Phase-Mediated Heavy Metal Adsorption from Aqueous Solutions Using Two-Dimensional Layered MoS2

吸附 金属 材料科学 相(物质) 水溶液 化学工程 热液循环 动力学 无机化学 物理化学 化学 冶金 有机化学 物理 量子力学 工程类
作者
Jinming Luo,Kaixing Fu,Meng Sun,Kai Yin,Dong Wang,Xia Liu,John C. Crittenden
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:11 (42): 38789-38797 被引量:90
标识
DOI:10.1021/acsami.9b14019
摘要

An understanding of the impacts regarding different phases of inorganic materials on heavy metal removal is indispensable, owing to the intrinsic structure of materials that can affect its properties. In this study, the distinct adsorption behaviors of heavy metals (Pb(II) and Cu(II)) on different phases of MoS2 (metallic phase (1T) and semiconducting phase (2H)) were theoretically and experimentally investigated. According to the computational results, both Pb(II) and Cu(II) have formed more stable complexes on 1T-MoS2 compared to those on 2H-MoS2 due to the lower adsorption energy (Ead). This phenomenon indicates that Pb(II) and Cu(II) were more preferably adsorbed onto 1T-MoS2. Based on the results of the computational studies, two-dimensional (2D) MoS2 nanosheets with identical 1T and 2H phases were synthesized via a facile hydrothermal reaction. As we surmised, 1T-MoS2 achieved excellent Pb(II) and Cu(II) adsorption capacities, which were 147.09 and 82.13 mg/g at 298 K, respectively, compared to those of 2H-MoS2 (i.e., 64.16 and 50.74 mg/g at 298 K). Moreover, 1T-MoS2 has shown other superior properties, such as (i) ultrafast adsorption kinetics and (ii) great anti-interference activity toward other existing cations, compared to 2H-MoS2. Extensive computations and characterizations of MoS2-Pb and -Cu adsorption complexes illustrated that the active S sites were indispensable for heavy metal adsorption. Overall, for the first time, we provide evidence that 1T-MoS2 is more functional in heavy metal removal compared to 2H-MoS2, which can guide and expand the applications of MoS2-based adsorbents in environmental remediation.
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
852应助郭宇采纳,获得10
刚刚
淡然的金针菇完成签到,获得积分20
刚刚
babyhead发布了新的文献求助10
3秒前
医学小王发布了新的文献求助10
4秒前
4秒前
eee应助HiNDT采纳,获得10
6秒前
fuiee完成签到,获得积分10
8秒前
8秒前
9秒前
郭宇发布了新的文献求助10
14秒前
Lsh173373完成签到 ,获得积分10
16秒前
16秒前
cxw发布了新的文献求助10
19秒前
毛豆爸爸发布了新的文献求助10
21秒前
士艳完成签到,获得积分10
21秒前
Akim应助丹丹采纳,获得30
22秒前
CipherSage应助晴天晒太阳采纳,获得10
23秒前
maggie完成签到 ,获得积分10
26秒前
27秒前
27秒前
28秒前
29秒前
凉白开发布了新的文献求助10
33秒前
fighting完成签到 ,获得积分10
33秒前
Anoxia发布了新的文献求助10
34秒前
34秒前
无限柠檬4519完成签到,获得积分10
36秒前
科研通AI5应助林狗采纳,获得10
38秒前
qiao应助Anoxia采纳,获得10
38秒前
冰魂应助郭宇采纳,获得10
39秒前
ll发布了新的文献求助10
39秒前
40秒前
40秒前
凉白开完成签到,获得积分10
42秒前
西西完成签到 ,获得积分10
43秒前
章鱼发布了新的文献求助10
45秒前
qiulong发布了新的文献求助10
46秒前
lucky完成签到 ,获得积分10
46秒前
lucky完成签到 ,获得积分10
46秒前
CC完成签到 ,获得积分10
47秒前
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
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
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
Mindfulness and Character Strengths: A Practitioner's Guide to MBSP 380
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 3776802
求助须知:如何正确求助?哪些是违规求助? 3322227
关于积分的说明 10209363
捐赠科研通 3037491
什么是DOI,文献DOI怎么找? 1666749
邀请新用户注册赠送积分活动 797627
科研通“疑难数据库(出版商)”最低求助积分说明 757976