In this work, we have systematically investigated the effect of the Al content on the number and location of bridging hydroxyls (Brønsted acid sites) and terminal hydroxyls (terminal silanol sites) in ZSM-5 zeolites with varying silica-alumina ratio (SAR ¼ SiO 2 /Al 2 O 3 ) using Diffuse Reflectance Infrared Fourier Transform Spectroscopy (DRIFTS) without molar extinction coefficients. Two base probe molecules with different kinetic diameters, pyridine (5.7Å) and collidine (7.4Å), were used. The total content of Brønsted acid sites is obtained by elemental analysis of the proton form and sodium exchanged form of ZSM-5. To quantify the number of internal and external Brønsted acid sites the change in area of the Brønsted acid site peak in the O-H stretching region is then used; thus, the need for molar extinction coefficients to quantify Brønsted acid sites is thereby eliminated. The results reported here show that for ZSM-5 the number of external Brønsted sites, in absolute terms, increases with increasing total Al content, as evidenced by collidine adsorption. The number of terminal silanol acid sites was found to be proportional to the external surface area probed by argon sorption experiments. In summary, this work shows that the use of DRIFTS in conjunction with elemental analysis is a valid alternative to qualitatively and quantitatively probe the number and location of hydroxyl acid sites without the use of molar extinction coefficients and gives a comprehensive picture of the effect of Al content on number and location of hydroxyl acid species in ZSM-5 zeolites with varying SAR. The work contributes to advancing the range of characterisation protocols for solid acid catalysts.
The diffusion of ammonia in commercial NH3-SCR catalyst Cu-CHA was measured and compared with H-CHA using quasielastic neutron scattering (QENS) and molecular dynamics (MD) simulations to assess the effect of counterion presence on NH3 mobility in automotive emission control relevant zeolite catalysts. QENS experiments observed jump diffusion with a jump distance of 3 Å, giving similar self-diffusion coefficient measurements for both Cu- and H-CHA samples, in the range of ca. 5-10 × 10(-10) m(2) s(-1) over the measured temperature range. Self-diffusivities calculated by MD were within a factor of 6 of those measured experimentally at each temperature. The activation energies of diffusion were also similar for both studied systems: 3.7 and 4.4 kJ mol(-1) for the H- and Cu-chabazite respectively, suggesting that counterion presence has little impact on ammonia diffusivity on the timescale of the QENS experiment. An explanation is given by the MD simulations, which showed the strong coordination of NH3 with Cu(2+) counterions in the centre of the chabazite cage, shielding other molecules from interaction with the ion, and allowing for intercage diffusion through the 8-ring windows (consistent with the experimentally observed jump length) to carry on unhindered.
The diffusion of ammonia in the small pore zeolite and potential commercial NH3-SCR catalyst levynite (LEV) was measured and compared with its mobility in the chabazite (CHA) topology (more established in NOx abatement catalysis), using quasielastic neutron scattering (QENS) and molecular dynamics (MD) simulations at 273, 323 and 373 K. The QENS experiments suggest that mobility in LEV is dominated by jump diffusion through the 8-ring windows between cages (as previously observed in CHA) which takes place at very similar rates in the two zeolites, yielding similar experimental self-diffusion coefficients (Ds). After confirming that the same characteristic motions are observed between the MD simulations and the QENS experiments on the picosecond scale, the simulations suggest that on the nanoscale, the diffusivity is higher by a factor of ∼2 in the CHA framework than in LEV. This difference between zeolites is primarily explained by the CHA cages having six 8-ring windows in the building unit, compared to only three such windows in the LEV cage building unit, thereby doubling the geometric opportunities to perform jump diffusion between cages (as characterised by the QENS experiments) leading to the corresponding increase in the MD calculated Ds. The techniques illustrate the importance of probing both pico- and nanoscale dynamics when studying intracrystalline diffusion in both NH3-SCR catalyst design, and in porous materials generally, where notable consistencies and differences may be found on either scale.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.