Pilot Scale Production of Mixed Alcohols from Wood

被引:15
作者
Bain, Richard L. [1 ]
Magrini-Bair, Kimberly A. [1 ]
Hensley, Jesse E. [1 ]
Jablonski, Whitney S. [1 ]
Smith, Kristin M. [1 ]
Gaston, Katherine R. [1 ]
Yung, Matthew M. [1 ]
机构
[1] Natl Bioenergy Ctr, Natl Renewable Energy Lab, Golden, CO 80401 USA
关键词
CATALYTIC HOT GAS; BIOMASS GASIFICATION; LIGNOCELLULOSIC BIOMASS; MOLYBDENUM SULFIDE; K/MOS2; CATALYSTS; FLUIDIZED-BEDS; NICKEL; ALKALI; SYNGAS; SULFUR;
D O I
10.1021/ie403631h
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
An integrated thermochemical biomass to ethanol process was demonstrated at the pilot scale at the National Renewable Energy Laboratory (NREL). A total of 233 h of pilot scale mixed alcohol production was achieved, comprising 81 h of continuous operation in methanol-derived syngas followed by 152 h of continuous operation in biomass-derived syngas. During this period the system generated 20 L of mixed alcohol product. The fully integrated biomass to mixed alcohol process was comprised of a solids feeder, fluidized bed indirect steam gasifier, thermal cracker, char collector, fluidized bed steam reformer, packed bed polishing steam reformer, scrubber, pressure-swing CO2 adsorber, and gas-phase continuously stirred tank gas-to-liquid reactor (CSTR). Additional pumps, compressors, and blowers were used to convey gases, solids, and liquids. Tars and methane were reformed using sequential steps: first in a fluidized bed using an NREL-developed Ni-based catalyst followed by a fixed bed reactor loaded with pelletized, precious metal catalyst developed by Johnson Matthey. Mixed alcohols (a mixture of methanol, ethanol, 1-propanol, etc.) were produced using a metal sulfide catalyst developed at NREL. Under steady state conditions, the steam reformers converted >99.9, 97.0, and 86% of tars, benzene, and methane, respectively, in the producer gas. A simulated partial recycle of carbon dioxide to the gasifier was used to reduce the H-2:CO ratio of the reformed syngas to 3:1 without adding water gas shift reactors to the process or coking the reforming catalysts. When operating on biomass-derived syngas in a CSTR, the fuel synthesis catalyst produced as much as 31 g of EtOH.kg of catalyst(-1).h(-1) at a CO2-free ethanol selectivity of 27% at 2000 psi, 300 degrees C, and 27% CO conversion. A bench scale packed bed reactor operated under analogous conditions produced 39 g of EtOH.kg of catalyst(-1).h(-1) at a CO2-free ethanol selectivity of 28% showing reasonable parity between bench scale and pilot scale.
引用
收藏
页码:2204 / 2218
页数:15
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