Influence of Bronsted Acid Site Proximity on Alkane Cracking in MFI Zeolites

被引:8
|
作者
Pham, Tram N. [1 ,2 ]
Nguyen, Vy [1 ]
Nguyen-Phu, Huy [1 ]
Wang, Bin [1 ]
Crossley, Steven [1 ]
机构
[1] Univ Oklahoma, Sch Chem Biol & Mat Engn, Norman, OK 73019 USA
[2] Univ Texas Austin, McKetta Dept Chem Engn, Austin, TX 78712 USA
基金
美国国家科学基金会;
关键词
zeolites; MFI framework; EFAL species; Br?nsted acid sites; alkane cracking; synergistic sites; SOLID-STATE NMR; FRAMEWORK ALUMINUM; CHABAZITE ZEOLITES; CATALYTIC-ACTIVITY; DOMINANT ROLE; ACTIVE-SITE; ZSM-5; DEALUMINATION; CONVERSION; IMPACT;
D O I
10.1021/acscatal.2c05291
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Extra-framework aluminum (EFAL) species generated during the hydrolysis of framework Al are believed to play a crucial role in the activity of alkane cracking on zeolites. The presence of these EFAL species can enhance the reactivity of the adjacent Bri nsted acid sites (BAS), resulting in the formation of the synergistic BAS-EFAL sites. Recently, we have demonstrated that water treatment in a pulse reactor can facilitate the mobility of existing EFAL species in the absence of framework hydrolysis. Here, we investigate the role of framework Al location and proximity on the generation of synergistic sites in MFI zeolites. Correlations are developed between the cracking rates and the rate enhancement under pulsing water treatment with the concentration of proximate framework Al species. In addition, it is illustrated that sodium and calcium can titrate proximate framework Al, which we reveal to be important precursors to synergistic site formation. This allows quantification of the number of synergistic sites, as well as the conclusion that these highly active sites are likely located at pore intersections within the MFI framework. In addition, the analysis of experimental and theorical transition-state energies suggests that these EFAL species facilitate n-hexane cracking by lowering activation enthalpies.
引用
收藏
页码:1359 / 1370
页数:12
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