首页> 外文期刊>The journal of physical chemistry, B. Condensed matter, materials, surfaces, interfaces & biophysical >Meaningful Differences in Spectral Performance, Thermal Behavior, and Heterogeneous Catalysis between Ammonium Molybdate Tetrahydrate and Its Adduct of β-Cyclodextrin
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Meaningful Differences in Spectral Performance, Thermal Behavior, and Heterogeneous Catalysis between Ammonium Molybdate Tetrahydrate and Its Adduct of β-Cyclodextrin

机译:四水合钼酸铵与β-环糊精加合物在光谱性能,热行为和非均相催化方面的有意义的区别

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摘要

A novel molecule-ion adduct of ammonium molybdate tetrahydarte (AMT) with β-cyclodextrin (CD) was prepared in this work. Significant differences in spectral properties between AMT and the adduct AMT—β-CD were observed by a series of experimental probes, such as powder X-ray diffraction, Fourier transformation infrared spectroscopy, and Raman spectroscopy. Field emission scanning electron microscopy showed that, although the crystal growth of AMT-β-CD was dominated by the molecular stacking of AMT, the size and morphology of the adduct were rather different from those seen in free AMT. The difference in stacking forms was attributed to the contribution of the molecule-ion interaction between AMT and β-CD. A drastic improvement in thermal stability of AMT and β-CD after adduct formation was observed by thermogravimetry analysis, which was confirmed by controlled sintering measurements. This revealed that the adduct interaction between them played an important role in mediating the thermal decomposition process of the adducted components. Furthermore, our results indicated that AMT and its adduct had a different performance in the catalytic desulfurization of thiophene and its derivatives. The fact that the catalytic efficiency of AMT was decreased after adduct formation implied there was a complexation between AMT and β-CD. Besides, several unusual molecular ions—NH_3~+, NH_2~+, and NH~+—were simultaneously found with gas chromatography coupled to time-of-flight mass spectrometry of free AMT.
机译:这项工作制备了一种新型的钼酸四氢铵(AMT)与β-环糊精(CD)的分子离子加合物。通过一系列的实验探针,如粉末X射线衍射,傅里叶变换红外光谱和拉曼光谱,观察到AMT和加合物AMT-β-CD的光谱性质存在显着差异。场发射扫描电子显微镜显示,尽管AMT-β-CD的晶体生长主要由AMT的分子堆叠所主导,但加合物的大小和形态与游离AMT所观察到的完全不同。堆积形式的差异归因于AMT和β-CD之间的分子离子相互作用。通过热重分析,观察到加合物形成后AMT和β-CD的热稳定性有了显着提高,这可通过控制烧结测量得到证实。这表明,它们之间的加合物相互作用在介导加合物的热分解过程中起着重要作用。此外,我们的结果表明,AMT及其加合物在噻吩及其衍生物的催化脱硫中具有不同的性能。加合物形成后AMT的催化效率降低的事实表明AMT与β-CD之间存在络合。此外,气相色谱-游离AMT的飞行时间质谱法同时发现了几种不常见的分子离子— NH_3〜+,NH_2〜+和NH〜+。

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