Enhanced fluoride removal from water by nanosized cerium oxides impregnated porous polystyrene anion exchanger

氟化物 吸附 聚苯乙烯 化学 聚偏氟乙烯 解吸 离子交换 化学工程 无机化学 废水 核化学 废物管理 有机化学 离子 聚合物 工程类
作者
Hao Dong,Huan Tang,Xinxing Shi,Wenlan Yang,Wenjing Chen,Han Li,Yu Zhao,Zhengyong Zhang,Ming Hua
出处
期刊:Chemosphere [Elsevier BV]
卷期号:287 (Pt 1): 131932-131932 被引量:35
标识
DOI:10.1016/j.chemosphere.2021.131932
摘要

Efficient elimination of fluoride from wastewater is an urgent need for ensuring water safety. In the present study, a stable and reusable nanocomposite (NCO@PAE) was synthesized by impregnating nanosized cerium oxides (NCO) inside a porous polystyrene anion exchanger (PAE) host for efficient fluoride removal from wastewater. The newly fabricated NCO@PAE exhibited excellent resistance to acid and alkali environment, allowing it to be utilized in a wide pH range (2–12). Fluoride uptake onto NCO@PAE was a pH-dependent process, which could reach the maximum capacity at pH 3.0. Compared with its host PAE, NCO@PAE showed conspicuous adsorption affinity towards fluoride in the coexistence of other competing anions at high concentrations. Adsorption kinetics confirmed its high efficiency for achieving equilibrium within 120 min. Fixed-bed adsorption runs demonstrated that the effective processing capacity of NCO@PAE for synthetic fluoride-containing wastewater (initial fluoride 2.5 mg/L) was about ~330 BV (bed volume), while only 22 BV for the host PAE. The exhausted NCO@PAE could be effectively revived by a simple in-situ desorption method for long-term cycle operation without conspicuous capacity loss. All the results indicated that NCO@PAE is a reliable and promising adsorbent for water defluoridation. • A stable and reusable nanocomposite NCO@PAE was fabricated for fluoride removal. • Nanosized Ce oxide was embedded in a porous polystyrene host to acquire selectivity. • NCO@PAE could selectively capture fluoride in the coexistence of competing anions. • As-laden NCO@PAE could be effectively revived for cyclic utilization.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
DZQ发布了新的文献求助10
刚刚
Quinta完成签到,获得积分10
刚刚
桐桐应助看看左右采纳,获得10
1秒前
15524333213发布了新的文献求助10
1秒前
黄先生完成签到,获得积分10
1秒前
科研通AI6.2应助sunny采纳,获得10
1秒前
bei完成签到,获得积分10
2秒前
壮壮发布了新的文献求助10
2秒前
可爱小张完成签到,获得积分20
2秒前
司空绝山完成签到,获得积分10
2秒前
科研通AI6.1应助西斯塔采纳,获得10
2秒前
2秒前
番茄鹅完成签到,获得积分10
3秒前
酷酷的傲之完成签到,获得积分10
3秒前
舒心的南珍完成签到,获得积分20
3秒前
zxdzaz完成签到 ,获得积分10
3秒前
酆百川完成签到,获得积分10
4秒前
4秒前
4秒前
小白完成签到,获得积分10
5秒前
Gladys完成签到,获得积分10
5秒前
5秒前
916应助1101592875采纳,获得10
5秒前
咖啡逗发布了新的文献求助10
7秒前
码头吃薯条完成签到,获得积分10
7秒前
che完成签到 ,获得积分10
7秒前
Zhihu完成签到,获得积分10
7秒前
风华正茂完成签到,获得积分10
7秒前
Frost发布了新的文献求助30
7秒前
浪费青春传奇完成签到 ,获得积分10
8秒前
慕青应助1111111采纳,获得10
8秒前
瞿访云完成签到,获得积分10
9秒前
痴情的银耳汤完成签到,获得积分10
9秒前
英吉利25发布了新的文献求助30
9秒前
可以完成签到,获得积分10
9秒前
领导范儿应助祝你发财采纳,获得10
10秒前
悦耳平文完成签到,获得积分10
10秒前
10秒前
10秒前
额威风完成签到,获得积分10
11秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Burger's Medicinal Chemistry and Drug Discovery 400
A Step-by-Step Guide to Qualitative Data Coding 2nd Edition 400
Impact of Storage Orientation and Duration on Prefilled Syringe Performance: Break-Loose and Glide Forces, and Injection Time Across Multiple Time Points 360
Programming for Chemical Engineers Using C, C++, and MATLAB 300
Upland Kenya wild flowers and ferns: a flora of the flowers, ferns, grasses, and sedges of highland Kenya 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6664434
求助须知:如何正确求助?哪些是违规求助? 8414206
关于积分的说明 17986334
捐赠科研通 5869625
什么是DOI,文献DOI怎么找? 2975436
邀请新用户注册赠送积分活动 1951357
关于科研通互助平台的介绍 1877831