RuO2-Ru/Hβ zeolite catalyst for high-yield direct conversion of xylose to tetrahydrofurfuryl alcohol

被引:38
作者
Insyani, Rizki [1 ]
Barus, Amsalia Florence [2 ]
Gunawan, Ricky [3 ]
Park, Jaeyong [2 ]
Jaya, Gladys Tiffany [2 ]
Cahyadi, Handi Setiadi [1 ]
Sibi, Malayil Gopalan [1 ,2 ,3 ]
Kwak, Sang Kyu [4 ]
Verma, Deepak [1 ,2 ,3 ]
Kim, Jaehoon [1 ,2 ,3 ]
机构
[1] Sungkyunkwan Univ, SKKU Adv Inst Nanotechnol SAINT, 2066 Seobu Ro, Suwon 16419, Gyeonggi Do, South Korea
[2] Sungkyunkwan Univ, Sch Mech Engn, 2066 Seobu Ro, Suwon 16419, Gyeonggi Do, South Korea
[3] Sungkyunkwan Univ, Sch Chem Engn, 2066 Seobu Ro, Suwon 16419, Gyeonggi Do, South Korea
[4] Ulsan Natl Inst Sci & Technol, Sch Energy & Chem Engn, 50 Unist Gil, Ulsan 44919, South Korea
基金
新加坡国家研究基金会;
关键词
Xylose; Furfural; Tetrahydrofurfuryl alcohol; Metal-metal oxide interface; Tandem catalyst; LIQUID-PHASE HYDROGENATION; SELECTIVE HYDROGENATION; FURFURYL ALCOHOL; ADSORPTION GEOMETRY; RUTHENIUM CATALYST; NICKEL-CATALYST; LEVULINIC ACID; RU-CATALYSTS; CU-CATALYSTS; BIOMASS;
D O I
10.1016/j.apcatb.2021.120120
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
Tetrahydrofurfuryl alcohol (THFOL), a valuable biomass-derived chemical, is an important precursor for producing linear diols and biodegradable solvents. Herein, we present the one-pot cascade conversion of xylose to THFOL over an H beta zeolite-supported RuO2-Ru (RuO2-Ru/H beta) catalyst. To elucidate the structure-property correlation of the RuO2-Ru/H beta catalyst and achieve a high THFOL yield via sequential isomerization, dehydration, and hydrogenation, several synthesis methods, namely incipient wetness impregnation, reductive deposition, activated reductive deposition, and post-oxidative activated reductive deposition (ARD-O) were used. The best catalytic performance was obtained over the RuO2-Ru/H beta-ARD-O catalyst. An almost complete conversion of xylose and a high THFOL yield of 61.8% were achieved after 1 h at 180 degrees C under an initial H-2 pressure of 3.0 MPa in tetrahydrofuran. In-depth analyses of the RuO2-Ru/H beta-ARD-O catalyst furfural (FFA)- and CO-probed diffuse reflectance infrared Fourier transform spectra indicated the formation of RuO2 at the corner and edge sites of Ru nanoparticles. The direct conversion of FFA to THFOL at interfacial RuO2-Ru sites without furfuryl alcohol (FOL) readsorption hindered the contact of FOL with the acidic support, which suppressed the formation of humin and other byproducts and led to a high THFOL yield.
引用
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页数:20
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