The hydration mechanism and performance of Modified magnesium oxysulfate cement by tartaric acid

被引:162
|
作者
Wu, Chengyou [1 ]
Chen, Wenhai [1 ]
Zhang, Huifang [2 ]
Yu, Hongfa [3 ]
Zhang, Wuyu [1 ]
Jiang, Ningshan [1 ]
Liu, Lianxin [1 ]
机构
[1] Qinghai Univ, Sch Civil Engn, Xining 810016, Peoples R China
[2] Chinese Acad Sci, Qinghai Inst Salt Lakes, Xining 810008, Peoples R China
[3] Nanjing Univ Aeronaut & Astronaut, Dept Civil Engn, 29 Yudao St, Nanjing 210016, Jiangsu, Peoples R China
关键词
Magnesium oxysulfate cement; Tartaric acid; Setting time; Compressive strength; 5Mg(OH)(2)center dot MgSO4 center dot 7H(2)O; CITRIC-ACID; PHOSPHORIC-ACID; PHOSPHATES;
D O I
10.1016/j.conbuildmat.2017.03.222
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
Magnesium oxysulfate (MOS) cement has the advantages of light weight, low alkalinity, fire resistance, and good decorative value. Large-scale applications of MOS cement in civil engineering have been restricted by its low strength, which can be improved by adding some proper additives. Here, the effects of tartaric acid on the setting time, compressive strength, flexural strength, and deformation of MOS cement have been studied. Fourier transform infrared spectra, pH changes, hydration-heat release rate, and impedance have been observed to determine the effects of tartaric acid on the hydration process of MOS cement. To a certain extent, the addition of tartaric acid extends the setting time of MOS cement by improving the stability of the hydration film of active MgO in magnesium sulfate. X-ray diffraction, scanning electron microscopy, and mercury intrusion porosimetry were used to examine the hydration products and pore-size distribution of MOS cement. The analysis results indicate that the main reason for the high strength of MOS cement with tartaric acid is that the addition of tartaric acid can promote the formation of the needle-like high-strength phase of 5Mg(OH)(2)center dot MgSO4 center dot 7H(2)O and inhibit the formation and growth of the Mg(OH)(2) crystal phase. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:516 / 524
页数:9
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