Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP), Université de Poitiers, UMR 7285 CNRS, 4 rue Michel Brunet, CEDEX 9, 86073 Poitiers, France.
LABPEMOL, Laboratorio de Peneiras Moleculares. Av. Sen. Salgado Filho, 3000-Lagoa Nova, Natal 59072-970, RN, Brazil.
Molecules. 2022 Dec 15;27(24):8934. doi: 10.3390/molecules27248934.
The possibility of crystallizing silicalite-1 (MFI) from the pore walls of as-synthesized MCM-41 via steam-assisted crystallization (SAC) was thoroughly investigated. A kinetic study was conducted through the impregnation of as-synthesized MCM-41 with the structure-directing agent tetrapropyl-ammonium hydroxide (TPAOH). Materials obtained after different SAC treatment times (1−288 h) were characterized by XRD, nitrogen physisorption at 77 K, TGA/DTA, and SEM. The achieved results allowed us to conclude that during SAC treatment, rapid destruction of the hexagonal mesophase occurs with the enlargement of mesopores, probably by their coalescence, until achieving non-porous amorphous silica. Only thereafter is the crystallization of the MFI phase evidenced through the development of micron-sized (>10 µm) MFI structured crystals. This study suggests the probable practical impossibility of even partial crystallization of the pore walls of mesoporous materials by SAC.
通过蒸汽辅助晶化(SAC)从合成的 MCM-41 的孔壁上彻底研究了结晶硅沸石-1(MFI)的可能性。通过用结构导向剂四丙基氢氧化铵(TPAOH)浸渍合成的 MCM-41 进行了动力学研究。在不同的 SAC 处理时间(1-288 h)后获得的材料通过 XRD、77 K 下的氮气物理吸附、TGA/DTA 和 SEM 进行了表征。所得结果使我们能够得出结论,在 SAC 处理期间,快速破坏六方介相伴随着介孔的扩大,可能通过它们的合并,直到达到无孔无定形二氧化硅。只有在此之后,通过开发微米级(>10 µm)的 MFI 结构晶体,才能证明 MFI 相的结晶。这项研究表明,即使通过 SAC,介孔材料的孔壁也几乎不可能部分结晶。