滴定法
化学
二价
离子
沸石
密度泛函理论
离子交换
结晶学
计算化学
功能(生物学)
离子键合
物理化学
化学物理
共振(粒子物理)
序列(生物学)
离子半径
无机化学
滴定曲线
对分布函数
作者
Wei Ge,Tania L. Class-Martínez,José Rebolledo-Oyarce,Alyssa McNarney,Songhyun Lee,Anshuman Goswami,Claire T. Nimlos,Ahmad Moini,Subramanian Prasad,Vivek Vattipalli,Anthony DeBellis,Sichi Li,Bradley F. Chmelka,Rajamani Gounder,William F. Schneider
标识
DOI:10.1021/acs.chemmater.5c03087
摘要
Co 2+ exchange is commonly used as a reporter of Al pair ensembles in zeolites. We combine density functional theory (DFT) calculations, statistical models, experimental titrations, and solid-state nuclear magnetic resonance (NMR) analyses to explore the utility of other 2+ ions as alternative reporters of proximal Al ensembles in the CHA zeolite. DFT calculations suggest that Ba 2+ will exchange into both eight- (8MR) and six-membered (6MR) CHA rings equally effectively, distinct from Co 2+, which exchanges solely into 6MR. Simulated titration curves highlight the potential for Co 2+ and Ba 2+ titrations to provide complementary information about specific proximal Al site ensembles as a function of Si/Al ratio. Experiments on CHA zeolites synthesized to express different Al distributions confirm that Ba 2+ uptake exceeds that of Co 2+ and that this uptake can be rationalized by Ba 2+ ions that titrate both 8MR and 6MR Al pair sites. Comparisons of absolute ion uptakes and two-dimensional NMR analyses of Al proximity with predictions reveal previously unrecognized differences in Al siting rules under different syntheses. These findings demonstrate that complementary titrations using divalent cations of differing ionic radii provide additional resolution on Al–Al pair ensembles and the underlying rules that govern Al distributions on zeolite frameworks.
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