Adsorption of sulfadiazine on novel bilayer porous resin: Synergism of micropore filling and anion exchange

Wei Sun, Guqing Xiao, Qiudong Meng
{"title":"Adsorption of sulfadiazine on novel bilayer porous resin: Synergism of micropore filling and anion exchange","authors":"Wei Sun, Guqing Xiao, Qiudong Meng","doi":"10.1016/j.mseb.2023.117039","DOIUrl":null,"url":null,"abstract":"<p>A novel bilayer porous resin with micropore filling and anion exchange (PsCH<sub>2</sub>BP) was synthesized. The aim was to investigate the adsorption of sulfadiazine on PsCH<sub>2</sub>BP. The micropore area of PsCH<sub>2</sub>BP was reduced by 73.91 % after the adsorption of sulfadiazine. PsCH<sub>2</sub>BP exhibited the synergism of micropore filling and anion exchange in the adsorption of sulfadiazine. Within the pH range of 7.29–13.31, the adsorption capacity trend of sulfadiazine on PsCH<sub>2</sub>BP was consistent with its ionization curve of pka 6.48. The adsorption of sulfadiazine on PsCH<sub>2</sub><span>BP was endothermic, spontaneous, entropy increase and heterogeneous multilayer adsorption, reflecting the bilayer pore structure of PsCH</span><sub>2</sub>BP. 100 % C<sub>2</sub>H<sub>5</sub>OH and 4 % NaCl could desorb 75.13 % and 65.06 % of sulfadiazine adsorbed on PsCH<sub>2</sub>BP, respectively, reflecting the synergism of the micropore filling and anion exchange in the adsorption of sulfadiazine on PsCH<sub>2</sub>BP. 100 % of desorption ratio of sulfadiazine adsorbed by PsCH<sub>2</sub>BP was achieved with 4 mol/LNaOH.</p>","PeriodicalId":501486,"journal":{"name":"Materials Science and Engineering: B","volume":"258 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-11-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Materials Science and Engineering: B","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.mseb.2023.117039","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

A novel bilayer porous resin with micropore filling and anion exchange (PsCH2BP) was synthesized. The aim was to investigate the adsorption of sulfadiazine on PsCH2BP. The micropore area of PsCH2BP was reduced by 73.91 % after the adsorption of sulfadiazine. PsCH2BP exhibited the synergism of micropore filling and anion exchange in the adsorption of sulfadiazine. Within the pH range of 7.29–13.31, the adsorption capacity trend of sulfadiazine on PsCH2BP was consistent with its ionization curve of pka 6.48. The adsorption of sulfadiazine on PsCH2BP was endothermic, spontaneous, entropy increase and heterogeneous multilayer adsorption, reflecting the bilayer pore structure of PsCH2BP. 100 % C2H5OH and 4 % NaCl could desorb 75.13 % and 65.06 % of sulfadiazine adsorbed on PsCH2BP, respectively, reflecting the synergism of the micropore filling and anion exchange in the adsorption of sulfadiazine on PsCH2BP. 100 % of desorption ratio of sulfadiazine adsorbed by PsCH2BP was achieved with 4 mol/LNaOH.

Abstract Image

新型双层多孔树脂对磺胺嘧啶的吸附:微孔填充与阴离子交换的协同作用
合成了一种具有微孔填充和阴离子交换功能的双层多孔树脂(PsCH2BP)。目的是研究磺胺嘧啶在PsCH2BP上的吸附。吸附磺胺嘧啶后,PsCH2BP的微孔面积减少了73.91%。PsCH2BP在吸附磺胺嘧啶过程中表现出微孔填充和阴离子交换的协同作用。在pH为7.29 ~ 13.31的范围内,磺胺嘧啶在PsCH2BP上的吸附量趋势与pka 6.48的电离曲线一致。磺胺嘧啶在PsCH2BP上的吸附是吸热、自发、熵增和非均相的多层吸附,反映了PsCH2BP的双层孔结构。100% C2H5OH和4% NaCl对吸附在PsCH2BP上的磺胺嘧啶的解吸率分别为75.13%和65.06%,反映了微孔填充和阴离子交换对PsCH2BP吸附磺胺嘧啶的协同作用。在4 mol/LNaOH条件下,PsCH2BP对磺胺嘧啶的解吸率达到100%。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信