Pyrazine substituted chitosan: an adsorbent material for the efficient removal of anionic dyes from aqueous solutions

IF 2.6 4区 化学 Q3 POLYMER SCIENCE
S. M Anush, C. S Kaliprasad, Gangadhar Gowda P H, B. H Gayathri, Y. R Girish, K Prashantha, Subramaniyan Ramasundaram, Mohammad Altaf, Tae Hwan Oh, Mani Durai
{"title":"Pyrazine substituted chitosan: an adsorbent material for the efficient removal of anionic dyes from aqueous solutions","authors":"S. M Anush,&nbsp;C. S Kaliprasad,&nbsp;Gangadhar Gowda P H,&nbsp;B. H Gayathri,&nbsp;Y. R Girish,&nbsp;K Prashantha,&nbsp;Subramaniyan Ramasundaram,&nbsp;Mohammad Altaf,&nbsp;Tae Hwan Oh,&nbsp;Mani Durai","doi":"10.1007/s10965-024-04173-3","DOIUrl":null,"url":null,"abstract":"<div><p>In the present work, a novel pyrazine based chitosan material was synthesized by functionalizing chitosan with chloroacetyl chloride and further modification with ethylene 1,2 diamine, thus a polymer matrix is obtained. Further the adsorbent material was characterized and verified using analytical techniques such as XRD, SEM, FTIR and TGA. The adsorbent material was analyzed for the adsorptive take-up process with a initial dye concentration varying from 20–100 mgL<sup>−1</sup> and the adsorptive process occurred due to the electrostatic interaction between the nitrogen atom of chitosan and the methyl orange dye molecule. The equilibrium adsorptive capacity obtained for the synthesized adsorbent material was 45.45 mg g<sup>−1</sup>. The adsorptive mechanism predicted the electrostatic interaction between the two atoms and the increased in the adsorption efficiency is contributed by the increased number of hetero atoms in the chitosan structure and the adsorption kinetics was found to be pseudo-second-order kinetics and with a monolayer coverage process indicating the Langmuir adsorption isothermal fit. Further, the evaluated thermodynamic parameters showed the adsorption process to be non-spontaneous and endothermic in nature. A regeneration and reusability study was achieved for the composite material using convenient stripping solutions and the adsorbent was successfully regenerated.</p></div>","PeriodicalId":658,"journal":{"name":"Journal of Polymer Research","volume":"31 11","pages":""},"PeriodicalIF":2.6000,"publicationDate":"2024-10-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://link.springer.com/content/pdf/10.1007/s10965-024-04173-3.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Research","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s10965-024-04173-3","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
引用次数: 0

Abstract

In the present work, a novel pyrazine based chitosan material was synthesized by functionalizing chitosan with chloroacetyl chloride and further modification with ethylene 1,2 diamine, thus a polymer matrix is obtained. Further the adsorbent material was characterized and verified using analytical techniques such as XRD, SEM, FTIR and TGA. The adsorbent material was analyzed for the adsorptive take-up process with a initial dye concentration varying from 20–100 mgL−1 and the adsorptive process occurred due to the electrostatic interaction between the nitrogen atom of chitosan and the methyl orange dye molecule. The equilibrium adsorptive capacity obtained for the synthesized adsorbent material was 45.45 mg g−1. The adsorptive mechanism predicted the electrostatic interaction between the two atoms and the increased in the adsorption efficiency is contributed by the increased number of hetero atoms in the chitosan structure and the adsorption kinetics was found to be pseudo-second-order kinetics and with a monolayer coverage process indicating the Langmuir adsorption isothermal fit. Further, the evaluated thermodynamic parameters showed the adsorption process to be non-spontaneous and endothermic in nature. A regeneration and reusability study was achieved for the composite material using convenient stripping solutions and the adsorbent was successfully regenerated.

吡嗪取代壳聚糖:一种从水溶液中高效去除阴离子染料的吸附材料
在本研究中,通过用氯乙酰氯对壳聚糖进行官能化,并用乙烯-1,2-二胺进一步改性,合成了一种新型吡嗪基壳聚糖材料,从而获得了一种聚合物基体。此外,还利用 XRD、SEM、傅立叶变换红外光谱和热重分析等分析技术对吸附材料进行了表征和验证。在初始染料浓度为 20-100 mgL-1 的情况下,对吸附材料的吸附吸收过程进行了分析,吸附过程是由于壳聚糖的氮原子与甲基橙染料分子之间的静电作用而发生的。合成吸附材料的平衡吸附容量为 45.45 mg g-1。吸附机理预测两个原子之间存在静电作用,壳聚糖结构中杂质原子数量的增加有助于提高吸附效率。此外,评估的热力学参数表明,吸附过程是非自发的,具有内热性质。使用方便的剥离溶液对复合材料进行了再生和可再利用性研究,吸附剂成功再生。
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
Journal of Polymer Research
Journal of Polymer Research 化学-高分子科学
CiteScore
4.70
自引率
7.10%
发文量
472
审稿时长
3.6 months
期刊介绍: Journal of Polymer Research provides a forum for the prompt publication of articles concerning the fundamental and applied research of polymers. Its great feature lies in the diversity of content which it encompasses, drawing together results from all aspects of polymer science and technology. As polymer research is rapidly growing around the globe, the aim of this journal is to establish itself as a significant information tool not only for the international polymer researchers in academia but also for those working in industry. The scope of the journal covers a wide range of the highly interdisciplinary field of polymer science and technology, including: polymer synthesis; polymer reactions; polymerization kinetics; polymer physics; morphology; structure-property relationships; polymer analysis and characterization; physical and mechanical properties; electrical and optical properties; polymer processing and rheology; application of polymers; supramolecular science of polymers; polymer composites.
×
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