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Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution

A series of methylamine-modified hyper-cross-linked resins were fabricated from chloromethylated polystrene-co-divinylbenzene by two continuous reactions (Friedel-Crafts alkylation and amination). The BET surface area and pore volume of the as-prepared resins took a positive correlation to the react...

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Autores principales: Peng, Xiaoqiang, Yang, Pengpeng, Dai, Kun, Chen, Yong, Chen, Xiaochun, Zhuang, Wei, Ying, Hanjie, Wu, Jinglan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295785/
https://www.ncbi.nlm.nih.gov/pubmed/32541885
http://dx.doi.org/10.1038/s41598-020-66592-8
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author Peng, Xiaoqiang
Yang, Pengpeng
Dai, Kun
Chen, Yong
Chen, Xiaochun
Zhuang, Wei
Ying, Hanjie
Wu, Jinglan
author_facet Peng, Xiaoqiang
Yang, Pengpeng
Dai, Kun
Chen, Yong
Chen, Xiaochun
Zhuang, Wei
Ying, Hanjie
Wu, Jinglan
author_sort Peng, Xiaoqiang
collection PubMed
description A series of methylamine-modified hyper-cross-linked resins were fabricated from chloromethylated polystrene-co-divinylbenzene by two continuous reactions (Friedel-Crafts alkylation and amination). The BET surface area and pore volume of the as-prepared resins took a positive correlation to the reaction time and temperature during alkylation reaction while lessened during amination process. When running batch adsorption experiments for adsorption of citric acid, the methylamine-modified resin named HM-65-2 showed higher adsorption capacity of 136.3 mg/g and selectivity of 6.98 (citric/glucose) than the precursor resins. The pseudo-second-order rate model fitted better than the pseudo-first-order model, implying the adsorption sites distributed on the resins surface tended to be heterogeneous. Subsequently, the interactions between citric acid and the resin were investigated by means of molecular simulation. Simulation result showed the addition of nitrogen-containing groups significantly enhanced the adsorption performance of citric acid. Lastly, the dynamic column experiments were performed to obtain the suitable operating conditions for the citric acid adsorption.
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spelling pubmed-72957852020-06-17 Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution Peng, Xiaoqiang Yang, Pengpeng Dai, Kun Chen, Yong Chen, Xiaochun Zhuang, Wei Ying, Hanjie Wu, Jinglan Sci Rep Article A series of methylamine-modified hyper-cross-linked resins were fabricated from chloromethylated polystrene-co-divinylbenzene by two continuous reactions (Friedel-Crafts alkylation and amination). The BET surface area and pore volume of the as-prepared resins took a positive correlation to the reaction time and temperature during alkylation reaction while lessened during amination process. When running batch adsorption experiments for adsorption of citric acid, the methylamine-modified resin named HM-65-2 showed higher adsorption capacity of 136.3 mg/g and selectivity of 6.98 (citric/glucose) than the precursor resins. The pseudo-second-order rate model fitted better than the pseudo-first-order model, implying the adsorption sites distributed on the resins surface tended to be heterogeneous. Subsequently, the interactions between citric acid and the resin were investigated by means of molecular simulation. Simulation result showed the addition of nitrogen-containing groups significantly enhanced the adsorption performance of citric acid. Lastly, the dynamic column experiments were performed to obtain the suitable operating conditions for the citric acid adsorption. Nature Publishing Group UK 2020-06-15 /pmc/articles/PMC7295785/ /pubmed/32541885 http://dx.doi.org/10.1038/s41598-020-66592-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Peng, Xiaoqiang
Yang, Pengpeng
Dai, Kun
Chen, Yong
Chen, Xiaochun
Zhuang, Wei
Ying, Hanjie
Wu, Jinglan
Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
title Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
title_full Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
title_fullStr Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
title_full_unstemmed Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
title_short Synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
title_sort synthesis, adsorption and molecular simulation study of methylamine-modified hyper-cross-linked resins for efficient removal of citric acid from aqueous solution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7295785/
https://www.ncbi.nlm.nih.gov/pubmed/32541885
http://dx.doi.org/10.1038/s41598-020-66592-8
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