Muslim Dvoyashkin

Future Challenges in Heterogeneous Catalysis: Understanding Catalysts under Dynamic Reaction Conditions

In the future, (electro‐)chemical catalysts will have to be more tolerant towards a varying supply of energy and raw materials. This is mainly due to the fluctuating nature of renewable energies. For example, power‐to‐chemical processes require a shift from steady‐state operation towards operation under dynamic reaction conditions. This brings along a number of demands for the design of both catalysts and reactors, because it is well‐known that the structure of catalysts is very dynamic. However, in‐depth studies of catalysts and catalytic reactors under such transient conditions have only started recently. This requires studies and advances in the fields of 1) operando spectroscopy including time‐resolved methods, 2) theory with predictive quality, 3) kinetic modelling, 4) design of catalysts by appropriate preparation concepts, and 5) novel/modular reactor designs. An intensive exchange between these scientific disciplines will enable a substantial gain of fundamental knowledge which is urgently required. This concept article highlights recent developments, challenges, and future directions for understanding catalysts under dynamic reaction conditions.

Freezing of fluids in disordered mesopores

Freezing and melting behaviors of a fluid confined to pores of mesoporous silicon with a modulated structure have been studied using NMR techniques. The molecular self-diffusivities, measured along the freezing and melting transitions, unveiled essential differences in the configuration of the frozen domains. This suggests that freezing is dominated by a pore-blocking mechanism. Freezing kinetics is found to exhibit very slow long-time dynamics, following a ln(2)(t) dependence. This type of time dependence may result if the front of the frozen phase is assumed to propagate in the random potential field created by the disorder of the porous silicon channels, similar to the mechanism of Sinai diffusion. The free energy barriers calculated from the kinetic measurements and estimated using a thermodynamical model yield a consistent picture of the freezing process in the presence of quenched disorder.

The Mechanism of Pseudomorphic Transformation of Spherical Silica Gel into MCM-41 Studied by PFG NMR Diffusometry

The pseudomorphic transformation of spherical silica gel (LiChrospher® Si 60) into MCM-41 was achieved by treatment at 383 K for 24 h with an aqueous solution of cetyltrimethylammonium hydroxide (CTAOH) instead of hexadecyltrimethylammonium bromide (CTABr) and NaOH. The degree of transformation was varied via the ratio of CTAOH solution to initial silica gel rather than synthesis duration. The transformed samples were characterized by N2 sorption at 77 K, mercury intrusion porosimetry, X-ray diffraction (XRD) and scanning electron microscopy (SEM). Thus, MCM-41 spheres with diameters of ca. 12 μm, surface areas >1000 m2 g−1, pore volumes >1 cm3 g−1 and a sharp pore width distribution, adjustable between 3.2 and 4.5 nm, were obtained. A thorough pulsed field gradient nuclear magnetic resonance (PFG NMR) study shows that the diffusivity of n-heptane confined in the pores of the solids passes through a minimum with progressing transformation. The final product of pseudomorphic transformation to MCM-41 does not exhibit improved transport properties compared to the initial silica gel. Moreover, the PFG NMR results support that the transformation occurs via formation and subsequent growth of domains of <1 μm containing MCM-41 homogeneously distributed over the volume of the silica spheres.

Structural characterization of porous solids by simultaneously monitoring the low-temperature phase equilibria and diffusion of intrapore fluids using nuclear magnetic resonance

Nuclear magnetic resonance (NMR) provides a variety of tools for the structural characterization of porous solids. In this paper, we discuss a relatively novel approach called NMR cryodiffusometry, which is based on a simultaneous assessment of both the phase state of intraporous liquids at low temperatures, using NMR cryoporometry, and their transport properties, using NMR diffusometry. Choosing two model porous materials with ordered and disordered pore structures as the host systems, we discuss the methodological and fundamental aspects of the method. Thus, with the use of an intentionally micro-structured mesoporous silicon, we demonstrate how its structural features give rise to specific patterns in the effective molecular diffusivities measured upon progressive melting of a frozen liquid in the mesopores. We then present the results of a detailed study of the transport properties of the same liquid during both melting and freezing processes in Vycor porous glass, a material with a random pore structure.

Diffusion of guest molecules in MCM-41 agglomerates

The pulsed field gradient nuclear magnetic resonance method has been used to study self-diffusion of cyclohexane in a commercial MCM-41 material at different external gas pressures from zero to saturated vapor pressure. It is found that the effective diffusivities exhibit three different regions with increasing pressure: decrease at low pressures, a sudden drop at intermediate pressures, and increase at higher pressures. In addition, in the region of irreversible adsorption (hysteresis loop) the diffusivities are also found to differ on the adsorption and the desorption branches. A simple analytical model taking account of different molecular ensembles with different transport properties due to the complex architecture of the porous structure is developed which provides a quantitative prediction of the experimental data. The analysis reveals that the effective diffusivity is predominantly controlled by the adsorption properties of the individual mesoporous MCM-41 crystallites which, in combination with high transport rates, provide a simple instrument for fine tuning of the transport properties by a subtle variation of the external conditions.

Diffusion NMR of Fluids Confined to Mesopores under High Pressures

Supercritical fluids are extensively used in various chemical applications including processes involving porous solids. The knowledge of their transport in bulk as well as under spatial confinements is critical for modeling and optimizing chemical reactions. In this contribution, we describe a high‐pressure cell designed for pulsed field gradient NMR studies of diffusion of supercritical solvents in mesoporous materials. Some preliminary results on diffusion properties of ethane in bulk phase and confined to pores of mesoporous silicon obtained in a broad range of pressures below and above the critical temperature are reported.

In Situ and In Operando Characterization of Mixing Dynamics in Liquid-Phase Reactions by ¹²⁹Xe NMR Spectroscopy

129 Xe NMR spectroscopy is applied under in situ and in operando conditions to study the mixing process in a multicomponent liquid mixture with partially miscible components. The process of mixing of an oil-methanol mixture was triggered by an industrially relevant catalytic transesterification reaction to form fatty acid methyl esters and glycerol. Up to date, kinetic limitations in liquid-phase reactions originating from the poor miscibility of the reacting species have been addressed solely under ex situ conditions, typically by chromatography. In the approach presented here, xenon gas, solvated in the reacting species, acts as a sensor, providing information on the progress of mixing and on the composition during the course of the catalytic reaction. We believe that this study offers a new tool to the set of established techniques for addressing mixing and/or separation processes in liquids, including but not limited to the ones resulting from catalytic reactions.