1995
DOI: 10.1515/zna-1995-2-310
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On the Use of Pulsed Field Gradients in a High-Field NMR Spectrometer to Study Restricted Diffusion in Zeolites

Abstract: A probe system is described which allows the application of magnetic field gradient pulses with amplitudes up to 24 T/m for self-diffusion measurements by means of a PFG NMR spectrometer operating at a proton resonance frequency of 400 MHz. It is demonstrated that PFG NMR measurements in the high field of a superconducting magnet necessitate precautions which are of minor relevance for measurements with iron magnets. Taking advantage of the large gradient intensity and the high sensitivity in signal detection … Show more

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Cited by 64 publications
(45 citation statements)
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“…The pulsed field gradient NMR self-diffusion measurements with the pulse program mentioned above were performed on a home-built spectrometer with a superconducting magnet at a proton NMR frequency of W, = 400 MHz (13). In the experiment, the field gradient g was varied (maximum value 25 T/m) at fixed pulse width 6 (between 0.3 ms and 2 ms) and diffusion time A.…”
Section: Nmr Experimentsmentioning
confidence: 99%
“…The pulsed field gradient NMR self-diffusion measurements with the pulse program mentioned above were performed on a home-built spectrometer with a superconducting magnet at a proton NMR frequency of W, = 400 MHz (13). In the experiment, the field gradient g was varied (maximum value 25 T/m) at fixed pulse width 6 (between 0.3 ms and 2 ms) and diffusion time A.…”
Section: Nmr Experimentsmentioning
confidence: 99%
“…diffusion, 11,12 anisotropic diffusion 13,14 and diffusion of different phases with individual diffusion coefficients. 15 Ordinary diffusion is well known and describes the behavior of isotropic systems such as bulk liquids.…”
Section: Introductionmentioning
confidence: 99%
“…The PFG NMR measurements were performed on a FEGRIS 400 laboratory-built spectrometer 11 at a proton resonance frequency of 400 MHz, using the conventional Hahn echo /2 sequence 1,3 -5 with observation times of 0.5-2 ms. Applying sufficiently large zeolite crystallites (with diameters ½30 and 100 µm for NaX, ½15 µm for NaA and ½1 mm for natural chabazite and a size ½200 ð 30 ð 30 µm 3 for ZSM-5), irrespective of the large diffusivities, the relatively short observation times ensured that the observed diffusivities were controlled by intracrystalline transport.…”
Section: Introductionmentioning
confidence: 99%