2012
DOI: 10.1016/j.biortech.2012.02.053
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Aqueous phase hydrogenolysis of glycerol to bio-propylene glycol over Pt–Sn catalysts

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Cited by 78 publications
(51 citation statements)
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“…This explains the why the reforming ratio of hydrogen to carbon dioxide was lower for the case of 1 g of 5% Pt/Al 2 O 3 . In a similar work under N 2 pressure, the PtSn0.2 catalyst showed 55% of glycerol conversion to liquid with 59% selectivity to propylene glycol leading to the highest yield to propylene glycol 32% [48]. The conversion to gaseous products, to liquids products and total conversion as a function of the reaction time, for three different catalyst weights (0.5, 1, 2.5 g of 5% Pt/Al 2 O 3 ) and 1 wt.% glycerol solution at 240 C are shown in Fig.…”
Section: Effect Of Catalyst Concentrationmentioning
confidence: 88%
“…This explains the why the reforming ratio of hydrogen to carbon dioxide was lower for the case of 1 g of 5% Pt/Al 2 O 3 . In a similar work under N 2 pressure, the PtSn0.2 catalyst showed 55% of glycerol conversion to liquid with 59% selectivity to propylene glycol leading to the highest yield to propylene glycol 32% [48]. The conversion to gaseous products, to liquids products and total conversion as a function of the reaction time, for three different catalyst weights (0.5, 1, 2.5 g of 5% Pt/Al 2 O 3 ) and 1 wt.% glycerol solution at 240 C are shown in Fig.…”
Section: Effect Of Catalyst Concentrationmentioning
confidence: 88%
“…Further, Barbelli et al. [58] demonstrated the use of a bimetallic catalyst (Pt/SiO 2 ) in the hydrogenolysis of glycerol yielded 83% of 1,2-PD at 200°C under 16 bar H 2 -pressurized conditions.…”
Section: Propylene Glycolmentioning
confidence: 97%
“…Propylene glycol [1,2-propanediol (1,2-PD)] is a chemical product originally derived from propylene oxide through hydrolysis [58,59]. 1,2-PD is a potential replacement for ethylene glycol.…”
Section: Propylene Glycolmentioning
confidence: 99%
“…This reaction produces principally 1,2-propylene glycol (1,2-PG), through a mechanism that may proceed in the following ways: (i) a first dehydration on the metal site or acid sites on the support to produce acetol as intermediate and (ii) hydrogenation of acetol on the metal site to generate 1,2-PG (Scheme 1). It was found that for a support presenting strong acid properties, the reaction can lead to a strong dehydration that produces acrolein [29], whereas when glycerol reacts directly with hydrogen by a C-C cleavage, the reaction produces ethylene glycol (EG) and other degradation products, such as methanol and ethanol, which are favored with temperature [30]. Accordingly, the hydrogenolysis tests were carried out at 200 °C to favor the production of 1,2-PG.…”
Section: Catalytic Activity: Glycerol Hydrogenolysis To Glycolsmentioning
confidence: 99%