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Carbon monoxide direct release

These operations carry energy penalties, and the heat of combustion released when burning the methane, hydrogen, or carbon monoxide produced is less than the energy that would have been released had the coal been burned directly. To produce heavier liquids, the equimolar mixture of hydrogen and carbon monoxide (water gas, also known as synthesis... [Pg.1115]

In addition to tobacco smokers, individuals who have had previous exposure to materials containing methylene chloride, such as degreasers, solvents, paint removers, and furniture strippers, are at greater risk because of an existing body burden of carbon monoxide. Approximately one-fourth to one-third of inhaled methylene chloride vapor is metabolized in the liver to carbon monoxide. In addition, methylene chloride is readily stored in body tissue. This stored material is released over time and results in elevated levels of carbon monoxide for extended periods, in some cases more than twice as long as compared with direct carbon monoxide inhalation. [Pg.257]

However, burning hydrogen is less desirable than using it in a fuel cell. The direct combustion of hydrogen releases carbon monoxide, hydrocarbons and some particulates, although these are only about 0.1 of that from the burning of fossil fuels. [Pg.135]

Some pollutants fall in both categories. Nitrogen dioxide, which is emitted directly from auto exhaust, is also formed in the atmosphere photochemically from NO. Aldehydes, which are released in auto exhausts, are also formed in the photochemical oxidation of hydrocarbons. Carbon monoxide, which arises primarily from autos and stationary sources, is likewise a product of atmospheric hydrocarbon oxidation. [Pg.411]

Fig. 3.2(d) Post smoking— broken and microswitch released. Pump of NDIR Analyser samples vapour phase from collecting bag to give direct reading of carbon monoxide concentration. Puff counts and carbon monoxide concentration to the computer. Cambridge filter removed for chemical analysis. [Pg.74]

Palladium-catalyzed carbonylation reactions with aryl halides are powerful methods of generating aromatic amides, hydrazides, esters and carboxylic acids [25]. We have previously reported the exploitation of Mo(CO)6 as a robust carbon monoxide-releasing reagent in palladium-catalyzed carbonylation reactions [26-29]. This stable and inexpensive solid delivers a fixed amount of carbon monoxide upon heating or by the addition of a competing molybdenum coordinating ligand (for example DBU). This allows for direct liberation of carbon monoxide in the reaction mixture without the need for external devices. [Pg.106]

SIPs are intended to prevent air pollution emergency episodes. Tlie phuis are directed toward preventing e.xcessive buildup of air pollutants tliat are known to be harmful to the population and the enviroiuiient when concentrations exceed certain limits. The compounds affected under the implementation plans are sulfur dioxide, particulate matter, carbon monoxide, nitrogen dioxide, and ozone. A contingency plan, which will outline the steps to be taken in tlie event tliat a particular pollutant concentration reaches die level at wliich it can be considered to be harmful, must be included in each implementation plan. Tlie implementation plans are solely based on tlie continuous emission of tlie previously stated air pollutants. Tliey do not mandate any actions to be taken in tlie event of an accidental toxic release. [Pg.73]

SAFETY PROFILE Most carbonyls are highly toxic. The toxicity of carbonyls depends in part, but not always endrely, on their ready decomposition, which releases carbon monoxide. Symptoms are due in part to carbon monoxide and in part to the direct irritating action of the carbonyl. See specific carbonyl in question. Many carbonyl metals ignite spontaneously in air, some with a delay period. Others are moderate fire and explosion hazards when exposed to heat or flame. Carbonyls of alkali metals are potentially explosive. Hypergolic reaction... [Pg.291]

Hydrogeochemical cycles couple atmosphere, land, and water. The atmosphere is an important conveyor belt for many pollutants. The atmosphere reacts most sensitively to anthropogenic disturbance because it represents a much smaller reservoir than land and water furthermore, the residence times of many constituents of the atmosphere are smaller than those in the other exchange reservoirs. Water and atmosphere are interdependent systems. Many pollutants, especially precursors of acids and photooxidants, originate directly or indirectly from the combustion of fossil fuels. Hydrocarbons, carbon monoxides, and nitrogen oxides released in thermal power plants and, above all, by automobile engines can produce, under the influence of sunlight, ozone and other photooxidants. [Pg.206]

The slow heat release appliances are operated in an insulated and air cooled calorimeter room (Fig. 3), where the heat output can be measured directly. In parallel, the efficiency is determined indirectly with measurement of flue gas temperature and concentrations of carbon dioxide (CO3) and carbon monoxide (CO) in the flue gas, in accordance with the CEN/prEN flue loss method. [Pg.617]

An ingenious extension of the Tsuji-Trost reaction was the cornerstone of Oppolzer s enantioselective synthesis of a heteroyohimbine alkaloid, (-t-j-B-isorauniticine (267) [117]. Substrate 263 was prepared from a commercially available glycinate equivalent by Malkylation, installation of the sultam chiral auxiliary followed by a sultam-directed C-alkylation. As illustrated in Scheme 48, the crucial double cyclization was accomplished by the treatment of 263 with Pd(dba), Bu,P, in the presence of carbon monoxide (1 atm) in acetic acid to give enone 264 and two other stereoisomers in a 67 22 11 ratio. In this case, an allyl carbonate, rather than an allyl acetate, was used as the allyl precursor. Since carbonate is an irreversible leaving group, formation of the n-allylpalladium complex occurs readily. In the presence of Pd(0), the allylic carbonate is converted into a n-allylpalladium complex with concurrent release of CO, and... [Pg.489]

The required ionization energy to form carbon ions in an oxyhydrogen flame mostly results from the high carbon oxidation energy released during the combustion reaction of carbon to carbon monoxide and carbon dioxide. The flame temperature itself is insufficient for a direct atom or molecule ionization. [Pg.184]

The experiments hitherto described dealt with catalytically active electrons and positive holes released by light. They allow only indirect conclusions regarding thermal catalysis. It is felt that direct observations are necessary in the present stage more than ever. Some work along these lines has been mentioned in the Introduction. Other observations on semiconductors of the ferrite type (d) have shown that the carbon monoxide oxidation, a donor reaction, is catalyzed best by inverse spinels, in which ferric ions, situated in octahedral positions, chemisorb carbon monoxide. Zinc ferrite, in which all the occupied octahedral positions carry ferric ions, showed a... [Pg.235]

The gas from any gasification process is inherently toxic, because of essential components such as carbon monoxide and unwanted components. However, this inherent toxicity is not the reason for gas cleaning because the gas should never be released to the atmosphere directly. [Pg.627]


See other pages where Carbon monoxide direct release is mentioned: [Pg.264]    [Pg.34]    [Pg.195]    [Pg.236]    [Pg.169]    [Pg.141]    [Pg.293]    [Pg.68]    [Pg.1]    [Pg.5]    [Pg.226]    [Pg.32]    [Pg.1]    [Pg.13]    [Pg.135]    [Pg.42]    [Pg.120]    [Pg.34]    [Pg.261]    [Pg.689]    [Pg.495]    [Pg.847]    [Pg.1060]    [Pg.766]    [Pg.479]    [Pg.113]    [Pg.204]    [Pg.195]    [Pg.203]    [Pg.175]    [Pg.161]    [Pg.226]    [Pg.89]    [Pg.64]   


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