The colloidal stability of molybdenum disulfide nanosheets in different natural surface waters: Combined effects of water chemistry and light irradiation

被引:2
作者
Chen, Kexin [1 ]
Xu, Xiaoyun [1 ]
Li, Xing [1 ]
Gui, Xiangyang [1 ]
Zhao, Ling [1 ]
Qiu, Hao [1 ]
Cao, Xinde [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Environm Sci & Engn, Shanghai 200240, Peoples R China
[2] Natl Field Observat & Res Stn Erhai Lake Ecosyst, Yunnan, Peoples R China
[3] Shanghai Inst Pollut Control & Ecol Secur, Shanghai 200092, Peoples R China
基金
中国国家自然科学基金;
关键词
MoS2; nanosheets; Colloidal stability; Water chemistry; Dissolved organic matter; Photochemical transformation; MOS2; NANOSHEETS; AGGREGATION; NANOPARTICLES; DISSOLUTION; OXIDES;
D O I
10.1016/j.watres.2024.121973
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
With the increasing production and application, more molybdenum disulfide (MoS2) nanosheets could be released into environment. The aggregation and dispersion of MoS2 nanosheets profoundly impact their transport and transformation in the aquatic environment. However, the colloidal stability of MoS2 remains largely unknown in natural surface waters. This study investigated the colloidal stability of MoS2 nanosheets in six natural surface waters affected by both light irradiation and water chemistry. Compared to that of the pristine MoS2 nanosheets, the colloidal stability of MoS2 photoaged in ultrapure water declined. Light irradiation induced the formation of Mo-O bonds, the release of SO42- species, and the decrease in 1T/2H ratio(,) which reduced negative charge and enhanced hydrophobicity. However, the colloidal stability of MoS2 photoaged in natural surface waters was increased relative to that in ultrapure water not only for the smaller extent of photochemical transformation but more importantly the surface modification by water chemistry. Furthermore, the colloidal stability of MoS2 photoaged in natural surface waters followed the order of sea water > lake water > river water. The abundant cations (e.g., Ca2+ and Mg2+) in sea water facilitated the covalent grafting (S-C bonds) of more dissolved organic matter (DOM) on MoS2 via charge screening and cation bridging, thus inducing stronger electrostatic repulsion and steric effect to stabilize nanosheets. The crucial role of the covalent grafting of DOM was further confirmed by the positive correlation between the critical coagulation concentration values and S-C ratios (R-2 = 0.82, p < 0.05). Our results highlighted the dominant role of water chemistry than light irradiation in dictating the colloidal stability of MoS2 photoaged in natural surface waters, which provided new insight into the environmental behavior of MoS2 in aquatic environment.
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页数:10
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