99181-63-2Relevant academic research and scientific papers
Direct Conversion of 5-Hydroxymethylfurfural to Furanic Diether by Copper-Loaded Hierarchically Structured ZSM-5 Catalyst in a Fixed-Bed Reactor
Hu, Hualei,Xue, Tingting,Zhang, Zhenxin,Gan, Jiang,Chen, Liangqi,Zhang, Jian,Qu, Fengzuo,Cai, Weijie,Wang, Lei
, p. 3461 - 3469 (2021/06/01)
The highly-efficient conversion of 5-hydroxymethylfurfural (HMF) to 2,5-bis(ethoxymethyl)furan (BEMF) was achieved over the copper-loaded hierarchically structured ZSM-5 (Cu/HSZ) catalysts in the continuous fixed-bed reactor. The main reaction path for BEMF synthesis on the Cu/HSZ catalysts was confirmed as following: HMF was firstly hydrogenated to BHMF intermediates over metal sites and then the formed BHMF was etherified by acid sites. Benefiting from the ammonia evaporation (AE) method promoted the dispersion of copper and reduced the acidity, the Cu/HSZ-AE catalyst exhibited more excellent BEMF yield and stability than the catalyst prepared by conventional incipient-wetness impregnation (Cu/HSZ-IW). Indeed, the inactivation of Cu/HSZ-IW catalyst was mainly attributed to the deactivation of copper by carbon species deposition.
Synthetic method of 2,5-furan dimethanol and etherified product of 2,5-furan dimethanol
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Paragraph 0032-0033; 0037, (2017/08/31)
The invention discloses a synthetic method of 2,5-furan dimethanol and an etherified product of 2,5-furan dimethanol and relates to 2,5-furan dimethanol. The synthetic method comprises the following steps of: adding organic alcohol into a reaction substrate; putting the obtained mixture as a raw material in a high pressure reaction kettle; adding a certain amount of a molecular sieve supported catalyst; and performing a heating reaction to obtain 2,5-furan dimethanol and the etherified product of 2,5-furan dimethanol. By using alcohol as a hydrogen donor and a reaction substrate, no external hydrogen source does not needed. By adjusting the acid-base property of a catalyst through an active metal component, 2,5-furan dimethanol can be obtained by selectively catalyzing transfer hydrogenation of 5-hydroxymethylfurfural or 2,5-dialkoxyl methyl furan is obtained by further etherification. The catalyst is cheap and easily available and good in repeatability, no excessively hydrogenated product exists, and the whole reaction is hydrogenated in a hydrogen environment, and the synthetic method has relatively strong operating safety of industrial production and very good industrial application potential.
Catalytic transfer hydrogenation of biomass-derived 5-hydroxymethyl furfural to the building block 2,5-bishydroxymethyl furan
Hao, Weiwei,Li, Weifeng,Tang, Xing,Zeng, Xianhai,Sun, Yong,Liu, Shijie,Lin, Lu
, p. 1080 - 1088 (2016/02/27)
An efficient process for the catalytic transfer hydrogenation of biomass-derived 5-hydroxymethyl furfural (HMF) to 2,5-bishydroxymethyl furan (BHMF) is presented using ethanol as a hydrogen donor and solvent over low-cost ZrO(OH)2. A HMF conversion of 94.1% and a DHMF selectivity of 88.9% were achieved at 423 K in 2.5 h. The fresh, spent, and regenerated catalysts were characterized comprehensively, and the OH group of ZrO(OH)2 as sites for ligand exchange with ethanol was considered to be important for the activity.
A continuous flow strategy for the coupled transfer hydrogenation and etherification of 5-(hydroxymethyl)furfural using lewis acid zeolites
Lewis, Jennifer D.,Van De Vyver, Stijn,Crisci, Anthony J.,Gunther, William R.,Michaelis, Vladimir K.,Griffin, Robert G.,Roman-Leshkov, Yuriy
, p. 2255 - 2265 (2014/11/08)
Hf-, Zr- and Sn-Beta zeolites effectively catalyze the coupled transfer hydrogenation and etherification of 5-(hydroxymethyl)furfural with primary and secondary alcohols into 2,5-bis(alkoxymethyl)furans, thus making it possible to generate renewable fuel
Cascade of liquid-phase catalytic transfer hydrogenation and etherification of 5-hydroxymethylfurfural to potential biodiesel components over Lewis acid zeolites
Jae, Jungho,Mahmoud, Eyas,Lobo, Raul F.,Vlachos, Dionisios G.
, p. 508 - 513 (2014/03/21)
We report a one-step process for the production of diesel fuel from biomass-derived 5-hydroxymethylfurfural (HMF). The reaction proceeds through the sequential transfer hydrogenation and etherification of HMF to 2,5-bis(alkoxymethyl)furan, a potential biodiesel additive, catalyzed by a Lewis acid zeolite, such as Sn-Beta or Zr-Beta. An alcohol is used as a hydrogen donor and as a reactant in etherification. This cascade reaction can selectively produce high yields of the biodiesel additive (>80 % yield) from HMF with the Sn-Beta catalyst and secondary alcohols, such as 2-propanol and 2-butanol. Diesel addiction: Biomass-derived 5-hydroxymethylfurfural (HMF) is converted to 2,5-bis(alkoxymethyl)furan, a potential biodiesel additive, through sequential transfer hydrogenation and etherification reactions catalyzed by a Lewis acid zeolite, such as Sn-Beta or Zr-Beta. Sn-Beta selectively produces high yields of the biodiesel additive (>80 % yield) with secondary alcohols, such as 2-propanol and 2-butanol, as hydrogen donors and as etherification agents. Copyright
