High adsorption capacities for dyes by a pH-responsive sodium alginate/sodium lignosulfonate/carboxylated chitosan/polyethyleneimine adsorbent

吸附 壳聚糖 化学 靛蓝胭脂红 亚甲蓝 柠檬黄 阳离子聚合 甲基蓝 核化学 有机化学 色谱法 光催化 催化作用
作者
Hui Wang,Kun Dai,Houle Xiang,Jingwei Kou,Han Guo,Hanjie Ying,Jinglan Wu
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:278 (Pt 3): 135005-135005 被引量:23
标识
DOI:10.1016/j.ijbiomac.2024.135005
摘要

Dyes are indispensable for the rapid development of society, but untreated dye wastewater can threaten human health. In this study, an adsorbent (SA/SL/CCS/PEI@MNPs) was synthesized by one-pot method using magnetic nanoparticles (MNPs), sodium alginate (SA), sodium lignosulfonate (SL), carboxylated chitosan (CCS) and polyethyleneimine (PEI). The adsorbent was mesoporous micrometer-sized particles with pore size of 34.92 nm, which was favorable for dynamic column experiments. SA/SL/CCS/PEI@MNPs possessed pH-responsive performance. Under acidic condition, the maximum adsorption capacities for anionic dyes (tartrazine, reactive black-5, indigo carmine) reached >550 mg/g. Under alkaline condition, those for cationic dyes (methylene blue, methyl violet, neutral red) exceeded 1900 mg/g. The function of the various modifiers was investigated. The results indicated that the incorporation of SL, CCS and PEI was able to provide plenty of sulfonate, carboxylate and amino/imine reactive groups so that adsorption capacities of dyes were improved. The adsorption mechanism was explored by FTIR and XPS. At the same time, the adsorption mechanism was more deeply analyzed using molecular dynamics simulations and radial distribution function. It was demonstrated that the dyes adsorption on the SA/SL/CCS/PEI@MNPs was mainly due to electrostatic attraction and π-π interaction. In addition, the adsorbent had good reusability, and the removal still reached over 90 % after five cycles. In conclusion, the adsorbent displayed a broad prospect for the adsorption of organic dyes.
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
刚刚
起点完成签到,获得积分10
1秒前
Joey发布了新的文献求助10
2秒前
xiaojie发布了新的文献求助10
2秒前
小周没有篮完成签到 ,获得积分10
2秒前
2秒前
3秒前
友好的士萧完成签到 ,获得积分10
4秒前
yuHS发布了新的文献求助10
4秒前
ShawnLeo发布了新的文献求助10
5秒前
风琴完成签到,获得积分10
5秒前
爱喝水的乌鸦完成签到 ,获得积分10
5秒前
Ciil完成签到,获得积分10
5秒前
5秒前
宋66完成签到,获得积分10
6秒前
6秒前
冷傲雅绿完成签到,获得积分20
6秒前
6秒前
自由惜芹应助zhiwei采纳,获得10
7秒前
高贵振家发布了新的文献求助10
7秒前
tester_gater发布了新的文献求助20
8秒前
栗栗子发布了新的文献求助10
10秒前
kjdgahdg完成签到,获得积分10
10秒前
烂漫煎饼完成签到,获得积分10
10秒前
luoshi94完成签到,获得积分10
11秒前
地球发布了新的文献求助10
11秒前
lingzi1015发布了新的文献求助20
11秒前
桐桐应助ddddd采纳,获得10
12秒前
spongxin完成签到,获得积分10
14秒前
Orange应助糖醋鱼采纳,获得10
14秒前
15秒前
栗栗子完成签到,获得积分10
15秒前
16秒前
Ava应助科研通管家采纳,获得10
16秒前
赘婿应助科研通管家采纳,获得10
16秒前
8R60d8应助科研通管家采纳,获得10
16秒前
爆米花应助科研通管家采纳,获得30
16秒前
研友_VZG7GZ应助科研通管家采纳,获得10
16秒前
CodeCraft应助科研通管家采纳,获得10
17秒前
顾矜应助科研通管家采纳,获得10
17秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
The Organometallic Chemistry of the Transition Metals 800
Chemistry and Physics of Carbon Volume 18 800
The Organometallic Chemistry of the Transition Metals 800
The formation of Australian attitudes towards China, 1918-1941 640
Signals, Systems, and Signal Processing 610
全相对论原子结构与含时波包动力学的理论研究--清华大学 500
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 6442171
求助须知:如何正确求助?哪些是违规求助? 8256014
关于积分的说明 17579996
捐赠科研通 5500741
什么是DOI,文献DOI怎么找? 2900393
邀请新用户注册赠送积分活动 1877328
关于科研通互助平台的介绍 1717144