Molecular Dynamics Simulations of Chloride and Sulfate Ion Transport in C-S-H gel and γ-FeOOH Nanopores

被引:3
|
作者
Tu, Yongming [1 ,2 ,3 ]
Yuan, Lei [1 ]
Liu, Dongyun [1 ,3 ]
Cao, Jie [1 ]
Ding, Yihui [1 ,3 ]
Das, Oisik [3 ]
Forsth, Michael [3 ]
Sas, Gabriel [3 ,4 ]
Elfgren, Lennart [3 ]
机构
[1] Southeast Univ, Sch Civil Engn, Key Lab Concrete & Prestressed Concrete Struct, Minist Educ, Nanjing 211189, Peoples R China
[2] Southeast Univ, Natl Engn Res Ctr Prestressing Technol, Nanjing 211189, Peoples R China
[3] Lulea Univ Technol, Dept Civil Environm & Nat Resources Engn, Div Struct & Fire Engn, S-97187 Lulea, Sweden
[4] SINTEF Narvik AS, N-8517 Narvik, Norway
基金
中国国家自然科学基金;
关键词
CALCIUM-SILICATE-HYDRATE; WATER-MOLECULES; CEMENT PASTE; CARBON-STEEL; NANO-SCALE; ADSORPTION; CONCRETE; HYDROXIDE; CORROSION; BEHAVIOR;
D O I
10.3151/jact.20.720
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Interactions between Cl-, SO42-and cementitious materials, reinforcement passive films influence the durability of rein-forced concrete structures. Transport of three solutions (NaCl, Na2SO4, mixed) in calcium silicate hydrate (C-S-H) gel, gamma- FeOOH nanopores was investigated using molecular dynamics. Solution transport in gamma-FeOOH nanopores is slower than in C-S-H gel nanopores because of the lesser hydrophilicity of gamma-FeOOH surface. SO42-can form ion clusters to hinder the solution transport and atomic motion, and the ion clusters appear in the solution more frequently than at the interface. Temporary adsorption of Cl-, SO42-on substrate surfaces occurs during transport because of Ca-Cl, Ca-SO4 ionic bonds on the C-S-H surface and Ho (hydroxyl hydrogen atoms)-Cl, Ho-SO4 hydrogen bonds on the gamma-FeOOH surface, and these bonds are influenced by the local structure. Two substrates interact with water, Cl-, SO42-via distinct microscopic mech-anisms.
引用
收藏
页码:720 / 731
页数:12
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