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Manufacturing honeycomb-structured catalysts require a careful understanding of the microstructure of the solid substrate and its dependence on thermalprocessing conditions. Herein, it is the thermal responses of microcracks in an uncoated microcracked aluminum titanate honeycomb catalyst is investigated by analyzing the material's resonance frequency using the high-temperature impulse excitation technique. The resonance frequencies are presented as Young's modulus values to avoid sample size effects. Dynamic Young's modulus measurements show closed-loop hysteresis due to microcracks healing and reopening, causing a reversible response. The hysteresis is further used to understand microcracks' dependence on critical thermal-processing conditions used in a catalyst manufacturing plant, including peak operating temperature (800--1000 °C), dwell period (1--3 h), and heating rates (1--5 °Cmin-1). Microcracks are observed to have two healing responses: instantaneous and delayed healing. Both responses significantly influence the design of catalyst manufacturing. Complete reopening of microcracks from their healing temperature (1150 °C) is a very time-consuming process (50--60 h).However, it is shown in the analysis that microcrack relaxation is a critical phenomenon that must be considered in quality-controlled environments. [ABSTRACT FROM AUTHOR]

We demonstrate a modified sol‐immobilization procedure using (MeOH)x/(H2O)1‐x solvent mixtures to prepare Pd/TiO2 catalysts that are able to reduce the formation of acid catalyzed products, e. g. ethers, for the hydrogenation of furfural. Transmission electron microscopy found a significant increase in polyvinyl alcohol (PVA) deposition at the metal‐support interface and temperature programmed reduction found a reduced uptake of hydrogen, compared to an established Pd/TiO2 preparation. We propose that the additional PVA hinders hydrogen spillover onto the TiO2 support and limits the formation of Brønsted acid sites, required to produce ethers. Elsewhere, the new preparation route was able to successfully anchor colloidal Pd to the TiO2 surface, without the need for acidification. This work demonstrates the potential for minimizing process steps as well as optimizing catalyst selectivity – both important objectives for sustainable chemistry. [ABSTRACT FROM AUTHOR]

We demonstrate a modified sol‐immobilization procedure using (MeOH)x/(H2O)1‐x solvent mixtures to prepare Pd/TiO2 catalysts that are able to reduce the formation of acid catalyzed products, e. g. ethers, for the hydrogenation of furfural. Transmission electron microscopy found a significant increase in polyvinyl alcohol (PVA) deposition at the metal‐support interface and temperature programmed reduction found a reduced uptake of hydrogen, compared to an established Pd/TiO2 preparation. We propose that the additional PVA hinders hydrogen spillover onto the TiO2 support and limits the formation of Brønsted acid sites, required to produce ethers. Elsewhere, the new preparation route was able to successfully anchor colloidal Pd to the TiO2 surface, without the need for acidification. This work demonstrates the potential for minimizing process steps as well as optimizing catalyst selectivity – both important objectives for sustainable chemistry. [ABSTRACT FROM AUTHOR]