TY - JOUR
T1 - New design approaches to ultra-clean diesel fuels by deep desulfurization and deep dearomatization
AU - Song, Chunshan
AU - Ma, Xiaoliang
N1 - Funding Information:
We are grateful to Prof. Harold H. Schobert of PSU for many helpful general discussions on fuel chemistry, and to our co-workers including Dr. Uday Turaga, Mr. Gang Wang, Dr. Jian Zheng, and Mr. Michael Sprague of PSU for helpful discussions on diesel fuel desulfurization and hydrogenation. We would like to acknowledge the US Department of Energy, National Energy Technology Laboratory, the US Air Force Office of Scientific Research, and the US Department of Defense Advanced Research Project Agency (DARPA) for partial financial support of various portions of our research.
PY - 2003/3/10
Y1 - 2003/3/10
N2 - This paper is a selective review on design approaches and associated catalysis and chemistry for deep desulfurization and deep dearomatization (hydrogenation) of hydrocarbon fuels, particularly diesel fuels. The challenge for deep desulfurization of diesel fuels is the difficulty of removing the refractory sulfur compounds, particularly 4,6-dimethyldibenzothiophene, with conventional hydrodesulfurization processes. The problem is exacerbated by the inhibiting effect of polyaromatics and nitrogen compounds, which exist in some diesel blend stocks on deep HDS. With the new Environmental Protection Agency (EPA) Tier II regulations to cut the diesel sulfur from current 500 ppmw down to 15 ppmw by June 2006, refineries are facing major challenges to meet the fuel sulfur specification along with the required reduction of aromatics contents. The principles and problems for the existing hydrodesulfurization processes, and the concepts, advantages and disadvantages of various new approaches will be discussed. Specifically, the following new design approaches for sulfur removal will be discussed: (1) novel catalysts for ultra-deep hydrodesulfurization under conventional HDS process conditions; (2) new design concept for sulfur-tolerant noble metal catalysts for low-temperature hydrogenation; (3) new desulfurization process by sulfur adsorption and capture under H2; (4) new desulfurization process by selective adsorption at ambient temperature without H2 and a related integrated process concept; (5) oxidative desulfurization in liquid-phase; and (6) biodesulfurization.
AB - This paper is a selective review on design approaches and associated catalysis and chemistry for deep desulfurization and deep dearomatization (hydrogenation) of hydrocarbon fuels, particularly diesel fuels. The challenge for deep desulfurization of diesel fuels is the difficulty of removing the refractory sulfur compounds, particularly 4,6-dimethyldibenzothiophene, with conventional hydrodesulfurization processes. The problem is exacerbated by the inhibiting effect of polyaromatics and nitrogen compounds, which exist in some diesel blend stocks on deep HDS. With the new Environmental Protection Agency (EPA) Tier II regulations to cut the diesel sulfur from current 500 ppmw down to 15 ppmw by June 2006, refineries are facing major challenges to meet the fuel sulfur specification along with the required reduction of aromatics contents. The principles and problems for the existing hydrodesulfurization processes, and the concepts, advantages and disadvantages of various new approaches will be discussed. Specifically, the following new design approaches for sulfur removal will be discussed: (1) novel catalysts for ultra-deep hydrodesulfurization under conventional HDS process conditions; (2) new design concept for sulfur-tolerant noble metal catalysts for low-temperature hydrogenation; (3) new desulfurization process by sulfur adsorption and capture under H2; (4) new desulfurization process by selective adsorption at ambient temperature without H2 and a related integrated process concept; (5) oxidative desulfurization in liquid-phase; and (6) biodesulfurization.
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U2 - 10.1016/S0926-3373(02)00212-6
DO - 10.1016/S0926-3373(02)00212-6
M3 - Article
AN - SCOPUS:0037429552
SN - 0926-3373
VL - 41
SP - 207
EP - 238
JO - Applied Catalysis B: Environmental
JF - Applied Catalysis B: Environmental
IS - 1-2
ER -