Probing the hydration behavior of tricalcium aluminate under the in situ polymerization of acrylic acid

被引:11
|
作者
Liu, Qing [1 ]
Ming, Xing [2 ]
Wang, Miaomiao [3 ]
Wang, Qiao [4 ]
Li, Yunjian [2 ]
Li, Zongjin [2 ]
Hou, Dongshuai [5 ]
Geng, Guoqing [1 ]
机构
[1] Natl Univ Singapore, Dept Civil & Environm Engn, Singapore 117576, Singapore
[2] Macau Univ Sci & Technol, Fac Innovat Engn, Ave Wai Long, Taipa 999078, Macau, Peoples R China
[3] Yancheng Inst Technol, Sch Mat Sci & Engn, Yancheng 224051, Peoples R China
[4] Hebei Univ Technol, Sch Civil & Transportat Engn, 5340 Xiping Rd, Tianjin 300401, Peoples R China
[5] Qingdao Univ Technol, Coll Civil Engn, Qingdao 266000, Peoples R China
关键词
Tricalcium aluminate; Hydration; In situ polymerization; Ab initio molecular dynamics; AL-27 MAS NMR; CARBONATION RESISTANCE; RAMAN-SPECTROSCOPY; PORTLAND-CEMENT; POLYMERS; C(3)A; PHASES; SUPERPLASTICIZERS; PSEUDOPOTENTIALS; INTERCALATION;
D O I
10.1016/j.cemconres.2024.107429
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The early hydration of Portland cement is profoundly affected by the mineral phase of tricalcium aluminate (C3A), but how in situ polymerization of monomers influences the hydration of C3A remains unclear. Herein, we probed the effect of in situ polymerization of acrylic acid (AA) on the hydration behavior of cubic C3A from experiment and ab initio molecular dynamics simulation (AIMD). Our findings reveal that in situ polymerization of AA retarded C3A hydration, which was corroborated by the AIMD result that polyacrylic acid (PAA) reduced the charge transfer between C3A and water and inhibited the dissolution of Ca ions from C3A surfaces by adsorbing on the C3A. Additionally, in situ polymerized PAA improves the carbonation resistance of C3A hydrates, accompanied by lowering their crystallinity. Hopefully, our findings can provide valuable guidance on the theory for implementing in situ polymerization of monomers in cement -based materials.
引用
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页数:13
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