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Carbon monoxide, from oxidation

A new route to ethylene glycol from ethylene oxide via the intermediate formation of ethylene carbonate has recently been developed by Texaco. Ethylene carbonate may be formed by the reaction of carbon monoxide, ethylene oxide, and oxygen. Alternatively, it could be obtained by the reaction of phosgene and methanol. [Pg.193]

Carbon monoxide from automobile exhausts Photochemical oxidants, particularly ozone (Los Angeles)... [Pg.121]

The stable gases produced by incineration are primarily carbon dioxide and water. Depending on waste composition, however, small quantities of carbon monoxide, nitrogen oxides, HC1, and other gases may form. Also, if combustion is not complete, compounds known as products of incomplete combustion (PICs) may be emitted. RCRA regulations control the amount of HC1 released from the APCD. [Pg.961]

Photochemical elimination reactions include all those photoinduced reactions resulting in the loss of one or more fragments from the excited molecule. Loss of carbon monoxide from type I or a-cleavage of carbonyl compounds has been previously considered in Chapter 3. Other types of photoeliminations, to be discussed here, include loss of molecular nitrogen from azo, diazo, and azido compounds, loss of nitric oxide from organic nitrites, and loss of sulfur dioxide and other miscellaneous species. [Pg.548]

Novacon An adsorptive process for removing oxides of sulfur and nitrogen, and carbon monoxide, from combustion gases. The adsorbent is an active form of natural marble. [Pg.191]

The first scheme was ruled out by showing that, at room temperature, a surface formed by very brief exposure of the oxygen-saturated surface to carbon monoxide is stable after removal of the carbon monoxide from the reaction chamber. In other words, no further surface carbide formed by lateral reactions of adsorbed carbon monoxide with surface oxygen atoms. The second scheme was ruled out by showing that exposure of the surface formed in the latter experiment to oxygen had no effect. Consequently the third scheme is believed to represent the mechanism of oxidation of carbon monoxide at the step and kink sites of platinum. [Pg.177]

Air emissions may arise from fugitive propane emissions and process vents. These include heater stack gas (carbon monoxide, sulfur oxides, nitrogen oxides, and particulate matter) as well as hydrocarbon emission, such as fugitive propane and fugitive solvents. Steam stripping wastewater (oil and solvents) and solvent recovery wastewater (oil and propane) are also produced. [Pg.107]

The time-series analysis results of Merz et were expressed in first-order empirical formulas for the most part. Forecasting expressions were developed for total oxidant, carbon monoxide, nitric oxide, and hydrocarbon. Fitting correlation coefficients varied from 0.547 to 0.659. As might be expected, the best results were obtained for the primary pollutants carbon monoxide and nitric oxide, and the lowest correlation was for oxidant. This model relates one pollutant to another, but does not relate emission to air quality. For primary pollutants, the model expresses the concentrations as a function of time. [Pg.225]

The PCC oxidation of 3-amino-4,5-diphenyl-2(3//)-oxazolone 96 affords mono-diazobenzyl 286 as the primary decomposition product obtained via loss of carbon monoxide from the postulated A -nitrenolactam 285. Oxidation of 96 with tert-BuOCl/NEt3 at 108 °C results in a deep green solution of 285, which reacts with dimethyl sulfoxide (DMSO) to give the sulfoximide 288 (Fig. 5.68). ... [Pg.42]

Meyer, J. (1981). Comparison of carbon monoxide, nitric oxide, and nitrite as inhibitors of the nitrogenase from Cbstridium pasteurianum. Arch. Biochem. Biophys. 210, 246-256. [Pg.171]

Thermolysis of indenone oxides (151) is an equally useful route to the betaines (150). Dimethyl acetylenedicarboxylate and compound 151 (R = R = Ph) at 175°C give adduct 153, and cyclohexanone at 150 C gives adduct 154. - Similarly, 1,3-dipolar adducts (e.g., 155) have been obtained using a wide variety of olefins—including cis- and [rans-, 2-dichloroethylene, dimethyl maleate, dimethyl fumarate, maleic anhydride, cis- and tran -stilbene, fran -dibenzoylethylene, tra .y-l,2-dicyanoethylene, A -phenylmaleimide, vinylene carbonate, acenaphthylene, and norbor-nadiene. With cis olefins the endo adduct (155) is usually the predominant isomer. Diphenylcyclopropenone gives compound 156 by spontaneous elimination of carbon monoxide from the initial adduct (157). Adduct 156... [Pg.28]

The continental biosphere is a large source of hydrocarbons. Quantification of these sources in toms of geophysical (e.g. temperature, humidity, light levels) and biogeochemical (soil physical and chemical properties, land use) parameters is much needed for inclusion in atmospheric models. The hydrocarbon oxidation mechanisms in the atmosphere should also be better understood, so that formation of ozone, carbon monoxide, partially oxidized gaseous hydrocarbons, and organic aerosol can be better quantified. The formation of organic aerosol from hydrocarbon precursors and then-capability to serve as cloud condensation nuclei are issues which need to be studied in depth. [Pg.9]

Because of the extensive reuse of combustion air in the process at Calaveras facility, the fabric filter exhaust is the only point of emissions for the kiln, clinker cooler, and raw mill. Exhaust gases from the fabric filter are monitored continuously for carbon monoxide, nitrogen oxides, and hydrocarbons. Calaveras has tested toxic pollutants while burning 20 percent TDF. Table 4-5 summarizes these test results, giving emission factors for metals, hazardous air pollutants, polyaromatic hydrocarbons, dioxins and... [Pg.210]

However, most fuel cell systems can tolerate methane concentrations up to at least 1% in the reformate, no special purification reactions are required. In contrast, hence, removing small residual amounts of carbon monoxide from pre-purifled reformate applying the methanation reaction may be considered as an alternative to the preferential oxidation of carbon monoxide, provided that the CO concentration is low enough to have no significant impact on the hydrogen yield. However, no applications of methanation for CO clean-up in micro structured devices appear to have been reported, hence the issue is not discussed in depth. Finally, during hydrocarbon reforming all hydrocarbon species (saturated and unsaturated) smaller than the feed molecule may be formed. [Pg.290]

The removal of low concentrations of carbon monoxide from the pre-cleaned reformate of hydrocarbon and ethanol reformers is commonly performed by oxidation with air. Owing to the lower carbon monoxide concentration achieved by the low temperatures of methanol reforming, in this case the reformate goes directly to the preferential CO oxidation (PrOx) ... [Pg.342]


See other pages where Carbon monoxide, from oxidation is mentioned: [Pg.405]    [Pg.48]    [Pg.480]    [Pg.481]    [Pg.86]    [Pg.524]    [Pg.112]    [Pg.652]    [Pg.1113]    [Pg.962]    [Pg.157]    [Pg.122]    [Pg.107]    [Pg.377]    [Pg.118]    [Pg.373]    [Pg.90]    [Pg.113]    [Pg.213]    [Pg.224]    [Pg.177]    [Pg.255]    [Pg.295]    [Pg.717]    [Pg.526]    [Pg.698]    [Pg.480]    [Pg.481]    [Pg.543]    [Pg.22]    [Pg.1041]    [Pg.458]   


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