Iron reaction with carbon monoxide

The negative sign of AG° implies that although Fe203 does not spontaneously decompose, it can be converted to iron by reaction with carbon monoxide. This is in fact the reaction used in the blast furnace when iron ore consisting mainly of Fe203 is reduced to iron (Chapter 20). 

Reaction with carbon monoxide to form iron carbonyls [2.23] which can be decomposed to give high-purity iron... 

An alternative method for preparing pure iron from Fc203 (Problem 3.59) is by reaction with carbon monoxide ... 

Most of the microsomal reactions can be classified as oxidations by what are referred to as mixed-function oxidases utilizing molecular oxygen and cofactors. The key enzyme is an iron-hemecytochrome P-450, a flavoprotein dependent in its reduction and reoxidation on the NADPH to NADP reaction. The 450 notation is based on the 450 nm absorption peak the enzyme exhibits on reaction with carbon monoxide. Thus, drug interactions with this enzyme system can be evaluated by measuring absorption spectra changes. 

Le Ch telier noted that many industrial processes of his time could be improved by an understanding of chemical equilibria. For example, the reaction of iron oxide with carbon monoxide was used to produce elemental iron and CO2 according to the reaction... 

Notice that in the reaction of iron oxide with carbon monoxide, oxygen has added to the carbon monoxide to produce carbon dioxide—the carbon monoxide has been oxidized. Here is a fundamental concept of chemistry— oxidation and reduction always occur together. If one reactant is oxidized, another must be reduced. 

In other reactions, it s easier to see reduction as the loss of oxygen in going from reactant to product. For example, iron ore (primarily rust, Fe20s) is reduced to iron metal in a blast furnace by a reaction with carbon monoxide ... 

A similar study has been made of reaction of the 14-ane and 15-ane (12 and 13, respectively) complexes of iron(II) with carbon monoxide and with... 

With an atomic number of 28 nickel has the electron conflguration [Ar]4s 3c (ten valence electrons) The 18 electron rule is satisfied by adding to these ten the eight elec Irons from four carbon monoxide ligands A useful point to remember about the 18 electron rule when we discuss some reactions of transition metal complexes is that if the number is less than 18 the metal is considered coordinatively unsaturated and can accept additional ligands... 

Ma.nufa.cture. Nickel carbonyl can be prepared by the direct combination of carbon monoxide and metallic nickel (77). The presence of sulfur, the surface area, and the surface activity of the nickel affect the formation of nickel carbonyl (78). The thermodynamics of formation and reaction are documented (79). Two commercial processes are used for large-scale production (80). An atmospheric method, whereby carbon monoxide is passed over nickel sulfide and freshly reduced nickel metal, is used in the United Kingdom to produce pure nickel carbonyl (81). The second method, used in Canada, involves high pressure CO in the formation of iron and nickel carbonyls the two are separated by distillation (81). Very high pressure CO is required for the formation of cobalt carbonyl and a method has been described where the mixed carbonyls are scmbbed with ammonia or an amine and the cobalt is extracted as the ammine carbonyl (82). A discontinued commercial process in the United States involved the reaction of carbon monoxide with nickel sulfate solution. 

Potential Processes. Sulfur vapor reacts with other hydrocarbon gases, such as acetjiene [74-86-2] (94) or ethylene [74-85-1] (95), to form carbon disulfide. Higher hydrocarbons can produce mercaptan, sulfide, and thiophene intermediates along with carbon disulfide, and the quantity of intermediates increases if insufficient sulfur is added (96). Light gas oil was reported to be successflil on a semiworks scale (97). In the reaction with hydrocarbons or carbon, pyrites can be the sulfur source. With methane and iron pyrite the reaction products are carbon disulfide, hydrogen sulfide, and iron or iron sulfide. Pyrite can be reduced with carbon monoxide to produce carbon disulfide. 

Mesitaldehyde may be prepared from mesitylmagnesium bromide by the reaction with orthoformate esters3 or ethoxy-methyleneaniline 3 from acetylmesitylene by oxidation with potassium permanganate,4 from mesitoyl chloride by reduction,5 from mesityllithium by the reaction with iron pentacarbonyl and from mesitylene by treatment with formyl fluoride and boron trifluoride,7 by treatment with carbon monoxide, hydrogen chloride, and aluminum chloride,8 or by various applications of the Gatterman synthesis.9-11... 

FIGURE 16.39 The reduction of iron ore takes place in a blast furnace containing a mixture of the ore with coke and limestone. Different reactions take place in different zones when the blast of air and oxygen is admitted. The ore, an oxide, is reduced to the metal by reduction with carbon monoxide produced in the furnace. 

The preparation of carbonylmetals by treating a transition metal halide either with carbon monoxide and zinc, or with iron pentacarbonyl is well-known and smooth. However, a violent eruptive reaction occurs if a methanolic solution of a cobalt halide, a rhodium halide or a ruthenium halide is treated with both zinc and iron pentacarbonyl. 

The above reaction occurs in two different steps, with carbon monoxide (CO) formed as an intermediate product. Temperature is a very important parameter at temperatures higher than 800 °C, there can be excess CO produced, while at temperatures lower than 500 °C, CH4 and other hydrocarbons are formed. In order to catalyse the reaction, finely powdered iron ( 10 pm) is usually used. Unless removed, the water produced may react... 

Iron(III) oxide reacts with carbon monoxide to produce elemental iron and carbon dioxide. Determine the enthalpy change of this reaction, using Icnown enthalpies of formation. 

Other aspects of solvation have included the use of surfactants (SDS, CTAB, Triton X-100), sometimes in pyridine-containing solution, to solubilize and de-aggregate hemes, i.e., to dissolve them in water (see porphyrin complexes, Section 5.4.3.7.2). An example is provided by the solubilization of an iron-copper diporphyrin to permit a study of its reactions with dioxygen and with carbon monoxide in an aqueous environment. Iron complexes have provided the lipophilic and hydrophilic components in the bifunctional phase transfer catalysts [Fe(diimine)2Cl2]Cl and [EtsBzNJpeCU], respectively. 

This enzyme [EC 1.2.99.2], also known as acetyl-CoA synthase, catalyzes the reaction of carbon monoxide with water and an acceptor to produce carbon dioxide and the reduced acceptor. The cofactors of this enzyme include nickel and zinc ions as well as non-heme iron. Methyl viologen can act as the acceptor substrate. The enzyme is isolated from Clostridium sp. Interestingly, it also catalyzes an exchange reaction of carbon between Cl of acetyl-CoA and carbon monoxide. The protein participates in the synthesis of acetyl-CoA from carbon dioxide and hydrogen in the organisms. 

The cyanide ion, CN, is isoelectronic with carbon monoxide and has an extensive chemistry of reaction with transition metals (e.g. the formation of the hexacyanoferrate(III) ion, [Fe(CN)63 ] by reaction with iron(III) in solution) but, unlike CO, it shows a preference for the positive oxidation states of the elements. This is mainly because of its negative charge. 

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