共 52 条
Aggregation behavior of graphitic C3N4 nanosheets in aqueous environment: Kinetics and mechanisms
被引:10
作者:
Dong, Shunan
[1
]
Cai, Wangwei
[1
]
Sheng, Liting
[1
]
Wang, Weimu
[1
]
Liu, Hui
[1
]
Xia, Jihong
[1
]
机构:
[1] Hohai Univ, Coll Agr Sci & Engn, Nanjing 210098, Peoples R China
基金:
中国国家自然科学基金;
关键词:
g-C3N4;
nanosheets;
Aggregation kinetics;
CCC values;
pH;
Electrolytes;
GRAPHENE OXIDE NANOMATERIALS;
CARBON NITRIDE NANOSHEETS;
DISSOLVED ORGANIC-MATTER;
HUMIC-ACID;
PHOTOCATALYTIC ACTIVITY;
G-C3N4;
NANOSHEETS;
POROUS-MEDIA;
STABILITY;
NANOPARTICLES;
ADSORPTION;
D O I:
10.1016/j.envpol.2020.114646
中图分类号:
X [环境科学、安全科学];
学科分类号:
08 ;
0830 ;
摘要:
The aggregation behaviors of graphitic carbon nitride (g-C3N4) nanosheets under various electrolytes and pH conditions were systematically investigated. The aggregation of g-C3N4 nanosheets was significantly enhanced with increasing electrolyte concentrations. The divalent electrolytes (CaCl2 and MgCl2) were more effective than monovalent electrolytes (NaCl and KCl) in promoting the aggregation of g-C3N4 nanosheets. At the same valence, cations with higher atomic weight were more effective in enhancing the aggregation of g-C3N4 nanosheets. The measured critical coagulation concentrations (CCC) of g-C3N4 nanosheets were 4.7 mM KCl, 9.2 mM NaCl, 1.0 mM CaCl2 and 1.9 mM MgCl2 at pH 6.0, which were lower than some of other two-dimensional nanoparticles. The CCC values of g-C3N4 nanosheets were decreased to 5.5 mM NaCl at pH 2.0, but increased to 29.0 mM NaCl and 2.1 mM CaCl2 at pH 10.0, indicating that the aggregation degree of g-C3N4 nanosheets was decreased with increasing pH. The Fe/Al hydrated complexes generated at the specific pH inhibited the aggregation of g-C3N4 nanosheets and enhanced the stability. Overall, findings from this study demonstrated that the electrolytes and pH conditions played important and combined roles on the aggregation of g-C3N4 nanosheets. In addition, the aggregation behaviors of g-C3N4 nanosheets could be well predicted with the DLVO theory. (c) 2020 Elsevier Ltd. All rights reserved.
引用
收藏
页数:9
相关论文