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Synthesis of nanoporous carbohydrate metal-organic framework and encapsulation of acetaldehyde

机译:纳米多孔碳水化合物金属 - 有机骨架的合成及乙醛包封

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摘要

Gamma cyclodextrin (γ-CD) metal organic frameworks (CDMOFs) were synthesized by coordinating γ-CDs with potassium hydroxide (KOH), referred hereafter as CDMOF-a, and potassium benzoate (C7H5KO2), denoted as CDMOF-b. The obtained CDMOF structures were characterized using nitrogen sorption isotherm, thermo-gravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy (SEM). High surface areas were achieved by the γ-CD based MOF structures where the Langmuir specific surface areas (SSA) of CDMOF-a and CDMOF-b were determined as 1376 m2 g−1 and 607 m2 g−1; respectively. The dehydrated CDMOF structures demonstrated good thermal stability up to 250 °C as observed by the TGA studies. XRD results for CDMOF-a and CDMOF-b reveal a body centered-cubic (BCC) and trigonal crystal system; respectively. Due to its accessible porous structure and high surface area, acetaldehyde was successfully encapsulated in CDMOF-b. During the release kinetic studies, we observed peak release of 53 μg of acetaldehyde per g of CDMOF-b, which was 100 times greater than previously reported encapsulation in β-CD. However, aldol condensation reaction occurred during encapsulation of acetaldehyde into CDMOF-a. This research work demonstrates the potential to encapsulate volatile organic compounds in CDMOF-b, and their associated release for applications including food, pharmaceuticals and packaging.
机译:通过与氢氧化钾(KOH)配合γ-CD来合成γ环糊精(γ-CD)金属有机框架(CDMOFS),以后称为CDMOF-A和苯甲酸钾(C7H5KO2),表示为CDMOF-B。使用氮吸附等温线,热重分析(TGA),X射线衍射(XRD)和扫描电子显微镜(SEM)所获得的CDMOF结构。通过基于γ-Cd的MOF结构实现高表面积,其中CDMOF-A和CDMOF-B的Langmuir比表面积(SSA)确定为1376m 2 G-1和607m 2 G-1;分别。脱水Cdmof结构明显高达250°C的良好热稳定性,如TGA研究所观察到的。 CDMOF-A和CDMOF-B的XRD结果显示了一个身体中心立方(BCC)和Trigonal Crystal系统;分别。由于其可移的多孔结构和高表面积,乙醛在Cdmof-b中成功包封。在释放动力学研究期间,我们观察到每G CDMOF-B的53μg乙醛的峰释放,其比以前报道的β-CD中的包封量大于100倍。然而,在将乙醛封装到CDMOF-A期间发生醛醇缩合反应。该研究工作证明了在CDMOF-B中封装挥发性有机化合物的可能性,以及它们的相关释放,包括食品,药物和包装。

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