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Carbon monoxide agents

Reference to Figure 3.4 shows that the reduction is not feasible at 800 K. but is feasible at 1300 K. However, we must remember that energetic feasibility does not necessarily mean a reaction will go kinetic stability must also be considered. Several metals are indeed extracted by reduction with carbon, but in some cases the reduction is brought about by carbon monoxide formed when air, or air-oxygen mixtures, are blown into the furnace. Carbon monoxide is the most effective reducing agent below about 980 K, and carbon is most effective above this temperature. [Pg.69]

Lead(II) oxide is easily reduced to the metal when heated with a reducing agent such as hydrogen, carbon or carbon monoxide, for example ... [Pg.193]

As the equation indicates, it is the anhydride of iodic-acid(V), which is re-formed when water is added to the pentoxide. Mixed with concentrated sulphuric acid and silica, it is a quantitative oxidising agent for carbon monoxide at room temperature ... [Pg.337]

The process of extraction requires first smelting (to obtain the crude metal) and then refining. In smelting, iron ore (usually an oxide) is mixed with coke and limestone and heated, and hot air (often enriched with oxygen) is blown in from beneath (in a blast furnace). At the lower, hotter part of the furnace, carbon monoxide is produced and this is the essential reducing agent. The reduction reactions occurring may be represented for simplicity as ... [Pg.391]

In the presence of aluminum chloride and a small amount of cuprous haUde, a mixture of hydrogen chloride and carbon monoxide serves as a formyl a ting agent of aromatics (Gattermann-Koch reaction) (107) ... [Pg.559]

Intermediate formation of formyl chloride is not necessary since the actual alkylating agent, HCO", can be produced by protonation of carbon monoxide or its complexes. However, it is difficult to obtain an equimolar mixture of anhydrous hydrogen chloride and carbon monoxide. Suitable laboratory preparations involve the reaction of chlorosulfonic acid with formic acid or the reaction of ben2oyl chloride with formic acid ... [Pg.559]

The reaction is mn for several hours at temperatures typically below 100°C under a pressure of carbon monoxide to minimise formamide decomposition (73). Conversions of a-hydroxyisobutyramide are near 65% with selectivities to methyl a-hydroxyisobutyrate and formamide in excess of 99%. It is this step that is responsible for the elimination of the acid sludge stream characteristic of the conventional H2SO4—ACH processes. Because methyl formate, and not methanol, is used as the methylating agent, formamide is the co-product instead of ammonium sulfate. Formamide can be dehydrated to recover HCN for recycle to ACH generation. [Pg.252]

In primary smelting, carbon (in the form of coal or fuel oil) is the reducing agent. During heat-up, carbon monoxide is formed by reaction with... [Pg.57]

The sihcates formed in reactions 2 and 3 fuse with the added fluxes to form a Hquid slag at which point carbon monoxide loses its effectiveness as a reducing agent. Unreacted carbon from the fuel then becomes the predominant reductant in reducing both staimous siUcate to tin and ferrous siUcate to iron. The metallic iron, in turn, reduces tin from stannous siUcate ... [Pg.58]

Low Oxidation State Chromium Compounds. Cr(0) compounds are TT-bonded complexes that require electron-rich donor species such as CO and C H to stabilize the low oxidation state. A direct synthesis of Cr(CO)g, from the metal and CO, is not possible. Normally, the preparation requires an anhydrous Cr(III) salt, a reducing agent, an arene compound, carbon monoxide that may or may not be under high pressure, and an inert atmosphere (see Carbonyls). [Pg.134]

Gaseous. True gases such as sulfur dioxide, nitrogen oxide, ozone, carbon monoxide, etc. vapors such as gasoline, paint solvent, diy cleaning agents, etc. [Pg.2172]

Air-poUutant effects on neural and sensory functions in humans vary widely. Odorous pollutants cause only minor annoyance yet, if persistent, they can lead to irritation, emotional upset, anorexia, and mental depression. Carbon monoxide can cause death secondary to the depression of the respiratory centers of the central nervous system. Short of death, repeated and prolonged exposure to carbon monoxide can alter sensory protection, temporal perception, and higher mental functions. Lipid-soluble aerosols can enter the body and be absorbed in the lipids of the central nervous system. Once there, their effects may persist long after the initial contact has been removed. Examples of agents of long-term chronic effects are organic phosphate pesticides and aerosols carrying the metals lead, mercury, and cadmium. [Pg.2179]

Fire Hazards - Flash Point Not flammable Flammable Limits in Air (%) Not flammable Fire Extinguishing Agents Not pertinent Fire Extinguishing Agents Not To Be Used Not pertinent Special Hazards of Combustion Products Toxic carbon monoxide gas may form in fire Behavior in Fire Not pertinent Ignition Temperature Not pertinent Electrical Hazard Not pertinent Burning Rate Not pertinent. [Pg.95]

Another formylation reaction, which is named after Gattermann, is the Gatter-mann-Koch reaction. This is the reaction of an aromatic substrate with carbon monoxide and hydrogen chloride (gas) in the presence of a Lewis acid catalyst. Similar to the Gattermann reaction, the electrophilic agent 9 is generated, which then reacts with the aromatic substrate in an electrophilic aromatic substitution reaction to yield the formylated aromatic compound 10 ... [Pg.134]

The reaction of an alkyne 1 and an alkene 2 in the presence of dicobaltoctacar-bonyl to yield a cyclopentenone 3 is referred to as the Pauson-Khand reaction Formally it is a [2 + 2 + 1 ]-cycloaddition reaction. The dicobaltoctacarbonyl acts as coordinating agent as well as a source of carbon monoxide. [Pg.223]

Exit gases from the shift conversion are treated to remove carbon dioxide. This may be done by absorbing carbon dioxide in a physical or chemical absorption solvent or by adsorbing it using a special type of molecular sieves. Carbon dioxide, recovered from the treatment agent as a byproduct, is mainly used with ammonia to produce urea. The product is a pure hydrogen gas containing small amounts of carbon monoxide and carbon dioxide, which are further removed by methanation. [Pg.142]

With less active metals, a chemical reducing agent can be used to reduce a metal cation to the element. The most common reducing agent in metallurgical processes is carbon, in the form of coke or, more exactly, carbon monoxide formed from the coke. [Pg.537]

Tricarbonyl(chloro)cyclopentadienylmolybdenum 6 reacts with 3-bromo-l-propene under phase transfer conditions at 45 °C to give directly the dicarbonyl(j)3-2-propenyl) complex 8 whereas at lower temperature the tricarhonyl(>/I-2-propenyl) complex 7 is obtained14. It was proposed that the carbon monoxide acts as the reducing agent. [Pg.446]


See other pages where Carbon monoxide agents is mentioned: [Pg.81]    [Pg.308]    [Pg.508]    [Pg.433]    [Pg.440]    [Pg.547]    [Pg.504]    [Pg.506]    [Pg.521]    [Pg.169]    [Pg.311]    [Pg.142]    [Pg.102]    [Pg.89]    [Pg.113]    [Pg.331]    [Pg.48]    [Pg.53]    [Pg.62]    [Pg.403]    [Pg.483]    [Pg.75]    [Pg.512]    [Pg.215]    [Pg.527]    [Pg.392]    [Pg.84]    [Pg.177]    [Pg.213]    [Pg.955]    [Pg.51]    [Pg.69]   
See also in sourсe #XX -- [ Pg.115 ]




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