>Hu, Jiarui</au><au>Liang, Xueting</au><au>Zhang, Daohong</au><au>Bien Tan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Carbonate-based hyper-cross-linked polymers with pendant versatile electron-withdrawing functional groups for CO2 adsorption and separation</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2022-07-19</date><risdate>2022</risdate><volume>10</volume><issue>28</issue><spage>15062</spage><epage>15073</epage><pages>15062-15073</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>The simple and highly efficient preparation of porous hyper-cross-linked polymers (HCPs) with high surface area and manifold functionalities for high-performance CO2 uptake and selective separation has drawn significant attention in the past decade. Herein, three low-cost carbonates rich in electron-withdrawing carbonyl and ester groups, fluorine atoms and electron-donating heteroatoms such as N, were used as building blocks to fabricate a series of novel and functional HCPs via the typical one-step Friedel–Crafts alkylation reaction under mild conditions, which has been scarcely reported to date. The resulting functional polymers were permanently microporous and the polymer enriched with nitrogen atoms and carbonyl and ester groups possessed the highest BET surface area of 1367 m2 g−1, Langmuir surface area of up to 2058 m2 g−1, CO2 uptake of 14.61 wt% at 273.15 K/1.00 bar, H2 adsorption of 1.28 wt% at 77.3 K/1.00 bar, and CH4 storage of 1.79 wt% at 273.15 K/1.00 bar. Besides, the structurally accessible functional groups and heteroatoms were able to endow the resultant polymers with improved gas adsorption selectivity for CO2/N2 (20.16) and CO2/CH4 (41.84) at 273.15 K and a low-pressure coverage of less than 0.3 bar according to Henry's law (initial slope ratio). In addition, it was found that by fine tuning the molecular structure of the employed building blocks, the texture property and gas capturing capacity of the obtained polymers can also be rationally tuned, and detailed insight from the viewpoint of structure–property relationships has been provided.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/d2ta02774g</doi><tpages>12</tpages></addata></record> |
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source | Royal Society Of Chemistry Journals 2008- |
subjects | Adsorption Alkylation Carbon dioxide Carbonates Carbonyl compounds Carbonyls Crosslinking Electrons Fluorine Functional groups Henrys law Low pressure Methane Molecular structure Nitrogen atoms Polymers Selectivity Separation Surface area Surface chemistry |
title | Carbonate-based hyper-cross-linked polymers with pendant versatile electron-withdrawing functional groups for CO2 adsorption and separation |
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