Aggregation behavior of graphitic C3N4 nanosheets in aqueous environment: Kinetics and mechanisms

被引:8
|
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
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页数:9
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