Solvent structure and dynamics over Brønsted acid MWW zeolite nanosheets.

In the liquid phase of heterogeneous catalysis, solvent plays an important role and governs the kinetics and thermodynamics of a reaction. Although it is often difficult to quantify the role of the solvent, it becomes particularly challenging when a zeolite is used as the catalyst. This difficulty arises from the complex nature of the liquid/zeolite interface and the different solvation environments around catalytically active sites. Here, we use ab initio molecular dynamics simulations to probe the local solvation structure and dynamics of methanol and water over MWW zeolite nanosheets with varying Brønsted acidity. We find that the zeolite framework and the number and location of the acid sites in the zeolite influence the structure and dynamics of the solvent. In particular, methanol is more likely to be in the vicinity of the aluminum (Al3+) at the T4 site than at T1 due to easy accessibility. The methanol oxygen binds strongly to the Al at the T4 site, weakening the Al-O for the bridging acid site, which results in the formation of the silanol group, significantly reducing the acidity of the site. The behavior of methanol is in direct contrast to that of water, where protons can easily propagate from the zeolite to the solvent molecules regardless of the acid site location. Our work provides molecular-level insights into how solvent interacts with zeolite surfaces, leading to an improved understanding of the catalytic site in the MWW zeolite nanosheet.

Insights into Sorption and Molecular Transport of Aqueous Glucose into Zeolite Nanopores.

Liquid-phase heterogeneous catalysis using zeolites is important for biomass conversion to fuels and chemicals. There is a substantial body of work on gas-phase sorption in zeolites with different topologies; however, studies investigating the diffusion of complex molecules in liquid medium into zeolitic nanopores are scarce. Here, we present a molecular dynamics study to understand the sorption and diffusion of aqueous ß-d-glucose into ß-zeolite silicate at T = 395 K and P = 1 bar. Through 2-µs-long molecular dynamics trajectories, we reveal the role of the solvent, the kinetics of the pore filling, and the effect of the water model on these properties. We find that the glucose and water loading is a function of the initial glucose concentration. Although the glucose concentration increases monotonically with the initial glucose concentration, the water loading exhibits a nonmonotonic behavior. At the highest initial concentration (∼20 wt %), we find that the equilibrium loading of glucose is approximately five molecules per unit cell and displays a weak dependence on the water model. Glucose molecules follow a single-file diffusion in the nanopores due to confinement. The dynamics of glucose and water molecules slows significantly at the interface. The average residence time for glucose molecules is an order of magnitude larger than that in the bulk solution, while it is about twice as large for the water molecules. Our simulations reveal critical molecular details of the glucose molecule's local environment inside the zeolite pore relevant to catalytic conversion of biomass to valuable chemicals.

Solvation effect on binding modes of model lignin dimer compounds on MWW 2D-zeolite.

Lignin as a potential renewable source of biofuels, chemicals, and other value-added products has gained much attention. However, the complexity of lignin structure poses a significant challenge for developing efficient valorization techniques. As most processes involve solvothermal conditions to minimize energy cost, lignin depolymerization is governed by reaction conditions (temperature and pressure) and solvents. In this work, binding of ß-O-4 linkage consisting lignin dimers on MWW two-dimensional (2D) zeolite is investigated using periodic density functional theory. Furthermore, the effect of different terminated surfaces (H:OH% = 100:0; 50:50; 0:100%), different temperatures (323, 353, 373 K), and different solvents (water and methanol) on the binding modes is quantified. Our work shows that in the gas phase the binding strength increases 10-15 kcal/mol upon increasing the number of hydroxyl groups on the surface. Also, the phenolic dimer binds more strongly than the nonphenolic dimer, and the binding strength of model compounds increases in the presence of the solvent. Analysis of structural changes in the presence of the solvent reveals that the aromatic rings are parallel to the zeolite surface and primary interaction with zeolite is through the hydroxyl groups near the ß-O-4 linkage. Furthermore, while the solvation energy decreases with increasing temperature, the opposite trend is observed for the binding energy with the surface.