Effect of Al content on the strength of terminal silanol species in ZSM-5 zeolite catalysts: a quantitative DRIFTS study without the use of molar extinction coefficients

被引:30
作者
Brauer, Pierre [1 ]
Situmorang, Olivia [1 ]
Ng, Pey Ling [1 ]
D'Agostino, Carmine [1 ,2 ]
机构
[1] Univ Cambridge, Dept Chem Engn & Biotechnol, Pembroke St, Cambridge CB2 3RA, England
[2] Univ Manchester, Sch Chem Engn & Analyt Sci, Sackville St, Manchester M13 9PL, Lancs, England
关键词
TEMPERATURE-PROGRAMMED DESORPTION; SOLID-STATE NMR; MULTIPLE ALUMINUM ENVIRONMENTS; ACID SITES; PROBE MOLECULES; SURFACE-ACIDITY; MAS NMR; FT-IR; THEORETICAL CALCULATION; INVISIBLE ALUMINUM;
D O I
10.1039/c7cp07826a
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
The strength of terminal hydroxyl Si-OH groups (silanols) in zeolites is important for many non-size-selective catalytic reactions occurring onto the external surface of the zeolite crystals and may often be responsible for catalyst deactivation, e.g., coke formation. A quantitative analysis of Si-OH strength and its link with the Al content, hence varying silica-to-alumina ratio (SAR = SiO2/Al2O3), has not been established yet. Various hypotheses have been proposed in the literature; nonetheless, the role of Al content in determining silanol strength remains still unclear and the object of speculation. In this work, we have systematically investigated the effect of the Al content on the strength of terminal silanol sites in ZSM-5 zeolite catalysts with varying SAR using Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) at variable temperatures without molar extinction coefficients. Two base probe molecules with different proton affinity values, pyridine and collidine, were used. To quantify the strength of terminal silanol sites the change of the terminal silanol peak in the OH stretching region, together with data on elemental analysis, was used. With this experimental protocol, unlike most IR studies, the use of molar extinction coefficients, often difficult to obtain, is not needed for quantification. The results reported here show for the first time that for ZSM-5 zeolite catalysts the fraction of occupied terminal silanol acid sites for both pyridine and collidine increases with increasing concentration of external Bronsted acid sites, hence establishing a clear link between the two types of acid sites. In summary, this work shows that the use of DRIFTS without molar extinction coefficients is able to quantitatively probe the strength of terminal silanol acid sites and establishes a link between the external Bronsted Al content and the strength of terminal silanol species in ZSM-5 zeolites with varying SAR at elevated temperatures.
引用
收藏
页码:4250 / 4262
页数:13
相关论文
共 69 条
[1]   Effects of crystal size and Si/Al ratio on the surface properties of H-ZSM-5 zeolites [J].
Armaroli, T. ;
Simon, L. J. ;
Digne, M. ;
Montanari, T. ;
Bevilacqua, M. ;
Valtchev, V. ;
Patarin, J. ;
Busca, G. .
APPLIED CATALYSIS A-GENERAL, 2006, 306 :78-84
[2]   FTIR study of the interaction of some branched aliphatic molecules with the external and internal sites of H-ZSM5 zeolite [J].
Armaroli, T ;
Trombetta, M ;
Alejandre, AG ;
Solis, JR ;
Busca, G .
PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2000, 2 (14) :3341-3348
[3]   A study of the external and internal sites of MFI-type zeolitic materials through the FT-IR investigation of the adsorption of nitriles [J].
Armaroli, T ;
Bevilacqua, M ;
Trombetta, M ;
Milella, F ;
Alejandre, AG ;
Ramírez, J ;
Notari, B ;
Willey, RJ ;
Busca, G .
APPLIED CATALYSIS A-GENERAL, 2001, 216 (1-2) :59-71
[4]   STUDY OF THE ACIDITY OF ZSM-5 ZEOLITE BY MICRO-CALORIMETRY AND INFRARED SPECTROSCOPY [J].
AUROUX, A ;
BOLIS, V ;
WIERZCHOWSKI, P ;
GRAVELLE, PC ;
VEDRINE, JC .
JOURNAL OF THE CHEMICAL SOCIETY-FARADAY TRANSACTIONS I, 1979, 75 :2544-2555
[5]   Conversion of methanol to hydrocarbons over zeolite H-ZSM-5: On the origin of the olefinic species [J].
Bjorgen, Morten ;
Svelle, Stian ;
Joensen, Finn ;
Nerlov, Jesper ;
Kolboe, Stein ;
Bonino, Francesca ;
Palumbo, Luisa ;
Bordiga, Silvia ;
Olsbye, Unni .
JOURNAL OF CATALYSIS, 2007, 249 (02) :195-207
[6]   STUDY OF THE STATE OF ALUMINUM IN ZEOLITE-BETA [J].
BOURGEAT-LAMI, E ;
MASSIANI, P ;
DIRENZO, F ;
ESPIAU, P ;
FAJULA, F ;
COURIERES, TD .
APPLIED CATALYSIS, 1991, 72 (01) :139-152
[7]   Solid-state NMR Spectroscopy of Quadrupolar Nuclei in Inorganic Chemistry [J].
Braeuniger, Thomas ;
Jansen, Martin .
ZEITSCHRIFT FUR ANORGANISCHE UND ALLGEMEINE CHEMIE, 2013, 639 (06) :857-879
[8]   Effect of Al content on number and location of hydroxyl acid species in zeolites: a DRIFTS quantitative protocol without the need for molar extinction coefficients [J].
Brauer, Pierre ;
Ng, Pey Ling ;
Situmorang, Olivia ;
Hitchcock, Iain ;
D'Agostino, Carmine .
RSC ADVANCES, 2017, 7 (83) :52604-52613
[9]  
Broach R.W., 2010, Zeolites in industrial separation and catalysis, DOI DOI 10.1002/9783527629565
[10]   Role of Lewis acid sites of ZSM-5 zeolite on gaseous ozone abatement [J].
Brodu, Nicolas ;
Manero, Marie-Helene ;
Andriantsiferana, Caroline ;
Pic, Jean-Stephane ;
Valdes, Hector .
CHEMICAL ENGINEERING JOURNAL, 2013, 231 :281-286