4.7 Article

Variable anchoring of boron in zeolite beta

Journal

MICROPOROUS AND MESOPOROUS MATERIALS
Volume 79, Issue 1-3, Pages 215-224

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.micromeso.2004.10.035

Keywords

boron; zeolite beta; solid state NMR; REDOR; IR spectroscopy

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The transformation of boron species in H-B-beta and H,Na-B-beta zeolites has been studied by B-11 and H-1 MAS NMR as well as H-1{B-11} Rotational Echo Double Resonance in combination with infrared spectroscopy. Tetrahedral and trigonal boron are found in the hydrated zeolites. Only trigonal boron is observed in the pure proton form for the dehydrated zeolite. The degree of boron anchoring in the framework (number of B-O-Si bridges) increases with higher dehydration temperature. The B-11 isotropic chemical shift of trigonal boron correlates with the number of B-O-Si connectivities, and can be utilized to identify B(OSi)(x)(OH)(3-x) species with different degrees of framework anchoring, x: 10.5 +/- 0.7ppm (x = 3), 15.4 +/- 0.5ppm (x = 1), and 18.5 +/- 0.6ppm (x = 0). The transformation of boron anchoring and coordination numbers is reversible, depending on the conditions (temperature, humidity). Five H-1 NMR and four IR lines are resolved for H-B-beta and assigned to three different classes of OH groups: class A are defect silanol groups (1.7ppm/3745cm(-1)), class B are Si-OH center dot center dot center dot B-[3] sites and weakly hydrogen bonded SiOH and BOH groups (2.0, 2.3ppm/3735cm(-1)), and class C groups are due to hydrogen bonded SiOH, BOH and possibly water (3.0, 4.3ppm/similar to 3680, 3530cm-1). (c) 2004 Elsevier Inc. All rights reserved.

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