Biodiesel Glycerin Valorization into Oxygenated Fuel Additives

被引:7
作者
Dias, Ana Paula Soares [1 ]
Fonseca, Frederico Gomes [2 ]
Catarino, Monica [1 ]
Gomes, Joao [1 ,3 ]
机构
[1] Univ Lisbon, Inst Super Tecn, CERENA, IDMEC, Av Rovisco Pais 1, P-1049001 Lisbon, Portugal
[2] Karlsruhe Inst Technol KIT, Inst Catalysis Res & Technol IKFT, D-76344 Eggenstein Leopoldshaven, Germany
[3] Inst Politecn Lisboa, Inst Super Engn Lisboa, ADEQ, R Conselheiro Emidio Navarro 1, P-1959007 Lisbon, Portugal
关键词
Biodiesel; Catalysis; Valorization; Fuel additives; Acetylation; Acetins; SOLID ACID CATALYSTS; ENGINE PERFORMANCE; ACETYLATION; ESTERIFICATION; SILICA;
D O I
10.1007/s10562-021-03646-0
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Current industrial methods of biodiesel production lead to an excess of crude glycerin which requires costly purification before commercialization. Production of oxygenated fuel additives is a potential route for glycerin valorization. Glycerin acetylation was carried out over heterogeneous acid catalysts (15%, glycerol weight basis) using glacial acetic acid (molar ratio=9). The catalysts, containing different amounts of phosphate species (P/Si from 10 to 20 atomic ratio), were prepared by wet impregnation of commercial silica with aqueous solutions of diammonium phosphate and ortho-phosphoric acid. X-ray diffraction patterns of calcined solids presented amorphous patterns like raw silica. The prepared catalysts presented, at 120 degrees C, glycerol conversion higher than 89.5% after 1 h of reaction, been diacetin the major product, with triacetin selectivities lower than 26.1%. Diacetin selectivity was found to be almost invariant with catalyst acidity thus underlining the relevance of catalyst porosity due to the large acetins molecules sizes. The slow rate of triacetin diffusion in narrow pores of catalyst might be responsible for the relatively low yield obtained. Surface phosphate species showed a slow rate of leaching in the reaction medium showing high catalyst stability. [GRAPHICS] .
引用
收藏
页码:513 / 522
页数:10
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