Studying effects of chemical admixtures on the workability retention of zeolitic Portland cement mortar

被引:36
作者
AzariJafari, Hessam [1 ]
Kazemian, Ali [2 ]
Ahmadi, Babak [3 ,5 ]
Berenjian, Javad [4 ]
Shekarchi, Mohammad [5 ]
机构
[1] Univ Sherbrooke, Dept Civil Engn, Sherbrooke, PQ J1K 2R1, Canada
[2] Univ So Calif, Sonny Astani Dept Civil & Environm Engn, Los Angeles, CA USA
[3] Amirkabir Univ Technol, Dept Civil & Environm Engn, Tehran, Iran
[4] Tabari Inst Higher Educ, Dept Civil Engn, Babol Sar, Iran
[5] Univ Tehran, Coll Engn, Sch Civil Engn, Construct Mat Inst, Tehran, Iran
关键词
Natural zeolite; Chemical admixture; Compatibility; Zeta potential; Adsorption isotherm; ALKALI-SILICA REACTION; NATURAL ZEOLITE; BLENDED CEMENTS; COMPETITIVE ADSORPTION; DURABILITY PROPERTIES; HIGH-VOLUME; IN-SITU; CONCRETE; SUPERPLASTICIZER; FUME;
D O I
10.1016/j.conbuildmat.2014.09.020
中图分类号
TU [建筑科学];
学科分类号
0813 ;
摘要
In this paper, the effects of three superplasticizers, namely, poly-carboxylate ether, calcium ligno-sulfonate, and Naphthalene Sulfonate Formaldehyde, on the workability retention of NZ blended mortars were investigated. In addition, simultaneous inclusion of either tripolyphosphate type retarder or Na2SO4 admixtures was examined as a measure to mitigate the workability loss of NZ blended mortars. Thereafter, the compatibility of zeolitic cement with three different superplasticizers was studied in more details by performing adsorption isotherm test, zeta potential test and also pH measurement of pastes at different time intervals. Obtained results indicated that for ligno-sulfonate and naphthalene sulfonate superplasticizers, reduction in the amount of electrostatic charge (which occurred by NZ inclusion) is an influential parameter contributing to the higher workability loss. On the other hand, for poly-carboxylate ether admixture, the results implied that the significantly high polymer adsorption is the major reason for the observed workability loss of NZ blended mortars. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:262 / 269
页数:8
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