INFLUENCE OF HYDROGEN AND CATALYST ON DISTILLATE YIELDS AND THE REMOVAL OF HETEROATOMS, AROMATICS, AND CCR DURING CRACKING OF ATHABASCA BITUMEN RESIDUUM OVER A WIDE-RANGE OF CONVERSIONS

Authors
Citation
Ec. Sanford, INFLUENCE OF HYDROGEN AND CATALYST ON DISTILLATE YIELDS AND THE REMOVAL OF HETEROATOMS, AROMATICS, AND CCR DURING CRACKING OF ATHABASCA BITUMEN RESIDUUM OVER A WIDE-RANGE OF CONVERSIONS, Energy & fuels, 8(6), 1994, pp. 1276-1288
Citations number
17
Categorie Soggetti
Engineering, Chemical","Energy & Fuels
Journal title
ISSN journal
08870624
Volume
8
Issue
6
Year of publication
1994
Pages
1276 - 1288
Database
ISI
SICI code
0887-0624(1994)8:6<1276:IOHACO>2.0.ZU;2-I
Abstract
The percent conversion of sulfur, nitrogen, vanadium, nickel, aromatic s, and CCR (Conradson carbon residue) has been analyzed as a function of residuum conversion for five series of reactions carried out in a b atch reactor under nitrogen, hydrogen, or hydrogen in the presence of a residuum hydrotreating catalyst, over residuum conversions ranging f rom 38 to 86%. Sulfur, nitrogen, and CCR conversions could be divided into three categories, up to 50% residuum conversion, 50-70% residuum conversion, and greater than 70% residuum conversion. Sulfur conversio n in the first category was from the distillable liquids and resulted from a combination of thermal, hydrogenation, and hydrogen atom additi on reactions. Nitrogen removal in the first category was due to incorp oration of nitrogen into reactor solids in the early stages of the rea ction and was therefore suppressed by hydrogen in the absence of a cat alyst. In the presence of hydrogen, CCR conversion was largely due to hydrogen atom addition. Without hydrogen, CCR conversion was negative through the first two categories of conversion. Aromatics in the resid ua fractions increased steadily as residuum Conversion increased, but increased faster in the coking case. Sulfur, nitrogen, and CCR convers ions were all rapid after approximately 70% residuum conversion and we re explained in terms of thermal reactions. Metals removal appeared to be due to thermal reactions with the solids in the reactor acting as a collector. Catalytic reactions did not appear to play a role. Overal l, the main role of catalyst was the removal of sulfur from distillabl e liquids produced in the early stages of the residuum conversion reac tion, and in CCR conversion, again in the early stages of the reaction .