Synthesis, acid properties and catalysis by niobium oxide nanostructured materials

被引:44
|
作者
Luisa Marin, M. [1 ,2 ,3 ]
Hallett-Tapley, Geniece L. [1 ,2 ]
Impellizzeri, Stefania [1 ,2 ]
Fasciani, Chiara [1 ,2 ]
Simoncelli, Sabrina [1 ,2 ,4 ,5 ]
Netto-Ferreira, Jose Carlos [1 ,2 ,6 ]
Scaiano, Juan C. [1 ,2 ]
机构
[1] Univ Ottawa, Dept Chem, Ottawa, ON K1N 6N5, Canada
[2] Univ Ottawa, Ctr Catalysis Res & Innovat, Ottawa, ON K1N 6N5, Canada
[3] Univ Politecn Valencia, CSIC, Inst Univ Mixto Tecnol Quim, Valencia 46022, Spain
[4] Univ Buenos Aires, Fac Ciencias Exactas & Nat, INQUIMAE, RA-1428 Buenos Aires, DF, Argentina
[5] Univ Buenos Aires, Fac Ciencias Exactas & Nat, Dept Quim Inorgan Analit Quim Fis, RA-1428 Buenos Aires, DF, Argentina
[6] Inst Nacl Metrol Qualidade & Tecnol INMETRO, Div Metrol Quim, BR-25250020 Rio De Janeiro, Brazil
基金
加拿大自然科学与工程研究理事会;
关键词
5-HYDROXYMETHYL-2-FURALDEHYDE; DEHYDRATION; PHOSPHATE; SILICA;
D O I
10.1039/c4cy00238e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Several forms of niobium oxide were prepared, including nanostructured mesoporous materials, and their acidity properties were comprehensively investigated and compared with commercially available materials. The composites were characterized by a variety of techniques, including XRD, TEM, N-2 adsorption and Hammett acid indicator studies. The acidity of the niobium oxide derivatives was also investigated by the ability of the materials to successfully promote the halochromic ring-opening of an oxazine-coumarin probe that was specifically designed for use in fluorescence imaging studies. The ring-opening reaction was easily monitored using UV-visible, fluorescence and NMR spectroscopy. Single molecule microscopy was employed to gain a more in-depth understanding of the niobium oxide acid catalysis pathway. Using this technique, the rate of niobium oxide mediated protonation was estimated to be 1.8 x 10(-13) mol m(-2) s(-1). Single molecule analysis was also used to obtain a detailed map of Bronsted acid sites on the niobium oxide surface. The active sites, located by multiple blinking events, do not seem to be localized on any area of the material, but rather randomly distributed throughout the solid state surface. As the reaction proceeds, the sites with the highest acidity and accessibility are gradually consumed, making the next tier of acid sites available for reaction. The phenomenon was more closely characterized by using time lapsed reactivity maps.
引用
收藏
页码:3044 / 3052
页数:9
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