Accelerated Synthesis of Nanolayered MWW Zeolite by Interzeolite Transformation.

Hierarchical zeolites can offer substantial benefits over bulk zeolites in catalysis. A drawback towards practical implementation is their lengthy synthesis, often requiring complex organic templates. This work describes an accelerated synthesis of nanolayered MWW zeolite based on the combination of interzeolite transformation (IZT) with a dual-templating strategy. FAU zeolite, hexamethyleneimine (HMI), and cetyltrimethylammonium bromide (CTAB) were respectively employed as Al source and primary zeolite, structure directing agent, and exfoliating agent. This approach allowed to reduce the synthesis of nanolayered MWW to 48 h, which is a considerable advance over the state of the art. Tracking structural, textural, morphological, and chemical properties during crystallization showed that 4-membered-ring (4MR) units derived from the FAU precursor are involved in the faster formation of MWW in comparison to a synthesis procedure from amorphous precursor. CTAB restricts the growth of the zeolite in the c-direction, resulting in nanolayered MWW. Moreover, we show that this approach can speed up the synthesis of nanolayered FER. The merits of nanolayered MWW zeolites are demonstrated in terms of improved catalytic performance in the Diels-Alder cycloaddition of 2,5-dimethylfuran and ethylene to p-xylene compared to bulk reference MWW sample.

Preparation of Metal-Supported Nanostructured Zeolite Catalysts and their Applications in the Upgrading of Biomass-Derived Furans: Advances and Prospects.

The development of platform chemicals derived from biomass, in particular, 5-hydroxymethylfurfural (5-HMF) and furfural (FUR), is of crucial importance in biorefinery. Over the past decades, metal-supported nanostructured zeolites, in particular, metal-supported hierarchically porous zeolites or metal-encapsulated zeolites, have been extensively elaborated because of their multiple functionalities and superior properties, for example, shape-selectivity, (hydro)thermal stability, tunable acidity and basicity, redox properties, improved diffusion, and intimacy of multiple active sites. In this review, the effects of such properties of metal-supported nanostructured zeolites on the enhanced catalytic performances in furanic compound upgrading are discussed. In addition, the recent rational design of metal-supported nanostructured zeolites is exemplified. Consequently, the ongoing challenges for further developing metal-supported nanostructured zeolites-based catalysts and their applications in HMF and FUR upgrading are identified.

Transformation of CO2 to Carbon Nanotubes by Catalytic Chemical Vapor Deposition using a Metal-Supported Hierarchical Zeolite Template.

The conversion of CO2 into valuable substances is a topic of great interest in current research. Carbon nanotubes (CNT) have emerged as highly promising materials for CO2 conversion. In this study, we successfully developed a catalyst by loading active transition metals (Fe or Ni) onto hierarchical zeolite for CNT synthesis. Our catalyst demonstrated excellent performance under synthetic conditions. The most favorable CNT was obtained using the 25 wt.% FeHieFAU catalyst, which exhibited a diameter size of 23.1 nm, a CNT yield of 15.4 %, and an ID /IG ratio of 0.56, indicating high quality. Additionally, we investigated the beneficial effects of the synthesized CNT by testing their current response. Notably, the current response of the synthesized CNT surpassed that of commercial CNT when using a 0.5 M H2 SO4 supporting electrolyte and cyclic voltammetry (V vs. Ag/AgCl). These findings highlight the significant contributions of the small diameter and superior quality of our synthesized pure CNT, which offer potential improvements in current response compared to commercial CNT. This research opens new avenues for utilizing CNT in CO2 conversion and electrochemical applications.

Mild Hydrogenation of 2-Furoic Acid by Pt Nanoparticles Dispersed in a Hierarchical ZSM-5 Zeolite.

Hydrogenation of biobased compounds can add value to platform molecules obtained from biomass refining. Herein, we explore the hydrogenation of 2-furoic acid (2-furancarboxylic acid, FCA), a derivative of furfural, with H2 generated in situ by NaBH4 hydrolysis at ambient conditions. Nearly complete conversion of FCA was obtained with tetrahydrofuroic acid (THFA) and 5-hydroxyvaleric acid (5-HVA) as the only two reaction products over Pt nanoparticles supported on hierarchical ZSM-5. Small Pt nanoparticles (2 to 3 nm) were stabilized by ZSM-5 nanosheets. At an optimized Pt loading, the Pt nanoparticles can catalyze the hydrolysis of NaBH4 and the subsequent hydrogenation of FCA with the assistance of Brønsted acid sites. Nanostructuring ZSM-5 into nanosheets and its acidity contributes to the stability of the dispersed Pt nanoparticles. Deactivation due to NaBO2 deposition on the Pt particles can be countered by a simple washing treatment. Overall, this approach shows the promise of mild hydrogenation of biobased feedstock coupled with NaBH4 hydrolysis.

Synthesis and Characterization of Sn, Ge, and Zr Isomorphous Substituted MFI Nanosheets for Glucose Isomerization to Fructose.

Invited for a cover feature this month is the research group of Asst. Prof. Dr. Chularat Wattanakit from School of Energy Science and Engineering, Vidyasirimedhi Institute of Science and Technology (VISTEC), Thailand. The cover picture shows the facile synthesis of Sn, Ge, and Zr isomorphously substituted MFI with hierarchical structures by a one-pot hydrothermal process. These designed materials illustrate the promising catalytic performance in glucose isomerization to fructose. More information can be found in the Full Paper by Chularat Wattanakit, and co-workers.

Synthesis and Characterization of Sn, Ge, and Zr Isomorphous Substituted MFI Nanosheets for Glucose Isomerization to Fructose.

Various metals including Sn, Ge, and Zr have been successfully incorporated into the MFI nanosheets via a one-pot synthesis. The as-synthesized zeolites exhibit high external surface area and mesopore volume without large metal oxides aggregated on zeolite surfaces. Interestingly, the successful introduction of heteroatoms in MFI nanosheets can be confirmed by shifted XRD peaks corresponding to the unit cell expansion due to the replacement of metals into the framework. In addition, the UV-Vis absorbance spectra reveal that at the suitable metal loading the incorporated tetrahedral coordination of metal species in the zeolite framework has been obtained. To illustrate the benefits of the prepared catalysts, the glucose isomerization to fructose was carried out in a water/dioxane system. Obviously, the SnMFI-NS samples, containing the high dispersion of metal isomorphous species demonstrate the outstanding catalytic behavior in term of fructose selectivity (>85 %).