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Carbon dioxide, purification

Chemical Applications. Cesium metal is used in carbon dioxide purification as an adsorbent of impurities in ferrous and nonferrous metallurgy (qv) it can be used as a scavenger of gases and other impurities. [Pg.378]

Voids and Honti (1974) described the incident. A carbon dioxide purification plant in Rdpcelak, Hungary, produced carbon dioxide from natural sources. It was liquefied and supercooled after purification by ammonia refrigeration, then stored in tanks under a pressure of 15 bar (220 psi) at a temperature of — 30°C ( —22°F). [Pg.27]

Backus process -carbon dioxide purification [CARBON DIOXIDE] (Vol 5)... [Pg.85]

The chief danger and main source of error in a combustion is that of moving the Bunsen forward a little too rapidly and so causing much of the substance to burn very rapidly, so that a flash-back occurs. This usually causes an explosion wave to travel back along the tube towards the purification train, some carbon dioxide and water vapour being carried with it. If these reach the packing of the purification train they will, of course, be absorbed there and the results of the estimation will necessarily be low. [Pg.479]

The technology of urea production is highly advanced. The raw materials requited ate ammonia and carbon dioxide. Invariably, urea plants ate located adjacent to ammonia production faciUties which conveniently furnish not only the ammonia but also the carbon dioxide, because carbon dioxide is a by-product of synthesis gas production and purification. The ammonia and carbon dioxide ate fed to a high pressure (up to 30 MPa (300 atm)) reactor at temperatures of about 200°C where ammonium carbamate [111-78-0] CH N202, urea, and water ate formed. [Pg.220]

The gases leaving the purification system are scmbbed with water to recover solvent and a continuous small purge of solvent gets rid of polymers. The acetylene purity resulting from this system is 99%. The main impurities in the acetylene are carbon dioxide, propadiene, and a very small amount of... [Pg.390]

The most overlooked hazard and contaminant is water (99). Water reacts with isocyanates at room temperature to yield both ureas and large quantities of carbon dioxide. The presence of water or moisture can produce a sufficient amount of CO2 to overpressurize and mpture containers. As Httle as 30 mL of water can result in 40 L of carbon dioxide which could result in pressures of up to 300 kPa (40 psi). For these reasons, the use of dry nitrogen atmospheres is recommended during handling. If a plant air system must be used, purification equipment, such as oil traps and drying beds, should be installed between the source and the isocyanate vessel. [Pg.457]

Gas Reduction. The use of a gaseous reduciag agent is attractive because the metal is produced as a powder that can easily be separated from the solution. Carbon dioxide, sulfur dioxide, and hydrogen can be used to precipitate copper, nickel, and cobalt, but only hydrogen reduction is appHed on an iadustrial scale. In the Sherritt-Gordon process, the excess ammonia is removed duting the purification to achieve a 2 1 ratio of NH iNi ia solution. Nickel powder is then precipitated by... [Pg.171]

Gas purification processes fall into three categories the removal of gaseous impurities, the removal of particulate impurities, and ultrafine cleaning. The extra expense of the last process is only justified by the nature of the subsequent operations or the need to produce a pure gas stream. Because there are many variables in gas treating, several factors must be considered (/) the types and concentrations of contaminants in the gas (2) the degree of contaminant removal desired (J) the selectivity of acid gas removal required (4) the temperature, pressure, volume, and composition of the gas to be processed (5) the carbon dioxide-to-hydrogen sulfide ratio in the gas and (6) the desirabiUty of sulfur recovery on account of process economics or environmental issues. [Pg.209]

Steam-Reforming Natural Gas. Natural gas is the single most common raw material for the manufacture of ammonia. A typical flow sheet for a high capacity single-train ammonia plant is iadicated ia Figure 12. The important process steps are feedstock purification, primary and secondary reforming, shift conversion, carbon dioxide removal, synthesis gas purification, ammonia synthesis, and recovery. [Pg.345]

Carbon Dioxide Removal. The effluent gases from the shift converters contain about 17—19 vol % (dry) carbon dioxide (qv) which is ultimately reduced to a few ppm by bulk CO2 removal, followed by a final purification step. Commercial CO2 removal systems can be broadly classified as... [Pg.348]

Final Purification. Oxygen containing compounds (CO, CO2, H2O) poison the ammonia synthesis catalyst and must be effectively removed or converted to inert species before entering the synthesis loop. Additionally, the presence of carbon dioxide in the synthesis gas can lead to the formation of ammonium carbamate, which can cause fouHng and stress-corrosion cracking in the compressor. Most plants use methanation to convert carbon oxides to methane. Cryogenic processes that are suitable for purification of synthesis gas have also been developed. [Pg.349]

Ammonium bicarbonate is produced as both food and standard grade and the available products are normally very pure. Although purification is possible by sublimation at low temperatures, it is more economical to prepare the desired product directiy by using ammonia and carbon dioxide of high purity. [Pg.363]

Essentially no waste products are formed ia the USP process if hydriodic acid and either sodium hydroxide or sodium carbonate are used as reactants. Water results from use of the former a mole equivalent quantity of carbon dioxide is produced from the latter reagents. Higher quaUty grades may require some purification steps which may result ia wastes from the treatment. Disposal of these impurities must then be carried out. [Pg.190]

First Carbonation. The process stream OH is raised to 3.0 with carbon dioxide. Juice is recycled either internally or in a separate vessel to provide seed for calcium carbonate growth. Retention time is 15—20 min at 80—85°C. OH of the juice purification process streams is more descriptive than pH for two reasons first, all of the important solution chemistry depends on reactions of the hydroxyl ion rather than of the hydrogen ion and second, the nature of the C0 2 U20-Ca " equiUbria results in a OH which is independent of the temperature of the solution. AH of the temperature effects on the dissociation constant of water are reflected by the pH. [Pg.26]

Second Carbonation. Calcium is reduced to the practical minimum by the addition of carbon dioxide at a OH of 4.5 at a temperature of as near to 100°C as possible. This is the maximum temperature in the purification process and the retention time is only long enough to effect the OH... [Pg.26]

Methods of Purification. Although carbon dioxide produced and recovered by the methods outlined above has a high purity, it may contain traces of hydrogen sulfide and sulfur dioxide, which cause a slight odor or taste. The fermentation gas recovery processes include a purification stage, but carbon dioxide recovered by other methods must be further purified before it is acceptable for beverage, dry ice, or other uses. The most commonly used purification methods are treatments with potassium permanganate, potassium dichromate, or active carbon. [Pg.22]

Ethylene Oxide Purification. The main impurities ia ethylene oxide are water, carbon dioxide, and both acetaldehyde and formaldehyde. Water and carbon dioxide are removed by distillation ia columns containing only rectifying or stripping sections. Aldehydes are separated from ethylene... [Pg.459]


See other pages where Carbon dioxide, purification is mentioned: [Pg.85]    [Pg.803]    [Pg.805]    [Pg.847]    [Pg.803]    [Pg.805]    [Pg.847]    [Pg.166]    [Pg.427]    [Pg.41]    [Pg.305]    [Pg.85]    [Pg.803]    [Pg.805]    [Pg.847]    [Pg.803]    [Pg.805]    [Pg.847]    [Pg.166]    [Pg.427]    [Pg.41]    [Pg.305]    [Pg.474]    [Pg.478]    [Pg.172]    [Pg.694]    [Pg.89]    [Pg.508]    [Pg.10]    [Pg.390]    [Pg.422]    [Pg.456]    [Pg.10]    [Pg.369]    [Pg.481]    [Pg.226]    [Pg.534]    [Pg.21]    [Pg.21]    [Pg.460]   
See also in sourсe #XX -- [ Pg.113 , Pg.115 ]




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