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Carbon dioxide thermal decomposition

Carbon dioxide acid -1- carbonate/hydrogencarbonate salt -i-water -i- carbon dioxide Thermal decomposition of carbonate/ hyd rogenca rbonate... [Pg.298]

The production of steel begins when iron ore is fed into a blast furnace (Fig. 16.39). The furnace, which is approximately 40 m high, is continuously replenished from the top with a mixture of ore, coke, and limestone. Each kilogram of iron produced requires about 1.75 kg of ore, 0.75 kg of coke, and 0.25 kg of limestone. The limestone, which is primarily calcium carbonate, undergoes thermal decomposition to calcium oxide (lime) and carbon dioxide. The calcium oxide, which contains the Lewis base O2", helps to remove the acidic (nonmetal oxide) and amphoteric impurities from the ore ... [Pg.809]

Example Calculate the volume of carbon dioxide obtained, at room temperature and pressure, when 25 g of calcium carbonate undergo thermal decomposition (relative atomic masses Ca = 40, C = 12,... [Pg.23]

The catalysts are prepared from hydroxides or carbonates by thermal decomposition. Equilibrium pressures for decomposition of carbonates and peroxides are shown in Fig. 3.4. lb obtain oxides from hydroxides or carbonates, high temperature pretreatment is required. During pretreatment, evolution of H2O, CO2, and O2 occurs. Evolution of H2O begins at about 673 K as Mg(OH)2, Ca(OH)2, and commercially available BaO are heat-treated in vacuo Carbon dioxide starts to evolve at a temperature slightly higher than that for H2O evolution. From commercially available... [Pg.29]

Figure 11.8 In a rotating lime kiln, calcium carbonate undergoes thermal decomposition to form calcium oxide and carbon dioxide. Figure 11.8 In a rotating lime kiln, calcium carbonate undergoes thermal decomposition to form calcium oxide and carbon dioxide.
There are three essential factors in the thermal decomposition of limestone (/) the stone must be heated to the dissociation temperature of the carbonates (2) this minimum temperature (but in practice a higher temperature) must be maintained for a certain duration and (J) the carbon dioxide evolved must be removed rapidly. [Pg.170]

Lithium Oxide. Lithium oxide [12057-24-8], Li20, can be prepared by heating very pure lithium hydroxide to about 800°C under vacuum or by thermal decomposition of the peroxide (67). Lithium oxide is very reactive with carbon dioxide or water. It has been considered as a potential high temperature neutron target for tritium production (68). [Pg.226]

Decomposition and Decarboxylation. Maleic anhydride undergoes anaerobic thermal decomposition in the gas phase in a homogeneous unimolecular reaction to give carbon monoxide, carbon dioxide, and acetylene [74-86-2] in equimolar amounts. The endothermic... [Pg.451]

Thermal decomposition of hydroxyalkyl hydroperoxyalkyl peroxides produces mixtures of starting carbonyl compounds, mono- and dicarboxyHc acids, cycHc diperoxides, carbon dioxide, and water. One specific hydroxyalkyl hydroperoxyalkyl peroxide from cyclohexanone (2, X = OH, Y = OOH) is a soHd that is produced commercially as a free-radical initiator and bleaching agent (see Table 5). On controlled decomposition, it forms 1,12-dodecanedioic acid (150). [Pg.116]

Solutions of these fire retardant formulations are impregnated into wood under fliU cell pressure treatment to obtain dry chemical retentions of 65 to 95 kg/m this type of treatment greatly reduces flame-spread and afterglow. These effects are the result of changed thermal decomposition reactions that favor production of carbon dioxide and water (vapor) as opposed to more flammable components (55). Char oxidation (glowing or smoldering) is also inhibited. [Pg.329]

Acryhc elastomers are normally stable and not reactive with water. The material must be preheated before ignition can occur, and fire conditions offer no hazard beyond that of ordinary combustible material (56). Above 300°C these elastomers may pyrolize to release ethyl acrylate and other alkyl acrylates. Otherwise, thermal decomposition or combustion may produce carbon monoxide, carbon dioxide, and hydrogen chloride, and/or other chloiinated compounds if chlorine containing monomers are present ia the polymer. [Pg.478]

The reaction is carried out over a supported metallic silver catalyst at 250—300°C and 1—2 MPa (10—20 bar). A few parts per million (ppm) of 1,2-dichloroethane are added to the ethylene to inhibit further oxidation to carbon dioxide and water. This results ia chlorine generation, which deactivates the surface of the catalyst. Chem Systems of the United States has developed a process that produces ethylene glycol monoacetate as an iatermediate, which on thermal decomposition yields ethylene oxide [75-21-8]. [Pg.433]

Thermal decomposition is a major route to smaller perfluonnated molecules Tetrafluoroethylene pyrolyzed at 1100-1300 °C with carbon dioxide gives a mixture of tetrafluoromethane (19 9%), hexafluoroethane (61 3%), and carbonyl fluoride (18 6%) [87]... [Pg.919]

Reaction of the glycol, 70, affords an oxazolidinone rather than the expected carbamate (71) on fusion with urea. It has been postulated that the urea is in fact the first product formed. This compound then undergoes 0 to N migration with loss of carbon dioxide reaction of the amino alcohol with the isocyanic acid known to result from thermal decomposition of urea affords the observed product, mephenoxolone (74) this compound shows activity quite similar to that of the carbamate. An analogous reaction on the glyceryl ether, 75, affords metaxa-lone (76). [Pg.119]

This process is only of historical interest, because not more than 5 % of the blacks are produced via this route. In this process, the feed (e.g., natural gas) is burned in small burners with a limited amount of air. Some methane is completely combusted to carbon dioxide and water, producing enough heat for the thermal decomposition of the remaining natural gas. The two main reactions could be represented as ... [Pg.119]

Carbon dioxide is present in steam as a result of the thermal decomposition of bicarbonates in the boiler. [Pg.285]

Where FW contains bicarbonate or carbonate alkalinity (as calcium, magnesium, or sodium salts), these salts undergo thermal decomposition in the boiler, and the steam-volatile contaminant gas carbon dioxide is introduced into the steam distribution system, as shown ... [Pg.288]

M.l When limestone, which is principally CaCO, is heated, carbon dioxide and quicklime, CaO, are produced by the reaction CaC03(s) A > CaO(s) + C02(g). If 17.5 g of C02 is produced from the thermal decomposition of 42.73 g of CaCO , what is the percentage yield of the reaction ... [Pg.123]

The formation of carbodiimide from 2 molecules of MDI is shown in Equation 1. Carbodiimide formation is accompanied by the evolution of carbon dioxide, and this reaction is believed to be the primary source of pressure upon the thermal decomposition of MDI. [Pg.429]

A full development of the rate law for the bimolecular reaction of MDI to yield carbodiimide and CO indicates that the reaction should truly be 2nd-order in MDI. This would be observed experimentally under conditions in which MDI is at limiting concentrations. This is not the case for these experimements MDI is present in considerable excess (usually 5.5-6 g of MDI (4.7-5.1 ml) are used in an 8.8 ml vessel). So at least at the early stages of reaction, the carbon dioxide evolution would be expected to display pseudo-zero order kinetics. As the amount of MDI is depleted, then 2nd-order kinetics should be observed. In fact, the asymptotic portion of the 225 C Isotherm can be fitted to a 2nd-order rate law. This kinetic analysis is consistent with a more detailed mechanism for the decomposition, in which 2 molecules of MDI form a cyclic intermediate through a thermally allowed [2+2] cycloaddition, which is formed at steady state concentrations and may then decompose to carbodiimide and carbon dioxide. Isocyanates and other related compounds have been reported to participate in [2 + 2] and [4 + 2] cycloaddition reactions (8.91. [Pg.435]

Although undoubtedly capable of generating carbon dioxide by thermal decomposition, the editor has heard of no pressurisation problems arising from this. [Pg.417]

During the vacuum fractional distillation of bulked residues (7.2 t containing 30-40% of the bis(hydroxyethyl) derivative, and up to 900 ppm of iron) at 210-225°C/445-55 mbar in a mild steel still, a runaway decomposition set in and accelerated to explosion. Laboratory work on the material charged showed that exothermic decomposition on the large scale would be expected to set in around 210-230°C, and that the induction time at 215°C of 12-19 h fell to 6-9 h in presence of mild steel. Quantitative work in sealed tubes showed a maximum rate of pressure rise of 45 bar/s, to a maximum developed pressure of 200 bar. The thermally induced decomposition produced primary amine, hydrogen chloride, ethylene, methane, carbon monoxide and carbon dioxide. [Pg.983]

Calcium oxide can be produced from extensive heating of limestone. Primarily composed of calcium carbonate, limestone is extracted from both underground and surface mines and heated to temperatures exceeding 180°F to convert the calcium carbonate into calcium oxide. This thermal decomposition reaction also generates carbon dioxide gas. [Pg.65]

Attempted syntheses of trifluoromethyl derivatives of germanium, tin, and lead by thermal decarboxylation either resulted in decomposition of the trifluoroacetate without forming carbon dioxide (22,39,40) or gave carbon dioxide but no trifluoromethyl organometallic (22). In the latter case, the metal fluoride was detected. This suggests that the trifluoromethyl compound is thermally unstable and decomposes by fluoride abstraction. [Pg.245]

Continuous monitoring of the carbon monoxide and carbon dioxide evolved during thermal decomposition of brominated polyester resin samples, has been carried out using a simultaneous thermal analysis-mass spectrometry technique. In order to allow measurement of the carbon monoxide evolved, the atmosphere chosen for these runs was 21% oxygen in argon, since the peak at 28 atomic mass units (amu)... [Pg.204]

Potassium Bicarbonate. Potassium bicarbonate has become available in commercial quantities for food use. The only reason for using it is that the sodium content of the resulting product is reduced. As the molecular weight of potassium bicarbonate is greater (100.11 for KHC03 compared with 84.01 for NaHC03) some 19% more is required to produce the same volume of carbon dioxide. Potassium bicarbonate is also more expensive. The reaction for its thermal decomposition is ... [Pg.71]

The sulfuric acid sludge from sulfuric acid treatment is used frequently as a source (through thermal decomposition) to produce sulfur dioxide (SO2, which is returned to the sulfuric acid plant) and sludge acid coke. The coke, in the form of small pellets, is nsed as a snbstitute for charcoal in the manufacture of carbon disulfide. Sulfuric acid coke is different from other petrolenm coke in that it is pyrophoric in air and also reacts directly with snlfnr vapor to form carbon disulfide. [Pg.82]


See other pages where Carbon dioxide thermal decomposition is mentioned: [Pg.222]    [Pg.22]    [Pg.64]    [Pg.507]    [Pg.115]    [Pg.240]    [Pg.238]    [Pg.481]    [Pg.208]    [Pg.48]    [Pg.908]    [Pg.328]    [Pg.84]    [Pg.693]    [Pg.99]    [Pg.693]    [Pg.86]    [Pg.63]    [Pg.79]    [Pg.382]    [Pg.52]    [Pg.121]    [Pg.45]   
See also in sourсe #XX -- [ Pg.237 ]




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