Advances in the green and controllable synthesis of MWW zeolite.

MWW zeolite is one of the commercialized zeolites that shows great promise in heterogeneous catalysis and other interdisciplinary application fields due to its coexisting multi-channel system. The green and controllable synthesis of MWW zeolite is conducive to its more efficient and broader application. Many researchers focus on precisely controlling the dimension, interlayer hydroxyl condensation, and aluminum siting, as well as obtaining MWW with low-toxicity, readily available organic structure directing agents (OSDAs) or without OSDAs.

Unlocking Enhanced Butadiene Selectivity: The Crucial Role of Zeolite Channel Confinement in the Selective Decarbonylation of γ-Valerolactone.

Herein, we report a highly selective production route for butadiene from γ-valerolactone over zeolite catalysts. The catalytic performance of eight zeolites with different framework topologies were compared, revealing that zeolites with narrower 10-membered ring channels exhibit enhanced selectivity of butadiene. Specifically, ZSM-35 and ZSM-22, featuring the narrowest 10-membered ring channels, demonstrate the highest butadiene selectivity to 61 % and 59 %, respectively.

Construction of diverse hollow MFI zeolites through regulating the micropore filling agents.

Constructing hollow structure into microporous zeolites can improve the accessibility of acid sites located at the inner part and the diffusion property. Hence, the development of an efficient synthesis strategy to acquire zeolites with tunable hollow structures and acidity has attracted much attention. In this work, an innovative tandem synthesis route was proposed to prepare MFI zeolites with diverse hollow structure while maintaining solid yields exceeding 90 %.

Unconventional seed-assisted strategy for Al-rich hierarchical ZSM-48 zeolite.

Inferior diffusion capacity and insufficient acid density hinder the practical application of ZSM-48 zeolite. Finding a simple and practical strategy to simultaneously address these two defects remains a challenge. In response to this dilemma, we developed an unconventional seed-assisted synthesis strategy for Al-rich hierarchical ZSM-48 zeolite.

Construction of a One-Dimensional Al-Rich ZSM-48 Zeolite with a Hollow Structure.

Diffusion limitation and acid deficiency are two main challenges that the ZSM-48 zeolite faces in practical application. To date, there have been few effective strategies to solve both problems, simultaneously. Also, it is also a challenge to construct a hollow structure in a one-dimensional (1D) zeolite.

Direct Preparation of *MRE Zeolites with Ultralarge Mesoporosity: Strategy and Working Mechanism.

Introduction of mesopore is critical for applications where mass-transport limitations within microporous networks, especially for zeolite with one-dimensional microporous network, hinder their performance. Generally, the creation of mesopore in zeolite through a direct synthesis route is strongly dependent on complex and expensive organic molecules, which limits their commercial application. Here, we successfully developed a facile synthesis route for preparing ZSM-48 zeolite (*MRE topology) with ultralarge mesoporosity in which typical 1,6-hexylenediamine worked as an organic structure-directing agent, innovatively assisted by a simple crystal growth modifier (tetraethylammonium bromide, TEABr).

A Highly Ion-Selective Zeolite Flake Layer on Porous Membranes for Flow Battery Applications.

Zeolites are crystalline microporous aluminosilicates with periodic arrangements of cages and well-defined channels, which make them very suitable for separating ions of different sizes, and thus also for use in battery applications. Herein, an ultra-thin ZSM-35 zeolite flake was introduced onto a poly(ether sulfone) based porous membrane. The pore size of the zeolite (ca.

Metathesis of 1-Butene to Propene over Mo/Al2O3@SBA-15: Influence of Alumina Introduction Methods on Catalytic Performance.

A series of Mo-based catalysts for 1-butene metathesis to propene were prepared by supporting Mo species on SBA-15 premodified with alumina. The effects of the method of introduction of the alumina guest to the host SBA-15 on the location of the Mo species and the corresponding metathesis activity were studied. As revealed by N2 adsorption isotherms and TEM results, well-dispersed alumina was formed on the pore walls of SBA-15 if the ammonia/water vapor induced hydrolysis (NIH) method was employed.