Catalytic routes for the conversion of biomass into liquid hydrocarbon transportation fuels

被引:715
作者
Carlos Serrano-Ruiz, Juan [1 ]
Dumesic, James A. [2 ]
机构
[1] Univ Alicante, Dept Inorgan Chem, Adv Mat Lab, E-03080 Alicante, Spain
[2] Univ Wisconsin, Dept Chem & Biol Engn, Madison, WI 53706 USA
关键词
C COUPLING REACTIONS; GAMMA-VALEROLACTONE; OXYGENATED HYDROCARBONS; LIGNOCELLULOSIC BIOMASS; ALDOL-CONDENSATION; CARBOXYLIC-ACIDS; FAST PYROLYSIS; LACTIC-ACID; KETONIZATION; CHEMICALS;
D O I
10.1039/c0ee00436g
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Concerns about diminishing fossil fuel reserves along with global warming effects caused by increasing levels of CO2 in the atmosphere are driving society toward the search for new renewable sources of energy that can substitute for coal, natural gas and petroleum in the current energy system. Lignocellulosic biomass is abundant, and it has the potential to significantly displace petroleum in the production of fuels for the transportation sector. Ethanol, the main biomass-derived fuel used today, has benefited from production by a well-established technology and by partial compatibility with the current transportation infrastructure, leading to the domination of the world biofuel market. However, ethanol suffers from important limitations as a fuel (e.g., low energy density, high solubility in water) than can be overcome by designing strategies to convert non-edible lignocellulosic biomass into liquid hydrocarbon fuels (LHF) chemically similar to those currently used in internal combustion engines. The present review describes the main routes available to carry out such deep chemical transformation (e. g., gasification, pyrolysis, and aqueous-phase catalytic processing), with particular emphasis on those pathways involving aqueous-phase catalytic reactions. These latter catalytic routes achieve the required transformations in biomass-derived molecules with controlled chemistry and high yields, but require pretreatment/hydrolysis steps to overcome the recalcitrance of lignocellulose. To be economically viable, these aqueous-phase routes should be carried out with a small number of reactors and with minimum utilization of external fossil fuel-based hydrogen sources, as illustrated in the examples presented here.
引用
收藏
页码:83 / 99
页数:17
相关论文
共 134 条
[1]
Catalytic conversion of a biofuel to hydrocarbons: Effect of mixtures of HZSM-5 and silica-alumina catalysts on product distribution [J].
Adjaye, JD ;
Katikaneni, SPR ;
Bakhshi, NN .
FUEL PROCESSING TECHNOLOGY, 1996, 48 (02) :115-143
[2]
Aehle W., 2004, ENZYMES IND PRODUCTI, P198
[3]
DFT studies for cleavage of C-C and C-O bonds in surface species derived from ethanol on Pt(111) [J].
Alcalá, R ;
Mavrikakis, M ;
Dumesic, JA .
JOURNAL OF CATALYSIS, 2003, 218 (01) :178-190
[4]
Production of liquid hydrocarbon transportation fuels by oligomerization of biomass-derived C9 alkenes [J].
Alonso, David Martin ;
Bond, Jesse Q. ;
Serrano-Ruiz, Juan Carlos ;
Dumesic, James A. .
GREEN CHEMISTRY, 2010, 12 (06) :992-999
[5]
[Anonymous], GLOB OIL DEPL REP
[6]
[Anonymous], 2009, International Energy Outlook
[7]
[Anonymous], 2003, EN Official Journal of the European Communities
[8]
[Anonymous], 2008, [No title captured], Patent No. [2008142127, WO 2008142127A1.]
[9]
[Anonymous], 2005, BIOMASS FEEDSTOCK BI
[10]
Astm D 4806, 2010, D4806 ASTM INT, DOI [10.1520/D4806-10, DOI 10.1520/D4806-10]