LICP OpenIR  > 环境材料与生态化学研究发展中心
Enhanced adsorptive removal of methylene blue from aqueous solution by alkali-activated palygorskite
Department环境材料与生态化学研究发展中心
Wang WB(王文波)1,2; Wang FF(王方方)1; Kang YR(康玉茹)1; Wang AQ(王爱勤)1,2; Wang AQ(王爱勤)
2015
Source PublicationWater Air and Soil Pollution
ISSN0049-6979
Volume226Issue:3Pages:83(1-13)
Abstract

Silicate clay materials are promising natural adsorbents with abundant, low cost, stable, and ecofriendly advantages, but the limited adsorption capacity restricts their applications in many fields. Herein, palygorskite (PAL) was facilely activated with alkali to enhance its adsorptive removal capability for methylene blue (MB). The effects of alkali activation on the microstructure, physicochemical, and adsorption properties of PAL for MB were intensively investigated. It was found that the moderate alkali activation can partially remove the metal cations (i.e., Al3+, Mg2+) and Si in the crystal backbone of PAL by which new Badsorption sites^ were created and the surface negative charges increased. The adsorption capacity and rate of PAL for MB were evidently enhanced due to the effective activation. The adsorption isotherms were described by Freundlich isotherm model very well, and the adsorption kinetics can be accurately presented by a pseudo-second-order model. It can be inferred from the fitting results that the overall adsorption process was controlled by external mass transfer and intra-particle diffusion (the dominant role). The multiple adsorption interactions (hydrogen bonding, electrostatic interactions, mesopore filling, and complexing) were turned out to be the dominant factors to improve the adsorption properties. It was revealed that the activated PAL could be used as a potential adsorption candidate for environmental applications.

KeywordPalygorskite Alkali Activation Adsorption Methylene Blue
Subject Area环境材料与生态化学
DOI10.1007/s11270-015-2355-0
Funding Organization“863” Project of the Ministry of Science and Technology, People’s Republic of China (No. 2013AA032003);the National Natural Science Foundation of China (No. 51403221);the open funds of Key Laboratory for Palygorskite Science and Applied Technology of Jiangsu Province (No. HPK201201)
Indexed BySCI
If1.554
Language英语
Funding Project功能复合材料组
compositor第一作者单位
Citation statistics
Cited Times:48[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.licp.cn/handle/362003/7213
Collection环境材料与生态化学研究发展中心
Corresponding AuthorWang AQ(王爱勤)
Affiliation1.Chinese Acad Sci, Lanzhou Inst Chem Phys, R&D Ctr Xuyi Attapulgite Appl Technol, Xuyi 211700, Peoples R China
2.Huaiyin Inst Technol, Key Lab Palygorskite Sci & Appl Technol Jiangsu P, Huaian 223003, Peoples R China
Recommended Citation
GB/T 7714
Wang WB,Wang FF,Kang YR,et al. Enhanced adsorptive removal of methylene blue from aqueous solution by alkali-activated palygorskite[J]. Water Air and Soil Pollution,2015,226(3):83(1-13).
APA Wang WB,Wang FF,Kang YR,Wang AQ,&王爱勤.(2015).Enhanced adsorptive removal of methylene blue from aqueous solution by alkali-activated palygorskite.Water Air and Soil Pollution,226(3),83(1-13).
MLA Wang WB,et al."Enhanced adsorptive removal of methylene blue from aqueous solution by alkali-activated palygorskite".Water Air and Soil Pollution 226.3(2015):83(1-13).
Files in This Item:
File Name/Size DocType Version Access License
water air soil pollu(2431KB)期刊论文出版稿开放获取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
[Wang WB(王文波)]'s Articles
[Wang FF(王方方)]'s Articles
[Kang YR(康玉茹)]'s Articles
Baidu academic
Similar articles in Baidu academic
[Wang WB(王文波)]'s Articles
[Wang FF(王方方)]'s Articles
[Kang YR(康玉茹)]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[Wang WB(王文波)]'s Articles
[Wang FF(王方方)]'s Articles
[Kang YR(康玉茹)]'s Articles
Terms of Use
No data!
Social Bookmark/Share
File name: water air soil pollu.pdf
Format: Adobe PDF
All comments (0)
No comment.
 

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