An Efficient Way to Synthesize Hiroshima University Silicate-1 (HUS-1) and the Selective Adsorption Property of Ni2+ from Seawater

An alternative and efficient way to synthesize HUS-1 (Hiroshima University Silicate-1, Si10O24H8·2[(CH3)4N]), and a new notable function of HUS-1 are reported. HUS-1, which is an ast-type layered silicate, was originally synthesized through a complicated process from two kinds of dealuminated zeolit...

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Published inBulletin of the Chemical Society of Japan Vol. 87; no. 1; pp. 160 - 166
Main Authors Honda, Koutaro, Ide, Yusuke, Tsunoji, Nao, Torii, Masato, Sadakane, Masahiro, Sano, Tsuneji
Format Journal Article
LanguageEnglish
Published Tokyo The Chemical Society of Japan 01.01.2014
Chemical Society of Japan
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Summary:An alternative and efficient way to synthesize HUS-1 (Hiroshima University Silicate-1, Si10O24H8·2[(CH3)4N]), and a new notable function of HUS-1 are reported. HUS-1, which is an ast-type layered silicate, was originally synthesized through a complicated process from two kinds of dealuminated zeolites, FAU and *BEA, with tetramethylammonium (TMA) and benzyltrimethylammonium hydroxides, respectively. In this article, the synthesis of HUS-1 by using only amorphous silica and TMA as a silica source and a structure directing reagent, respectively, with varied temperature, time, and composition of a starting mixture containing water, TMA hydroxide, sodium hydroxide, and amorphous silica, in the presence or the absence of a seed crystal was examined to find that HUS-1 successfully formed for a wide range of NaOH/SiO2 (0.2–0.6) and TMA/SiO2 (0.2–0.8) ratios and reaction time (3–21 days) at a H2O/SiO2 ratio of 5.5 and reaction temperature of 140 °C in the presence and the absence of a seed crystal. The particle size and crystallinity of HUS-1 varied depending on the synthetic conditions. The obtained HUS-1 selectively adsorbed Ni2+ from a mixed electrolytes solution mimicking seawater. The maximum amount of the adsorbed Ni2+ on HUS-1 was dependent on the synthetic conditions.
ISSN:0009-2673
1348-0634
DOI:10.1246/bcsj.20130251