Effect of nano-silica on the efflorescence of waste based alkali-activated inorganic binder

被引:60
作者
Wang, Jinbang [1 ]
Zhou, Tongtong [2 ]
Xu, Dongyu [1 ]
Zhou, Zonghui [1 ]
Du, Peng [1 ]
Xie, Ning [1 ]
Cheng, Xin [1 ]
Liu, Yu [3 ]
机构
[1] Univ Jinan, Engn Ctr Adv Bldg Mat, Shandong Prov Key Lab Preparat & Measurement Bldg, Minist Educ, Jinan 250022, Shandong, Peoples R China
[2] Shandong High Speed Rd & Bridge Maintenance Co Lt, Jinan 250022, Shandong, Peoples R China
[3] Shenzhen Gang Chuang Bldg Mat Co Ltd, Shenzhen 518035, Peoples R China
基金
中国国家自然科学基金;
关键词
Nano-silica; Efflorescence; Waste; Alkali-activated inorganic binder; FLY-ASH; MECHANICAL-PROPERTIES; COMPRESSIVE STRENGTH; PORE STRUCTURE; CEMENT PASTES; SI/AL RATIO; SLAG; METAKAOLIN; NANO-SIO2; MICROSTRUCTURE;
D O I
10.1016/j.conbuildmat.2018.02.006
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
The efflorescence caused by carbonate weathering is one of the dominant causes of deterioration of alkali-activated inorganic materials. In order to inhibit the efflorescence of waste based alkali-activated inorganic binder, the effects of nano-silica on the compressive strength, carbonate ions concentration, hydration rate and pore size distribution of the obtained alkali-activated inorganic binder have been investigated, and the efflorescence inhibition mechanism has been also analyzed. The results revealed that compressive strength and microstructural properties could be further developed with inclusion of nano-silica in alkali-activated inorganic binder. In addition, the efflorescence decreased with increasing nano-silica content and decreasing of the nano-silica particle size. Besides, the hydration rate results indicated that the hydration of waste based alkali-activated inorganic binder was accelerated before hydration for 3d with the incorporation of nano-silica. The suggested inhibition mechanisms discussed were mainly; micro-aggregate filling effect, induced nucleation, and accelerated hydration effects of nano-silica. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:381 / 390
页数:10
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