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Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A
Deep eutectic solvent molecularly imprinted polymer (DES-MIP) was synthesized by bulk polymerization via free radical polymerization using bisphenol A (BPA) as a template, DES as a functional monomer, ethylene glycol dimethyl acrylate (EGDMA) as a crosslinker and benzoyl peroxide as initiator. DES f...
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Published in: | Journal of polymer research 2023-06, Vol.30 (6), Article 205 |
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description | Deep eutectic solvent molecularly imprinted polymer (DES-MIP) was synthesized by bulk polymerization via free radical polymerization using bisphenol A (BPA) as a template, DES as a functional monomer, ethylene glycol dimethyl acrylate (EGDMA) as a crosslinker and benzoyl peroxide as initiator. DES functional monomer was prepared by the combination of choline chloride methacrylic acid (ChCl-MAA). The synthesized DES-MIP was then compared with conventional molecularly imprinted polymer (MIP) synthesized using methacrylic acid (MAA) as a functional monomer. The DES-MIP has a higher selectivity for BPA (17.72 mg/g) than competing chemicals, including bisphenol AP (9.78 mg/g), 2-naphthol (8.25), and 4-tertiary butyl-phenol (6.98 mg/g). The optimization parameters include the effects of pH, adsorption kinetics, adsorption isotherm, and thermodynamic studies were investigated. DES-MIP showed the highest binding capacity at pH 7. The kinetic and isotherm studies demonstrated good agreement with a pseudo-second-order kinetic model and Langmuir isotherm models, respectively. The thermodynamic study proved that the adsorption of BPA on DES-MIP was exothermic and spontaneous with
ΔH
0
(-23.734 × kJ/mol) and
ΔG
0
(-2.929 kJ/mol
−
). Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. As a result, it proved that the contribution of DES as a functional monomer alternative in MIP synthesis considerably improved the recognition of BPA adsorption. |
doi_str_mv | 10.1007/s10965-023-03581-1 |
format | article |
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ΔH
0
(-23.734 × kJ/mol) and
ΔG
0
(-2.929 kJ/mol
−
). Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. As a result, it proved that the contribution of DES as a functional monomer alternative in MIP synthesis considerably improved the recognition of BPA adsorption.</description><identifier>ISSN: 1022-9760</identifier><identifier>EISSN: 1572-8935</identifier><identifier>DOI: 10.1007/s10965-023-03581-1</identifier><language>eng</language><publisher>Dordrecht: Springer Netherlands</publisher><subject>Adsorption ; Analysis ; Benzoyl peroxide ; Bisphenol A ; Bulk polymerization ; Characterization and Evaluation of Materials ; Chemistry ; Chemistry and Materials Science ; Choline ; Ethylene glycol ; Free radical polymerization ; Free radicals ; Imprinted polymers ; Industrial Chemistry/Chemical Engineering ; Isotherms ; Methacrylic acid ; Monomers ; Optimization ; Original Paper ; Phenols ; Polymer industry ; Polymer Sciences ; Polymerization ; Polymers ; Solvents ; Synthesis ; Thermal properties ; Thermodynamics</subject><ispartof>Journal of polymer research, 2023-06, Vol.30 (6), Article 205</ispartof><rights>The Polymer Society, Taipei 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>COPYRIGHT 2023 Springer</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c358t-b5c427cbb5ced822a36062572a6c8c1af921ab49eeba040ba38a0e69878387773</citedby><cites>FETCH-LOGICAL-c358t-b5c427cbb5ced822a36062572a6c8c1af921ab49eeba040ba38a0e69878387773</cites><orcidid>0000-0002-4421-1745</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Shah, Syed Asim Hussain</creatorcontrib><creatorcontrib>Asman, Saliza</creatorcontrib><title>Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A</title><title>Journal of polymer research</title><addtitle>J Polym Res</addtitle><description>Deep eutectic solvent molecularly imprinted polymer (DES-MIP) was synthesized by bulk polymerization via free radical polymerization using bisphenol A (BPA) as a template, DES as a functional monomer, ethylene glycol dimethyl acrylate (EGDMA) as a crosslinker and benzoyl peroxide as initiator. DES functional monomer was prepared by the combination of choline chloride methacrylic acid (ChCl-MAA). The synthesized DES-MIP was then compared with conventional molecularly imprinted polymer (MIP) synthesized using methacrylic acid (MAA) as a functional monomer. The DES-MIP has a higher selectivity for BPA (17.72 mg/g) than competing chemicals, including bisphenol AP (9.78 mg/g), 2-naphthol (8.25), and 4-tertiary butyl-phenol (6.98 mg/g). The optimization parameters include the effects of pH, adsorption kinetics, adsorption isotherm, and thermodynamic studies were investigated. DES-MIP showed the highest binding capacity at pH 7. The kinetic and isotherm studies demonstrated good agreement with a pseudo-second-order kinetic model and Langmuir isotherm models, respectively. The thermodynamic study proved that the adsorption of BPA on DES-MIP was exothermic and spontaneous with
ΔH
0
(-23.734 × kJ/mol) and
ΔG
0
(-2.929 kJ/mol
−
). Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. As a result, it proved that the contribution of DES as a functional monomer alternative in MIP synthesis considerably improved the recognition of BPA adsorption.</description><subject>Adsorption</subject><subject>Analysis</subject><subject>Benzoyl peroxide</subject><subject>Bisphenol A</subject><subject>Bulk polymerization</subject><subject>Characterization and Evaluation of Materials</subject><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Choline</subject><subject>Ethylene glycol</subject><subject>Free radical polymerization</subject><subject>Free radicals</subject><subject>Imprinted polymers</subject><subject>Industrial Chemistry/Chemical Engineering</subject><subject>Isotherms</subject><subject>Methacrylic acid</subject><subject>Monomers</subject><subject>Optimization</subject><subject>Original Paper</subject><subject>Phenols</subject><subject>Polymer industry</subject><subject>Polymer Sciences</subject><subject>Polymerization</subject><subject>Polymers</subject><subject>Solvents</subject><subject>Synthesis</subject><subject>Thermal properties</subject><subject>Thermodynamics</subject><issn>1022-9760</issn><issn>1572-8935</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9UU1LxDAQLaLg-vEHPAU8VydJ2yTHRfwCwYueQ5qdapc0qUmr7L83awVvMocZwntv8uYVxQWFKwogrhMF1dQlMF4CryUt6UGxorVgpVS8PswzMFYq0cBxcZLSFqCuRSNXRbz9NG42Ux88CR3ZII4E5wnt1FuSgvtEPxGTiCEev8gQfBgwki7EPDu0szPR7Ug_jLH3E27IGNwuI9IPJOIQsvxeuO3T-I4-OLI-K4464xKe__bT4vXu9uXmoXx6vn-8WT-VNjuYyra2FRO2zR03kjHDG2hYtmQaKy01nWLUtJVCbA1U0BouDWCjpJBcCiH4aXG56I4xfMyYJr0Nc_R5pWaScgDaKJpRVwvqzTjUve_CFI3NtcGht8Fj1-f3tagUpVWl6kxgC8HGkFLETmfvg4k7TUHvw9BLGDqHoX_C0PstfCGl_aHeMP795R_WN6uujbw</recordid><startdate>20230601</startdate><enddate>20230601</enddate><creator>Shah, Syed Asim Hussain</creator><creator>Asman, Saliza</creator><general>Springer Netherlands</general><general>Springer</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope><orcidid>https://orcid.org/0000-0002-4421-1745</orcidid></search><sort><creationdate>20230601</creationdate><title>Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A</title><author>Shah, Syed Asim Hussain ; Asman, Saliza</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c358t-b5c427cbb5ced822a36062572a6c8c1af921ab49eeba040ba38a0e69878387773</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adsorption</topic><topic>Analysis</topic><topic>Benzoyl peroxide</topic><topic>Bisphenol A</topic><topic>Bulk polymerization</topic><topic>Characterization and Evaluation of Materials</topic><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Choline</topic><topic>Ethylene glycol</topic><topic>Free radical polymerization</topic><topic>Free radicals</topic><topic>Imprinted polymers</topic><topic>Industrial Chemistry/Chemical Engineering</topic><topic>Isotherms</topic><topic>Methacrylic acid</topic><topic>Monomers</topic><topic>Optimization</topic><topic>Original Paper</topic><topic>Phenols</topic><topic>Polymer industry</topic><topic>Polymer Sciences</topic><topic>Polymerization</topic><topic>Polymers</topic><topic>Solvents</topic><topic>Synthesis</topic><topic>Thermal properties</topic><topic>Thermodynamics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shah, Syed Asim Hussain</creatorcontrib><creatorcontrib>Asman, Saliza</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of polymer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shah, Syed Asim Hussain</au><au>Asman, Saliza</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A</atitle><jtitle>Journal of polymer research</jtitle><stitle>J Polym Res</stitle><date>2023-06-01</date><risdate>2023</risdate><volume>30</volume><issue>6</issue><artnum>205</artnum><issn>1022-9760</issn><eissn>1572-8935</eissn><abstract>Deep eutectic solvent molecularly imprinted polymer (DES-MIP) was synthesized by bulk polymerization via free radical polymerization using bisphenol A (BPA) as a template, DES as a functional monomer, ethylene glycol dimethyl acrylate (EGDMA) as a crosslinker and benzoyl peroxide as initiator. DES functional monomer was prepared by the combination of choline chloride methacrylic acid (ChCl-MAA). The synthesized DES-MIP was then compared with conventional molecularly imprinted polymer (MIP) synthesized using methacrylic acid (MAA) as a functional monomer. The DES-MIP has a higher selectivity for BPA (17.72 mg/g) than competing chemicals, including bisphenol AP (9.78 mg/g), 2-naphthol (8.25), and 4-tertiary butyl-phenol (6.98 mg/g). The optimization parameters include the effects of pH, adsorption kinetics, adsorption isotherm, and thermodynamic studies were investigated. DES-MIP showed the highest binding capacity at pH 7. The kinetic and isotherm studies demonstrated good agreement with a pseudo-second-order kinetic model and Langmuir isotherm models, respectively. The thermodynamic study proved that the adsorption of BPA on DES-MIP was exothermic and spontaneous with
ΔH
0
(-23.734 × kJ/mol) and
ΔG
0
(-2.929 kJ/mol
−
). Reusability experiments show that the DES-MIP can be recycled five times without significantly diminishing its adsorption capacity. As a result, it proved that the contribution of DES as a functional monomer alternative in MIP synthesis considerably improved the recognition of BPA adsorption.</abstract><cop>Dordrecht</cop><pub>Springer Netherlands</pub><doi>10.1007/s10965-023-03581-1</doi><orcidid>https://orcid.org/0000-0002-4421-1745</orcidid></addata></record> |
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subjects | Adsorption Analysis Benzoyl peroxide Bisphenol A Bulk polymerization Characterization and Evaluation of Materials Chemistry Chemistry and Materials Science Choline Ethylene glycol Free radical polymerization Free radicals Imprinted polymers Industrial Chemistry/Chemical Engineering Isotherms Methacrylic acid Monomers Optimization Original Paper Phenols Polymer industry Polymer Sciences Polymerization Polymers Solvents Synthesis Thermal properties Thermodynamics |
title | Evaluation of deep eutectic solvent as a new monomer for molecularly imprinted polymers for removal of bisphenol A |
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