Strategically Designed Ternary Nanohybrids of Titanate Nanosheet and Polydopamine-Coated Carbon Nanotubes for Highly Efficient Enrichment of Uranium(VI).

IF 3.7 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2024-12-05 eCollection Date: 2024-12-17 DOI:10.1021/acsomega.4c05253
Zhiyang Jiang, Yuzhi Zhou, Wenshuo Wang, Zheng Yin, Mingze Zhao, Lei Yu, Sijie Ren, Han Xiao, Yanfang Ma
{"title":"Strategically Designed Ternary Nanohybrids of Titanate Nanosheet and Polydopamine-Coated Carbon Nanotubes for Highly Efficient Enrichment of Uranium(VI).","authors":"Zhiyang Jiang, Yuzhi Zhou, Wenshuo Wang, Zheng Yin, Mingze Zhao, Lei Yu, Sijie Ren, Han Xiao, Yanfang Ma","doi":"10.1021/acsomega.4c05253","DOIUrl":null,"url":null,"abstract":"<p><p>A strategically designed ternary nanohybrid (TNS-PDA/CNT), consisting of titanate nanosheet (TNS) and polydopamine-modified multiwalled carbon nanotube (PDA/CNT composite), was synthesized by the facile hydrothermal method and wet impregnation method for removal of U(VI) from aqueous solution and were characterized by transmission electron microscopy (TEM), scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray diffraction (XRD), Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman spectroscopy, Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS). TNSs were introduced into the PDA/CNT composite, which effectively averted the agglomeration of the CNT and further exposed more adsorption sites. PDA thin layer exposing more active sites was conducive to enhance adsorption capacity and kinetic. The adsorption process was largely influenced by pH values and weakly affected by ionic strength, indicating that the adsorption process was controlled by inner-sphere surface complexes because of TNS-PDA/CNT with multiple functional groups, including imine, catechol, amine, and hydroxyl groups. The isotherm data could be well described by the Langmuir model, and the monolayer maximum adsorption was determined to be 309.60 mg/g at pH = 5.0 and temperature = 45 °C. Thermodynamic parameters (Δ<i>G</i>° < 0, Δ<i>S</i>° > 0, and Δ<i>H</i>° < 0) showed that the nature of adsorption was endothermic and spontaneous. By XRD, FT-IR, and XPS analyses, the adsorption mechanism mainly involved surface complexation and ion exchange. In summary, the TNS-PDA/CNT materials are fully qualified as a satisfactory adsorbent for the purification and recovery of U(VI) from wastewater.</p>","PeriodicalId":22,"journal":{"name":"ACS Omega","volume":"9 50","pages":"49108-49120"},"PeriodicalIF":3.7000,"publicationDate":"2024-12-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11656379/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Omega","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsomega.4c05253","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/12/17 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

A strategically designed ternary nanohybrid (TNS-PDA/CNT), consisting of titanate nanosheet (TNS) and polydopamine-modified multiwalled carbon nanotube (PDA/CNT composite), was synthesized by the facile hydrothermal method and wet impregnation method for removal of U(VI) from aqueous solution and were characterized by transmission electron microscopy (TEM), scanning electron microscopy-energy-dispersive X-ray spectroscopy (SEM-EDS), X-ray diffraction (XRD), Fourier transform infrared (FT-IR), thermogravimetric analysis (TGA), Raman spectroscopy, Brunauer-Emmett-Teller (BET), and X-ray photoelectron spectroscopy (XPS). TNSs were introduced into the PDA/CNT composite, which effectively averted the agglomeration of the CNT and further exposed more adsorption sites. PDA thin layer exposing more active sites was conducive to enhance adsorption capacity and kinetic. The adsorption process was largely influenced by pH values and weakly affected by ionic strength, indicating that the adsorption process was controlled by inner-sphere surface complexes because of TNS-PDA/CNT with multiple functional groups, including imine, catechol, amine, and hydroxyl groups. The isotherm data could be well described by the Langmuir model, and the monolayer maximum adsorption was determined to be 309.60 mg/g at pH = 5.0 and temperature = 45 °C. Thermodynamic parameters (ΔG° < 0, ΔS° > 0, and ΔH° < 0) showed that the nature of adsorption was endothermic and spontaneous. By XRD, FT-IR, and XPS analyses, the adsorption mechanism mainly involved surface complexation and ion exchange. In summary, the TNS-PDA/CNT materials are fully qualified as a satisfactory adsorbent for the purification and recovery of U(VI) from wastewater.

战略性设计钛酸盐纳米片和聚多巴胺包覆碳纳米管的三元纳米杂化物用于铀的高效富集(VI)。
采用水热法和湿浸渍法合成了由钛酸盐纳米片(TNS)和聚多巴胺修饰的多壁碳纳米管(PDA/CNT复合材料)组成的三元纳米杂化物(TNS-PDA/CNT),并通过透射电子显微镜(TEM)、扫描电子显微镜-能量色散x射线能谱(SEM-EDS)、x射线衍射(XRD)、傅里叶变换红外(FT-IR)、热重分析(TGA)、拉曼光谱、布鲁诺尔-埃米特-泰勒光谱(BET)和x射线光电子能谱(XPS)。将tns引入到PDA/CNT复合材料中,有效地避免了CNT的团聚,并进一步暴露出更多的吸附位点。PDA薄层暴露出更多的活性位点,有利于提高吸附容量和动力学。吸附过程受pH值影响较大,受离子强度影响较小,说明由于TNS-PDA/CNT具有亚胺、儿茶酚、胺和羟基等多个官能团,吸附过程受球内表面配合物控制。等温线数据可以用Langmuir模型很好地描述,在pH = 5.0,温度= 45℃时,单层最大吸附量为309.60 mg/g。热力学参数(ΔG°< 0,ΔS°>,ΔH°< 0)表明吸附是吸热自发的。通过XRD、FT-IR和XPS分析,发现其吸附机理主要为表面络合和离子交换。综上所述,TNS-PDA/CNT材料完全可以作为一种令人满意的吸附剂净化和回收废水中的U(VI)。
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
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
×
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