In Situ Formation of Zeolitic Imidazolate Frameworks on Nanocellulose Revealed by Time-Resolved Synchrotron Small-Angle and Wide-Angle X-ray Scattering

IF 8.2 2区 材料科学 Q1 MATERIALS SCIENCE, MULTIDISCIPLINARY
Salvatore Lombardo*, Houssine Khalili, Shun Yu, Sritama Mukherjee, Kim Nygård, Zoltan Bacsik and Aji P. Mathew*, 
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Abstract

Metal–organic frameworks such as ZIF-8, grown in situ on nanocellulose (NC), have gained significant attention in recent years due to the versatility of the processing route and multifaceted application in the field of environmental remediation and biomedical applications. However, insights into the interactions between NC and MOF precursors and MOF structure evolution during in situ synthesis are limited or nonexistent. We report the kinetics of ZIF-8 formation on a nanocellulose (NC) aqueous suspension and in water at room temperature, monitored in real time after the addition of ZIF-8 precursors. This is the first study revealing the mechanism of ZIF-8 formation in the presence of nanocellulose. A combination of synchrotron-based small-angle (SAXS) and wide-angle X-ray scattering (WAXS) enabled us to compare the time evolution of the radius of gyration obtained from SAXS and the extent of crystallization determined by WAXS. Based on the SAXS data, we propose a new model that accounts for the initial rapid formation of primary particles, which subsequently evolve into medium-range structures before growing into the final product. Scanning electron microscopy images supported this mechanism, showing smaller particles at the beginning of the reaction and confirmed interparticle interactions, showing nanocellulose particles decorating the surface of the final ZIF-8 crystals. We demonstrate that the concentration of the starting metal salt significantly influences the kinetics of the reaction but has little effect on the ZIF-8 particle size. In contrast, increasing the NC concentration led to a reduction in the final ZIF-8 particle size, while having a negligible impact on the reaction rate and affording a minor decrease in surface area and micropore volume. We show that at the lower NC concentration that was studied the ZIF-8 particles were covered by NC, and no reduction in porosity was observed. Moreover, the kinetics of formation was shown to be independent of the NC functional group and morphology under the conditions used in this study.

时间分辨同步加速器小角和广角x射线散射研究纳米纤维素上咪唑酸沸石骨架的原位形成。
近年来,在纳米纤维素(NC)上原位生长的金属有机骨架(如ZIF-8)因其加工路线的多功能性和在环境修复和生物医学领域的多方面应用而受到广泛关注。然而,对NC和MOF前体之间的相互作用以及原位合成过程中MOF结构演变的见解有限或不存在。我们报道了室温下ZIF-8在纳米纤维素(NC)水悬浮液和水中形成的动力学,并在添加ZIF-8前体后实时监测。这是首次揭示纳米纤维素存在下ZIF-8形成机制的研究。结合基于同步加速器的小角x射线散射(SAXS)和广角x射线散射(WAXS),我们可以比较SAXS获得的旋转半径的时间演变和WAXS确定的结晶程度。基于SAXS的数据,我们提出了一个新的模型来解释初级粒子最初的快速形成,随后在成长为最终产品之前演变成中等结构。扫描电镜图像支持这一机制,显示了反应开始时较小的颗粒,并证实了颗粒间的相互作用,显示纳米纤维素颗粒修饰了最终ZIF-8晶体的表面。研究表明,起始金属盐的浓度对反应动力学有显著影响,但对ZIF-8的粒径影响不大。相比之下,增加NC浓度导致最终ZIF-8粒径减小,而对反应速率的影响可以忽略不计,并且表面积和微孔体积略有减少。我们发现,在较低NC浓度下,ZIF-8颗粒被NC覆盖,孔隙率没有降低。此外,在本研究中使用的条件下,形成动力学被证明与NC官能团和形态无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Applied Materials & Interfaces
ACS Applied Materials & Interfaces 工程技术-材料科学:综合
CiteScore
16.00
自引率
6.30%
发文量
4978
审稿时长
1.8 months
期刊介绍: ACS Applied Materials & Interfaces is a leading interdisciplinary journal that brings together chemists, engineers, physicists, and biologists to explore the development and utilization of newly-discovered materials and interfacial processes for specific applications. Our journal has experienced remarkable growth since its establishment in 2009, both in terms of the number of articles published and the impact of the research showcased. We are proud to foster a truly global community, with the majority of published articles originating from outside the United States, reflecting the rapid growth of applied research worldwide.
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