LICP OpenIR  > 环境材料与生态化学研究发展中心
Ag(I)-triggered one-pot synthesis of Ag nanoparticles onto natural nanorods as a multifunctional nanocomposite for efficient catalysis and adsorption
Department环境材料与生态化学研究发展中心
Tian GY(田光燕)1,2; Wang WB(王文波)1,3; Mu B(牟斌)1,3; Kang YR(康玉茹)1,3; Wang AQ(王爱勤)1,3; Wang WB(王文波); Wang AQ(王爱勤)
2016
Source PublicationJournal of Colloid and Interface Science
ISSN0021-9797
Volume473Pages:84-92
Abstract

A multifunctional palygorskite/polyaniline/Ag nanoparticles (PAL/PANI/AgNPs) nanocomposite was prepared at room temperature using a simple one-pot in-situ polymerization reaction of aniline monomers triggered by Ag(I) on the surface of natural PAL nanorods. Ag(I) served as both the oxidant and the precursor of the AgNPs, which initiated the polymerization of aniline monomers on PAL nanorods while simultaneously being reduced to form Ag0 nanoparticles (AgNPs). The in-situ formed AgNPs were evenly distributed on the surface of the PAL nanorods because the interfacial effect of PAL prevents their aggregation. The density and size of the AgNPs and the catalytic activity of the nanocomposites could be controlled by altering the molar ratio of aniline to Ag(I). The performance evaluation revealed that the nanocomposites could be used as highly active catalysts, which rapidly catalyzed the reduction of 4-nitrophenol (4-NP) within 2 min and Congo red (CR) within 10 min. The nanocomposites are also an effective adsorbent for H2PO4 able to remove 99.40% of H2PO4 (only 61.77% for raw PAL) from a solution with an initial concentration of 50 mg/L. This multifunctional nanocomposite synthesized by a simple one-pot approach is a promising material for environmental applications.

KeywordPalygorskite Ag Nanoparticles Nanocomposite Catalysis Adsorption
Subject Area环境材料与生态化学
DOI10.1016/j.jcis.2016.03.058
Funding Organization“863” Project of the Ministry of Science and Technology, PR China (No. 2013AA032003);National Natural Science Foundation of China (No. 51403221);Natural Science Foundation of Gansu Province (No. 1308RJZA308);Youth Innovation Promotion Association CAS (No. 2016370)
Indexed BySCI
If4.233
Language英语
Funding Project功能复合材料组
compositor第一作者单位
Citation statistics
Cited Times:24[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/19801
Collection环境材料与生态化学研究发展中心
Corresponding AuthorWang WB(王文波); Wang AQ(王爱勤)
Affiliation1.Chinese Acad Sci, Lanzhou Inst Chem Phys, Ctr Ecomat & Green Chem, Lanzhou 730000, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Chinese Acad Sci, Lanzhou Inst Chem Phys, R&D Ctr Xuyi Palygorskite Appl Technol, Xuyi 211700, Peoples R China
Recommended Citation
GB/T 7714
Tian GY,Wang WB,Mu B,et al. Ag(I)-triggered one-pot synthesis of Ag nanoparticles onto natural nanorods as a multifunctional nanocomposite for efficient catalysis and adsorption[J]. Journal of Colloid and Interface Science,2016,473:84-92.
APA Tian GY.,Wang WB.,Mu B.,Kang YR.,Wang AQ.,...&王爱勤.(2016).Ag(I)-triggered one-pot synthesis of Ag nanoparticles onto natural nanorods as a multifunctional nanocomposite for efficient catalysis and adsorption.Journal of Colloid and Interface Science,473,84-92.
MLA Tian GY,et al."Ag(I)-triggered one-pot synthesis of Ag nanoparticles onto natural nanorods as a multifunctional nanocomposite for efficient catalysis and adsorption".Journal of Colloid and Interface Science 473(2016):84-92.
Files in This Item:
File Name/Size DocType Version Access License
jcis.pdf(2864KB)期刊论文作者接受稿开放获取CC BY-NC-SAView Application Full Text
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[Tian GY(田光燕)]'s Articles
[Wang WB(王文波)]'s Articles
[Mu B(牟斌)]'s Articles
Baidu academic
Similar articles in Baidu academic
[Tian GY(田光燕)]'s Articles
[Wang WB(王文波)]'s Articles
[Mu B(牟斌)]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Tian GY(田光燕)]'s Articles
[Wang WB(王文波)]'s Articles
[Mu B(牟斌)]'s Articles
Terms of Use
No data!
Social Bookmark/Share
File name: jcis.pdf
Format: Adobe PDF
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.