Liquefaction co-processing of coal shale oil at - Argonne National ...
Liquefaction co-processing of coal shale oil at - Argonne National ...
Liquefaction co-processing of coal shale oil at - Argonne National ...
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TWO-STAGE COAL LIQUEFACTION<br />
WITHOUT GAS-PHASE HYDROGEN<br />
H. P. Stephens<br />
Sandia N<strong>at</strong>ional Labor<strong>at</strong>ories<br />
Albuquerque, New Mexi<strong>co</strong> 87185<br />
INTRODUCTION<br />
Current two-stage direct <strong>co</strong>al liquefaction processes require the use<br />
<strong>of</strong> high-pressure purified hydrogen to hydrogen<strong>at</strong>e either the solvent<br />
or a <strong>co</strong>al/solvent slurry. This paper describes techniques to<br />
elimin<strong>at</strong>e the direct use <strong>of</strong> hydrogen gas in the solvent production<br />
and primary <strong>co</strong>al liquefaction stages. The approach employs the<br />
w<strong>at</strong>er-gas shift (WGS) reaction to gener<strong>at</strong>e liquefaction hydrogendonor<br />
solvents <strong>at</strong> low temper<strong>at</strong>ures and pressures in a c<strong>at</strong>alytic<br />
solvent production stage, followed by reaction <strong>of</strong> the solvent with<br />
<strong>co</strong>al, in the absence <strong>of</strong> hydrogen, in a thermal primary liquefaction<br />
stage.<br />
Previous researchers (1,2) have used mixtures <strong>of</strong> carbon monoxide and<br />
steam to <strong>co</strong>nverg <strong>co</strong>al .in single-stage processes oper<strong>at</strong>ed <strong>at</strong> high<br />
temper<strong>at</strong>ures (380 to 475 C) and pressures (to 5000 psi). Although<br />
pilot tests with high-reactivity, low-rank <strong>co</strong>als achieved moder<strong>at</strong>e<br />
<strong>co</strong>nversions to benzene-soluble products, yields <strong>of</strong> distill<strong>at</strong>e <strong>oil</strong>s<br />
were low (3).<br />
In an initial portion <strong>of</strong> this study it was proposed (4) th<strong>at</strong> a<br />
significant improvement in <strong>co</strong>al liquefaction using CO/H 0 mixtures<br />
may be realized by separ<strong>at</strong>ing, or staging, the &GS-solvent<br />
production and <strong>co</strong>al liquefaction reactions, allowing each to be<br />
performed <strong>at</strong> an optimum temper<strong>at</strong>ure. Results <strong>of</strong> thermodynamic<br />
calcul<strong>at</strong>ions and greliminary experiments proved th<strong>at</strong> use <strong>of</strong> low<br />
temper<strong>at</strong>ures (