Ammonia Titration Methods To Quantify Bronsted Acid Sites in Zeolites Substituted with Aluminum and Boron Heteroatoms

Ammonia titration methods were developed to discriminate and quantify Bronsted acid sites of different strength that compensate aluminum and boron heteroatoms incorporated within zeolite frameworks. Borosilicate and MFI zeolites (B-Al-MFI) were synthesized with different Al contents and crystallite sizes, which are typically correlated structural properties in aluminosilicates synthesized hydrothermalfy, but independently varied here by incorporating boron as a second framework heteroatom and using ethylenediamine as a structure directing agent. Temperature-programmed desorption (TPD) of ammonia from B-Al-MFI samples saturated via liquid-phase NH(4)N0(3) ion exchange resOlted in quantifying the total number of Al and B heteroatoms. In contrast, TPD performed after NH4-form B-Al-MFI samples were purged in flowing helium (433 K), or after gas-phase NH3 adsorption (433 K) onto H-form B-Al-MFI samples, quantified only protons charge-compensating framework Al heteroatoms. Turnover rates for methanol dehydration to dimethyl ether, when measured in zero-order kinetic regimes that are sensitive predominantly to Bronsted acid strength, are dependent only on the number of protons compensating framework Al atoms in B-Al-MFI zeolites. The NH3 titration methods developed here are useful in rigorously normalizing turnover rates of Bronsted acid-catalyzed reactions in boroaluminosilicate zeolites, which have been recognized previously to be dependent solely on Al content. The incorporation of B heteroatoms into zeolite frameworks, which generate protons that are essentially unreactive, provides a strategy to influence crystallite sizes independently of Al content, especially relevant in cases where catalytic behavior is influenced by intracrystalline transport phenomena.