Deng F, Yue Y, Ye C
Laboratory of Magnetic Resonance and Atomic and Molecular Physics, Wuhan Institute of Physics, the Chinese Academy of Sciences.
Solid State Nucl Magn Reson. 1998 Jan;10(3):151-60. doi: 10.1016/s0926-2040(97)00028-3.
Aluminum species in several dealuminated zeolites (ultrastable HY, HZSM-5 and mordenite) were investigated in detail by means of the newly introduced 1H/27Al TRAPDOR method in combination with 27Al MAS NMR, and the quadrupole coupling constants (Q[CC]s) for aluminum atoms associated with these species were obtained. A signal at ca. 6.8 ppm, due to water molecules adsorbed on Lewis acid sites, was observed in the 1H MAS spectra for all the three zeolites. The TRAPDOR NMR provides direct evidence that there is a strong interaction between the adsorbed water molecules and the aluminum atoms of the Lewis-acid sites. The Q(CC) values for this aluminum species of 8.3, 6.7 and 11.3 MHz were determined from the TRAPDOR profiles for the ultrastable HY, HZSM-5 and mordenite zeolites, respectively. The Q(CC)s calculated from the TRAPDOR curves are usually larger than 10 MHz for both Bronsted-acid sites (SiOHAI) and non-framework aluminum species in the three zeolites. Three narrow peaks at 54, 30 and 0 ppm are separately superimposed on a broad hump in the 27Al MAS spectra of the three dehydrated zeolites, while the latter is associated with the 'NMR invisible' Al. The NMR experimental results suggest that the three kinds of aluminum species (non-framework aluminum species, Bronsted- and Lewis-acid sites) are all responsible for the resonance of the broad hump in dehydrated zeolites, which makes it difficult to explain the 27Al MAS spectra. Fortunately, the TRAPDOR NMR provides a direct method for individually studying different aluminum species with large Q(CC)s via their dipolar coupling to nearby proton nuclei.
通过新引入的1H/27Al TRAPDOR方法结合27Al MAS NMR,对几种脱铝沸石(超稳HY、HZSM-5和丝光沸石)中的铝物种进行了详细研究,并获得了与这些物种相关的铝原子的四极耦合常数(Q[CC]s)。在所有三种沸石的1H MAS谱中均观察到一个约6.8 ppm处的信号,该信号归因于吸附在路易斯酸位点上的水分子。TRAPDOR NMR提供了直接证据,表明吸附的水分子与路易斯酸位点的铝原子之间存在强相互作用。分别从超稳HY、HZSM-5和丝光沸石的TRAPDOR谱图中确定了该铝物种的Q(CC)值,分别为8.3、6.7和11.3 MHz。从TRAPDOR曲线计算得到的Q(CC)s对于三种沸石中的布朗斯特酸位点(SiOHAI)和非骨架铝物种通常都大于10 MHz。在三种脱水沸石的27Al MAS谱中,三个窄峰分别位于54、30和0 ppm处,并叠加在一个宽峰上,而后者与“NMR不可见”的Al相关。NMR实验结果表明,三种铝物种(非骨架铝物种、布朗斯特酸和路易斯酸位点)均对脱水沸石中宽峰的共振有贡献,这使得难以解释27Al MAS谱。幸运的是,TRAPDOR NMR提供了一种直接方法,可通过它们与附近质子核的偶极耦合来单独研究具有大Q(CC)s的不同铝物种。