Hydrogenolysis of glycerol to propylene glycol by in situ produced hydrogen from aqueous phase reforming of glycerol over SiO2-Al2O3 supported nickel catalyst

被引:62
作者
Seretis, A. [1 ]
Tsiakaras, P. [1 ]
机构
[1] Univ Thessaly, Sch Engn, Dept Mech Engn, Volos 38334, Volos, Greece
关键词
Glycerol; Aqueous phase reforming; Hydrogenolysis; Nickel; Hydrogen; Propylene glycol; RENEWABLE HYDROGEN; CONVERSION; 1,2-PROPANEDIOL; PROPANEDIOLS; APR;
D O I
10.1016/j.fuproc.2015.10.013
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
In the present work, the reactions of glycerol's aqueous phase reforming (APR) and Aqueous Phase Hydrogenolysis (APR) in a batch reactor containing SiO2-Al2O3 supported 65% Ni catalyst are performed. The effect of: i) the reaction time (30-240 min), ii) the operating temperature (200-240 degrees C), iii) the glycerol concentration (1 or 10 wt.%), iv) the catalyst weight (0.5-10 g) and v) the gas to liquid phase volume ratio (1.4 or 5 ml/ml) on: a) the gaseous and liquid product selectivities and b) the glycerol's conversion is investigated. The main gaseous products are found to be H-2, CH4 and CO2, while the main liquid products are found to be propylene glycol (PG), ethylene glycol (EG), ethanol and acetol. Glycerol's conversion increases with the reaction evolution and the increase of the temperature, reaching a plateau. It is found that hydrogen yield is maximized at short reaction times, low glycerol concentrations and increased gas to liquid phase volume ratios, reaching up to 23.5%. On the contrary, the PG yield is favored under the inverse conditions, reaching up to 22%. The higher conversion to gaseous products is found to be similar to 73.6% and the higher conversion to liquid products similar to 35.6%. It is also found that, the increased catalyst concentration favors the C-C bond cleavage and the formation of ethylene glycol, ethanol and CH4. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:135 / 146
页数:12
相关论文
共 48 条
[1]   Hydrogen production from glycerol: An update [J].
Adhikari, Sushil ;
Fernando, Sandun D. ;
Haryanto, Agus .
ENERGY CONVERSION AND MANAGEMENT, 2009, 50 (10) :2600-2604
[2]   Reaction mechanism of the glycerol hydrogenolysis to 1,3-propanediol over Ir-ReOx/SiO2 catalyst [J].
Amada, Yasushi ;
Shinmi, Yasunori ;
Koso, Shuichi ;
Kubota, Takeshi ;
Nakagawa, Yoshinao ;
Tomishige, Keiichi .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2011, 105 (1-2) :117-127
[3]   Pt catalyst supported on α-Al2O3 modified with CeO2 and ZrO2 for aqueous-phase-reforming of glycerol [J].
Barbelli, Maria L. ;
Pompeo, Francisco ;
Santori, Gerardo F. ;
Nichio, Nora N. .
CATALYSIS TODAY, 2013, 213 :58-64
[4]   Aqueous phase hydrogenolysis of glycerol to bio-propylene glycol over Pt-Sn catalysts [J].
Barbelli, Maria L. ;
Santori, Gerardo F. ;
Nichio, Nora N. .
BIORESOURCE TECHNOLOGY, 2012, 111 :500-503
[5]   Pt-Re synergy in aqueous-phase reforming of glycerol and the water-gas shift reaction [J].
Ciftci, Aysegul ;
Ligthart, D. A. J. Michel ;
Sen, A. Oben ;
van Hoof, Arno J. F. ;
Friedrich, Heiner ;
Hensen, Ernie J. M. .
JOURNAL OF CATALYSIS, 2014, 311 :88-101
[6]   Hydrogen from catalytic reforming of biomass-derived hydrocarbons in liquid water [J].
Cortright, RD ;
Davda, RR ;
Dumesic, JA .
NATURE, 2002, 418 (6901) :964-967
[7]   Low-pressure hydrogenolysis of glycerol to propylene glycol [J].
Dasari, MA ;
Kiatsimkul, PP ;
Sutterlin, WR ;
Suppes, GJ .
APPLIED CATALYSIS A-GENERAL, 2005, 281 (1-2) :225-231
[8]   Influence of the nature of the support on the catalytic properties of Pt-based catalysts for hydrogenolysis of glycerol [J].
Delgado, Severine Noe ;
Yap, David ;
Vivier, Laurence ;
Especel, Catherine .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2013, 367 :89-98
[9]   Hydrogen production from catalytic steam reforming of biodiesel byproduct glycerol: Issues and challenges [J].
Dou, Binlin ;
Song, Yongchen ;
Wang, Chao ;
Chen, Haisheng ;
Xu, Yujie .
RENEWABLE & SUSTAINABLE ENERGY REVIEWS, 2014, 30 :950-960
[10]   Recent Improvement on H2 Production by Liquid Phase Reforming of Glycerol: Catalytic Properties and Performance, and Deactivation Studies [J].
El Doukkali, M. ;
Iriondo, A. ;
Cambra, J. F. ;
Arias, P. L. .
TOPICS IN CATALYSIS, 2014, 57 (10-13) :1066-1077