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Combustors carbon monoxide

A diagram for one implementation of this process (61,62) is shown in Eigure 11. Recovered potassium sulfate is converted to potassium formate [590-29 ] by reaction with calcium formate [544-17-2] which is made by reacting hydrated lime, Ca(OH)2, and carbon monoxide. The potassium formate (mp 167°C), in hquid form, is recycled to the combustor at about 170°C. Sulfur is removed as soHd calcium sulfate by filtration and then disposed of (see... [Pg.423]

The authors developed a multi-layered microreactor system with a methanol reforma- to supply hydrogen for a small proton exchange membrane fiiel cell (PEMFC) to be used as a power source for portable electronic devices [6]. The microreactor consists of four units (a methanol reformer with catalytic combustor, a carbon monoxide remover, and two vaporizers), and was designed using thermal simulations to establish the rppropriate temperature distribution for each reaction, as shown in Fig. 3. [Pg.67]

Emissions from hazardous waste combustors are regulated under two statutory authorities RCRA and the CAA. The MACT standards set emission limitations for dioxins, furans, metals, particulate matter, total chlorine, hydrocarbons/carbon monoxide, and destruction and removal efficiency (DRE) for organics. Once a facility has demonstrated compliance with the MACT standards by conducting its comprehensive performance test (CPT) and submitting its notification of compliance (NOC), it is no longer subject to the RCRA emission requirements with a few exceptions. RCRA-permitted facilities, however, must continue to comply with their permitted emissions requirements until they obtain modifications to remove any duplicative emissions conditions from their RCRA... [Pg.460]

The rate of catalytic "NO" reduction by hydrogen and carbon monoxide over a char surface was measured and compared with the rate of noncatalytic "NO" reduction by char which has been previously reported to have a significant effect on "NO" emission control in a fluidized bed combustor of coal. [Pg.347]

In the presence of hydrogen and carbon monoxide, the surface catalyzed reduction of "NO" controlled the overall "NO" destruction. Thus the presence of hydrogen and carbon monoxide decreased the corn-sumption of carbon to nearly zero. The rate was significantly enhanced by hydrogen over the temperature range employed for the fluidized bed combustor. [Pg.347]

Fig. 1 Carbon monoxide emissions as a function of fuel moisture content for stoker combustor with primary air only for all fuel types. Fig. 1 Carbon monoxide emissions as a function of fuel moisture content for stoker combustor with primary air only for all fuel types.
MW of power. Utilization of DME for power generation offers tremendous environmental benefits, in terms of CO SO and NO emissions. It burns in conventional gas turbines without modifications to the turbine or the combustors. Emissions produced by combustion of conventional fuels in gas turbines include nitrogen oxides, carbon monoxide, unburned hydrocarbons, and sulfur oxides. Dimethyl ether produces no sulfur oxide emission, as the fuel is sulfur free. It generates the least amount of NO CO, and unburned hydrocarbons as compared with natural gas and distillate, and lower CO2 emissions than the distillates. [Pg.710]

Pacific Northwest National Laboratory s (USA) microchannel reactor unit consisting, in part, of a combustor/evaporator made of stainless steel with an overall size of 41 x 60 x 20mm, with micro-machined combustor channels of 300 p x 500 p x 35 mm, is used to perform methane partial oxidation reaction at 900°C to produce carbon monoxide and hydrogen. Methane conversion efficiencies were more than 85% and 100% with 11 and 25ms residence times, respectively. [Pg.164]

Subsequently, a meso-scaled combined reformer/catalytic combustor with 10-kW power output was realised by GM/OPEL, which was not presented in detail. For this bigger reactor, the carbon monoxide content of the reformate increased, as expected, with increasing reformer outlet temperature from 0.5% at 250 °C to 2% at 300 °C. Increasing the residence time increased the carbon monoxide concentration of the reformate due to the reverse water-gas shift reaction. Increasing the S/C ratio from 1.2 to 1.8 at a 300 °C reaction temperature increased the hydrogen concentration in the reformate slightly from 72 to 73% and decreased the carbon monoxide content from 1.5 to 1.0%, which originated from the beneficial effect of steam addition on the equilibrium of the water-gas shift reaction. [Pg.249]


See other pages where Combustors carbon monoxide is mentioned: [Pg.112]    [Pg.1176]    [Pg.316]    [Pg.274]    [Pg.535]    [Pg.542]    [Pg.543]    [Pg.544]    [Pg.547]    [Pg.454]    [Pg.125]    [Pg.369]    [Pg.358]    [Pg.160]    [Pg.481]    [Pg.303]    [Pg.88]    [Pg.180]    [Pg.209]    [Pg.210]    [Pg.215]    [Pg.317]    [Pg.318]    [Pg.533]    [Pg.603]    [Pg.3]    [Pg.477]    [Pg.55]    [Pg.185]    [Pg.221]    [Pg.120]    [Pg.204]    [Pg.138]    [Pg.672]    [Pg.149]    [Pg.1684]    [Pg.351]    [Pg.200]    [Pg.241]    [Pg.314]    [Pg.335]   
See also in sourсe #XX -- [ Pg.392 ]




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