Bio-fuel reformation for solid oxide fuel cell applications. Part 3: Biodiesel-diesel blends

被引:13
作者
Lin, Jiefeng
Trabold, Thomas A. [1 ]
Walluk, Mark R.
Smith, Daniel F.
机构
[1] Rochester Inst Technol, Golisano Inst Sustainabil, Rochester, NY 14623 USA
关键词
Biodiesel-diesel blends; Auto-thermal reforming; Carbon formation; Hydrogen production; Solid oxide fuel cell; HYDROGEN-PRODUCTION; PREFERENTIAL OXIDATION; THERMODYNAMIC ANALYSIS; LIQUID HYDROCARBONS; CARBON FORMATION; METHANE; CATALYSTS; GAS; BIOETHANOL; PROCESSOR;
D O I
10.1016/j.ijhydene.2013.10.093
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
The auto-thermal reforming (ATR) performance of diesel blended with biodiesel (e.g., B5, B10, B20, B40, and B80) was investigated and compared to pure diesel and biodiesel ATR in a single-tube reformer with ceramic monolith wash-coated rhodium/ceria-zirconia catalyst. The initial operating condition of the ATR of all studied fuels was set as total moles of oxygen from air, water, and fuel per mole of carbon (O/C) = 1.47, moles of water to carbon (H2O/C) = 0.6, and gas hourly space velocity = 33,950 h(-1) at 1223 K reformer temperature, to achieve the same syngas (H-2 + CO) production rate. A direct photo-acoustic micro-soot meter was applied to quantify the dynamic evolution of carbon formation and a mass spectrometer was used to measure the gas composition of reformer effluents. The blends with more biodiesel content were found to have a lower syngas production rate and reforming efficiency, and require more air and higher reformer temperature to avoid carbon formation. Strong correlations between ethylene and solid carbon concentration were observed in the reformation of all the fuels and blends, with more biodiesel content tending to have higher ethylene production. This study is one component of a three-part investigation of bio-fuel reforming, also including fuel vaporization and reactant mixing (Part 1) and biodiesel (Part 2). Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:196 / 208
页数:13
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