posted on 2015-04-01, 00:00authored byEnhui Xing, Yanchun Shi, Aiguo Zheng, Jin Zhang, Xiuzhi Gao, Dongyun Liu, Mudi Xin, Wenhua Xie, Fengmei Zhang, Xuhong Mu, Xingtian Shu
The transformation from NaA (LTA)
to MCM-49 (MWW) zeolite was achieved
in the synergism of hexamethyleneimine (HMI), NaOH, and SiO2, in spite of no common composite build units between LTA (lta, sod, and d4r) and
MWW (mel and d6r) structure. NaA
(SiO2/Al2O3 = 2.0) was employed as
the parent zeolite. The samples prepared at different crystallization
stages were characterized by XRD, SEM, 29Si/27Al/13C MAS NMR, and STEM-EDS to investigate the intermediates
during the transformation from NaA to MCM-49. As shown in SEM and
STEM-EDS images, MCM-49 was proposed to be transformed gradually from
the exterior to the interior of NaA, which was clearly observed by
the core (LTA, low SiO2/Al2O3)–shell
(MWW, high SiO2/Al2O3) coexisting
zeolites as intermediates. With high relative crystallinity and the
uniform sizes of crystals, the final MCM-49 was featured by Si enrichment
on the external surface, which was proved by the shell (SiO2/Al2O3 = 45.4) wrapping around the core (SiO2/Al2O3 = 22.0). For transformed H-MCM-49
zeolite, the uniform sizes of crystals and the increase of total acid
sites contributed to better accessibility of active centers, which
achieved simultaneous improvement in ethylene conversion and ethylbenzene
selectivity in the liquid-phase alkylation of benzene with ethylene.