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Novel Design of an Integrated Pulp Mill Biorefinery for the ...

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3.3.2.4 CO conversion <strong>an</strong>d efficiency<br />

Fig. 15. shows <strong>the</strong> effect <strong>of</strong> H2/CO ratio on syngas conversion <strong>an</strong>d product selectivity.<br />

The dependence <strong>of</strong> one-through conversion on <strong>the</strong> reaction pressure <strong>an</strong>d temperature are shown<br />

in Fig.6[48]. From Fig.3.3.4, when H2/CO ratio is 0.8, <strong>the</strong> DME selectivity is more th<strong>an</strong> 95% <strong>an</strong>d<br />

syngas conversion is more th<strong>an</strong> 50%. From Fig.16., at 270 o C <strong>an</strong>d 50 bar, <strong>the</strong> CO conversion is<br />

about 60%. There<strong>for</strong>e, we suppose our CO conversion is 60%, <strong>an</strong>d hence <strong>the</strong> syngas to DME<br />

efficiency is about 51%.<br />

Figure 16: CO conversion as a function <strong>of</strong> temperature <strong>an</strong>d pressure.<br />

3.3.3 Product separation <strong>an</strong>d purification<br />

The separation scheme design is based on <strong>the</strong> invention <strong>of</strong> Peng. et al[105]. The DME<br />

reactor effluent, which is a mixture <strong>of</strong> DME, meth<strong>an</strong>ol, CO2 <strong>an</strong>d water <strong>an</strong>d unconverted syngas<br />

will be cooled <strong>an</strong>d fed to a high-pressure flash column. The high-pressure flash column will<br />

separate <strong>the</strong> polar molecules <strong>an</strong>d non-polar molecules. The vapor phase containing DME, CO2<br />

<strong>an</strong>d unconverted syngas (non-polar molecules) will pass through a scrubbing column. DME is<br />

used as <strong>the</strong> scrubbing solvent to remove DME <strong>an</strong>d CO2 <strong>an</strong>d meth<strong>an</strong>ol from <strong>the</strong> unconverted<br />

syngas. The mixture <strong>of</strong> DME <strong>an</strong>d CO2 from <strong>the</strong> bottom <strong>of</strong> <strong>the</strong> scrubbing column is fed to a<br />

DME-CO2 distillation column to separate CO2 from <strong>the</strong> product DME.<br />

3.4 Fischer-Tropsch syn<strong>the</strong>sis<br />

This section will describe <strong>an</strong>d elaborate on a design <strong>for</strong> <strong>the</strong> production FTD, based on<br />

black liquor <strong>an</strong>d coal feed stocks. Comp<strong>an</strong>y such as Sasol <strong>an</strong>d Texaco, which produce large<br />

amount <strong>of</strong> FTD, do not share <strong>the</strong> specifics <strong>of</strong> <strong>the</strong>re pl<strong>an</strong>t designs. For this reason, scraps <strong>of</strong><br />

in<strong>for</strong>mation that are found in literature must be pieced toge<strong>the</strong>r with assumptions to create a<br />

design.<br />

Figure 28 list all <strong>of</strong> <strong>the</strong> major parameters <strong>of</strong> <strong>the</strong> FTD production design. LTFT was used<br />

because it produces a greater yield <strong>of</strong> FTD <strong>the</strong>n HTFT. A slurry-phase bubbling-bed reactor was<br />

chosen because <strong>of</strong> its higher efficiency compared to a fixed bed reactor. Slurry-phase bubblingbed<br />

reactors also have responsive temperature control <strong>an</strong>d low down time in <strong>the</strong> case <strong>of</strong> catalyst<br />

poisoning. An iron based catalyst was chosen because <strong>of</strong> its low H2/CO ratio requirement, so that<br />

<strong>an</strong> external water gas shift was not necessary. An α <strong>of</strong> 0.94 was used to maximize wax<br />

production <strong>an</strong>d minimize light hydrocarbon production.<br />

56

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