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the coking properties of coal at elevated pressures. - Argonne ...

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could not be assumed constant. Thus a fluidized bed reactor with a continuous<br />

feed and discharge <strong>of</strong> carbon (150mm height) was used to analyze<br />

<strong>the</strong> r<strong>at</strong>e for higher oxygen concentr<strong>at</strong>ion; namely, a large value <strong>of</strong> a<br />

and a higher temper<strong>at</strong>ure. Fur<strong>the</strong>rmore, <strong>the</strong> reduction <strong>of</strong> “NO“ in a<br />

Simul<strong>at</strong>ed combustion product containing C02 was studied. A remarkable<br />

result from <strong>the</strong>se experiments is th<strong>at</strong> a significant reduction <strong>of</strong> “NO“<br />

was realized even under an excess air condition in which oxygen remained<br />

in <strong>the</strong> outlet flow.<br />

The simplified bubbling bed model by Kunii and Levenspiel was used<br />

to evalu<strong>at</strong>e <strong>the</strong> reaction r<strong>at</strong>e in <strong>the</strong> presence <strong>of</strong> oxygen. First, <strong>the</strong><br />

effective bubble diameter was calcul<strong>at</strong>ed as an adjustable parameter by<br />

curvefitting <strong>the</strong> experimental d<strong>at</strong>a obtained in <strong>the</strong> absence <strong>of</strong> oxygen to<br />

<strong>the</strong> curve calcul<strong>at</strong>ed <strong>the</strong>oretically by <strong>the</strong> above model and <strong>the</strong> kinetic<br />

d<strong>at</strong>a shown previously. Then <strong>the</strong> increased r<strong>at</strong>e in <strong>the</strong> presence <strong>of</strong><br />

oxygen was evalu<strong>at</strong>ed by changing <strong>the</strong> r<strong>at</strong>e, but by keeping <strong>the</strong> o<strong>the</strong>r parameter,<br />

including <strong>the</strong> effective bubble diameter, constant.<br />

In this evalu<strong>at</strong>ion <strong>of</strong> <strong>the</strong> r<strong>at</strong>e, <strong>the</strong> effect <strong>of</strong> fuel “NO” formed by<br />

<strong>the</strong> simultaneously occuring combustion <strong>of</strong> char was compens<strong>at</strong>ed for. The<br />

details are shown elsewhere. The estim<strong>at</strong>ed r<strong>at</strong>e is shown in Fig. 5. An<br />

increased r<strong>at</strong>e <strong>of</strong> “NO“ reduction was observed in <strong>the</strong> presence <strong>of</strong> oxygen<br />

<strong>at</strong> both 60OoC and 750°C. The r<strong>at</strong>e was not significantly reduced by <strong>the</strong><br />

presence <strong>of</strong> oxygen <strong>at</strong> 8OO0C. At 853’C <strong>the</strong> r<strong>at</strong>e <strong>of</strong> “NO“ destruction was<br />

reduced by coexisting oxygen. The extent <strong>of</strong> “NO“ reduction by both char<br />

and activ<strong>at</strong>ed carbon in both <strong>the</strong> absence and presence <strong>of</strong> oxygen was measured<br />

over a temper<strong>at</strong>ure ronge <strong>of</strong> 700Q990O0C where <strong>the</strong> heiyht <strong>of</strong> <strong>the</strong> bed<br />

was 150mm. The results toge<strong>the</strong>r with <strong>the</strong> extent <strong>of</strong> oxygen consumption<br />

is shown in Fig. 7. The increased r<strong>at</strong>e for char was verified up to<br />

approxim<strong>at</strong>ely 75OoC and th<strong>at</strong> for <strong>the</strong> activ<strong>at</strong>ed carbon up to 95OoC.<br />

Reduction <strong>of</strong> “NO” in <strong>the</strong> presence <strong>of</strong> carbon monoxide and hydrogen8’12)<br />

The preliminary investig<strong>at</strong>ion concerning <strong>the</strong> reduction <strong>of</strong> nitric<br />

oxide by char in <strong>the</strong> presence <strong>of</strong> hydrogen or carbon monoxide was carried<br />

out over a temper<strong>at</strong>ure range <strong>of</strong> 700-800°C in a fixed bed reactor mentioned<br />

previously. The reaction was first order with respect to nitric<br />

oxide. Ammonia was formed in <strong>the</strong> nitric oxide hydrogen-char system.<br />

The presence <strong>of</strong> hydrogen and carbon monoxide decreased <strong>the</strong> consumption<br />

<strong>of</strong> carbon to nearly zero, as:<br />

NO + CO+COz + %N2<br />

NO .+ Hg+H20 + ‘/2 Nz<br />

NO tV2H2-+NHB + H2 0<br />

(1)<br />

(2)<br />

(3)<br />

The r<strong>at</strong>es and activ<strong>at</strong>ion energies obtained for <strong>the</strong> above c<strong>at</strong>alytic reac-<br />

tions for (1) or (2) + (3) agreed with <strong>the</strong> r<strong>at</strong>e <strong>of</strong> nonc<strong>at</strong>alytic reduction<br />

<strong>of</strong> nitric oxide by char within <strong>the</strong> experimental error. This strongly<br />

suggested th<strong>at</strong> <strong>the</strong> activ<strong>at</strong>ed adsorption <strong>of</strong> nitric oxide on <strong>the</strong> char sur-<br />

face controlled <strong>the</strong> overall r<strong>at</strong>es. The r<strong>at</strong>io <strong>of</strong> ammonia formed by<br />

reaction (3) to <strong>the</strong> consumed nitric oxide which is found to be constant<br />

<strong>at</strong> each temper<strong>at</strong>ure is decreased with an increased temper<strong>at</strong>ure.<br />

271

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