Adsorption of P-Nitrophenol Onto Partially Reduced Graphene Oxide: An Experimental and Theoretical Study

IF 2.1 4区 化学 Q3 CHEMISTRY, PHYSICAL
Mengzhi Yang, Meiling Wang
{"title":"Adsorption of P-Nitrophenol Onto Partially Reduced Graphene Oxide: An Experimental and Theoretical Study","authors":"Mengzhi Yang, Meiling Wang","doi":"10.3184/146867818X15233705894374","DOIUrl":null,"url":null,"abstract":"This study investigated the adsorption process of p-nitrophenol (p-NP) onto partially reduced graphene oxide (prGO) using both experiment and theoretical calculations. The maximum adsorption capacity of prGO at pH 6.0 and 293 K for p-NP was 29.94 mg g−1 which was significantly higher than previously reported using a metal-doped reduced graphene oxide composite. Systematic, comparative theoretical calculations were used to investigate the adsorption mechanism of p-NP onto graphene oxide, prGO and graphene nanosheet (GN). Calculations revealed three types of adsorption site and indicated that the adsorption force and sites were significantly affected by the quantity and type of oxygen-containing functional groups on the GN. The adsorption affinity was mainly derived from hydrogen bonds and π-π stacking which was further demonstrated by FTIR analysis. Due to its excellent adsorption performance, good recyclability and easy separation, prGO can be a promising adsorbent for the efficient elimination of p-NP from wastewater in the future.","PeriodicalId":20859,"journal":{"name":"Progress in Reaction Kinetics and Mechanism","volume":"1 1","pages":"189 - 200"},"PeriodicalIF":2.1000,"publicationDate":"2018-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Progress in Reaction Kinetics and Mechanism","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.3184/146867818X15233705894374","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 2

Abstract

This study investigated the adsorption process of p-nitrophenol (p-NP) onto partially reduced graphene oxide (prGO) using both experiment and theoretical calculations. The maximum adsorption capacity of prGO at pH 6.0 and 293 K for p-NP was 29.94 mg g−1 which was significantly higher than previously reported using a metal-doped reduced graphene oxide composite. Systematic, comparative theoretical calculations were used to investigate the adsorption mechanism of p-NP onto graphene oxide, prGO and graphene nanosheet (GN). Calculations revealed three types of adsorption site and indicated that the adsorption force and sites were significantly affected by the quantity and type of oxygen-containing functional groups on the GN. The adsorption affinity was mainly derived from hydrogen bonds and π-π stacking which was further demonstrated by FTIR analysis. Due to its excellent adsorption performance, good recyclability and easy separation, prGO can be a promising adsorbent for the efficient elimination of p-NP from wastewater in the future.
部分还原氧化石墨烯吸附对硝基苯酚的实验与理论研究
本研究通过实验和理论计算研究了对硝基苯酚(p-NP)在部分还原氧化石墨烯(prGO)上的吸附过程。在pH 6.0和293 K条件下,prGO对p-NP的最大吸附量为29.94 mg g - 1,显著高于先前报道的金属掺杂还原氧化石墨烯复合材料。采用系统的、比较的理论计算研究了p-NP在氧化石墨烯、氧化石墨烯和石墨烯纳米片(GN)上的吸附机理。计算发现了三种类型的吸附位点,并表明吸附力和吸附位点受GN上含氧官能团数量和类型的显著影响。吸附亲合力主要来源于氢键和π-π堆积,FTIR分析进一步证实了这一点。由于其优异的吸附性能,良好的可回收性和易于分离,prGO有望成为未来有效去除废水中p-NP的吸附剂。
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
2.10
自引率
0.00%
发文量
5
审稿时长
2.3 months
期刊介绍: The journal covers the fields of kinetics and mechanisms of chemical processes in the gas phase and solution of both simple and complex systems.
×
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