Institut für Physikalische Chemie, Westfälische Wilhelms-Universität Münster, Corrensstrasse 28/30, 48149, Münster, Germany.
Chevron Energy Technology Company, Richmond, CA, 94802, USA.
Angew Chem Int Ed Engl. 2016 Nov 7;55(46):14459-14463. doi: 10.1002/anie.201607428. Epub 2016 Oct 14.
Internal defect SiOH and SiO groups evolve during the structure formation of high-Si zeolites in the presence of a cationic organic structure-directing agent (SDA). These negatively charged defects do not completely disappear upon calcination. Herein we investigate the clustering of defect groups and their location within the pore walls of four zeolites. ZSM-12, ZSM-5, and SSZ-74 have three clustered SiOH groups which are hydrogen-bonded to SiO , whereas SSZ-24 has only two. These defects interact with the structure-directing quaternary ammonium ions preferably close to the charge center, unless steric shielding is present. The framework topologies of ZSM-12, ZSM-5, and SSZ-24 have connected six-rings where the organics interact with the defects. It is suggested that these six-ring patterns form connectivity defects. SSZ-74 is unique, it does not contain an extended six-ring motif, so vacancy defects form instead.
在阳离子有机结构导向剂(SDA)的存在下,高硅沸石的结构形成过程中会出现 SiOH 和 SiO 内部缺陷。这些带负电荷的缺陷在煅烧后不会完全消失。本文研究了缺陷群的聚集及其在四种沸石孔壁内的位置。ZSM-12、ZSM-5 和 SSZ-74 具有三个聚集的 SiOH 基团,它们与 SiO 通过氢键结合,而 SSZ-24 只有两个。这些缺陷与结构导向的季铵离子相互作用,优选靠近电荷中心,除非存在空间位阻屏蔽。ZSM-12、ZSM-5 和 SSZ-24 的骨架拓扑结构具有相互连接的六元环,有机物与缺陷相互作用。有人认为,这些六元环模式形成了连通性缺陷。SSZ-74 是独特的,它不包含扩展的六元环结构,因此形成了空位缺陷。