Selective conversion of furfural into tetrahydrofurfuryl alcohol using a heteropoly acid-based material as a hydrogenation catalyst

被引:15
|
作者
Koley, Paramita [1 ,2 ]
Rao, B. Srinivasa [2 ]
Sabri, Ylias M. [1 ]
Bhargava, Suresh K. [1 ]
Tardio, James [1 ]
Lingaiah, N. [2 ]
机构
[1] RMIT Univ, Sch Appl Sci, Ctr Adv Mat & Ind Chem CAMIC, GPO BOX 2476, Melbourne, Vic 3001, Australia
[2] Indian Inst Chem Technol, CSIR, Catalysis & Fine Chem Div, Uppal Rd, Hyderabad 500007, Andhra Pradesh, India
关键词
SUBSTITUTED POLYOXOMETALATE; METAL-CATALYSTS; FUEL ADDITIVES; BIOMASS; SILICA; PHASE; REDUCTION; 1,5-PENTANEDIOL; OXIDATION; CHEMICALS;
D O I
10.1039/d0se00861c
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 (THFAL) is a green solvent as well as a significant platform chemical which can be obtained from biomass derived furfural. In this study, new palladium exchanged vanadium incorporated supported heteropoly molybdate (PdMPAV(2)) catalysts were synthesized using a simple wet impregnation method and studied for selective hydrogenation of furfural. Six different catalysts were investigated: PdMPAV(2)/Al2O3, PdMPAV(2)/TiO2, PdMPAV(2)/SiO2, PdMPAV(2)/ZrO2, PdMPAV(2)/Nb2O5 and Pd/Al2O3. Of the catalysts studied the PdMPAV(2)/Al(2)O(3)catalyst was able to achieve the highest selectivity of THFAL (95%) under moderate reaction conditions (150 degrees C, 2.5 MPa, 6 h) using isopropanol as a solvent and the weight percentage of palladium is only 0.5% which is the least among all the previously reported catalysts. The other catalysts investigated achieved yields of 50-75% under the same reaction conditions. The higher selectivity obtained using the alumina supported catalyst was explained using a range of physicochemical methods: XRD, temperature programmed reduction (H-2-TPR), CO pulse chemisorption, BET surface area analysis and SEM. The H-2-TPR results showed that PdMPAV(2)/Al(2)O(3)contained a significant amount of Pd that was reduced at the lowest temperature (similar to 100 degrees C) observed for all the materials investigated, which indicated that this catalyst most likely contained a significantly greater amount of more highly dispersed/higher surface area Pd than the other catalysts investigated which is also supported by CO pulse chemisorption results. XPS results supported the presence of Pd(0) which is stabilized by a heteropoly acid framework, and TEM and CO chemisorption results illuminated the fact that the well dispersed and smaller palladium cluster is one of the crucial factors for the better activity of PdMPAV(2)/Al2O3. The effects of the variation of temperature, pressure, time and catalyst concentration were investigated for the best performing catalyst (PdMPAV(2)/Al2O3).
引用
收藏
页码:4768 / 4779
页数:12
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