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Liquefaction co-processing of coal shale oil at - Argonne National ...

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c<strong>at</strong>alytic stage in Run 2506, whereas in Run 244 approxim<strong>at</strong>ely 45 wt % was produced by the<br />

c<strong>at</strong>alytic hydrotre<strong>at</strong>er (Table 3). Higher quality products are made by the c<strong>at</strong>alytic<br />

stage.<br />

Subsequent oper<strong>at</strong>ion in CC-ITSL was devoted to study <strong>of</strong> performance <strong>of</strong> a new c<strong>at</strong>alyst,<br />

Amoc<strong>at</strong> 1C. As noted previously, interstage vapor separ<strong>at</strong>ion was employed throughout this<br />

period. A <strong>co</strong>mparison <strong>of</strong> "all-distill<strong>at</strong>e'' oper<strong>at</strong>ion <strong>at</strong> the same <strong>co</strong>al feed r<strong>at</strong>e for Shell<br />

324 and Amoc<strong>at</strong> 1C revealed th<strong>at</strong> distill<strong>at</strong>e and hydrocarbon gas yields were similar (Run<br />

2508 versus Run 250C). An altern<strong>at</strong>e deashing solvent was used in Run 250C in order to<br />

maintain stable perfonnance while <strong>processing</strong> the highly soluble feed gener<strong>at</strong>ed by the<br />

fresh Amoc<strong>at</strong> c<strong>at</strong>alyst. This resulted in gre<strong>at</strong>er rejection <strong>of</strong> resid to ash <strong>co</strong>ncentr<strong>at</strong>e<br />

with <strong>co</strong>n<strong>co</strong>mitantly less TSL resid produced. A lower hydrogen <strong>co</strong>nsumption was observed<br />

for Run 250C. This phenomenon <strong>co</strong>uld be <strong>at</strong>tributed to the effect <strong>of</strong> interstage separ<strong>at</strong>ion<br />

(i.e., not hydrotre<strong>at</strong>ing all distill<strong>at</strong>e products) and/or to rel<strong>at</strong>ively lower hydrogen<strong>at</strong>ion<br />

activity <strong>of</strong> the Amoc<strong>at</strong> c<strong>at</strong>alyst.<br />

Higher system space velocities were explored by increasing <strong>co</strong>al feed r<strong>at</strong>es. The goal was<br />

to demonstr<strong>at</strong>e the production <strong>of</strong> high quality (CC-ITSL) distill<strong>at</strong>es <strong>at</strong> reduced <strong>co</strong>st. Yield<br />

d<strong>at</strong>a are reported for Run 250 Periods C, 0, and E in Table 1. Product quality d<strong>at</strong>a and<br />

unit <strong>co</strong>ntributions to distill<strong>at</strong>e production for Period D are given in Tables 2 and 3,<br />

respectively. The d<strong>at</strong>a clearly indic<strong>at</strong>e th<strong>at</strong> "all-distill<strong>at</strong>e'' yield sl<strong>at</strong>es were produced<br />

<strong>at</strong> increased throughputs by <strong>co</strong>mpens<strong>at</strong>ory increases in reactor temper<strong>at</strong>ures. Product<br />

quality did not change significantly <strong>at</strong> the higher r<strong>at</strong>es. It should also be noted th<strong>at</strong><br />

products from higher space velocity CC-ITSL were substantially better than those from<br />

lower space velocity ITSL.<br />

Near the <strong>co</strong>nclusion <strong>of</strong> Run 250, a test <strong>of</strong> solids (un<strong>co</strong>nverted <strong>co</strong>al and ash-cresol insolu-<br />

bles) recycle was performed (Figure 3). The objective was to decrease size <strong>of</strong> the<br />

critical solvent deashing unit by deashing a higher solids <strong>co</strong>ntent vacuum bottoms stream.<br />

Deashed resid was recycled as a <strong>co</strong>mponent <strong>of</strong> the liquefaction solvent. Lower organic<br />

rejection to the ash <strong>co</strong>ncentr<strong>at</strong>e was demonstr<strong>at</strong>ed with the <strong>co</strong>ncentr<strong>at</strong>ed feed. Based on<br />

this result, the <strong>co</strong>ncept <strong>of</strong> solids recycle may be investig<strong>at</strong>ed in a future close-<strong>co</strong>upled<br />

run using c<strong>at</strong>alyst in both reactors.<br />

B<strong>at</strong>ch deactiv<strong>at</strong>ion trends for resid <strong>co</strong>nversion in the c<strong>at</strong>alytic reactor were developed for<br />

the ITSL (deashed bituminous)- Shell 324 and CC-ITSL (close-<strong>co</strong>upled bituminous)-Amoc<strong>at</strong> 1C<br />

modes, using a first order resid <strong>co</strong>nversion model (1). The trends are plotted in Figure 4<br />

together with b<strong>at</strong>ch deactiv<strong>at</strong>ion d<strong>at</strong>a from Wilsonville Run 247 ("simul<strong>at</strong>ed" close-<br />

<strong>co</strong>upled). The trends showed initial periods <strong>of</strong> rapid deactiv<strong>at</strong>ion, followed by slower<br />

deactiv<strong>at</strong>ion r<strong>at</strong>es. Higher resid <strong>co</strong>nversion r<strong>at</strong>e <strong>co</strong>nstants were observed for close-<br />

<strong>co</strong>upled oper<strong>at</strong>ion using the Amoc<strong>at</strong> 1C c<strong>at</strong>alyst. The close-<strong>co</strong>upled residlhoc<strong>at</strong> <strong>co</strong>mbina-<br />

tion was more reactive than the other feedlc<strong>at</strong>alyst (Shell 324) <strong>co</strong>mbin<strong>at</strong>ions. Figure 5<br />

further illustr<strong>at</strong>es this point in an Arrhenius plot.<br />

RELATIVE ECONOMICS<br />

Results from an e<strong>co</strong>nomic screening study performed by Lummus Crest Inc. indic<strong>at</strong>ed a<br />

reduction in the required product selling price for CC-ITSL products <strong>co</strong>mpared to ITSL<br />

products (Table 41. The study was based on a <strong>co</strong>nceptual <strong>co</strong>mnercial 10,000 TPD plant using<br />

Illinois No. 6 <strong>co</strong>al. The rel<strong>at</strong>ively lower price was due to higher distill<strong>at</strong>e production<br />

and improved distill<strong>at</strong>e quality for the close-<strong>co</strong>upled case (2).<br />

241

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