Fabrication of a nitrogen-rich GO composite for selective removal of Cu2+ in aqueous solutions

IF 5.9 3区 工程技术 Q1 CHEMISTRY, MULTIDISCIPLINARY
Mei-Yi Duan , Bi Yang , Yi-Ping Liu , Guo-Cong Liu , Yong-Kun Li , Jin-Gang Yu
{"title":"Fabrication of a nitrogen-rich GO composite for selective removal of Cu2+ in aqueous solutions","authors":"Mei-Yi Duan ,&nbsp;Bi Yang ,&nbsp;Yi-Ping Liu ,&nbsp;Guo-Cong Liu ,&nbsp;Yong-Kun Li ,&nbsp;Jin-Gang Yu","doi":"10.1016/j.jiec.2025.05.030","DOIUrl":null,"url":null,"abstract":"<div><div>Graphene oxide (GO) based composites are renowned for their adsorption properties toward metal ions from mono-/multi-component systems. However, it is difficult for a newly-developed adsorbent to possess high adsorption capacity and good selectivity. By modifying GO with a nitrogen-rich organic molecule, 3,5-diamino-1,2,4-triazole (DAT), through a facile nucleophilic reaction, the developed GO-DAT composite could selectively adsorb Cu<sup>2+</sup> of low concentrations from aqueous solutions with high efficiency. Several characterization techniques confirmed that DAT was successfully bound to GO through the formation of C=N bonds, which greatly improved its thermal stability. In addition, more active adsorption sites could be also offered to complex with Cu<sup>2+</sup> to achieve excellent adsorption effects. The adsorption investigation was implemented in-depth by evaluating the conditional parameters (Contact time, initial adsorbate concentration, temperature, and pH effect) on the adsorption process. For the kinetic and isothermal studies, the adsorption data could be better fitted by the linear pseudo-second-order model and linear Langmuir model, respectively, suggesting the chemical adsorption dominated the intermolecular interactions between GO-DAT composite and Cu<sup>2+</sup>, and a higher adsorption capacity of 0.63mmol g<sup>−1</sup> at equilibrium could be observed. The proposed GO-DAT composite also exhibited excellent reusability, implying that it is an effective adsorbent for the removal of Cu<sup>2+</sup> from aqueous solutions.</div></div>","PeriodicalId":363,"journal":{"name":"Journal of Industrial and Engineering Chemistry","volume":"152 ","pages":"Pages 614-624"},"PeriodicalIF":5.9000,"publicationDate":"2025-05-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Industrial and Engineering Chemistry","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1226086X25003417","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Graphene oxide (GO) based composites are renowned for their adsorption properties toward metal ions from mono-/multi-component systems. However, it is difficult for a newly-developed adsorbent to possess high adsorption capacity and good selectivity. By modifying GO with a nitrogen-rich organic molecule, 3,5-diamino-1,2,4-triazole (DAT), through a facile nucleophilic reaction, the developed GO-DAT composite could selectively adsorb Cu2+ of low concentrations from aqueous solutions with high efficiency. Several characterization techniques confirmed that DAT was successfully bound to GO through the formation of C=N bonds, which greatly improved its thermal stability. In addition, more active adsorption sites could be also offered to complex with Cu2+ to achieve excellent adsorption effects. The adsorption investigation was implemented in-depth by evaluating the conditional parameters (Contact time, initial adsorbate concentration, temperature, and pH effect) on the adsorption process. For the kinetic and isothermal studies, the adsorption data could be better fitted by the linear pseudo-second-order model and linear Langmuir model, respectively, suggesting the chemical adsorption dominated the intermolecular interactions between GO-DAT composite and Cu2+, and a higher adsorption capacity of 0.63mmol g−1 at equilibrium could be observed. The proposed GO-DAT composite also exhibited excellent reusability, implying that it is an effective adsorbent for the removal of Cu2+ from aqueous solutions.

Abstract Image

制备富氮氧化石墨烯复合材料选择性去除水溶液中的Cu2+
氧化石墨烯(GO)基复合材料以其对单组分/多组分体系中的金属离子的吸附性能而闻名。然而,新开发的吸附剂很难具有高的吸附容量和良好的选择性。用富氮有机分子3,5-二氨基-1,2,4-三唑(DAT)修饰氧化石墨烯,通过易发生的亲核反应,制备的GO-DAT复合材料可高效选择性吸附低浓度水溶液中的Cu2+。几种表征技术证实,DAT通过形成C=N键成功地与GO结合,从而大大提高了其热稳定性。此外,配合物还可以提供更多的活性吸附位点,以达到良好的吸附效果。通过考察条件参数(接触时间、初始吸附浓度、温度和pH值)对吸附过程的影响,对吸附过程进行了深入的研究。在动力学和等温实验中,GO-DAT复合物与Cu2+的吸附数据分别用线性拟二阶模型和线性Langmuir模型拟合较好,表明化学吸附主导了GO-DAT复合物与Cu2+的分子间相互作用,达到了0.63mmol g−1的平衡吸附量。所提出的GO-DAT复合材料还具有良好的可重复使用性,这意味着它是一种有效的吸附剂,可以从水溶液中去除Cu2+。
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
CiteScore
10.40
自引率
6.60%
发文量
639
审稿时长
29 days
期刊介绍: Journal of Industrial and Engineering Chemistry is published monthly in English by the Korean Society of Industrial and Engineering Chemistry. JIEC brings together multidisciplinary interests in one journal and is to disseminate information on all aspects of research and development in industrial and engineering chemistry. Contributions in the form of research articles, short communications, notes and reviews are considered for publication. The editors welcome original contributions that have not been and are not to be published elsewhere. Instruction to authors and a manuscript submissions form are printed at the end of each issue. Bulk reprints of individual articles can be ordered. This publication is partially supported by Korea Research Foundation and the Korean Federation of Science and Technology Societies.
×
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:604180095
Book学术官方微信