Synthesis and structural properties of titanium containing microporous/mesoporous silicate composite (Ti, Al)-Beta/MCM-48

被引:21
作者
Mazaj, Matjaz
Logar, Natasa Zabukovec
Mali, Gregor
Tusar, Natasa Novak
Arcon, Iztok
Ristic, Alenka
Recnik, Aleksander
Kaucic, Venceslav
机构
[1] Natl Inst Chem, Ljubljana 1000, Slovenia
[2] Univ Nova Gorica, Nova Gorica 5000, Slovenia
[3] Jozef Stefan Inst, Ljubljana 1000, Slovenia
关键词
microporous; mesoporous; microporous/mesoporous composite; (Ti; Al)-beta/MCM-48; Ti EXAFS; Ti XANES; NMR; nitrogen adsorption; HRTEM;
D O I
10.1016/j.micromeso.2006.08.028
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Thermally stable titanium-containing microporous/mesoporous composite (Ti, Al)-Beta/MCM-48 was synthesised hydrothermally in the presence of structure-directing agents cetyltrimethylammonium bromide (CTABr), polyoxyethylene(8) isooctylhexyl ether (Triton(D X-114) and tetraethylammonium hydroxide (TEAOH) in the absence of sodium cations. The presence of both microporous and mesoporous phases was determined by XRD and HRTEM measurements and by the analysis of nitrogen adsorption isotherm based on the oc-plot method. The mass percentage (p) of the microporous material in the composite is approximately 6.5%. NMR investigations showed that acid sites related to framework aluminium were generated by calcination of the as-synthesised (Ti, Al)-Beta/MCM-48. Local environment of titanium incorporated into the microporous/mesoporous silicate material was investigated by X-ray absorption spectroscopy. XANES studies showed the presence of tetrahedrally-coordinated Ti4+ cations in the template-free sample. EXAFS analysis revealed that titanium cations were coordinated to four oxygens in the first coordination shell, to one oxygen at 1.73(1) angstrom and three oxygens at 1.86(1) angstrom. In the second coordination sphere three silicon atoms were found at distances 3.18(2) angstrom and 3.48(2) angstrom, respectively. These results indicated framework Ti and thus the presence of Ti oxidation centres within the composite material. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:3 / 13
页数:11
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