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

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esults would be expected to be similar to those previously reported<br />

for naphthas from single stage processes (7).1<br />

Jet. To make jet fuel meeting the ASTM smoke point specific<strong>at</strong>ion<br />

<strong>of</strong> 20mm.(minimum), most <strong>of</strong> the arom<strong>at</strong>ics in the <strong>co</strong>al liquids had to<br />

be hydrogen<strong>at</strong>ed.<br />

Figure 4 is a plot <strong>of</strong> smoke point versus arom<strong>at</strong>ic <strong>co</strong>ntent <strong>of</strong><br />

kerosene jet fuels from the various syncrudes. The results fall into<br />

two rough groups, those from Wyodak <strong>co</strong>al and those from Illinois <strong>co</strong>al.<br />

At a given arom<strong>at</strong>ics <strong>co</strong>ntent, those from Wyodak <strong>co</strong>al had smoke points<br />

2-3 mm higher than those from Illinois <strong>co</strong>al, a <strong>co</strong>nsequence <strong>of</strong> the<br />

higher Wyodak paraffin <strong>co</strong>ntent. [The Wyodak jet <strong>co</strong>ntained about 10<br />

LV% paraffins; the Illinois jet, 1-3 LV%.] The Illinois jet fuels met<br />

the jet smoke specific<strong>at</strong>ion <strong>of</strong> 20 mm <strong>at</strong> 10% arom<strong>at</strong>ics or lower; the<br />

Wyodak jet fuels met the specific<strong>at</strong>ion <strong>at</strong> about 16 LV% arom<strong>at</strong>ics.<br />

[Some <strong>of</strong> the sc<strong>at</strong>ter in results for products from a given <strong>co</strong>al was due<br />

to different b<strong>oil</strong>ing distributions. Those jet fuels <strong>co</strong>ntaining more<br />

low b<strong>oil</strong>ing m<strong>at</strong>erial had somewh<strong>at</strong> higher smoke points.]<br />

Jet fuels from <strong>co</strong>al <strong>of</strong>fer some unique advantages over those from<br />

petroleum. Because they <strong>co</strong>ntain high <strong>co</strong>ncentr<strong>at</strong>ions <strong>of</strong> naphthenes,<br />

they are very dense and have high he<strong>at</strong>ing values by volume.<br />

Therefore, they <strong>co</strong>uld have specialized uses, such as for military<br />

fuels. FOK example, Figure 5 shows the densities <strong>of</strong> narrow b<strong>oil</strong>ing<br />

fractions <strong>of</strong> hydrotre<strong>at</strong>ed ITSL <strong>oil</strong>. Jet fuel <strong>of</strong> a desired density<br />

<strong>co</strong>uld be made by adjusting the b<strong>oil</strong>ing range. The ASTM specific<strong>at</strong>ion<br />

for jet fuel gravity is 37OAPI (minimum). However, this specific<strong>at</strong>ion<br />

is probably unnecessary for aircraft with modern flow <strong>co</strong>ntrollers, and<br />

lower gravity (higher density) fuels <strong>co</strong>uld be acceptable. Also, these<br />

jet fuels have unusually low freezing points, because <strong>of</strong> low normal<br />

paraffin <strong>co</strong>ntents.<br />

Diesel. Diesel products from both single-stage and two-stage<br />

procemet typical ASTM specific<strong>at</strong>ions. A rel<strong>at</strong>ively high degree<br />

<strong>of</strong> hydrogen<strong>at</strong>ion was needed to meet the cetane-number specific<strong>at</strong>ion <strong>of</strong><br />

40 (minimum).<br />

Figure 6 shows the rel<strong>at</strong>ionship for cetane number versus<br />

arom<strong>at</strong>ics <strong>co</strong>ntent for products from single-stage and two-stage<br />

processes. With the two-stage <strong>oil</strong>s, the specific<strong>at</strong>ion was met with an<br />

arom<strong>at</strong>ics <strong>co</strong>ntent <strong>of</strong> about 20 Lv%; with single-stage <strong>oil</strong>s, an arom<strong>at</strong>ic<br />

<strong>co</strong>ntent <strong>of</strong> less than 10 LV% was needed. These differences, however,<br />

were not necessarily the result <strong>of</strong> single-stage versus two-stage<br />

<strong>processing</strong>. R<strong>at</strong>her, they appear to be due to changes in b<strong>oil</strong>ing<br />

ranges <strong>of</strong> the diesels. For example, Table VI <strong>co</strong>mpares pairs <strong>of</strong><br />

samples <strong>of</strong> different b<strong>oil</strong>ing ranges. The arom<strong>at</strong>ics and paraffin<br />

<strong>co</strong>ntents within a given pair were about the same. Within each pair,<br />

the higher b<strong>oil</strong>ing sample had the higher cetane number. Also, in<br />

other <strong>co</strong>mparisons (1). the more paraffinic diesels had higher cetane<br />

numbers, when other properties were about equal.<br />

AS with the jet fuels described above, these <strong>co</strong>al-derived diesel<br />

fuels had excellent <strong>co</strong>ld we<strong>at</strong>her properties, and high volumetric<br />

energy <strong>co</strong>ntents.<br />

287

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