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Tacoma filtrate

Hydrotreating of Tacoma filtrate was investigated over both an inert, low-surface-area alumina and a silica-promoted cobalt-molybdena (Co-Mo) on alumina catalyst. The filtrate feed used in this study was from a run made at Tacoma on June 21,1976 operating with Kentucky Colonial coal as feed at 843°F, 1500 psig at a solvent to coal ratio of 1.6 1. This... [Pg.128]

However, the heptane insolubility of 850° F+ SRC residue from Tacoma (see Table I) showed little change when subjected to the same treatment as the filtrate from Tacoma. The 850°F+ SRC residue received from Tacoma had 81% heptane insolubles while the 850°F+ residue from the distillation of the reconstituted SRC filtrate, which is described below, had 87% heptane insolubles. This was a 6% increase in heptane insolubles in Tacoma residual SRC after thermal treatment compared with a 40% increase for the Tacoma filtrate heptane insolubles after the same treatment. [Pg.130]

Table VI. Results on Tacoma Filtrate Using 850°F Cut Point for Co-Mo... Table VI. Results on Tacoma Filtrate Using 850°F Cut Point for Co-Mo...
Authentic and synthetic solvent-refined coal filtrates were processed upflow in hydrogen over three different commercially available catalysts. Residual (>850°F bp) solvent-refined coal versions up to 46 wt % were observed under typical hydrotreating conditions on authentic filtrate over a cobalt-molybdenum (Co-Mo) catalyst. A synthetic filtrate comprised of creosote oil containing 52 wt % Tacoma solvent-refined coals was used for evaluating nickel-molybdenum and nickel-tungsten catalysts. Nickel-molybdenum on alumina catalyst converted more 850°F- - solvent-refined coals, consumed less hydrogen, and produced a better product distribution than nickel-tungsten on silica alumina. Net solvent make was observed from both catalysts on synthetic filtrate whereas a solvent loss was observed when authentic filtrate was hydroprocessed. Products were characterized by a number of analytical methods. [Pg.124]

Apparently the increase in heptane insolubles resulted from thermal repolymerization during distillation. The filtrate readily underwent this reaction but Tacoma 850° F+ SRC residue was unreactive because it already had been exposed to high temperature when isolated by distilla-... [Pg.130]

An 850°F cut point was used at the Tacoma plant when this filtrate was generated. [Pg.135]

Processing Reconstituted SRC Filtrate. A synthetic blend of 850°F+ residual SRC in a coal-derived creosote oil was prepared and used in catalyst evaluation studies when SRC filtrate became unavailable. The synthetic blend was a 52 wt % mixture of residual Tacoma 850°F+ SRC dissolved in Koppers Tar creosote oil. [Pg.136]

The process operates without catalysts, since the catalytic activity of the finely divided pyrites in the coal feedstock is sufficient. Hydrogen consumption is around 2%. The undissolved residue is separated by pressure filtration. A pilot plant was started up at Fort Louis in Tacoma/Wash., USA in 1974, with a throughput of 50 t/d of coal. By increasing the severity of cracking, this method can also be used to produce heavy heating oil (SRC-II process). [Pg.52]


See other pages where Tacoma filtrate is mentioned: [Pg.130]    [Pg.131]    [Pg.127]    [Pg.128]    [Pg.129]    [Pg.130]    [Pg.131]    [Pg.127]    [Pg.128]    [Pg.129]   


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Heptane insolubles Tacoma filtrate

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