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As mentioned above, many adsorption structures for aromatic molecules on MFI-type zeolites have been determined.
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As a first step, we examined the adsorption of the amino acids glycine (gly), l-alanine (ala) and l-lysine (lys) on MFI-type zeolite (MFI).
The adsorption structures of dimethyl ether (DME) on silicalite-1 zeolite (MFI-type) are determined using single-crystal X-ray diffraction.
The SAS were evaluated comprehensively for various Brønsted acid sites including bridging hydroxyl (BH), nest hydroxyl (NH), and terminal silanol (TS) in the internal pores and on the external surfaces of MFI-type zeolite.
Further investigations about other chain molecules are needed to reveal the adsorption behavior in the MFI-type zeolites.
Structured copper-containing MFI-type (Cu-MFI) zeolite catalysts on paper-like sintered stainless fiber (PSSF) were prepared by a secondary hydrothermal synthesis method and resulting in Cu-MFI coating with good relative crystallinity (80.7%), high BET surface area (237.5 m2/g) and uniform pore size distribution (2 3 nm).
Using a new fabrication method based on microelectronic fabrication and zeolite thin film technologies, MFI-type zeolites with engineered structures were incorporated as catalyst, membrane and structural material within the design architecture of a microreactor, membrane microseparator and microeletrochemical cell.
Selective production of aromatics from the heavier n-paraffins was studied on nano-structured (ns) catalysts consisting of ns alumina and MFI-type H-galloaluminosilicate (H-GaAlMFI) zeolite.
The configuration of guest molecules (linear or bent) plays an important role in determining where the stable sorption site is in the pore system of MFI-type zeolites.
MFI-type zeolitic membranes were prepared by a vapor-phase transport method on porous α-alumina flat disks.
The aim of the current study is to investigate pure silica MFI-type zeolites nanoparticles with sizes of 50 nm and 100 nm (samples MFI-50 and MFI-100) under suspended conditions and their toxicological effects on human lung alveolar (A549) cells under in vitro conditions.
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