Processing of Primary Fischer-Tropsch Products - University of Alberta
Processing of Primary Fischer-Tropsch Products - University of Alberta
Processing of Primary Fischer-Tropsch Products - University of Alberta
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increased, the overall distillate yield first increased, passed through a maximum<br />
and subsequently decreased. The higher pressure inhibits secondary cracking and<br />
lighter product formation. The pour points <strong>of</strong> diesels produced from this program<br />
varied between -12~ and -37~ UOP reported that the FT Diesel derived was<br />
<strong>of</strong> extremely high quality, with a very high Cetane number, which can be<br />
blended with low-value refinery products such as light cycle oil to increase the<br />
volume <strong>of</strong> the diesel pool. The hydrocracking catalyst used in this program was a<br />
commercial sulphided catalyst designed for petroleum refining.<br />
Keeping some differences in mind, comparable trends were reported<br />
processing a comparatively light feed- it contained ca 61% wt <strong>of</strong> material<br />
already in the distillates range [68]. The catalyst used was platinum (0.3 mass%)<br />
on amorphous mesoporous silica-alumina. This program included testing over<br />
the same pressure range (35 to 70 bar) at temperatures between 330-355~ The<br />
degree <strong>of</strong> isomerisation in the hydrocracked products increased with an increase<br />
in the conversion. As a consequence, the freezing point <strong>of</strong> the kerosene was a<br />
very low -50~ and the pour point <strong>of</strong> the diesel -30~ remarkable figures<br />
considering the high fraction <strong>of</strong> linear light species in the feed.<br />
This approach <strong>of</strong> using a noble metal on amorphous silica alumina is<br />
likely to be the preferred approach for maximum production <strong>of</strong> highly desirable<br />
diesel blending material. It is likely that all the C14+ material will be treated<br />
using such catalysts due to the enhancement in cold flow properties resulting<br />
from the simultaneous isomerisation. A high blending Cetane value is retained<br />
and very little <strong>of</strong> the diesel range material in the feed is degraded into naphtha<br />
and kerosene.<br />
There are many technology licensors for hydroconversion processes<br />
including ChevronTexaco, UOP, IFP (Axens) and Haldor-Topsoe. Additionally<br />
catalysts can be obtained from these companies as well as from Akzo Nobel,<br />
Stid-Chemie and Axens among others.<br />
6.2.2 Hydrotreating <strong>of</strong> FT paraffins<br />
The quality <strong>of</strong> the primary FT products, both condensate and wax, can be<br />
improved by hydrotreating as Sasol has been doing commercially for many<br />
years. The primary objective <strong>of</strong> this process is to saturate olefins and oxygenates<br />
to the corresponding paraffins. This hydrogenation results in a hydrocarbon<br />
product that is stable when stored for long periods. Stability during storage is the<br />
primary objective for the hydrogenation <strong>of</strong> the hydrocarbon condensate or<br />
fractions there<strong>of</strong>. In the case <strong>of</strong> LTFT wax, the resulting product has better<br />
colour and stability. It is also possible, depending on the reaction conditions, to<br />
transform some <strong>of</strong> the linear hydrocarbons into branched species. In this case the<br />
crystallization temperature <strong>of</strong> the wax can also be influenced. These results are<br />
similar to those attainable when hydrotreating petroleum wax in a similar way<br />
[69]. However, as it was mentioned for hydrocracking, the required process<br />
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