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The representative geopolymerization product was fabricated through alkaline- or alkali-silicate-activated metakaolin, which has a wide range of compositions represented by M2O-mAl2O3-nSiO2, where (usually) m ¡Ö 1, 2 ¡Ü n ¡Ü 6, and M represents one or more alkali metals. To obtain geopolymers with a low Si/Al ratio and to overcome the disadvantages associated with the use of impure raw materials; amorphous Al2O3-SiO2 powder was first prepared through a sol-gel method in accordance with chemical compositions that were specifically designed in our work. The composition of the geopolymers is similar to that of the NaA zeolites when n = 2 and M = Na [15-16]. During this fabrication process, sodium silicate was used as an alkali activator (SiO2:Na2O molar ratio = 1.0), and the molar ratio of SiO2 in the synthetic powders to that of the sodium silicate was 1:1. Therefore, the chemical composition of the resulting geopolymers was Al2O3-2SiO2-Na2O. The zeolite crystal structure was obtained through the hydrothermal processing of Al2O3-2SiO2-Na2O at 90ºC for 6 h. The XRD patterns and the MAS NMR spectra of the calcined Al2O3-SiO2 powders, the chemosynthetic Al2O3-2SiO2-Na2O geopolymers, and the hydrothermal samples are presented in Fig. 2. Traditional alkali-based geopolymers typically exhibit one ¡°hump¡± centered at approximately 26.0¡ã to 29.0¡ã (2¦È) in their XRD patterns [17-19]. However, the XRD pattern of the as-prepared Al2O3-2SiO2-Na2O geopolymer has one ¡°hump¡± centered at approximately 28.5¡ã, which indicates a trend of crystallization. The HRTEM results from the analysis of the Al2O3-2SiO2-Na2O geopolymer confirm the existence of nanoscale ordered structures within the amorphous geopolymer gel [15-16]. After the hydrothermal process, the XRD results indicate that the majority of the Al2O3-2SiO2-Na2O geopolymers transformed into NaA zeolite crystals with good crystallinity (see Fig. 2a). The most important observation from our results is that the crystalline zeolite seeds already exist in a solid geopolymer gel. Key evidence supporting this conclusion was also obtained from the MAS NMR spectra. |
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- ×¢²á: 2005-06-04
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hellen7256: ½ð±Ò+30, ·ÒëEPI+1, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-06-17 21:40:53
hellen7256: ½ð±Ò+30, ·ÒëEPI+1, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-06-17 21:40:53
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