Direct hydrothermal synthesis and stabilization of high-silica mordenite (Si∶Al = 25) using tetraethylammonium and fluoride ions

2003 ◽  
Vol 13 (5) ◽  
pp. 1173-1179 ◽  
Author(s):  
Hitoshi Sasaki ◽  
Yasunori Oumi ◽  
Keiji Itabashi ◽  
Baowang Lu ◽  
Toshiharu Teranishi ◽  
...  
2017 ◽  
Vol 17 (3) ◽  
pp. 1173-1179 ◽  
Author(s):  
Maeva Borel ◽  
Mathias Dodin ◽  
T. Jean Daou ◽  
Nicolas Bats ◽  
Bogdan Harbuzaru ◽  
...  

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

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 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.


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

2004 ◽  
Vol 16 (2) ◽  
pp. 286-291 ◽  
Author(s):  
Baowang Lu ◽  
Tomohiro Tsuda ◽  
Hitoshi Sasaki ◽  
Yasunori Oumi ◽  
Keiji Itabashi ◽  
...  

1999 ◽  
Vol 77 (12) ◽  
pp. 2099-2104 ◽  
Author(s):  
Rémi Valéro ◽  
Bernard Durand ◽  
Jean-Louis Guth ◽  
Thierry Chopin

The solubility of zirconia gels versus pH is studied in order to state first the influence of F- ions alone, then the influence of the simultaneous presence of F- and amorphous silica. Two concentrations of F- ions are chosen, 0.094 and 0.314 mol L-1, corresponding to initial molar ratios F/Zr = 0.6 and 2.0. Metal fluorocomplexes formed at pH 0.5 and 2.5 are characterized by 19F NMR. The influence of F- on the solubility of zircon is also studied. It is shown that the formation of silicon complexes rich in fluorine shifts the equilibriums between the zirconium fluorocomplexes toward the complexes poor in fluorine and that, in the presence of F-, the crystallization of zircon by hydrothermal synthesis can be forecasted, for pH values in the range 0-10.Key words: zirconia gels, silica, zircon, fluoride ions, solubility, 19F NMR.


2005 ◽  
Vol 81 (1-3) ◽  
pp. 365-374 ◽  
Author(s):  
Baowang Lu ◽  
Yasunori Oumi ◽  
Keiji Itabashi ◽  
Tsuneji Sano

ChemInform ◽  
2004 ◽  
Vol 35 (15) ◽  
Author(s):  
Baowang Lu ◽  
Tomohiro Tsuda ◽  
Hitoshi Sasaki ◽  
Yasunori Oumi ◽  
Keiji Itabashi ◽  
...  

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