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首页> 外文期刊>RSC Advances >Inorganic–organic hybrid sorbent for aromatic desulfurization of hydrocarbons: regenerative adsorption based on a charge-transfer complex
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Inorganic–organic hybrid sorbent for aromatic desulfurization of hydrocarbons: regenerative adsorption based on a charge-transfer complex

机译:用于烃的芳族脱硫的无机 - 有机杂交吸附剂:基于电荷转移复合物的再生吸附

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摘要

A new series of inorganic–organic hybrid materials as sorbents for the adsorption of dibenzothiophene (DBT) and 4,6-dimethyldibenzothiophene (4,6-DMDBT) have been prepared by functionalizing mesoporous silica with 9,10-anthraquinone derivatives. A selected sorbent was fully characterized via ~(13) C and ~(29) Si cross-polarization magic-angle solid-state nuclear magnetic resonance (CP-MAS NMR), FTIR spectroscopy, powder X-ray diffraction (PXRD) and thermal analysis (TGA-DTA). The prepared materials were used to adsorb DBT and 4,6-DMDBT from C _(7) hydrocarbons under ambient conditions. The results show that the hybrid material prepared by the functionalization of mesoporous silica with 9,10-dioxo-5-((3-(triethoxysilyl)-propyl)amino)-1,5-dichloro-4,8-dinitroanthraquinone is an efficient and regenerable sorbent for adsorption of DBT and 4,6-DMDBT by π–π interaction. To demonstrate the adsorption of DBT and 4,6-DMDBT through π–π interaction, a charge-transfer complex (CTC) of 1,5-dichloro-4,8-dinitroanthraquinone and 4,6-DMDBT was prepared and characterized by FT-IR, ~(1) H and ~(13) C NMR spectroscopy, MS, TGA-DTA and single-crystal X-ray diffraction. The results show that 1,5-dichloro-4,8-dinitroanthraquinone produces a CTC with 4,6-DMDBT, and when it is grafted on Si-MCM-41, it produces a hybrid material with the capability of adsorbing only aromatic DBT and 4,6-DMDBT rather than anthracene, naphthalene and xylene. In contrast, 1,5-dichloroanthraquinone and 1,5-dicyanoanthraquinone neither produce a CTC nor adsorb DBT, 4,6-DMDBT, anthracene, naphthalene and xylene after they are grafted on Si-MCM-41. This study proves that the hybrid material prepared from mesoporous silica and 9,10-dioxo-5-((3-(triethoxysilyl)-propyl)amino)-1,5-dichloro-4,8-dinitroanthraquinone is an efficient, environmentally benign and regenerable sorbent for the removal of DBT and 4,6-DMDBT from C _(7) hydrocarbons.
机译:通过将介孔二氧化硅与9,10-蒽醌衍生物官能化,通过官能化二氧化硅制备新的一系列新的无机 - 有机杂化材料作为吸附二苯并噻吩(DBT)和4,6-二甲基二苯甲酸噻吩(4,6-DMDBT)。通过〜(13)C和〜(29)Si交叉偏振魔角固态核磁共振(CP-MAS NMR),FTIR光谱,粉末X射线衍射(PXRD)和热量,完全表征了一种选择的吸附剂。分析(TGA-DTA)。在环境条件下,制备的材料用于从C _(7)烃中的DBT和4,6-DMDBT吸附。结果表明,通过介孔二氧化硅的官能化制备的杂化材料与9,10-二氧化硅-5-((3-(三乙氧基甲硅烷基) - 丙基)氨基)-1,5-二氯-4,8-​​二硝基蒽醌是有效的通过π-π相互作用吸附DBT和4,6-DMDBT的可再生吸附剂。为了证明DBT和4,6-DMDBT通过π-π相互作用的吸附,制备1,5-二氯-4,8-​​ Dinitroanthraquinnone和4,6-DMDBT的电荷转移复合物(CTC),并通过FT表征 - 〜(1)H和〜(13)C NMR光谱,MS,TGA-DTA和单晶X射线衍射。结果表明,1,5-二氯-4,8-​​DINITroantraquinons产生具有4,6-DMDBT的CTC,并且当它接枝在Si-MCM-41上时,它产生杂种材料,仅具有吸附芳香DBT的能力和4,6-DMDBT而不是蒽,萘和二甲苯。相比之下,1,5-二氯醌醌和1,5-二氰基蒽醌均未产生CTC,也不会在嫁接Si-MCM-41上后产生CTC也不是吸附DBT,4,6-DMDBT,蒽,萘和二甲苯。本研究证明,由介孔二氧化硅和9,10-二氧氧-5-((3-(三乙氧基甲硅烷基) - 丙基)氨基)-1,5-二氯-4,8-​​二硝基蒽醌的杂化材料是有效的,环境良性可再生吸附剂,用于从C _(7)碳氢化合物中除去DBT和4,6-DMDBT。

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