首页> 外文期刊>ChemSusChem >Selective Aerobic Oxidation of 5-Hydroxymethylfurfural to 2,5-Diformylfuran or 2-Formyl-5-furancarboxylic Acid in Water by using MgO center dot CeO2 Mixed Oxides as Catalysts
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Selective Aerobic Oxidation of 5-Hydroxymethylfurfural to 2,5-Diformylfuran or 2-Formyl-5-furancarboxylic Acid in Water by using MgO center dot CeO2 Mixed Oxides as Catalysts

机译:通过使用MgO中心DOT CEO2混合氧化物作为催化剂,在水中选择性有氧氧化5-羟甲基糠醛或2-甲酰基-5-FurancarBoxic酸

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摘要

Mixed oxides based on MgOCeO2 were used as efficient catalysts in the aerobic oxidation of 5-hydroxymethylfurfural (5-HMF) to afford, with very high selectivity, either 2,5-diformylfuran (DFF, 99%) or 2-formyl-5-furancarboxylic acid (FFCA, 90%), depending on the reaction conditions. 5-Hydroxymethyl-2-furancarboxylic acid (HMFCA, 57-90%) was formed only at low concentration of 5-HMF (< 0.03 M) or in presence of external bases. The conversion of 5-HMF ranged from a few percent to 99%, according to the reaction conditions. The oxidation was performed in water, with O-2 as oxidant, without any additives. The surface characterization of the catalysts gave important information about their acid-base properties, which drive the selectivity of the reaction towards DFF. FFCA was formed from DFF at longer reaction times. Catalysts were studied by XPS and XRD before and after catalytic runs to identify the reason why they undergo reversible deactivation. XRD showed that MgO is hydrated to Mg(OH)(2), which, even if not leached out, changes the basic properties of the catalyst that becomes less active after some time. Calcination of the recovered catalyst allows recovery of its initial activity. The catalyst is thus recoverable (> 99%) and reusable. The use of mixed oxides allows tuning of the basicity of the catalysts, avoiding the need for external bases for efficient and selective conversion of 5-HMF and waste formation, resulting in an environmentally friendly, sustainable process.
机译:基于MGOceO 2的混合氧化物用作5-羟甲基糠醛(5-HMF)的有氧氧化的有效催化剂,得到非常高的选择性,2,5-二甲基呋喃(DFF,99%)或2-甲酰基-5-根据反应条件,FurancarBoxylic acid(FFCA,90%)。仅在低浓度为5-HMF(<0.03μm)或外部碱的低浓度下形成5-羟甲基-2-呋喃甲酸(HMFCA,57-90%)。根据反应条件,5-HMF的转化率从少量达到99%的范围内。氧化在水中进行,用O-2作为氧化剂,没有任何添加剂。催化剂的表面表征对其酸碱性质具有重要信息,这使得反应的选择性朝向DFF驱动。在更长的反应时间内由DFF形成FFCA。催化剂通过XPS和XRD进行,然后催化在催化作用之前和之后进行识别它们经历可逆失活的原因。 XRD显示MgO水合成Mg(OH)(2),即使不浸出,也改变催化剂的基本性质在一段时间后变得较小。回收的催化剂的煅烧允许恢复其初始活性。因此,催化剂可回收(> 99%)和可重复使用。混合氧化物的使用允许调节催化剂的碱度,避免外部碱的需要,以便有效和选择性转化为5-HMF和废物形成,导致环境友好,可持续的过程。

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