Geopolymerization of halloysite via alkali-activation: Dependence of microstructures on precalcination
Geopolymerization of halloysite via alkali-activation: Dependence of microstructures on precalcination
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通过碱活化进行埃洛石的地质聚合:微观结构对预分解的依赖性
DOI:
10.1016/j.clay.2019.105375
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发表时间:
2020-02
影响因子:
5.6
通讯作者:
Liu Dong
中科院分区:
文献类型:
--
作者:
Zhang Baifa;Guo Haozhe;Yuan Peng;Li Yun;Wang Qiang;Deng Liangliang;Liu Dong
Halloysite has a chemical composition very similar to that of kaolinite, but it possesses a special nanotubular structure and surface reactivity. This work focuses on the geopolymerization of halloysite via alkali-activation, and investigates the effects of precalcination temperatures ranging from 450 °C to 1000 °C on the microstructures and mechanical properties of halloysite-based geopolymer. The products obtained were characterized using a combination of techniques including X-ray diffraction, Fourier-transform infrared spectroscopy, scanning electron microscopy, N2physisorption analysis, and nuclear magnetic resonance. The results show that halloysite underwent minimal structural changes when calcined at 450 °C, and its alkali-activation product showed poor mechanical properties due to the formation of hydrosodalite with a porous structure. The dehydroxylation that occurred at calcination temperatures between 650 °C and 850 °C could improve the reactivity of halloysite with alkaline solution. The formation of geopolymer with a compact structure resulted in increased compressive strength. When halloysite was calcined at 1000 °C, geopolymerization also occurred, but to a lesser extent because of the formation of nanosized γ-Al2O3. This resulted in a decreased compressive strength in the product. These results indicate that the microstructures and properties of halloysite-based geopolymers are greatly dependent upon the precalcination of halloysite and that the optimal temperature is around 750 °C to ensure a high degree of dehydroxylation with high reactivity, which is favorable for geopolymerization.
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影响因子:
3.5
作者:
K. Heide;M. Földvári
通讯作者:
K. Heide;M. Földvári
DOI:
10.1007/s11595-009-1132-6
发表时间:
2009-03
期刊:
Journal of Wuhan University of Technology-Mater. Sci. Ed.
影响因子:
--
作者:
Zuhua Zhang;X. Yao;Huajun Zhu;Sudong Hua;Yue Chen
通讯作者:
Zuhua Zhang;X. Yao;Huajun Zhu;Sudong Hua;Yue Chen
影响因子:
3.9
作者:
Lee, WKW;van Deventer, JSJ
通讯作者:
van Deventer, JSJ
影响因子:
3.9
作者:
Chen, Xu;Sutrisno, Andre;Struble, Leslie J.
通讯作者:
Struble, Leslie J.
影响因子:
2.2
作者:
P. Yuan;Daoyong Tan;F. Annabi-Bergaya;Wenchang Yan;Mingde Fan;Dong Liu;Hongping He
通讯作者:
P. Yuan;Daoyong Tan;F. Annabi-Bergaya;Wenchang Yan;Mingde Fan;Dong Liu;Hongping He