Direct Synthesis of Cubic Benzene-Bridged Mesoporous Organosilica Functionalized with Mercaptopropyl Groups as an Effective Adsorbent for Mercury and Silver Ions

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題名:	Direct Synthesis of Cubic Benzene-Bridged Mesoporous Organosilica Functionalized with Mercaptopropyl Groups as an Effective Adsorbent for Mercury and Silver Ions
作者:	Wu,HY;Chen,CT;Hung,IM;Liao,CH;Vetrivel,S;Kao,HM
貢獻者:	化學學系
關鍵詞:	MOLECULAR-SCALE PERIODICITY;SILICA SBA-1;LARGE-PORE;HETEROGENEOUS CATALYSTS;SELECTIVE ADSORPTION;ACIDIC CONDITIONS;SULFONIC-ACIDS;ORGANIC GROUPS;CHANNEL WALLS;SURFACTANT
日期:	2010
上傳時間:	2012-03-27 18:08:01 (UTC+8)
出版者:	國立中央大學
摘要:	Well-ordered cubic (Pm (3) over barn symmetry) benzene-bridged periodic mesoporous organosilicas (PMOs) functionalized with variable contents of thiol groups were successfully synthesized via a one-step co-condensation of 1,4-bis(triethoxysilyl)benzene (BTEB) and 3-mercaptopropyltrimethoxysilane (MPTMS) in a highly acidic medium with use of cetyltrimethylammonium bromide (CTMABr) as the structure-directing agent. The materials thus obtained exhibited ordered and uniformed mesopores up to 25 mol % of MPTMS in the initial mixture. Direct evidence of the simultaneous presence of chemically attached thiol and benzene moieties was provided by solid-state (29)Si and (13)C NMR spectroscopy. The present cubic PMOs can be synthesized with a wide temperature window from 0 to 100 degrees C without any undesirable phase transformation. On the contrary, this is not possible when BTEB was replaced by tetraethoxysilane (TEOS) as the silicon source for the conventional synthesis of SBA-1 with Pm (3) over barn symmetry. It suggests that the benzene-linking spacer of BTEB has a beneficial effect on the enlargement of effective head group of the surfactant against the temperature changes and thus prevents phase transformation to a hexagonal mesophase. These thiol-functionalized benzene-silica materials exhibited high adsorption affinity toward metal ions such as Hg(2+) and Ag(+) but not for Cd(2+), Co(2+), and Pb(2+). Of particular interest is that the (13)C NMR chemical shift of the carbon atom adjacent to the -SH group is sensitive to the Hg(2+) and Ag(+) ion bindings, shifting from 27 ppm to 37 and 34 ppm, respectively. Such a significant NMR shift provides clear evidence that there are strong interactions between the thiol groups and the Hg(2+) and Ag(+) ions.
關聯:	JOURNAL OF PHYSICAL CHEMISTRY C
顯示於類別:	[化學學系] 期刊論文

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