Suitable commercial catalysts for the synthesis of oxymethylene dimethyl ethers

被引:8
|
作者
Mantei, Franz [1 ]
Kopp, Sebastian [1 ]
Holfelder, Anna [1 ]
Flad, Elisa [1 ]
Kloeters, Daniela [1 ]
Kraume, Matthias [2 ]
Salem, Ouda [1 ]
机构
[1] Fraunhofer Inst Solar Energy Syst, Thermochem Proc Dept, Div Hydrogen Technol, Heidenhofstr 2, D-79110 Freiburg, Germany
[2] Tech Univ Berlin, Chair Chem Engn, Str 17 Juni 135,MAR 2-1, D-10623 Berlin, Germany
关键词
CHEMICAL-EQUILIBRIUM; REACTION-KINETICS; FORMALDEHYDE; WATER;
D O I
10.1039/d2re00508e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
OME have diesel fuel like properties with almost soot-free combustion, which can enable a reduction of nitrogen oxides. This makes them promising candidates for internal combustion engines as blends or neat fuel. Moreover, OME are addressed as environmentally benign solvents and as hydrogen dense carriers for fuel cells. OME are produced from methanol which can be produced sustainably, allowing a significant overall reduction of CO2 emissions. Various catalysts have been investigated for OME synthesis focusing on selectivity and activity. This study concentrates on commercial heterogeneous catalysts and compares not only the conversions, selectivities and the target product yield but also the activity, side product formation and thermal stability of the synthesis products. Various ion exchange resins, zeolites and Nafion catalysts were applied for the OME synthesis in a batch autoclave at 60 degrees C for the aqueous reaction systems methanol/paraformaldehyde and the anhydrous reaction system OME1/trioxane. Investigations of the synthesis products in a micro distillation setup showed that all applied catalysts lead to active species in the synthesis product, negatively impacting its thermal stability. This indicates that a synthesis product handling step is necessary prior to the downstream purification. Based on these investigations, ion exchange resins are identified as the most suitable for industrial OME synthesis due to their higher activity and lower side product formation.
引用
收藏
页码:917 / 932
页数:16
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