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Carbon dioxide removal from gases

The commercial microporous hydrophobic membranes used for carrying out tests on carbon dioxide removal from gas streams are mainly made of polypropylene (PP) and PVDF. [Pg.774]

E4. The kinetics demonstrate that PZ can be an effective promoter for carbon dioxide removal from gas streams. [Pg.48]

This leaves a hydrogen stream ready for ammonia synthesis, after a final cleanup. The nitrogen required is normally taken from a part of the gas stream obtained from the heating, coke combustion phase of the water-gas reaction sequence, which is depleted in oxygen. Carbon dioxide removal from the nitrogen feed component is achieved in the same manner as from the hydrogen. [Pg.328]

Heintz YJ, Sehabiague L, Morsi BI et al (2009) Hydrogen sulfide and carbon dioxide removed from dry fuel gas streams using an ionic liquid as a physical solvent. Energy Fuel 23 4822 830... [Pg.166]

Carbon-dioxide removal from various gas streams. [Pg.237]

The vast majority of current power plants use coal or natural gas as the fuel source and air as the source of oxygen. In these plants, the stack gas is at essentially atmospheric pressure and contains a large concentration of nitrogen (76 mol%). A small amount of excess air is used, which gives a stack composition of 4.8 mol% O2. The carbon dioxide concentration is only 13.2 mol%. The principal proven method for carbon dioxide removal from a low-concentration, low-pressme gas uses amine absorption, which involves chemical reaction of carbon dioxide with an amine, such as monoethanolamine (MEA). [Pg.399]

Feed gas is fed to the bottom of the absorber and the lean solvent is fed to the top. The amount of carbon dioxide removed from the gas depends on the flow rate and concentration of the solvent fed. The fat solvent leaving the bottom of the absorber is fed to a distillation column in which it is heated, driving off the carbon dioxide and regenerating the solvent for circulation back to the top of the absorber. The heat input to the reboiler is the major energy consumption of the process. [Pg.400]

A13 Absorption process Carbon dioxide removal from Magnesium hydroxide absorbent Greenhouse gas [141... [Pg.135]

Lindmark, J. and Hedlund, J. (2010) Carbon dioxide removal from synthesis gas using MFI membranes. J. Membr. [Pg.917]

However, the ability of these and other forms of plant life to absorb carbon dioxide is not keeping up with the increase in carbon dioxide. Most scientists agree that the primary source of the increase of carbon dioxide is the burning of fossil fuels such as gasoline, coal, and natural gas. The cutting and burning of trees in the rain forests (deforestation) also reduces the amount of carbon dioxide removed from the atmosphere. [Pg.90]

Carbon oxides removal from gas streams in ammonia synthesis processes, by catalytic conversion and subsequent absorption of carbon dioxide. T. A. Semenova. SU 436075 (1975). [Pg.417]

Carbon Dioxide and Water Removal from Ethylene, 1076 Carbon Dioxide Removal from Cryogenic Plant Feed Gas, 1076 Removal of Sulfur Compounds, 1078 Hydrogen Purification by Pressure Swing Adsorption (PSA), 1081... [Pg.1022]

Carbon Dioxide Removal from Cryogenic Plant Feed Gas... [Pg.1076]

Meyer, H. S., and Gamez, J. P., 1995, Gas Separation Membranes Coming of Age for Carbon Dioxide Removal from Natural Gas, Proceedings of the 45th Annual Laurance Reid Gas Conditioning Conference, Norman, OK, Feb. 26-March 1, pp. 284-306. [Pg.1294]

The solvents most used in carbon dioxide removal from ammonia synthesis gas can be characterized according to the nature of the absorption process. Chemical absorption, i.e. processes where the carbon dioxide reacts with the solvent by a chemical reaction which is reversed in the solvent regeneration stage, is most often based on the use of alkanolamines, mainly MEA (mono-ethanolamine) [273], or hot solutions of potassium carbonate [274] as solvents. [Pg.214]

Hydrogen sulfide and carbon dioxide removal from dry fuel gas streams... [Pg.614]

The saturated, cleaned raw synthesis gas from a Texaco partial oxidation system is first shifted by use of a sulfur resistant catalyst. Steam required for shifting is already present ia the gas by way of the quench operation ia the generator. The shifted gas is then processed for hydrogen sulfide and carbon dioxide removal followed by Hquid nitrogen scmbbiag. [Pg.343]

Mounting electrodes in a bioreactor is costly, and there is an additional contamination risk for sensitive cell cultures. Some other sensors of prac ticai importance are those for dissolved oxygen and for dissolved carbon dioxide. The analysis of gas exiting from a bioreactor with an infrared unit that detects carbon dioxide or a paramagnetic unit that detects oxygen (after carbon dioxide removal) has been replaced by mass spec trophotometry. Gas chromatographic procedures coupled with a mass spectrophotometer will detect 1 the volatile components. [Pg.2148]

Direct hydrogen cyanide (HCN) gas in a fuel oil gasification plant to a combustion unit to prevent its release. 4. Consider using purge gases from the synthesis process to fire the reformer strip condensates to reduce ammonia and methanol. 5. Use carbon dioxide removal processes that do not release toxics to the environment. When monoethanolamine (MEA) or other processes, such as hot potassium carbonate, are used in carbon dioxide removal, proper operation and maintenance procedures should be followed to minimize releases to the environment. [Pg.68]

The carbon dioxide removed in synthesis gas preparation can be reacted with ammonia, to lonn urea CO(NH2)2- This is an excellent fertilizer, highly concentrated in nitrogen (46.6%) and also useful as an additive in animal feed to provide the nitrogen for formation of meat protein. Urea is also an important source of resins and plastics by reacting it with formaldehyde from methanol. [Pg.265]

Fig. 8.7 shows a second example (Cycle A2) of carbon dioxide removal by chemical absorption from a CCGT plant, but one in which the semi-closed concept is introduced— exhaust gas leaving the HRSG is partially recirculated. This reduces the flow rate of the gas to be treated in the removal plant, so that less steam is required in the stripper and the extra equipment to be installed is smaller and cheaper. This is also due to the better removal efficiency achievable—for equal reactants flow rate—when the volumetric fraction of CO2 in the exhaust gas is raised from the 4-6% value typical of open cycle gas turbines to about 12% achievable with semi-clo.sed operation. [Pg.146]


See other pages where Carbon dioxide removal from gases is mentioned: [Pg.581]    [Pg.349]    [Pg.502]    [Pg.348]    [Pg.2838]    [Pg.262]    [Pg.838]    [Pg.135]    [Pg.5687]    [Pg.313]    [Pg.6]    [Pg.375]    [Pg.1190]    [Pg.1214]    [Pg.172]    [Pg.929]    [Pg.115]    [Pg.62]    [Pg.419]    [Pg.422]    [Pg.341]    [Pg.341]    [Pg.342]    [Pg.430]    [Pg.20]    [Pg.21]    [Pg.460]    [Pg.157]   
See also in sourсe #XX -- [ Pg.147 ]




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