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Adsorptive desulfurization from the model fuels by functionalized UiO-66(Zr)

机译:通过功能化的UiO-66(Zr)对模型燃料进行吸附脱硫

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摘要

Metal organic frameworks (MOFs) have recently emerged as promising candidates for efficient removal of sulfur-containing compounds (SCCs) from liquid fuels. In this study, adsorptive desulfurization (ADS) is performed by adsorbing thiophene (TP) and benzothiophene (BT) from model fuels over pristine and functionalized UiO-66 (Zr). The introduction of amino (-NH2) and carboxylic (-COOH) groups reduces the porosity of UiO-66. However, the adsorption capacities of functionalized UiO-66 improved remarkably. Especially for the adsorbent functionalized with amino moieties (UiO-66-NH2), its maximum adsorption capacities for TP (29.5 mg S/g) and BT (35.7 mg S/g) are 1.7 and 1.8 times to that of bare UiO-66. The superior performance of UiO-66-NH2 is ascribed to the higher availability of hydrogen-bond donor sites in the surface and the favorable interactions between H atoms of -NH2 and sulfur species. UiO-66-COOH is beneficial for the adsorption of SCCs than that of pristine UiO-66 because of the existence of acid-base interactions. Moreover, the reusability of UiO-66-NH2 is confirmed by regenerating it via a simple solvent washing.
机译:金属有机骨架(MOF)最近作为有效从液体燃料中去除含硫化合物(SCC)的有前途的候选者而出现。在这项研究中,吸附脱硫(ADS)是通过从原始燃料和功能化的UiO-66(Zr)上吸附模型燃料中的噻吩(TP)和苯并噻吩(BT)来进行的。氨基(-NH2)和羧基(-COOH)的引入降低了UiO-66的孔隙率。但是,官能化的UiO-66的吸附能力显着提高。特别是对于被氨基部分(UiO-66-NH2)功能化的吸附剂,其对TP(29.5 mg S / g)和BT(35.7 mg S / g)的最大吸附容量分别是裸UiO-66的1.7和1.8倍。 UiO-66-NH2的优异性能归因于表面中氢键供体位点的更高可用性以及-NH2的H原子与硫物种之间的良好相互作用。由于存在酸碱相互作用,所以UiO-66-COOH比原始UiO-66对SCC的吸附更有利。此外,UiO-66-NH2的可重复使用性通过简单的溶剂洗涤使其再生而得到确认。

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