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首页> 外文期刊>Microporous and mesoporous materials: The offical journal of the International Zeolite Association >ZSM-5 and ferrierite synthesized by magadiite conversion method in 1, 6-hexamethylenediamine system
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ZSM-5 and ferrierite synthesized by magadiite conversion method in 1, 6-hexamethylenediamine system

机译:1,6-六亚甲基二胺体系中通过magadiite转化法合成的ZSM-5和镁碱沸石

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摘要

ZSM-5 and ferrierite have been successfully synthesized by magadiite conversion method using 1, 6-hexamethylenediamine (HMD) as structure directing agent. The binary crystallization phase diagram was obtained by various reactant ratios of H2O/SiO2 and SiO2/Al2O3 and the regular phase transformations were also demonstrated. The optimized reactant HMD/SiO2 ratio was 0.6. The high crystalline ZSM-5 was composed of coffin-shaped crystallite with length of 4 gm where as ferrierite exhibited platelike crystallite having a diameter of 8 mu m. The C-13 MAS NMR spectra revealed that the HMD which can be used as a structure directing agent in the conversion process was held tenaciously inside the pores of ZSM-5 and ferrierite. The formula of as-obtained ZSM-5 and ferrierite could be vertical bar K-2.1(C6H16N2)(4.2)(H2O)(16.9)H-8.4 vertical bar[Si85.5Al10.5O192] and vertical bar K-2.1(C6H16N2)(0.9)(H2O)(6.4)H-2.2 vertical bar[Si31.7Al4.3O72] respectively based on the compositional analysis. More over the structure of prepared ZSM-5 and ferrierite were collapsed when the temperature rose up to 1200 degrees C and 1100 degrees C respectively; both are exceptionally stable towards strong acid. (C) 2015 Elsevier Inc. All rights reserved.
机译:以1,6-六亚甲基二胺(HMD)为结构导向剂,通过菱铁矿转化法成功合成了ZSM-5和镁碱沸石。通过H2O / SiO2和SiO2 / Al2O3的不同反应物比得到二元结晶相图,并证明了规则的相变。优化的反应物HMD / SiO 2比为0.6。高结晶性ZSM-5由长度为4gm的棺材状微晶组成,其中作为镁碱沸石具有直径为8μm的板状微晶。 C-13 MAS NMR光谱表明,可以在转化过程中用作结构导向剂的HMD牢固地保持在ZSM-5和镁碱沸石的孔中。所获得的ZSM-5和镁碱沸石的配方可以是垂直棒K-2.1(C6H16N2)(4.2)(H2O)(16.9)H-8.4垂直棒[Si85.5Al10.5O192]和垂直棒K-2.1(C6H16N2)根据组成分析)分别为(0.9)(H2O)(6.4)H-2.2竖线[Si31.7Al4.3O72]。当温度分别升至1200℃和1100℃时,所制备的ZSM-5和镁碱沸石的结构进一步塌陷。两者对强酸都格外稳定。 (C)2015 Elsevier Inc.保留所有权利。

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