Facile synthesis of chitosan membranes for visible-light-driven photocatalytic degradation of tetracycline hydrochloride

盐酸四环素 降级(电信) 壳聚糖 光催化 四环素 盐酸盐 可见光谱 化学 化学工程 核化学 光化学 材料科学 有机化学 催化作用 计算机科学 光电子学 生物化学 抗生素 工程类 电信
作者
Huimin Liang,Caizhi Lv,Hanjiao Chen,Lan Wu,Xiandeng Hou
出处
期刊:RSC Advances [Royal Society of Chemistry]
卷期号:10 (73): 45171-45179 被引量:17
标识
DOI:10.1039/d0ra08358e
摘要

Due to the film-forming ability of polymers, a variety of photocatalytic membranes (PMs) based on polymers easily being separated and reused have been constructed for wastewater contaminant treatment. During their construction processes, chitosan (CS) as a bio-polymer with its distinct merits of abundant resources, low-cost and environmental-friendliness, as well as formability and ease of modification, has attracted great attention. However, the role of CS was mostly believed to be just a support or an adsorbent for fixing or dispersing photocatalysts. Whether CS possessed photocatalytic activity or not still remained vague. Herein, in this work, CS membranes (CSM) were facilely prepared for photocatalytic degradation of tetracycline hydrochloride (TC, a model organic pollutant) in aqueous solution, and its photocatalytic performance was investigated and compared with that of CSP (CS powder) and TiO2-P25 (a commercially used photocatalyst). The results showed that the single-phased CSM exhibited a better visible light photocatalytic activity. After visible light irradiation for 60 minutes, the degradation efficiency of TC can reach above 90% when the CSM was used as a photocatalyst, while with the same irradiation time interval, less TC could be degraded over both CSP and TiO2-P25. Through radical scavenging and EPR experiments, ˙O2 - and h+ were found to be the main active oxygen species generated in the reaction system for TC degradation. After being washed with 2 wt% NaOH solution, the CSM revealed a good recyclability implying its potential for practical applications. This study would provide a certain theoretical and data basis for the future development of CS-based PMs and photocatalysts.
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
MMP发布了新的文献求助50
1秒前
4秒前
ding应助小AB采纳,获得10
6秒前
攀攀完成签到,获得积分10
6秒前
QR发布了新的文献求助10
6秒前
单身的青柏完成签到 ,获得积分10
12秒前
搜集达人应助圈圈黄采纳,获得10
13秒前
简单面包完成签到,获得积分10
14秒前
西柚完成签到 ,获得积分10
18秒前
XHX完成签到,获得积分10
20秒前
bkagyin应助狂野的若雁采纳,获得10
21秒前
可爱的函函应助阿然采纳,获得10
24秒前
蟲先生完成签到 ,获得积分0
28秒前
29秒前
扬xue完成签到,获得积分20
31秒前
唐宝完成签到 ,获得积分10
33秒前
35秒前
jin发布了新的文献求助10
35秒前
扬xue发布了新的文献求助30
36秒前
非要叫我起个昵称完成签到,获得积分10
37秒前
LZY发布了新的文献求助10
38秒前
shunshun51213完成签到,获得积分10
38秒前
zxy完成签到 ,获得积分10
39秒前
李健的小迷弟应助安白采纳,获得10
42秒前
hbb完成签到 ,获得积分10
46秒前
汉堡包应助科研通管家采纳,获得10
46秒前
back you up应助科研通管家采纳,获得30
46秒前
科研通AI2S应助科研通管家采纳,获得10
46秒前
慕青应助科研通管家采纳,获得10
46秒前
zhu97应助科研通管家采纳,获得20
46秒前
汉堡包应助科研通管家采纳,获得10
46秒前
科研通AI5应助科研通管家采纳,获得10
46秒前
充电宝应助沁阳采纳,获得10
48秒前
LZY完成签到,获得积分10
49秒前
fdwang完成签到 ,获得积分10
51秒前
56秒前
57秒前
1分钟前
1分钟前
1分钟前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Maneuvering of a Damaged Navy Combatant 650
Mixing the elements of mass customisation 300
the MD Anderson Surgical Oncology Manual, Seventh Edition 300
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3778003
求助须知:如何正确求助?哪些是违规求助? 3323643
关于积分的说明 10215259
捐赠科研通 3038839
什么是DOI,文献DOI怎么找? 1667661
邀请新用户注册赠送积分活动 798341
科研通“疑难数据库(出版商)”最低求助积分说明 758339