SDA-Free Hydrothermal Synthesis of High-Silica Ultra-nanosized Zeolite Y

2017 ◽  
Vol 17 (3) ◽  
pp. 1173-1179 ◽  
Author(s):  
Maeva Borel ◽  
Mathias Dodin ◽  
T. Jean Daou ◽  
Nicolas Bats ◽  
Bogdan Harbuzaru ◽  
...  
2016 ◽  
Vol 52 (86) ◽  
pp. 12765-12768 ◽  
Author(s):  
Dawei He ◽  
Danhua Yuan ◽  
Zhijia Song ◽  
Yansi Tong ◽  
Yaqi Wu ◽  
...  

Zeolite Y with a SiO2/Al2O3 ratio of 7.76 and outstanding thermal stability and hydrothermal stability is synthesized using TEAOH as an SDA.


1997 ◽  
Vol 15 (4) ◽  
pp. 289-299 ◽  
Author(s):  
Ivar M. Dahl ◽  
Elisabeth Myhrvold ◽  
Åse Slagtern ◽  
Michael Stöcker

Two dealuminated β-zeolites, zeolite Y and MCM-22 as well as silicalite, MCM-41 and AlPO4-5 have been studied as hydrophobic adsorbents in water solutions. Dealuminated β-zeolite, MCM-22 and silicalite all adsorb alcohols from water solutions. Enhanced adsorption is obtained for alcohols with longer alkyl chains. Adsorption in the practically most interesting 10–80% range of zeolite filling may adequately be described by Langmuir isotherms. The Langmuir adsorption constants are similar for β-zeolite, MCM-22 and silicalite. This indicates that the adsorption is independent of the pore structure for the alcohols tested in this study. The surface silanol density is however important, such that a low SiOH density is required to give lipophilic properties. In line with this, dealuminated zeolite Y, as prepared here, and MCM-41 give only a poor preference for alcohols from water. For the β-zeolite, the dealumination procedure is important for retaining the micropore volume and adsorption capacity of the zeolite. AlPO4-5 shows no potential as an adsorbent for alcohols from water solutions.


2008 ◽  
Vol 16 (3) ◽  
pp. 299-306 ◽  
Author(s):  
Young Chang Kim ◽  
Ji Yeon Jeong ◽  
Ji Yeong Hwang ◽  
Shin Dong Kim ◽  
Wha Jung Kim

2004 ◽  
Vol 112 (1306) ◽  
pp. 332-337
Author(s):  
Tomohiro TSUDA ◽  
Baowang LU ◽  
Yasuyuki YAO ◽  
Yasunori OUMI ◽  
Keiji ITABASHI ◽  
...  

Langmuir ◽  
2010 ◽  
Vol 26 (12) ◽  
pp. 9524-9532 ◽  
Author(s):  
Ilaria Braschi ◽  
Giorgio Gatti ◽  
Geo Paul ◽  
Carlo E. Gessa ◽  
Maurizio Cossi ◽  
...  

2020 ◽  
Vol 12 (2) ◽  
pp. 173-179 ◽  
Author(s):  
Supinya Nijpanich ◽  
Takeshi Hagio ◽  
Yuki Kamimoto ◽  
Ryoichi Ichino

MFI-type zeolite is a crystalline microporous aluminosilicate with an intersecting two-dimensional pore structure and well-defined windows of approximately 0.55 nm. It generally crystallizes in high silica to alumina ratios, leading to a rather hydrophobic character. This makes it an attractive adsorbent for removing organic pollutants from wastewater. However, separating the conventional powdery-zeolites from the media after treatment is difficult because they require considerable time to settle. They also trigger filter clogging. In this work, high silica MFI-type zeolite, namely, silicalite-1, was synthesized on the surfaces of hollow glass microspheres to develop a floating adsorbent with high hydrophobicity. Tetraethylorthosilicate and tetrapropylammonium hydroxide were used as the additional silica source and structure directing agent, respectively. The crystallization of silicalite-1 on hollow glass microspheres was performed using hydrothermal synthesis at 180 °C or 150 °C for 40 h using a precursor sol with a molar composition of 3SiO2:1TPA:14EtOH:286H2O. The surface coverage and crystallinity of the as-prepared samples were optimized, and the floatability and adsorption performance of the optimized sample were investigated. Well-covered microspheres were obtained when hydrothermal synthesis was conducted at 180 °C using 0.5 g of hollow glass microspheres and 15 g of a precursor sol adjusted to pH 12.5. The balance between the dissolution rate of the hollow glass microspheres and the crystallization rate of silicalite-1 appeared to be the key factor in the successful synthesis.


2016 ◽  
Vol 43 ◽  
pp. 302-312 ◽  
Author(s):  
I. Braschi ◽  
S. Blasioli ◽  
E. Buscaroli ◽  
D. Montecchio ◽  
A. Martucci

2016 ◽  
Vol 45 (8) ◽  
pp. 919-921 ◽  
Author(s):  
Naoto Nakazawa ◽  
Satoshi Inagaki ◽  
Yoshihiro Kubota

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