Effect of cure temperature on the formation of metakaolinite-based geopolymer

被引:140
作者
Aredes, F. G. M. [1 ]
Campos, T. M. B. [1 ]
Machado, J. P. B. [1 ,2 ]
Sakane, K. K. [2 ]
Thim, G. P. [1 ]
Brunelli, D. D. [1 ]
机构
[1] Inst Tecnol Aeronaut, Div Ciencias Fundamentais, Sao Jose Dos Campos, SP, Brazil
[2] Univ Vale Paraiba, Inst Pesquisa & Desenvolvimento, Sao Jose Dos Campos, SP, Brazil
关键词
Porosity; Geopolymer; Metakaolin; FLY-ASH; WATER; MICROSTRUCTURE; STRENGTH;
D O I
10.1016/j.ceramint.2015.02.022
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
A series of metakaolinite-based geopolymer was prepared at several curing temperatures and its relationship with porosity, infrared spectrometry (FT-IR) and mechanical properties was investigated. The samples were cured at the following temperatures: 55, 65 and 80 degrees C for 1 h. After a post cure of 28 days, the samples were investigated by using the following techniques: compressive strength, mercury intrusion porosimetry (MP), helium pycnometry, X-ray diffraction (XRD), scanning electron microscopy (SEM) and infrared spectrometry (FT-IR). All samples were amorphous by XRD. The sample thermally treated at 65 degrees C (C65) presented the highest values of compressive strength and relative integrated area of peak at 792 cm(-1). This peak was attributed to a higher concentration of tetra-coordinated aluminum, indicating a higher efficiency of the geopolymeric reaction. The C65 also presented the lowest volume of closed pores. The values of the skeletal and the true densities for C65 were very similar and consistent with the volume of the closed pores. On the other hand, this sample showed the highest bulk density obtained by MW and the greatest difference between the open and closed porosity measured by MW and helium pycnometry, respectively. All these results are coherent and clearly indicate that the amount of open pores is directly related to a better mechanical performance of the geopolymeric sample. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:7302 / 7311
页数:10
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