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paul9979

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The starting materials were synthesized using a sol-gel method with tetraethyl orthosilicate (TEOS) and aluminum nitrate nonahydrate (ANN). Anhydrous ethanol (EtOH) and the other starting materials were mixed at the following molar ratios: Al2O3:SiO2 = 1:1 and EtOH:SiO2 = 20:1. The gel was obtained by the addition of a solution of ANN and EtOH to a solution of TEOS and EtOH with stirring. The gel was sealed in a beaker and placed in a water bath at 70ºC for approximately 13 h until a transparent, homogeneous gel was formed. After aging for 36 h at room temperature, the gel was dried in air at 105ºC for 6 h. The dried gel was calcined at 800ºC for 2 h. A sodium silicate solution (modulus = 1.0) was obtained with the water glass (solid mass fraction = 39%, modulus = 3.15) and sodium hydroxide. The Na-geopolymer specimens were prepared using pure Al2O3-SiO2 powder, sodium silicate solution, and distilled water by mechanically mixing the solid (aluminosilicate powder) with the liquid (sodium silicate solution) at a mass ratio of 1.0. The molar composition of the resulting geopolymer slurry was Al2O3-2SiO2-Na2O. After mechanically stirring the geopolymer slurry, the homogenous geopolymer paste was cast into different molds to fabricate membranes with different shapes. In this work, a disk mold (diameter = 40 mm, thickness = 10 mm) was used. The thickness of the geopolymer membrane can be controlled by different volumes of geopolymer paste casting. The disks mold were sealed and cured at 60ºC for 24 h. The cured geopolymer circular plates were removed from the molds and placed into 100 ml Teflon bottles with 50 ml of water at 90ºC for 6 h. After the hydrothermal process was performed, self-supporting NaA zeolite membranes were obtained. The thickness of zeolite membrane could be decided by casting weight of geopolymer slurry. Different weight slurry could get different thickness. The self-supporting zeolite membranes were found to be supported by crystalline materials (NaA zeolite). The structural characterizations of the geopolymeric materials and the crystalline specimens were conducted using XRD, SEM, and NMR techniques. The micropores and mesopores were measured by both adsorption and desorption isotherm analyses using high-speed surface area and pore size analyzers (NOVA® e Series 2000, Quantachrome Instruments USA).

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paul9979: ½ð±Ò+35, ·­ÒëEPI+1, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸, лл 2015-06-16 21:58:54
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