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Carbon dioxide iron carbonate formation

The importance of carbon dioxide in the formation of the iron complexes of the human serum transferrin was shown early by Fiala and Burk (46) and Schade et al. 117). Warner and Weber (133), by an indirect but exquisite method, proved the participation of CO2 in the formation of the complex, and also that it was in the form of bicarbonate or carbonate. This was done through experiments in which the iron complex was formed in the absence of CO2, or by the addition of small amounts, of gaseous CO2, and noting the red color of the complex was formed only very slowly. However, when the enzyme carbonic anhydrase was added, together with the CO2, the red color of the complex appeared rapidly. In addition the same workers showed by the use of C1402 that one mole of CO2 was bound per mole of iron bound. [Pg.172]

Using formate, Sutton and Winterbourn [111,132,133] also presented evidence that the reaction of Fe2+-edta and aqueous, unchelated, iron(II) with hydrogen peroxide involves in part a higher oxidation state of iron. This experiment involves a chain of reactions, which on the basis of the known rate constants, would have a very large number of cycles before it would come to an end. Instead, fewer than 10 cycles were observed, see below. These experiments have been extended to other ligands. In rapid-mix experiments a solution of iron(II) complex [or iron(II)], formate and PQ + is mixed with hydrogen peroxide and the ratio of carbon dioxide produced per paraquat oxidised (the number of cycles) is determined. Alternatively, paraquat radicals are generated... [Pg.16]

EXPLOSION and FIRE CONCERNS noncombustible liquid, but will support combustion NFPA rating (NA) contact with hot iron causes formation of toxic carbon tetrachloride vapor contact with hot water causes formation of hydrochloric acid, sulfur and carbon dioxide decomposes rapidly at elevated temperatures to give carbon tetrachloride and sulfur monochloride may decompose rapidly on contact with alkalies and amines will attack some forms of plastics, rubber, and coatings hazardous decomposition products include carbon tetrachloride, sulfur monochloride, hydrogen chloride, sulfur dioxide, and carbon monoxide use alcohol foam, dry chemical, or carbon dioxide for firefighting purposes. [Pg.823]

These earlier facilities were also plagued by corrosion due to the sulfur compounds, to carbon dioxide (as carbonic acid solution), or to hydrogen embrittlement, or to iron carbonyl formation from the high pressure-low temperature carbon monoxide containing gases. These problems were for the most part solved, but the iron carbonyl problem remains and seems to defy an economic solution. [Pg.353]

The rate of corrosion of cast iron is directly linked to oxygen content. Carbon dioxide accelerates the formation of scales in fresh water. Cast iron and carbon steels are sensitive to attack by hydrogen sulfide even in the absence of oxygen. Corrosion rates of low carbon steels and cast iron accelerate with velocity, if the water is not treated with inhibitors. [Pg.510]

Iron carbonate formation reduces the rate of corrosion. The pH of the condensate is increased by reduction in the amount CO2 in solution. However, the pipe material is dissolved by the formation of iron carbonate (FeC03). As the condensate is replenished, the pipes continue to corrode. When oxygen is present, ferrous carbonate and bicarbonate decomposes, forming ferric oxide and hydroxide deposits, and releasing more and more carbon dioxide which lowers the pH. [Pg.593]

Syntheses from Dry Metals and Salts. Only metaUic nickel and iron react direcdy with CO at moderate pressure and temperatures to form metal carbonyls. A report has claimed the synthesis of Co2(CO)g in 99% yield from cobalt metal and CO at high temperatures and pressures (91,92). The CO has to be absolutely free of oxygen and carbon dioxide or the yield is drastically reduced. Two patents report the formation of carbonyls from molybdenum and tungsten metal (93,94). Ruthenium and osmium do not react with CO even under drastic conditions (95,96). [Pg.67]

Heal content, 110. 116 change (luring a reaction, 110 of a substance, 109 Heat of combustion of diamond, 122 graphite, 122 hydrazine, 47 hydrogen, 40 methane, 123 Heat of formation, 113 Heat of reaction, 135 between elements, table, 112 oxidation of HC1, 160 oxidation of sulfur dioxide, 161 predicting, 112 Heat of reaction to form ammonia, 112 Br atoms, 290 carbon dioxide, 112 carbon monoxide, 112 Cl atoms, 290 CO + Hi, 110 ethane, 112 F atoms, 290 H atoms, 274 hydrogen chloride, 160 hydrogen iodide, 112 iron(Ill) oxide, 162 Li atoms, 290 Li + Br, 290 Li + F, 290 Na + Cl, 290 NHs products, 114 Na atoms, 290 NO, 112 NOj, 112... [Pg.460]

The formation of a passive film of iron oxide (magnetite, Fe304), under sulfite or hydrazine reducing conditions, is optimized at pH of 11 to 12. The downside is that the decomposition of carbonates and bicarbonates produces carbon dioxide, the primary cause of condensate system corrosion. [Pg.227]

The oxygen in the blast penetrates but a short distance above the tuyere level. It is all consumed in burning the carbon of the coke to CO. Most of the carbon in the coke descends through the shaft of the furnace until it reaches the tuyere zone, where it is met by the blast and burned to carbon monoxide. The high temperature precludes the formation of carbon dioxide. Some of the carbon, however, through actual contact with iron oxide, is oxidized (either to CO or C02) in the upper part of the furnace. This oxidation, of course, liberates heat above, instead of in, the smelting zone where it is most needed and likewise tends to decrease the proportion of carbon fully oxidized to C02 in the furnace and thereby the quantity of heat developed in the furnace. [Pg.367]

The primary function of the mammalian red blood cell is to maintain aerobic metabolism while the iron atom of the heme molecule is in the ferrous (Fe+2) oxidation state however, copper is necessary for this process to occur (USEPA 1980). Excess copper within the cell oxidizes the ferrous iron to the ferric (Fe+3) state. This molecule, known as methemoglobin, is unable to bind oxygen or carbon dioxide and is not dissociable (Langlois and Calabrese 1992). Simultaneous exposure of sheep to mixtures of cupric acetate, sodium chlorite, and sodium nitrite produced a dose-dependent increase in methemoglobin formation (Calabrese et al. 1992 Langlois and Calabrese 1992). [Pg.137]

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. [Pg.253]

Iron, in the form of fine filings, will burn and ean be used to produee attraetive gold sparks, such as in the traditional wire sparkler. The small percentage (less than 1%) of carbon in steel ean eause an attraetive branching of the sparks due to earbon dioxide gas formation as the metal particles bum in air. [Pg.148]

When heated in a closed vessel to 200° C., thiocarbonyl tetrachloride decomposes with formation of sulphur chloride. It dissolves chlorine without being attacked. Water at 160° C. decomposes it entirely into carbon dioxide, hydrogen chloride and sulphur. It is also decomposed at ordinary temperatures by contact with metallic iron, the products being ferrous chloride and carbon tetrachloride,5 although according to de Fazi5 the reaction may, under special conditions, proceed according to the equation ... [Pg.273]


See other pages where Carbon dioxide iron carbonate formation is mentioned: [Pg.48]    [Pg.796]    [Pg.183]    [Pg.54]    [Pg.508]    [Pg.164]    [Pg.522]    [Pg.530]    [Pg.955]    [Pg.242]    [Pg.337]    [Pg.743]    [Pg.744]    [Pg.100]    [Pg.66]    [Pg.368]    [Pg.767]    [Pg.37]    [Pg.214]    [Pg.924]    [Pg.122]    [Pg.237]    [Pg.245]    [Pg.249]    [Pg.279]    [Pg.272]    [Pg.413]    [Pg.189]    [Pg.268]    [Pg.924]    [Pg.161]    [Pg.712]    [Pg.522]    [Pg.239]    [Pg.142]   
See also in sourсe #XX -- [ Pg.593 ]




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